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SMITHSONIAN CONTRIBUTIONS TO ZOOLOGY • NUMBER 559

The Intermuscular Bones and Ligaments of Teleostean Fishes

Colin Patterson and G. David Johnson

SMITHSONIAN INSTITUTION PRESS

Washington, D.C.

1995

ABSTRACT

Patterson, Colin, and G. David Johnson. The Intermuscular Bones and Ligaments of Teleostean Fishes. Smithsonian Contributions to Zoology, number 559, 85 pages, 16 figures, 2 plates, 8 tables, 1995.—Intermuscular bones are found only in teleostean fishes. They are segmental ossifications in the myosepta and generally are associated with ligaments. That association takes three forms: ontogenetic or structural continuity, when intermuscular bones ossify within ligament and/or are attached to the axial skeleton by ligament; serial homology, when a series of bones is continued rostrally or caudally by a series of ligaments; and homology, when a series of bones in one teleost is homologous with a series of ligaments in another. We recognize three series of intermusculars, epineurals, epicentrals, and epipleurals. Epineurals and epicentrals develop in a rostrocaudal gradient, whereas epipleurals develop rostrally and caudally from the region of the first caudal vertebra. We create a notation for recording the distribution and form of intermuscular bones and ligaments, and we map them in about 125 genera of teleosts from over 100 families, covering all major groups. The primitive state of Recent teleostean intermusculars is exemplified by Hiodon, in which all ossified epineurals are fused with the neural arches, and all epicentrals and epipleurals are ligaments. Some or all epineural bones are free (unfused) from the neural arches in other teleosts, and in many lower (nonacanthomorph) elopocephalans they develop an anteroventral branch so that they are forked proximally. Epineurals are primitively dorsolaterally directed, but the first one to three are deflected ventrally in a few nonacanthomorphs (argentinoids, some aulopiforms, Neoscopelus) and in lampridiform acanthomorphs. In Polymixia, the first epineural is displaced ventrally into the horizontal septum, and in all other acanthomorphs several or all epineurals are so displaced; the bones generally called epipleurals in acanthomorphs are epineurals. Epicentrals lie in the horizontal septum, and are primitively ligamentous. There are ossified epicentrals in Notopterus, Megalops, clupeiforms, gonorynchiforms, gymnotoids, Thymallus, and the aulopiforms Parasudis, Alepisaurus, and Omosudis. Epicentral ligaments sometimes include a cartilage rod distally (salmonoids, osmeroids, Maurolicus, Polymixia), and in many clupeoids the distal tip of each anterior epicentral bone is associated with a separate superficial chevron of cartilage. Anterior epicentrals are lacking in some aulopiforms and among acanthomorphs in beryciforms, some zeiforms, and primitive percomorphs, so that the series of ligaments begins on the posterior abdominal vertebrae. All epicentrals are absent in some aulopiforms, in all examined paracanthopterygians and stephanoberyciforms, and in many percomorphs. A series of segmental, anterolaterally directed ligaments, “POTs,” attaches to epicentrals in the horizontal septum of many teleosts. In percomorphs and zeiforms the anterior POTs acquire a new association, attaching to epineural bones secondarily positioned in the horizontal septum. Epipleurals lie below the horizontal septum and are posteroventrally directed. There are ossified epipleurals in Heterotis, elopomorphs, clupeomorphs, esocoids, ostariophysans, argentinoids, stomiiforms, aulopiforms, myctophiforms, and Polymixia. Like the epineurals, in many lower (nonacanthomorph) elopocephalan teleosts the epipleural bones develop an anterodorsal branch so that they are forked proximally. Epipleurals are unossified in salmonoids and osmeroids (except Spirinchus and some galaxiines), and this, together with cartilaginous epicentrals in those groups, indicates that they are sister groups. Aulopiforms are uniquely characterized by attached epipleurals that extend forward to the first or second vertebra. In many aulopiforms, the anterior epipleurals are displaced dorsally into the horizontal septum, the reverse of the acanthomorph situation (epineurals displaced ventrally), and in most aulopiforms the primitive bidirectional pattern of epipleural development is replaced by a rostrocaudal gradient. The epipleural series is lost in all acanthomorphs except Polymixia and holocentrids. The distribution and structure of ribs and Baudelot's ligament also are mapped. The potential systematic value of the intermusculars is illustrated by a parsimony analysis of Aulopiformes, and intermuscular characters of many other groups are enumerated.

OFFICIAL PUBLICATION DATE is handstamped in a limited number of initial copies and is recorded in the Institution's annual report, Smithsonian Year. SERIES COVER DESIGN: The coral Montastrea cavernosa (Linnaeus).

Library of Congress Cataloging-in-Publication Data

Patterson, Colin

The intermuscular bones and ligaments of teleostean fishes / Colin Patterson and G. David Johnson.

p. cm. — (Smithsonian contributions to zoology ; no. 559)

Includes bibliographical references (p. 76).

1. Osteichthyes—Anatomy. 2. Bones. 3. Ligaments. 4. Muscles. I. Johnson, G. David. II. Title. III. Title: Teleostean fishes. IV. Series.

QL1.S54 no. 559 [QL639] 591 s—dc20 [597′.50447] 94–10700

art The paper used in this publication meets the minimum requirements of the American National Standard for Permanence of Paper for Printed Library Materials Z39.48–1984.

The Intermuscular Bones and Ligaments of Teleostean Fishes

Colin Patterson and G. David Johnson

“In studying the skeleton, we generally give too little attention to the ligaments. The oversight is regrettabe. When two organic systems have such close mutual relations as the bones and the ligaments, and especially when the elements of one system may happen to take on the characters of the other, to study one without taking account of the other will often create the most serious difficulties. In morphology there is no such thing as insignificant detail; each observation, no matter how trifling, may carry the germ of an explanation for others of much greater consequence.”

Émile Baudelot (1868:84, our translation from the French)

_________________

Colin Patterson, The Natural History Museum, London, SW7 5BD, England. G. David Johnson, National Museum of Natural History, Smithsonian Institution, Washington, DC 20560.

Reviewers: Victor G. Springer, Smithsonian Institution; Gareth Nelson and Melanie J. Stiassny, The American Museum of Natural History; George Lauder, The University of California, Irvine.

Introduction

The work reported here began with an attempt by Patterson to understand the intermuscular bones and ligaments in Polymixia, the genus currently regarded as the sister taxon of all other Acanthomorpha (Rosen, 1985; Stiassny, 1986). Alone among Recent acanthomorphs, Polymixia has been described as having two sets of intermuscular bones, epineurals and epipleurals (Starks, 1904a; Patterson, 1964; Zehren, 1979). Other Recent acanthomorphs have either a single series of bones, generally called epipleurals, or they lack intermuscular bones (bothid and samarid pleuronectiforms and aulostomid gasterosteiforms are exceptional in having extra autapomorphous series of bones; Amaoka, 1969; Hensley and Ahlstrom, 1984; Jungersen, 1910:270; and below). The work expanded into the present collaboration after Johnson saw a draft manuscript by Patterson and thereupon pointed out that intermuscular ligaments are much more widely distributed than Patterson had realized. We began a wider survey of teleostean intermuscular bones and ligaments and soon found that interpreting and recording details of the form and distribution of those structures in cleared-and-stained specimens can be extremely difficult and is best undertaken by two people, alternating as observer and as critic and recorder. The plan of the paper is first to consider historical and current terminology, next to give a detailed description of conditions in Polymixia, and then to summarize our observations and interpretations in separate sections on lower (nonacanthomorph) and acanthomorph teleosts. We recognize that the results presented here do no more than scratch the surface of a very complex subject; we believe that the intermuscular bones and ligaments hold promise as a source of characters of systematic value, and we hope that others will pursue and realize that promise.

TERMINOLOGY AND MATERIAL

Intermuscular bones, which occur only in teleosts amongst Recent vertebrates, are segmental, serially homologous ossifications in the myosepta. Their position in the myosepta distinguishes them from (pleural) ribs, which (with a few exceptions) are found not in myosepta but in the peritoneal membrane. In this paper we concentrate on the three principal series of intermusculars—epineurals, epicentrals, and epipleurals—that attach to the axial skeleton and which we show to be homologous throughout teleosts. In a few teleosts there are two or more additional series of intermusculars, the myorhabdoi (Chapman, 1944), which are commonest in the dorsal and ventral forward flexures of the myoseptum; however, myorhabdoi do not attach to the axial skeleton and are autapomorphous for those taxa in which they occur.

The terms “epineural,” “epicentral,” and “epipleural” were introduced by Richard Owen. “Epipleural” dates from 1846 (Owen, 1846:66), for bones “attached to, or near to, the heads of the ribs, [which] extend upward, outward, and backward, between the dorsal and lateral masses of muscles.” “Epineural” and “epicentral” were introduced in 1866 (Owen, 1866:43), and this division of the intermusculars into three series generally has been followed since. Owen's “type locality” for the three series was the herring, Clupea (Owen, 1866, fig. 37), which has epineurals above the horizontal septum, epipleurals below it, and epicentrals in it. Owen did not mention the horizontal septum as a criterion, but he named the three series “according to the vertebral element they may adhere to” (Owen, 1866:43), i.e., neural arch or spine for the epineural, centrum for the epicentral, and rib for the epipleural. But he acknowledged that this criterion is not definitive because “each may shift its place, rising or falling gradually along the series of vertebrae.” Owen wrote that Esox and Thymallus have epineurals and epicentrals, Cyprinus has epineurals and epipleurals, Salmo has epineurals together with “gristly representatives of epipleurals,” whereas Perca and Gadus have only epicentrals. We regard the first of those three statements as partially true (of Thymallus; Esox has ossified epineurals and epipleurals), the second (Cyprinus) as true, the third (Salmo) as false (Salmo has epineurals and “gristly” (cartilaginous) epicentrals, not epipleurals), and the fourth (Perca, Gadus) as a pointer to one of the conclusions of this paper. We both initially thought Owen right, but we now think him wrong; the intermuscular bones of Perca (and other percomorphs) and Gadus (and other paracanthopterygians) are epineurals.

When all three series of intermuscular bones are present, as in Clupea, discriminating them is easy, and the horizontal septum (containing the epicentrals) is a useful criterion. When one (or two) series is missing and the remaining series modified, naming becomes problematic; we postpone the question of defining criteria of the different series until the concluding section of the paper, after their modifications have been discussed.

Several other names have been applied to series of intermuscular bones in teleosts. In English, these include epimerals, hypomerals, and dorsal ribs. Monod (1963:271) gave a partial synonymy of these terms and others in French and German.

The epipleural series normally is easily distinguished from epicentrals and epineurals by an ontogenetic criterion. Whereas epineurals and epicentrals develop in a rostrocaudal gradient, first appearing and being most strongly developed on the anterior vertebrae, epipleurals develop both rostrally and caudally from about the level of the first caudal vertebra. The distribution of epipleurals in Polymixia (Figure 1) and in many lower teleosts (Tables 3–5) illustrates the restriction of the series to the middle of the body. Inference of rostral and caudal development is borne out by the developmental series of Albula in Table 3 and (to a lesser extent) by the series of Polymixia in Table 1.

One principal aim of this paper, implied by our epigraph, is to expand the concept of intermusculars to include ligaments as well as bones. We have found that teleostean intermuscular bones almost invariably are associated with ligaments (e.g., Figure 1, Plate 1A). That association takes three forms. First, each intermuscular bone is generally an ossification within a ligament (e.g., Plate 2H), and intermuscular bones frequently are joined to the axial skeleton proximally by ligament (especially toward the caudal end of the series) and may be continued distally by ligament. Second, in a given teleostean fish each series of intermuscular bones (epineural, epicentral, epipleural) often is part of a more extensive series of ligaments; the epineural, epicentral, and epipleural series of bones may be continued both rostrally and caudally by a series of ligaments (e.g., Plate 1A). Third, where a teleost appears to lack one of the three series of intermuscular bones, that series (most commonly the epicentral series) may be represented by ligaments alone (e.g., Plate 1B,C, Plate 2C,E,F). These three types of association between intermuscular bones and ligaments may be summarized as (1) ontogenetic or anatomical continuity; (2) serial homology; or (3) homology. Intermuscular ligaments occasionally are indicated in illustrations (e.g., Goodrich, 1909, fig. 336; Kishinouye, 1923, pls. 13–15) or mentioned in descriptions (e.g., Phillips, 1942:489; Nursall, 1956:139; Taverne, 1978:209; Fink and Weitzman, 1982:61), but we found almost no account of them in the literature, even in the classics of detailed anatomy (e.g., Allis, 1903, 1909). In fact, the one account we found (through the help of Mark Westneat, FMNH; also Westneat et al., 1993) is in Japanese (Kafuku, 1950) and deals only with ligaments in the horizontal septum, which contains the epicentral series in lower teleosts and the series of bones generally called epipleurals in acanthomorphs.

FIGURE 1.—Intermuscular system of bones and ligaments in adult Polymixia lowei Günther, based on BMNH 1987.12.7.1 (128 mm SL). The intermuscular bones are in solid black, the ligaments are shaded, and the epicentral cartilages are indicated by dots. (Scale bar in mm.)

Kafuku studied the structure of the horizontal septum in representatives of 40 families of teleosts, including an elopomorph (Anguilla), three clupeomorphs (Clupea, Sardinella, Clupanodon), several ostariophysans (Chanos, three cyprinids, a cobitid) and other lower euteleosts (Oncorhynchus, Plecoglossus), an aulopiform (Saurida), and a range of acanthomorphs, including paracanthopts (Gadus, Pterophryne), smegmamorphs (a mugilid, an exocoetid, a scombresocid), scorpaeniforms (representatives of four families), perciforms (representatives of about 20 families), a pleuronecti- form, and three tetraodontiforms. In all of these fishes he found that each vertebra gives origin to two tendons that lie in the horizontal septum, and he named them the anterior oblique and posterior oblique tendons (AOT, POT). Each AOT runs from the anteroventral part of the vertebral centrum out to the superficial lateralis muscle; according to Kafuku (1950:95) it often is cartilaginous distally, and sometimes it is called a “dorsal rib,” “intermuscular bone,” or “accessory rib.” Kafuku found that each POT originates on the posteroventral part of the vertebral centrum and also runs out to the superficial lateralis muscle, but the POT attaching to that muscle at the same point as a given AOT may come from the centrum located two (Scomber), three (Cyprinus), or up to eight (Katsuwonus, Thunnus) vertebrae posterior to that on which the given AOT originates; in general, AOTs extend directly posterolaterally to the superficial muscle, and POTs run more obliquely anterolaterally, penetrating through the AOTs on their way so that AOTs and POTs form an interconnected sliding latticework. That latticework is particularly well developed in scombroids (Westneat et al., 1993) and is beautifully illustrated in pls. 13–15 of Kishinouye (1923). The number of POTs crossing a given AOT indicates the number of vertebrae separating the origin of that AOT from the origin of the POT inserting at its tip.

Kafuku (1950) made his observations of the ligaments in the horizontal septum on parboiled formalin-fixed specimens. He gave no sizes for his specimens, but they were presumably large fishes. Westneat et al. (1993) also used large, dissected fishes. We worked mainly with cleared-and-stained specimens, most of them counterstained for cartilage and bone by the method of Dingerkus and Uhler (1977). In such specimens, we found POTs to be much more spotty in their distribution than the ubiquity documented by Kafuku (1950). We also found that when POTs occur, their distribution in a fish is more complex than the uniformity throughout the vertebral column implied by Kafuku's work. POTs certainly are easier to find in larger specimens than in the small individuals usually selected for clearing and staining, and differences between our observations and those of Kafuku and Westneat et al. may in part be due to different methods of investigation. However, in general we find that the system of intermuscular bones and ligaments is fully developed in quite small individuals of the species where we have studied ontogenetic variation or size ranges (examples may be found in Tables 1, 3, 8). Furthermore, we know of no instance where study of large specimens is necessary in order to find an intermuscular bone. The only probable exception is the development of cartilage rods within epicentral ligaments; we have found well-developed rods in salmonoids and osmeroids at 40–50 mm SL, but in Polymixia the rods do not become visible until about 100 mm SL, and they may develop in larger individuals of other taxa.

On nomenclature, Kafuku (1950) technically was correct to call the AOTs and POTs tendons because they connect muscle (superficial lateralis) and bone (vertebra). But when an intermuscular bone or cartilage lies in one of these tendons and is not directly attached to the axial skeleton, exactitude demands that one names the proximal portion (between the intermuscular bone or cartilage and the centrum; i.e., connecting bone or cartilage to bone) a ligament and the distal portion (connecting muscle to intermuscular bone or cartilage) a tendon. We avoid this and other problems of terminology by calling them all ligaments, whether or not an intermuscular bone or cartilage is involved. Kafuku (1950) dealt only with the horizontal septum, and in that septum intermuscular bones or cartilages develop only in his AOTs. Ligaments with a broadly similar posterolateral orientation to the AOTs may occur above and below the horizontal septum, in series with or including epineural and epipleural bones. We call these epineural and epipleural ligaments, and we call the AOTs epicentral ligaments. We refer to the proximal attachment of an intermuscular ligament, on the axial skeleton, as its origin, and we call its distal attachment, if any, its insertion. We comment on the POTs in our descriptive sections, but they never contain bone or cartilage and are not part of the intermuscular skeleton on which we concentrate.

As noted above, our material is mainly cleared-and-stained specimens and, where possible, is counterstained for cartilage and bone by the method of Dingerkus and Uhler (1977). We worked primarily by surveying the BMNH and USNM collections, borrowing material from other institutions where necessary. (Institutional abbreviations follow Leviton et al. (1985).) Rather than give a full list of material examined (which would run to many pages), in Appendices 1 and 2 we give alphabetical and systematic lists of all genera cited in the text and in Tables 1–5, 7, and 8. We examined specimens of many other genera beyond those listed in the Appendices. In addition to cleared-and-stained specimens, we studied some that were alizarin-stained without clearing before dissection, some dissected spirit specimens, and many dried skeletal preparations and radiographs of larger specimens. In Tables 3–5, 7, and 8, summarizing the intermusculars and associated structures in a wide variety of teleosts, we generally record structures on the left side of the specimen. Where there is noticeable variation between the two sides of a specimen, we record the state that appears normal, especially when we had access to more than one individual.

Although there can be little argument about the distribution of intermuscular bones in cleared-and-stained specimens, we cannot pretend that observing and recording intermuscular ligaments is an entirely objective procedure, particularly toward the caudal end of a series of ligaments, where they decrease in size and coherence. We have found that the condition of the specimen is important (how well digested and/or bleached), as is the lighting and the quality of the optical equipment. Incident light, in addition to or instead of transmitted light, often is useful in resolving the ligaments (e.g., Plate 2A–C), but too much reliance on incident light may overemphasize connective tissue sheets that do not deserve the term ligament. Transferring cleared-and-stained specimens to alcohol may render the ligaments more opaque, and so more visible. We have found that Leitz stereomicroscopes give the best resolution and may be essential in resolving details of ligaments in small specimens. In cases of doubt, we have changed illumination and observer until agreement was reached. Nevertheless, the observations of ligaments recorded in our tables include an unknown quantity of subjectivity, and we will be glad to see all or any of them checked by others. Our decisions, also recorded in the tables, on whether the pleural ribs of a specimen are preformed in cartilage or are membrane bone is based on the distinction between a rib tip that is an open, cartilage-capped cylinder and one that ends in a bony point. That distinction may be hard to draw in ribs that are very slender, or poorly stained, or decalcified, and there is an element of subjectivity.

A NOTE ON THE TABLES

In Tables 1–3, 7, and 8 we record features of the intermuscular bones and ligaments, and other aspects of the vertebral column, in about 125 genera of teleosts from over 100 families. The entries in those tables are, in effect, maps of the vertebral column or a form of illustration in which symbols stand in for objects. As with maps, some effort is necessary to learn the conventions. It will help readers who intend to study or use the tables, in conjunction with either our text or their own specimens, to make a photocopy of the “Key to the Tables” (p. 50), a photocopy of Table 3, which is printed as a foldout, and photocopies of Tables 4, 5, 7, and 8 which may be cut and pasted to make the equivalent of foldouts of those tables.

ACKNOWLEDGMENTS

For the loan of specimens, we are most grateful to William D. Anderson Jr., Douglas P. Begle, Edward J. Crossman, M. Norma Feinberg, Anthony C. Gill, Karsten E. Hartel, Dannie A. Hensley, Robert K. Johnson, Gareth Nelson, Muneo Okiyama, James W. Orr, John R. Paxton, William J. Richards, Richard H. Rosenblatt, Darrell J. Siebert, Melanie L.J. Stiassny, Kenneth J. Sulak, Yoshiaki Tominaga, James C. Tyler, and Richard Winterbottom. For unpublished information we thank Lance Grande, Tony Harold, Gordon J. Howes, P. Humphry Greenwood, John E. Olney, Lynne R. Parenti, Darrell J. Siebert, and Mark W. Westneat. For help in translating Japanese we are indebted to Louise and Seiji Arimatsu. We thank John Harshbarger for preparing histological sections. For reviewing the manuscript and providing many constructive suggestions for its improvement we are particularly grateful to George V. Lauder, Gareth Nelson, Victor G. Springer, Melanie J. Stiassny, and Richard L. Zusi. And for technical and logistic support of many kinds we are most obliged to Carole C. Baldwin.

Intermusculars in Polymixia

The description that follows is based on four counterstained specimens of P. lowei Günther: MCZ 64773, 12 mm SL; MCZ 95714, 28 mm SL; USNM 308378, 72 mm SL; and BMNH 1987.12.7.1, 128 mm SL; features of osteology also were checked in dried skeletons of P. japonica Günther and P. nobilis Lowe. Polymixia (Figure 1, Plate 2A–D) does not have two series of intermusculars (Starks, 1904a; Patterson, 1964; Zehren, 1979), rather it has three: epineurals above the horizontal septum, epicentrals in that septum, and epipleurals below it. Ligaments occur in association with all three series.

In the adult, the entire upper, or epineural, series of bones and ligaments extends over about 24 vertebrae, from the first vertebra (V1) back to about the twelfth caudal (PU5). The epineural bone on V1 differs from its successors in being larger and in lying in the horizontal septum, so that it is in series positionally with the epicentral ligaments behind it; we anticipate our discussion of the problem of its homology (p. 33) in describing it as an epineural. The first epineural is a stout bone, originating in a socket at the base of the (autogenous) first neural arch, at a level slightly ventral to the articulation of the epineural on the second neural arch (Rosen, 1985, fig. 18). The bone extends posterolaterally in the horizontal septum and ends immediately beneath the lateral line nerve, at the level of V4. On V2 the epineural articulates at the base of the (fused) neural arch, but on V3–10 the epineurals originate on the centrum. On V3–8 the attachment is on the upper edge of the parapophysis, just above the head of the rib, and on the succeeding one or two vertebrae (V9–10) it is at or just above the midpoint of the anterior margin of the centrum. On V 11 the epineural originates on the base of the neural arch, at about the same level as on V2, and on more posterior vertebrae the point of attachment of the epineural rises successively higher on the neural arch and spine. The last five to seven epineural bones are attached to the axial skeleton by ligaments that are progressively longer on more posterior vertebrae, and in the adult there are ligaments, with no included bone, on about four more neural spines, so that the entire series extends back to about PU5.

FIGURE 2.—First five vertebrae and attached intermusculars in Polymixia lowei, based on BMNH 1987.12.7.1 (128 mm SL) and supplemented by USNM 308378 (72 mm SL). (Scale bar (1 mm) refers to the larger specimen.)

The lowermost, or epipleural, series of bones in Polymixia extends over some 10 vertebrae, from about V9 back to V19 (the seventh caudal). The first and the last one or two epipleural bones have no direct articulation with the axial skeleton but are attached by ligaments, and in front of the first ossified epipleural and behind the last there are from one to three ligaments with no included bone (Plate 2G). The remaining epipleurals attach near the heads of the last two or three pleural ribs and at successively lower points on the first five or six haemal spines (Figure 1).

Between the upper and lower intermuscular series of Polymixia there is a middle series, the epicentrals. As noted above, the first epineural lies in the horizontal septum. Behind and in series with this stout bone in the horizontal septum there is a row of epicentral ligaments (Plate 2B–D), one in each myocomma, extending from V2 back to the posterior caudal vertebrae (to about PU5 in the adult). Our epicentral ligaments are the anterior oblique tendons (AOTs) of Kafuku's (1950) account of the teleostean horizontal septum. In Polymixia they are stout, cylindrical ligaments, whereas the posterior oblique tendons (POTs of Kafuku, 1950) are very feeble, each consisting of several strands. As shown in Figure 3, three POTs cross each epicentral ligament, and the POT inserting with a given epicentral ligament originates on the vertebra four behind that on which the epicentral ligament originates. The first epicentral ligament (Figure 2) originates immediately below the attachment of the epineural on V2. On V3 and succeeding abdominal vertebrae the ligament originates on the head of the rib, immediately below the origin of the epineural on the parapophysis. On anterior caudal vertebrae the ligament originates at the base of the haemal spine, and from about the sixth caudal vertebra onward it originates on the centrum. In the distal part of the second to sixteenth of these ligaments (V3–17) in our 128 mm SL specimen there is a series of cartilaginous rods (Plate 2D). We identify the tissue of these rods as cartilage by histology (in thin section and in squash preparations; it is cellular with much extracellular matrix), by comparing its reaction with alcian blue (deeply stained) with that of undoubted cartilage in the same specimen, and by comparison with similar rods in Salmo (Plate 1D and below), both in thin section and in double-stained specimens, where cartilage previously has been verified histologically (Emelianov, 1935). Like the epineural bone on V1, each of these cartilaginous rods ends distally beneath the lateral line nerve. They are most strongly chondrified distally, where their tips are often bifid, and they grow progressively shorter posteriorly.

FIGURE 3.—Epicentral ligaments and posterior oblique ligaments (POTs) in horizontal septum in abdominal region of Polymixia lowei. The sketch, in dorsolateral view, shows the parapophyses and rib heads of V5–10 in BMNH 1987.12.7.1, with the epicentrals and POTs attaching to them. The cartilage in epicentral ligaments is shown by open circles. The vertebrae are numbered. (Scale bar in mm.)

Associated with the epicentral ligaments of Polymixia are the posterior oblique tendons (POT) of Kafuku (1950). The POTs lie in the horizontal septum and are clearly visible in our 128 mm specimen (Figure 3). Working back from the head, the first two POTs insert on the epicentral ligament of V5; one POT inserts about two-thirds of the way along that epicentral and another inserts at its tip where the epicentral ends in the lateralis muscle. These two POTs originate respectively on the head of the rib of V8 and the parapophysis of V9. Another slender POT originates on the head of the rib of V9 and inserts on the epicentral of V6. V10 gives origin to no POT. A POT originating on the parapophysis of V11 ends on the epicentral of V7. The POT originating on the parapophysis of V12 (the last abdominal) inserts on the epicentral ligament of V8, and the POT originating on the haemal arch of V13 inserts on the epicentral of V9. This pattern is repeated back into the caudal region, with the POT inserting on a given epicentral ligament originating on the vertebra four behind. From V11 back, the point of insertion of the POT is always at the tip of the epicentral ligament rather than some distance from its tip as it may be more anteriorly. Passing back along the column, the point of origin of the POTs rises from the haemal spine to the anteroventral margin of the centrum, and at V19–20 it shifts to the posterior part of the preceding centrum, so that V19 carries two POTs, one from the anteroventral and one from the posteroventral part of the centrum. From this point back to the last epicentral ligament (on V24) epicentrals and POTs show the pattern described by Kafuku (1950) as general in teleosts, with the epicentral originating at the front of a centrum and the POT at the rear. This pattern exists only on about five centra in Polymixia. The last visible POT originates on V25 (PU4). The POTs of Polymixia are very feeble in comparison with the epicentral ligaments. The epicentrals are stout cylinders, lying on the dorsal surface of the horizontal septum, whereas the POTs are feeble, dorsoventrally compressed, strap-like ligaments lying within the horizontal septum. The POTs pass ventral to the epicentral ligaments (although attached to the epicentral by connective tissue) and do not pass through or penetrate the epicentrals, which is the situation described by Kafuku (1950) in other teleosts. In the middle of the trunk, at approximately the first caudal vertebra, POTs are about half the size of the epicentral ligament originating on the same centrum. As they pass forward, these POTs break up into two or three slender strap-like ligaments. Posteriorly, near the end of the series, each POT divides into five or six separate strap-like ligaments almost immediately after its origin from the centrum. Anteriorly, at the front of the series, where the epicentral ligaments are more robust than posteriorly, the contrast between their size and the diminutive POTs is even more obvious (Figure 3). The anterior POTs divide into two or three branches, like those in the middle of the series. In our 72 mm SL specimen, POTs show much the same pattern as in the 128 mm SL specimen. We have not succeeded in seeing POTs in our two smaller specimens of Polymixia (12 and 28 mm SL).

The ribs of Polymixia extend from V3 to V12. All are ossified in cartilage.

Table 1 introduces our method of recording intermuscular bones and ligaments in teleosts and shows the conditions in four specimens of Polymixia ranging from 11 to 128 mm SL.

Intermusculars in Nonacanthomorph Teleosts

Polymixia has three sets of intermusculars that match Owen's (1866) topographic criteria for epineurals, epicentrals, and epipleurals. The situation in Polymixia is relatively uncomplicated because all the intermuscular bones are simple; none shows the proximal or distal forking or branching that occurs in many lower teleosts, which may render their topography and relationships more difficult to decipher. In this section we first describe the intermusculars in the gonorynchiform Gonorynchus, as an example of a nonacanthomorph with the most extreme complications of that sort. (In keeping with our epigraph, the intricacies of the intermuscular bones and ligaments in Gonorynchus are not necessarily mere worthless detail for they may be phylogenetically informative.) We then review the structure and distribution of the three series of intermusculars and some associated structures in nonacanthomorph teleosts, and finally we comment on the significance of variation in the intermusculars within and between some major groups of nonacanthomorphs.

Gonorhynchus

The description that follows is based on SIO 70-275, 146 mm SL (Figures 4, 6); we also include a drawing of a smaller double-stained specimen (Figure 5) made by one of us some years ago. Monod (1963) gave a full account of intermuscular bones in larger specimens (∼300 mm SL). The situation in Gonorynchus is so complex that in the description we do not try to take account of variation among individuals (which certainly occurs, and may include interspecific variation, cf. Howes, 1985:280). We compare our observations with Monod's (1963) at the end of the description.

The epineural series in Gonorynchus ostensibly extends from the fourth vertebra (V4) back to about V47 (PU9), but as we will show, epineurals extend anterior to V4. In our 146 mm specimen there are ossified epineurals that attach to neural arches of V5–40 and unattached epineural bones on V41–47. These epineural bones are all associated with or ossified within ligaments, and those on V5–40 are attached to the anterior part of the neural arch by ligament (Figures 5, 6). Those on V5–35 are forked proximally (Figures 4–6), with a primary anteromdial branch attaching to the neural arch and a secondary anteroventral branch passing toward the transverse process (fused parapophysis) of the next vertebra in front. Passing back along the series, the point at which the epineural bifurcates becomes gradually more remote from its attachment to the neural arch, and at V36, in the region of the origin of the dorsal fin, the anteromedial branch ceases to join the distal part and anteroventral branch; beyond this point there are five or six short, simple epineurals attached to the neural arch by ligament, and lateral to them is a corresponding series of long bones that represent the distal portions and anteroventral branches of the posterior epineurals. This series of bones extends back to V47. At the anterior end of the epineural series there is a similar separation of the epineurals into two parts. On V4 there is a short, simple epineural bone (En 4, Figure 4), which differs from its successors in attaching to the anterodorsal part of the centrum, not to the neural arch, and in articulating directly with the vertebra, with no intervening ligament. If one traces the distal parts of the epineurals forward in sequence, it is evident that this short and simple epineural on V4 is merely the isolated anteromedial branch of an epineural, and that the distal part and anteroventral branch of this epineural exists as a long, separate bone (Vo 4, Figures 4, 5), extending down (like its successors) toward the region of the parapophysis of the next vertebra in front, V3. That vertebra bears the first rib, which is enlarged and articulates with a short transverse process. The tip of the epineural branch of V4 is directed toward the head of the rib rather than toward the transverse process. On V3 there is a ligament attaching to the centrum (En 3, Figure 4), a little lower than the attachment of the epineural bone on V4, and on the right side of our 146 mm specimen there is a diminutive epineural bone within the ligament. No epineural bone or ligament attaches to V1 or V2. However, the epineurals of V1 and V2, which appear to be missing when only vertebrae are considered, are represented by their distal parts and anteroventral branches, each directed proximally toward the axial skeleton of the segment in front. But on V1–3 there is an additional complication in that the anterior ends of these three epineural branches are fused or coossified with the anterior members of the epicentral series; these epineural branches are described with the epicentral series, below.

The epicentral series of Gonorynchus extends from the cranium back to about V50, having about the same posterior extent as the epineurals. In our 146 mm SL specimen there are epicentral bones back to V40 and epicentral ligaments thereafter. Epicentral bones and ligaments attach to the tips of the transverse processes of abdominal vertebrae, to the base of the haemal arch of the first caudal vertebra (V43), and to the centrum on posterior caudal vertebrae. They lie in the horizontal septum, and all epicentral bones are simple, unbifurcated rods except for those on the occiput and V1–2, which are modified and associated with the anteroventral branches of the first few epineurals. On V4 the epicentral is a substantial bone (Ec 4, Figures 4, 5) that attaches to the anterior margin of the large transverse process. On V3, which carries the enlarged first rib, there is apparently no epicentral. On V2 there is no rib, but there is a bifid transverse process. Attached by ligament to the posterior limb of the transverse process is a substantial intermuscular bone (Ec 2 + Vo 3, Figures 4, 5). That bone bifurcates almost immediately into a posterodorsal branch and a posterolateral branch. The posterodorsal branch is in series posteriorly with the epineural bones, and it is the detached distal part and anteroventral branch of the epineural of V3. The posterolateral branch is in series posteriorly with the epicentrals, and it is the epicentral of V2. V1 also has a bifid transverse process, like V2, and attached by ligament to the two limbs of the process are two large intermuscular bones. The proximal end of both may be bifid or trifid, and the bones are closely associated just beyond their attachment. The more posterior of the two bones (Ec 1 + Vo 2, Figure 5) splits into two branches, directed respectively posterodorsally and posterolaterally and agree with the epineural and epicentral branches of the intermuscular on V2 (this epineural branch on V1 represents the epineural of V2). The more anterior intermuscular on V1 is directed posteroventrally in the peritoneal membrane, so that it lies in the plane of the ribs distally, where it breaks up into a brush-like termination, with about seven branches passing out into the musculature; we interpret this bone as the serial homologue of the two “cranial ribs” (below). Anterior to these complex intermusculars on V1 there are seven more intermusculars, which insert on the cranium. These include the “cranial ribs” of previous descriptions of Gonorynchus (Chabanaud, 1931; Monod, 1963). The two most posterior of these bones insert close together on the basioccipital, just anterior to the lower margin of the occipital condyle. The more dorsal of the two (Ec Boc + V₀ 1, Figures 4, 5) bifurcates into two branches, one posterodorsal and one posterolateral, respectively matching the epineural and epicentral branches of the succeeding bones (so that the epineural branch represents the epineural of V1). The more ventral bone is directed posteroventrally, breaks up into a brush-like termination in the peritoneal membrane, and is a cranial rib, matching the anterior intermuscular on V1 in orientation and configuration. The next two intermusculars insert close together on the exoccipital, immediately beneath the vagus foramen. They show the same pattern as the two bones on the basioccipital, with the more dorsal bone (Ec Exo + V₀ 0, Figure 4) bifurcating into epineural and epicentral branches and the more ventral ending in a bony brush in the peritoneal membrane in series with those of the two succeeding cranial ribs. Passing forward on the cranium, the next two intermusculars (Ec Exo, En Exo, Figures 4, 5) insert close together on the exoccipital just above and lateral to the vagus foramen. They are smaller than the bones behind them on the cranium, and together they match the upper of the two intermusculars on the exoccipital and on the basioccipital; the upper bone matches their epineural branch, and the lower matches their epicentral branch. The lower, epicentral, bone bifurcates and both limbs attach to the medial face of the supracleithrum. The last intermuscular on the cranium (En Ic, Figures 4, 5) is a slender bone attached to the intercalar; this intermuscular bifurcates distally, with an outer branch attaching to the medial face of the posttemporal and an inner dorsolateral branch (which bifurcates again) passing back into the musculature in series with the epineurals. Ridewood (1904:66) homologised this last intermuscular with the intercalar limb of the posttemporal, which he thought was otherwise absent in Gonorynchus, but we believe that the intercalar limb is represented by a stout, strap-like ligament that originates on the intercalar immediately beneath the point of origin of the epineural intermuscular and passes out to the posttemporal (Figure 4).

FIGURE 4.—Gonorynchus ? gonorynchus (L.), SIO 70-275, 146 mm SL. Ventral view of the first six vertebrae and the rear of the braincase, with the intermuscular bones in solid black. The ribs are removed on the left side (right side of figure). The left “cranial ribs” on the occiput and V1, and the epicentral (lower) branch of left compound intermuscular on V1 are drawn as if they were cut through near their origin. The left posttemporal and supracleithrum are included, with the supracleithrum drawn as if it was cut through. The only ligaments shown are those representing the intercalar limb of the posttemporal and the epineural ligament of V3, which includes a diminutive bone on the right side. (Scale bar in mm.) (Abbreviations: Boc, basioccipital; Ec, epicentral; En, epineural; Exo, exoccipital; Ic, intercalar; Pas, parasphenoid; Vo, intermuscular representing unattached anteroventral limb and posterior body of an epineural. Plus signs between symbols indicate fusion. Intermusculars and ribs are numbered or labeled according to the vertebra (number) or bone (abbreviation) with which they are associated.)

FIGURE 5.—Gonorynchus ? gonorynchus. Anterior vertebrae and intermuscular bones in left dorsolateral view of RUSI 15048, 95 mm SL. The intermuscular bones are in solid black. The only ligament shown is that attaching the fifth epineural to the neural arch. (Scale bar 1 mm.) (Abbreviations: Boc, basioccipital; Ec, epicentral; En, epineural; Exo, exoccipital; Ic, intercalar; Vo, intermuscular representing unattached anteroventral limb and posterior body of an epineural. Plus signs between symbols indicate fusion. Intermusculars and ribs are numbered or labeled according to the vertebra (number) or bone (abbreviation) with which they are associated.)

FIGURE 6.—Gonorynchus? gonorynchus, same specimen as Figure 4. Lateral view of vertebrae 25 and 26 (left) and of vertebrae 34 and 35 (right), with attached intermuscular bones and ligaments. The intermuscular bones are in solid black. (Scale bar in mm.) (Notation Do (as in Table 2) denotes unattached bones that are homologous with anterodorsal branch of an epipleural.)

The epipleural series in our 146 mm SL Gonorynchus ostensibly extends from V11 back to V35 (the level of the pelvic-fin insertion), but, as we will show, it extends much further posteriorly. All the epipleurals to V35 are ossified, and there appears to be no rostral or caudal extension of the series in ligament. The bones are simple rods, attached by short ligaments to the tips of transverse processes (Figure 6). They are directed slightly posterodorsally, and most of them extend back in the musculature for a distance equal to about one-and-one-half vertebrae. The first few and last few bones are shorter than those in the middle of the series and are attached to the transverse process by longer ligaments. Beginning at V30, and extending posteriorly to V52, there is another series of epipleural bones that clearly mirror the detached anteroventral branches of the posterior epineural bones. These bones (D₀. Figure 6) lie unattached (free) in the lateral musculature above the epipleurals and lateral to the middle part of the epicentrals; they are oriented obliquely ventrolaterally, and, in the anterior part of the series, each begins close to the middle part of the epicentral bone of the preceding vertebra. The first few bones are short (about the length of a vertebra), but they lengthen posteriorly (up to about two vertebrae long) and become oriented more horizontally.

We have not found any posterior oblique tendons (POTs) in Gonorynchus, and Baudelot's ligament also is absent.

Ribs of Gonorynchus extend from V3 to V34. The first is enlarged and is preformed in cartilage. The remainder are slender and ossified as membrane bone.

Table 2 illustrates our method of recording intermuscular bones and ligaments as applied in Gonorynchus.

Monod (1963) gave an excellent account of intermuscular bones in Gonorynchus based on dissected specimens two or three times as large as ours (∼300 mm SL). His observations match our own in most respects. Monod's specimen has 62 preural vertebrae, whereas our 146 mm specimen has 55. He used an alphabetical notation (a1–50, b1-50, etc.) for the different series, but he concluded that his a series comprised epineurals, his b series epicentrals, his c series ribs, and his d and e series epipleurals. Monod's e series extends from V33 into the caudal region, and posteriorly from V49 onward each e bone is fused with the tip of an epipleural (Monod's d), so that his e bones correspond to the anterodorsal branch of the epipleural (D₀ in Table 2 and Figure 6). In our smaller specimen (146 mm SL), principal epipleurals (attached to the axial skeleton) extend only to V35, overlap the e series (beginning at V30) for only a few segments, and are nowhere fused with them. Fusion between the two may occur in larger individuals, as the series of principal epipleurals extends to more posterior vertebrae. Monod found that the principal (anteromedial) and distal (anteroventral branch + posterior body of the bone; notation V₀ in Table 2 and Figure 6) branches of epineurals did not separate until about V51, and that the medial branch did not disappear until V54 (cf. V36 and V41 in our specimen). On the back of the cranium and the first few vertebrae, where the intermusculars of Gonorynchus are most intricate, Monod's observations and interpretations agree with our own in most details.

Monod included three “cranial ribs” in his c series, two originating on the cranium and one on V1. We can find no other interpretation for these three bones, which (as noted above) appear to lie in the peritoneal membrane. We have not found cranial ribs in any other teleost (the supposed “cranial ribs” of Chanos and other gonorynchiforms are epicentrals, Table 4) and infer that they are autapomorphous for gonorynchids. We do not believe that they are homologous with “true” ribs, and we use a different symbol for them in Table 2.

Monod failed to notice that the anteroventral (secondary) limb of each epineural is directed toward the transverse process of the vertebra in front of that to which the primary (anteromedial) limb attaches. He also referred to the primary limb, attaching to the neural arch, as the accessory branch, and he took the anteroventral limb and the posterior part of each epineural to represent the principal part of the bone. He found no intermusculars on V2 and sought to explain this by a phylogenetic shift of the intermusculars from the posterior part of one centrum to the anterior part of its successor. Intermusculars exist on V2 in our specimens, so no such explanation is necessary. The absence of an epicentral on V3 seems more to demand explanation, and we return to it below, in the section on ostariophysans.

Gonorynchus has an intermuscular system more intricate and challenging than that of any other teleost in our sample.

THE INTERMUSCULAR SERIES AND ASSOCIATED STRUCTURES IN OTHER NONACANTHOMORPH TELEOSTS

Tables 3–5 record the distribution and form of intermuscular bones and ligaments in a range of nonacanthomorphs. In this section we comment on the three series of intermusculars in those fishes and on their POTs, ribs, and certain other features recorded in the tables.

EPINEURALS.—The primitive teleostean condition with regard to intermuscular bones is to have epineurals alone (Patterson and Rosen, 1977:129; Schaeffer and Patterson, 1984:61). Actinopterygian epineurals are primitively developed as short, broad outgrowths of the anterior neural arches that are preformed in cartilage and ossify perichondrally (in cartilage bone) so that in fossil actinopterygians they are hollow and open at the tip, which was cartilage-capped in life. Short epineural processes of this type occur on the first few vertebrae in Devonian lungfishes (Rosen et al., 1981, fig. 54) and palaeoniscoids (Gardiner, 1984, figs. 121–124) and may well be primitive for osteichthyans. Short, cartilage-tipped epineural processes occur on about the first 20 vertebrae in the Jurassic neopterygian Hulettia (Schaeffer and Patterson, 1984, figs. 15, 17C). It is synapomorphous for teleosts to have much longer epineurals, equal in length to several vertebrae (e.g., the early Jurassic Pholidophorus bechei, Schaeffer and Patterson, 1984, fig. 17D). These long epineurals were still hollow and cartilage-tipped in Pholidophorus, a condition that we observed in P. bechei (the type species), the early Jurassic P. germanicus, and two late Jurassic species, “P.” macrocephalus and the species described by Patterson (1975) as “the Callovian Pholidophorus sp.” The cartilaginous anlagen of the epineurals evidently have regressed in all Recent teleosts, as have those of some or all the pleural ribs in many teleosts (Emelianov, 1935; Tables 2–5, 7, 8). We have seen no sign of cartilage in epineurals of any Recent teleost (including the developmental series of some taxa), and Emelianov (1935) found no cartilage in epineural bones of the teleosts that he investigated, which included Salmo and a clupeoid. It is therefore synapomorphous for Recent teleosts to have solid, membrane bone epineurals, and this derived condition also characterizes some Jurassic stem-group teleosts. We observed solid, membrane bone epineurals, without cartilage cores or tips, in the late Jurassic “leptolepids” Ascalabos, Tharsis, and the species described by Patterson (1975) as “the Callovian Leptolepis sp.,” as well as in the late Jurassic ichthyodectiform Allothrissops and the late Jurassic elopocephalan Anaethalion. However, in the early Jurassic Leptolepis coryphaenoides (type species of the genus), the epineurals are hollow and evidently had a cartilage core in life, but their tips are fully ossified, so that there was no cartilage cap. In the early Jurassic Proleptolepis, the epineurals seem to show the same condition: they are hollow, but the tips of at least the most posterior ones (our material is incomplete) are fully ossified. Solid, membrane bone epineurals, therefore, seem to characterize the node above Leptolepis coryphaenoides in the cladogram in Patterson and Rosen (1977, fig. 54), or ichthyodectiforms, Ascalabos, Tharsis, and all higher teleosts, and epineurals with a cartilage core but without a cartilage tip characterize a node above Pholidophorus bechei and below Leptolepis coryphaenoides in that cladogram. Those two taxa are separated by Pholidolepis dorsetensis in the cladogram. We examined the available material of that species, and although we can confirm that the epineurals had a wide cartilaginous core, we could see no well-preserved epineural tips; the lack of distal tapering of the epineurals is suggestive of the condition in Pholidophorus (cartilage-tipped) rather than that in Leptolepis (solid tips).

Primitive continuity between epineurals and neural arches persists in all epineurals of Pholidophorus bechei and of Leptolepis coryphaenoides. In both genera, epineurals are confined to the abdominal region. In the derived late Jurassic “Pholidophorus” macrocephalus, only about the first eight epineurals are continuous with the neural arch, and the remainder (they extend back to about V22, and the first caudal is V27) are free, articulating with a socket on the neural arch. In the ichthyodectiforms Thrissops (Taverne, 1977a) and Allothrissops, all epineurals are continuous with the neural arch; they extend back to the third or fourth caudal vertebra. In Tharsis, epineurals extend back to about the first caudal vertebra, and there appear to be two or three free epineurals posteriorly, articulating with the neural spine. In Ascalabos, epineurals extend to about the fifth caudal vertebra, and, as in Tharsis, the last two or three are free and articulate with the neural spine. As in the above stem-group teleosts, primitive continuity between anterior epineurals and neural arches persists in various more-derived fossil and living teleosts (e.g., the Jurassic Anaethalion and Recent Elops, Arratia, 1987, figs. 3, 31; Hiodon, Taverne, 1977b, figs. 22, 23; Pantodon, Taverne, 1978, figs. 49–53; Esox, Figure 8; Alepocephalus, Gosline, 1969, fig. 11; Clupea, Figure 7A, and Ramanujam, 1929:389; stomiiforms, Weitzman, 1974, fig. 85; Fink and Weitzman, 1982, fig. 5). In all these forms (except the osteoglossomorphs Hiodon, where all epineurals are fused to the neural arch (Table 3), and Pantodon, where all but the first are so fused (Taverne, 1978)), the more posterior epineurals articulate with the neural arch or spine, and the most posterior ones are either free or connected with the neural spine by ligament. In more-derived teleosts, anterior epineurals are separate, either articulating with the vertebra (e.g., Rosen, 1985, figs. 9, 11, 13, 15–17) or attaching to it by ligament, and posterior epineurals are free from the vertebral column and often are forked proximally (e.g., Figures 4, 5, 8, Plate 1E,F Weitzman, 1962, fig. 14; Jollie, 1962, fig. 6.40, “epimerals”), a condition that we take to be synapomorphous for elopocephalans. When epineurals are forked anteriorly (as in Gonorynchus, above), there is an anteromedial branch that represents the primitive connection with the neural arch and an anteroventral branch that passes forward in the myoseptum, roughly parallel to the vertebral column, into the epaxial forward flexure of the myomere (Nursall, 1956, fig. 8).

Epineurals are virtually universal in nonacanthomorph teleosts, occurring in all “leptolepids,” ichthyodectiforms, osteoglossomorphs, elopomorphs, and clupeomorphs, in ostariophyans (except siluroids), in esocoids, argentinoids, osmeroids (osmeroids sensu Rosen, 1974, were said by Rosen to lack intermusculars, but all osmeroids that we have examined have epineurals), salmonoids, stomiiforms, aulopi- forms, and myctophiforms (cf. Tables 3–5).

The only nonacanthomorphs lacking epineural bones among those recorded in Tables 3–5 are the southern osmeroids Stokellia and Lepidogalaxias, the salangid Salangichthys, and the umbrid Novumbra (they also are lacking in Dallia). In Stokellia, Novumbra, Dallia, and salangids, the epineural series is represented by a series of ligaments with the same distribution as epineural bones in other lower euteleosts. We found the same condition in Retropinna, and it may be a synapomorphy corroborating the sister-group relationship between that genus and Stokellia (Begle, 1991), but McDowall (1971, 1976) reported that ossified epineurals also are absent in Aplochiton, Lovettia, and Prototroctes. In Lepidogalaxias, there are no epineural bones or ligaments, a unique condition. In other osmeroids (Osmerus, Hypomesus, Table 4) and various other lower euteleosts (e.g., the stomiiform Diplophos and the aulopiforms Ahliesaurus, Scopelosaurus, Scopelarchoides, Synodus, and Trachinocephalus, Table 5), the series of epineural bones is extended caudally by a series of ligaments, without included bone. In the evermanellid aulopiform Coccorella, there is only one epineural bone (true of all evermanellids according to Johnson, 1982:55), and the epineural series is continued caudally as ligament.

Epineurals are posterodorsally inclined in the epaxial backward flexure of the myoseptum (Nursall, 1956, fig. 8), and their distal tips are normally (and primitively) all aligned at the same level. But in Polymixia (Figure 2), the bone that we interpret as the first epineural is out of alignment with the rest of the series and lies in the horizontal septum. In a few nonacanthomorphs, the distal part of the first one or more epineurals also is displaced ventrally relative to their successors, although, in contrast to Polymixia, they are always above the horizontal septum. We have observed this ventral displacement in alepocephaloids, argentinoids, several aulopiforms, and the neoscopelid Neoscopelus (notation b¹, or f¹ in Tables 4, 5). In alepocephaloids and argentinoids, the tips of the first three (Glossanodon, Leptoderma, Searsia) or four (Argentina) epineurals are displaced, a unique condition that we take to be synapomorphous, corroborating the sister-group relationship of these two taxa (Greenwood and Rosen, 1971; Begle, 1991). In aulopiforms, the tips of the first one to three epineurals may be displaced, and in Neoscopelus only that of the first is displaced (none is displaced in the other neoscopelid genera, Scopelengys and Solivomer).

In Polymixia, the proximal articulation of the epineurals on V3–10 is not on the neural arch but on the centrum (V9–10) or parapophysis (V3–8). The proximal ends of some anterior epineurals also are displaced ventrally in a few nonacanthomorphs. Among osteoglossomorphs, most epineurals originate on the centrum in mormyrids and in the notopterids Xenomystus (Table 3) and Papyrocranus. Among the elopomorphs in our sample, a few anterior epineurals originate on the centrum in Notacanthus, and among clupeomorphs about 15 do so in Anchoa (notation B₂ in Table 3). In euteleosts, Esox has 20 or more epineurals originating on the centrum, from about V10 onward (Table 4), and the aulopiforms Scopelosaurus, Ahliesaurus (both Notosudidae), Scopelarchoides (Scopelarchidae), Coccorella (Evermanellidae), Bathysaurus, and Gigantura have a number of epineurals originating on the centrum or (in Scopelosaurus) on the parapophysis (Table 5).

EPIPLEURALS.—As noted above, the epipleural series generally is easily distinguished from epicentrals and epineurals by ontogeny and distribution; epineurals and epicentrals develop in a rostrocaudal gradient, first appearing and being most strongly developed on anterior vertebrae, whereas epipleurals develop both rostrally and caudally from about the level of the first caudal vertebra.

Epipleural bones are absent in the most primitive teleosts, such as Mesozoic pholidophorids, early Jurassic leptolepids, and the Mesozoic ichthyodectiforms. When epipleurals first appear in the geological record, in late Jurassic “leptolepids,” such as Ascalabos, Tharsis, and Todiltia, they are confined to the last few abdominal and first few caudal vertebrae. In small Todiltia (37 mm SL), for example, there are five pairs of epipleurals in that region, and in the largest specimens (60–80 mm SL) there are seven or eight (Schaeffer and Patterson, 1984:54). Ascalabos and Tharsis have about six epipleurals in that region, Anaethalion has about 12, and Elops has up to about 40 (Taverne, 1974). Osteoglossomorphs generally lack epipleurals, but in Heterotis they occur on up to 10 vertebrae (V26–36, Taverne, 1977b; cf. Table 3), and notopterids have been described as having a long series of them (Taverne, 1978). However, we interpret notopterid “epipleurals” differently; we consider them to be myorhabdoi (see section on osteoglossomorphs, below). Epipleurals generally are present in elopomorphs (elopids, megalopids, albulids, halosaurs, notacanths, anguilliforms) and in clupeomorphs (Denticeps, clupeoids) (Table 3); in clupeoids, the epipleural series may extend along the entire vertebral column (Table 3, Chirocentrus; Figure 7A). In euteleosteans, epipleurals occur as bones in gonorynchiforms, cypriniforms, characiforms, esocoids, alepocephaloids, stomiiforms, aulopiforms (where they always extend forward to V2 and often to V1), myctophiforms, and Polymixia (Tables 4, 5, 7). In many of these groups some epipleurals are forked proximally, like the epineurals above them (e.g., Plate 1E,G). When epipleurals have a proximal fork, orientation of the branches is the reverse of that in epineurals. There is an anteromedial branch, representing the primitive connection with the axial skeleton (rib, parapophysis, or haemal spine), and an anterodorsal branch that passes forward in the myoseptum, roughly parallel to the vertebral column, into the hypaxial forward flexure of the myomere. Toward the rostral and caudal ends of the epipleural series, the anteromedial branch is often absent, so that anterior and posterior epipleurals are rod-like bones, unconnected with the axial skeleton, representing the anterodorsal branch and the posterior body of the bone (notation D₀ in Tables 2–5).

Epipleural bones are absent in Hiodon and Osteoglossum (Table 3), Dallia and Novumbra (Table 4), and salmonoids (Sanford, 1990; Table 4) and osmeroids (McDowall, 1969, 1971, 1976; Rosen, 1974; Table 4; the osmeroid Spirinchus and the galaxiines Galaxias and Paragalaxias are exceptions, McDowall, 1969, 1978). In Hiodon, Osteoglossum, Dallia, Novumbra, and in all salmonoids and osmeroids (except Lepidogalaxias, Stokellia, and Retropinna) that we examined, we found the epipleural series to be represented by a series of ligaments (Tables 3, 4), with broadly the same distribution and attachment to the axial skeleton as the epipleural series of bones in other lower teleosts. There is a similar series of ligaments in the stomiiform Pollichthys (Table 5). Furthermore, in lower teleosts with epipleural bones, the series may be extended rostrally (e.g., Megalops, Albula, Notacanthus, Anguilla, Esox, Tables 3, 4, Plate 1A) or caudally (e.g., Diplophos and many aulopiforms, Table 5, Plate 2G) by a series of ligaments without ossification. To our knowledge, these epipleural ligaments have not been recorded previously.

Presence of epipleural bones evidently is a relatively derived feature in teleosts, because these bones are absent in pholidophorids, Proleptolepis, Leptolepis sensu stricto, and ichthyo- dectiforms (Patterson and Rosen, 1977). Among Recent osteoglossomorphs, they are absent except in Heterotis (we interpret the “epipleurals” of notopterids as myorhabdoi; see below in section on osteoglossomorphs). The epipleurals of Heterotis have the same form as in other teleosts; they are rod-like bones in direct continuity with the epipleural ligament (as in Plate 2G,H). Epipleural bones also are absent in Mesozoic osteoglossomorphs, such as Lycoptera, Paralycoptera, Plesiolycoptera, Asiatolepis, Jiaohichthys, Yanbiania, and the Huashiidae (Huashia, Kuntulunia) (Chang and Chou, 1976, 1977; Ma, 1983, 1986; Li, 1987). According to Chang and Chou (1977), some of these Mesozoic forms (Asiatolepis, Paralycoptera) are more closely related to osteoglossoids than to hiodontids, whereas some (Lycoptera, Plesiolycoptera) are immediately related to hiodontids. According to Ma (1983, 1986), other Mesozoic osteoglossomorphs (huashiids, Jiaohichthys) are incertae sedis within the group. A parsimony argument therefore implies that absence of epipleural bones is primitive for osteoglossomorphs, but that is inconsistent with Patterson and Rosen's (1977) and Schaeffer and Patterson's (1984) use of the presence of a few epipleurals in the middle of the trunk as a character grouping Tharsis (and possibly other Mesozoic stem-group teleosts, e.g., Ascalabos and Todiltia) with all Recent teleosts (osteoglossomorphs, elopocephalans). Because Hiodon and osteoglossoids have a series of epipleural ligaments, we assume that they also were present in Mesozoic stem-group teleosts and were the site of ossification of epipleural bones when they first appeared. We therefore regard the presence of a series of epipleural ligaments as primitive for teleosts (we have not found them in Amia or Lepisosteus), but because they are not preserved in fossils we cannot say when they first occurred. There are two possible interpretations of the distribution of ossification within those ligaments. Either it is synapomorphous for all taxa possessing epipleural bones, or it is homoplastic and has occurred independently in more than one lineage. The first interpretation (as in Patterson and Rosen, 1977) requires multiple losses in osteoglossomorphs (in Arapaima, the osteoglossid lineage, and in notopteroids according to Lauder and Liem's (1983, fig. 19) cladogram). The second interpretation requires multiple gains (Heterotis, elopocephalans, and at least one in “leptolepids”). We are unable to choose between the alternatives.

Patterson and Rosen (1977:126) and Lauder and Liem (1983) used presence of a long series of epipleural bones as a character of Elopocephala. The character remains uncontradicted (Tables 3, 4), and we add to it here the presence of proximally forked (with anterodorsal branches) epipleurals along some part of the series. Within elopocephalans, it is clear that epipleural bones have regressed, leaving only ligaments, on more than one occasion (e.g., the esocoid Novumbra and the stomiiform Pollichthys, Tables 4, 5). A decision on whether absence of epipleural bones in salmonoids and osmeroids (Table 4) is primary (primitive) or due to secondary loss can only be based on parsimony. Because they occur in elopomorphs, clupeomorphs, esocoids, ostariophysans, stomiiforms, and aulopiforms, we infer that epipleural bones were primitively present in elopocephalans, clupeocephalans, euteleosts, and neoteleosts, and that their absence in salmonoids and osmeroids is therefore secondary.

A more-derived state is complete absence of the epipleural series (no ligaments or bones). In nonacanthomorphs that we checked, epipleurals are completely absent only in Lepidogalaxias, Stokellia, and Retropinna.

The epipleural series of aulopiforms (Table 5) shows remarkable modifications that are discussed in detail in the section on aulopiforms below (p. 28). In brief, all aulopiforms are uniquely characterized by having epipleurals that extend forward to V1 or V2, and available evidence indicates that they have a different developmental pattern from that in other teleosts, where epipleurals develop rostrally and caudally from the region of the first caudal vertebra. In aulopiforms, epipleurals develop caudally from V3, V2, or V1. Furthermore, in most aulopiforms (all except Bathypterois and Parasudis in our sample) several or many of the anterior epipleurals have moved dorsally into the horizontal septum (notation B₃ in Table 5). As a consequence, the epicentral series is truncated rostrally in various aulopiforms.

Alepocephaloids have epipleurals that extend unusually far forward, to V3, and in at least some alepocephaloids the distribution of epipleurals (virtually confined to the abdominal region) is such that they evidently do not develop from around the first caudal vertebra but from a more anterior focus. Data on development are lacking for alepocephaloids.

EPICENTRALS.—As bones, epicentrals are the most restricted of the three classes of intermusculars in lower teleosts. They lie in the transverse septum, and, like epineurals, they generally develop in a rostrocaudal gradient, from the anterior vertebrae backward. Unlike epineurals and epipleurals, they are almost always simple rods, without the proximal or distal forking that occurs in the other two series (we have observed distal forking of epicentral bones only in Chanos and kneriid gonorynchiforms). Epicentral bones do not occur in osteoglossomorphs, except in the notopterid Notopterus where the epicentrals are Taverne's (1978) “supraventrales”; they extend from the occiput to about V30 (see the section on osteoglossomorphs, below). Among elopomorphs, epicentral bones occur only in Megalops (Table 3; Forey, 1973; Rosen, 1985, fig. 9A). They occur in all clupeomorphs (Table 3; Greenwood, 1968 on Denticeps; Owen, 1866, Phillips, 1942, Yabumoto and Uyeno, 1982, and Whitehead and Teugels, 1985 on clupeoids; Greenwood, and Whitehead and Teugels call the epicentrals epipleurals). In many clupeoids there is a broad, vertical chevron of cartilage at the distal end of the anterior epicentral bones (Figure 7A′, Plate 1G, and below). Among ostariophysans, epicentrals occur as bones in all gonorynchiforms except the diminutive Grasseichthys (Table 4; Patterson, Fink, and Fink, ms) and in gymnotoids (Mago Leccia, 1978, as “costillas dorsales”; our observations on cleared-and-stained specimens of Eigenmannia, Gymnotus, Hypopygus, and Sternopygus). Among aulopiforms, ossified epicentrals occur in the chlorophthalmid Parasudis, in Alepisaurus (Table 5), and in Omosudis.

As with epipleurals, when epicentral bones are absent in nonacanthomorphs, we find a series of ligaments with broadly the same distribution as the bones. These are the anterior oblique tendons (AOTs) of Kafuku (1950), who reported their presence in Anguilla, clupeoids, ostariophysans, Oncorhynchus, Plecoglossus, and Saurida among nonacanthomorphs. Kafuku did not discuss the distribution of epicentral ligaments (AOTs) along the vertebral column of those fishes. As Tables 3–5 show, epicentral ligaments often begin on the occiput, attach to the centrum, parapophysis, or rib head on abdominal vertebrae, and to the centrum on caudal vertebrae. The only fishes in Tables 3–5 in which we failed to find epicentral bones or ligaments are the umbrid Novumbra (of which we had only poor specimens) and derived aulopiforms, such as paralepidids, Bathysaurus, and Gigantura (Table 5 and below).

The primitive pattern of epicentral ligaments and/or bones is a rostrocaudal gradient, with the structures extending caudally from the occiput or anterior vertebrae. Major exceptions to that pattern are found in Umbra and many aulopiforms. In Umbra krameri (Table 4) the epicentral series is interrupted, with ligaments from the occiput to V5 (the last one or two weaker than their predecessors) and then a gap back to V17; in U. pygmaea we failed to find epicentral ligaments anteriorly and the series appears to begin at V18. In many aulopiforms (Table 5) the epicentral series is truncated rostrally.

Anterior epicentral ligaments contain distal cartilaginous rods, similar to those of Polymixia, in many salmonoids and most osmeroids (Table 4). In salmonoids, the cartilage rods occur both in coregonids (Coregonus lavaretus, Prosopium williamsoni, Stenodus leucichthys) and salmonids (Salvelinus alpinus, Salvelinus malma, Salmo salar, Salmo trutta, Figure 7B, Plate 1D, Thymallus thymallus, see below), implying that they are primitive for the group according to Sanford's (1990) cladogram. Their ontogeny is well known in Salmo (Emelianov, 1935). In the salmonid Thymallus, we have observed cartilaginous rods in about the first 10 epicentral ligaments in small specimens of T. thymallus (40–45 mm SL), but they are not evident in larger specimens (∼70–100 mm SL) of that species and of T. arcticus. In large Thymallus arcticus, Norden (1961) described and illustrated a series of “epipleural” bones that originate at the bases of the first eight ribs (V3–10) and are continuous with the head of the rib (like the anterior epicentrals in Clupea, Figure 7A). In our small specimens of Thymallus these bones are absent, and in larger specimens they are variable in number, and some or all of them may be independent of the rib (Table 4). We interpret the bones as epicentrals and as autapomorphous for Thymallus within salmonoids. (Norden (1961:736) reported a similar series of bones, apparently fused to the rib, in five out of 14 specimens of Salvelinus fontinalis, where they occurred on from 15 to 23 ribs. They were absent in other species of Salvelinus. The Salvelinus we examined (S. alpinus and S. malma) have cartilaginous rods in the epicentral ligaments and no epicentral bones.) In osmeroids, cartilaginous epicentrals occur both in northern taxa (Osmeroidea of Begle, 1991; Hypomesus, Mallotus, Plecoglossus, Figure 7C, in which they are particularly well developed) and in southern taxa (Galaxioidea of Begle, 1991; Galaxias, Plate 1H, Prototroctes, Retropinna, Stokellia). As with salmonoids, the distribution of cartilaginous epicentrals in osmeroids implies that they are primitive for the group according to Begle's (1991) cladogram. In Lepidogalaxias, which Begle (1991) placed as the sister group of Salangidae + Galaxiidae, the first six epicentral ligaments contain bone distally (Table 4), and the bone has the form of the epicentral cartilages in other osmeroids and in salmonoids, i.e., it is superficial, irregular in outline, and forked distally. We predict that it ossifies as cartilage bone, and it is an autapomorphic state of the osmeroid/salmonoid cartilaginous epicentral. Cartilaginous epicentrals also occur in the stomiiform Maurolicus, but not in the other stomiiforms that we have checked (Table 5).

FIGURE 7.—Anterior vertebra and its appendages with associated epicentral cartilages in A and A′, Clupea harengus L.; B, Salmo salar L.; and C, Plecoglossus altivelis Temminck and Schlegel. Cartilage is stippled and intermuscular bones are in solid black. A, Fourth vertebra of BMNH 1970.2.17.22, ~ 65 mm SL. In Clupea, epicentrals are fused with the head of the pleural rib on anterior vertebrae and do not become independent until about the 20th vertebra. Anterior epipleurals lie free in the musculature (notation B₀, as in Table 3) so that the apparent epicentral position of the epipleural is illusory. A′, Tip of epicentral and associated cartilage chevron, after Göppert (1895, fig. 4; Göppert gave no scale or indication of size of fish from which he made the preparation). B, Fifth vertebra of BMNH 1981.9.22.11, 57 mm SL. C, Fourth vertebra of BMNH 1984.12.6.16, - 65 mm SL. (Scale bar 1 mm.).

Ontogeny of the epicentral cartilages in Salmo was the basis for Emelianov's (1935) distinction of ventral (our pleural) ribs from dorsal ribs (our epicentrals) by the criterion of centrifugal development (ventral ribs) versus centripetal development (dorsal ribs). Epicentral cartilages of Salmo first appear at about 30 mm TL as cartilaginous anlagen in the distal part of the horizontal septum, immediately beneath the lateral line nerve (Emelianov, 1935, fig. 20). They later extend medially toward the vertebrae as cartilage rods in the horizontal septum (Figure 7B); Lepidogalaxias (above) is the only fish known to us in which epicentral cartilages ossify. Emelianov regarded the ossifed epicentral of clupeoids (Clupea, Alosa) and the associated distal cartilage chevron (Figure 7A,A′) as together homologous with the cartilaginous epicentral in Salmo. But our observations of the clupeoid cartilage chevron indicate that there is no histological continuity or structural association between it and the epicentral bone, whose distal tip is merely surrounded by the cartilage, not in continuity with it. In salmonoids and osmeroids, the distal part of the cartilaginous epicentral is bifid, resembling the superficial cartilage chevron in clupeoids (Figure 7A′,B,C, Plate 1D,G,H).

In summary, there are four kinds of epicentrals: (1) epicentral ligaments, which we take to be the primitive teleostean condition; (2) epicentral bones (Notopterus, Megalops, clupeomorphs, gonorynchiforms, Thymallus, Parasudis, Alepisaurus, Omosudis, gymnotoids), which are membrane bones within the epicentral ligament; (3) ligaments containing rod-like epicentral cartilages (salmonoids, osmeroids, Maurolicus, Polymixia); (4) superficial ossifications in the distal part of the ligament (Lepidogalaxias), which we take to be ossified epicentral cartilages. Epicentral cartilages (3) develop centripetally, whereas epicentral bones (2), judging by their configuration, develop centrifugally except in the special case of Lepidogalaxias (4). The cartilaginous chevrons associated with the tips of epicentral bones in clupeoids are merely superficial and are not associated with epicentral ligaments. Because epicentral bones and cartilage chevrons coexist in clupeoids, with no structural or developmental continuity between them, they cannot be homologous. Emelianov (1935) therefore was mistaken in using the clupeoid condition as an intermediate stage in generalising the centripetal development of the epicentral cartilages in Salmo; the antithetic states of centripetally developed cartilage (e.g., salmonoids, Polymixia) and centrifugally developed bone (e.g., gonorynchiforms, Parasudis) imply that these two kinds of epicentrals (2, 3) are not homologous.

POSTERIOR OBLIQUE TENDONS (POTs of Kafuku, 1950).—Among lower teleosts considered in this section, Kafuku (1950) recorded POTs in one elopomorph (Anguilla), three clupeomorphs (Clupea, Sardinella, Clupanodon), several ostariophysans (Chanos, three cyprinids, a cobitid), a salmonoid (Oncorhynchus), an osmeroid (Plecoglossus), and an aulopiform (Saurida). We confirm Kafuku's observation that in Cyprinus POTs penetrate the intervening epicentral ligaments en route to their insertion in the lateralis muscles.

Our most complete observations of POTs in lower teleosts were in the 164 mm SL Albula recorded in Table 3; significantly, this is about the largest of our cleared-and-stained specimens. In this fish the POTs in the abdominal region originate below the epicentral ligaments, from the ribs anteriorly and the parapophyses posteriorly. Each of them fans out immediately into a large number of small ligaments, so that in the abdominal region the horizontal septum is filled by evenly spaced, close-packed subdivisions of the POTs, all running obliquely forward at an acute angle to the long axis of the fish. Each epicentral ligament is crossed by the subdivided POTs originating on about 10 vertebrae behind that on which it originates. The epicentral ligaments lie on the upper side of the horizontal septum, dorsal to the POTs, which lie in that septum, and the segmental vessels run out on the underside of the septum, beneath the POTs. In the caudal region, POTs become less subdivided, more coherent and so easier to individualize. As an example, the epicentral ligament originating on V51 (PU21) is attached distally to subdivisions of the POTs from V58 and V59 (PU14–13). The last epicentral ligament originates on V53 (PU 19). It is short and is attached distally to the innermost branch of the POT from V59. We have observed POTs in Hiodon, Osteoglossum, notopterids, Elops, Anguilla, clupeoids, Umbra, Chanos, cypriniforms, and stomiiforms, but not in Esox or Gonorynchus and in no salmonoids or osmeroids, no aulopiforms (except Synodus), and no myctophiforms. We failed to find POTs in small cleared-and-stained Amia and Lepisosteus. However, Westneat et al. (1993) reported POTs (and AOTs or epicentral ligaments) in the salmonid Oncorhynchus, in Amia, Lepisosteus, and even in sharks (Carcharhinus). They gave no size range for the fishes examinined.

MYORHABDOI.—In various lower teleosts there are one or two extra series of unattached intermuscular bones, developed respectively in the uppermost and lowermost forward flexures of the myosepta. These bones, which were named myorhabdoi by Chapman (1944), occur, for example, in Notopterus (Taveme, 1978, and the section on osteoglossomorphs, below), some species of the congrid eel Ariosoma (Smith 1989, figs. 516, 517), many clupeoids (which generally have only the dorsal series, or have that series much better developed than the ventral series; Grande, 1985, figs. 10, 11; Chapman, 1944, fig. 14), gymnotoids (Mago Leccia, 1978; our observations on several genera), and the stomiiform Triplophos. Notopterids have two additional series that we interpret as myorhabdoi: one in the epineural position, following behind the true or attached epineurals, and one in the epipleural position (see the section on osteoglossomorphs, below). Notopterus has two further series of myorhabdoi: one (Taverne's, 1978, “centro-vertébrales”) oriented obliquely posteroventrally between the epineurals and epicentrals on about V1–25, and one associated with the anterior epicentrals, on the occiput and about V1–5 (see the section on osteoglossomorphs, below). In our opinion, myorhabdoi are adventitious structures, typical of long-bodied, laterally compressed fishes. Anchoa and Xenomystus are the only tabulated genera that have them, and we have entered them (notation M, Table 3) only in the latter.

OCCIPUT, CRANIAL RIBS AND INTERMUSCULARS, AND ACCESSORY NEURAL ARCH.—There has been much debate, historical and recent, over the composition of the occiput in teleosts. It frequently has been asserted that one or more vertebrae, or a “half-centrum,” have fused with the occiput in one teleost or another. Rosen (1985) gives the most recent review of the question.

Allis (1898, 1903) showed that in Scomber the configuration of the anteriormost myotomes and the attachment of their myosepta to the occiput are the same as in Amia, given that in Amia two vertebrae fuse with the occiput during ontogeny. One useful landmark in homologising occipital structures is the internal limb of the posttemporal, which lies in the first myoseptum (between myomeres 1 and 2) and attaches to the intercalar proximally. Among teleosts surveyed in Tables 3–5, the only one with an intermuscular originating on the intercalar is Gonorynchus (En Ic, Figure 4). There, the bone is in series with the epineurals, and, together with the internal limb of the posttemporal (represented only in ligament in Gonorynchus), it passes out toward the posttemporal and must lie in the myoseptum. In Scomber, the second and third myosepta attach to the occiput close behind (i.e., posteromedial to) the first myoseptum, and Baudelot's ligament lies in the third myoseptum; the fourth myoseptum attaches to the first vertebra and contains the first epineural (Allis, 1898, 1903). The match between anterior myosepta in Amia and Scomber (Allis, 1898) implies that the pattern in Scomber is general for teleosts. If so, no teleost should have more than three serially homologous intermusculars on the braincase, unless one or more vertebrae are fused into the occiput, and none we know of has more than three. Among lower teleosts surveyed in Tables 3–5, Albula, Chanos, and Gonorynchus have three such bones. In Albula, the three are in series with the epineurals; the first two are branched proximally and extend into the posttemporal fossa without direct attachment to the braincase, and the third attaches to the exoccipital by ligament. They must lie in myosepta 1–3. In Chanos, the three bones are also in series with the epineurals, but they represent only the anteroventral branches of those bones; like the first two bones in Albula, they extend into the posttemporal fossa without direct attachment to the braincase, and they must lie in myosepta 1–3. In Gonorynchus, the first of the three bones is an epineural in myoseptum 1 (above), and the other two each represent fusion between an epicentral and the anteroventral branch of an epineural; these two originate respectively on the exoccipital and basioccipital and must lie in myosepta 2 and 3. There is thus no evidence from the segmental intermusculars that any teleost has a vertebra fused into the braincase, and the constancy of origin of the first rib on V3 (Tables 3–5) is corroborative. In fact, among lower teleosts that we survey in Tables 3–5, there is evidence of ontogenetic fusion of a vertebra into the occiput only in Heterotis (Daget and D’Aubenton, 1957). That fusion is reflected in the ligaments and ribs, because both Baudelot's ligaments (double in Heterotis) originate on the braincase, and the first rib is on V2. In one specimen of Heterotis, the BMNH skull described by Ridewood (1905), the fusion is incomplete, and the second Baudelot's ligament (ossified) remains on the vertebral centrum. The example of Heterotis implies that where a vertebral fuses with the braincase in lower teleosts, it will carry Baudelot's ligament. In Esox, Jollie (1975:78) wrote that the basioccipital “includes the first vertebral body,” but he presented no developmental evidence for this apart from presence of an accessory neural arch (see below). Baudelot's ligament is on V1 in Esox (Figure 8, Table 4).

Fink and Fink (1981:326) pointed out that an unattached neural arch in front of that of V1 (Rosen's, 1985, accessory neural arch; abbreviated ANA here and in Tables 3–5) probably is primitive for teleosts and is absent in all ostariophysans. They recorded presence of ANA in Elops, the clupeoids Dorosoma, Harengula, and Anchoa, and in Esox and the stomiiform Diplophos. Tables 3 and 4 show that ANA is absent in the osteoglossomorphs in our sample, absent in Megalops, Albula, Halosaurus, Notacanthus, and Anguilla amongst elopomorphs, present in Clupea and Chirocentrus, but absent in Denticeps, Clupeichthys, and Jenkinsia amongst the clupeomorphs in our sample, absent in Umbra and Novumbra, and, according to our sample, is present in salmonids, alepocephaloids, and northern osmeroids, but absent in argentinoids and southern osmeroids. In stomiiforms, ANA is present in a number of genera (in addition to Diplophos), which are rated as primitive members of the group on other criteria (A.S. Harold, pers. comm., 1993). Among aulopiforms (Table 5), ANA is present in Aulopus, synodontids, and harpadontids but is absent elsewhere. It does not occur in ctenosquamates (myctophiforms plus acanthomorphs). We note that Rosen (1985, fig. 9) illustrated an ANA in Albula, but we have examined several specimens, including an ontogenetic series, and have not found the structure.

Fink and Fink (1981:326) also reported ANA in Polypterus and Amia, implying that the structure is primitive for actinopterygians. There is no ANA in those fishes, because the occipital neural arch(es) is associated with vertebrae fused into the occiput during ontogeny (Jollie, 1984a, 1984b). We have not observed ANA, nor is one reported, in Mesozoic stem group teleosts such as pholidophorids, leptolepids, and ichthyodectiforms.

Given the mosaic pattern of presence and absence of ANA in lower teleostean groups, there are two possible interpretations: either it is synapomorphous at some level and has been lost repeatedly, or it has arisen repeatedly and is nonhomologous from group to group. If it is synapomorphous, according to the information summarized above and in our tables, it appears to be an elopocephalan character, as it is not recorded in osteoglossomorphs or nonteleostean actinopterygians. Treating ANA as an elopocephalan character would require that it be lost at least 10 times (at least once in elopomorphs, at least twice in clupeomorphs, and in at least seven different euteleostean lineages—ostariophysans, esocoids, argentinoids, osmeroids, stomiiforms, aulopiforms, ctenosquamates). Treating ANA as independently acquired demands that it arose once in Elops, at least once in clupeoids, in Esox, in alepocephaloids, in salmonoids and/or osmeroids, and in stomiiforms and/or aulopiforms, with subsequent loss within several of those groups. A choice between these alternatives ultimately will have to be made on grounds of parsimony, presumably with differential weighting for gain and loss of ANA. We need a more robust cladogram of teleosts and a more extensive survey for ANA before any rational decision is possible, but in our analysis of aulopiforms (Figure 11, Table 6) ANA was resolved as a derived character.

We have no useful conjecture on the origin of ANA, although we are convinced, for reasons discussed at the beginning of this section, that it does not represent the remains of a missing vertebra.

BAUDELOT'S LIGAMENT.—Baudelot's ligament is the name now given to the stout ligament that originates on the ventrolateral aspect of an anterior vertebra (usually the first) or the occiput (usually the basioccipital) proximally and inserts on the supracleithrum distally, usually after looping around the upper part of the cleithrum. As an aside, we think it worth clarifying the origin and history of the term, so far as we have been able to understand it.

Baudelot (1868:83–84) seems to have been the first to notice the ligament, and he named it the “scapulo-vertébral” ligament. That name was used by subsequent late nineteenth- and early twentieth-century European authors (e.g., Siebenrock, 1901), and it was used in the early 1960s by Monod (1960:631, with a reference to Baudelot, 1868; 1963:271, as “ligamentum scapulo-vertébrale de BAUDELOT”). Baudelot's term was not used by early twentieth-century Anglophone authors, such as Starks (1904b:258–259; 1923:267) or Allis (1903:103, 110; 1909:36, 57, as “occipito-supraclavicular ligament”). In 1962, Weitzman (1962:42) called it the “trans-scapular ligament,” and Rosen (1962:8) called it the “ligamentous support.” Thus, the name “Baudelot's ligament” does not seem to have been current in the early 1960s. The earliest use of the term that we have found is in Rosen (1964:241) when he stated that “the shoulder girdle is attached by a ligament (Baudelot's ligament) to the basicranium.” In Greenwood et al. (1966) the term “Baudelot's ligament” is used several times (pp. 352, 353, 354, 388, 389, 392), but on p. 386, in a part written by Weitzman, the structure is called the “transscapular ligament,” as in Weitzman's earlier (1962) work. Our guess is that the term “Baudelot's ligament” was coined by Rosen (1964:241), perhaps intentionally but more probably through misreading of Monod's (1963:271) phrase “ligamentum scapulo-vertébrale de BAUDELOT.” The term soon gained general acceptance through repeated use in the widely read paper by Greenwood et al. (1966).

FIGURE 8.—Anterior vertebrae and associated structures in A, Esox lucius L., ROM 598 CS, 62 mm SL; B, Esox americanus Gmelin, BMNH 1982.11.60.16, 61 mm SL. The intermuscular bones are in solid black, except for proximal parts of anterior epineurals that are broadly fused to neural arches, where fusion is indicated by stipple. The ligaments are shaded. (Scale bars 1 mm.) (Abbreviations: ANA, accessory neural arch; V₀, intermuscular representing unattached anteroventral limb and posterior body of an epineural. Intermusculars and ribs are numbered or labeled according to vertebra (number) with which they are associated.)

Tables 3–5 show that the origin of Baudelot's ligament on V1 is remarkably constant in lower (nonacanthomorph) teleosts. The only exceptions that we have found are as follows. In the osteoglossomorphs Heterotis and Osteoglossum and the cobitid Acanthopsoides there are two ligaments, one on the basioccipital and one on V1 (that on V1 is ossified in Heterotis, in which V1 is fused with the basioccipital). In Galaxias there are also two ligaments, one from the basioccipital and one from V1, which join distally before attaching to the supracleithrum. In the characoid Alestes, the ligament is on the basioccipital; according to Fink and Fink (1981:335) this is true of all characiphysans (characiforms and siluriforms) and of several cypriniforms. In the paralepid aulopiforms Paralepis and Macroparalepis there is a ligament with an origin extending from V1 to V2, whereas the aulopiform Alepisaurus has the origin of the ligament extending from V2 to V4 (we have observed the same condition in Omosudis). The clupeoid Chirocentrus has an ossified ligament with a double attachment, to the anteroventral corner of V3 and to the posteroventral corner of V2. The ligament on V1 is ossified in the engraulid Anchoa, the stomiiform Diplophos, and the harpadontid aulopiforms Harpadon and Saurida among our sample. It also is ossified in Dallia (Nelson, 1972; Wilson and Veilleux, 1982). Finally, Baudelot's ligament is absent in Notacanthus, gonorynchiforms, the catostomid Hypentilium, and the aulopiform Gigantura; in Anguilla a sheet of ligament with origins on V1-5 attaches to the supracleithrum; some or all of these may be homologous with Baudelot's ligament.

RIBS.—Ribs of teleosts are primitively preformed in cartilage and ossify as cartilage bones, but in many teleosts some or all ribs ossify as membrane bone (Emelianov, 1935; Faruqi, 1935). Although our criterion for distinguishing ribs formed in cartilage from those formed in membrane bone (the configuration of the tip in cleared-and-stained specimens) is less refined in comparison with the serial sectioning used by Emelianov, Faruqi, and others, the survey in Tables 3–5 is probably the most extensive yet published. All ribs are preformed in cartilage in the osteoglossomorphs, elopomorphs, and clupeomorphs in our sample, with two exceptions. The first is a diminutive rib in membrane on V2 in our Heterotis and Osteoglossum and on V3 in Xenomystus. The second includes the elopomorphs Halosaurus, in which most ribs are in membrane but the last dozen are in ligament, Notacanthus, where 911 the ribs are in ligament, and Anguilla, where the first few ribs are in ligament and the remainder are in membrane. Among nonacanthomorph euteleosts, all the ribs are preformed in cartilage in Chanos and in the salmonoids, alepocephaloid, osmerids, retropinnid, galaxiid, stomiiforms, and myctophiforms in our sample (Tables 4, 5). In Esox, the first one (E. americanus) to three (E. lucius) ribs form in membrane bone and are coossified with the parapophysis, a configuration that occurs elsewhere (to our knowledge) only in the highly modified first two ribs (tripus, on V3, and transformator process, on V4) of otophysans. In Umbra and Novumbra, the first rib is in membrane and the rest (or all but the last) are in cartilage. Among gonorynchiforms, Gonorynchus has all but the first rib in membrane, whereas Parakneria has the first and about the last eight in membrane. The ribs (other than those on V3 and V4) are in cartilage in the otophysans in our sample, except in the cobitid Acanthopsoides, where they are all in bone. The argentinoid Glossanodon has about the last 10 ribs in membrane, and Lepidogalaxias has them all in membrane. In aulopiforms, the condition ranges from the last few ribs in membrane (Parasudis, Scopelosaurus, Coccorella) or only the first in membrane (Bathysaurus), through most of them in membrane (Chlorophthalmus, Bathypterois, Ahliesaurus, Scopelarchoides), to all ribs in membrane (the remainder of the genera sampled in Table 5).

Ribs of nonacanthomorph teleosts are, in our experience, restricted to the abdominal region, where they always lie in the peritoneal membrane.

As with the origin of Baudelot's ligament on V1, origin of the first rib on V3 is remarkably constant in lower teleosts. Exceptions in Tables 3–5 are the first rib on V1 in the aulopiforms Paralepis and Alepisaurus (and Omosudis); first rib on V2 in Heterotis, Osteoglossum, all esocoids, Searsia, Osmerus, Lepidogalaxias, Galaxias, Bathypterois, and Harpadon; on V4 in Megalops and Pseudotrichonotus; on V5 in Halosaurus and the aulopiforms Macroparalepis, Synodus, and Trachinocephalus; on V6 in Elops; and on V15 in Notacanthus, in which all ribs are in ligament. In Paralepis, Alepisaurus, and Omosudis, the only teleosts we have found with ribs on V1, the ribs on V1 and V2 are fused to the centrum (Table 5), another unique feature of these genera.

The “cranial ribs” of Gonorynchus (two pairs on the occiput, one on V1) lie in the peritoneal membrane, which is the position of ribs, but we do not believe that they are serially homologous with ribs. They appear to be an extra series of intermuscular bones, which is autapomorphous for gonorynchids.

COMMENTS ON INDIVIDUAL GROUPS AMONG LOWER TELEOSTS

In this section we comment on aspects of the intermuscular bones, ligaments, and cartilages in various major groups that may bear on relationships.

OSTEOGLOSSOMORPHS.—We recorded the intermuscular bones and ligaments in only four osteoglossomorphs, Hiodon, Osteoglossum, Heterotis, and Xenomystus (Table 3), and our specimens were far from ideal. Nevertheless, it is worth noting that Hiodon exhibits what we take to be the most primitive condition found in any Recent teleost, with all epineurals unbranched and fused to the neural arches proximally, epineural ligaments extending the epineural series caudally, a series of epicentral ligaments from the occiput back into the caudal region, and a short series of epipleural ligaments in the middle part of the trunk. Osteoglossum, Heterotis, and Xenomystus are more derived, with all (Heterotis, Xenomystus) or most (Osteoglossum) of the epineurals free from the neural arches, and Heterotis has all the epipleurals ossified whereas Xenomystus has two series of bones that we interpret as myorhabdoi (below), one succeeding the epineurals and one in the epipleural position. The osteoglossoid Pantodon agrees with Hiodon in having all the epineurals (except the first) fused with the neural arch (Taverne, 1978), but we have seen no good cleared-and-stained material of Pantodon, and so we cannot comment on its ligaments. Arapaima (Taverne, 1977b, and our observations) is derived in lacking epineurals on about the first 20 vertebrae, and in having the anterior epineurals on the parapophysis.

Among notopteroids, in addition to Xenomystus (Table 3), we examined specimens of mormyroids (Gymnarchus, Isichthys, Marcusenius) and the other two notopterid genera (Notopterus, Papyrocranus), and Taverne (1972, 1978) has given good descriptions of the osteology of all genera in the two groups. The two groups agree in having only a short series of epineural bones that are attached (not fused) to the neural arches (in Notopterus and Gymnarchus) or centra (in mormyrids, Xenomystus, and Papyrocranus): on V4 to about V15 in Gymnarchus, VI to about V10 in mormyrids, V1 to about V13 in Notopterus, V1–16 in Papyrocranus, and V1–7 in Xenomystus. In mormyrids and notopterids (except Notopterus) there are epineural ligaments beyond the short series of attached epineural bones. In mormyrids there are no further epineural bones, but in Xenomystus and Papyrocranus each epineural ligament fans out distally, and beginning immediately behind the last attached epineural bone there is a long series of superficial, lath-like bones that are remote from the vertebrae and loosely attached to the diffuse ligaments; we interpret them as myorhabdoi (notation M in Table 3, and see below). In Notopterus, where there are no epineural ligaments behind the last attached epineural bone (~V13), there is an abrupt transition from attached epineural bones to superficial, unattached bones that are deeply subdivided or frayed anteriorly; as with the lath-like bones in other notopterids, we interpret them as myorhabdoi. A long series of epicentral ligaments and a short series of epipleural ligaments are present in mormyrids and notopterids, and in Notopterus the epicentrals are ossified on about V1–30 (Taverne's, 1978, “supraventrales,” below).

In notopterids, Taverne (1978) described a long series of epipleural bones in each of the three genera. Our interpretation differs. The epipleurals of the osteoglossoid Heterotis have the same form as in other teleosts; they are rod-like bones, in direct continuity with the epipleural ligament (as in Plate 2H). But in notopterids they have a different configuration, and they differ between the three genera. In Papyrocranus, the most anterior “epipleural” is about at the level of the first caudal vertebra (~V16), and epipleural ligaments are present from about V14 to about V35. The “epipleural” bones are superficial and lath-like. The epipleural ligaments fan out distally, and, in segments with both “epipleurals” and ligaments, the diffuse ligament attaches loosely and broadly to the posterior end of the bone. In Xenomystus (Table 3), the “epipleural” bones extend forward to about V4, but, as in Papyrocranus, epipleural ligaments extend forward only to the antepenultimate abdominal vertebra (V9); they extend back to about V22. In segments with both epipleural ligaments and bones, the bones are shaped rather like a single-blade propellor, and, as in Papyrocranus, the epipleural ligaments fan out distally, but they attach broadly to the middle of the bone rather than to its posterior end. Thus, in Xenomystus and Papyrocranus the “epipleural bones” have the same relationships as the unattached “epineural bones” above them. Because the “epipleural bones” do not resemble the epipleurals in any other teleosts, and because we know of no other teleost in which there is an abrupt transition from an attached epineural on one vertebra to a superficial, lath-like epineural on the next, we believe that both series of bones are myorhabdoi (notation M in Table 3), which is autapomorphous for notopterids.

In Notopterus, the intermusculars are much more complex than in Xenomystus and Papyrocranus. Taverne (1978) described six series of epipleurals. The uppermost and lowermost series (Taverne's “supradorsales” and “infraventrales”) resemble and correspond to the myorhabdoi of clupeoids and gymnotoids. As described above, behind the last attached epineural (~V13) there are no epineural ligaments, and there is an abrupt transition from attached epineural bones to unattached, superficial bones that we interpret as myorhabdoi, as in Xenomystus and Papyrocranus. The epicentrals are ossified from the occiput to about V30 (Taverne's “supraventrales”), and on the occiput and the first four or five vertebrae they are accompanied by extra ossifications (myorhabdoi), so that there may be up to four additional bones in the myoseptum lateral to the epicentral (Taverne, 1978, figs. 76, 77). Between the epicentrals and the epineurals, from the occiput to about V25, there is a further series of small, irregular, unattached intermusculars (Taverne's “centro-vertébrales”) that are inclined posteroventrally. The anterior members of this series are more dorsally placed, rising upward medial to the epineurals and decreasing in size anteriorly. We take them to be another series of myorhabdoi, which is autapomorphous for Notopterus. Finally, Notopterus has the series of intermusculars described as epipleurals by Taverne (1978). They extend from about V8 back to the tail, and most of them resemble the epineural myorhabdoi above them, being brush-like or fimbriate at both ends (Taverne, 1978, figs. 78–80). There are epipleural ligaments from about V8 to V30. Most of these ligaments fan out distally and attach loosely or diffusely to the middle part of the “epipleurals,” as in Papyrocranus, but the ligamentous attachment moves toward the anterior part of the bone in the anterior “epipleurals,” and the first two or three members of the “epipleural” series (∼V8–10) are small, rod-like bones attached to the ligament by their anterior tips. Thus, the first two or three members of this series resemble true epipleurals (as in Plate 2G,H or Heterotis, for example), but the great majority of them resemble the lath-like bones in the epipleural position in Xenomystus and Papyrocranus that we interpret as myorhabdoi. In other lower teleosts with epipleural bones, the ligamentous attachment is best developed in the middle of the series (examples in Tables 3, 4), not in its first few members. Thus, in Notopterus, as in Xenomystus and Papyrocranus, the “epipleurals” do not agree with those bones in other teleosts, and as in those genera, we interpret them as myorhabdoi. In short, among notopterids, Xenomystus and Papyrocranus have two series of myorhabdoi, one in the epineural and one in the epipleural position, whereas Notopterus has six series of them: one dorsal and one ventral, corresponding to the myorhabdoi of other teleosts (e.g., clupeoids, gymnotoids); one in the epineural and one in the epipleural position, corresponding to the myorhabdoi in other notopterids; and two autapomorphous series, one between the epicentrals and epineurals and one accompanying the epicentrals on the occiput and first few vertebrae.

Although there are reasons to believe that Hiodon is related to notopteroids, it generally is agreed that “of all osteoglossomorphs, the Hiodontidae show the greatest aggregate of primitive characters” (Greenwood, 1973:314). The intermusculars bear out this assessment.

ELOPOMORPHS.—We record the intermuscular bones and ligaments in Elops, Megalops, Albula, Halosaurus, Notacanthus, and Anguilla (Table 3). In comparison with the basic generality of Hiodon, these elopomorphs share several derived features with clupeomorphs and lower euteleosts: (1) some epineurals are not fused with the neural arch; (2) some epineurals are forked proximally (not found in Anguilla, but present in many other eels, e.g., Smith, 1989, figs. 516, 517); (3) there is an extensive series of epipleural bones, covering at least one-third of the abdominal region and most of the caudal region; (4) some epipleurals are forked proximally (again, not found in Anguilla but present in many other eels). Characters (2) and (4) almost always co-occur, but Esox (Table 4) shows that co-occurrence is not consistent.

In Halosaurus, the last dozen ribs are in ligament, whereas in Notacanthus all ribs are in ligament; this derived condition is probably synapomorphous for halosaurs and notacanths. Albula, Notacanthus, and Anguilla share an extensive series of anterior epipleural ligaments, extending forward to V10 in Albula and Notacanthus, and to V7 in Anguilla. In Halosaurus there are epipleural ligaments from V37 to V57 and bones thereafter.

CLUPEOMORPHS.—We record the intermusculars in Denticeps and five clupeoids, the clupeine Clupea, the pellonuline clupeid Clupeichthys, the dussumieriine clupeid Jenkinsia, the engraulid Anchoa, and the chirocentrid Chirocentrus (Table 3). All have ossified epicentrals, but in other respects Denticeps (the only member of the suborder Denticipitoidei) is very different from clupeoids. Denticeps lacks epineurals on V1–11, has epineural ligaments on V12–19, and the first ossified epineural on V20; these conditions are unique among the teleosts we have sampled, although Arapaima, with the first epineurals on the parapophyses of V21 (Taverne, 1977b:229) or V22–24 (pers. obs.) approaches it. The epipleural series in Denticeps is confined to the caudal region, whereas in clupeoids it extends very far forward (to V3 in Clupeichthys, to V2 in Clupea, Jenkinsia, and Anchoa, and even to the occiput in Chirocentrus, where there are two cranial epipleurals, each fused proximally with one of the two epicentrals on the occiput). The epicentral series in the three clupeids and Chirocentrus share one feature that is almost unique among the teleosts that we record in Tables 3–5: fusion of the epicentral with anterior ribs. That fusion occurs on about the first 20 ribs in Clupea and Clupeichthys (recorded in Clupea by Chabanaud, 1942; also present in Sardinops, Phillips, 1942; and observed by us in the clupeines Harengula, Opisthonema, and Sprattus), on about 8–10 ribs in Jenkinsia (as in the dussumieriine Spratelloides; observed on about 12–15 ribs in Etrumeus), and on 6–7 ribs in Chirocentrus. This rib/epicentral fusion also may occur on a few ribs in the salmonid Thymallus (Table 4 and below). It does not occur in pristigasterids that we checked (Chirocentrodon, Ilisha, Odontognathus, Opisthopterus, Pellona), or in other engraulids (Engraulis, Cetengraulis) or in the coiliids (sensu Grande and Nelson, 1985) Setipinna and Thryssa; the derived coiliid Coilia is an exception, for the first rib is enlarged and fused with the epicentral. The rib/epicentral fusion occurs on about the first 20 ribs in alosines (Alosa, Brevoortia) and on the first few ribs (up to about eight) in dorosomatines (Anodontostoma, Dorosoma). In Clupea, the fusion is ontogenetic, at about 40 mm TL (Ramanujam, 1929). It may not occur in the diminutive pellonuline Sierrathrissa (Whitehead and Teugels, 1985, figs. 33, 34), which reaches only 30 mm SL. This rib/epicentral fusion certainly is derived, and it suggests that chirocentrids and clupeids (clupeines, alosines, dorosomatines, dussumieriines, and pellonulines) form a monophyletic group. This would give further support to Grande's (1985, fig. 9) scheme, in which he cited only one character supporting that grouping (Clupeoidea), “increase in pleural rib to preural vertebrae ratio,” a character that may not be derived.

Cartilage chevrons at the tips of epicentrals are recorded in all clupeoids except Chirocentrus in Table 3. They are found only in clupeoids among lower teleosts, although similar structures are associated with epineurals in holocentrids and the stephanoberyciform Rondeletia (Table 7 and below). Emelianov (1935) recorded cartilage chevrons in Clupea (Clupeinae) and Alosa (Alosinae); we have observed them in other clupeids (e.g., Cynothrissa, Plate 1G, Pellonula, Sierrathrissa) and engraulids (Engraulis, and in Stolephorus at 40 mm SL, although not in Cetengraulis at 55 mm) and in the coiliid Thryssa (although not in Setipinna at 80 mm SL). Lance Grande (pers. comm., 1992) has observed them in the clupeines Harengula and Sardinella and the dorosomatine Dorosoma, but not in his specimens of the clupeine Lile, the dorosomatine Nematalosa, the dussumieriine Etrumeus, or the coiliid Coilia (in our Coilia, BMNH 1979.8.24.133-4, ∼110 mm SL, there are diminutive chevrons on the first five or six epicentrals in one specimen but none in the other). Cartilage chevrons do not occur in the pristigasterids we checked (Chirocentrodon, Ilisha, Odontognathus, Opisthopterus, Pellona) or in the three double-stained Chirocentrus that we have seen. They might be synapomorphous, indicating that Engrauloidea are more closely related to Clupeoidea than are Pristigasteroidea (cf. Grande, 1985, fig. 9), but their distribution, so far as we have been able to check, is not congruent with the epicentral/rib fusion discussed above, which groups Chirocentrus with clupeids. We have not seen enough double-stained clupeoids (the cartilage chevrons are detectable only with alcian blue) to resolve this conflict.

The intermusculars of clupeoids show some remarkable complications (e.g., Whitehead and Teugels, 1985, on Sierrathrissa) and a comprehensive study could well be profitable.

OSTARIOPHYSANS.—Fink and Fink (1981) gave further substance to the idea, first proposed by Rosen and Greenwood (1970), that gonorynchiforms are the sister group of otophysans; the two groups together make up the Ostariophysi. The anterior intermusculars, which were not considered by Fink and Fink (those of Chanos and Gonorynchus were discussed by Rosen and Greenwood, 1970), are relevant here. In Table 4 we record the intermusculars of four otophysans, a characiform (Alestes), and three cypriniforms: a cyprinid (Hemibarbus), a cobitid (Acanthopsoides), and a catostomid (Hypentelium). In these forms, intermusculars of the first four or five vertebrae are modified, evidently in association with development of the Weberian apparatus. In all four genera the epicentral series is interrupted or truncated anteriorly in the region of the Weberian apparatus. In all four genera the epineurals are forked proximally (back to about V30 in Alestes, Hemibarbus, and Hypentelium, and to about V25 in Acanthopsoides), and the anteromedial (primary) branch of the epineural is attached to the neural arch by ligament. There are no medial branches or ligaments anterior to V5 in Alestes, V6 in Acanthopsoides, and V12 in Hypentelium. But in Hemibarbus, epineurals are attached by ligament forward to VI (except on V2, which lacks an epineural). Epineurals without medial branches or ligaments on anterior vertebrae are represented only by the anteroventral branch and the posterior body (notation V₀ in Table 4). The anterior tips of these epineurals tend to establish connections with other structures.

In Alestes, the epineural of V4 has an extra bifid or trifid ventral branch from its proximal end, with ligaments running down to the swimbladder from the tips of those branches, and the epineural of V3 has a ligament from its proximal end running to the anterior tip of the transverse process of the third neural arch (which is a structure unique to characiforms; character 71 of Fink and Fink, 1981:329). The anterior tips of the epineurals of V1 and V2 in Alestes are without obvious ligamentous attachment, and anterior to them there is one further epineural passing forward into the posttemporal fossa.

In Acanthopsoides, where the first epineural with a (primitive) anteromedial branch to the neural arch is on V6, the anteroventral tip of that epineural is bifid and extends downward toward the proximal part of the rib of V5, where it attaches to the epicentral ligament. The anteroventral tip of the epineural of V5 is expanded and bifid, and it is attached to the epicentral ligament of V5 close to its origin on the proximal part of the rib. The anteroventral tip of the epineural of V4 is much expanded and attaches (presumably by a ligament belonging to the epicentral series) to the posterodorsal surface of the capsule formed from the parapophyses of the fourth vertebra (Sawada, 1982, figs. 58, 62C), and the tip of the epineural of V3 is attached by ligament to the tip of the horizontal process from the fused second and third vertebrae (Sawada, 1982, figs. 58, 62C). In front of this there are three more strap-like epineurals (V1, V2, and one occipital) passing forward and attaching by ligaments to the occiput.

A fuller survey of the anterior intermusculars in otophysans is desirable, but features common to Alestes and Acanthopsoides include loss of the medial branch and the proximal attachment on the first four or five epineurals, and development of ligamentous attachments between tips of the anteroventral branches of the anterior epineurals and structures ventral to them; those structures include the swimbladder and transverse process of the third neural arch in Alestes, and the epicentral ligaments, capsule (fourth parapophyses), transverse process of the fused second and third vertebrae, and occiput in Acanthopsoides.

Some gonorynchiforms show similar modifications of the anterior intermusculars, but the situation is more complex than in otophysans because gonorynchiforms have epicentrals as well as epineurals on the anterior vertebrae. We describe the anterior intermusculars of Gonorynchus above, and those of Chanos and Parakneria are recorded in Table 4.

In Chanos (Rosen and Greenwood, 1970, figs. 3, 5, 6; Table 4), as in Gonorynchus and otophysans, epineurals are forked proximally (back to about V30 in Chanos, about V35 in Gonorynchus), and the anteromedial branch of the epineural is attached to the neural arch by ligament. The first anteromedial branch of an epineural is attached by ligament to the neural arch of V2. In front of this there are four more epineurals, each represented only by the anteroventral branch and posterior part of the bone; they have brush-like posterior ends and variously subdivided anterior ends. The first two of these pass forward into the posttemporal fossa. The epicentrals of Chanos are unusual in being widely forked distally (Rosen and Greenwood, 1970, fig. 3), a condition we have seen elsewhere only in kneriids (Lenglet, 1974; Table 4). They attach to the head of the rib on the anterior rib-bearing vertebrae and, by means of a long ligament, to the first two centra. There are two occipital epicentrals (the cranial ribs of Rosen and Greenwood, 1970), an enlarged one attached by ligament to the basioccipital, and one similarly attached to the exoccipital, just below the vagus foramen. Each of these has an anterodorsal branch, passing forward in the myoseptum into the rear of the posttemporal fossa. Both occipital epicentrals attach by ligament to the dorsal tip of the cleithrum distally. There is no Baudelot's ligament.

The intermuscular bones of kneriids were described by Lenglet (1974). Epineurals of our Parakneria (Table 4) are forked proximally from V7 back, and the anterior ones are attached by ligament low on the anterior margin of the expanded neural arches. Passing forward from V7, epineurals become more and more weakly ossified, and some of them are mere discontinuous slips of bone, remote from the neural arch, in the epineural ligament. On V3, the epineural ligament attaches to the centrum, just above the parapophysis, and contains a slip of bone distally. On V2, the right side of our specimen shows two ligaments originating together, low on the centrum, with a small slip of bone distally in the upper one, which we take to be the epineural, and the lower one leading to the epicentral. On the left side of the specimen there are two ligaments originating on the centrum, each leading to the head of one of the proximal branches of the epicentral; we assume that the epineural is fused here with the epicentral. There is no epineural on V1. Epicentrals of Parakneria are forked distally, like those of Chanos (cf. Lenglet, 1974, figs. 17–19; Rosen and Greenwood, 1970, fig. 3), and attach to the rib head on anterior rib-bearing vertebrae. On V2, the proximal end of the left epicentral is trifid, with an anterodorsal branch attaching to the centrum by a separate ligament, as noted above; we take this branch to be the incorporated epineural. The head of the epicentral of V1 is single and attaches to the centrum by ligament. There is one occipital epicentral (the cranial rib of Lenglet, 1974), a stout bone, forked distally, attaching to the exoccipital just behind the vagus foramen. Kneria has virtually the same configuration of the intermusculars as Parakneria (Lenglet, 1974). Among other gonorynchiforms, Phractolaemus (Thys van den Audenaerde, 1961) and Cromeria have the epicentral series represented only by a “cranial rib,” and the diminutive Grasseichthys lacks epicentrals (and other intermuscular bones).

In Gonorynchus (described above; Figures 4–6), the anterior intermusculars are modified in ways comparable to those of kneriids. The attachment of the epineurals to the vertebra descends from the neural arch (V5 and successors) to the centrum (V3, 4). On VI-2 the epineurals are unattached. The anteroventral branches of an occipital epineural and of the epineurals of VI–3 fuse with the epicentral of the segment in front. There is no epicentral on V3; we have seen a comparable gap in an intermuscular series only in otophysans (e.g., no epineural on V3 in Hemibarbus, no epicentral on V4 in Alestes, no epicentral on V2–4 in Hemibarbus and Hypentilium; Table 4), in Umbra (no epicentral on V6–16; Table 4), and in some specimens of the aulopiform Pseudotrichonotus (no epineural on V3; Table 5).

To sum up, gonorynchiforms are shown to be monophyletic by the presence of epicentral bones (in addition to other features listed by Fink and Fink, 1981). Within gonorynchiforms, Chanos shows the most generalized condition, but it lacks medial branches on the three occipital epineurals and that of VI. Gonorynchus and kneriids show more extensive modifications of the anterior intermusculars, including associations between epineurals and epicentrals and descent of the epineural attachment on to the centrum. In otophysans, the anterior intermusculars are modified in connection with the Weberian apparatus. In our sample, the cyprinid Hemibarbus shows the most generalized condition, but both the epineural and epicentral series are interrupted in the region of the Weberian apparatus. The other genera have the anterior epineurals modified by loss of their medial branches, and in Acanthopsoides and Alestes the anteroventral branches of the anterior epineurals develop associations with structures ventral to them. One could sum up the generality common to otophysans and gonorynchiforms as a clearing away of intermuscular attachments to the dorsal parts of the first few vertebrae; in otophysans that clearing away is associated with development of the Weberian apparatus. The gonorynchiform condition is presumably a plesiomorphic version of the otophysan condition, as supposed on other grounds by Greenwood et al. (1966) and Rosen and Greenwood (1970).

ESOCOIDS.—In Table 4 we record the intermuscular bones and ligaments of four esocoids, two species of Esox and one each of Umbra and Novumbra. The relationships of esocoids are problematic. To date, the only proposal with any support (loss of a single character) is that esocoids are the sister group of all other euteleosts, including ostariophysans, all of which lack a fourth basibranchial toothplate, a structure present in esocoids (Fink, 1984). The intermusculars and anterior vertebrae may bear on this problem.

In Umbra the intermusculars are unremarkable, except for modification of the epicentral series. The anterior epineurals are simple; the first is in ligament in U. krameri and in bone in U. pygmaea. The posterior epipleurals and epineurals are unattached, and some of them are forked proximally. The epicentrals are all in ligament. Umbra krameri is unique among taxa we examined in having an extensive gap in the epicentral series, with ligaments from the occiput to V5 (the last one or two weaker than their predecessors) and then nothing until the series reappears at V17. In U. pygmaea, we found epicentral ligaments only on a few vertebrae in the middle of the trunk. In Novumbra, all epineurals and epipleurals are in ligament (they may ossify in larger specimens, Wilson and Veilleux, 1982), and we could find no epicentral ligaments.

In Esox (Figure 8) things are much more complex, including differences between E. lucius and E. americanus (respectively representing the species groups assigned to the subgenera Esox and Kenoza by Nelson, 1972). In E. lucius, the first four (or occasionally the first five, Figure 8) epineurals and in E. americanus the first two epineurals are broadly fused to the base of the neural arch. Both subgenera show epineurals attached to the centrum rather than the neural arch from about V10–25; this is an unusual specialization, which we record elsewhere only in Xenomystus (Table 3), Anchoa (Table 3), and in notosudid, scopelarchid, and evermanellid aulopiforms (Table 5) among lower (nonacanthomorph) teleosts. In E. lucius, epineurals are forked proximally from V7–8 onward and are attached to the neural arch or centrum by ligament (Figure 8A). In E. americanus, epineurals are like those of E. lucius from about V10 onward, but those of V3–8 are modified (Figure 8B). The epineurals of V3–6 are unbranched and consist only of the anteroventral limb and the posterodorsal body of the bone (V₀ 6, Figure 8B). The ligamentous connection to the neural arch remains on V3 and V7. The anteroventral tips of the epineurals of V3–8 are attached to the head of the rib of the same vertebra by means of the epicentral ligament (Figure 8B), and on V4–6, where the ligament to the neural arch is missing, this attachment to the epicentral ligament is the only attachment of the bone. Esox has only one anterior supraneural (Figure 8), an expanded, ovoid plate over the second and third neural arches (a series of small, unmodified supraneurals begins over about V10). In E. americanus, the second neural arch is swollen in the transverse plane and rostrocaudally expanded, extending back over the third centrum (Figure 8B); in E. lucius, the third (not the second) neural arch is similarly swollen and expanded (Figure 8A). The first rib is on V2 in all esocoids. In E. americanus, the first rib is coossified with the parapophysis in membrane bone, the ribs on V3–20 ossify in cartilage, and those on V21–31 ossify in membrane. In E. lucius, the first three ribs (on V2–4) are coossified with the parapophysis in membrane bone, and all but the last of the remaining ribs ossify in cartilage. These differences between E. lucius and E. americanus seem to be constant for the two subgenera; E. masquinongy and E. reicherti (subgenus Esox) show the lucius pattern, and E. niger (subgenus Kenoza) shows the americanus pattern.

When we first studied the intermusculars of Esox, it happened that we had access only to cleared-and-stained specimens with the Kenoza pattern (E. americanus, E. niger), showing an association between the anterior epineurals and the epicentrals. As Table 4 and the discussion in the preceding section indicate, gonorynchiforms (Chanos excepted) and otophysans are the only other teleosts in which we have found modifications of the intermusculars on the first few vertebrae that include association between the epineurals and the epicentrals (indicated by vertical lines in Table 4). We therefore jumped to the conclusion that the epineural/epicentral association was synapomorphous, and that in Esox we had found the sister group of the ostariophysans. We had to discard that idea for three reasons. First, species of the subgenus Esox (E. lucius, E. niger, E. reicherti), when they became available, proved to have no epineural/epicentral association, and there is good evidence that Esox is monophyletic (Nelson, 1972; Wilson, 1984). Second, there is no epineural/epicentral association in umbrids, and there is reasonable evidence that esocoids are monophyletic (Nelson, 1972; Rosen, 1974; Wilson, 1984). Third, Chanos and the cypriniforms we sampled have no epineural/epicentral association (Table 4), and there is good evidence that ostariophysans, gonorynchiforms, and otophysans are each monophyletic (Fink and Fink, 1981). The epineural/epicentral association therefore must be homoplastic in Esox (Kenoza), gonorynchoids, and otophysans. But we think it worth pointing out that beyond the epineural/epicentral association, Esox shares three other specializations of the anterior vertebrae with some or all ostariophysans.

The first of those is the presence of only one anterior supraneural, which is expanded (compared with the primitive rod-like or sigmoid supraneural) and is situated over the second and third neural arches, of which either the second (Kenoza) or third (Esox) is expanded. In kneriid gonorynchoids (including Phractolaemus) there is also a single expanded supraneural over the third neural arch (Thys van den Audenaerde, 1961; Lenglet, 1974), whereas in gonorynchids (including several Cretaceous forms) there is a series of four or five supraneurals over V2–5 or V2–6, with that over V2 or V3 enlarged in some Cretaceous genera (Gayet and Chardon, 1987). In otophysans there are one (characiphysans) or two (cypriniforms) enlarged supraneurals (the neural complex), those over V3 or V2–3 (Fink and Fink, 1981; Patterson, 1984). The derived condition of only one (Esox, kneriids, characiphysans) or two (cypriniforms) enlarged anterior supraneurals is certainly homoplastic in esocoids, gonorynchiforms, and otophysans because there are numerous unmodified supraneurals in umbrids (Wilson and Veilleux, 1982), Chanos, the Paleocene Esox tiemani (Wilson, 1984), and the Eocene otophysan Chanoides, which has unmodifed supraneurals over V5–10 in addition to the enlarged supraneurals forming the neural complex over V1–4 (Patterson, 1984).

The second anterior vertebral modification shared by Esox and ostariophysans is expansion of the anterior neural arches. Fink and Fink (1981:325, character 63) described the ostariophysan condition and stated that “the dorsomedial portions of the anterior neural arches are expanded and abut against each other and the posterior margin of the exoccipital, forming a roof over the neural canal. In other primitive teleosts, the neural arches are smaller and do not meet each other or the exoccipital.” As Figure 8 shows, Esox shares this condition, with the difference that the accessory neural arch (ANA, Figure 8) is present, separating the first neural arch from the exoccipital. The anterior neural arches are not expanded in umbrids (Wilson and Veilleux, 1982, fig. 12), so that if esocoids are monophyletic, the derived state is homoplastic in Esox and ostariophysans.

The third anterior vertebral modification shared by Esox and some ostariophysans is coossification of the rib and parapophysis on V2 (Kenoza) or on V2–4 (Esox). In gonorynchiforms, the foremost rib (on V3) and parapophysis are not coossified (Greenwood et al., 1966; Rosen and Greenwood, 1970), but that coossification appears to be a necessary precondition for formation of the tripus (V3) and os supensorium (V4) in otophysans (Rosen and Greenwood, 1970; Fink and Fink, 1981; Patterson, 1984). Again, the esocoid and otophysan conditions must be homoplastic becaue the anterior ribs are unmodified in umbrids and gonorynchiforms.

We checked Esox and esocoids against Fink and Fink's (1981) list of fifteen ostariophysan characters. Esocoids share one of them (absence of basisphenoid, Fink and Fink's character no. 7); Esox shares two more (absence of supraneural in front of first neural arch, no. 58; expansion and abutment of anterior neural arches, no. 63, above and Figure 8); esocoids either lack the remaining ostariophysan characters (Fink and Fink's characters 8, 20, 54, 55, 57, 64, 111, 118), or those characters do not characterize ostariophysans (no. 41, as discussed in Patterson, 1984; no. 56).

Current opinion (Fink and Weitzman, 1982; Fink, 1984; Begle, 1992; Figure 9A) is that esocoids are the sister group of all other euteleosts, including ostariophysans. As noted above, the single (loss) character proposed in support of that grouping is absence of a toothplate on the fourth basibranchial (BB4) in all euteleosts except esocoids. In discussing this character, Fink and Weitzman (1982) reported that among clupeomorphs the toothplate occurs only in Chirocentrus, which would weaken it as primitive for clupeomorphs according to Grande's (1985) cladograms. However, Nelson (1970a) also recorded the toothplate in the pristigasteroid Pellona (but not in other pristigasteroids) and recorded fragmentary toothplates over BB4 in several engrauloids, rendering the assessment of the primitive state problematic. We note that the only ostariophysans with any basibranchial teeth or toothplates are Gonorynchus and characiforms; a toothplate over BB4 occurs only in certain characiforms, where reacquisition is inferred (Fink and Weitzman, 1982). In our view, the character is questionable. Fink and Weitzman (1982) and Fink (1984) placed the ostariophysans in a tetrachotomy, the other three branches of which are salmonoids, argentinoids + osmeroids, and neoteleosts (Fink and Weitzman, 1982), or argentinoids, osmeroids, and salmonoids + neoteleosts (Fink, 1984). Rosen (1985) placed ostariophysans in a trichotomy whose other two branches are argentinoids, and salmonoids + osmeroids + neoteleosts. We discuss the salmonoids, osmeroids, and argentinoids below, and we argue that they form a monophyletic group within which salmonoids and osmeroids are sister taxa (Figure 9B). That grouping simplifies Fink and Weitzman's (1982) and Fink's (1984) tetrachotomies and modifies Rosen's (1985) trichotomy; the result is a trichotomy whose three branches are ostariophysans, salmoniforms (argentinoids, salmonoids + osmeroids), and neoteleosts. We have suggested (Johnson and Patterson, 1993:600) that this trichotomy may be resolved by the median caudal cartilages (CMC) of Fujita (1990, table 3). CMC are unknown in osteoglossomorphs, elopomorphs, clupeomorphs, esocoids, and ostariophysans (except for a cartilage in the position of a lower CMC in Fujita's specimen of the cyprinid Tanakia). CMC are present in argentinoids, osmeroids, salmonoids, and in stomiiform, aulopiform, and myctophiform neoteleosts; they are absent (secondarily) in acanthomorphs (Johnson and Patterson, 1993). We regard CMC as synapomorphous for Euteleostei minus esocoids and ostariophysans, a group for which we here (Figure 9) adopt the name Neognathi (Rosen, 1973; Rosen's usage differed from ours by including esocoids).

FIGURE 9.—Cladograms contrasting Begle's (1991, 1992) view of the interrelationships of lower euteleosts (left) with that proposed here (right).

Within the Clupeocephala, there are thus four monophyletic groups: (1) Clupeomorpha, (2) Ostariophysi, (3) Esocoidei, (4) Neognathi. We know of no morphological character that unambiguously groups any two of these four. The adipose fin, nuptial tubercles, and a stegural have been used to group (2) + (3) + (4) (Patterson and Rosen, 1977; Lauder and Liem, 1983), but the adipose and nuptial tubercles do not occur in esocoids, and their stegural is as dubious as that of ostariophysans. Molecular evidence from nucleotide sequences of partial large subunit ribosomal RNA (Le et al., 1993) and ependymins (Müller-Schmid et al., 1993) favors grouping (1) + (2), but esocoids are not yet sampled for ribosomal RNA, and the sampling in ependymins also is poor (Clupea, Esox, Oncorhynchus, and two cyprinids). Although we have found no convincing evidence that ostariophysans (2) and esocoids (3) belong together, and are unwilling to appeal to “underlying synapomorphies” (Saether, 1983), we believe that the anterior vertebral modifications unique to some or all esocids and some or all ostariophysans are sufficiently striking to encourage further search for ostariophysan/esocoid synapomorphies.

SALMONOIDS, OSMEROIDS, AND ARGENTINOIDS.—Salmonoids and osmeroids share cartilaginous rods in the epicentral ligaments (see p. 14 and Table 4, Plate 1D,H), and, as noted above, the distribution of those structures in both groups implies that they are primitive for each according to Sanford's (1990) cladogram of salmonoids and Begle's (1991) cladogram of osmeroids. Salmonoids and osmeroids also share the absence of ossified epipleurals; the osmerid Spirinchus (pers. obs.) and the galaxiines Galaxias and Paragalaxias (McDowall, 1969, 1978) are exceptions, but Spirinchus and the galaxiines are each among the most derived members of their clades (Begle, 1991; Wilson, 1992), and, as each has several successive outgroups that lack epipleurals, their epipleural bones must be interpreted as reversals. Although we infer that absence of epipleural bones is primitive for teleosts, the universality of a long series of epipleural bones in elopomorphs, clupeomorphs, esocoids, ostariophysans, argentinoids, stomiiforms, aulopiforms, and myctophiforms (Tables 3–5) shows that their absence in salmonoids and osmeroids is secondary or derived and so potentially synapomorphous. Thus, there are two intermuscular characters, presence of epicentral cartilages and absence of epipleural bones, implying that salmonoids and osmeroids are related.

At present, the relationships of salmonoids are unresolved (Fink and Weitzman, 1982; Fink, 1984; Rosen, 1985; Sanford, 1990; Begle, 1992). A sister-group relationship between osmeroids and argentinoids (Argentinoidea + Alepocephaloidea; Greenwood and Rosen, 1971; Begle, 1991, 1992) was indicated in Fink and Weitzman's (1982, fig. 23) cladogram, but no support was given for that node (cf. Fink, 1984). However, Begle (1991, 1992) cited characters supporting the monophyly of his Osmerae (Argentinoidei + Osmeroidei; Figure 9A). Argentinoids lack epicentral cartilages, so far as we know, and have epipleural bones. Thus, there are two sets of contradictory characters bearing on the relationships of osmeroids: the features listed by Begle as relating them to argentinoids and the two features of the intermusculars (cartilaginous epicentrals, no epipleurals) indicating that they are immediately related to salmonoids. Because of this conflict, we evaluate the characters proposed by Begle (1991, 1992; his character numbers are given in square brackets).

In his 1991 paper, Begle (figs. 2, 3) cited four characters relating osmeroids and argentinoids: (1) “loss” of nuptial tubercles [33]; (2, 3) “loss” of basisphenoid [57] and orbitosphenoid [58]; and (4) presence of a ventral cartilaginous vane on the first basibranchial [64]. In a second paper, Begle (1992) diagnosed the Osmerae (Argentinoidei + Osmeroidei) by characters 2 (rephrased as “reduction/loss of basisphenoid” [57]) and 4 [64] in the above list, and by a new one: (5) fusion of rudimentary neural arches to ural centra [5]. Begle's (1992:353) character 1 [33] in the above list appears as an “additional character…that may occur at this node under alternative optimization schemes,” together with: (6) loss of endopterygoid teeth [3]; (7) reduced pterosphenoids [63]; and (8) basihyal teeth [106] (four states are found in osmeroids and argentinoids, Begle, 1992:363). In addition, Begle (1992) cited two further characters uniting Osmerae and Neoteleostei, which therefore distinguish Osmerae from salmonoids: (9) extended alveolar process of premaxilla [83]; and (10) reduction in laminar bone on anterior margin of hyomandibular [100]. Evaluation or criticism of these 10 characters follows; asterisks indicate characters listed as diagnostic by Begle (1992), with the implication that he acknowledged ambiguity in the distribution of characters without asterisks.

1. Absence of nuptial tubercles. As Begle (1991:39) noted, nuptial tubercles occur among osmeroids in Osmeridae, Lovettia, Stokellia, and Retropinna. The character is ambiguous.

2, *3. Absence of orbitosphenoid and basisphenoid. Both of these bones occur in argentinoids. They were described in alepocephaloids by Gosline (1969:198, with references to Gegenbaur's earlier work) and in argentinids by Chapman (1942), and we have confirmed that both bones are well developed in dried skeletons of Argentina and Alepocephalus. Begle (1992:362) also acknowledged that the basisphenoid and orbitosphenoid are present in a range of argentinoids. In our view the characters are mistaken.

*4. Ventral cartilaginous vane on first basibranchial. Begle (1991, fig. 5) explained this character by means of drawings of the first basibranchial (B1) in the salmonoid Thymallus, the osmerid Thaleichthys, and the platytroctid Sagamichthys. Thymallus has a small, cuboid, ossified B1 (Begle's “unmodified” state), whereas the other two genera have a larger, cartilaginous B1 with a ventral vane or keel (Begle's “modified” state). There are several conditions of B1 in osmeroids and argentinoids. Begle (1991, fig. 3) noted that B1 shows the unmodified state in Lepidogalaxias and more-derived galaxioids, and we find that it also is unmodified in the argentinoids Glossanodon, Argentina, and Opisthoproctus (cartilaginous in the first, ossified in the other two), whereas we find in the osmerids Allosmerus and Plecoglossus it has the modified shape but is ossified. The character is ambiguous.

5. Reduction or loss of endopterygoid teeth. Osmeroids (except salangids and Lepidogalaxias) have a band of enlarged teeth along the medial margin of the endopterygoid, whereas argentinoids, salangids, and Lepidogalaxias have the endopterygoid toothless. We see two characters here: absence (versus presence) of teeth and modification (versus uniformity) of dentition.

*6. Fusion of rudimentary neural arches to ural centra. In his 1991 paper (page 48), Begle treated this as a two-state character, with the derived state (“uroneural 1 fuses to compound centrum, followed in some forms by fusion with neural arches”) found only in Osmeroidea. In the 1992 paper (page 361), it became a three-state character, with state 1 (recorded in argentinoids, most alepocephaloids, and in southern osmeroids) as “rudimentary neural arches fuse to centrum, followed in some cases by fusion to first uroneural,” and state 2 (recorded in northern osmeroids) as “rudimentary neural arches fuse first to uroneural, followed in some cases by fusion to centrum” (“followed” is used here with reference to ontogeny, Fink and Weitzman, 1982:83; Begle, 1992:356). This character originated with Patterson (1970), who used the alternative derived states to distinguish argentinoids, alepocephaloids, and galaxiids (state 1, distinct neural arch on PU1 and often on U1) from northern osmeroids, Prototroctes, and Retropinna (state 2, no neural arch on PU1 or U1). Begle (1992:356) writes that “fusion of the rudimentary neural arches to the centrum is unambiguously the primitive condition for the Osmerae,” implying that state 2 is a modification of state 1. But this follows only if the Osmerae are demonstrably monophyletic. Given that retropinnids (Rosen, 1974, fig. 27), Lovettia (Rosen, 1974, fig. 19), and salangids (Rosen, 1974, fig. 26; Roberts, 1984) show the northern osmeroid pattern, with no caudal neural arches (state 2), Begle's (1991) cladogram indicates that the caudal neural arches (state 1, supposedly primitive) in galaxiines and Aplochiton are nonhomologous with those in argentinoids.

Rudimentary caudal neural arches (assignable to PU1 or U1) do not occur in neoteleosts (Fujita, 1990), and in salmonoids they occur only occasionally (as individual variants, commonest in Prosopium and Thymallus; Arratia and Schultze, 1992).

7. Reduced pterosphenoids. The reduced state is characterized by Begle (1992:362) as “widely separated, not meeting at midline.” In our view, the latter is the primitive state. The pterosphenoids are widely separated and fail to meet in the midline in Jurassic pholidophorids and leptolepids (Patterson, 1975, figs. 63, 72, 79, 89), and in Hiodon, Elops, esocoids, salmonids, etc.

8. Basihyal teeth. Begle (1992) acknowledged that this feature is ambiguous, with state 1 (marginal fangs) occurring in salmonids and osmeroids, and state 4 (teeth absent) in most argentinoids.

*9. Extended alveolar process of premaxilla. Begle (1991, 1992) illustrated this character by comparing the pattern in osmeroids, argentinoids, and a stomiatoid with that in salmonids, where the premaxilla and maxilla are in tandem, with no extension of the premaxilla beneath the maxilla; the salmonid pattern was taken to be primitive. As with number 6 above, we regard the polarity as inverted here because there is an extended alveolar process in (for example) Hiodon, Elops, Megalops, Albula, most clupeoids, all esocoids, etc.

*10. Reduction in laminar bone on anterior margin of hyomandibular. This is a difficult character to evaluate because it is one of degree. Begle (1992) noted that laminar bone is present among alepocephaloids in Leptochilichthys and Narcetes (which occupy two of the three basal nodes in his cladogram of the group) and among osmeroids in Plecoglossus and Prototroctes (both derived members of the group in his cladogram). Laminar bone also is well developed in Alepocephalus (Gosline, 1969, fig. 5 and a dried skeleton). The problem of evaluating the character is exemplified by Sanford (1988:134), who judged that an anterior laminar extension of the hyomandibular is present in all argentinoids, and he wrote that “this mosaic distribution indicates that an anterior laminar extension…has arisen, and perhaps been lost, many times amongst teleosts.”

From this survey, we conclude that there is, as yet, no unequivocal support for argentinoid-osmeroid relationships, and we offer the alternative that salmonoids are the sister group of osmeroids (Figure 9B) because of the presence in both of cartilaginous epicentrals and the absence in both of ossified epipleurals.

Within argentinoids, the intermusculars suggest one synapomorphy corroborating the sister-group relationship between alepocephaloids and argentinoids: the tips of the first three (Glossanodon, Leptoderma, Searsia) or four (Argentina) epineurals are displaced ventrally relative to their successors. The intermusculars also provide a character corroborating the monophyly of alepocephaloids: the epipleurals extend unusually far forward, to V3 (recorded in Searsia in Table 4, and observed also in Bathytroctes, Leptochilichthys, Rinoctes, Talismania). Developmental implications of this feature are mentioned below in the section on aulopiforms.

Salmoniformes: Salmoniformes as circumscribed by Greenwood et al. (1966) now are seen to be nonmonophyletic (e.g., Rosen 1974; Fink, 1984). But after removal of the esocoids, stomiatoids (= Stomiiformes), and myctophoids (= Aulopiformes and Myctophiformes), there remain three groups: salmonoids (Sanford, 1990), argentinoids (Argentinoidea + Alepocephaloidea; Greenwood and Rosen, 1971; Begle 1992), and osmeroids (Osmeroidea + Galaxioidea; Begle, 1991). Sanford (1990:149) proposed two characters indicating that these three form a monophyletic group: absence of radii on the scales (a character that we have not tried to evaluate) and well-developed marginal teeth on the basihyal (a character discussed by Nelson, 1970b, Fink and Weitzman, 1982, and Begle, 1992). Jamieson's (1991) review of spermatozoan structure provided one further salmoniform synapomorphy, a single, annular mitochondrion, recorded in two alepocephaloids (Argentinoidei), in salmonids, and in Galaxias (Osmeroidei); however, the mitochondria are not annular in Lepidogalaxias. The intermusculars provide one further hint that these three groups may be related.

In elopomorphs, clupeomorphs, and ostariophysans, the posterior epineurals and epipleurals are forked proximally (Tables 3, 4). Among esocoids, Esox has the epineurals forked proximally but not the epipleurals (Table 4). Argentinoids, salmonoids, and osmeroids are unique among lower (non-neoteleost) elopocephalans in lacking proximal forking of epineurals and epipleurals, and this might be a synapomorphy of Salmoniformes. The character is weakened because proximal forking of epineurals and epipleurals also is lacking in stomiiforms (Table 5; Weitzman, 1974; Fink and Weitzman, 1982) and is unusual in aulopiforms (recorded only in Chlorophthalmus and Parasudis, Table 5). It is general in myctophiforms (Table 5).

If the Salmoniformes are monophyletic, their intermusculars indicate that argentinoids are the most primitive members of the group. They retain an extensive series of epineurals fused to the neural arches (V1-27 in Alepocephalus, V1-23 in Searsia, V1-21 in Argentina, V1-20 in Glossanodon), lack epicentral cartilages, and have epipleural bones.

Lepidogalaxias: The relationships of Lepidogalaxias have long been a problem (Rosen, 1974; Fink and Weitzman, 1982; Fink, 1984). Begle (1991) placed Lepidogalaxias among galaxioid osmeroids, as the sister group of salangids + galaxiids. Although salangids lack ossified intermusculars (Salangichthys, Table 4; Roberts, 1984, fig. 1), the intermusculars of Lepidogalaxias give general support to this proposal. Lepidogalaxias (Table 4) shows several unique features in the intermusculars: there are no epineurals or epipleurals in either bone or ligament, and the only intermusculars are epicentrals, which are represented by a series of ligaments but with those on V1-6 containing bone distally. These bones are remote from the vertebrae and are forked distally, just beneath the skin. Distal forking of the epicentral bones occurs elsewhere only in Chanos and kneriids, so far as we know, and as argued above (p. 14), we believe that the bones in Lepidogalaxias are cartilage bones, ossifications of the epicentral cartilages present in other osmeroids. Apart from Lepidogalaxias, the only other genus that lacks epineural bones in Tables 3–5 is the retropinnid Stokellia, where epineurals are represented by ligament (Retropinna and Salangichthys show the same condition). The ribs of Lepidogalaxias are all in membrane bone, another unusual (although not unique) condition in non-neoteleosts, and the first rib is on V2, as in Galaxias.

Neoteleosts and Eurypterygians: We found no features of the intermusculars bearing on monophyly of the Neoteleostei (Stomiiformes + Aulopiformes + Myctophiformes + Acanthomorpha) or Eurypterygii (Neoteleostei minus Stomiiformes). Characters corroborating the monophyly of these groups recently were enumerated by Johnson (1992).

We had hoped that the intermusculars might provide some information about the relationships of ateleopodids, which were placed in an unresolved trichotomy with stomiiforms and eurypterygians by Olney et al. (1993). Unfortunately, our observations on two cleared-and-stained specimens of Ateleopus indicate that ateleopodids lack all intermuscular bones and ligaments, and they also lack ribs and Baudelot's ligament. We have not included comments on absence in ateleopodids in our sections discussing the distribution of components of the intermuscular system and associated structures.

AULOPIFORMS.—We record the intermusculars of 18 aulopiforms in Table 5, a wide sample illustrating the remarkable variations within this group and their potential value in systematics. Our sample covers members of 13 of the 15 nominal families (Okiyama, 1984; Johnson, 1992) or families and subfamilies (Nelson, 1984) currently recognised in the Aulopiformes, i.e., all except the monotypic Anotopteridae (included in Paralepididae by Johnson, 1992) and Omosudidae. Aspects of the intermuscular bones in Anotopterus and Omosudis are illustrated by Rofen (1966a, 1966b). Omosudis is held to be closely related to Alepisaurus by Johnson (1992); we comment on the structure and relationships of Omosudis below on the basis of a small cleared-and-stained O. lowei (USNM 219982, 81 mm SL), which was not decipherable in sufficient detail for entry in Table 5.

Aulopiforms are uniquely characterized by having epipleural bones extending far forward, always to V2 and frequently to V1 (Table 5). The only other groups with epipleurals extending forward to the anterior vertebrae are alepocephaloids (to V3, recorded in Searsia in Table 4, and observed also in Bathytroctes, Binghamichthys, Leptochilichthys, Rinoctes, and Talismania) and clupeoids (Table 3), and, in the latter, the anterior epipleurals are unattached to the axial skeleton (notation D₀ or B₀ in Table 3). In aulopiforms, well-developed, attached epipleurals extend forward to V1 or V2. This specialization forms the basis for other remarkable modifications within the group. Although we have little evidence bearing on the ontogeny of epipleural bones in aulopiforms, their mode of development evidently differs from that observed or inferred in other teleosts, where epipleurals develop rostrally and caudally from the region of the first caudal vertebra. In larval Saurida, epipleurals ossify caudally from V3, with that on V2 ossifying later than that on V3; the pattern in Aulopus (Table 5), with a small, unattached epipleural on V2, implies that development is as in Saurida. In other aulopiforms, the pattern of epipleurals in Ahliesaurus, Coccorella, Paralepis, and Alepisaurus (Table 5) is such that the bones can have developed only in a rostrocaudal gradient; in Ahliesaurus and Coccorella epipleural bones are almost or completely confined to the abdominal region, with a long series of ligaments extending into the caudal region, and in Paralepis and Alepisaurus the epipleurals on V1-2 are fused to the centrum, and the series passes back either into a long series of ligaments (Alepisaurus) or a long series of unattached bones (Paralepis). This change in mode of development may be due to associations between anterior epipleurals and the horizontal septum and its contained epicentrals that occur in various aulopiforms. These associations are discussed below.

In alepocephaloids, the only other group with attached epipleurals extending almost as far forward as in aulopiforms (V3 vs. V1-2), we have no information on development; however, because in Searsia (Table 4) the epipleural series is confined to the abdominal region (the last bone is attached by ligament to the first caudal vertebra), it is evident that the series does not develop from the primitive focus, at about the level of the first caudal vertebra. In Rinoctes the pattern is similar, with the last epipleural bone attached by ligament to the first haemal spine and about 10 ligaments, without included bone, beyond it. It may be that some or all alepocephaloids have altered the mode of development of epipleurals in a way comparable (although obviously nonhomologous) with that in aulopiforms.

Bathypterois (Ipnopidae) shows what seems to be the most generalised pattern of intermusculars in our sample of aulopiforms, with long, coextensive series of epineural (V1 to ∼V50) and epipleural (V2 to ∼V50) bones and epicentral ligaments. Bathypterois lacks the accessory neural arch, a structure present in Aulopus (Aulopidae), Harpadon, Saurida (both Harpadontidae), and Synodus and Trachinocephalus (both Synodontidae). Aulopus, generally taken to be the most primitive aulopiform, has a significant modification of the epicentral ligaments and epipleural bones in the abdominal region: from about V5 back to about V20 epicentral ligaments originate not on the centrum but on the epipleural bone (notation LE in Table 5), near its base anteriorly and posteriorly but at up to about one-third of the length of the epipleural on about V10–15. The implication of this association is that the proximal part of these epipleurals is in the horizontal septum, not below it as is normal.

The larval Scopelarchoides (Scopelarchidae) illustrated in Figure 10 illuminates the condition in Aulopus and several other aulopiforms. In this Scopelarchoides (35 mm SL) all the intermusculars are still in ligament. On V1-11 there are only two ligaments on each vertebra, the epineural, originating on the neural arch (V1-3) or centrum (V4–11), and one that originates on the parapophysis and lies in the horizontal septum. On V7 the lower ligament bifurcates near its tip, and on V8–11 the bifurcation is successively closer to the centrum. From V12 onward there are two lower ligaments on each vertebra, an epicentral in the horizontal septum and an epipleural below it. In adult Scopelarchoides (Table 5) there are epipleural bones forward to V1, and those on V2–10 have an epicentral ligament closely applied to their upper surface. Both bone and ligament lie in the horizontal septum, but posteriorly (beyond V10) the bones and ligaments diverge, with the epicentrals moving up on to the centrum and the bones down on to the haemal arch. Here, ontogeny shows that the epicentral and epipleural series have coalesced anteriorly, with the anterior epipleurals displaced dorsally into the horizontal septum; the situation is the inverse of that in beryciform acanthomorphs (discussed below), where the anterior epineurals are displaced ventrally into the horizontal septum. In Table 5, epipleural bones lying in the horizontal septum are indicated in bold type (e.g., B₃ for one originating on the parapophysis), just as in Tables 7 and 8 bold type indicates epineurals in the horizontal septum.

FIGURE 10.—Anterior vertebrae and associated intermuscular ligaments in larval Scopelarchoides signifer Johnson, USNM 274385, 35 mm SL. At this stage, the only ossified structures are centra (including the parapophyses) and tips of neural and haemal spines. All intermusculars are ligaments, and the one rib visible is the first, on V3, which is the only one ossifying in cartilage. Every fifth vertebra is numbered. (Scale bar 1 mm.)

In the notosudid Scopelosaurus (Table 5), the epipleurals on V2–24 are in the horizontal septum, and the region where they turn ventrally and leave the septum is indicated by distal bifurcation of the bones on V20–24, with the upper branch lying in the horizontal septum and the lower branch below it. The first epicentral ligament occurs on V20, together with the first bifurcate epipleural. and its distal part is applied to the upper branch of the epipleural. Posteriorly, behind V24, epicentrals and epipleurals diverge, with the epicentral ligaments moving up on to the centrum and the epipleurals down on to the haemal arch. In Ahliesaurus, the other notosudid that we sample in Table 5, there is distal bifurcation of a single epipleural, the last one in the horizontal septum (on V19); epicentral ligaments first appear four vertebrae in front of this, as in Scopelosaurus, but the five ligaments that overlie epipleurals in the horizontal septum are closely applied to the upper margin of the bones. In the evermanellid Coccorella (Table 5), the epipleurals on V1–12 lie in the horizontal septum, and epicentral ligaments are applied to the upper surface of the bones on V6–12. The notosudids, scopelarchid, and evermanellid in our sample share epineural bones whose origin descends from the neural arch to the centrum (and even to the parapophysis in Scopelosaurus; also in Scopelarchus (USNM 234988) and Evermanella (Rofen, 1966c, fig. 185)) from about V5 back to at least V15.

According to Johnson et al. (1989), morphological evidence not including the intermusculars indicates that Pseudotrichonotus is the sister taxon of the Synodontoidea, represented in Table 5 by the synodontids Synodus and Trachinocephalus and the harpadontids Harpadon and Saurida. These genera agree in having the anterior epipleurals in the horizontal septum, on about V2–10 in Harpadon, V2–20 in Pseudotrichonotus, V2–25 in Trachinocephalus and Saurida, and V2–35 in Synodus. Pseudotrichonotus, Synodus, and Trachinocephalus also agree, and differ from other aulopiforms, in having an abrupt and obvious transition between epipleurals in the horizontal septum and below it. In other aulopiforms with dorsally displaced epipleurals, such as the notosudids, scopelarchid, and evermanellid discussed above, there is a gradual transition between the bones in and below the septum, typified by the successively more deeply forked ligaments on V8–11 in larval Scopelarchoides (Figure 10) and the successively more deeply forked bones on V20–24 in Scopelosaurus. In Pseudotrichonotus, Synodus, and Trachinocephalus the point where the epipleurals leave the horizontal septum is marked by an abrupt transition, with a stout, posterolaterally directed bone closely associated with an epicentral ligament on one vertebra, and a slender, ventrolaterally inclined bone with a free epicentral ligament above it on the next. Epicentral ligaments first appear above the last three or four dorsally displaced epipleurals in Pseudotrichonotus and Trachinocephalus, above the last six or seven in Harpadon and Saurida, and above about the last 10 in Synodus. In Synodus, these first 10 epicentral ligaments are short and insert on the upper surface of the proximal part of the epipleural bone, so that the bone appears to be slung from the centrum by a short ligament. The same pattern occurs in Saurida, Trachinocephalus, and Pseudotrichonotus in the epicentral ligaments overlying dorsally displaced epipleurals (notation pL in Table 5). In some specimens of Synodus the first free epicentral ligament (above the first ventrolaterally inclined epipleural) is ossified so that there is a single epicentral bone, but this condition is not constant, even on both sides of a specimen.

As noted above, Johnson et al. (1989) treated Aulopus as the sister group of Pseudotrichonotus + synodontoids. Synodontoids share with Aulopus the accessory neural arch (absent in Pseudotrichonotus) and ventral displacement of the distal part of the first one to three epineurals (notation b₁ in Table 5). Aulopus has the first three epineurals modified in this way, Pseudotrichonotus has the first two modified and the third absent (Table 4) or the first three modified (ZUMT 55678), Synodus has the first two or three modified, Trachinocephalus the first, and in Saurida the first is modified in S. brasiliensis and S. suspicia but not in S. gracilis nor S. normani (the species recorded in Table 5). The first epineural is unmodified in Harpadon.

Other aulopiforms sampled in Table 5 (apart from the ipnopid, aulopid, synodontoids, notosudids, scopelarchid, and evermanellid discussed above) are the chlorophthalmids Chlorophthalmus and Parasudis, the paralepids Paralepis and Macroparalepis, and Alepisaurus, Bathysaurus, and Gigantura, each representing a monotypic family. In Chlorophthalmus and Parasudis, many epineurals and epipleurals are forked proximally, and the posterior epineurals and epipleurals lack the anteromedial fork and so are unattached to the axial skeleton (notation V₀ and D₀ in Table 5). This is a pattern, common in lower elopocephalans (Tables 3, 4), that we have not observed elsewhere in aulopiforms. But in other respects Chlorophthalmus and Parasudis are very different. Chlorophthalmus has the first two epineurals modified in the same way as Aulopus and most synodontoids (notation b₁ in Table 5), and it has the first five or six epipleurals displaced dorsally into the horizontal septum. In other aulopiforms showing this displacement, the epicentral series of ligaments begins above the last epipleurals in the horizontal septum, but in Chlorophthalmus the first obvious epicentral ligament occurs at about V15, well behind the last dorsally displaced epipleural (in some specimens we saw indications of very small ligaments inserting on epipleurals anterior to this point, suggesting the pattern in Aulopus, but after examining a series of cleared-and-stained specimens of more than one species we were unable to convince ourselves that the ligaments were real). In contrast, Parasudis has an extensive series of epicentral bones from the occiput back to about V30 (continued caudally by a few ligaments), has no epipleurals in the horizontal septum, and has the first epineurals unmodified. Thus, the pattern in Parasudis most closely resembles the generalized pattern in Bathypterois, with the difference that the epicentrals are ossified.

Epicentral bones also occur in Alepisaurus (and Omosudis), where there is a long series from V3 onward. Alepisaurus, Paralepis, and Omosudis agree in having the first rib on V1, in having the rib and epipleural of V1 and V2 fused to the centrum, and in having most epineurals unattached to the axial skeleton; in Paralepis and Omosudis, most epipleurals also are unattached, whereas they are normal in Alepisaurus. The paralepid Macroparalepis differs from Paralepis in having only a few epineurals (in bone on V1–4 and in ligament on V5–7) and epipleurals (V1–5) and in having the first rib on V5, but it shares with Paralepis a fused epineural, one free epipleural (many in Paralepis), and Baudelot's ligament attaching broadly to V1 and V2.

Gigantura is unique in having many epineurals and epipleurals bifid proximally (a few epineurals are trifid), with both branches attaching to the centrum, and in having no ribs; only the first epipleural appears to be in the horizontal septum. Finally, in Bathysaurus, which is conventionally allied with or included in the Synodontidae, the pattern is as strange as in Gigantura, with which Bathysaurus shares absence of epicentral bones or ligaments. In Bathysaurus, the first few epipleurals (V1–8) are in the horizontal septum, almost all the epineurals originate on the centrum (rather than the neural arch) and are fused to it, and all but the first of the ribs originate not on the parapophyses but by ligament on the epipleurals (notation LBE in Table 5).

Table 6 shows a matrix for 26 characters, all but one drawn from the data on aulopiforms in Table 5, and Figure 11 shows cladograms derived from that matrix (see caption to Figure 11 for procedures). Although we do not pretend that Figure 11 contains the truth on aulopiform interrelationships, we contend that it may be nearer the truth than other schemes currently available (Johnson, 1982; Okiyama, 1984; Hartel and Stiassny, 1986). In Johnson's (1982, fig. 20) scheme, Aulopus is remote from all other aulopiforms; notosudids, scopelarchids, chlorophthalmids, and ipnopids are placed with myctophiforms in the pattern [[Myctophidae, Neoscopelidae] [Notosudidae [Scopelarchidae, Chlorophthalmidae, Ipnopidae]]]; the remaining aulopiform families are placed in a third group in the pattern [[Bathysauridae [Synodontidae, Harpadontidae]] [[Paralepididae, Anotopteridae] [Evermanellidae [Omosudidae, Alepisauridae]]]]; and giganturids are not included. In Okiyama's (1984, table 69) phenetic scheme, aulopiforms fall into four groups: Aulopidae; Chlorophthalmidae + Ipnopidae + Notosudidae + Scopelarchidae; Bathysauridae + Harpadontidae + Synodontidae; and Alepisauridae + Anotopteridae + Evermanellidae + Omosudidae + Paralepididae. Okiyama's groups are, therefore, the same as the four major aulopiform components of Johnson's scheme, and again, giganturids are not included. According to Hartel and Stiassny (1986), Parasudis is the sister taxon of Chlorophthalmus, those two genera comprising the Chlorophthalmidae (Hartel and Stiassny transferred Bathysauropsis from Chlorophthalmidae to Ipnopidae). Parasudis differs from Chlorophthalmus and most other aulopiforms in having a full series of epicentral bones, including (in our specimen) one on the occiput and one on the notochordal sheath in the “cervical gap” of Rosen (1985) (Hartel and Stiassny, 1986, fig. 6A, illustrated a Parasudis truculentus in which there is no occipital epicentral and the first bone originates on the centrum of V1). Aulopiforms were nonmonophyletic for Hartel and Stiassny (1986), as they were for Rosen (1985). That notion is contradicted by the aulopiform synapomorphies listed by Johnson (1992) and by the unique pattern of epipleurals in the group. As for Hartel and Stiassny's (1986) Chlorophthalmidae (Chlorophthalmus and Parasudis), evidence from the intermusculars indicates that they might be monophyletic (Figure 11B, monophyly supported only by proximally forked epineurals and epipleurals, with the posterior members of each series unattached) or nonmonophyletic (Figure 11C). The link between Chlorophthalmus and synodontoids in Figure 11C is very weak (supported only by descent of the anterior epineurals), but in that tree a number of more substantial characters distinguish Chlorophthalmus from Parasudis.

The relationships of Gigantura are unknown. Giganturids were not included in the Aulopiformes by Okiyama (1984), and R.K. Johnson's (1984; Johnson and Bertelsen, 1991:27) comments suggest that they might be the sister taxon of aulopiforms. The dorsal gill arches of giganturids are greatly reduced (Rosen, 1973) and do not show the features used by Johnson (1992) to characterize aulopiforms. Nevertheless, the intermusculars indicate that Gigantura belongs within aulopiforms, specifically with alepisauroids, and that it may be linked with Bathysaurus, usually placed in the synodontoids.

Within alepisauroids, the implication of paralepidid paraphyly in Figure 11 may be artifactual and due only to reduction of the intermusculars in Macroparalepis.

We hope that Figure 11 may be enough to spur those interested in showing our errors to produce better schemes based on other aspects of aulopiform morphology.

Ctenosquamates: The Ctenosquamata comprise the Myctophiformes and Acanthomorpha (Johnson, 1992). Two features of the intermusculars are consistent with ctenosquamate monophyly, although both are subject to so much homoplasy in other teleostean groups that they can hardly be used as characters or synapomorphies.

First, the accessory neural arch is consistently absent in ctenosquamates. However, as discussed above, the mosaic pattern of distribution of ANA among lower teleosts casts doubt on its homology, and therefore on the validity of its absence as a ctenosquamate character.

The second ctenosquamate feature is absence of fusion between anterior epineurals and neural arches. Fusion of epineurals is the primitive teleostean condition (e.g., Hiodon), and it persists in elopomorphs, some clupeomorphs, on a few vertebrae in Esox, on many in argentinoids, and on several or many in stomiiforms and some aulopiforms (Tables 3–5). It never occurs in ctenosquamates.

FIGURE 11.—Cladograms of aulopiforms based on the data in Table 6. Family names in current use for the genera in our sample are added after the generic names in C. A, Strict consensus of 24 equally parsimonious shortest trees (length 74 steps, CI 0.68, RI 0.76) found the implicit enumeration option in Hennig86 (Farris, 1988), rooted on the “ancestor” in Table 6. B, Single shortest tree found by three-item analysis with fractional weighting (Nelson and Ladiges, 1992b) using the program TAX, version 3.1 (Nelson and Ladiges, 1992a). The matrix produced by TAX contains 1434 characters; weights were multiplied by a factor of 100, and the matrix was analyzed by PAUP version 3.0 (Swofford, 1990). The PAUP tree has a length of 135351, CI 0.857, RI 0.834. When fitted to our data, the tree has a length of 82, an increase of seven steps or 9.3% over the shortest trees, but it is interesting in that it maintains a monophyletic Chlorophthalmidae (Chlorophthalmus, Parasudis), it places notosudids, evermanellids, and scopelarchids with alepisauroids, and it presents a novel pattern within alepisauroids. C, A consensus of two among the 24 equally parsimonious shortest trees combined in A. The two trees were selected from the 24 by discarding three sets of trees. First, we discarded trees in which Pseudotrichonotus is placed as the sister group either of Aulopus + Harpadontidae + Synodontidae or of Synodontidae alone, because both of those patterns are contradicted by other characters not considered here (Johnson et al., 1989). Second, we discarded trees in which Gigantura is placed as the sister group of paralepids + Alepisaurus + Omosudis; that pattern is favored only by state 1 of character 18 (some unattached epipleurals posteriorly), whereas the link between Gigantura and Bathysaurus shown here is favored by state 1 of character 24 (very few caudal vertebrae) and by possible homology between states 2 and 3 of character 3 (all or most of the epineurals originate on the centrum). Third, we discarded trees in which the group comprising Coccorella and Scopelarchoides is placed as the sister group of alepisauroids. The latter grouping is supported by state 2 of character 16 (epipleurals extend forward to VI), whereas the grouping shown here is supported by state 1 of character 3 (epineurals on ∼ V5–15 originate on the centrum or parapophysis); both seem to be “good” characters, unique and unreversed in their respective trees. Which of them is homoplastic might be discovered by checking further members of the families concerned, but at present our choice of the grouping shown is arbitrary, although it agrees with Nelson's result in B. Characters supporting the nodes are indicated by numbers referring to Table 6, with change from state 0 to state 1 implied unless otherwise indicated. Character states are in subscript; inferred reversals are indicated by <; and characters appearing twice on the cladogram (homoplasies) are underlined. Autapomorphies (including homoplasy and/or reversal) in terminal taxa are not indicated. Presence of ANA (state 0 of character 0) in synodontoids is resolved as a reversal, and epicentrals of Alepisaurus and Omosudis (state 1 of character 10) are resolved as secondarily reacquired.

Myctophiforms: The pattern of the epineurals in the myctophiforms that we have sampled (Table 5) is a generalized one, and we see nothing in the intermusculars that bears on the problem of myctophiform monophyly (Johnson, 1992).

Intermusculars in Acanthomorph Teleosts

Tables 7 and 8 record the intermuscular series in a range of acanthomorphs, including Polymixia, with which this paper began. The overall pattern of the intermusculars in Polymixia, with epineural bones in a series beginning behind the head, epipleural bones in the middle part of the trunk, and a series of epicentral ligaments from V2 back into the caudal region with rod-like cartilages in them from V3–16, is not precisely matched in any other teleost that we have seen. Nevertheless, there is no problem of homology between the three series in Polymixia and those in lower teleosts. The only major differences in Polymixia concern the anterior epineurals because the bone that we interpret as the first epineural is enlarged and lies in the horizontal septum, and the epineurals of V3–10 originate on the parapophysis or centrum. In nonacanthomorphs (Tables 3–5) anterior epineurals generally originate on the neural arch and lie well above the horizontal septum. Some anterior epineurals originate on the centrum in a few nonacanthomorphs, e.g., Xenomystus, Anchoa, Esox, notosudids, scopelarchids (Tables 3–5), and in the aulopiform Scopelosaurus some anterior epineurals (on ∼ V6–11) originate on the parapophyses, just as in Polymixia. In the osteoglossoid Arapaima, where the first epineural is on V21 (Taverne, 1977b:229) or V22–24 (pers. obs.), the first few epineurals also originate on the parapophyses (Taverne, 1977b, fig. 141). The distal parts of the first one or more epineurals are displaced ventrally relative to their successors in argentinoids, several aulopiforms, and in Neoscopelus (notation b₁ or f₁ in Tables 4, 5), although they lie above the horizontal septum.

Thus, the ventrally displaced anterior epineurals of Polymixia are not entirely original in comparison with those of nonacanthomorphs. In any case, the intermuscular bones on V3–8 in Polymixia must be epineurals because there are epicentral ligaments below them. The only question of homology, therefore, concerns the intermuscular on V1: is it the serial homologue of the epineural bones on succeeding vertebrae, which it resembles in structure (bone), or of the epicentral ligaments on succeeding vertebrae, which it resembles in position (horizontal septum)? There is no decisive test to settle problems of serial homology, like the congruence test for problems of homology as synapomorphy, but ontogeny is the most useful criterion (Mabee, 1988, 1993). As Table 1 shows, the bone on V1 of Polymixia develops in series with the epineurals and is fully formed at 12 mm SL, before the epicentrals are recognizable. Furthermore, as Tables 3–5 show, there is no lower teleost in which the epicentral series contains just one bone on V1 followed by a series of ligaments; when epicentral bones occur, they form a complete series anteriorly (Megalops, clupeomorphs, gonorynchiforms, Parasudis). Both lines of evidence indicate that the bone on V1 of Polymixia is an epineural displaced ventrally into the horizontal septum, not an epicentral. We take that conclusion as the starting point for our comparisons of the intermusculars in Polymixia with those of other acanthomorphs, and we use a description of the intermusculars in holocentrid beryciforms and centropomid perciforms as an introduction to those comparisons.

FIGURE 12.—Intermuscular system of bones and ligaments in Holocentrus diadema Lacépède, based on BMNH 1960.3.15.117 (40 mm SL). The intermuscular bones are in solid black, the ligaments are shaded. Every fifth vertebra is numbered. (Scale bar in mm.)

HOLOCENTRIDS

As stated in the “Introduction,” all Recent acanthomorphs except Polymixia have only one series of ossified intermusculars, or no such bones. Holocentrids (Figures 12, 13) are used here to exemplify the primitive form of that acanthomorph condition. Within holocentrids, we construe Holocentrus in a broad sense, as including species currently placed in Sargocentron or Adioryx, as Stewart (1984) was unable to find any apomorphies distinguishing those species, and they are evidently paraphyletic relative to the two species (H. ascensionis, H. rufus) currently grouped in Holocentrus by an apomorphic ear/swimbladder linkage. The description that follows is based on the illustrated counterstained specimen of Holocentrus diadema Lacépède, a counterstained specimen of H. spiniferum Forskål (BMNH 1960.3.15.169), three alizarin-stained specimens of H. vexillaris (USNM 269533), and counterstained and alizarin-stained specimens of Ostichthys and Myripristis. In the Holocentrus illustrated (Figures 12, 13), the series of ossified intermusculars extends over 12 vertebrae. On V1 (cf. Rosen, 1985, fig. 20, where it is called an epineural) the bone originates rather high on the (autogenous) neural arch, extends posterolaterally in the horizontal septum, and ends immediately below the lateral line nerve at the level of the junction between the third and fourth centra. This bone has the same relations as the epineural on V1 in Polymixia, but it differs from that in one respect: its distal tip is surrounded by (but is not continuous with) an irregular superficial plate of cartilage (Figure 13). The intermuscular on V2 in Holocentrus has an enlarged head (Rosen, 1985, fig. 20, where it is called a pleural rib). It originates in a socket at the extreme base of the (fused) neural arch, extends posterolaterally in the horizontal septum, and ends beneath the lateral line nerve. Like the first intermuscular, the distal tip of the second is surrounded by an irregular but smaller superficial plate of cartilage (Figure 13). The next five intermusculars, on V3–7, each originate on the head of the rib, and their distal end is successively further above the lateral line nerve; the distal tip of the third is associated with a small, superficial blob of cartilage (Figure 13), but there is no cartilage at the tip of the others. On V8–10 the intermusculars originate at successively higher points on the parapophysis and centrum rather than on the rib (Figure 12): at the base of the parapophysis on V8, on the centrum, by means of a short ligament, on V9, and on the base of the neural arch, by means of a ligament, on V10. The distal ends of these intermusculars lie at successively higher levels above the horizontal septum, a condition first noted in holocentrids by Owen (1846:66; also Günther, 1859:24, 38, on Myripristis and Holocentrus). The last two intermuscular bones are attached by long ligaments to neural spines of V11–12. Like their predecessors, they end distally at successively higher levels, with the last one terminating closer to the tip of the neural spine than to the lateral line. On V13 and V14 there are epineural ligaments on the neural spines; the epineural ligament on V13 has a sliver of included bone distally on the right side only.

FIGURE 13.—First four vertebrae of Holocentrus diadema, same specimen as Figure 12, to show superficial cartilage (indicated by open circles) at tips of first three epineurals. In larger Holocentrus (e.g., the 74 mm SL individual recorded in Table 7), cartilage also occurs on the fourth epineural.

In holocentrids, as in Polymixia (Figure 1, Plate 2A–D) and most lower teleosts, there are epicentral ligaments extending from the vertebrae in the horizontal septum (Plate 2E,F). The first is on V9, and it originates on the parapophysis, just in front of the rib head. The last two rib-bearing vertebrae, V10–11, have closed haemal canals, and the epicentral ligament originates above the rib on the haemal arch. On the first three caudal vertebrae, V12–14, the epicentral ligament originates at successively higher points on the base of the haemal spine, and on V15–17 it is on the anteroventral part of the centrum. On more posterior vertebrae, the point of origin of the ligament shifts toward the middle of the centrum, and the last detectable epicentral is on V24 (PU5).

Posterior oblique ligaments (POTs) are present in Holocentrus. The most anterior one originates anteroventral to the epicentral ligament on the haemal spine of the second caudal vertebra (VI3), passes forward beneath three epicentral ligaments, and inserts on the lateralis musculature together with the epicentral ligament of V9 (the most anterior member of the epicentral series). On succeeding caudal vertebrae the POTs have the same pattern, inserting with the epicentral of the vertebra four in front. On vertebrae behind V13, the point of origin of the POT moves up the haemal arch on to the anteroventral corner of the centrum, and more posteriorly (at about V17) the origin of the POT shifts across the intervertebral joint on to the posteroventral comer of the preceding centrum. The last detectable POT is on V25 (PU4). The POTs in holocentrids are dorsoventrally flattened, strap-like ligaments, about half the size of the epicentral ligaments anteriorly, and about equal in size to them posteriorly.

There are generally no epipleural bones in holocentrids, but in specimens of H. diadema, H. spinifer, and H. vexillaris there are ligaments in the epipleural position on haemal spines of the first two caudal centra (V12–13), and in one individual (the largest, 77 mm SL) among the three in USNM 269533 (H. vexillaris) there is a sizeable bone in the first of these ligaments on both sides of the specimen. We have not seen an epipleural bone in any other holocentrid or beryciform, although we have examined many cleared-and-stained specimens as well as dried skeletons and radiographs of large specimens, nor is one recorded in previous descriptions (Starks, 1904a; Zehren, 1979; Stewart, 1984), and we therefore regard the single epipleural bone in this individual as anomalous or atavistic.

Other holocentrids show only trivial differences from the pattern described above and shown in Figures 12 and 13. A counterstained specimen of H. spiniferum (76 mm SL) has 13 rather than 12 intermusculars, with that on the 8th vertebra attaching to the rib rather than the parapophysis, and that on the 11th vertebra attaching directly to the neural spine rather than by ligament, and it has the fourth intermuscular ending in a small superficial plate of cartilage, like the first three in the illustrated specimen (Figure 13).

A counterstained specimen of Myripristis pralinius (BMNH 1974.5.25.699,65 mm SL) and the alizarin-stained M. murdjan illustrated in Plate 2E,F indicate that intermuscular bones and ligaments of Myripristis show the same pattern as in Holocentrus in every detail except that no cartilage is detectable at the tips of anterior intermusculars. As in Holocentrus, epipleural ligaments are present on the first two caudal haemal spines.

CENTROPOMIDS

In Table 8 we record the intermusculars in two species of the centropomid Lates, one L. sp. (from a cleared-and-stained lot of 11 planktonic young of L. longispinis or L. niloticus from near Kigoma, Lake Tanganyika; introduced populations, determination by P.H. Greenwood) and an adult L. calcarifer. Lates sp. is illustrated in Figure 14. In our specimens there are four (L. calcarifer) or five (L. sp.) intermuscular bones; Greenwood (1976) found eight intermusculars in adult L. niloticus and five in L. (Luciolates) stappersi. These bones have the same distribution as anterior epineurals in holocentrids: all lie in the horizontal septum, with the first two originating on the neural arch (epineurals of Greenwood, 1976) and the remainder on the rib (epipleurals of Greenwood, 1976). Behind these intermuscular bones there is a gap of four (L. sp.) to seven (L. calcarifer) vertebrae before the first epicentral ligament, which originates on the parapophysis (forming a closed haemal arch) of V10 in L. sp., and on that of V12, the first caudal vertebra, in L. calcarifer. In L. sp. there are nine more epicentral ligaments and in L. calcarifer there are seven more epicentral ligaments, with the last on V19 in both species. Passing posteriorly along the column, the origin of the epicentrals moves from the base of the haemal spine to the middle of the centrum, as shown in Figure 14.

Posterior oblique ligaments (POTs) are well developed in Lates. In our juvenile L. sp., the first POT originates on the parapophysis of V7 and inserts on the distal part of the intermuscular of V4. The POT from the parapophysis of V8 inserts on the tip of the intermuscular of V5 (the last intermuscular, which is attached to the centrum by ligament), and POTs from V9–12 insert at the lateral junction of the myoseptum and horizontal septum. The point of origin of POTs shifts from the parapophysis (placed anteriorly on the vertebra) to the posterior part of the preceding centrum at about V11, so that in the anterior caudal region there is an epicentral ligament originating anteriorly on each centrum and a POT originating posteriorly, the pattern described by Kafuku (1950). The first epicentral ligament, on V10, inserts with the POT from the centrum of V11. The last obvious POT originates on PU7, with the last epicentral ligament, and inserts with the epicentral ligament from PU8. In our adult Lates calcarifer, the first detectable POT originates on V9.

FIGURE 14. Intermuscular system of bones and ligaments in Lates sp. (L. longispinus Worthington or L. niloticus (L.)), based on unregistered BMNH pelagic larvae, 35–40 mm SL. The intermuscular bones are in solid black, the ligaments are shaded. Every fifth vertebra is numbered. (Scale bar 1 mm.)

There are no epipleural bones or ligaments in Lates.

Table 8 also records the intermusculars in the centropomid Psammoperca waigiensis. The pattern in Psammoperca agrees with that in Lates in most details. There are eight epineurals, as in adult L. niloticus, but epicentrals begin on V10 (the last abdominal), on the same vertebra as the first epicentral in Lates sp., so that there is a gap of only one vertebra between the epineural and epicentral series. The first POT originates on the parapophysis of V6 and inserts on the fourth epineural. As in Lates, there are no epipleurals in Psammoperca.

Centropomus (we checked C. ensiferus) has six (our C. ensiferus) or seven (Fraser, 1968) epineural bones and the first epicentral ligament originates on V10 (the last abdominal). The first POT also originates on V10, and inserts on the epineural of V6.

COMPARISON BETWEEN THE INTERMUSCULAR BONES AND LIGAMENTS IN Polymixia, HOLOCENTRIDS, AND CENTROPOMIDS

Figure 15A–C summarizes the condition of the intermuscular bones and ligaments in Polymixia, a holocentrid, and a centropomid. As shown above, the pattern in Polymixia is readily homologized with that in nonacanthomorph teleosts (aulopiforms in particular), and the only unique difference is that the first epineural of Polymixia is displaced ventrally into the horizontal septum.

The intermusculars of holocentrids differ from those of Polymixia in six ways: (1) the first five to seven epineurals (rather than just the first) lie in the horizontal septum; (2) epineurals on V3 to V7–8 originate on the rib, not the parapophysis; (3) epicentral ligaments are absent on V1–8 (rather than just V1); (4) there are no cartilage rods in the epicentral ligaments, although there may be superficial cartilage plates at the tips of the first few epineurals; (5) the first POT is on the second caudal vertebra (V13) and inserts on the first epicentral ligament, on V9 (in Polymixia the first POT is on V9 and inserts on the epicentral ligament of V5); and (6) there are no epipleural bones in holocentrids (except a single bone in one anomalous individual), just epipleural ligaments on the first two caudal vertebrae. We interpret five of these six differences as derived conditions in holocentrids relative to those in Polymixia. In holocentrids the second to seventh epineurals have descended into the horizontal septum (1), so eliminating epicentrals of the anterior vertebrae (3) and anterior POTs (5); origin of the epineurals on V3 to V7 or V8 has shifted from parapophysis to rib (2); and the epipleural series is greatly reduced (6). The other difference (4), concerning cartilage in the epicentrals or at the tip of the anterior epineurals, may merely reflect autapomorphic conditions in both Polymixia and holocentrids; a wider survey of double-stained acanthomorphs, particularly of relatively large specimens, is necessary before anything useful can be concluded.

FIGURE 15.—Comparative summary of intermuscular patterns in acanthomorphs. A, Primitive euacanthomorph pattern in Polymixia lowei, as in Figure 1; B, Primitive acanthopterygian pattern in Holocentrus diadema, as in Figure 12; C, Lates sp., as in Figure 14, exemplifying the pattern we take to be primitive for percomorphs; D, Pseudanthias squamipinnis (Peters), based on BMNH 1975.4.5.14 (29 mm SL), exemplifying the pattern we take to be derived in percomorphs. Ossified intermusculars are in solid black, cartilaginous epicentrals in Polymixia are stippled. (Scale bars in mm.)

The intermusculars of centropomids differ from those of holocentrids in five ways: (1) epineurals are confined to the first four (Lates calcarifer) to eight (L. stappersi, Psammoperca) vertebrae, and they all lie in the horizontal septum; (2) there is no cartilage at the tip of anterior epineurals; (3) epicentral ligaments are absent on V1–9 (Psammoperca, Centropomus, Lates sp.) or V1–11 (Lates calcarifer) so that there is a gap of from one (Psammoperca) to seven (L. calcarifer) vertebrae between the last epineural and the first epicentral; (4) the first POT originates on V6 (Psammoperca), V7 (L. sp.), V9 (L. calcarifer), or V10 (Centropomus), in front of or beneath (Centropomus) the first epicentral ligament, and the most anterior POTs insert on epineural bones rather than epicentral ligaments; and (5) there are no epipleural ligaments. We interpret four of these five differences as derived conditions in centropomids relative to those in holocentrids. In centropomids the epineural series is truncated caudally (1) and the epicentral series is further truncated rostrally (3) so that the two series no longer overlap; the POTs have extended rostrally beyond the epicentrals and have established a new relationship with the epineurals in the horizontal septum (4); and the epipleural series is lost (5). The remaining difference, concerning absence of cartilage at the tips of anterior epineurals (2), probably reflects autapomorphic conditions in holocentrids, as surmised above.

THE INTERMUSCULAR SERIES AND ASSOCIATED STRUCTURES IN OTHER ACANTHOMORPH TELEOSTS

Tables 7 and 8 record the distribution and form of the intermuscular bones and ligaments in a range of acanthomorphs. In the corresponding section on nonacanthomorphs (p. 11) we commented separately on the three series of intermusculars in those fishes. Acanthomorphs lack epipleurals (excepting Polymixia, ligaments on the first two caudal vertebrae in holocentrids, and questionable ligaments in the lampridiform Velifer, p. 43) so there is no need for further comment on those. We discuss the two other series, the epineurals and epicentrals, together, because we believe that they are indistinguishable in some acanthomorphs. We also comment on acanthomorph POTs, ribs, and certain other features recorded in the tables.

EPINEURALS AND EPICENTRALS.—The preceding comparisons between the intermusculars of Polymixia, holocentrids, and centropomids showed three patterns of the epineurals and epicentrals (Figure 15A–C). We regard these three conditions as a morphocline. As Tables 7 and 8 show, the pattern in Polymixia is approximated only in lampridiforms among acanthomorphs. Lampridiforms are discussed separately below, and the Polymixia pattern needs no further comment here.

The holocentrid pattern is matched only in other beryciforms, notably in the berycid Centroberyx and the anomalopid Anomalops (Table 7). Essentials of this pattern are a series of epineurals that originate on ribs anteriorly and ascend to neural arches and spines posteriorly, and a series of epicentral ligaments that begin on the posterior abdominal vertebrae, at about V9. Because the epicentral series overlaps the epineural series over several vertebrae there is no problem of serial homology. Variants of the holocentrid pattern recorded in Table 7 include that in the trachichthyid Trachichthys and the anomalopid Photoblepharon, where the epineural series is interrupted, with bones on the first two vertebrae and ligaments beginning at V6–7, and that in Monocentris, where epineurals do not begin until V8. Stephanoberyciforms (Table 7) show a different pattern, with few epineurals (the eight in Gibberichthys and 10 in Rondeletia are exceptional) and no epicentrals (except for a questionable bone on the centrum of V2 in our specimen of Barbourisia, probably an individual anomaly).

The pattern in centropomids, with a gap of one to several vertebrae between the last epineural and the first epicentral, is matched in three other percoids in Table 8: Morone (Moronidae), Doederleinia (Acropomatidae), and Drepane (Drepanidae), although in Drepane epineurals extend to the second caudal vertebra (where they originate on the haemal arch) and epicentrals begin on the fifth caudal vertebra. The centropomid pattern also is matched in the zeiform Xenolepidichthys (Table 7), in the mugiloids Agonostomus (Table 8) and Liza (Table 8), and in a 14 mm SL larva of the scombroid (sensu Johnson, 1986) Sphyraena (Table 8).

A much more common pattern among the percomorphs (sensu Johnson and Patterson, 1993) in Table 8 is that shown, for example, by the atherinomorphs Bedotia, Menidia, and Exocoetus, by the serranid Pseudanthias (Figure 15D), the caproids Antigonia and Capros, the acanthuroid Siganus (and other acanthuroids illustrated in Tyler et al., 1989, figs. 23–29), the anabantoid Colisa, the cottoid Cottus, and the carangoids Caranx and Rachycentron. In this pattern there is only a single, uninterrupted series of intermusculars, originating on the ribs on anterior rib-bearing vertebrae (except in Menidia and Exocoetus, where they are on the parapophyses), on the parapophysis and/or haemal arch more posteriorly, and usually ascending to the centrum on caudal vertebrae. The series may be all in bone (e.g., Elassoma, Bedotia, Exocoetus, Pseudanthias, Cottus) or may be in bone anteriorly and ligament caudally (e.g., Menidia, caproids, Siganus, Colisa, carangoids). A similar pattern occurs among nonpercomorph acanthomorphs (Table 7) in gadiforms and in the stephanoberyciform Rondeletia. There is an obvious problem of homology with the elements (bones, ligaments) of this pattern: are they all epineurals, serial homologues, or are anterior members of the series epineurals and posterior members epicentrals (the ligaments, perhaps), in which case they are not all serial homologues?

We have come to the conclusion that in most cases this question is meaningless, and we have decided to call them all epineurals (they are entered as such in Tables 7 and 8). The question is analogous to the problem of “phylogenetic fusion” between bones (discussed by Patterson, 1977), with the added dimension or complication of serial homology. Where there is evidence of ontogenetic fusion between two bones, there is no real difficulty. A compound name for the resultant single bone sometimes may be thought appropriate (e.g., the intertemporosupratemporal of Polyodon, Grande and Bemis, 1991:6), or the compound name is not found necessary, as with the teleostean pterotic (ontogenetic fusion between dermopterotic and autopterotic in some teleosts, Patterson, 1977:98), palatine (ontogenetic fusion between dermopalatine and autopalatine in some teleosts, Patterson, 1977:100), and quadrate (ontogenetic fusion between quadrate and quadratojugal in some teleosts, Patterson, 1977:100). But when there is no evidence of ontogenetic fusion, and a single bone in one form or group is held to be homologous with two bones in outgroup taxa, is it better to assume that the two bones have “fused” in phylogeny, and so prefer the compound name, or has one of the two bones been lost or “captured” by the other, so that a single name is more appropriate? ∅rvig (1962) and Nelson (1969, 1973) concluded that distinction between phylogenetic fusion and loss in such cases was meaningless (“merely semantic,” Nelson, 1973:339) and opted for fusion “for want of a better word” (Nelson, 1969:10). Patterson (1977:96) argued that the hypothesis of phylogenetic fusion was preferable, “when supported by evidence of ontogenetic fusion in some forms,” because the alternative, i.e., loss of one bone through “capture” or “invasion” by the other, was irrefutable and therefore untestable.

In our case, the question of distinction between epineurals and epicentrals concerns serial homology as well as taxic homology and is, therefore, different from discriminating between fusion or loss for two bones. As with fusion between bones, ontogeny provides the best test, and fusion and loss hypotheses are both testable because each makes different predictions. For example, we have evidence of ontogenetic fusion between the epineural and epicentral series in the primitive scombroid (sensu Johnson, 1986) Sphyraena (Table 8). In a 14 mm SL larva, there are only three epineural bones, on V1–3, and the epicentral series of ligaments occupies V9–15. In a 79 mm SL subadult, the epineural series of bones occupies V1–7 (that on V7 is attached by ligament) and that series is continued caudally by ligaments on V8–19. Thus, in Sphyraena we have evidence that the epineural series has developed rostrocaudally and has become continuous with a pre-existing series of epicentral ligaments. In Table 8, we enter bones on V1–7 of the subadult as epineurals and ligaments on V8–19 as epicentrals. But it will be evident that there is some arbitrariness here, i.e., is the ligament on V8 (which does not exist in our 14 mm larva) “really” the last epineural or is it the first epicentral? We have no solution. And in cases like Menidia, caproids, and carangoids, where in our specimens there is continuity between intermuscular bones anteriorly and ligaments posteriorly and where we have no ontogenetic series, no rational decision is yet possible on whether some or all of the ligaments are “truly” epicentrals. We expect that ontogeny will be decisive here. For example, it will be interesting to learn from ontogeny whether the pattern in gadiforms like Raniceps and Gaidropsarus (Table 7) is the result of craniocaudal development of a single series of structures (epineurals) or is the result of coalescence of two separate series (epineurals and epicentrals, as in Sphyraena). Because we have not found epicentral ligaments in any paracanthopterygian, we predict that larvae of these gadiforms will show craniocaudal development of a single series of epineurals.

There are two instances among the percomorphs in Table 8 where we have entered overlapping series of epineurals and epicentrals: the scombrid Scomberomorus and the polynemid Polydactylus. Westneat et al. (1993) have described intermuscular bones and ligaments in Scomberomorus and several other scombrids. We confirm their description (p. 188) of the condition in Scomberomorus: “An AOT [our epicentral ligaments] is a single band of fibers attaching to the posterior edge of the epipleural ribs [our epineurals] in the anterior region of the body. The anterior epipleural ribs have reduced AOTs in comparison to the thicker AOTs that attach to the posterior epipleural ribs.” But Westneat et al. (1993:193) note that in Sarda, Euthynnus, and Thunnus “most AOTs…surround epipleural ribs….Bands of AOT fibers occur on both the posterior and anterior edge of each epipleural rib.” Thus, in these scombrids the epineural bones appear to be ossifications within or surrounded by ligaments, rather than distinct from them (as in Scomberomorus). As with the ligament on V8 in Sphyraena (above), it will be evident that the distinction between epineurals and epicentrals in scombrids is more-or-less arbitrary. Westneat et al. (1993:188) suggest that “epipleural ribs are likely to be ossified serial homologues of the AOTs that occur in the main horizontal septum.” This is an accurate statement of the topographic relations between intermuscular bones and ligaments in many percomorphs, but we hope we have shown that in the phylogenetic sense the single series of intermusculars in those fishes comprises two series, the epineurals and epicentrals, that are distinct in polymixiids, beryciforms, centropomids, and some other percomorphs. Ontogenetic evidence is necessary to determine whether the two series “fuse” during development (as in Sphyraena) or are no longer distinguishable.

The second instance of overlapping epineural and epicentral series in Table 8 is the polynemid Polydactylus. Here there is a series of decended epineural bones on V1–7, and that series is continued caudally by a series of ligaments on V8–15. The point of origin of the last two epineural bones ascends from rib to parapophysis, a frequent pattern for posterior epineurals in percomorphs (e.g., Psammoperca, Pseudanthias; Figure 15D, Table 8). Following these bones is the series of ligaments on V8–15, but the anterior members of that series (V8–10) originate not on the parapophysis but more ventrally, on the rib, and the remainder originate on the haemal spine. These ligaments do not lie in the main horizontal septum, beneath the lateral line, but in the ventral secondary horizontal septum (described by Westneat et al., 1993, in scombrids), which is particularly well developed in Polydactylus. Furthermore, the first two of these ligaments, originating on the ribs of V8–9, are weaker and more diffuse than their successors, implying that the series of ligaments expresses a different developmental gradient from the epineural series of bones. Above these ligaments, there is another series of ligaments beginning on V10 and entered as epicentrals in Table 8. The first of these originates at the anteroventral corner of the centrum of V10, and the points of origin of its successors ascend to the centrum in the normal pattern of epicentral ligaments; the series extends into the caudal region, to PU4. Polydactylus also has a series of “neoneural” ligaments (notation Nn in Table 8; see below).

The situation in Polydactylus does not match any other genus in Table 8, and we do not yet fully understand it. The interpretation that we favor is that the epineurals and epicentrals show the pattern that we take to be primitive for percomorphs, as described above in centropomids, Morone, mugilids, and larval Sphyraena, where the epineural and epicentral series are discontinuous; in Polydactylus the discontinuity would be the gap between the last epineural bone on V7 and the first epicentral ligament on V10. Ligaments on the ribs of V8–10 and the haemal spines of V11–15 lie in the ventral secondary horizontal septum, in the position of epipleurals, and the fact that anterior members of the series are weaker than their successors implies that they develop in the same way as epipleurals, rostrally and caudally from the region of the first caudal vertebra. If they are epipleural ligaments, we do not believe that they are homologous with the primitive epipleural series, which is absent in all percomorphs and is represented in acanthopterygians only by two ligaments in holocentrids. We therefore suggest that these ligaments in Polydactylus are a neoformation, analogous to the “neoneural” ligaments found above the vertebral column in Polydactylus, Ammodytes, and the mullid Upeneus (Table 8 and below); they might be called “neopleurals.” Further work is necessary to determine whether a similar series of ligaments occurs in other percomorphs and whether the interpretation just proposed is valid.

Owen (1866:44), in first discriminating the three series of intermuscular bones, wrote that “in Glyphysodon [= Abudefduf, Pomacentridae] the epipleurals [= epineurals] are anchylosed to the ribs.” The pomacentrid Dascyllus is included in Table 8 and confirms Owen's observation. An epineural is fused to every rib. In a 12 mm SL specimen of Abudefduf biocellatus, all the epineurals are ossified, but none is yet fused with a rib.

POSTERIOR OBLIQUE LIGAMENTS (POTs).—Our survey of POTs in acanthomorphs has been more cursory than our survey of their epineurals and epipleurals.

POTs occur in Polymixia and lampridiforms, and those two taxa are unique among acanthomorphs in having POTs that originate on abdominal vertebrae and insert on anterior epicentral ligaments (the first POT originates on V9 in Polymixia and Velifer and inserts on the epicentral of V5 in Polymixia and of V3 in Velifer).

We have found no POTs in any paracanthopterygian in our sample, which included percopsiforms, ophidiiforms, gadiforms, batrachoidiforms, and lophiiforms. In stephanoberyciforms, POTs occur only in melamphaids, where the first originates on V9 in Poromitra, on V10 in Scopelogadus, and on V12 in Melamphaes. Because these fishes have no epicentrals (like all stephanoberyciforms), POTs of melamphaids do not cross any other ligaments in passing anterolaterally to the lateralis musculature.

Among beryciforms, holocentrids have POTs (described above) from V13 (second caudal vertebra) back to about PU4. The POT originating on V13 inserts on the first epicentral ligament, from V9. In Anomalops, the first POT originates on V11, posteroventral to the first epicentral ligament, which also originates on V11. Because there are no epicentrals anterior to this, POTs of V11–13 lie free in the horizontal septum (like those of melamphaids) as they pass forward after crossing the epicentral of V11; more posterior POTs insert on the epicentral from the vertebra four ahead of their origin.

In zeiforms, POTs show a pattern like that in percomorphs, with some anterior POTs originating on abdominal vertebrae and inserting on epineural bones. In Parazen, the first POT originates on V12 but extends forward past eight vertebrae to insert on the third epineural, which is unattached proximally (Table 7) but is aligned with V3. In Xenolepidichthys, the first POT originates on V6 and inserts on the first epineural, which is on V2.

In percomorphs (sensu Johnson and Patterson, 1993), the pattern described above in centropomids (and just mentioned in zeiforms) is common; in it some anterior POTs originate on abdominal vertebrae and insert on epineural bones. A few examples of that pattern follow. In Serranus cabrilla the first POT originates on V10 and inserts on the epineural of V6; in Morone the first POT runs from V9 to the epineural of V6; in Sphyraena the first POT runs from V8 to the epineural of V7 (the last epineural bone); in Drepane the first POT runs from V8 to the epineural of V5; in Antigonia the first POT runs from V7 to the epineural of V4; in Mulloidichthys (Mullidae) the first POT runs from V6 to the epineural of V3; in Caranx the first POT runs from V5 to the epineural of V3; and in Siganus the first POT runs from V3 to the epineural of V1.

All percomorphs named in the preceding paragraph have a series of ligaments in the caudal region (the AOTs of Kafuku, 1950, and Westneat et al., 1993), and that series of ligaments is either continuous with epineural bones anteriorly (adult Sphyraena, Antigonia, Mulloidichthys, Serranus, Siganus) or is separated from epineurals by a gap of several vertebrae (Morone, Drepane). There is another common percomorph pattern in which there are no detectable AOTs, only epineural bones, so that the anterior POTs insert on epineural bones and the posterior POTs insert on the lateralis musculature, without crossing any AOTs. Examples of that pattern include Epigonus (Epigonidae), where the first POT runs from V7 to the fourth (of six) epineurals, Cookeolus (Priacanthidae), with the first POT from V9 to the fifth epineural, Elassoma (Elassomatidae), with the first POT from V12 to the epineural of V9, and Cottus, with the first POT from V10 to the epineural of V5.

Finally, there is a third set of percomorphs in which we have found no POTs in the cleared-and-stained specimens that we have checked. These include the percoid Pseudanthias (Serranidae); the polyenemoid Polydactylus (Polynemidae); the scorpaeniforms Platycephalus (Platycephalidae), Hoplichthys (Hoplichthyidae), Anoplopoma (Anoplopomatidae), and Hexagrammus (Hexagrammidae); the trachinoids Champsodon (Champsodontidae), Trichodon (Trichodontidae), Trachinus (Trachinidae), Uranoscopus (Uranoscopidae), Bembrops and Hemerocoetes (both Percophididae), and Parapercis (Pinguipedidae); the blennioids Forsterygion (Tripterygiidae) and Dactyloscopus (Dactyloscopidae); the ammodytoid Ammodytes (Ammodytidae); and the callionymoid Synchiropus (Callionymidae). A wider and more thorough survey that includes larger specimens is necessary to determine whether absence of POTs in all or any of these genera is real or artefactual, and if real, whether it has any significance in characterizing groups.

MYORHABDOI.—The only acanthomorph in Tables 7 and 8 in which we observed myorhabdoi (series of unattached intermuscular bones in the uppermost and lowermost forward flexures of the myoseptum) is the pleuronectiform Bothus. Bothid pleuronectiforms have five series of intermuscular bones (Amaoka, 1969, figs. 120–122, 125), which are in a pattern resembling that in Notopterus amongst osteoglossomorphs (Taverne, 1978, and above) and in some clupeoids (Phillips, 1942). Samarid pleuronectiforms have three series of intermusculars (Hensley and Ahlstrom, 1984; Table 8), agreeing in position with the middle three of the five series in bothids. Amaoka (1969) took the numerous intermusculars of bothids to be primitive and to be evidence that pleuronectiforms are not related to percoids. Hensley (1977) and Hensley and Ahlstrom (1984) have argued, correctly in our view, that the extra intermuscular series in bothids (and samarids) are apomorphic. Psettodes, the sister group of other pleuronectiforms (Chapleau, 1993), has epineurals on V1-7 in a typical percomorph pattern (B₁, B₁, B₄, B₄, B₄, B₃, B₃ in the notation of Tables 7, 8; Amaoka, 1969, fig. 118). Citharids have epineurals on V1-10 or V1-11 and paralichthyids have them on V2–10 or V2–11, attaching to the centrum anteriorly and parapophyses or haemal arches posteriorly (Amaoka, 1969).

Myorhabdoi also are present in the gasterosteiform family Aulostomidae. They were described briefly in the single Recent genus Aulostomus by Jungersen (1910), and they are shown to have existed in the group since at least the Eocene by their presence in the genera Eoaulostomus, Jungersenichthys, and Synhypuralis, from Monte Bolca, Verona, Italy. Myorhabdoi also occur in gempylids (pers. obs.).

“NEONEURAL” LIGAMENTS AND BONES.—In six percomorphs in Table 8 we record a series of bones or ligaments against the symbol “Nn” meaning “neoneural.” The taxa are Ammodytes (Ammodytoidei), Dascyllus (Pomacentridae), Polydactylus (Polynemoidei), Upeneus (Mullidae), and the pleuronectiforms Samaris and Bothus. Neoneurals are all in ligament in the first four genera and are all in bone in Samaris and Bothus. In Upeneus, ligaments originate on the neural arch of V2–6 and rise to the neural spine on V8–14. In Dascyllus, the ligaments originate on the neural arch of V2–13 and rise on to the neural spine on V14–18. In Polydactylus, ligaments originate on the neural arch of V1-3, on the centrum of V4–8, and ascend to the neural spine posteriorly (V12). In Ammodytes, where the ligaments are very robust and obvious, they originate on the centra of V5–33 and ascend to the neural arch and spine posteriorly. We interpret these series of ligaments as neoformations, nonhomologous with anything in lower acanthomorphs and nonacanthomorphs. We are satisfied that they are not epineurals because all neoneural-bearing genera have a series of normal percomorph epineurals beneath the neoneurals. The distribution of these ligaments should be studied further. In a preliminary check we have found them (or something like them) in representatives of several other percomorph families: Teraponidae, Kuhliidae, Carangidae, Echeneidae, Lutjanidae, Caesionidae, Gerreidae, Sparidae, Lethrinidae, Sciaenidae, Haemulidae, Labridae, and Scaridae. We have found neoneural ligaments to be absent in representatives of a much larger range of percomorph families. Their presence may be significant, but more work is needed.

In Bothus and Samaris, neoneurals are ossified in a pattern mimicking epineurals of lower (nonacanthomorph) teleosts (for bothids, see Amaoka, 1969, figs. 120–122, 125). In our Bothus specimens, the first bone in the series attaches to the occiput by ligament. The second attaches by ligament to the reduced neural spine of V1, and the next to the neural arch of V2. There is no neoneural bone or ligament on V3 in the two specimens we examined. On V4–6, the bones are forked or spatulate proximally, where they attach to neural arches. On V7–10, the bones have anteromedial branches that attach to the neural arch and unattached anteroventral branches, like the proximally forked epineurals of many lower teleosts (notation vB₁ in Tables 3–5). These last seven bones (V4–10) are brush-like distally. Behind V10, the bones are unattached to the axial skeleton and are brush-like both proximally and distally. These unattached bones appear to be serially homologous with the anteroventral branch and posterior body of the bones on V7–10; the posterior epineurals of many lower teleosts show the same pattern (notation V₀ in Tables 3–5). In Samaris, the pattern of the neoneurals is similar but differs in detail. The first bone attaches by ligament to the first neural arch, which also (in our specimen) carries a second ligament with no included bone. There are bones attached by ligament to the second and third neural arches, and beyond that a series of unattached bones extends back to V32, some of them are forked proximally, some distally, and some at both ends (Table 8). We interpret this series of bones in Bothus and Samaris as a neoformation because there is a normal series of percomorph epineurals beneath them, on V2–9 in both genera. Amaoka (1969, figs. 120–122, 125) illustrates variants of the pattern in bothids.

In the section on acanthomorph epineurals and epicentrals, above, we described and commented on possible neopleurals in the polynemid Polydactylus, which may be ventral analogues of the neoneurals above the vertebral column.

OCCIPUT.—There are no intermuscular bones or ligaments on the occiput in any acanthomorphs in Tables 7 and 8, except for a ligament on the exoccipital in the stephanoberyciform Barbourisia and a neoneural bone attached by ligament to the occiput in the pleuronectiform Bothus (there may be two occipital neoneurals in bothids, Amaoka, 1969, figs. 120, 125). One or two intermuscular bones attach to the occiput in some scombroids (e.g., Collette and Chao, 1975).

BAUDELOT'S LIGAMENT.—Among acanthomorphs sampled in Tables 7 and 8, Baudelot's ligament originates on V1 in lampridiforms, Polymixia, paracanthopterygians, and stephanoberyciforms and on the occiput in beryciforms, zeiforms, and percomorphs (sensu Johnson and Patterson, 1993). The only exceptions to that statement in Tables 7 and 8 are the two veliferid lampridiforms and the stephanoberyciform Rondeletia, where the ligament is double, with part on V1 and part on the occiput (also in the xenisthmid gobioid Tyson; Springer, 1988, table 1); the hexagrammid scorpaeniform Hexagrammus, where the ligament is on V1; and taxa lacking the ligament, i.e., the beryciforms Anoplogaster and Monocentris, the four gasterosteiforms, and the gobiesocid Lepadogaster. We therefore believe that the point of origin of the ligament is a generally consistent and useful character, and we have used the occipital origin as a character of Euacanthopterygii (Johnson and Patterson, 1993; Percomorpha + Beryciformes and Zeiformes).

RIBS.—Among acanthomorphs sampled in Tables 7 and 8, the primitive teleostean condition (all ribs preformed in cartilage) persists in Polymixia, percopsiforms, stephanoberyciforms (Barbourisia has the last rib in membrane), several beryciforms (the last rib is in membrane in Diretmus, Holocentrus, Centroberyx, anomalopids), mugiloids, atherinomorphs, and various perciforms. All ribs are in membrane in zeiforms (or in ligament), Elassoma, gasterosteiforms, Ammodytes, Lepadogaster, and gobioids (Johnson and Brothers, 1993).

Ribs show the most remarkable modifications in the pleuronectiforms Bothus and Samaris, if our interpretation in Table 8 is correct. Amaoka (1969) interpreted bothids as lacking ribs, but Hensley and Ahlstrom (1984) suggested another interpretation, that Amaoka's “abdominal hypomerals” are pleural ribs. In Table 8, we interpret all Amaoka's hypomerals (not just those in the abdominal region) as ribs. According to that interpretation, the first rib of Bothus and Samaris is on V2, whereas in the other pleuronectiforms studied by Amaoka (1969) it is in the primitive position, on V3. In our Bothus specimens, the first three or four ribs are unmodified, but the fourth or fifth and its successors are brush-like distally. The sixth to ninth ribs (on V7–10) have an anterodorsal branch, just like that on the epipleurals of many lower teleosts (Tables 3–5), and from V11 onward the series is continued back into the caudal region by bones that are brush-like at both ends, are unattached to the axial skeleton, and appear to be serially homologous with the anterodorsal branch and posterior body of the bones on V7–10; the posterior epipleurals of many lower teleosts show the same pattern (notation D₀ in Tables 3–5). Amaoka's illustrations of bothids (1969, figs. 120–122, 125) show variants of this pattern. In Samaris, the first six ribs (on V2–7) are unmodified, the seventh (V8) is forked proximally, and those on V9–10 have anterodorsal branches passing medial to the proximal parts of the preceding ribs. On V11 (the first caudal) there is a similar bone, with a similar anterodorsal process, but it is not attached to the vertebra. The remaining members of the series are unattached, but on V12–14 the proximal end of the bone passes anterodorsally, medial to the proximal part of the preceding bone, like the anterodorsal branch on the bones on V9–11. The series extends back to V31 (PU9), with some bones forked or bifid distally, some proximally, and some simple. Extra slivers of unattached bone accompany the bones on V10–13. If these bones in the caudal region of bothids and Samaris are not ribs, the only alternative interpretation is that they are epipleurals, secondarily redeveloped in a pattern mimicking that in lower (nonacanthomorph) teleosts. Because of the perfect continuity between undoubted and unmodifed anterior ribs, modified posterior ribs, and the unattached bones in the caudal region, we prefer the interpretation that the ribs are modified in an autapomorphic pattern.

In the anabantoid Colisa (Table 8) ribs continue back into the caudal region (to PU5) as intermuscular bones, a condition resembling the caudal extension of ribs in bothids.

COMMENTS ON INDIVIDUAL GROUPS AMONG ACANTHOMORPHS

In this section we comment on aspects of the intermuscular bones and ligaments in various acanthomorph groups, which may bear on relationships.

ACANTHOMORPHA.—One feature of the intermusculars supports the monophyly of Acanthomorpha: absence in all acanthomorphs of proximal forking of epineurals and/or epipleurals. We take this proximal forking to be primitive for elopocephalans (above), and although it also is absent in argentinoids, salmonoids, osmeroids, stomiiforms, and most aulopiforms, it is present in myctophiforms, which currently are regarded as the sister group of acanthomorphs (Johnson, 1992).

LAMPRIDIFORMS.—In Table 7 we record the intermusculars in three lampridiforms, the veliferids Velifer and Metavelifer, and the lampridid Lampris (information on Lampris from a partially dissected specimen and radiographs only), which are the three cladistically most primitive genera of this monophyletic group (Olney et al., 1993). These three lampridiforms differ from all other acanthomorphs in having no epineurals in the horizontal septum, and Velifer and Metavelifer differ from other acanthomorphs in having all epineurals originating on the neural arch (anteriorly) or spine (posteriorly). Like some aulopiforms, the three lampridiforms have the first epineural displaced ventrally relative to its successors (notation b₁ in Tables 5, 7), but that bone is well above the horizontal septum. Furthermore, unlike all other acanthomorphs except Polymixia, these lampridiforms also have epicentral ligaments beginning on V1 (Velifer, Johnson and Patterson, 1993, fig. 1) or V3 (Metavelifer, Lampris). In Velifer, where POTs are easily seen in incident light in our 133 mm SL cleared-and-stained specimen, the first POT originates on the parapophysis of V9 and inserts at the tip of the epicentral ligament of V3. In Polymixia, the first POT also originates on V9, but it inserts on the epicentral of V5; thus Velifer agrees with Polymixia and differs from other acanthomorphs in having POTs that originate on abdominal vertebrae and insert on anterior epicentral ligaments. We have seen no epipleural bones or ligaments in lampridiforms, but we note that in veliferids the swimbladder extends behind the abdominal cavity in paired, horn-like processes that occupy the normal position of epipleurals, and that in Velifer the series of ribs is continued posteriorly into the caudal region by an extensive series of ligaments (Table 7). A review of other teleosts in our sample shows that in halosaurs and notacanths some (Halosaurus) or all (Notacanthus) ribs are in ligament (Table 3), in the cypriniform Hemibarbus the last eight ribs are attached by ligament (Table 4), in the aulopiform Scopelarchoides the last two ribs are in ligament (Table 5), in the beryciform Anoplogaster all ribs are attached by ligament (Table 7), and in the exocoetoid Exocoetus the last rib is attached by ligament (Table 8), but all these rib-like ligaments are within the abdominal region; in the beryciform Monocentris and the zeiforms Xenolepidichthys and Parazen anterior ribs are in ligament (Table 7). In other words, the situation in Velifer is unique among the teleosts that we have sampled, and we surmise that the ligaments behind the ribs represent the missing, but expected, epipleurals.

Thus, lampridiforms are more primitive than all other acanthomorphs in having no epineurals in the horizontal septum, and veliferids are more primitive than other acanthomorphs in having all epineurals originating on the neural arch or spine rather than some on the parapophysis, rib, or centrum. Lampridiforms agree with Polymixia in having epicentral ligaments on the first few vertebrae, and in having POTs originating on abdominal vertebrae and inserting on anterior epicentral ligaments. Velifer also may have an extensive series of epipleural ligaments. We therefore believe that lampridiforms are the sister group of all other acanthomorphs, Polymixia included. Elsewhere (Johnson and Patterson, 1993) we proposed the name Euacanthomorpha for the group comprising nonlampridiform acanthomorphs, and Holacanthopterygii for the Euacanthomorpha minus polymixiiforms; we argued there that polymixiiforms are the sister group of the Holacanthopterygii.

In Lampris (Table 7), epineurals of V3–6 (there are no epineural bones behind V6) originate on the rib, not on the neural arch as they do in veliferids; in this Lampris agrees with most euacanthomorphs (Table 7, 8). But in Lampris, epicentral ligaments of V3–5 originate on epineural bones (notation LN in Table 7); that pattern is unique to this genus among our entire sample, and it corroborates the inference that descent of anterior epineurals to ribs occurred independently in Lampris and in euacanthomorphs.

PARACANTHOPTERYGIANS.—There are reasons to believe that the Paracanthopterygii are the sister group of the Acanthopterygii (all other holacanthopterygians; Johnson and Patterson, 1993). Those reasons do not include features of paracanthopterygian intermuscular bones and ligaments, which are either uninformative on paracanthopterygian relationships or provide only conflicting evidence. In Table 7 we record the intermusculars in two percopsiforms (Percopsis, Aphredoderus) and two gadiforms (Raniceps, Gaidropsarus), and Markle (1989:73) summarizes the condition of the ribs and intermuscular bones in a range of paracanthopterygians. Percopsiforms show the pattern that we take to be primitive for the group: a short series of epineural bones (five in Percopsis, up to eight in Aphredoderus), all lying in the horizontal septum and originating on the rib from V3 onward. There are no epicentral ligaments and no epineural ligaments behind the series of epineural bones. The two gadiforms lack epineurals on V1–2, a synapomorphy of the group (Patterson and Rosen, 1989:19, as “epipleurals”; there is a small, unattached bone on one side of V1 in our Raniceps), but they have a long series of epineurals that extend back into the caudal region. Again there are no epicentral ligaments, and we have not succeeded in finding either epicentral ligaments or POTs in any paracanthopterygians we checked, including ophidiiforms, batrachoidiforms, and lophiiforms.

STEPHANOBERYCIFORMES.—In Table 7 we record the intermusculars of six stephanoberyciforms, representing six of eight families currently included in the group (the Stephanoberycoidei of Moore, 1993). There are from 0 (Stephanoberyx) to 10 (Rondeletia) epineural bones in stephanoberyciforms (melamphaids have 4–6), and those on rib-bearing vertebrae (V3 onward) originate on the parapophysis or centrum (Table 7), except in Barbourisia, where there are epineurals on the ribs of V3–5 (Table 7). In having epineurals of rib-bearing vertebrae on the parapophysis or centrum rather than the rib, stephanoberyciforms resemble Polymixia and differ from beryciforms and percomorphs, which have epineurals on the rib on anterior rib-bearing vertebrae. The major exception to the latter condition to be found in Tables 7 and 8 is that all epineurals of rib-bearing vertebrae are on the parapophysis in the atherinoid Menidia and the exocoetoid Exocoetus. We take this to be secondary because several anterior epineurals are on the rib in the atherinoid Bedotia and in mugiloids, gasterosteids, and Elassoma, taxa that include outgroups of Menidia and Exocoetus in our opinion (Johnson and Patterson, 1993). Other exceptions in Tables 7 and 8, such as the zeiform Xenolepidichthys, with ribs formed only in ligament, and Cottus, with ribs only on V9–11, are clearly secondary. We therefore take the origin of epineurals on the parapophysis in stephanoberyciforms to be a primitive condition, differentiating them from beryciforms and percomorphs (Johnson and Patterson, 1993). We interpret the descent of epineurals to the ribs in Barbourisia to be independent of their descent in beryciforms and percomorphs, given the cladistically derived position of Barbourisia in Moore's (1993) phylogeny of stephanoberyciforms (placed as the sister group of megalomycterids + cetomimids). Lampris (above) and paracanthopterygians provide other examples of independent descent of epineurals to ribs.

We have not found epicentral ligaments in any stephanoberyciform. We agree with Moore (1993) that melamphaids are the most primitive stephanoberyciforms, and they are the only members of the group in which we have found POTs; the first POT originates on V9 in Poromitra, on V10 in Scopelogadus, and on V12 in Melamphaes. Because there are no epicentral ligaments, the POTs of melamphaids do not cross any other ligaments in their passage to the lateralis musculature, and the anterior ones do not insert on epineurals.

Rondeletia is different from any other stephanoberyciform in our sample in several ways. It has epineural bones on V1–10, more than any other stephanoberyciform. All epineural bones lie in the horizontal septum, and the epineurals are continued caudally by a series of ligaments (V11–16) in the horizontal septum, originating on the haemal arch anteriorly and the centrum posteriorly. Finally, at the tip of the epineurals on V1–8 there are small, superficial plates of cartilage, like those in Holocentrus (Figure 13). Given the position of Rondeletia in Moore's (1993) phylogeny of stephanoberyciforms (as the sister group of Barbourisiidae and Megalomycteridae + Cetomimidae), we interpret these features of its intermusculars as autapomorphous, not primitive for the group (the features are all absent in melamphaids and Gibberichthys, for example).

EUACANTHOPTERYGII.—Elsewhere (Johnson and Patterson, 1993) we proposed the name Euacanthopterygii for a group comprising Beryciformes and an expanded Percomorpha (including Atherinomorpha). The only character of the intermusculars bearing on that grouping is the origin of epineurals on ribs (rather than on the parapophysis, centrum, or neural arch) of anterior rib-bearing centra. The character is questionable because the same origin of epineurals on the ribs is found in the lampridiform Lampris, the stephanoberyciform Barbourisia, and in paracanthopterygians.

ZEIFORMES.—Elsewhere (Johnson and Patterson, 1993) we argued that Zeiformes do not include caproids (Capros, Antigonia), and that caproids are percomorphs but zeiforms are not. As with paracanthopterygians (above), the intermusculars of zeiforms are uninformative or provide contradictory information on zeiform relationships. In Table 7 we record intermusculars of the grammicolepid Xenolepidichthys and the parazenid Parazen, two genera that we regard as relatively primitive zeiforms (Johnson and Patterson, 1993). Xenolepidichthys has epineural bones on V2–7 and a ligament on V8. There is then a gap of three vertebrae before a series of epicentral ligaments on the haemal arches of V12–20. None of the epineurals originates on a rib, but “ribs” are in ligament on V4–8, where they overlap the epineural series. Parazen shows a unique condition among the acanthomorphs in Tables 7 and 8; epineural bones are present on V1–13, but they are all unattached except for those on V5–6, which originate on the ligamentous ribs of those vertebrae. Unattached epineurals occur commonly in zeiforms (e.g., Cyttopsis, Zenion).

We interpret the separation of the epineural and epicentral series in Xenolepidichthys as relatively primitive, resembling the condition in centropomid percoids and in mugiloids. But absence of overlap between the epineural and epicentral series, and the fact that the epineurals have not ascended above the haemal arch by V8, give no support to the proposal by Johnson and Patterson (1993) that zeiforms fit between stephanoberyciforms and beryciforms in the acanthomorph cladogram, for beryciforms show a more primitive state than zeiforms in both these characters (Table 7). The POTs of zeiforms also show a pattern more like that in percomorphs than beryciforms, with some anterior POTs originating on abdominal vertebrae and inserting on epineural bones (as noted above, in Parazen the first POT originates on V12 and inserts on the epineural of V3, and in Xenolepidichthys the first POT originates on V6 and inserts on the epineural of V2).

BERYCIFORMES.—Table 7 records the intermusculars of nine beryciforms, including representatives of all seven families (unlike Stiassny and Moore, 1992, and Moore, 1993, we include the Berycidae and Holocentridae in Beryciformes; Johnson and Patterson, 1993). We take the pattern in holocentrids, described in detail above and illustrated in Figures 12 and 13, to be primitive for the group. Major components of that pattern include a series of epineural bones that originates on the ribs on anterior rib-bearing centra and ascends to the neural spine on posterior abdominal and caudal vertebrae and a series of epicentral ligaments beginning at about the first caudal vertebra. There are epipleural ligaments on the first two caudal vertebrae in holocentrids, but we have not seen similar structures in other beryciforms.

The holocentrid pattern of intermusculars is most closely matched in Anomalops and the berycid Centroberyx (Table 7). In the anomalopid Photoblepharon and in Trachichthys the pattern is similar, but the epineural series is interrupted, with bones on V1–2 and ligaments (with included bone posteriorly in Photoblepharon) from V6 or V7. Monocentris lacks epineurals on V1–7 and ribs on V3–4, and its posterior epineurals (identifiable as epineurals because there are epicentral ligaments beneath them) remain in the horizontal septum, rather than ascending on to the neural arch and spine as they do in other beryciforms. In Diretmus there is only one epineural, on V1, and in Anoplogaster, which appears to be the sister group of diretmids (Moore, 1993; Baldwin and Johnson, in press), there are no epineurals or epicentrals, no Baudelot's ligament, and all ribs are attached by ligament.

PERCOMORPHA (sensu Johnson and Patterson, 1993).—The Percomorpha may be rendered monophyletic by inclusion of the Atherinomorpha and exclusion of several groups (Lampridiformes, Stephanoberyciformes, Beryciformes, Zeiformes) (Johnson and Patterson, 1993). The Percomorpha in that sense share three derived features of the intermusculars (Table 8): (1) all epineurals lie in the horizontal septum, originating on the ribs anteriorly (V3 onward) and on the parapophyses, haemal arches, or centra posteriorly; (2) the epicentral series of ligaments, when present and distinct, never overlaps the epineural series; and (3) POTs in the abdominal region extend anteriorly beyond the epicentrals to insert on epineural bones. As with so many other characters in percomorphs and their relatives, the percomorph condition of all three characters occurs elsewhere in acanthomorphs. Regarding character (1), epineurals show the same pattern in paracanthopterygians (e.g., gadiforms, Table 7), in the stephanoberyciform Rondeletia, and in zeiforms. Regarding character (2), the zeiform Xenolepidichthys shows no overlap between epineurals and epicentrals (Table 7). And regarding character (3), zeiforms show the percomorph pattern.

The pattern of intermusculars that we interpret as primitive for percomorphs is that illustrated in Figure 14 and shown in Table 8 by centropomids, Morone, Drepane, larval Sphyraena, and mugiloids. In that pattern, the epineural and epicentral series are discrete, with a gap of from one (Psammoperca) to seven (Lates calcarifer) vertebrae between the last epineural and the first epicentral. In many percomorphs the epineural and epicentral series become indistinguishable (e.g., caproids, Siganus, Colisa, Rachycentron, Menidia; Table 8). The problem of distinguishing the two, the possible value of ontogeny in doing so, and our usage in Table 8 are discussed above (p. 38).

We believe that a wider and more thorough survey of percomorph intermusculars might well provide valuable information on relationships. As one example, the neoneural series of ligaments, recorded in Table 8 in the ammodytoid Ammodytes, the polynemoid Polydactylus, and the mullid Upeneus and discussed above (p. 41), may prove to be a useful feature when its distribution is better understood. Two further examples concern gobieseocids and uranoscopids. In Table 8, intermusculars of the gobiesocid Lepadogaster are recorded. They show a remarkable pattern, with all epineurals of rib-bearing vertebrae (V2–14) originating on the centrum, and with ribs originating on the epineural (notation BN) on V2–11 and lying free on V12–14. This pattern (ribs originating on epineurals) is evidently general in gobiesocids (Gosline, 1970:376) but does not occur in callionymids (Callionymus, Table 8), which are their close relatives (Winterbottom, 1993; Johnson and Patterson, 1993:614). Callionymids lack ribs, but they share with gobiesocids absence of an epineural on V1, an unusual feature (caproids and the zeiform Xenolepidichthys are the only other taxa in Tables 7 and 8 that lack the epineural on V1 but have one on V2).

Concerning uranoscopids, Figure 16 is a reinterpretation of Pietsch's (1989, fig. 31) drawing of the axial skeleton of Uranoscopus. In the illustrated specimen of Uranoscopus there are ribs on V3–12 and epineurals on V1–17. Pietsch (1989) interpreted the first four unattached epineurals as ribs and the first three ribs as epineurals (his epipleurals); based on our reinterpretation, he counted 10 pairs of ribs, missing the small ones of V12, and 15 pairs of intermusculars, missing the short epineural of V1. That bone is variable, being present only on the right side in the illustrated specimen, present on both sides in a second specimen and in that used by Starks (1923:279), and absent on both sides in a third. In the illustrated specimen, epineurals of V1–5 are unattached, and those of V6–17 originate on the parapophysis (anteriorly) or centrum (posteriorly). The ribs of V3–5 originate on the parapophysis in the normal way, but those of V6–12 are unattached, resembling the epineurals of V2–5 in form and orientation, but distinguishable from those by their position beneath the epineurals and by their cartilaginous tips. We have examined three other genera of uranoscopids. Gnathagnus has three attached ribs, so that the switch between attached ribs and attached epineurals is at V6, as in Uranoscopus. Kathetostoma has the first epineural associated with V2 and has the first four ribs attached, so that the switch is at V7. Astroscopus has the first epineurals associated with V1 but is otherwise like Kathetostoma, with the switch at V7. Okamura and Kishimoto (1993) described a new uranoscopid genus, Selenoscopus, and illustrated V9–14 in it and Uranoscopus. They described Selenoscopus as having nine pairs of pleural ribs and “epicentrals” and 10 pairs of epipleurals. Comparison of their illustrations with Figure 16 indicates that their “epipleurals” on V9–11 are ribs, their “pleural ribs” on V9–11 are epineurals, and their “epicentrals” are the epineurals of caudal vertebrae.

In Pietsch's (1989) cladogram, trachinids are the sister group of uranoscopids. Trachinus (Table 8) has epineurals from V1, all attached to the axial skeleton. There are only four ossified ribs, on V10–13, but there are ligaments in the position of ribs on several preceding vertebrae. The sister group of trachinids + uranoscopids in Pietsch's (1989) cladogram is the leptoscopids, whereas in Pietsch and Zabetian's (1990) cladogram it is ammodytids. In Leptoscopus there are no ribs, and epineurals extend from V2 back into the caudal region, all attached to the axial skeleton. In Ammodytes (Table 8) there are epineurals attached to the axial skeleton from V1 back into the caudal region, normal ribs, and a conspicuous series of neoneural ligaments from V5 back into the caudal region. The next group in Pietsch's (1989) and Pietsch and Zabetian's (1990) cladograms is Champsodontidae + Chiasmodontidae. Champsodon has a normal percoid pattern, with epineurals beginning on V1 and descending to the ribs from V3 onward. In Chiasmodon, the first epineural is on V1, and from V3 the rib and epineural are fused proximally at their common articulation with the parapophysis, and the body of the rib and epineural have almost the same horizontal orientation, diverging only slightly distally. In Dysalotus the pattern is the same except that the rib and epineural are not fused proximally.

FIGURE 16.—Ribs and intermuscular bones of Uranoscopus scaber L. A, “Semi-diagrammatic view of axial skeleton of…USNM 206551, 75 mm; ventral view, showing pleural and epipleural ribs of right side” as interpreted by Pietsch (redrawn from Pietsch, 1989, fig. 31, modified by emphasizing bones that he interpreted as intermusculars in solid black). B, Same drawing reinterpreted, with epineurals shown in solid black and epineural of V1 (present only on one side of specimen) and diminutive rib of V12 added. Every fifth vertebra is numbered.

We conclude from this that uranoscopids are characterized by a distinctive pattern, the switch between attached ribs and attached epineurals (Figure 16), and that the pattern of ribs and epineurals is considerably more variable among Pietsch's trachinoids than in any other percomorph group. We think it likely that further study of this complex will challenge the hypothesized monophyly and relationships of the Trachinoidei.

SMEGMAMORPHA.—The Smegmamorpha (Johnson and Patterson, 1993) comprise the Synbranchoidei (synbranchids and mastacembeloids), Mugilomorpha (of Stiassny, 1990, = Mugiloidei), Elassomatidae (Elassoma only), Gasterosteiformes (including Pegasus and Indostomus), and Atherinomorpha. Table 8 records the intermusculars in two mugiloids, Elassoma, three atherinomorphs, and four gasterosteiforms. The principal character of smegmamorphs is to have the first (or first and second) epineural originating at the tip of a lateral process from the first (or first and second) vertebra (notation BP in Table 8). To our knowledge, this character occurs in only two other teleosts, the carangoid Echeneis and the gobiid Gnatholepis. As Echeneis and Gnatholepis are each nested well within well-characterized monophyletic groups (carangoids, Johnson, 1984; gobioids, Winterbottom, 1993), we interpret the modified first epineural origin in them as independently derived.

PLEURONECTIFORMES.—We recorded the intermusculars in only two genera of pleuronectiforms, the bothid Bothus and the samarid Samaris. We chose those genera because bothids and samarids are known to have “extra” series of intermusculars (Hensley and Ahlstrom, 1984). According to our interpretation, Bothus (and other bothids, Amaoka, 1969) and Samaris uniquely share two derived features. The first is ossification of the neoneurals, which, to our knowledge, does not occur elsewhere in teleosts. The second is modification of the posterior ribs so that they come to resemble the epipleurals of lower teleosts and extend into the caudal region as intermuscular bones (see section on “Ribs,” above). In our sample, caudal extension of ribs occurs elsewhere only in the anabantoid Colisa (Table 8), where the bones do not show the proximal branching characteristic of the posterior ribs in bothids and Samaris. In addition, Bothus (and other bothids, Amaoka, 1969, as “hypomerals”) share with Samaris the derived condition of origin of the first rib on V2, rather than on V3, the primitive position, as in the other pleuronectiforms studied by Amaoka (1969).

Pleuronectiform interrelationships are still poorly resolved (Chapleau, 1993). Bothids and samarids are separated by two nodes in Chapleau's (1993) cladogram, with bothids in a polychotomy together with several other lineages, and samarids grouped with soleoids. The characters cited above imply that bothids and samarids are immediately related, and this should be taken into account in future studies of pleuronectiform interrelationships.

Conclusions and Summary of Systematic Consequences

We believe that the intermuscular bones and ligaments of teleosts have been neglected and are potentially of value in systematics. As an analogy, the teleostean caudal skeleton generally was neglected as a source of characters until the 1960s; for example, Gosline (1960:328) wrote that it was “usually either ignored or briefly dismissed in taxonomic papers.” The reason for that neglect was put nicely by Monod (1968:5): “Authors coming to the caudal skeleton in their osteological descriptions find themselves a little embarrassed or ill at ease because of the unfamiliar ground under their feet: is the ice, just here, enough to bear my weight? All those who have grappled with this part of the skeleton will have experienced the sensation to some extent” (our loose translation from the French). One of us can vouch for the truth of Monod's diagnosis in the 1950s and early 1960s, and the tentative and sketchy references to the caudal skeleton in Greenwood et al. (1966) confirm it. Yet today every ichthyologist is familiar with the caudal skeleton, and many details of it are widely used in systematics. Again, Monod (1968:5) correctly diagnosed one reason for that change: “The major obstacle…is above all the lack of a coherent and homogeneous terminology.” The second reason for the change was the lack (before Monod, 1968) of a broad comparative survey of the teleostean caudal skeleton. Once the kinds of variations in the caudal skeleton were mapped, and nomenclature was at hand to describe them, ichthyologists were happy, in Monod's simile, to venture on to the ice.

As one example of the current confusion over teleostean intermusculars we cite Whitehead and Teugel's (1985) account of the clupeoid Sierrathrissa, surely one of the best anatomical papers of the last decade. Yet when they came to the intermusculars, Whitehead and Teugels were lost; they called the epineurals by two different names (epicentrals, dorsal intermuscular bones), which were both wrong; they wrongly called the epicentrals epipleurals; and they wrongly called the epipleurals ventral intermuscular bones—the ice would not support them. These errors are no worse than those of earlier generations, as when Goodrich (1909, fig. 305; 1930, fig. 82), in adapting two figures of Salmo from Bruch (1861), converted the epicentral ligaments and cartilages into solid bones, which he called ribs, and wrongly called the epineurals epipleurals.

We do not pretend that this paper stands with Monod's (1968) monograph on the teleostean caudal skeleton. (Monod admitted that although he spent almost 10 years on that work, he still felt that he should have studied a hundred times as many species and 10 times as many specimens per species (1968:3); we feel the same about our more cursory survey of teleostean intermusculars.) Nevertheless, we hope that the information on variation in the intermusculars and the terminology that we have provided are enough to convince others that the ice will bear their weight, and that it is worth the effort of learning to read the intermuscular bones and ligaments.

By way of a concluding summary, we first describe the system of intermuscular bones and ligaments that we believe to be primitive for Recent teleosts, and then we summarise modifications of that system that characterize various major groups.

The primitive condition of the intermusculars is exemplified by Hiodon. The ossified epineurals are all fused with the neural arch proximally, and the epineural series is extended into the caudal region by about a dozen ligaments. Epicentrals are present only as ligaments, originate on the parapophysis on rib-bearing vertebrae, and extend into the caudal region where their origin ascends to the centrum. Epipleurals also are present only as ligaments, and they are confined to the middle of the body, where they originate on the last few ribs and the first few haemal arches.

Within osteoglossomorphs, there are many variations on the basic pattern seen in Hiodon (Taverne, 1977b, 1978, and above), but our survey has not been complete enough to determine the systematic significance of those variations. Elopocephalans (nonosteoglossomorph teleosts) generally share two features that are not found in any osteoglossomorph: a long series of epipleural bones and proximal forking of many of the epineural and epipleural bones. Fusion (continuity) between the epineural and the neural arch, true of all epineurals in Hiodon and of all but the first in Pantodon, persists on anterior vertebrae in many lower elopocephalans (Tables 3–5); epineurals fused to the neural arch never show proximal forking. There is sometimes (and probably primitively) an abrupt switch from a fused, simple epineural to a free, proximally forked one on the succeeding vertebra (Elops, Megalops); Clupea, Chirocentrus, and Esox lucius show a more gradual transition between the two conditions, over two to four vertebrae. The presence of epicentral bones in all clupeomorphs (including Denticeps) and all gonorynchiforms provides additional support for the monophyly of each of those groups. Derived fusion between anterior epicentrals and ribs in clupeids and chirocentrids supports the monophyly of that grouping, but it is incongruent with what we know about the distribution of cartilage chevrons at the tips of the anterior epicentrals, which implies a grouping of engraulids and clupeids. More double-stained material is necessary to resolve the conflict.

We take the presence of epipleural bones and of proximally forked epineurals and epipleurals to be primitive for elopocephalans because of the conditions in elopomorphs, clupeomorphs, Esox, and gonorynchiforms. The second of those characters is absent in argentinoids, salmonoids, and osmeroids, and that absence is conceivably a character of a group including only those taxa (Salmoniformes). Intermusculars provide stronger support for a relationship between salmonoids and osmeroids (sensu Begle, 1991, 1992) because those groups share absence of epipleural bones and presence of cartilaginous rods in the epicentral ligaments.

The intermusculars show remarkable variations in aulopiforms, and we use characters from them as the basis of a parsimony analysis. Results of that analysis (Figure 11) suggest some radical reinterpretations of aulopiform interrelationships.

In acanthomorphs, features of the intermusculars support monophyly of a group comprising all acanthomorphs except lampridiforms (Euacanthomorpha, defined by descent of one or more epineurals into the horizontal septum); one comprising all euacanthomorphs except polymixiids (Holacanthopterygii, defined by descent of several or all the epineurals into the horizontal septum and absence of epipleural bones); one comprising zeiforms and Percomorpha sensu Johnson and Patterson (1993; the characters are an association between POTs and epineural bones and absence of overlap between the epineural and epicentral series); and one comprising synbranchoids, mugiloids, Elassoma, gasterosteiforms, and atherinomorphs (Smegmamorpha, defined by origin of the first epineural on a transverse process of V1). There is weaker support from the intermusculars (weaker in the sense of involving more homoplasy in outgroups) for the monophyly of Acanthomorpha (absence of proximal forking of epineurals and/or epipleurals) and of Euacanthopterygii (Acanthopterygii minus stephanoberyciforms, defined by origin of anterior epineurals from the rib rather than the parapophysis).

Much work remains to be done on the intermuscular bones and ligaments, particularly within percomorphs, where features like the neoneural ligaments that we report in a few taxa and the possible neopleurals in Polydactylus suggest characters that may be of value in systematics.

Finally, there remains the question of whether it is possible to provide efficient anatomical definitions or diagnoses of the different series of intermusculars. In naming the epineural, epicentral, and epipleural series “according to the vertebral element they may adhere to,” Owen (1866:43) noted that this criterion failed because “each may shift its place, rising or falling gradually along the series of vertebrae.” When the intermuscular system is unmodified, the horizontal septum is the best criterion: epicentrals are in the horizontal septum, epineurals are above it, and epipleurals are below it. POTs, when present, are always in the horizontal septum, and their association with the epicentrals (AOTs) provides an additional guideline in the unmodified system.

A second criterion is developmental sequence. Epineurals and epicentrals develop in a rostrocaudal gradient, whereas epipleurals develop both rostrally and caudally from a focus around the first caudal vertebra. We know of no exception to the first part of that statement (concerning epineurals and epicentrals), although both series may be truncated rostrally. For example, the first epineural is on about V20 in Arapaima, V12 in Denticeps, V10 in Monocentris, V3–4 in Salangichthys and Stokellia, and V3 in Jenkinsia and gadiforms; the first epicentral is on about V15–20 in synodontids, Saurida, Pseudotrichonotus, Chlorophthalmus, and notosudids among aulopiforms, on about V5 in the aulopiforms Coccorella and Harpadon, on about V7–10 in Diretmus, Monocentris, trachichtyids, anomalopids, berycids and holocentrids among beryciforms, and in mugilids, centropomids, Sphyraena, and Polydactylus among percomorphs, and behind V10 in zeiforms and in Morone, Doederleinia, and Drepane among percomorphs. Ontogenetic information is lacking in many of these taxa with rostrally truncated epineural or epicentral series, and in those cases rostrocaudal development remains an untested assumption. Bidirectional development of the epipleural series is known to fail as a criterion in one group, aulopiforms, where we have limited developmental information, and it may fail in another group, alepocephaloids, where we lack that information.

The horizontal septum fails as a defining criterion in two taxa, aulopiforms and nonlampridiform acanthomorphs (Euacanthomorpha of Johnson and Patterson, 1993). In many aulopiforms, according to our interpretation, the anterior epipleurals lie in the horizontal septum, and in euacanthomorphs some (Polymixia, beryciforms) or all (paracanthopterygians, stephanoberyciforms, zeiforms, percomorphs) of the epineurals are in the horizontal septum. The attachment of POTs to epicentrals also fails as a criterion in zeiforms and percomorphs, where the POTs may attach to descended epineurals.

The problem of defining or diagnosing the intermuscular series in these modified groups is similar to the problem of deciding whether the ribs of a gnathostome are dorsal ribs or ventral (pleural) ribs (Rosen et al., 1981:242). With ribs, topographic criteria fail because the ribs may “wander” within the myoseptum from one part of the vertebral column to another in an individual or from species to species, and because the horizontal septum is absent in most tetrapods. According to our interpretations, the epineural and epipleural intermusculars also “wander” within the myoseptum and so come to lie in the horizontal septum in aulopiforms and euacanthopterygians. Because of these modifications, we are unable to give diagnoses or definitions of the epineural and epicentral series that will apply in all teleosts; in difficult cases, where one or more intermuscular series is lost or modified, identification of the remaining series will have to rely on comparative arguments, assessing details of structure and distribution within a cladistic framework.

Tables

KEY TO TABLES 1-5, 7, 8

Headings of rows and columns:

ANA

Accessory neural arch

Ec

Epicentral series

En

Epineural series

Ep

Epipleural series

Nn

“Neoneural” series in certain percomorphs (Table 8)

Occ

Occiput

R

Pleural ribs

1, 2, etc. vertebrae, numbered from the first

//

Symbols separate vertebral numbers to indicate that a series of vertebrae is ommitted (intermuscular elements unvaried in that series)

Entries in rows and columns:

B

Bone (intermuscular or rib) not preformed in cartilage(membrane bone)

B

Rib preformed in cartilage (cartilage bone)

B

Bone (intermuscular or rib) attached to axial skeleton by ligament

B

Epineural bone displaced ventrally into horizontal septum (acanthomorphs, Tables 6, 7) or epipleural bone displaced dorsally into horizontal septum (aulopiforms, Table 5)

B

As B above, but attached to axial skeleton by ligament

b

Anterior epineural bone placed lower (lower case) distally than its successors, but above the horizontal septum

C

Rib in cartilage (unossified)

D

Epipleural bone, a member of a series with anterodorsal branching, in which the medial branch, attaching to the axial skeleton, is lost, so that the remaining part represents only the anterodorsal branch and the posterior part of the bone

F

Intermuscular bone or rib fused to axial skeleton; epineural bones are primitively fused to the neural arches, epicentral bones are occasionally fused to ribs, and anterior ribs are rarely fused to parapophyses (Esox) or to centra (Alepisaurus, Paralepis)

F

Epineural bone displaced ventrally into horizontal septum and fused with a rib (Dascyllus, Table 8)

f

Anterior epineural bone fused to axial skeleton and placed lower (lower case) distally than its successors, but above the horizontal septum

L

Ligament attached to axial skeleton

L

Epicentral ligament containing a rod of cartilage distally

L

Epineural ligament displaced ventrally into horizontal septum

M

Myorhabdoi: unattached, superficial bones succeeding the epineurals and in the epipleural position in Xenomystus (Table 3)

PU

Number of preural centrum following the last element of the intermuscular system

S

Baudelot's ligament, originating on the occiput or first vertebra and inserting on the supracleithrum

s

Ossified Baudelot's ligament

V

Epineural bone, a member of a series with anteroventral branching, in which the medial branch, attaching to the axial skeleton, is lost, so that the remaining part represents only the anteroventral branch and the posterior part of the bone

X

“Cranial ribs” on occiput and VI of Gonorynchus

?>

In Lampris (Table 7), conditions unknown posteriorly, partially dissected specimen only

|,/,—

Fusion between elements connected or indicated by the symbol

Subscripts
As prefix:

c

With a chevron of cartilage distally

D

With a dorsal branch anteriorly

P

Epicentral ligament reduced to a short “sling” running from the centrum or parapophysis to the upper surface of an epipleural bone

V

With a ventral branch anteriorly

<

Branched or forked distally

>

Branched or forked proximally

X

Branched or forked at both ends (proximally and distally)

As suffix:

0

Unattached to axial skeleton

1

Attached to neural arch or spine

2

Attached to centrum

3

Attached to parapophysis

4

Attached to rib

5

Attached to haemal arch or spine

E

Attached to epipleural bone

N

Attached to epineural bone

P

Attached to lateral process of vertebra

TABLE 1.—Distribution of intermuscular bones and ligaments in Polymixia.

TABLE 2.—Distribution of intermuscular bones and ligaments in Gonorynchus.

EDITOR'S NOTE: For ease of use, Table 3 appears on page 85.

TABLE 4.—Distribution of intermuscular bones and ligaments in certain ostariophysan, esocoid, salmonoid, and osmeroid teleosts.

TABLE 5.—Distribution of intermuscular bones and ligaments in certain stomiiform, aulopiform, and myctophifrom neoteleosts.

TABLE 6.—Matrix for 26 characters of the intermusculars and vertebral column in 19 genera of aulopiforms, the stomiiform Diplophos, the myctophid Myctophum, and an “ancestor” (a row of zeros). Except for character 25, the data are taken from Table 5, with the addition of Omosudis, based on USNM 219982, SL 81 mm. Character 25, the median caudal cartilages, is taken from Fujita (1990) and study of specimens; it was added to reinforce the monophyly of Synodontoidea s.l. (Aulopidae, Pseudotrichonotidae, Synodontidae, Harpadontidae; Johnson et al., 1989), which is otherwise not well supported by our intermuscular characters.

Characters (* = run unordered):

0.   |  | ANA (accessory neural arch) present (0) or absent (1)
1*. |  | Baudelot's ligament originates on V1 (0), or on V1 and V2 (1), or on V2-4 (2), or is ossified (3), or absent (4)
2*. |  | Epineurals all independent (0), or the first five or fewer fused with the neural arch (1), or the first six or more fused with the neural arch (2), or the majority fused with the centrum (3)
3*. |  | Epineurals all originate on the neural arch (0), or those on –V5–15 originate on the centrum or parapophysis (1), or all beyond V5 originate on centrum (2), or all originate on centrum (3)
4*. |  | Epineurals all attached to the axial skeleton (0), or a few unattached epineurals posteriorly (1), or the majority unattached (2), or the unattached epineurals represent only the anteroventral fork and posterior body of bone (notation V₀ in Table 5) (3)
5.   |  | First epineural “descended” (notation b₁, in Table 5) (1) or none descended (0)
6.   |  | First two or three epineurals “descended” (1) or one or none descended (0)
7.   |  | Some epineurals forked proximally (1) or none forked (0) (autapomorphous condition in Gigantura coded (0)
8*. |  | All epicentrals in ligament (0), or all in bone from VI (1), or all in bone from V3 (2), or epicentrals absent (3)
9.   |  | Epicentral on VI in ligament (0), or in bone (1), or absent (2)
10.   |  | Epicentral series begins anteriorly at VI (0), or more posteriorly (1), or absent (2)
11.   |  | Epipleurals on VI and V2 fused with centrum (1) or free/absent (0)
12.   |  | Anterior epipleurals partially in (1) or entirely beneath (0) the horizontal septum
13*. |  | Transition between epipleurals in and beneath the horizontal septum absent (none are in the septum) (0), or gradual (1), or abrupt (2)
14.   |  | Number of epipleurals with distal end in horizontal septum zero (0), one (1), or more (2)
15.   |  | One or more epipleurals forked distally at the transition between epipleurals in and beneath the horizontal septum (1), or no forking/no epipleurals in horizontal septum (0)
16.   |  | Epipleural series confined to the middle region of the body (0), or extends anteriorly to V2 (1), or to VI (2)
17.   |  | Epipleural fused with VI and V2 (1) or unfused (0)
18*. |  | All epipleurals attached to the axial skeleton (0), or a few unattached epipleurals posteriorly (1), or the majority unattached (2), or the unattached epineurals represent only the anterodorsal fork and posterior body of the bone (notation D₀ in Table 5) (3)
19.   |  | Some epipleurals forked proximally (1), or all either unforked or forked only distally (0) (autapomorphous condition in Gigantura coded 0)
20.   |  | A brushlike posterodorsal outgrowth of the first neural arch present (1) or absent (0)
21*. |  | All ribs ossified in cartilage (0), or some ossified in membrane bone (1), or all in membrane bone (2), or ribs absent (3)
22*. |  | First rib originates on V3 (0), or V4 (1), or V5 (2). or V2 (3), or VI (4), or ribs absent (5)
23.   |  | Ribs on VI and V2 fused to centrum (1), or absent/free (0)
24*. |  | Ratio of number of abdominal vertebrae to number of caudal vertebrae 0.25–1.75 (0), <0.25 (1), >1.75 (2)
25.   |  | Median caudal cartilages (CMC of Kafuku, 1990) present (0) or absent (1)

TABLE 7.—Distribution of intermuscular bones and ligaments in certain lower acanthomorph neoteleosts.

TABLE 8.—Distribution of intermuscular bones and ligaments in certain percomorph teleosts.

Appendix 1

Alphabetical List of Neopterygian Genera Cited in Text and Tables

(Names in bold italic indicate genera for which we have studied the intermusculars; those in italic indicate genera studied by others. References to Tables 1–5, 7, and 8 are given so that the list provides an alphabetical index to those tables. Family names are given except where a genus is the type of a family. Names of extinct genera are preceded by a dagger (†), and names of extinct paraphyletic stem-group families are placed in quotation marks.)

 Abudefduf, Pomacentridae

 Acanthopsoides, Cobitidae

Table 4

 Adioryx, Holocentridae

 Agonostomus, Mugilidae

Table 8

 Ahliesaurus, Notosudidae

Table 5

 Albula

Table 3

 Alepisaurus

Table 5

 Alepocephalus

 Alestes, Characidae

Table 4

†Allothrissops

 Alosa, Clupeidae

 Amia

 Ammodytes

Table 8

†Anaethalion, Elopomorpha incertae sedis

 Anchoa, Engraulidae

Table 3

 Anguilla

Table 3

 Anodontostoma, Clupeidae

 Anomalops

Table 7

 Anoplogaster

Table 7

 Anoplopoma

 Anotopterus

 Antigonia, Caproidae

Table 8

 Aphredoderus

Table 7

 Aplochiton, Galaxiidae

 Arapaima

 Argentina

Table 4

 Ariosoma, Congridae

†Ascalabos, “Leptolepididae”

†Asiatolepis, Osteoglossoidei incertae sedis

 Astroscopus, Uranoscopidae

 Ateleopus

 Aulichthys, Aulorhynchidae

Table 8

 Aulopus

Table 5

 Aulorhynchus

Table 8

 Aulostomus

 Barbourisia

Table 7

 Bathypterois, Ipnopidae

Table 5

 Bathysaurus

Table 5

 Bathytroctes, Alepocephalidae

 Bedotia, Atherinidae

Table 8

 Bembrops, Percophididae

 Binghamichthys, Alepocephalidae

 Bothus

Table 8

 Brevoortia, Clupeidae

 Callionymus

Table 8

 Capros

Table 8

 Caranx

Table 8

 Centroberyx, Berycidae

Table 7

 Centropomus

 Centengraulis, Engraulidae

 Champsodon

 Chanos

Table 4

 Chiasmodon

 Chirocentrodon, Pellonidae

 Chirocentrus

Table 3

 Chlorophthalmus

Table 5

 Clupanodon, Clupeidae

 Clupea

Table 3

 Clupeichthys, Clupeidae

Table 3

 Coccorella, Evermanellidae

Table 5

 Coilia

 Colisa, Belontiidae

Table 8

 Cookeolus, Priacanthidae

 Coregonus

 Cottus

Table 8

 Cromeria, Kneriidae

 Culaea, Gasterosteidae

Table 8

 Cynothrissa, Clupeidae

 Cyprinus

 Cyttopsis, Zeidae

 Dactyloscopus

 Dallia, Umbridae

 Dascyllus, Pomacentridae

Table 8

 Denticeps

Table 3

 Diplophos, Gonostomatidae

Table 5

 Diretmus

Table 7

 Doederleinia, Acropomatidae

Table 8

 Dorosoma, Clupeidae

 Drepane

Table 8

 Dysalotus, Chiasmodontidae

 Echeneis

 Ectreposebastes, Scorpaenidae

Table 8

 Eigenmannia, Sternopygidae

 Elassoma

Table 8

 Elops

Table 3

 Engraulis

†Eoaulostomus, Aulostomidae

 Epigonus

 Esox

Table 4

 Exocoetus

Table 8

 Etrumeus, Clupeidae

 Euthynnus, Scombridae

 Evermanella

 Forsterygion, Tripterygiidae

 Gadus

 Gaidropsarus, Phycidae

Table 7

 Galaxias

Table 4

 Gibberichthys

Table 7

 Gigantura

Table 5

 Glossanodon, Argentinidae

Table 4

 Gnathagnus, Uranoscopidae

 Gnatholepis, Gobiidae

 Gonorynchus

Tables 2, 4

 Grasseichthys, Kneriidae

 Gymnarchus

 Gymnotus

 Halosaurus

Table 3

 Harengula, Clupeidae

 Harpadon

Table 5

 Hemerocoetes, Percophididae

 Hemibarbus, Cyprinidae

Table 4

 Heterotis, Arapaimidae

Table 3

 Hexagrammus

Table 8

 Hiodon

Table 3

 Hispidoberyx

Table 7

 Holocentrus

Table 7

 Hoplichthys

 Hoplostethus, Trachichthyidae

Table 7

†Huashia

†Hulettia, Halecostomi incertae sedis

 Hypentelium, Catostomidae

Table 4

 Hypomesus, Osmeridae

Table 4

 Hypoptychus, Aulorhynchidae

Table 8

 Hypopygus, Hypopomidae

 Ilisha, Pellonidae

 Indostomus

 Isichthys, Mormyridae

 Jenkinsia, Clupeidae

Table 3

†Jiaohichthys, Osteoglossomorpha incertae sedis

†Jungersenichthys, Aulostomidae

 Kathetostoma, Uranoscopidae

 Katsuwonus, Scombridae

 Kneria

†Kuntulunia, Huashiidae

 Lampris

Table 7

 Lates, Centropomidae

Table 8

 Lepadogaster, Gobiesocidae

Table 8

 Lepidogalaxias

Table 4

 Lepisosteus

 Leptochilichthys, Alepocephalidae

 Leptoderma, Alepocephalidae

†Leptolepis

 Leptoscopus

 Lile, Clupeidae

 Liza, Mugilidae

Table 8

 Lovettia, Galaxiidae

†Lycoptera, Hiodontidae

 Macroparalepis, Paralepididae

Table 5

 Mallotus, Osmeridae

 Marcusenius, Mormyridae

 Maurolicus, Sternoptychidae

Table 5

 Megalops

Table 3

 Melamphaes

 Menidia, Atherinidae

Table 8

 Metavelifer, Veliferidae

Table 7

 Micropercops, Odontobutidae

Table 8

 Monocentris

Table 7

 Morone

Table 8

 Mulloidichthys, Mullidae

 Myctophum

Table 5

 Myripristis, Holocentridae

 Nematalosa, Clupeidae

 Neoscopelus

Table 5

 Notacanthus

Table 3

 Notopterus

 Novumbra, Umbridae

Table 4

 Odontognathus, Pristigasteridae

 Omosudis

 Oncorhynchus, Salmonidae

 Opisthonema, Clupeidae

 Opisthoproctus, Bathylagidae

 Opisthopterus, Pristigasteridae

 Osmerus

Table 4

 Osteoglossum

Table 3

 Ostichthys, Holocentridae

 Pantodon

 Papyrocranus, Notopteridae

 Paragalaxias, Galaxiidae

 Parakneria, Kneriidae

Table 4

 Paralepis

Table 5

†Paralycoptera, Osteoglossoidei incertae sedis

 Parapercis, Pinguipedidae

 Parasudis, Chlorophthalmidae

Table 5

 Parazen

Table 7

 Pegasus

 Pellona

 Pellonula, Clupeidae

 Perca

 Percopsis

Table 7

†Pholidolepis, “Pholidophoridae”

†Pholidophorus

 Photoblepharon, Anomalopidae

Table 7

 Phractolaemus, Kneriidae

 Platycephalus

 Searsia, Alepocephalidae

Table 4

 Plecoglossus, Osmeridae

Table 4

†Plesiolycoptera, Hiodontidae

 Pollichthys, Photichthyidae

Table 5

 Polydactylus, Polynemidae

Table 8

 Polymixia

Tables 1, 7

 Poromitra, Melamphaidae

Table 7

†Proleptolepis, “Leptolepididae”

 Prosopium, Coregonidae

 Prototroctes, Retropinnidae

 Psammoperca, Centropomidae

Table 8

 Psettodes

 Pseudanthias, Serranidae

Table 8

 Pseudotrichonotus

Table 5

 Pterophryne, Antennariidae

 Rachycentron, Coryphaenidae

Table 8

 Raniceps

Table 7

 Retropinna

 Rinoctes, Alepocephalidae

 Rondeletia

Table 7

 Salangichthys, Salangidae

Table 4

 Salmo

Table 4

 Salvelinus, Salmonidae

 Samaris

Table 8

 Sarda, Scombridae

 Sardinella, Clupeidae

 Sardinops, Clupeidae

 Sargocentron, Holocentridae

 Saurida, Harpadontidae

Table 5

 Scomber

 Scomberomorus, Scombridae

Table 8

 Scopelarchoides, Scopelarchidae

Table 5

 Scopelengys, Neoscopelidae

 Scopelogadus, Melamphaidae

 Scopelosaurus, Notosudidae

Table 5

 Selenoscopus, Uranoscopidae

 Serranus

 Setipinna, Coiliidae

 Sierrathrissa, Clupeidae

 Siganus

Table 8

 Solivomer, Neoscopelidae

 Sphyraena

Table 8

 Spirinchus, Osmeridae

 Spratelloides, Clupeidae

 Sprattus, Clupeidae

 Stenodus, Coregonidae

 Stephanoberyx

Table 7

 Sternopygus

 Stokellia, Retropinnidae

Table 4

 Stolephorus, Engraulidae

 Synchiropus, Callionymidae

†Synhypuralis, Aulostomidae

 Synodus

Table 5

 Talismania, Alepocephalidae

†Tharsis, “Leptolepididae”

 Thrissops, Ichthyodectidae

 Thryssa, Coiliidae

 Thunnus, Scombridae

 Thymallus, Salmonidae

Table 4

†Todiltia, “Leptolepididae”

 Trachichthys

Table 7

 Trachinocephalus, Synodontidae

Table 5

 Trachinus

Table 8

 Trichodon

 Triplophos, Gonostomatidae

 Umbra

Table 4

 Upeneus, Mullidae

Table 8

 Uranoscopus

 Velifer

Table 7

 Xenolepidichthys, Grammicolepididae

Table 7

 Xenomystus, Notopteridae

Table 3

†Yanbiania, Hiodontidae

 Zenion

Appendix 2

Outline Classification of Neopterygians Including Genera Cited in Text and Tables

(Names in bold italic indicate genera for which we have studied the intermusculars; those in italic indicate genera studied by others. References to Tables 1–5, 7, and 8 are given so that the classification provides a systematic index to those tables. Classification follows Nelson (1984), Johnson and Gill (1994), Johnson and Patterson (1993), Patterson (1993), and some results of this paper. Extinct taxa are preceded by a dagger (†), and names of extinct paraphyletic stem-group families are placed in quotation marks.)

NEOPTERYGII

LEPISOSTEIFORMES

LEPISOSTEIDAE

Lepisosteus

HALECOSTOMI

incertae sedis

†Hulettia

AMIIFORMES

AMIIDAE

Amia

TELEOSTEI

†“PHOLIDOPHORIDAE”

Pholidophorus

Pholidolepis

†“LEPTOLEPIDIDAE”

Proleptolepis

Leptolepis

Ascalabos

Tharsis

Todiltia

†ICHTHYODECTIFORMES

Allothrissops

Thrissops

OSTEOGLOSSOMORPHA

incertae sedis

†Jiaohichthys

†HUASHIIDAE

Huashia

Kuntulunia

OSTEOGLOSSIFORMES

NOTOPTEROIDEI

HIODONTIDAE

Hiodon       Table 3

†Lycoptera

†Plesiolycopiera

†Yanbiania

NOTOPTERIDAE

Notopterus

Papyrocranus

Xenomystus       Table 3

MORMYRIDAE

Isichthys

Marcusenius

GYMNARCHIDAE

Gymnarchus

OSTEOGLOSSOIDEI

incertae sedis

†Asiatolepis

†Paralycoptera

PANTODONTIDAE

Pantodon

OSTEOGLOSSIDAE

Osteoglossum       Table 3

ARAPAIMIDAE

Arapaima

Heterotis       Table 3

ELOPOMORPHA

incertae sedis

†Anaethalion

ELOPIFORMES

ELOPIDAE

Elops       Table 3

MEGALOPIFORMES

MEGALOPIDAE

Megalops       Table 3

ANGUILLIFORMES

ALBULIDAE

Albula       Table 3

HALOSAURIDAE

Halosaurus       Table 3

NOTACANTHIDAE

Notacanthus       Table 3

ANGUILLIDAE

Anguilla       Table 3

CONGRIDAE

Ariosoma

CLUPEOMORPHA

CLUPEIFORMES

DENTICIPITOIDEI

DENTICIPITIDAE

Denticeps       Table 3

CLUPEOIDEI

ENGRAULOIDEA

COILIIDAE

Coilia

Setipinna

Thryssa

ENGRAULIDAE

Anchoa       Table 3

Cetengraulis

Engraulis

Stolephorus

PRISTIGASTEROIDEA

PELLONIDAE

Chirocentrodon

Ilisha

Pellona

PRISTIGASTERIDAE

Odontognathus

Opisthopterus

CLUPEOIDEA

CHIROCENTRIDAE

Chirocentrus       Table 3

CLUPEIDAE

DUSSUMIERIINAE

Etrumeus

Jenkinsia       Table 3

Spratelloides

PELLONULINAE

Clupeichthys       Table 3

Cynothrissa

Pellonula

Sierrathrissa

ALOSINAE

Alosa

Brevoortia

CLUPEINAE

Clupea       Table 3

Harengula

Lile

Opisthonema

Sardinella

Sardinops

Sprattus

DOROSOMATINAE

Anodontostoma

Clupanodon

Dorosoma

Nematalosa

OSTARIOPHYSI

ANOTOPHYSI

GONORYNCHIFORMES

CHANIDAE

Chanos       Table 4

GONORYNCHIDAE

Gonorynchus       Tables 2, 4

KNERIIDAE

Cromeria

Grasseichthys

Kneria

Parakneria       Table 4

Phractolaemus

OTOPHYSI

CYPRINIFORMES

CYPRINIDAE

Cyprinus

Hemibarbus       Table 4

COBITIDAE

Acanthopsoides       Table 4

CATOSTOMIDAE

Hypentelium       Table 4

CHARACIFORMES

CHARACIDAE

Alestes       Table 4

SILURIFORMES

GYMNOTOIDEI

STERNOPYGIDAE

Eigenmannia

Sternopygus

HYPOPOMIDAE

Hypopygus

GYMNOTIDAE

Gymnotus

EUTELEOSTEI

ESOCIFORMES

ESOCIDAE

Esox       Table 4

UMBRIDAE

Dallia

Novumbra       Table 4

Umbra       Table 4

SALMONIFORMES

ARGENTINOIDEI

ARGENTINOIDEA

ARGENTINIDAE

Argentina       Table 4

Glossanodon       Table 4

BATHYLAGIDAE

Opisthoproctus

ALEPOCEPHALOIDEA

ALEPOCEPHALIDAE

Alepocephalus

Bathytroctes

Binghamichthys

Leptochilichthys

Leptoderma

Rinoctes

Searsia       Table 4

Talismania

SALMONOIDEI

COREGONIDAE

Cortgonus

Prosopium

Stenodus

SALMONIDAE

Oncorhynchus

Salmo       Table 4

Salvelinus

Thymallus       Table 4

OSMEROIDEI

OSMEROIDEA

OSMERIDAE

Hypomesus       Table 4

Mallotus

Osmerus       Table 4

Plecoglossus       Table 4

Spirinchus

SALANGIDAE

Salangichthys       Table 4

GALAXIOIDEA

RETROPINNIDAE

Prototroctes

Retropinna

Stokellia       Table 4

LEPIDOGALAXIIDAE

Lepidogalaxias       Table 4

GALAXIIDAE

Aplochiton

Galaxias       Table 4

Lovettia

Paragalaxias

NEOTELEOSTEI

incertae sedis

ATELEOPODIDAE

Ateleopus

STOMIIFORMES

GONOSTOMATIDAE

Diplophos       Table 5

Triplophos

PHOTICHTHYIDAE

Pollichthys       Table 5

STERNOPTYCHIDAE

Maurolicus       Table 5

AULOPIFORMES

incertae sedis

IPNOPIDAE

Bathypterois       Table 5

CHLOROPHTHALMIDAE

Chlorophthalmus       Table 5

Parasudis       Table 5

SYNODONTOIDEI

AULOPIDAE

Aulopus       Table 5

PSEUDOTRICHONOTIDAE

Pseudotrichonotus       Table 5

SYNODONTIDAE

Synodus       Table 5

Trachinocephalus       Table 5

HARPADONTIDAE

Harpadon       Table 5

Saurida       Table 5

ALEPISAUROIDEI

EVERMANELLIDAE

Evermanella

Coccorella       Table 5

NOTOSUDIDAE

Ahliesaurus       Table 5

Scopelosaurus       Table 5

SCOPELARCHIDAE

Scopelarchoides       Table 5

PARALEPIDIDAE

Macroparalepis       Table 5

Paralepis       Table 5

ALEPISAURIDAE

Alepisaurus       Table 5

ANOTOPTERIDAE

Anotopterus

BATHYSAURIDAE

Bathysaurus       Table 5

GIGANTURIDAE

Gigantura       Table 5

OMOSUDIDAE

Omosudis

MYCTOPHIFORMES

MYCTOPHIDAE

Myctophum       Table 5

NEOSCOPELIDAE

Neoscopelus       Table 5

Scopelengys

Solivomer

ACANTHOMORPHA

LAMPRIDIFORMES

VELIFERIDAE

Metavelifer       Table 7

Velifer       Table 7

LAMPRIDIDAE

Lampris       Table 7

POLYMIXIIFORMES

POLYMIXIIDAE

Polymixia       Tables 1, 7

PARACANTHOPTERYGII

PERCOPSIFORMES

PERCOPSIDAE

Percopsis       Table 7

APHREDODERIDAE

Aphredoderus       Table 7

GADIFORMES

RANICIPITIDAE

Raniceps       Table 7

PHYCIDAE

Gaidropsarus       Table 7

GADIDAE

Gadus

LOPHIIFORMES

ANTENNARIIDAE

Pterophryne

STEPHANOBERYCIFORMES

MELAMPHAIDAE

Melamphaes

Poromitra       Table 7

Scopelogadus

STEPHANOBERYCIDAE

Stephanoberyx       Table 7

GIBBERICHTHYIDAE

Gibberichthys       Table 7

HISPIDOBERYCIDAE

Hispidoberyx       Table 7

BARBOURISIIDAE

Barbourisia       Table 7

RONDELETIIDAE

Rondeletia       Table 7

BERYCIFORMES

HOLOCENTRIDAE

Adioryx

Holocentrus       Table 7

Myripristis

Ostichthys

Sargocentron

BERYCIDAE

Centroberyx       Table 7

TRACHICHTHYIDAE

Hoplostethus       Table 7

Trachichthys       Table 7

MONOCENTRIDAE

Monocentris       Table 7

ANOMALOPIDAE

Anomalops       Table 7

Photoblepharon       Table 7

DIRETMIDAE

Diretmus       Table 7

ANOPLOGASTRIDAE

Anoplogaster       Table 7

ZEIFORMES

PARAZENIDAE

Parazen       Table 7

ZENIONTIDAE

Zenion

GRAMMICOLEPIDIDAE

Xenolepidichthys       Table 7

ZEIDAE

Cyttopsis

PERCOMORPHA

SMEGMAMORPHA

ELASSOMATIDAE

Elassoma       Table 8

MUGILIDAE

Agonostomus       Table 8

Liza       Table 8

AULORHYNCHIDAE

Aulichthys       Table 8

Aulorhynchus       Table 8

Hypoptychus       Table 8

INDOSTOMIDAE

Indostomus

PEGASIDAE

Pegasus

GASTEROSTEIDAE

Culaea       Table 8

AULOSTOMIDAE

Aulostomus

†Eoaulostomus

†Jungersenichthys

†Synhypuralis

ATHERINOMORPHA

ATHERINIDAE

Bedotia       Table 8

Menidia       Table 8

EXOCOETIDAE

Exocoetus       Table 8

SCORPAENIFORMES

SCORPAENIDAE

Ectreposebastes       Table 8

PLATYCEPHALIDAE

Platycephalus

HOPLICHTHYIDAE

Hoplichthys

ANOPLOPOMATIDAE

Anoplopoma

HEXAGRAMMIDAE

Hexagrammus       Table 8

COTTIDAE

Cottus       Table 8

PERCIFORMES

PERCOIDEI

CENTROPOMIDAE

Centropomus

Lates       Table 8

Psammoperca       Table 8

MORONIDAE

Morone       Table 8

ACROPOMATIDAE

Doederleìnìa       Table 8

SERRANIDAE

Pseudanthias       Table 8

Serranus

PERCIDAE

Perca

EPIGONIDAE

Epigonus

CAPROIDAE

Antigonia       Table 8

Capros       Table 8

PRIACANTHIDAE

Cookeolus

MULLIDAE

Mulloidichthys

Upeneus       Table 8

CARANGOIDEI

CARANGIDAE

Caranx       Table 8

ECHENEIDIDAE

Echeneis

CORYPHAENIDAE

Rachycentron       Table 8

POLYNEMOIDEI

POLYNEMIDAE

Polydactylus       Table 8

LABROIDEI

POMACENTRIDAE

Abudefduf

Dascyllus       Table 8

TRACHINOIDEI

TRICHODONTIDAE

Trichodon

PINGUIPEDIDAE

Parapercis

PERCOPHIDIDAE

Bembrops

Hemerocoetes

CHIASMODONTIDAE

Chiasmodon

Dysalotus

CHAMPSODONTIDAE

Champsodon

LEPTOSCOPIDAE

Leptoscopus

AMMODYTIDAE

Ammodytes       Table 8

TRACHINIDAE

Trachinus       Table 8

URANOSCOPIDAE

Astroscopus

Gnathagnus

Kathetostoma

Selenoscopus

Uranoscopus

BLENNIOIDEI

TRIPTERYGIIDAE

Forsterygion

DACTYLOSCOPIDAE

Dactyloscopus

CALLIONYMOIDEI

CALLIONYMIDAE

Callionymus       Table 8

Synchiropus

GOBIESOCOIDEI

GOBIESOCIDAE

Lepadogaster       Table 8

GOBIOIDEI

ODONTOBUTIDAE

Micropercops       Table 8

XENISTHMIDAE

Rotuma

GOBIIDAE

Gnatholepis

ACANTHUROIDEI

DREPANIDAE

Drepane       Table 8

SIGANIDAE

Siganus Tibie 8

SCOMBROIDEI

SPHYRAENIDAE

Sphyraena       Table 8

SCOMBRIDAE

Euthynnus

Katsuwonus

Sarda

Scomber

Scomberomorus       Table 8

Thunnus

ANABANTOIDEI

BELONTIIDAE

Colisa       Table 8

PLEURONECTIFORMES

PSETTODIDAE

Psettodes

BOTHIDAE

Bothus       Table 8

SAMARIDAE

Samaris       Table 8

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Plates

PLATE 1

A–C, Albula vulpes (L.), USNM 128509, 51 mm SL; D, Salmo trutta L., BMNH 1981.9.22.81, 52 mm SL; E, F, Myctophum obtusirostre Tåning, AMNH 29140 SW, 40 mm SL; G, Cynothrissa mento Regan, BMNH 1967.12.29.1, 100 mm SL; H, Galaxias fasciatus Gray, BMNH 1965.12.6.15, 84 mm SL. A shows the posterior abdominal region in Albula, with the epipleural series of ligaments (attaching to ribs) containing epipleural bones at right of picture but without bone at left. Epicentral series of ligaments (attaching to parapophysis in this region) are visible just below middle of vertebral centra. B and C show the epicentral series of Albula in close-up, with B in dorsolateral view to show ligaments against ribs, and C in lateral view to show them against centra, with epipleural ligaments attaching to ribs below them. E and F show the three series of intermusculars in Myctophum. E is in the caudal region, with faintly stained, proximally forked epineural and epipleural bones respectively above and below vertebral centra. Epicentral ligaments are shown against vertebral centra by incident light, and they are forked distally in this region. F is in the abdominal region, and it shows epineural bones attaching to neural arches and epicentral ligaments attaching to ribs or parapophyses. G is in the posterior abdominal region of the pellonuline clupeoid Cynothrissa, which shows cartilaginous chevrons at tips of epicentral bones. There are proximally forked epineural and epipleural bones respectively above and below the vertebral centra. D and H show cartilage rods in the distal part of epicentral ligaments in the abdominal region of a salmonoid (D) and an osmeroid (H). Both are in dorsolateral view, with epineurals seen as overlying vertebral centra, and epicentrals seen as overlying ribs. In H, the epineurals and ribs are unstained, although ossified.

PLATE 2

A–C, G, H, Polymixia lowei Günther, USNM 308378, 72 mm SL; D, Polymixia lowei Günther, BMNH 1987.12.7.1, 128 mm SL; E, F, Myripristis murdjan (Forskâl), AMNH 43444SW, 51 mm SL. A–C show the posterior abdominal and anterior caudal region in Polymixia under different lighting conditions. The epineural bones attach to the parapophysis at left of photographs and move up to the neural spines at right. The epipleural bones are at the bottom right, with the ligamentous attachment of the first one most clearly seen in B. The epicentral series of ligaments, attaching to rib (at left), parapophysis, or haemal arch, is invisible in A, visible in transmitted light in B, and emphasized by incident light in C. D shows the distal cartilaginous rods in anterior epicentral ligaments of a larger Polymixia. The epineural bones are at top of photograph and the lateral line nerve is at the tip of the epicentrals. E and F show the epicentral ligaments on the last few abdominal and first few caudal vertebrae in Myripristis, in transmitted light, with a close-up in F. The posterior epineural bones, visible in E, attach to the neural arches and spines. G and H show the posterior members of the epipleural series in Polymixia, with transition from a ligament containing bone distally to a ligament without bone in G, and close-up of a ligament with enclosed bone in H.

Table 3

Table 3.—Distribution of intermuscular bones and ligaments in certain osteoglossomorph, elopomorph and clupeomorph teleosts. Numbers in top horizontal row = vertebrae, numbered from the first.

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