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.
Non-Smithsonian authors should address inquiries to the appropriate department. If submission
is invited, the following format requirements of the Press should govern the preparation of copy.
Copy must be typewritten, double-spaced, on one side of standard white bond paper, with
1%" top and left margins, submitted in ribbon copy with a carbon or duplicate, and accom-
panied by the original artwork. Duplicate copies of all material, including illustrations, should
be retained by the author. There may be several paragraphs to a page, but each page should
begin with a new paragraph. Number all pages consecutively, including title page, abstract,
text, literature cited, legends, and tables. A manuscript should consist of at least thirty pages,
including typescript and illustrations.
The title should be complete and clear for easy indexing by abstracting services. 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.