Hippolyte catagrapha, Cédric, 2007

Cédric, 2007, New records of Atlantic Hippolyte, with the description of two new species, and a key to all Atlantic and Mediterranean species (Crustacea, Decapoda, Caridea), Zoosystema 29 (1), pp. 183-207 : 185-193

publication ID

https://doi.org/ 10.5281/zenodo.5397868

persistent identifier

https://treatment.plazi.org/id/03E4113B-FFE5-FF6F-FF76-FCDFFD8E56BE

treatment provided by

Marcus

scientific name

Hippolyte catagrapha
status

sp. nov.

Hippolyte catagrapha View in CoL n. sp.

( Figs 1-4 View FIG View FIG View FIG View FIG )

TYPE MATERIAL. — South AFrica. False Bay , 6-8 m depth, from the crinoid Tropiometra carinata (Lamarck, 1816) , collected by the scuba divers Georgina Jones, Peter Southwood and Guido Zsilavecz and made available for study by Charles L. Griffiths, 1.V.2005, ovigerous ♀ holotype (MNHN-Na16258) ; 1 ovigerous ♀ dissected paratype (MNHN-Na16259); 1 immature ♀ paratype (MNHN-Na16260).

ETYMOLOGY. — Catagrapha is the feminine of the Latin adjective catagraphus, which means painted, coloured, figured. The name alludes to the complex and variable colour pattern of the species.

DISTRIBUTION. — False Bay ( South Africa).

DESCRIPTION

Carapace moderately stout. Rostrum moderately high, straight, about as long as carapace, much longer than antennular peduncle. Rostrum without postrostral tooth, with a single dorsal teeth at 0.4 of rostrum length; two or three ventral teeth, distant from tip of rostrum. Hepatic tooth overreaching or not reaching anterior edge of carapace. Pterygostomial angle not protruding ( Fig. 1A, B View FIG ).

Third pleonite barely curved in lateral view. Ratio dorsal length/height of sixth pleonite: 1.8 in holotype ( Fig. 1A View FIG ). Distal border of telson with 10 well developed spines in dissected paratype (outer spines much shorter than others). First pair of dorsolateral spines on 0.5 or 0.6 of telson and second pair on 0.8 ( Fig. 1E, F View FIG ).

Unpigmented part of cornea slightly longer than broad ( Fig. 1C View FIG ). Cornea not reaching stylocerite apex ( Fig. 1A View FIG ). First article of antennular peduncle without distolateral tooth; stylocerite long, reaching or just overreaching tip of first article of antennular peduncle. Second article of antennular peduncle distinctly longer than broad in dorsal view, distinctly longer than third article in dorsal view. Inner antennular flagellum longer than outer flagellum ( Fig. 1C View FIG ). Scaphocerite 3.2 times as long as wide; distolateral spine of scaphocerite not reaching tip of blade; distolateral spine and blade separated by a distinct notch ( Fig. 1D View FIG ).

Mandibular incisor process with seven teeth ( Fig. 2B View FIG ). Third maxilliped reaching about 0.5 of scaphocerite ( Fig. 1A View FIG ). Ultimate article of third maxilliped with many long apical setae (looking like a paintbrush), with 10 conical spines on its apex and the distal third of its mesial border (the apical ones are difficult to see in dorsal view, being hidden by setae); 3 times as long as wide when dorsally measured; 1.5 times as long as penultimate; exopod of third maxilliped not reaching half of antepenultimate segment of endopod ( Fig. 3 View FIG A-D).

P1 ( Fig. 3E, F View FIG ) with outer edges of fingers of chela not denticulate (but with marginal tiny setules).

P2 ( Fig. 3G, H View FIG ) with first segment of carpus 2.1 times as long as third segment, 1.2 times as long as second and third segments combined; first segment 8.6 times as long as wide; second segment 3.6 times as long as wide; third segment 3.7 times as long as wide.

P3-P5 stout ( Fig. 4 View FIG ). Merus of P3-P4 with a single spine, in subdistal position; merus of P5 without spine; carpus of P3-P5 with spine; propodus with about two or three slender spinules on distal third, hidden by dense tufts of setae; dactylus short and very stout, with two terminal spines much shorter than dactylus (most anterior spine 2.5 times as long as next one), and with four or five more slender but rather well developed spines on flexor border.

No specimens with plumose setae on body (“fascigerous” specimens) were recorded.

A B

A

Colour pattern

Colour pattern very vivid but variable (photographs given by C. Griffiths).Some specimens have a colour pattern made up of longitudinal red and yellowish stripes, some stripes being interrupted and forming longitudinal series of spots. Others are spotted like a panther: black spots on a yellow background with a few small whitish marks. The different colour patterns mimic those (also varied) of the feather star Tropiometra carinata (Lamarck, 1816) .

Size

Total length up to 22 mm.

ECOLOGY

6-8 m depth, associated with the crinoid Tropiometra carinata , mimicking its various colour patterns.

REMARKS

Hippolyte catagrapha View in CoL n. sp. can be distinguished at first glance from the other South African Hippolyte View in CoL described by Barnard (1950) and Kensley (1970, 1972) by the whorl of setae of the tip of its third maxilliped. This character is shared with the rare European species H. leptometrae View in CoL . The two species are very similar but H. catagrapha View in CoL n. sp. lives in shallower waters than H. leptometrae View in CoL . Hippolyte catagrapha View in CoL n. sp. has only one dorsal rostral tooth (on the middle of the rostrum), whilst H. leptometrae View in CoL has in addition a subdistal tooth on the dorsal part of the rostrum. Hippolyte catagrapha View in CoL n. sp. is also stouter than H. leptometrae View in CoL , especially in the last three pereiopods and their dactyli.

The validity of the rostral ornamentation as a diagnostic character is variable within the genus Hippolyte View in CoL . There are species in which this character is very constant, e.g., H. varians View in CoL , and others, such as Hippolyte leptocerus (Heller, 1863) View in CoL , in which it is exceedingly variable (d’Udekem d’Acoz 1996). Griffiths (in litt.) who examined more specimens of H. catagrapha View in CoL n. sp. confirmed that there was one single dorsal rostral tooth in all his specimens, confirming the validity of this character for the species.

The existence of a pair of very similar species, one European and one South African is not unique amongst decapods. This is for example the case in Callianassa subterranea (Montagu, 1808) and C. australis Kensley, 1974 . In other cases there is a latitudinal succession of three related species, for example Polybius (Macropipus) tuberculatus (Roux, 1830) in Europe, P. (M.) rugosus Doflein, 1904 in West Africa and P. (M.) australis Guinot, 1961 in South Africa. Therefore it would not be unexpected if a third Hippolyte species of the group leptometrae would occur on crinoids of tropical West Africa.

Unlike H. catagrapha n. sp. and H. leptometrae , the third crinoid-associated Hippolyte species , the European H. prideauxiana Leach, 1815 (syn. H. huntii Gosse, 1877 ), has no dense whorl of setae on the tip of the third maxilliped. However H. prideauxiana shares other characters with H. catagrapha n. sp. and H. leptometrae , such as a very long and narrow first article of the carpus of P2 and the general morphology of the dactylus of P3-P5.

Hippolyte catagrapha View in CoL n. sp. exhibits either longitudinal stripes or a spotted colour pattern. H. leptometrae View in CoL is longitudinally striped (in the very few specimens observed alive) ( Noël 1983). Adult females of H. prideauxiana View in CoL are always transversally striped ( Smaldon et al. 1993). Hippolyte catagrapha View in CoL n. sp. probably is able to modify its colour pattern to match the variable colour of its host. Free-living Hippolyte species such as H. varians View in CoL are able to modify their colour pattern to match the substrate, in modifying their chromatophores (Chassard- Bouchaud 1965). So, it could also be the case in some symbiotic species.

Hippolyte leptometrae Ledoyer, 1969 View in CoL ( Figs 5 View FIG ; 6 View FIG )

Hippolyte leptometrae Ledoyer, 1969: 342 View in CoL , pl. 2. — Lagardère 1973: 80, 84. — Noël 1983: 37, fig.1. — D’Udekem d’Acoz 1996: 54, fig. 24.

MATERIAL EXAMINED. — France. Bay of Biscay,TROPHAL cruise, sample E3-TS03-F1 (daytime sampling), 46°56’N 004°30’W, medium-grained sand [“sables moyens”], 130-132 m depth, the occurrence of Leptometra celtica (McAndrew & Barrett, 1858) in the sample was noted (Jean-Claude Sorbe pers. comm.), 13.IX.2002, coll. J.-C. Sorbe, 1 ovigerous ♀ (MNHN-Na16261).

DISTRIBUTION. — Bay of Biscay ( Lagardère 1973; present data); Mediterranean (d’Udekem d’Acoz 1996).

ECOLOGY The species has been recorded between 95 and 130 m depth. It is associated with the crinoids Leptometra phalangium (J. Müller, 1841) in the Mediterranean ( Ledoyer 1969; Noël 1983) and presumably with Leptometra celtica in the eastern Atlantic, as the occurrence of L. celtica in the sample here examined was noted.

REMARKS

Hippolyte leptometrae has rarely been recorded, and all illustrations in the literature are based on Mediterranean specimens. The Biscayan specimen under study proves to be slightly more robust than the Mediterranean shrimp illustrated by d’Udekem d’Acoz (1996). In that paper, I indicated that I was unable to observe spines on the last article of the third maxilliped of the single specimen examined (which was not dissected). The dissection of the maxilliped of the present specimen (from the Bay of Biscay) indicates that such spines are indeed present but cannot be seen in dorsal view ( Fig. 6 View FIG A-C).

Kingdom

Animalia

Phylum

Arthropoda

Class

Malacostraca

Order

Decapoda

Family

Hippolytidae

Genus

Hippolyte

Loc

Hippolyte catagrapha

Cédric 2007
2007
Loc

Hippolyte leptometrae

NOEL P. Y. 1983: 37
LAGARDERE J. - P. 1973: 80
LEDOYER M. 1969: 342
1969
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