RAYMOND B. MANNB and FENNER A. CHACE, JR Shrimps of the Family Processidae from the f Northwestern Atlantic Ocean (Crustacea: A Decapoda: Caridea) SMITHSONIAN CONTRIBUTIONS TO ZOOLOGY NUMBER 89 SERIAL PUBLICATIONS OF THE SMITHSONIAN INSTITUTION The emphasis upon publications as a means of diffusing knowledge was expressed by the first Secretary of the Smithsonian Institution. In his formal plan for the Insti- tution, Joseph Henry articulated a program that included the following statement: "It is proposed to publish a series of reports, giving an account of the new discoveries in science, and of the changes made from year to year in all branches of knowledge." This keynote of basic research has been adhered to over the years in the issuance of thousands of titles in serial publications under the Smithsonian imprint, com- mencing with Smithsonian Contributions to Knowledge in 1848 and continuing with the following active series: Smithsonian Annals of Flight Smithsonian Contributions to Anthropology Smithsonian Contributions to Astrophysics Smithsonian Contributions to Botany Smithsonian Contributions to the Earth Sciences Smithsonian Contributions to Paleobiology Smithsonian Contributions to Zoology Smithsonian Studies in History and Technology In these series, the Institution publishes original articles and monographs dealing with the research and collections of its several museums and offices and of profes- sional colleagues at other institutions of learning. These papers report newly acquired facts, synoptic interpretations of data, or original theory in specialized fields. These publications are distributed by subscription to libraries, laboratories, and other in- terested institutions and specialists throughout the world. Individual copies may be obtained from the Smithsonian Institution Press as long as stocks are available. S. DILLON RIPLEY Secretary Smithsonian Institution SMITHSONIAN CONTRIBUTIONS TO ZOOLOGY NUMBER 89 Raymond B. Manning Shrimps of the Family and Fenner A. Chace, Jr. T . . 1 r - rrocessidae trom the Northwestern Atlantic Ocean (Crustacea: Decapoda: Garidea) SMITHSONIAN INSTITUTION PRESS CITY OF WASHINGTON 1971 ABSTRACT Manning, Raymond B., and Fenner A. Chace, Jr . Shrimps of the Family Processidae from the Northwestern Atlantic Ocean. (Crustacea: Decapoda: Caridea) Smithsonian Contributions to Zoology, number 89, 41 pages, 1971.?The processid shrimp fauna of the northwestern Atlantic Ocean is reviewed for the first time. Eleven species are recorded, of which eight are newly described. Ambidexter symmetricus, new genus, new species; Nikoides schmitti, new species; and six new species of Processa are described. Ambidexter is the only genus of the family in which both first pereiopods are chelate. Nikoides has not been recorded previously from outside of the Indo-West Pacific region. Keys to the species of Nikoides and to the Atlantic species of Processa are presented, and the Indo-West Pacific species of Processa are listed. Official publication date is handstamped in a limited number of initial copies and is recorded in the Institution's annual report, Smithsonian Year. UNITED STATES GOVERNMENT PRINTING OFFICE WASHINGTON : 1971 For sale by the Superintendent of Documents, U.S. Government Printing Offic Washington, D.C. 20402 - Price 50 cents (paper cover) Raymond B. Manning and Fenner A. Chace, Jr. Shrimps of the Family Processidae from the Northwestern Atlantic Ocean (Crustacea: Decapoda: Caridea) Introduction Shrimps of the family Processidae are small, nocturnal animals which are abundant in shallow-water habitats, primarily on grass flats. In the western Atlantic, at least, most of the species are found in the tropics or subtropics. We have seen no material from the American mainland north of North Carolina. The western Atlantic processids have never been studied in detail. Prior to our study, the only repre- sentatives of the family known with certainty from the western Atlantic were three species of Processa. Processa bermudensis (Rankin, 1900), the first to be described, was redescribed by Gurney (1936), who also gave an account of its larvae; it was known only from Bermuda until Williams (1965) recorded it from North Carolina. In 1941 Lebour described P. wheeleri and its larvae from Bermuda; it is still known only from her material. Holthuis (1959) described P. guyanae from the coast of Surinam; we have seen no further specimens of this species. Numerous lots of unidentified processids from various localities in the western Atlantic, which had accumulated in the collection of the Division of Crustacea, National Museum of Natural History (USNM), supplemented by collections made by one of us (RBM) in Florida and Puerto Rico, formed the basis of this report. Additional collections from Bermuda were made by one of us (RBM) in April 1970, because available study material from Bermuda, the type locality for two of the western Atlantic Raymond B. Manning and Fenner A. Chace, Jr., Department of Invertebrate ^oology, National Museum of Natural History, Smith- sonian Institution, Washington, D.C. species, was apparently limited to one damaged specimen of P. bermudensis collected by G. Brown Goode in 1876-1877. We describe below a new genus and species, a new species of Nikoides, a genus previously known only from the Indo-West Pacific region, and six new species of Processa. The eight new species, the presence of inadequate material of an additional new Processa, the occurrence of two unknown processid larvae at Bermuda (Lebour 1941), and the fact that we did not encounter two of the three previously known species from the study area suggest that not only was this review needed but that more is yet to be learned about the western Atlantic processids. We hope that this contribution to our knowledge of American processids will aid future work on members of this family. Until 1936 when Miss Lebour showed that the British species then called P. canaliculata actually com- prised two species, that species was thought to have a cosmopolitan distribution. Thus, most records of processids from the western Atlantic were identified as P. canaliculata, a species which does not occur out- side of the eastern Atlantic region (Nouvel and Holthuis 1957). Fortunately, we have been able to examine and reidentify most of the western Atlantic specimens recorded in the literature as P. canaliculata, and the synonymies given herein reflect these identifi- cations. Only two literature records could not be verified with certainty: Schmitt (1924) recorded a specimen of "P. canaliculata" from Caracas Bay, Curac,ao, and Hudson, Allen, and Costello (1970) listed Processa sp. from Florida Bay. We have exam- ined none of the material reported in these two papers. 1 SMITHSONIAN CONTRIBUTIONS TO ZOOLOGY In addition to our descriptive accounts of the western Atlantic processids, we have included a key to the known species of Nikoides, constructed from data in the literature, a list of the nominal Indo- West Pacific species of Processa, and a provisional key to the Atlantic species of Processa. Some of the species recorded from the eastern Atlantic may conceivably be found in the western Atlantic also, although no species is now known to occur in both. The descriptive accounts include a brief diagnosis designed to distinguish each species from other proces- sids in the western Atlantic. Complete descriptions and illustrations are given for all species except P. guyanae Holthuis and P. wheeleri Lebour. Holthuis (1959) gave a complete account for P. guyanae; we have seen no additional material of that species. We were unable to locate the type or any additional material of P. wheeleri. Measurements in all cases are carapace lengths in millimeters. The descriptions are composites, and include observed variations in the material examined. Acknowledgments We are pleased to acknowledge the aid of the follow- ing individuals: Dorothy Bliss, American Museum of Natural History, and Willard Hartman, Peabody Museum, Yale University, for tracking down speci- mens previously recorded from Bermuda; H. Levi, Museum of Comparative Zoology, Harvard Uni- versity (MCZ), for the loan of a specimen from the Bahamas; R. Ingle and A. L. Rice, British Museum (Natural History), for looking up the material from Bermuda reported by R. Gurney and M. Lebour; Carl Saloman, United States Fish and Wildlife Service, Saint Petersburg, Florida, and Larry Abele, Florida State University, for generously sharing col- lections; J . Rivero, University of Puerto Rico, Mayaguez, for making possible the visit by one of us (RBM) to Puerto Rico in 1961; Wolfgang Sterrer, director, Bermuda Biological Station, for making facilities available at the station in April 1970; and L. B. Holthuis, for funishing notes and illustrations made by H. Nouvel of the specimen reported from Guadeloupe as P. canaliculata by Monod (1939). Family PROCESSIDAE Ortmann, 1896 Processidae Ortmann, 1896: 415, 424.?Holthuis, 1955: 116 [and synonymy]. DEFINITION.?Body smooth. Rostrum short, apex bifid or simple, ventral border never armed. Carapace armed at most with antennal spines. Postorbitai groove present or absent. First abdominal somite neither armed nor denticulate. Fifth abdominal somite occasionally with posterolateral spine or spines on pleuron. Telson with 2 pairs of dorsal and 2 pairs of posterior spines, with pair of stout plumose setae between inner pair of posterior spines. Eyes relatively large, with well-developed cornea. Antennular peduncle with well-developed stylocerite; antennular flagella simple, ventromesial shorter than dorsolateral, with thickened setigerous portion proximally. Antennal scale well developed. Mandible lacking distinct incisor process and palp. First maxilla with 1 endite and palp. Second maxilla with endites reduced, palp and scaphognathite well developed. First maxilliped with palp, caridean lobe, epipod, and exopod. Second maxilliped with endite of 5 articles, exopod, and epipod. Third maxilliped with well-developed exopod. All pereiopods with pleurobranch; arthrobranch present or absent at base of first pereiopod; first pereiopod with (Nikoides) or without (Ambidexter, Processa) exopod. Both pereiopods of first pair chelate (Ambidexter) or with only 1 chelate (Nikoides, Processa), usually right, left with unopposed simple dactyl. Second pair of pereiopods chelate, slenderer than first; carpus always, merus usually, and ischium occasionally subdivided; ischium with inner basal enlargement; right second pereiopod usually stronger than left, sometimes equal. Third, fourth, and fifth pereiopods slender, termi- nating in simple dactyl. First pair of pleopods in male with foliaceous endopod sometimes bearing coupling lobe. Endopod of second pleopod in male with appendix interna and appendix masculina. Uropods elongate, exopods with transverse suture extending from lateral spine (adapted from Nouvel and Holthuis 1957.) DISCUSSION.?Discovery of a processid shrimp with both first pereiopods chelate has necessitated a re- definition of the family?previously defined by the presence of a simple dactyl on one of the first pereio- pods in all known species. The family can best be recognized by the form of the rostrum, which in most species is a simple projection of the carapace, terminating in an apical and a subapical tooth, in combination with usually asymmetrical first pereio- pods. The subapical tooth may be set some distance posterior to the apex of the rostrum (as in Nikoides maldivensis Borradaile and Processa jacobsoni De Man), or it may be absent (as in P. acutirostris Nouvel and Holthuis and Nikoides nanus Chace). NUMBER 89 In the key to families and superfamilies of caridean shrimp given by Holthuis (1955, couplet 16), in which the Processidae are separated from the other families in the superfamily Alpheoida (Hippolytidae, Ogyridi- dae, and Alpheidae), the following modification could be made: 16. First pair of pereiopods both chelate. Rostrum dentate or unarmed, not with single subdistal dorsal tooth ..17 Usually right first pereiopod chelate, left ending in simple clawlike dactylus. If both chelate, rostrum with distal setose notch formed by subdistal dorsal tooth Processidae Although the processids exhibit some superficial resemblance to the Hippolytidae, we believe that the form of the rostrum and the structure of the mouth- parts in the processids support the continued recogni- tion of these two groups of species as distinct families. All of the Atlantic processids are similar in basic facies; indeed, the western Atlantic species examined by us apparently have essentially identical mouth- parts?with the exception of the number of spinules on the posterior margin of the molar process of the mandible?and uropods. We have figured the mouth- parts of all but two of the western Atlantic species; they appear to be subsimilar to the mouthparts of Processa canaliculata Leach and P. edulis (Risso) as described by Lebour (1936). In view of these close similarities, it is not surprising that the genera are very similar, differing only in characters of the first pereiopods. Gurney (1937) pointed out the similarities of the larvae of Nikoides and Processa, noting that there is more difference between the larvae of Processa aequimana and those of other species of Processa than there is between the larvae of Nikoides and Processa. He also pointed out the similarities between the rostrums of Processa jacobsoni De Man and Nikoides maldivensis Borradaile, in which the dorsal tooth is widely separated from the apex; De Man (1921) did not mention the exopods on the first pereiopods, but his species could prove to be conspecific with N. maldivensis. Chace (1955: 10), in his discussion of Nikoides nanus, a small species with short exopods on the first pereiopods, pointed out that the occurrence of short exopods in his species possibly strengthened Gurney's suggestion that Nikoides could be maintained as a distinct genus if only for convenience. It seems likely that the genera recognized here are closely related natural units. It is also possible that additional study of Indo- West Pacific species will result in the recognition of additional genera. Processa molaris Chace has an un- usually enlarged mandible, and P. paucirostris and P. steinii, two species described by Edmondson, each have an unusually short, unarmed rostrum, not ex- tending much beyond the antennal spine. 2(1). Key to the Genera of the Processidae First pereiopods both chelate [first pereiopods lacking exopods; second pereiopods sym- metrical] Ambidexter Only one of first pair of pereiopods (usually right) chelate, other pereiopod with simple dactyl 2 First pereiopods with exopods Nikoides First pereiopods without exopods Processa Ambidexter, new genus DEFINITION.?Processid shrimp with both first pereiopods chelate and lacking exopods. TYPE-SPECIES.?Ambidexter symmetricus, new species (see below). GENDER.?Masculine. NUMBER OF SPECIES.?One, described below. Ambidexter symmetricus, new species FIGURES 1, 2 Processa sp. Tabb and Manning, 1961: 598 [listed; specimen from Flamingo].?Rouse, 1970: 140 [listed; part]. HOLOTYPE.?cT, 4.7 mm; Florida, Dade County, Miami, Biscayne Bay, Matheson Hammock Wading Beach; push net on grass flats, evening; C. F. E. Roper and R. B. Manning, col.; 7 July 1962; USNM 134097. PARATYPES.?19 c?1, 17 9 (16 ovigerous); data as in holotype; USNM.?1 9 ; same locality; R. B. Man- ming, col.; 21 February 1960; USNM.?1 ovigerous 9 ; same locality; sand, in sparse Diplanthera; R. B. Manning, col.; 10 May 1962; USNM.^c?1, 3 9 (1 ovigerous); same locality; L. P. Thomas, S. Dobkin, and R. B. Manning, col.; 28 June 1962; USNM.?6c?, 5 9 (3 ovigerous); same locality; D. R. Moore and R. B. Manning, col.; 13 July 1962; SMITHSONIAN CONTRIBUTIONS TO ZOOLOGY USNM.?1 ovigerous 9; Florida, Dade County, Biscayne Bay, Soldier Key; L. P. Thomas, col.; 3 July 1959; USNM.? 1 cf1; Florida, Monroe County, Everglades National Park, Florida Bay, off Flamingo, Sandy Key Basin; D. Tabb and R. B. Manning, col.; 16 April 1959; USNM.?Id", 1 9 ; Florida, Pinellas County, Boca Ciega Bay; BCG shovel; Carl H. Saloman, col.; 14 November 1963; USNM.?5d\ 10 9 ; Florida, Pinellas County, Point Pinellas, Tampa Bay; fine net, night; Carl H. Saloman, col.; 4 December 1965; USNM.?3 ovigerous 9 ; Florida, Levy County, Seahorse Key, in channel near marker 14; H. B. Herrick, col.; 28 May 1964; USNM.?3d\ 4 9 ; Florida, Levy County, Cedar Keys; found among grass between tides; H. Hemphill, col.; 1883; USNM. ?lcf; Florida, Franklin County, Bald Point; dug from sand-mud grass flat at low tide; M. Wass, col.; 31 January 1957; USNM.?1 9 ; Florida, Franklin County, Alligator Harbor, grass flats at mouth; L. Abele, col.; 29 January 1968; USNM.?1 9 ; Florida, Franklin County, Alligator Harbor; on bar, at mouth, in sand; may have come from Diopatra hole; L. Abele, col.; 18 November 1969; USNM.?5d\ 1 9 ; Louisi- ana, Chandeleur Island, Smack Channel; 29?51'N, 88?51'W; 17-18 feet; R. M. Darnell, col.; 28 March 1954; USNM.?2c?, 10 9 (8 ovigerous); Mexico, Tamaulipas, Punta Piedras (South), Laguna Madre del San Antonio; push net, night; 0-3 feet; H. Hildebrand, col.; 24 October 1953; USNM.?8c?, 119 (9 ovigerous); Puerto Rico, Lajas, La Parguera, east side of Maguey Island; evening, after dark, with push net on shallow Thalassia flats; R. B. Manning station PR 6-61; 24 June 1961; USNM.?1 ovigerous 9 ; Trinidad; shore; Albatross, col.; 30 January-2 February 1884; USNM. OTHER MATERIAL.? 1 juvenile; Trinidad, Coco- rite Swamp, northwest of Port of Spain; seaward mud flats; P. R. Bacon, col.; 31 August 1966; USNM. DIAGNOSIS.?Antennal spine present. Stylocerite rounded laterally, unarmed. (Both first pereiopods chelate, lacking exopods.) Second pereiopods sym- metrical, with 4 meral and 9-10 carpal articles. Carpus of fifth pereiopod longer than propodus. Fifth abdominal somite unarmed posterolaterally. Abdominal sternites unarmed. DESCRIPTION.?Rostrum (Figure \b) slightly de- flexed, not extending beyond anterior margin of eye, upper margin slightly convex; apex (Figure \c) bifid, lower tooth longer, short setae implanted in bifurca- tion; distal portion of lower margin of rostrum straight, lined with setae. Lower orbital angle ob- tusely rounded, inconspicuous. Antennal spine pres- ent. Lower anterior angle of carapace broadly rounded (Figure la). Abdomen (Figure Id) smooth, bare, ventral margins of pleura lined with fine setae. Fifth ab- dominal somite rounded or bluntly angled but un- armed posterolaterally. Sixth abdominal somite less than \y, j , m, X 12.5; k, n, X25; e, g, i, /, o, X63. nular peduncle. Basal segment of antenna lacking ventrolateral spine. Antennal flagellum more than ?Y<2, times carapace length. Third maxilliped (Figure 3o) overreaching antennal scale by slightly more than length of distal segment in males, by most of penultimate segment in females; ultimate segment with dorsal spines, apex sharp, about as long as penultimate segment but slightly less than 3^ as long as proximal segment. Exopod well developed. Posterior margin of mandible (Figures 3i, j) with 13 small spines. Remainder of mouthparts shown in Figures 3k-n. Right pereiopod of first pair (Figure 4a) chelate, falling short of tip of antennal scale, slightly over- reaching penultimate segment of antennular ped- uncle; fingers about Yi length of the palm in males, about % the length of palm in females; carpus sub- equal to or slightly shorter than palm; merus longer than carpus and chela combined. Left pereiopod of first pair (Figure Sb) with dactyl simple, extending about to end of antennal scale; dactyl less than % the length of propodus; carpus shorter than propodus; merus about as long as carpus, propodus, and dactyl combined. Exopods of first pereiopods not extending beyond midlength of merus. First pereiopods with arthrobranch. Second pereiopods (Figure 5) strongly asymmetrical. Right larger, overreaching antennal scale by chela, carpus, and Y2 of merus; ischium divided into 3, merus into 23-24, and carpus into 43-49 articles; fingers subequal to palm in males, slightly shorter than palm in females; carpus about 13 times as long as chela in males, about 10 times as NUMBER 89 11 long as chela in females; merus more than 7 times as long as chela in males, 5-7 times as long as chela in females; ischium shorter than merus. Left pereiopod of second pair (Figures Ac, 5b) overreaching antennal scale by chela and about J^ of carpus; ischium not noticeably segmented, merus with 5 and carpus with 17-18 articles; fingers subequal to palm; carpus more than 8 times as long as chela; merus about 5 times as long as chela; ischium subequal to merus. Third pereiopod (Figure Ad) overreaching antennal scale by dactyl, propodus, and ^ of carpus; dactyl (Figure Ae) slender, simple, with numerous apical setae; pro- podus more than 3 times as long as dactyl, unarmed, ornamented with few scattered setae; carpus about 2 times as long as propodus in males, about 2-3 times as long in females, unarmed; merus less than twice as long as propodus, with 4 movable spines on lateral surface; ischium shorter than merus, with 2 movable spines on lateral surface; combined length of propodus and carpus of third pereiopod about as long as that of ischium and merus in males, combined length of propodus and carpus slightly longer in large females. Fourth pereiopod (Figure 4/) overreach- ing antennal scale by dactyl, propodus, and ^ of carpus; dactyl (Figure 4 )^ slender, simple, with nu- merous apical setae; propodus less than 3 times as long as dactyl, unarmed, with few scattered setae on surface and several long, distal tufts of setae; outer margin of propodus not lined with short setae in males; carpus slightly more than twice as long as propodus, unarmed, with few scattered setae; merus slightly less than twice the length of propodus, with 2-8 movable spines on lateral surface; ischium shorter than merus, with 1-2 movable spines on lateral sur- face; combined length of propodus and carpus of fourth pereiopod greater than that of ischium and merus. Fifth pereiopod (Figure Ah) overreaching antennal scale by dactyl and 2"io of propodus in males, by dactyl and all of propodus in large females; dactyl (Figure 4i) slender, with rounded ventral tubercle distally and numerous long apical setae; propodus less than 3 times as long as dactyl, with scattered tufts of setae and 2 slender spines on flexor margin; upper margin of propodus not lined with short setae in males; carpus less than 1 J/? times as long as propodus in males, 1l/^ times as long in females, unarmed, with few scattered setae; merus about \}/, right second maxilliped; q, right third maxilliped; r, right first pereiopod; s, left first pereio- pod; t, right second pereiopod; u, left second pereiopod; v, right third pereiopod; w, right fourth pereiopod; x, right fifth pereiopod. Magnifications: d, X3; a, b,J, h,j, q-x, X6; e, m-p, X\2; g, I, k, X25; c, I, X63. nearly % longer than carapace, thickened setigerous portion consisting of 17-19 articles and amounting to % of total length, slender distal portion consisting of 26-29 articles. Ventromesial flagellum at least 2% times as long as carapace. Antennal scale (Figure 16/) slightly overreaching antennular peduncle, length of scale almost 4 times the greatest breadth; distal spine of scale extending slightly beyond lamella. Basal segment of antenna with ventral spine. Antennal peduncle extending to end of second segment of antennular peduncle. An- tennal flagellum at least as long as body. Third maxilliped (Figure 16 )^ overreaching anten- nal scale by slightly more than combined lengths of two distal segments; ultimate segment ornamented with short spines, apex sharp; ultimate segment longer than penultimate, slightly more than half as long as proximal segment. Exopod well developed. Mandible (Figures 16?, /) with row of 21 spines on posterior margin of molar process. Remainder of mouthparts (Figures \6m-p) as in P. bermudensis. Right pereiopod of first pair (Figure 16r) chelate, overreaching antennal scale by fingers and over 3^ of palm of chela; fingers about % the length of palm; carpus slightly shorter than palm; merus slightly shorter than carpus and chela combined. Left pereio- pod of first pair (Figure 16*) with simple dactyl, overreaching antennal scale by dactyl and % of pro- 30 SMITHSONIAN CONTRIBUTIONS TO ZOOLOGY podus; dactyl % the length of propodus; carpus slightly more than 3^> as long as propodus; merus about as long as carpus and propodus combined. No arthrobranch visible at base of first pereiopods. Second pereiopods asymmetrical, right (Figure 16/) stronger, overreaching antennal scale by chela, carpus, and ^ of merus; merocarpal articulation extending beyond eye; ischium with 3, merus with 17, and carpus with 39-43 articles; fingers slightly shorter than palm; carpus 10 times as long as chela; merus about 5 ^ times as long as chela; ischium slightly shorter than merus. Left pereiopod of second pair (Figure 16M) overreaching antennal scale by chela, carpus, and 2 distal articles of merus; ischium undivided, merus with 5-6 and carpus with 16-20 articles; fingers shorter than palm; carpus about 4J/? times as long as chela; merus about 2 ^ times as long as chela. Third pereiopod (Figure 16P) overreaching antennal scale by dactyl, propodus, and about J^ fo of carpus; dactyl slender, simple, with apical setae; propodus about 4 times as long as dactyl, unarmed, ornamented with tufts of setae along surface and at apex; carpus slightly more than 1}/% times as long as propodus, unarmed; merus less than 1 }/? times as long as propodus, with 4 movable spines on lateral face; ischium shorter than merus, with 2 movable spines on lateral face; combined lengths of propodus and carpus of third pereiopod greater than those of ischium and merus. Fourth pereiopod (Figure I6w) overreaching anten- nal scale by dactyl, propodus, and ?? of carpus; dactyl slender, simple, with apical tuft of setae; pro- podus 3% times as long as dactyl, unarmed, with tufts of setae along surface and at apex; carpus less than \}/2 times as long as propodus, unarmed; merus slightly longer than propodus, with 3 movable spines on lateral surface; ischium shorter than merus, with 2 movable spines on lateral surface; combined length of propodus and carpus of fourth pereiopod greater than that of ischium and merus. Fifth pereiopod (Figure 16x) overreaching antennal scale by dactyl and %o of propodus; dactyl slender, simple, with short apical tuft of setae; propodus almost 4 times as long as dactyl, surface with scattered setae, with 4?5 spines on flexor margin; carpus slightly shorter than pro- podus, unarmed; merus slightly longer than propodus, unarmed; ischium shorter than merus, unarmed; combined length of propodus and carpus of fifth pereiopod greater than that of ischium and merus. Abdominal sternites 1-5 with median spine in fe- males. Uropods (Figure 16/) as in P. bermudensis. Eggs small and numerous, 0.3-0.4 mm in diameter. SIZE.?Carapace lengths of females, 2.7-5.65 mm; of ovigerous females, 5.3-5.65 mm. COLOR.?Background white, with minute red chromatophores scattered over body; third maxilli- peds and first pereiopods tinged with orange distally; eggs light green. DISCUSSION.?Processa riveroi closely resembles P. Jimbriata, the only other western Atlantic species with a spine on the stylocerite, a posterolateral spine on the pleuron of the fifth abdominal somite, and spines on the abdominal sternites. It can, how- ever, be distinguished from that species by several features. Processa riveroi is a slenderer species, with noticeably smaller eyes; the cornea width is only slightly greater than the greatest width of the antennal scale, whereas in P. jimbriata it is usually twice as broad as the antennal scale. The distal portion of the dorsolateral antennal flagellum is longer than the proximal in P. riveroi, whereas the reverse is true in P. Jimbriata. The stylocerite of P. riveroi is armed at both internal and external angles, rather than the external angle only, and there are more spines (21 rather than 6-7) on the posterior margin of the man- dible. The pereiopods of P. riveroi are longer than those of P. Jimbriata: the right second pereiopod in P. riveroi extends beyond the antennal scale by two thirds of the merus, rather than by most of the carpus; the third pereiopod of P. riveroi overreaches the antennal scale by most of the carpus, whereas in P. Jimbriata it extends beyond the scale by the two distal seg- ments only. The numbers of articles in the second pereiopods are slightly different in the two species: in P. riveroi there are 17 meral and 39-43 carpal articles in the right pereiopod, 5-6 meral and 16-20 carpal articles in the left; in P. Jimbriata there are 13- 16 meral and 31^0 carpal articles in the right pereio- pod, 4-6 meral and 15-18 carpal articles in the left. There may also be a habitat difference in the two species, for P. riveroi was found free-living on shallow grass flats, whereas many of the specimens of P. fimbriata were found to be associated with sponges. Two other species, Ambidexter symmetricus and Pro- cessa bermudensis, were collected along with P. riveroi at Maguey Island; all three apparently live in the same habitat, Thalassia flats in shallow water, (water depth 1 meter or less) on a sandy substratum. NAME.?We are pleased to dedicate this species to NUMBER 89 31 Juan A. Rivero, University of Puerto Rico, who sup- ported the trip to Puerto Rico by one of us (RBM) to study the decapods in the collection of the Institute of Marine Biology at Mayaguez; during that trip the types of P. riveroi were collected. TYPE-LOCALITY.?Maguey Island, La Parguera, Puerto Rico. DISTRIBUTION.?Known only from the type-locality, Maguey Island, La Parguera, Puerto Rico, in shallow water. Processa tenuipes, new species FIGURES 17, 18 HOLOTYPE.?Ovigerous 9 , 9.65 mm; Gulf of Mex- ico, off west coast of Florida; 29?12'N, 84?22'W; 31 m; Oregon station 898; 8 March 1954; USNM 97415. PARATYPES.?5cf, 6 ovigerous 9 ; off North Caro- lina; 35?08'30"N, 75?1O'W; 90 m; grey sand; Alba- tross station 2596; 17 October 1885; USNM.?1 oviger- ous 9; off northern coast of Cuba; 23?H'45"N, 82?17'54"W; 331 m; fine brown sand; Albatross sta- tion 2327; 17 January 1885; USNM.?7 9 (5 oviger- ous); Gulf of Mexico; off west coast of Florida; 28?44'N, 85?06'W; 92 m; fine clay ooze; L. Abele col., LGA 70-5; 10 April 1970; USNM. DIAGNOSIS.?Antennal spine present. Stylocerite with at most lateral tubercle. (Right pereiopod of first pair chelate, left with simple dactyl; first pereio- pods lacking exopods.) Second pereiopod asymmetri- cal, right stronger. Right second pereiopods with 18-28 meral and 28-69 carpal articles, left second pereiopod with 5-9 meral and 17-26 carpal articles. Carpus of fifth pereiopod longer than propodus. Fifth abdominal somite unarmed posterolaterally. Ab- dominal sternites unarmed. DESCRIPTION.?Rostrum (Figure 17b) slender, con- vex dorsally, not extending to anterior margin of eye; apex deflexed, bifid, lower tooth longer, apex ob- scured by long setae. Lower orbital angle inconspicu- ous, broadly rounded. Antennal spine small but dis- tinct. Lower anterior angle of carapace broadly rounded (Figure 17a). Abdomen (Figure 11c) smooth, surface ornamented with few short setae, ventral margins of pleura lined with fine setae. Fifth abdominal somite bluntly angled posterolaterally. Sixth abdominal somite less than twice as long as fifth, angled posterolaterally; lobe above articulation of telson unarmed. Telson (Figure \7d) slightly more than \y% times as long as sixth abdominal somite, length slightly more than 3 times greatest width, with 2 pairs of dorsal and 3 pairs of distal spines; anterior pair of dorsal spines of telson set near end of proximal fourth, posterior pair beyond midlength; distance between anterior margin and anterior pair of spines more than ^ distance between pairs of spines; distal spines (Figure 17^ ) as in P. bermudensis; apex of telson produced into slender median spine. Eye (Figure 17a) of moderate size, cornea width subequal to length of stalk and cornea combined, more than double greatest width of antennal scale. Antennular peduncle (Figure 17/) extending be- yond rostrum by 2 distal segments and distalmost third of proximal segment; basal segment as long as combined lengths of distal segments, penultimate segment more than twice the length of ultimate seg- ment. Proximal segment of antennular peduncle with small ventral spine near midlength. Stylocerite (Fig- ure 17 )^ subtruncate .anteriorly, anterior margin sinu- ous, with lateral tubercle or bluntly angled promi- nence. Dorsolateral flagellum of antennule % as long as carapace, thickened setigerous portion consisting of 17-26 articles in females and 26-30 articles in males and amounting to % of length, slender distal portion consisting of 17-19 articles. Ventromesial flagellum of antennule at least 4 times as long as carapace. Antennal scale (Figure 17A) extending about to end of antennular peduncle, length of scale about 6}/? times greatest width; distal spine of scale small, not overreaching blade. Basal segment of antennal pe- duncle with small but distinct outer spine. Antennal peduncle extending about to midlength of second segment of antennular peduncle. Antennal flagellum about 4}/? times as long as carapace. Third maxilliped (Figure 17?) overreaching an- tennal scale by 2 distal segments; ultimate segment ornamented with spines, apex sharp, shorter than penultimate segment and less than 3^ as long as prox- imal segment; exopod well developed. Posterior mar- gin of molar process of mandible (Figure 17i) with row of 21 small spines. Remainder of mouthparts (Figures 1 lj-m) as in P. bermudensis. Right pereiopod of first pair (Figure 1 To) chelate, overreaching antennal scale by length of fingers; fingers slightly more than x/i the length of palm; 32 SMITHSONIAN CONTRIBUTIONS TO ZOOLOGY FIGURE 17.?Processa tenuipes, new species, holotype, ovigerous female, carapace length 9.65 mm: a, anterior region; b, distal portion of rostrum; c, abdomen; d, telson and uropods; e, end of telson; / , left antennule; g, same, stylocerite; k, left antenna; i, right mandible; j , right first maxilla; k, right second maxilla; /, right first maxilliped; m, right second maxilliped; n, left third maxilliped; o, right first pereiopod; p, left first pereiopod; q, right second pereiopod; r, left second pereiopod; s, right third pereiopod; t, same, dactyl; u, left fourth pereiopod (dactyl missing); v, left fifth pereiopod (dactyl and distal end of propodus missing). Magnifications: a, c, d,J, h, n-s, u, v, X4.2; j?m, X8.4; g, XI7.5; b, e, i, t, X35. NUMBER 89 33 carpus subequal to palm; merus longer than carpus and chela combined. Left pereiopod of first pair (Figure \lp) with simple dactyl, overreaching anten- nal scale by dactyl and fully y% of propodus; dactyl about }/? the length of propodus; carpus slightly shorter than propodus; merus longer than carpus, propodus, and dactyl combined. No arthrobranch visible at base of first pereiopods. Second pereiopods strongly asymmetrical, right longer. Right pereiopod of second pair (Figure \lg) overreaching antennal scale by chela, carpus, and slightly less than x/i of merus; merocarpal articulation of right pereiopod extending well beyond eye; ischium divided into 4 (sometimes indistinct), merus into 18-28, and carpus into 48-69 articles; fingers subequal to palm; carpus about \\y times as long as propodus, with 5 movable spines on lateral surface; ischium shorter than merus, with FIGURE 20.?Processa vicina, new species, paratype, male, from off Venezuela, carapace length 3.0 mm: a, anterior region; b, tclson and uropods; c, end of telson; d, stylocerite of right antennule; e, right first pereiopod; / , left first pereiopod; g, right second pereiopod; h, left second pereiopod; i, right third pereiopod; j , same, dactyl; k, right fourth pereiopod; /, left fifth pereiopod; m, endopod of right second pleopod. Magnifica- tions: a, b, e-i, k, I, X12.5; d, X25; c,j, m, X63. NUMBER 89 37 2 movable spines on lateral surface; combined length of propodus and carpus of fourth periopod much greater than that of ischium and merus. Fifth pereio- pod (Figure 20/) overreaching antennal scale by dactyl, propodus, and fully half of carpus; dactyl slender, simple, with subapical tufts of setae; propodus almost 4 times as long as dactyl, with scattered short setae on surface, longer apical setae, and 1 distal spine on flexor margin; outer margin of propodus not markedly more setose in males than in females; carpus % longer than propodus, unarmed; merus about l}4 times as long as propodus, unarmed; ischium shorter than merus, unarmed; combined length of propodus and carpus of fifth pereiopod greater than that of ischium and merus. Endopod of first male pleopod (Figures 19r, s) about x/l as long as exopod, tapering distally, apex acute, setose, retinacular lobe well developed, separated for most of its length; coupling hooks not seen. Appendix masculina of second male pleopod (Figures 19/-r>, 20m) with row of spinules on outer margin, apex with 4 distal spinules. Abdominal sternites unarmed. Uro- pods (Figures 19 ,^ 206) as in P. bermudensis. Eggs small and numerous, 0.5-0.6 mm in diameter. SIZE.?Carapace lengths of males, 2.8^1.0 mm; of females, 2.9-5.3 mm; of ovigerous females, 4.3-5.3 mm. COLOR.?Not recorded. DISCUSSION.?Processa vicina resembles P. bermudensis and differs from all other Atlantic species of Processa in lacking the antennal spine of the carapace. It dif- fers from P. bermudensis in having symmetrical second pereiopods, with 5 meral and 10-14 carpal articles on both; it further differs from P. bermudensis in having the rostrum deflexed anteriorly and in having broader eyes. Only three other species of Processa are known to have symmetrical second pereiopods: P. aequimana (Paulson), from the Red Sea; P. parva Holthuis, from the eastern Atlantic; and P. hemphilli, described herein from west Florida. These three species also have an antennal spine on the carapace. NAME.?The name is from the Latin, vicina, near, alluding to its presumed relationship with P. ber- mudensis. TYPE-LOCALITY.?Off North Carolina, in 59 m. DISTRIBUTION.?Western Atlantic, where it has been taken off North Carolina, in the Gulf of Mexico, and off Venezuela, in depths between 46 and 95 m. Processa wheeleri Lebour, 1941 Processa wheeleri Lebour, 1941: 403, figs. 1-9, 11-27.?Holthuis, 1959: 120 [discussion].?A. B. Williams, 1965: 87. DIAGNOSIS.?Antennal spine present. Stylocerite with lateral spine. (Right pereiopod of first pair che- late, left with simple dactyl; first pereiopods lacking exopods.) Second pereiopods asymmetrical, right stronger. Right second pereiopod with 7 meral and 23 carpal articles, left second pereiopod with 5 meral and 15 carpal articles. Carpus of fifth leg subequal in length to propodus. Fifth abdominal somite unarmed posterolaterally. (Abdominal sternites not described). DISCUSSION.?This species was not represented in the material available to us, and we were unable to locate the male holotype; it may prove to be at The Marine Laboratory, Plymouth. P. guyanae, P. profunda, and P. tenuipes (the other western Atlantic species with a spine on the stylo- cerite, an antennal spine, unarmed pleura on the fifth abdominal somite, and asymmetrical second chelae) all have longer pereiopods and have more than forty articles on the carpus of the right second pereiopod. Williams (1965) suggested that a few immature specimens of Processa collected in Bogue Sound, North Carolina, might prove to be P. wheeleri, but his speci- mens were too young to be identified with certainty. TYPE-LOCALITY.?Off Bermuda. DISTRIBUTION.?Western Atlantic, where it is known from Bermuda and possibly from off North Carolina. Literature Cited Allen, J . A. 1961. Observations on the Genus Processa from Northum- berland Waters. Annals and Magazine of Natural History, series 13, 4: 129-141, figures 1-7. Bacescu, M. 1967. Decapoda. Fauna Republicii Socialiste Romania, Crusta- cea, 4 (9): 1-351, figures 1-141. Academia Repub- licii Socialiste Romania. Baker, W. H. 1907. Notes on South Australian Decapod Crustacea, Part V. Transactions and Proceedings and Report of the Royal Society of South Australia, 31 : 173-191, plates 23-25. Barnard, K. H. 1947. Descriptions of New Species of South African De- capod Crustacea, and Notes on Synonymy and New Records. Annals and Magazine of Natural History, series 11, 13: 361-392. 38 SMITHSONIAN CONTRIBUTIONS TO ZOOLOGY 1950. Descriptive Catalogue of South African Decapod Crustacea. Annals of the South African Museum, 38: 1-837, figures 1-154. 1955. Additions to the Fauna-list of South African Crusta- cea and Pycnogonida. Annals of the South African Museum, 43: 1-107, figures 1-53. Bate, C. Spence 1888. Report on the Crustacea Macrura Collected by H. M. S. Challenger during the Years 1873-76. The Voyage of H. M. S. "Challenger," Zoology, 24: i-xc, 1-942, figures 1-76, plates 1-150. Borradaile, L. A. 1915. Notes on Carides. Annals and Magazine of Natural History, series 8, 15: 205-213. Bullis, Harvey R., Jr., and John R. Thompson 1965. Collections by the Exploratory Fishing Vessels Oregon, Silver Bay, Combat, and Pelican Made during 1956-1960 in the Southwestern North Atlantic. United States Fish and Wildlife Service, Special Scientific Report?Fisheries, number 510: iii, 1-130. Chace, Fenner A., Jr. 1937. Bermudian Crustacea, pages 55-57. In The Bermuda Biological Station for Research, Reports of Officers for the Years 1935 and 1936, Appendix I, Summaries of the Work of Visiting Scientists. 1955. Notes on Shrimps from the Marshall Islands. Pro- ceedings of the United States National Museum, 105 (3349): 1-22, figures 1-8. Dana, J. D. 1852. Crustacea, Part I. United States Exploring Expedition during the Tears 1838, 1839, 1840, 1841, 1842 under the Command of Charles Wilkes, UJ.N, 13: 1-685. Atlas, 1855: 1-27, plates 1-96. Philadelphia: C. Sherman. Edmondson, Charles H. 1930. New Hawaiian Crustacea. Bernice P. Bishop Museum, Occasional Papers, 9 (10): 1-18, figures 1-6, plate 1. 1935. New and Rare Polynesian Crustacea. Bernice P. Bishop Museum, Occasional Papers, 10 (24): 1-40, figures 1-11, plates 1-2. Gurney, Robert R. 1936. A Description of Processa bermudensis Rankin and Its Larvae, IV. Notes on Some Decapod Crustacea of Bermuda, I II -V. Proceedings of the Zoological Society of London, part 3, 1936: 621-630, plates 1-7. 1937. The Genus Processa. Notes on Some Decapod Crusta- cea from the Red Sea. Proceedings of the ?oo/o?jfa/ Society of London, series B, part 1, 1937: 85-101, plates 1-6. Haan, W. De 1833- Crustacea. In De Siebold, Fauna Japonica, sive De- 1850. scriptio Animalium, Quae in ltinere per Japoniam, Jusse et Auspiciis Superiorum, qui Summum in India Batavia 1m- perium Tenent, Suscepto, Annis 1823-1830 Collegit, Notis Observationibus et Adumbrationibus Illustravit, i-xvi, i - xxxi, vii-xvii, 1-243, plates A-Q, 1-55, circular 2. A. Arnz, Lugdunum Batavorum. Holthuis, L. B. 1951. The Caridean Crustacea of Tropical West Africa. Atlantide-Report, number 2: 7-187, figures 1-34. 1952. Crustaces Decapodes, Macrures. Resultats Scientifiques. Expedition Oceanographique Beige dans les Eaux Cotihres Africaines de VAtlantique Sud (1948-1949), 3 (2): 1-88, figures 1-21. 1955. The Recent Genera of the Caridean and Steno- podidean Shrimps (Class Crustacea, Order De- capoda, Supersection Natantia) with Keys for Their Determination. ?oologische Verhandelingen, number 26: 1-157, figures A - B , 1-105. 1959. The Crustacea Decapoda of Suriname. goologische Verhandelingen, number 44: 1-296, figures 1-68, plates 1-16. Hudson, J. Harold, Donald M. Allen, and T. J. Costello 1970. The Flora and Fauna of a Basin in Central Florida Bay. United States Fish and Wildlife Service, Special Scientific Report?Fisheries, number 604: 1-14, figures 1-2. Leach, W. E. 1815- Malacostraca Podophthalmata Britanniae; or Descriptions 1875. of such British Species of the Linnaean Genus Cancer as Have Their Eyes Elevated on Footstalks. 124 pages, 45 plates. London. Lebour, Marie V. 1936. Notes on the Plymouth Processa (Crustacea). Pro- ceedings of the Zoological Society of London, part 3, 1936: 609-617, plates 1-6. 1941. Notes on Thalassinid and Processid Larvae (Crusta- cea Decapoda) from Bermuda. Annals and Magazine of Natural History, series 11,7: 401-420, figures 1-45. Man, J. G. De 1918. Diagnoses of New Species of Macrurous Decapod Crustacea from the Siboga-Expedition. ?oologische Mededeelingen, 4 ( 3 ) : 159-166. 1920. Families Pasiphaeidae, Stylodactylidae, Hoplopho- ridae, Nematocarcinidae, Thalassocaridae, Panda- lidae, Psalidopidae, Gnathophyllidae, Processidae, Glyphocrangonidae, and Crangonidae. The De- capoda of the Siboga Expedition, Part IV. Siboga- Expeditie, monograph 39aJ: 1-318, plates 1-25. 1921. On Three Macrurous Decapod Crustacea, One of Which Is New to Science. Zpologische Mededeelingen, 6 (2): 92-96, 2 figures. 1924. On a Collection of Macrurous Decapod Crustacea, Chiefly Penaeidae and Alpheidae, from the Indian Archipelago. Archiv fur Naturgeschichte, 9 0 ( 1 ) : 1-60, figures 1-20. Monod, Th. 1939. Sur Quelques Crustaces de la Guadeloupe (Mission P. Allorge, 1936). Bulletin du Museum National d'Histoire Naturelle, Paris, series 2, 11 (6): 557-568, figures 1-11. Nobili, G. 1904. Diagnoses Prdliminaires de Vingt-huit Especes Nouvelles de Stomatopode et D6capodes de la Mer Rouge. Bulletin du Museum d'Histoire Naturelle, Paris, 10: 228-238. Nouvel, H. 1945. Description du Type de Processa coutierei Nobili, 1904. Bulletin du Museum National d'Histoire Naturelle, Paris, series 2, 17 (5): 395-398, figures 1-8, NUMBER 89 39 Nouvel, H., and L. B. Holthuis 1957. Les Processidae (Crustacea Decapoda Natantia) des Eaux Europ6ennes. ?oologische Verhandelingen, num- ber 32: 1-53, figures 1-220. O'Gower, A. K., and J. W. Wacasey 1967. Analysis of Communities in Relation to Water Movement. Animal Communities Associated with Thalassia, Diplanthtra, and Sand Beds in Biscayne Bay, I. Bulletin of Marine Science, 17 (1): 175-210. Ortmann, A. E. 1896. Das System der Decapoden Krebse. Zoologische Jahr- biicher, Systematik, Okologie und Geographie der Tiere, 9: 409-453. Parisi, B. 1915. Note su Alcuni Crostacei del Mediterraneo. Monitore Zpologico Italiano, 26: 62-66, figures 1-2. Paulson, O. 1875. Podophthalmata and Edriophthalmata (Cumacea), Part 1. Investigations on the Crustacea of the Red Sea with Notes on Crustacea of the Adjacent Seas. Pages i- xiv, 1-144, plates 1-21 (text in Russian). Pearse, A. S. 1932. Inhabitants of Certain Sponges at Dry Tortugas, VII. Papers from the Tortugas Laboratory, volume 28. Carnegie Institute of Washington, Publication Num- ber 435: 117-124, figure 1, plates 1-2. 1950. Notes on the Inhabitants of Certain Sponges at Bimini. Ecology, 31 (1): 149-151. Rankin, W. M. 1900. The Crustacea of the Bermuda Islands, with Notes on the Collections Made by the New York University Expeditions in 1897 and 1898. Annals of the New York Academy of Sciences, 12 (12): 521-548, plate 17. Rathbun, Mary J. 1901. The Brachyura and Macrura of Porto Rico. Bulletin of the United States Fish Commission, 20 (2) (for 1900): 1-127, figures 1-24, plate 1. Richardson, Harriet 1904. Contributions to the Natural History of the Isopoda. Proceedings of the United States National Museum, 27 (1350): 1-89, figures 1-92. Risso, A. 1816. Hisloire Naturelle des Crustaces des Environs de Nice. Pages 1-175, plates 1-3. Paris. Rouse, Wesley L. 1970. Littoral Crustacea from Southwest Florida. Quarterly Journal of the Florida Academy of Sciences, 32 (2) (for 1969): 127-152, figure 1. Schmitt, Waldo L. 1924. The Macruran, Anomuran and Stomatopod Crusta- cea. Bijdragen tot de Kennis der Fauna van Curacao. Resultaten eener reis van Dr. C. J. van der Horst in 1920. Bijdragen tot de Dierkunde uitgegeven door het Koninklijk ?oologisch genootschap Natura Artis Magistra te Amsterdam, 23: 61-81, figures 1-7, plate 8. 1935. Crustacea Macrura and Anomura of Puerto Rico and the Virgin Islands. New York Academy of Sciences, Scientific Survey of Porto Rico and the Virgin Islands, 15 (2): 125-227, figures 1-80. Sowinsky, V. 1882. The Crustacean Fauna of the Black Sea. gapiski Kievskago Obshchestva Estestvoispytatelei, 6: 220-254, plates 9-11 (text in Russian). Stimpson, W. 1860. Prodromus descriptionis animalium evertebratorum, quae in Expeditione ad Oceanum Pacificum Septen- trionalem, a Republica Federata Missa, C. Ring- gold et J. Rodgers ducibus, observavit et descripsit. Pars 8. Crustacea Macrura. Proceedings of the Academy of Natural Sciences of Philadelphia, 1860: 22-47. Tabb, Durbin C , and Raymond B. Manning 1961. A checklist of the" Flora and Fauna of Northern Florida Bay and Adjacent Brackish Waters of the Florida Mainland Collected During the Period July, 1957 Through September, 1960. Bulletin of Marine Science of the Gulf and Caribbean, 11 (4): 552-649, figures 1-8. Verrill, A. E. 1922. Macrura. Decapod Crustacea of Bermuda, Part II. Transactions of the Connecticut Academy of Arts and Sciences, 26: 1-179, figures 1-12, plates 1-48. Williams, Austin B. 1965. Marine Decapod Crustaceans of the Carolinas. Fishery Bulletin, United States Fish and Wildlife Service, 65 (1): xi, 1-298, figures 1-252. Yokoya, Yu. 1933. On the Distribution of Decapod Crustaceans In- habiting the Continental Shelf Around Japan. Chiefly Based Upon the Materials Collected by S. S. Soyo- Maru, During the Year 1923-30. Journal of the College of Agriculture, Tokyo Imperial University, 12 ( 1 ) : 1-226, figures 1-71. Index [Pages with principal accounts are in boldface] acutirostris, Processa, 2, 13 aequimana, Processa, 3, 12, 13, 25, 37 Ambidexter, 2, 3, 7, 25 symmetricus, 3, 5-7, 19, 25, 30 apodus, Lutjanus, 19 Aulospongus schoemus, 22 australiensis, Processa, 13 austroafricana, Processa, 13 bermudensis, Nika, 15 Processa, 1, 12, 14,15, 16, 18, 19, 21, 23-31, 33, 34, 36, 37 Processa canaliculata var., 15 borboronica, Processa, 15 canaliculata, Processa, 1-3, 12, 13, 15, 19, 23, 25, 28, 34 var. bermudensis, Processa, 15 coutierei, Processa, 13 danae, Nikoides, 7, 8, 12, 22 Diopatra, 4 Diplanthera, 3, 7 edulis, Processa, 3, 13 elegantula, Processa, 12, 14, 22 fimbriata, Processa, 12, 14, 19, 20-22, 30 gracilis, Processa, 13 guyanae, Processa, 1, 2, 12, 15, 22, 28, 33, 34, 37 Halimeda, 16 hawaiiensis, Processa, 13 hemphilli, Processa, 7, 12-14, 22, 23, 24, 25 Hircinia strobilina, 22 intermedia, Processa, 14 jacobsoni, Processa, 2, 3, 13 japonica, Processa, 13 kotiensis, Processa, 13 Lutjanus apodus, 19 macrodactyla, Processa, 14 macrognatha, Processa, 13 macrophthalma, Processa, 14 maldivensis, Nikoides, 2, 3, 8, 12 mediterranea, Processa, 15 molaris, Processa, 3, 13 nanus, Nikoides, 2, 3, 7, 12 Nika bermudensis, 15 Nikoides, 1-3,7, 12 danae, 7, 8, 12, 22 maldivensis, 2, 3, 8, 12 nanus, 2, 3, 7, 12 schmitti, 8, 9-12, 34 sibogae, 8, 12 parva, Processa, 12-14, 25, 37 paucirostris, Processa, 3, 13 pontica, Processa, 13, 14 Processa, 1-3,12, 13, 18, 37 acutirostris, 2, 13 aequimana, 3, 12, 13, 25, 37 australiensis, 13 austroafricana, 13 bermudensis, 1, 12, 14, 15, 16, 18, 19, 21, 23-31, 33, 34, 36, 37 borboronica, 15 canaliculata, 1-3, 12, 13, 15, 19, 23, 25, 28, 34 var. bermudensis, 15 coutierei, 13 edulis, 3, 13 elegantula, 12, 14, 22 fimbriata, 12, 14,19, 20-22, 30 gracilis, 13 guyanae, 1, 2, 12, 15, 22, 28, 33, 34, 37 hawaiiensis, 13 hemphilli, 7, 12-14, 22, 23, 24, 25 intermedia, 14 jacobsoni, 2, 3, 13 japonica, 13 kotiensis, 13 macrodactyla, 14 macrognatha, 13 macrophthalma, 14 mediterranea, 15 molaris, 3, 13 parva, 12-14, 25, 37 paucirostris, 3, 13 pontica, 13, 14 processa, 13, 15 profunda, 15, 25, 26-28, 37 riveroi, 12, 14, 19, 21, 22, 28, 29-31 robusta, 13 species, 1,8, 12, 15, 19 steinii, 3, 13 tenuipes, 12, 15, 28, 31, 32-34, 37 vicina, 12, 14, 18, 25, 34, 35-37 wheeleri, 1, 2, 14, 37 processa, Processa, 13, 15 processae, Urobopyrus, 22 profunda, Processa, 15, 25, 26-28, 37 riveroi, Processa, 12, 14, 19, 21, 22, 28, 29-31 robusta, Processa, 13 schmitti, Nikoides, 8, 9-12, 34 schoemus, Aulospongus, 22 sibogae, Nikoides, 8, 12 species, Processa, 1,8, 12, 15, 19 40 NUMBER 89 41 Spheciospongia vespara, 19, 22 steinii, Processa, 3, 13 strobilina, Hircinia, 22 symmetricus, Ambidexter, 3, 5-7, 19, 25, 30 tenuipes, Processa, 12, 15, 28, 31, 32-34, 37 Thalassia, 4, 7, 16, 19, 28, 30 Urobopyrus processae, 22 vespara, Spheciospongia, 19, 22 vicina, Processa, 12, 14, 18, 25, 34, 35-37 wheeled, Processa, 1,2, 14, 37 ?& U.S. GOVERNMENT PRINTING OFFICEi 1971 O?410-847 Publication in Smithsonian Contributions to Zoology Manuscripts for serial publications are accepted by the Smithsonian Institution Press subject to substantive review, only through departments of the various Smithsonian museums. 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Taxonomic titles will carry a final line indicating the higher categories to which the taxon is referable: "(Hymenoptera: Sphecidae)." Include an abstract as an introductory part of the text. Identify the author on the first page of text with an unnumbered footnote that includes his professional mailing address. A table of contents is optional. An index, if required, may be supplied by the author when he returns page proof. Two headings are used: (1) text heads (boldface in print) for major sections and chapters and (2) paragraph sideheads (caps and small caps in print) for subdivisions. Further headings may be worked out with the editor. In taxonomic keys, number only the first item of each couplet; if there is only one couplet, omit the number. For easy reference, number also the taxa and their corresponding headings throughout the text; do not incorporate page references in the key. In synonymy, use the short form (taxon, author, date, page) with a full reference at the end of the paper under "Literature Cited." Begin each taxon at the left margin with subse- quent lines indented about three spaces. Within a taxon, use a period-dash (.?) to separate each entry. Enclose with square brackets any annotation in or at the end of the taxon. For synonymy and references within the text, use the author-date system: "(Jones 1910)." Use the colon system for page references: "(Jones 1910:122)," and abbreviate further data: "(Jones 1910:122, fig. 3, pi. 5: fig. 1)." Simple tabulations in the text (e.g., columns of data) may carry headings or not, but they should not contain rules. Formal tables must be submitted as pages separate from the text, and each table, no matter how large, should be pasted up as a single sheet of copy. Use the metric system instead of (or in addition to) the English system. Illustrations (line drawings, maps, photographs, shaded drawings) usually can be in- termixed throughout the printed text. They will be termed Figures and should be numbered consecutively; however, if a group of figures is treated as a single figure, the individual com- ponents should be indicated by lowercase italic letters on the illustration, in the legend, and in text references: "Figure 9*." Submit all legends on pages separate from the text and not attached to the artwork. An instruction sheet for the preparation of illustrations is available from the Press on request. In the bibliography (usually called "Literature Cited"), spell out book, journal, and article titles, using initial caps with all words except minor terms such as "and, of, the." (For capital- ization of titles in foreign languages, follow the national practice of each language.) Under- score (for italics) book and journal titles. Use the colon-parentheses system for volume number and page citations: "10(2) :5-9." Spell out such words as "figures," "plates," pages." For free copies of his own paper, a Smithsonian author should indicate his requirements on "Form 36" (submitted to the Press with the manuscript). A non-Smithsonian author will receive fifty free copies; order forms for quantities above this amount, with instructions for payment, will be supplied when page proof is forwarded.