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A new species of the hermit crab genus Paguristes Dana, 1851 (Crustacea: Decapoda: Anomura: Diogenidae) from southwestern India

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A new species of the hermit crab genus Paguristes Dana, 1851 (Diogenidae), P. luculentus, is described and illustrated on the basis of three male specimens collected from off the Kerala State, southwestern India. It belongs to the species group characterized by the posterior lobes of the telson unarmed on the terminal margins, but the characteristic armature of the chelae and carpi of the chelipeds, consisting of a covering of numerous small corneous-tipped spines, and the presence of numerous small corneous-tipped or corneous spines on the mesial faces of the dactyli of the second pereopods immediately distinguish the new species from other congeneric species. The new species represents the ninth of the genus known from Indian waters.
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Accepted by S. Ahyong: 23 Jan. 2015; published: 26 Mar. 2015
ZOOTAXA
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http://dx.doi.org/10.11646/zootaxa.3937.3.5
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A new species of the hermit crab genus Paguristes Dana, 1851 (Crustacea:
Decapoda: Anomura: Diogenidae) from southwestern India
TOMOYUKI KOMAI
1
, REMA RESHMI
2
& APPUKUTTANNAIR BIJU KUMAR
2
1
Natural History Museum and Institute, Chiba, 955-2 Aoba-cho, Chuo-ku, Chiba, 260-8682 Japan. E-mail: komai@chiba-muse.or.jp
2
Department of Aquatic Biology & Fisheries, University of Kerala, Thiruvananthapuram 695581, Kerala, India.
E-mail: resmirema@gmail.com, bijupuzhayoram@gmail.com
Abstract
A new species of the hermit crab genus Paguristes Dana, 1851 (Diogenidae), P. l uc u le nt us , is described and illustrated on
the basis of three male specimens collected from off the Kerala State, southwestern India. It belongs to the species group
characterized by the posterior lobes of the telson unarmed on the terminal margins, but the characteristic armature of the
chelae and carpi of the chelipeds, consisting of a covering of numerous small corneous-tipped spines, and the presence of
numerous small corneous-tipped or corneous spines on the mesial faces of the dactyli of the second pereopods immedi-
ately distinguish the new species from other congeneric species. The new species represents the ninth of the genus known
from Indian waters.
Key words: Paguristes luculentus, taxonomy, Kerala State, Indian Ocean
Introduction
The hermit crab genus Paguristes Dana, 1851 is still most species-rich in the family Diogenidae, currently
represented by 118 species worldwide (McLaughlin et al. 2010; Ayón-Parente & Hendrickx 2013), although
several species previously assigned to the genus have been recently transferred to Areopaguristes Rahayu &
McLaughlin, 2010 (replacement name for Stratiotes Thompson, 1899), Pseudopaguristes McLaughlin, 2002 or
Tetralobistes Ayón-Parente & Henderickx, 2010 (Rahayu 2005; Komai 2009; Ayon-Parente & Hendrickx 2013).
These four genera are typically characterized by having paired first and second pleopods, modified as gonopods, in
the male, and paired first pleopods in the female. Paguristes is primarily differentiated from Areopaguristes and
Pseudopaguristes by having 13 pairs of gills, in contrast to 12 pairs in Areopaguristes and reduced to eight pairs in
Pseudopaguristes. Tetralobistes is differentiated from Paguristes by the four-lobed posterior lobes of the telson
(Ayon-Parente & Hendrickx 2010, 2013). Taxonomic identities of species of these four genera have been
substantially clarified by recent studies (Forest & McLaughlin 2000; Komai 2001, 2009, 2010; McLaughlin 2004,
2008; McLaughlin & Rahayu 2005; Rahayu 2005, 2006, 2007; Rahayu & McLaughlin 2006; Rahayu & Forest
2009; Ayón-Parente & Hendrickx 2013). From waters around India, the following eight species of Paguristes s.s.
are known (Alcock 1905; Thomas 1989; McLaughlin & Dworschak 2001): P. balanophilus Alcock, 1905, P. ca l vu s
Alcock, 1905,P. ciliatus Heller, 1862, P. incomitatus Alcock, 1905, P. mundus Alcock, 1905, P. longirostris Dana,
1851, P. pusillus Henderson, 1896, and P. puniceus Henderson, 1896. Of these, P. balanophilus, P. c a l v u s , P.
ciliatus, P. pusillus and P. puniceus have been redescribed recently at modern standard (cf. McLaughlin &
Dworschak 2001; McLaughlin 2004; McLaughlin & Rahayu 2005; Rahayu & McLaughlin 2006). McLaughlin
(2002) presented a diagnosis for P. longirostris sufficient for species recognition, but without figures. Modern
descriptions or diagnoses are not available yet for P. mundus and P. incomitatus.
In this article, we describe a new species of Paguristes s.s. on the basis of three male specimens collected from
off the Kerala State, southwestern India, during the course of the faunal investigations conducted by the second and
third authors. The new species, P. luculentus, is referred to one of the two informal species groups proposed by
McLaughlin & Provenzano (1975) (group B) because of the unarmed terminal margins of the posterior lobes of the
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telson, but the characteristic armature of the chelipeds and ambulatory legs readily distinguishes the new species
from other Indo-West Pacific species placed in the group B. It is the fourth new species of hermit crab (Paguroidea)
described from material collected during the project by the junior authors (Komai et al. 2012, 2013a, b).
Material examined in this study is deposited in the Zoological Survey of India Western Ghat Regional Centre
(ZSI/WGRC), India; Natural History Museum and Institute, Chiba (CBM), Japan; and the museum collections of
the Department of Aquatic Biology and Fisheries, University of Kerala (DABFUK), India. Descriptive
terminology follows McLaughlin (2008), except for numbering of thoracic sternites. Shield length (sl), measured
from the tip of the rostrum to the midpoint of the posterior margin of the shield, indicates specimen size.
Taxonomic account
Family Diogenidae
Genus Paguristes Dana, 1851
Paguristes luculentus
n. sp.
(Figs. 1–7)
Material examined. Holotype: male (sl 12.1 mm), off Kollam, Kerala State, India, 08°34'24.85"N, 76°20'25.32"E,
100–110 m, 21 November 2012, commercial trawl, ZSI/WGRC/IR/INV.4148.
Paratypes: 1 male (sl 10.5 mm), same data as holotype, CBM-ZC 12589; 1male (sl 11.9 mm), same data,
DABFUK-AR-AN 95.
Description. Thirteen pairs of deeply quadriserial gills.
Shield (Fig. 1A) about 1.2 times as long as wide; rostrum narrowly triangular, usually distinctly overreaching
lateral projections and overreaching midlength of ocular acicles; lateral projections broadly triangular, with or
without marginal spinule; anterior margin between rostrum and lateral projections evenly concave; anterolateral
margins sloping; lateral margins slightly convex; dorsal surface with granules and several tufts of moderately short
to long setae laterally; gastric elevations clearly delimited, rugose and punctate. Anterodorsal portion of
branchiostegite well calcified, with row of minute denticles or spinules on dorsal and anterior margins (Fig. 1D).
Posteromedian plate (Fig. 1B) well calcified, noticeably narrowed posteriorly.
Ocular peduncles (Fig. 1A) relatively slender, subequal or slightly unequal (left longer than right), 0.7 times as
long as shield, slightly inflated basally, bearing longitudinal row of tufts of moderately long setae dorsomesially;
corneas not dilated, slightly wider than basal width of ocular peduncle, corneal diameter less than 0.2 of peduncular
length. Ocular acicles triangular, each terminating in simple, sharp spine.
Antennular peduncles (Fig. 1A, C) just reaching or slightly overreaching distal corneal margins; basal segment
with small spine on distolateral margin of statocyst lobe, ventrodistal margin produced and terminating in sharp
spine partially obscured by tuft of long setae; penultimate segment unarmed on ventral margin; ultimate segment
about 1.4 times as long as penultimate segment. Dorsal flagellum slightly shorter than ultimate peduncular
segment.
Antennal peduncles (Fig. 1A, D) reaching corneal bases, but not reaching distal corneal margins; first segment
unarmed on lateral face, ventromesial distal angle produced into rounded process; second segment with
dorsolateral distal angle produced, terminating in bifid spine, dorsomesial distal angle with small spine, mesial half
of dorsal surface not particularly elevated; third segment with strongly produced, sharply pointed ventromesial
distal angle; fourth segment with minute spine at distolateral angle; fifth segment moderately slender, unarmed.
Antennal acicle moderately slender, slightly falling short of distal end of fifth peduncular segment, terminating in
simple or bifid spine, mesial margin with row of 4–6 small spines, lateral margin with 3 or 4 similarly small spines.
Antennal flagellum (Fig. 1E) slightly exceeding twice length of shield, consisting of more than 60 articles, each
article with several short setae on distal margin (at most 2.5 times as long as one article).
Third maxilliped (Fig. 2A) moderately slender; carpus with minute dorsolateral distal and ventrolateral distal
spinules; merus with row of 5 small spines on ventrolateral margin, but unarmed on dorsodistal margin; ischium
with small ventrodistal spine, and with well-developed crista dentata consisting of row of sharp triangular corneous
teeth; coxa with 2 spinules at ventrodistal angle. Exopod slightly overreaching distal margin of carpus.
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FIGURE 1. Paguristes luculentus n. sp., holotype, male (sl 12.1 mm), ZSI/WGRC/IR/INV.4148. A, shield and cephalic
appendages, dorsal view (right setae omitted); B, carapace, dorsal view (setae omitted); C, left antennule, lateral view; D,
anterior part of left branchiostegite and antennal peduncle, lateral view; E, left antennal flagellum, dorsal view; F, telson, dorsal
view. Scale bars: 5 mm for A, B, E; 2 mm for C, D, F.
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FIGURE 2. Paguristes luculentus n. sp., holotype, male (sl 12.1 mm), ZSI/WGRC/IR/INV.4148 A, left third maxilliped,
lateral view; B, dactylus and propodus of left fourth pereopod, lateral view; C, left first gonopod, ventral view; D, same, dorsal
view; E, left second gonopod, ventral view. Scale bars: 2 mm for A; 1 mm for B–F.
Chelipeds slightly unequal, somewhat dissimilar (left stouter); armature and setation generally similar; spines
on palms and carpi mostly corneous-tipped. Left cheliped (Fig. 3A–E) with propodal/carpal articulation rotated
counterclockwise about 15° from horizontal. Chela subtriangular in dorsal view, about 1.7 times as long as wide.
Dactylus1.6 times as long as palm, slightly curved ventrally; dorsomesial margin bluntly delimited by double row
of small spines, dorsal surface with numerous scattered small spines decreasing in size distally and sparse short
setae; mesial face shallowly depressed proximally, covered with closely set numerous small spines becoming blunt
and smaller ventrally, continuing to ventral surface; cutting edge with row of small blunt calcareous teeth in
proximal 0.7 (proximalmost 2 teeth prominent, molariform; 1–3 tiny corneous teeth interspersed by these
calcareous teeth) and row of small, partially fused corneous teeth in distal 0.3, terminating in small corneous claw;
inner surface below cutting edge broad, somewhat concave, with row of small rounded teeth or tubercles on ventral
margin; no hiatus between dactylus and fixed finger when closed. Palm with row of spines on dorsomesial margin
(these spines not particularly strong, though still stronger than those on dorsal surface of palm), slightly convex
dorsal surface with covering of scattered small spines and short sparse setae, dorsolateral margin bluntly delimited
by double or triple row of small spines extending onto fixed (these spines directed laterally); lateral face of palm
and fixed finger broadly concave around base of fixed finger, with scattered corneous-tipped tubercles diminishing
in size distally; mesial face of palm sloping to ventral surface, with numerous scattered small tubercles becoming
smaller and lower ventrally and tufts or individual very short setae; ventral surface generally convex, with small to
large corneous-tipped tubercles arranged in 3 irregular rows along mesial concavity and sparse tufts of short to long
setae. Fixed finger very slightly curved ventrally; cutting edge with row of closely spaced, blunt calcareous teeth
interspersing minute corneous teeth; inner surface below cutting edge also broad, concave, with row of rounded
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tubercles on ventral margin and tufts of long setae. Carpus with row of moderately strong spines on dorsomesial
margin, dorsolateral margin not delimited; dorsal and lateral surfaces with numerous, scattered minute to small
spines and tufts of short setae not obscuring armature, ventrolateral distal angle with small spine; mesial face with
several small spines or tubercles in dorsal half, otherwise almost smooth; ventral surface shallowly depressed,
distal margin weakly tuberculate. Merus triangular in cross section, with row of multifid spines on dorsal margin,
decreasing in size and becoming obsolete proximally; subdistal transverse groove delimited proximally by row of
small spines or multifid tubercles; distal margin with row of small spines, dorsal spines strongest; lateral face with
scattered tiny multifid tubercles or simple granules and tufts or individual short setae; mesial face nearly smooth;
ventral surface with armature including scattered numerous minute to small spines becoming larger laterally and
prominent low protuberance at proximomesial portion, and with numerous tufts of long setae. Ischium with row of
denticles on ventromesial margin; laterodistal margin minutely denticulate. Coxa with patch of spinules on ventral
surface posteriorly.
Right cheliped (Fig. 4A–D) without noticeable rotation of propodal/carpal articulation. Chela elongate
subovate in dorsal view, about 2.3 times as long as wide. Dactylus 1.9 times as long as palm. Palm somewhat
compressed laterally; dorsomesial margin with row of strong spines; lateral surface perpendicular, faintly concave
entirely. Merus with trace of protuberance on proximomesial portion of ventral surface.
Second pereopods (Figs. 5A) moderately slender, similar from right to left, right overreaching tip of right
cheliped by 0.7 length of dactylus; spines mostly corneous-tipped. Dactyli 1.7 times as long as propodi, 7.7 times
as long as wide, gently arcuate but not twisted, terminating in small corneous claw; dorsal margins each with row
of moderately long, bristle-like setae and row of small spines in proximal half mesial to setal row (Fig. 6A); lateral
surfaces convex transversely, with scattered minute individual setae and tufts of short stiff setae; mesial surfaces
each with sets of 2 or 3 short bristle-like setae adjacent to dorsal margin, tiny spines arranged in several irregular
longitudinal rows (these spines erect or forwardly curved) and tufts of stiff setae adjacent to ventral margin (Fig.
6A, B); ventral margins each with more than 50 minute, slender corneous spinules becoming more widely spaced
proximally (Fig. 6A, B). Propodi each with single row of prominent spines and tufts of short stiff setae on dorsal
margin; lateral faces each with row of smaller spines and tuft of stiff setae adjacent to dorsal row of spines and
median row of tufts of setae; mesial faces each with small spines, arranged in irregular 2 rows, adjacent to dorsal
row of spines, and sparse minute to small row protuberances bearing very short setae (Fig. 6B); ventral surfaces
each with sparse scale-like, corneous spines and few short setae. Carpi each with row of moderately strong spines
on dorsal margin; lateral faces each with faint, sinuous sulcus and row of tufts of short setae along midline, and
some additional tiny to small spines adjacent to dorsal spines; mesial faces (Fig. 6C) also with some additional
small spines adjacent to dorsal spines, otherwise unarmed, almost glabrous; ventral surfaces each with some
minute spinules. Meri strongly compressed laterally, with tufts of setae on dorsal margins, arising from very low
protuberances; lateral faces with sparse tufts of short setae; mesial faces nearly glabrous, only with few tufts of
setae; ventral margins each with double rows of small spines and tufts of long setae mesially (Fig. 6D). Ischia
unarmed, with numerous setae on dorsal and ventral margins. Ischia with few small spines or tubercles and tufts on
setae on dorsal margin; ventral margin with row of tiny spines mesial to fine row of long setae (Fig. 6D). Coxae
with few minute spinules on anteromesial angles.
Third pereopods (Fig. 5B) similar from right to left, somewhat differing from second pereopods mainly in
armature. Dactyli somewhat twisted, thus ventral corneous spinules hardly visible in lateral view; dorsal margin
without conspicuous spines (Fig. 6E); mesial faces each with row of short spiniform setae (setae in proximal half
usually paired) and sets of 2 or 3 short to long bristle-like setae becoming longer and more narrowly spaced distally
and minute, stout corneous spines in proximal half adjacent to ventral margin (Fig. 6E). Propodi each with low,
marginally spinose or denticulate protuberances and tufts of short setae on dorsal surface; mesial surfaces each
with sparse, minute, scale-like, corneous spines (Fig. 6F). Carpi each with double row of small spines diminishing
in size proximally on dorsal margin mesially (Fig. 6F). Meri unarmed or armed with few minute spinules on ventral
margin. Ischium without conspicuous spines on ventral margin.
Fourth pereopods (Fig. 2B) each with prominent, rod-like preungual process (not reaching beyond terminal
claw) followed by row of several corneous teeth on ventral margin of dactylus. Propodal rasp consisting of at most
4 rows of rounded corneous scales beyond midlength of ventral margin. Carpi without dorsodistal spine.
Pleon dextrally twisted. In males, lateral margin of third tergite with dense long setae. Male first pleopods (Fig.
2C, D) strongly twisted; inferior lamella broad, with double row of small spines on rounded distal margin (larger
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FIGURE 3. Paguristes luculentus n. sp., holotype, male (sl 12.1 mm), ZSI/WGRC/IR/INV.4148, left cheliped (setae mostly
omitted). A, chela and carpus, dorsal view; B, same, mesial view; C, same, lateral view; D, merus, mesial view; E, same, lateral
view. Scale bar: 5 mm.
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FIGURE 4. Paguristes luculentus n. sp., holotype, male (sl 12.1 mm), ZSI/WGRC/IR/INV.4148, right cheliped (setae mostly
omitted). A, chela, dorsal view; B, entire right cheliped, mesial view; C, same, lateral view; D, carpus, dorsal view. Scale bar: 5
mm.
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FIGURE 5. Paguristes luculentus n. sp., holotype, male (sl 12.1 mm), ZSI/WGRC/IR/INV.4148, ambulatory legs. A, right
second pereopod, lateral view; B, left third pereopod, lateral view. Scale bar: 5 mm.
distal spines strongly curved, hooked), followed by row of short stiff setae on lateral margin; internal lobe with
rounded distal portion, bearing dense short to long setae on margin and inner surface; external lobe relatively
slender, not reaching distal margin of inferior lamella. Second pleopod (Fig. 2E) with basal segment naked; distal
segment slightly twisted, endopod rather clearly delimited, bearing prominent tuft of stiff setae distally; appendix
masculina moderately narrow, rounded terminally, with numerous marginal or submarginal setae. Third to fifth
pleopods subequal in length, each with well-developed, moderately slender exopod and rudimentary endopod.
Telson (Fig. 1F) with deep lateral indentations; median cleft relatively deep, narrow; posterior lobes strongly
asymmetrical, subtriangular with rounded tips, terminal and lateral margins unarmed, each with row of long setae.
Female unknown.
Colouration in life. Shield entirely orange; calcified median part of posterior carapace orange, lateral parts
whitish. Ocular peduncles orange, corneas dark gray. Antennular and antennal peduncles also orange, antennal
flagellum red. Ambulatory legs with large white spots on red ground colour.
Distribution. At present known only from off Kerala coast, southwestern India; at depths of 100–110 m.
Habitat. The three individuals all used shells of Fusinus colus (Linnaeus) (Mollusca: Gastropoda:
Fasciolariidae). No association with coelenterates was seen.
Etymology. The specific epithet luculentus (= colourful) refers to the vivid living colour of the new species.
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FIGURE 6. Paguristes luculentus n. sp., holotype, male (sl 12.1 mm), ZSI/WGRC/IR/INV.4148. A–D, right second pereopod,
mesial view; E–G, left third pereopod, mesial view (setae mostly omitted). A, E, dactyli; B, F, same, details of tip; C, G, propodi
and carpi; D, merus. Scale bars: 2 mm for A, C–E, G; 1 mm for B, F.
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FIGURE 7. Paguristes luculentus n. sp., holotype, male (sl 12.1 mm), ZSI/WGRC/IR/INV.4148, image showing colouration
in life.
Remarks. Only three male specimens have been available for study, and they are very similar, not showing
significant intraspecific variation.
As McLaughlin & Provenzano (1975) argued, Paguristes can be divided into two groups on the basis of the
armature of the posterior lobes of the telson (with or without spines on the terminal margins). The diagnostic value
of this character has been supported by subsequent workers (e.g., Miyake 1978; Komai 2001; McLaughlin &
Rahayu 2005; Rahayu 2006; Rahayu & McLaughlin 2006; McLaughlin 2008). Paguristes luculentus n. sp. has
unarmed posterior lobes of the telson, and thus is referred to the group B as defined by McLaughlin & Provenzano
(1975). The new species is easily distinguished from the 27 Indo-West Pacific species referred to the group B (see
Tab. 1) by the dense covering of small corneous-tipped spines on the dorsal surfaces of chela and carpi of the
chelipeds and numerous tiny corneous-tipped or corneous spines, arranged in several irregular longitudinal rows,
on the mesial faces of the dactyli of the second pereopods. No other species placed in the group B display such
characteristics (Komai 2001, 2010; McLaughlin & Rahayu 2005; Rahayu 2006, 2007; Rahayu & McLaughlin
2006; McLaughlin 2008; Rahayu & Forest 2009). The armature of the mesial surfaces of the cheliped dactyli also
appears characteristic to the new species: the mesial faces are covered with numerous scattered small spines
becoming smaller and blunt ventrally, none arranged in distinct row(s).
Among the 54 Indo-West Pacific species of the genus (Tab. 1), the armature of the telson remains unknown for
P. barnardi Forest, 1954, P. gamianus (H. Milne Edwards, 1836), P. incomitatus, P. macrotrichus Forest, 1954, P.
mundus and P. seminudus Stimpson, 1858. Paguristes barnardi and P. gamianus are easily distinguished from P.
luculentus n. sp. by the quite different armature and dense setation of the right second pereopod (cf. Forest 1954:
pl. IV).
Paguristes incomitatus is readily separated from the new species by the antennular peduncles distinctly
overreaching the distal corneal margins, the short antennal flagellum (shorter than the shield) and the chelae with
sparse spines and dense setation on the dorsal surface (Alcock 1905). The short antennal flagellum suggests that P.
incomitatus might belong to the group A, or other genus such as Areopaguristes or Pseudopaguristes, although the
gill formula needs to be verified for P. incomitatus.
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TABLE 1. List of species of Paguristes Dana, 1851 known from the Indo-West Pacific, with summary of geographic range and species group assignment. Group A (with spines on
terminal margins of posterior lobes of telson); group B (without spines on terminal margins of posterior lobes of telson).
Species Geographical range
Group assignment References
Paguristes acanthomerus Ortmann, 1892 Japan, Korea, Taiwan B Komai (2001); McLaughlin et al. (2007)
Paguristes aciculus Grant, 1905 Australia, Indonesia A Rahayu (2006); McLaughlin (2008)
Paguristes albimaculatus Komai, 2001 Japan, Taiwan, Philippines B Komai (2001); McLaughlin et al. (2007);
Rahayu & Forest (2009)
Paguristes alegrias Morgan, 1987 Northern and Western Australia AMorgan (1987b); McLaughlin (2008)
Paguristes alcocki McLaughlin & Rahayu, 2005 Westrm Australia, Indonesia, Philippines BMcLaughlin & Rahayu (2005);
McLaughlin (2008)
Paguristes antennarius Rahayu, 2006 Madagascar, Indonesia, Taiwan ARahayu (2006; 2007); McLaughlin et al.
(2007)
Paguristes arostratus Rahayu, 2006 Taiwan, Indonesia, Philippines BRahayu (2006); McLaughlin et al. (2007);
Rahayu & Forest (2009)
Paguristes aulacis Rahayu & Forest, 2009 Philippines BRahayu & Forest (2009)
Paguristes balanophilus Alcock, 1905 Gulf of Oman, Andaman Sea BRahayu & McLaughlin (2006)
Paguristes barbatus (Heller, 1862) New Zealand AForest & McLaughlin (2000)
Paguristes barnardi Forest, 1954 South Africa unknown Forest (1954)
Paguristes brachyrostris Rahayu, 2006 Indonesia, Philippines BRahayu (2006); Rahayu & Forest (2009)
Paguristes brevirostris Baker, 1905 Southeastern Australia AMcLaughlin (2008)
Paguristes calvus Alcock, 1905 Red Sea, Bay of Bengal, Andaman Sea, Philippines,
Taiwan
BRahayu & McLaughlin (2006);
McLaughlin et al. (2007); Rahayu &
Forest (2009)
Paguristes ciliatus Heller, 1862 Nicobar Islands, eastern Indian Ocean AMcLaughlin & Dworschak (2001)
Paguristes crinitimanus McLaughlin, 2008 Queensland, Australia B McLaughlin (2008)
Paguristes dampierensis McLaughlin, 2008 Western Australia A McLaughlin (2008)
Paguristes digitalis Stimpson, 1858 Japan, Korea, Far Eastern Russia A Komai (2001)
……continued on the next page
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TABLE 1. (Continued)
Species Geographical range
Group assignment References
Paguristes doederleini Komai, 2001 Japan, Taiwan A Komai (2001); McLaughlin et al. (2007)
Paguristes frontalis (H. Milne Edwards, 1836) South and Western Australia B McLaughlin (2008)
Paguristes gamianus (H. Milne Edwards, 1836) South Africa unknown Forest (1954)
Paguristes geminatus McLaughlin, 2008 Queensland, Australia A McLaughlin (2008)
Paguristes gonagrus (H. Milne Edwards, 1836) Japan to Philippines B Rahayu & Forest (1999); Komai (2010)
Paguristes incomitatus Alcock, 1905 Gulf of Aden, Maldives, India, Sri Lanka unknown Alcock (1905); Thomas (1989)
Paguristes jalur Morgan, 1992 Cocos (Keeling) Islands, Christmas Islands, Japan,
Mariana Islands
B Morgan (1992); Osawa & Takeda (2004);
McLaughlin (2008)
Paguristes jousseaumei Bouvier, 1892 Red Sea A Dechancé (1963)
Paguristes kimberleyensis Morgan & Forest, 1991 Western Australia B Morgan & Forest (1991); McLaughlin
(2008)
Paguristes lauriei McLaughlin & Hogarth, 1998 Seychelles, Réunion B McLaughlin & Hogarth (1996); Rahayu
(2007)
Paguristes lewinsohni McLaughlin & Rahayu, 2005 Red Sea to Arabian coast, Philippines B McLaughlin & Rahayu (2005); Rahayu &
Forest (2009)
Paguristes longirostris Dana, 1851 India, Andaman Sea, Singapore A Alcock (1905); McLaughlin (2002)
Paguristes longisetosus Morgan, 1987 Tasmania, South and Western Australia A Morgan (1987a); McLaughlin (2008)
Paguristes macrops Rahayu & Forest, 2009 Philippines, Japan B Rahayu & Forest (2009); Osawa &
Rahayu (2012)
Paguristes macrotrichus Forest, 1954 South Africa unknown Forest (1954)
Paguristes miyakei Forest & McLaughlin, 1998 Western Australia, Japan, Taiwan A Forest & McLaughlin (1998); McLaughlin
et al. (2007); McLaughlin (2008)
Paguristes mundus Alcock, 1905 Andamans, eastern Indian Ocean unknown Alcock (1905)
Paguristes ocellus Komai, 2010 Japan B Komai (2010)
Paguristes ortmanni Miyake, 1978 Japan, Korea, Far East Russia A Komai (2001)
……continued on the next page
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TABLE 1. (Continued)
Species Geographical range
Group assignment References
Paguristes palythophilus Ortmann, 1892 Madagascar to Japan B Komai (2001); McLaughlin et al. (2007);
McLaughlin (2008); Rahayu & Forest
(2009)
Paguristes petalodactylus Rahayu, 2007 Madagascar B Rahayu (2007)
Paguristes pugil McCulloch, 1913 Southeastern Australia A McLaughlin (2008)
Paguristes puniceus Henderson, 1896 Madagascar, Bay of Bengal, Andaman Sea,
Indonesia, Australia, Taiwan
A McLaughlin (2004; 2008); McLaughlin et
al. (2007); Rahayu (2007)
Paguristes purpureantennatus Morgan, 1987 Western Australia B Morgan (1987b); McLaughlin (2008)
Paguristes pusillus Henderson, 1896 Off Sri Lanka B McLaughlin & Rahayu (2005)
Paguristes runyanae Haig & Ball, 1988 Indonesia, Philippines B Haig & Ball (1988); Rahayu & Forest
(2009)
Paguristes seminudus Stimpson, 1858 Japan unknown Stimpson (1858, 1907)
Paguristes simplex Rahayu & McLaughlin, 2006 Madagascar, Western Australia B Rahayu & McLaughlin (2006);
McLaughlin (2008)
Paguristes sinensis Tung & Wang, 1966 China A Tung & Wang (1966); Komai (2009)
Paguristes squamosus McCulloch, 1913 New South Wales, Australia A McLaughlin (2008)
Paguristes subpilosus Henderson, 1888 New Zealand A Forest & McLaughlin (2000)
Paguristes sulcatus Baker, 1905 Southern Australia A McLaughlin (2008)
Paguristes tosaensis Komai, 2010 Japan B Komai (2010)
Paguristes triton McLaughlin, 2008 Northwestern Australia B McLaughlin (2008)
Paguristes versus Komai, 2001 Japan, Taiwan, Philippines B Komai (2001); McLaughlin et al. (2007);
Rahayu & Forest (2009)
Paguristes zhejiangensis Wang & Tung, 1982 East China Sea B Wang & Tung (1982); McLaughlin et al.
(2010)
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Paguristes macrotrichus differs from P. l u c u l e n t u s n. sp. in the short rostrum only exceeding as far as the
lateral projections and the dactylus of the second pereopod being devoid of small spines on the mesial face and
bearing fewer (apparently less than 15) and longer corneous spines on the ventral margin (Forest 1954).
Paguristes mundus is superficially similar to P. luculentus n. sp. in the long antennal flagellum and the general
armature of the chelipeds (cf. Alcock 1905: pl. III, fig. 5), but differs in the short, broadly triangular rostrum,
multidenticulate ocular acicles, the left cheliped being smaller than the right cheliped, and the presence of a row of
fine setae on the ventral margins of ambulatory dactyli.
The specific identity of P. seminudus is obscure. The type material of Stimpson’s (1958) taxon is no longer
extant (Evans 1967; Manning & Reed 2006), and it is difficult to establish its taxonomic identity without
examination of topotypic specimens that match the descriptions by Stimpson (1858, 1907). Nevertheless, the
description by Stimpson (1907) provides some characters that distinguish our new taxon from P. seminudus: “Eyes
very stout for the genus, but long, considerably longer than the front is wide, and much overreaching the peduncle
of the antennulae”; “Antennae shorter than carapax”; Cheliped “carpus and hand densely hairy and spinulose”;
“Color olive or brownish; antennae annulated; maxillipeds spotted with white; tips of all the feet white”. As
discussed by McLaughlin (2008), identifications of P. seminudus by subsequent authors (Miyake 1978; Miyake &
Imafuku 1980; Baba 1986; McLaughlin et al. 2007) are not correct. Specimens referred to P. seminudus by these
authors most probably represent P. zejiangensis Wang & Tung, 1982 (Komai, unpublished data).
As mentioned above, eight species of Paguristes have been recorded from Indian waters, and thus the new
species is the ninth of the genus to be recorded from the area.
Acknowledgments
We thank the Kerala State Council for Science, Technology and Environment for the financial support of the
project.
References
Alcock, A. (1905) Anomura. Fasc. I. Pagurides. In:Catalogue of the Indian Decapod Crustacea in the Collection of the Indian
Museum. Vol. 2. Indian Museum, Calcutta, pp. 1–197.
Ayon-Parente, M. & Hendrickx, M.E. (2010) A new genus and new species of hermit crab (Crustacea: Anomura: Paguroidea:
Diogenidae) from the eastern tropical Pacific. Zootaxa, 2677, 49–59.
Ayon-Parente, M. & Hendrickx, M.E. (2013) Redescription and taxonomic status of Paguristes weddellii (H. Milne Edwards)
(Crustacea: Anomura: Paguroidea: Diogenidae) from the eastern Pacific. Zootaxa, 3616 (6), 587–596.
http://dx.doi.org/10.11646/zootaxa.3616.6.5
Baba, K., Hayashi, K.-I. & Toriyama, M. (1986) Decapod Crustaceans from Continental Shelf and Slope around Japan: The
Intensive Research of Unexploited Fishery Resources on Continental Slopes. Japan Fisheries Resource Conservation
Association, Tokyo, 336 pp.
Dechancé, M. (1963) Sur des Paguristes littoraux de l’ouest de l’oceanIndien: P. jousseaumei Bouvier, P. perspicax Nobili et P.
abbreviatus sp. nov. (Crustacea Decapoda Paguridea). Bulletin du Muséum national d’Histoire naturelle, Série 2
e
, 35,
291–301.
Evans, A.C. (1967) Syntypes of Decapoda described by William Stimpson and James Dana in the collections of the British
Museum (Natural History). Journal of Natural History, 1, 399–411.
http://dx.doi.org/10.1080/00222936700770391
Forest, J. (1954) Les Paguristes des côtes occidentales et méridionales d’ Afrique. Annals of the South African Museum, 41,
159–213.
Forest, J. & McLaughlin, P.A. (1998) Descriptions of two new Japanese hermit crabs (Decapoda: Paguridae [sic]: Diogenidae).
Proceeding of the Biological Society of Washington, 111, 188–198.
Forest, J. & McLaughlin, P.A. (2000) Superfamily Coenobitoidea, families Pylochelidae and Diogenidae. In: Forest, J., de Saint
Laurent, M., McLaughlin, P.A. & Lemaitre, R. (Eds.), The Marine Fauna of New Zealand: Paguridea (Decapoda:
Anomura) Exclusive of the Lithodidae. NIWA Biodiversity Memoir, 114, pp. 31–103.
Haig, J. & Ball, E. (1988) Hermit crabs from northern Australian and eastern Indonesian waters (Crustacea Decapoda:
Anomura: Paguroidea) collected during the 1975 Alpha Helix Expedition. Records of the Australian Museum, 40,
151–196.
http://dx.doi.org/10.3853/j.0067-1975.40.1988.153
Zootaxa 3937 (3) © 2015 Magnolia Press
·
531
A NEW SPECIES OF PAGURISTES
Komai, T. (2001)A review of the north-western Pacific species of the genus Paguristes (Decapoda: Anomura: Diogenidae), I.
Five species initially reported by Ortmann (1892) from Japan. Journal of Natural History, 35, 357–428.
http://dx.doi.org/10.1080/002229301300009603
Komai, T. (2009) A review of the northwestern Pacific species of the genus Paguristes (Decapoda: Anomura: Diogenidae). II.
Species transferred to the genus Stratiotes, with descriptions of two new species. Natural History Research, 10, 59–92.
Komai, T. (2010) A review of the northwestern Pacific species of the genus Paguristes (Decapoda: Anomura: Diogenidae). III.
Clarification of the identity of a species heretofore referred to Paguristes balanophilus Alcock and descriptions of two new
species from Japan. Natural History Research, 11, 9–33.
Komai, T., Reshmi, R. & Biju Kumar, A. (2012) A new species of the hermit crab genus Ciliopagurus Forest (Crustacea:
Decapoda: Anomura: Diogenidae) from southern India. Zootaxa, 3266, 53–61.
Komai, T., Reshmi, R. & Biju Kumar, A. (2013a) A new species of the hermit crab genus Diogenes (Crustacea: Decapoda:
Anomura: Diogenidae) from southern India. Zootaxa, 3613 (4), 380–390.
http://dx.doi.org/10.11646/zootaxa.3613.4.5
Komai, T., Reshmi, R. & Biju Kumar, A. (2013b) Rediscovery and range extension of Ciliopagurus liui Forest, 1995 and
description of a new species of Pagurus Fabricius, 1775 (Crustacea: Decapoda: Anomura: Paguroidea) from the Kerala
State, southwestern India. Zootaxa, 3710 (5), 467–484.
http://dx.doi.org/10.11646/zootaxa.3710.5.5
Manning, R.B. & Reed, K.J. (2006) Decapod crustaceans deposited in the Zoological Museum of Copenhagen by William
Stimpson in 1859. Raffles Bulletin of Zoology, 54, 283–293.
McLaughlin, P.A. (2002) A review of the hermit-crab (Decapoda: Anomura: Paguridea) fauna of southern Thailand, with
particular emphasis on the Andaman Sea, and descriptions of three new species. Phuket Marine Biological Center Special
Publication, 23, 385–460.
McLaughlin, P.A. (2004) Paguristes puniceus Henderson, 1896 (Decapoda: Anomura: Paguroidea: Diogenidae): a study in
intraspecific variability. Zootaxa, 742, 1–28.
McLaughlin, P.A. (2008) Australian hermit crabs of the genera Paguristes Dana, Stratiotes Thomson, and Pseudopaguristes
McLaughlin (Crustacea: Anomura: Paguroidea: Diogenidae). In: Jones, D.S. (Ed.), Crustaceans Collected by the Western
Australian Museum/Woodside Energy Ltd. Partnership to Explore the Marine Biodiversity of the Dampier Archipelago,
Western Australia, 1998–2002. Records of the Western Australian Museum, 73 (Supplement), 185–273.
McLaughlin, P.A. & Dworschak, P. (2001) Reappraisal of hermit crab species (Crustacea: Anomura: Paguridea) reported by
Camille Heller in 1861, 1862 and 1865. Annalen des Naturhistorischen Museum in Wien, 103B, 135–176.
McLaughlin, P.A., Komai, T., Lemaitre, R. & Rahayu, D.L. (2010) Annotated checklist of Anomuran decapod crustaceans of
the world (exclusive of the Kiwaoidea and families Chirostylidae and Galatheidae of the Galatheoidea) Part 1 –
Lithodoidea, Lomisoidea and Paguroidea. Raffles Bulletin of Zoology, Supplement, 23, 5–107.
McLaughlin, P.A. & Provenzano, A.J. Jr. (1975) Hermit crabs of the genus Paguristes (Crustacea: Decapoda: Diogenidae) from
the western Atlantic. Part II. Descriptions of six new species. Bulletin of Marine Science, 24, 885–938.
McLaughlin, P.A. & Rahayu, D.L. (2005) Two new species of Paguristes sensu stricto (Decapoda: Anomura: Paguroidea:
Diogenidae) and a review of Paguristes pusillus Henderson. Zootaxa, 1083, 37–62.
McLaughlin, P.A., Rahayu, D.L., Komai, T. & Chan, T.-Y. (2007) A Catalog of the Hermit Crabs (Paguroidea) of Taiwan.
National Taiwan Ocean University, Keelung, viii + 365 pp.
Morgan, G.J. (1987a) Two new species of Paguristes (Decapoda: Anomura: Diogenidae) from southwestern Australia.
Proceedings of the Biological Society of Washington, 100, 726–734.
Morgan, G.J. (1987b) Hermit crabs (Decapoda, Anomura: Coenobitidae, Diogenidae, Paguridae) of Darwin and Port Essington,
Northern Australia. The Beagle, Records of the Northern Territory Museum of Arts and Sciences, 4, 165–186.
Morgan, G.J. (1992) The hermit crabs (Crustacea: Decapoda: Coenobitidae, Diogenidae, Paguridae) of Christmas and Cocos
(Keeling) Islands, Indian Ocean, with description of a new species of Paguristes. Raffles Bulletin of Zoology, 40, 163–174.
Morgan, G.J. & Forest, J. (1991) Seven new species of hermit crabs from northern and western Australia (Decapoda, Anomura,
Diogenidae). Bulletin du Muséum national d'Histoire naturelle, Series 4A, 12, 649–689.
Miyake, S. (1978) The Crustacean Anomura of Sagami Bay. Biological Laboratory, Imperial Household, Tokyo, 200 pp.
(English), 161 pp. (Japanese).
Miyake, S. & Imafuku, M. (1980) Hermit crabs from Kii Peninsula I. Nankiseibutu, 22, 1–7. [in Japanese with English
summary]
Osawa, M. & Takeda, M. (2004) Hermit crabs (Crustacea: Decapoda: Anomura: Paguroidea) from submarine caves in the
Ryukyu Islands, south-western Japan. Journal of Natural History, 38, 1097–1132.
http://dx.doi.org/10.1080/0022293031000079589
Rahayu, D.L. (2005) Additions to the Indonesian fauna of the hermit crab genus Pseudopaguristes McLaughlin and a further
division of the genus Paguristes Dana (Crustacea: Decapoda: Paguroidea: Diogenidae). Zootaxa, 831, 1–42.
Rahayu, D.L. (2006) The genus Paguristes (Crustacea, Decapoda, Diogenidae) from Indonesia. In: Richer de Forges, B. &
Justine, J.-L. (Eds.), Tropical Deep-Sea Benthos. Vol. 24. Mémoires du Muséum national d’Histoire naturelle, 193,
349–374.
Rahayu, D.L. (2007) The hermit crabs Paguristes Dana, 1851 s.l. (Crustacea, Decapoda, Anomura, Diogenidae) from the
western Indian Ocean. Zoosystema, 29, 515–534.
KOMAI ET AL.
532
·
Zootaxa 3937 (3) © 2015 Magnolia Press
Rahayu, D.L. & Forest, J. (2009) Le genre Paguristes Dana aux Philippines avec la description de deux nouvelles espèces
(Decapoda, Anomura, Diogenidae). Crustaceana, 82, 1307–1338.
http://dx.doi.org/10.1163/001121609X12475745628388
Rahayu, D.L. & McLaughlin, P.A. (2006) Clarifications of the identities of Paguristes balanophilus Alcock, 1905 and P. calvus
Alcock, 1905 (Crustacea, Decapoda, Anomura, Paguroidea, Diogenidae), and the description of another broadly
distributed new species. Zoosystema, 28, 865–886.
Rahayu, D.L. & Osawa, M. (2012) Hermit crabs (Crustacea: Decapoda: Diogenidae) from the KUMEJIMA 2009 Expedition,
Japan. Zootaxa, 3367, 176–190.
Stimpson, W. (1858) Prodromus descriptionis animalium evertebratorum, quae in Expeditione ad Oceanum Pacificum
Septentrionalem, a Republica Federatamissa, Cadwaladaro Ringgold et Johanne Rodgers ducibus, observavit et descripsit.
Pars VII. Crustacea Anomura. Proceedings of the Academy of Natural Sciences, Philadelphia, 10, 225–252.
Stimpson, W. (1907) Report on the Crustacea (Brachyura and Anomura) collected by the North Pacific Exploring Expedition,
1853–1856. Smithsonian Miscellaneous Collections, 49, 1–240, pls. 1–26.
Thomas, M.M. (1989) On a collection of hermit crabs from the Indian waters. Journal of the Marine Biological Association of
India, 31, 59–79.
Tung, Y.-M. & Wang, F.-T. (1966) A new species of the hermit crab from the East China Sea. Acta Zootaxonomica Sinica, 3,
95–97, pl. 1.
Wang, F.-Z. & Tung, Y.-M. (1982) New subspecies and new records of hermit crabs (Crustacea, Anomura) from China. Acta
Zootaxonomica Sinica, 7, 368–371. [in Chinese with English summary]
... Recent collaborations among Indian and international researchers have yielded 11 new species from the Indian EEZ, including two chirostyloids (Komai et al. 2019a;Padate et al. 2020b), two galatheoids Macpherson et al. 2020a), one lithodoid (Padate et al. 2020a) and six paguroids (Komai et al. 2012(Komai et al. , 2013a(Komai et al. , 2013b(Komai et al. , 2015. In addition, 20 species were recorded for the first time from India including two hippoids (Marimuthu et al. 2015;Kumar et al. 2020), six galatheoids (Prakash et al. 2013a;Kumaralingam et al. 2015;Beleem et al. 2016;Josileen et al. 2020;Macpherson et al. 2020a;Padate et al. 2020b) and 12 paguroids (Reshmi & Bijukumar 2011Komai et al. 2013b;Reshmi 2014;Gosavi et al. 2017;Kachhiya et al. 2017;Patel et al. 2020). ...
... no. not mentioned (Alcock 1905a) Red India (Komai et al. 2015) Paguristes mundus Alcock, 1905 Paguristes mundus Alcock, 1905a Andaman Sea, off Port Blair, Andamans, 112 fathoms (205 m), Andaman and Nicobar Islands (Alcock 1905a) India, Eastern Indian Ocean (Komai et al. 2015) Paguristes (Alcock 1905a) India Tomopaguropsis lanata Alcock, 1905 Tomopaguropsis lanata Alcock, 1905a Arabian Sea, off Travancore coast, 360 fathoms (659 m), Kerala (Alcock 1905a) Indian Ocean ...
... no. not mentioned (Alcock 1905a) Red India (Komai et al. 2015) Paguristes mundus Alcock, 1905 Paguristes mundus Alcock, 1905a Andaman Sea, off Port Blair, Andamans, 112 fathoms (205 m), Andaman and Nicobar Islands (Alcock 1905a) India, Eastern Indian Ocean (Komai et al. 2015) Paguristes (Alcock 1905a) India Tomopaguropsis lanata Alcock, 1905 Tomopaguropsis lanata Alcock, 1905a Arabian Sea, off Travancore coast, 360 fathoms (659 m), Kerala (Alcock 1905a) Indian Ocean ...
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An annotated checklist of the anomuran crustaceans recorded from Indian waters is compiled from available published literature. A total of 231 species belonging to 58 genera, 15 families and five superfamilies are listed. The highest number of species was seen in the Andaman and Nicobar Islands Ecoregion (114 species, 37 genera, 14 families), followed by the South India Ecoregion (111 species, 41 genera, 14 families), West India Ecoregion (93 species, 36 genera, 14 families), Eastern India Ecoregion (76 species, 29 genera, 12 families), Maldives Ecoregion (34 species, 15 genera, 10 families) and Northern Bay of Bengal Ecoregion (22 species, nine genera, five families). Notes on the questionable identifications and records of some anomuran crabs are also provided.
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A redescription of Paguristes aztatlanensis Glassell, 1937 is presented together with the description of Paguristes turkayi n. sp. from the Mexican Pacific. Paguristes turkayi n. sp. is close to P. digueti and P. sanguinimanus, but can be separated from these two species by the following: P. turkayi features a slender rostrum; the ocular peduncles are proportionally larger relative to the shield in P. turkayi n. sp. than in P. digueti, but proportionally shorter than in P. sanguinimanus; the anterodorsal plates of the carapace are unarmed in Paguristes turkayi n. sp. and P. sanguinimanus (versus armed with small teeth in P. digueti); in P. turkayi n. sp., the palm and carpus of the chelipeds bear fewer but larger spines and tufts of very long setae, while in P. digueti and P. sanguinimanus the chelipeds are armed with many small spines and very short setae.
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Annotated checklists of the world's Recent anomuran crustacean superfamilies Aegloidea, Hippoidea, Lithodoidea, Lomisoidea, Paguroidea and galatheoid family Porcellanidae are presented. Each is accompanied by brief reviews of the historical aspects of its classification, general external morphology, features of larval development and current phylogenetic status. This presentation is divided into four parts because the only unifying threads among the Aegloidea, Hippoidea, Porcellanidae and the crab-like Lithodoidea and Lomisoidea are their shared anomuran apomorphies and mutually exhibited, but independently evolved, carcinization. That carcinization similarly links the latter two superfamilies with the Paguroidea is still a passionately debated matter that will be briefly addressed, but certainly not resolved. The checklists include all currently recognized valid species, primary synonyms and homonyms, notes on matters of confusion and/or misunderstanding, and complete bibliographic references to all original descriptions. The lists are enhanced by a collection of photographs depicting the variety exhibited by members of these taxa.
Article
The availability of 45 adult specimens from single population of the hermit crab Paguristes puniceus Henderson, 1896, together with ten specimens from other localities, has made it possible to investigate intraspecific variability in morphological characters heretofore considered diagnostic for species of the genus. Fifty-one attributes deemed important by previous investigators, were examined and/or measured. However, when variations in segmental armature were found in the two pairs of ambulatory legs, the segments were scored individually, for a total of 77 characters. The results of the analysis demonstrated conclusively that most, if not all, previously employed characters were subject to intraspecific variation, and that for some, variability rendered them ineffective in discriminating among closely related taxa. Just as a suite of characters is usually needed to define a taxon, a similar suite is needed to differentiate one closely related taxon from another. In addition to discussing the ranges of variation observed for each of the characters, P. puniceus has been redescribed to include this variability. A second taxon, P. puniceus unispinosa Balss has been found to be a junior subjective synonym of P. puniceus. Paguristes puniceus also has been compared with three very similar Japanese species, P. miyakei Forest & McLaughlin, 1998, P. doederleini Komai, 2001, and Paguristes sp.
Article
An in-depth study of the genera Paguristes Dana, 1851 and Pseudopaguristes McLaughlin, 2002 in Indonesian waters has resulted in refined hypotheses of some of the evolutionary trajectories within the Paguroidea. Not only has the observed reduction in pleurobranch and arthrobranch number in three species, Paguristes hians Henderson, 1888, P. kuekenthali De Man, 1902 and P. monoporus Morgan, 1987 required the transfer of these taxa to Pseudopaguristes, they, and two new species, have required an emendation of the genus itself. Additionally, the investigation has also revealed anintermediate evolutionary change that heretofore has gone unrecognized. In several, apparently less derived, representatives of Paguristes, the characteristic gill number of 13 pairs (ten of arthrobranchs and three pleurobranchs) has been reduced to 12, with the loss of the pleurobranch on the wall of fifth thoracic somite. Only one of these recognized species, Paguristes tuberculatus Whitelegge, 1900, occurs in Indonesian waters. The genus Stratiotes, Thomson, 1899, erected for Pagurus setosus Filhol, 1885, a junior synonym of Paguristes setosus (H. Milne Edwards, 1848), is reinstated because its type species has proved to have 12 pairs of gills. Three new species are included in Stratiotes: S. micheleae n. sp., S. breviantennatus n. sp., and S. ngochoae n. sp. The new species assigned to Pseudopaguristes are P. asper n. sp. and P. gracilis n. sp.
Article
A new species of the hermit crab genus Paguristes, sensu stricto, Paguristes alcock n. sp., is described and illustrated from materials collected in Australia, Indonesia and the Philippine Islands. It is proposed that this taxon, or a species identified simply as Paguristes sp. by Lewinsohn (1969) in his monograph of Red Sea Anomura, may be conspecific with the species incorrectly referred by Alcock (1905) and several subsequent carcinologists to Paguristes ciliatus Heller, 1862. Lewinsohn subsequently re-identified his material of Paguristes sp. as Paguristes ciliatus sensu Alcock, 1905 and P. pusillus Henderson, 1896. Alcock’s single specimen of P. ? ciliatus from the Persian Gulf was not available for reexamination. Lewinsohn’s specimens however, have been reviewed and compared with the present authors Indo-Pacific species and with a specimen identified by Henderson as P. pusillus. Lewinsohn’s Red Sea specimens are described and illustrated herein as P. lewinsohni n. sp., as are the specimens identified as P. pusillus by Thompson (1943) from the John Murray Expedition. An illustrated description of P. pusillus is also provided to facilitate recognition of these superficially similar species. Paguristes pusillus zhejiangensis Wang & Tung, 1982 is considered to be a distinct taxon, not a subspecies of P. pusillus, and is herein elevated to full specific rank.
Article
The availability of 45 adult specimens from single population of the hermit crab Paguristes puniceus Henderson, 1896, together with ten specimens from other localities, has made it possible to investigate intraspecific variability in morphological characters heretofore considered diagnostic for species of the genus. Fifty-one attributes deemed important by previous investigators, were examined and/or measured. However, when variations in segmental armature were found in the two pairs of ambulatory legs, the segments were scored individually, for a total of 77 characters. The results of the analysis demonstrated conclusively that most, if not all, previously employed characters were subject to intraspecific variation, and that for some, variability rendered them ineffective in discriminating among closely related taxa. Just as a suite of characters is usually needed to define a taxon, a similar suite is needed to differentiate one closely related taxon from another. In addition to discussing the ranges of variation observed for each of the characters, P. puniceus has been redescribed to include this variability. A second taxon, P. puniceus unispinosa Balss has been found to be a junior subjective synonym of P. puniceus. Paguristes puniceus also has been compared with three very similar Japanese species, P. miyakei Forest & McLaughlin, 1998, P. doederleini Komai, 2001, and Paguristes sp.
Article
Two hermit crab species, Canceling investigatoris Alcock and Paguristes setosus (H. Milne Edwards), have been reported on a number of occasions from Japanese waters. Neither Japanese taxon has been correctly identified, and both are now recognized as new species. The true Cancellus investigatoris appears to be restricted in its distribution to Sri Lanka, whereas the true Paguristes setosus is endemic to New Zealand. The Japanese species are described herein as Cancellus mayoae new species, and Paguristes miyakei new species. Sources of the earlier mistakes are discussed.
Article
An in-depth study of the genera Paguristes Dana, 1851 and Pseudopaguristes McLaughlin, 2002 in Indonesian waters has resulted in refined hypotheses of some of the evolutionary trajectories within the Paguroidea. Not only has the observed reduction in pleurobranch and arthrobranch number in three species, Paguristes hians Henderson, 1888, P. kuekenthali De Man, 1902 and P. monoporus Morgan, 1987 required the transfer of these taxa to Pseudopaguristes, they, and two new species, have required an emendation of the genus itself. Additionally, the investigation has also revealed an intermediate evolutionary change that heretofore has gone unrecognized. In several, apparently less derived, representatives of Paguristes. the characteristic gill number of 13 pairs (ten of arthrobranchs and three pleurobranchs) has been reduced to 12. with the loss of the pleurobranch on the wall of fifth thoracic somite. Only one of these recognized species, Paguristes tuberculatus Whitelegge. 1900, occurs in Indonesian waters. The genus Stratiotes, Thomson, 1899, erected for Pagurus setosus Filhol, 1885. a junior synonym of Paguristes setosus (H. Milne Edwards, 1848), is reinstated because its type species has proved to have 12 pairs of gills. Three new species are included in Stratiotes: S. micheleae n. sp., S. breviantennatus n. sp., and 5. ngochoae n. sp. The new species assigned to Pseudopaguristes are P. asper n. sp. and P. gracilis n. sp.