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First Record of the Sponge-Dwelling Palaemonid Shrimp, Anchistioides compressus (Crustacea: Decapoda: Palaemonidae) in Korea PDF

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Anim. Syst. Evol. Divers. Vol. 36, No. 4: 319-329, October 2020 https://doi.org/10.5635/ASED.2020.36.4.045 Review article First Record of the Sponge-Dwelling Palaemonid Shrimp, Anchistioides compressus (Crustacea: Decapoda: Palaemonidae) in Korea Jin-Ho Park1,*, Damin Lee1, Sang-Hui Lee2, Sammy De Grave3 1College of Natural Sciences, Seoul National University, Seoul 08826, Korea 2National Marine Biodiversity Institute of Korea, Seocheon 33662, Korea 3Oxford University Museum of Natural History, Parks Road, Oxford, OX1 3PW, UK ABSTRACT The sponge-dwelling shrimp, Anchistioides compressus Paulson, 1875, is recorded from Munseom Islet, Jejudo Island, Korea for the first time. All specimens were collected inside the orange coloured sponges by trimix diving at depth from 36-45 m on the rocky reef slope. Anchistioides compressus is characterized by the shape of the rostrum, the posterolateral teeth of the sixth somite, stylocerite being well developed, the anterior margin of the scaphocerite sharply produced, and the biunguiculate dactyli of the ambulatory pereiopods, as well as the proportions of the fingers of the second pereiopods. An illustrated description of the specimens and colour photo are provided to aid future recognition. Keywords: Jejudo Island, symbiotic, range extension, taxonomy, Korean fauna INTRODUCTION compressus was collected from an unidentified host sponge species from Munseom Islet, Jejudo Island in 2018 (Fig. 1B). The genus Anchistioides Paulson, 1875 currently comprises The species is herein recorded as new to the Korean fauna, three species: the widespread Indo-West Pacific species An- and an illustrated description is provided to aid future recog- chistioides compressus Paulson, 1875 (Fig. 1A), A. willeyi nition. (Borradaile, 1900), and the western Atlantic A. antiguensis (Schmitt, 1924). All three species are known to associate with a variety of demosponges and calcareous sponges, inhabiting MATERIALS AND METHODS their spongocoel (Miyake and Fujino, 1967; Marin, 2009; De Grave and Anker, 2017; Fransen, in press). Although for During extensive sampling of palaemonid shrimps from Je- many decades the genus was placed in its own family, An- judo Island, Korea in 2018, six specimens of Anchistioides chistioididae, recently Chow et al. (2020) synonymized the compressus were collected by trimix diving at depths from family with Palaemonidae Rafinesque, 1815, based on a phy- 36-45 m. All symbiotic shrimps were collected with host logenetic study and a review of the morphological and devel- sponges and preserved in 80% ethanol. Shrimps were ob- opmental reasoning to support the family. served using a stereo microscope (M125; Leica, Germany) The original description of A. compressus, the type species and light microscope (BX51; Olympus, Japan). Digital illus- of genus Anchistioides, was brief and sparingly illustrated on trations were done using a microscope digital camera (Mc170; the basis of a single male specimen, collected from an un- Leica), Helicon focus software (Helicon focus 7.5.6, Ukraine) known location in the Red Sea (Paulson, 1875). Since then, and a drawing tablet (Intuos Pro PTH-660; Wacom, China) relatively more detailed descriptions have been done in litera- with Adobe Illustrator CC (Adobe Systems, USA), follow- ture (Kemp, 1925; Gordon, 1935; Miyake and Fujino, 1967), ing Coleman (2006). Postorbital carapace length (pocl) was with the species extensively described and illustrated by measured from the postorbital margin to the posterior dorsal Fransen (in press). During fieldwork in Korea, Anchistioides margin of the carapace. Material is deposited in the Marine This is an Open Access article distributed under the terms of the Creative *To whom correspondence should be addressed Commons Attribution Non-Commercial License (http://creativecommons.org/ Tel: 82-2-887-0752, Fax: 82-2-872-1993 licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, E-mail: [email protected], [email protected] and reproduction in any medium, provided the original work is properly cited. eISSN 2234-8190 Copyright The Korean Society of Systematic Zoology Jin-Ho Park, Damin Lee, Sang-Hui Lee, Sammy De Grave B A Fig. 1. Map of Indo West Pacific Ocean (IWP): A, Distribution of Anchistioides compressus Paulson, 1875; B, Collection locality of Jejudo Island, Korea. Red, previous record; Blue, present records; ?, not specified type locality. Arthropod depository Bank of Korea in Seoul National Uni- 120531_002); 1♀, 2♂♂ (pocl 3.2, 3.9, 3.8 mm), same data versity (MADBK), Seoul and National Institute of Biological (NIBRIV0000837765 to 837767). Resources (NIBR), Incheon. Description of Korean specimens. Body (Figs. 2, 8A) me- dium-sized, subcylindrical form. Rostrum (Figs. 2, 3A, B) straight, stout, about 1.1 times as SYSTEMATIC ACCOUNTS long as pocl, overreaching distal end of scaphocerite; dorsal margin with 9-10 teeth, most posterior one at about 0.2 of Family Palaemonidae Rafinesque, 1815 rostrum length; ventral margin deep at medial part, with 7-9 Genus 1*Anchistioides Paulson, 1875 teeth. Carapace (Fig. 3A, B) smooth, antennal tooth present, he- 2*Anchistioides compressus Paulson, 1875 (Figs. 2-8) patic tooth absent, with conical postorbital tubercle; inferior Anchistioides compressus Paulson, 1875: 115 (type locality: orbital angle minutely produced medially; pterygostomial an- Red Sea); Nobili, 1906: 54; Kemp, 1925: 339; Gordon, gle rounded. 1935: 339; Holthuis, 1952: 18; Bruce, 1967: 570, 1974: Abdomen (Fig. 2) smooth, first segment without anterome- 463, 1979: 241, 1981: 2, 1984: 199, 2007: 98; Miyake and dian dorsal lobe; first five pleonites ventrally rounded; sixth Fujino, 1967: 279; Li, 1996: 231; Nomura et al., 1996: 10; somite (Fig. 3C) about 1.2 times as long as fifth, with well-de- Poupin, 1998: 11; Hayashi, 1999: 389; Davie, 2002: 220; veloped posterolateral margin with two sharp teeth on each Li et al., 2007, 43; De Grave and Fransen, 2011: 308; Fran- side, posteroventral angles sharply pointed. sen (in press). Telson (Figs. 2, 3C) about 0.6 of pocl, about 1.4 times lon- ger than sixth somite length, about 3.0 times longer than max- Material examined. Korea: 1♀ (pocl 4.2 mm), Jejudo Is- imal width, tapering posteriorly; two pairs of dorsal spiniform land, Munseom Islet, 33°13.617′N, 126°34.133′E, depth: setae, at about 0.4 and 0.6 of telson length, respectively; pos- 36 m, 17 Jan 2018, leg. JH Park (MADBK120531_003; 1♂ terior margin (Fig. 3D) entire without median tooth, furnished (pocl 3.3 mm), Jejudo Island, Munseom Islet, 33°13.610′N, with three pairs of spiniform setae, lateral pair short, about 0.3 126°34.161′E, depth: 45 m, 20 Jun 2018, leg. JH Park (MA- of length of median pair, intermediate pair stout, about 0.55 D BK120531_001, GenBank accession no: MK602862; of submedian pair; submedian pair long and slender, setulose. Park et al., 2019; 1♀ (pocl 4.0 mm), same data (MADBK Eye (Figs. 2, 3E) with corneal diameter about 0.25 of pocl, Korean name: 1*해면더부살이새우속 (신칭), 2*작은손해면더부살이새우 (신칭) 320 Anim. Syst. Evol. Divers. 36(4), 319-329 First Records of Anchistioides compressus from Korea Fig. 2. Anchistioides compressus Paulson, 1875, lateral aspect. Female pocl 3.3 mm (MADBK 120531_002). Scale bar 3.0 mm. = corneal length about 0.6 of diameter, without nebenauge; nathite well developed, about 3 times longer than central stalk short, tapering proximally, medial length slightly longer width, with marginal plumose setae. than corneal length. First maxilliped (Fig. 4D) with coxal and basal endites Antennule (Figs. 2, 3F) with peduncle extending middle fused, suture demarcated, medially with serrulate and sim- of scaphocerite, flagella well developed; stylocerite reach- ple setae; palp simple, with rounded distal lobe, extending to ing to middle of basal segment, lateral margin straight, with distal margin of basis endite, without seta; exopod flagellum acute distal tooth; basal segment with slightly convex lateral short, reduced, about 3.6 times longer than maximal width, margin, distolateral tooth reaching to middle of distal seg- distally with one plumose seta; caridean lobe about 2.7 times ment, medial margin with strong ventromedial tooth at about longer than central width, marginally with plumose setae; epi- middle of segment length; intermediate and distal segment pod large, feebly bilobed, about 3.7 times longer than central short, subequal, about 0.3 of proximal segment length, with- width. out special features; upper flagellum biramous, proximal 4 or Second maxilliped (Fig. 4E) with epipod well-developed, 5 segments fused, short ramus with 5 or 6 segments, with 17 without podobranch; exopod well-developed, with eight groups of long aesthetascs; longer ramus slender, with about plumose terminal setae; endopod with coxal segment, with 30 segments, lower flagellum similar with about 35 segments. two simple setae; ischial and basal segments fused; meral Antenna (Fig. 3G) with basicerite distodorsally rounded, segment without special features; carpal segment tapering ventrolateral margin with long setae; ischiocerite and mero- proximally, with simple setae distally; propodal segment with cerite unarmed; carpocerite reaching to about 0.3 of scapho- long simple setae distally and medially; dactylar segment cerite length; scaphocerite about 2.6 times as long as maximal with serrulate and simple setae medially. width, lateral margin slightly convex, anterior margin sharply Third maxilliped (Fig. 4F) without exopod and rudimenta- pointed, medial margin convex, distolateral tooth large, not ry exopod, slightly overreaching distal margin of merocerite; exceeding lamella. coxa reduced; lateral plate convex; ischiomerus completely Mandible (Fig. 4A) without palp; incisor process with three fused to basis, suture demarcated, ischiomerus about 5 times distally acute teeth, central tooth smaller than marginal ones; longer than proximal width, medially and laterally with long molar process robust, apex subquadrate, with four blunt mar- simple setae; penultimate segment about 0.45 as long as is- ginal teeth, without setal bristles. chiomeral length, about 4.4 times as long as proximal width, Maxillula (Fig. 4B) with bilobed palp, lower palp lobe distally with four long simple setae; ultimate segment as long rounded, with tubercle, upper lobe rounded; upper lacinia as penultimate segment, tapering distally, with long serrulate broad, with 6 stout and simple spines, with simple setae dis- setae. tally; lower lacinia robust with long, strong, simple terminal All pereiopods without rudimentary exopod on basis. First setae. pereiopods (Fig. 5A) subequal in shape and size, reaching to Maxilla (Fig. 4C) without basal endite; palp long, simple, 0.9 of distal margin of scaphocerite; coxa and basis without with rounded lobe, five plumose setae laterally; scaphog- special features; ischium short, about half as long as merus, Anim. Syst. Evol. Divers. 36(4), 319-329 321 Jin-Ho Park, Damin Lee, Sang-Hui Lee, Sammy De Grave C A D D C B E-G E A, B F G Fig. 3. Anchistioides compressus Paulson, 1875, female pocl 3.3 mm (MADBK 120531_002): A, Carapace, lateral; B, Same, dorsal; C, Sixth pleonal segment, telson, and right uropod, dorsal; D, Posterior margin of telson, dorsal; E, Eye, dorsal; F, Antennule, dorsal; G, Antenna, ventral. Scale bars: A, B 2.0 mm, C, E-G 1.0 mm, D 0.3 mm. = = = unarmed; merus about 1.1 times as long as carpus, unarmed; mesially completely covered with group of setae; movable carpus slightly tapering proximally, about 1.3 times as long finger with acute tooth, distinctly demarcated, with group of as chela; carpo-propodal brush well developed; chela with setae distally. palm about 1.3 times as long as fingers, simple, cutting edges Second pereiopods (Figs. 5B, 7A) subequal in shape and entire; fixed finger with acute tooth, distinctly demarcated, tip size, overreaching distal margin of scaphocerite by entire 322 Anim. Syst. Evol. Divers. 36(4), 319-329 First Records of Anchistioides compressus from Korea C A F B D E A-F Fig. 4. Anchistioides compressus Paulson, 1875, female pocl 3.3 mm (MADBK 120531_002): A, Mandible; B, Maxillula; C, Maxilla; D, First maxilliped; E, Second maxilliped; F, Third maxilliped. Scale bars: A-F 0.5 mm. = length of dactylus; coxa proximally rounded; basis short, maximal width, unarmed; carpus short, slightly tapering prox- without special features; ischium short, about 0.7 times as imally, about 1.4 times as long as maximal width, about 0.4 long as merus, unarmed; merus slightly swollen proximally, as long as chela; chela (Fig. 5C) about 0.6 of pocl, about 1.6 about 1.8 times as long as carpus, about 2.9 times longer than times as long as merus; palm smooth, subcylindrical, about 1.4 Anim. Syst. Evol. Divers. 36(4), 319-329 323 Jin-Ho Park, Damin Lee, Sang-Hui Lee, Sammy De Grave A B D A, B, D, F, H E F E, G, I I G H C C Fig. 5. Anchistioides compressus Paulson, 1875, female pocl 3.3 mm (MADBK 120531_002): A, First pereiopod, lateral; B, Second pereiopod, lateral; C, Same, chela, mesial; D, Third pereiopod, lateral; E, Same, dactylus and distal propodus, ventromesial; F, Fourth pereiopod; G, Same, dactylus and distal propodus, ventromesial; H, Fifth pereiopod, lateral; I, Same, dactylus and distal propodus, ventromesial. Scale bars: A, B, D, F, H 1.5 mm, E, G, I 0.3 mm, C 0.5 mm. = = = times as long as fingers; fingers with subspatulate concavity times as long as carpus, with single spiniform setae on ventral on mesial side; fixed finger laterally expanded, with angular margin, with a pair of stout spiniform setae on distoventral proximal process mesially, distally with acute strong tooth, flexor margin; dactylus about 0.2 as long as propodus, biun- distinctly demarcated; movable finger with acute strong tooth guiculate, dorsal unguis larger than ventral one, flexor margin distally, distinctly demarcated. entire. Ambulatory pereiopods (Fig. 2) subequal in shape and size. Fourth pereiopod (Fig. 5F, G) with merus about 1.5 times Third pereiopod (Fig. 5D, E) overreaching distal end of sec- as long as ischium, unarmed; carpus about half as long as ond article of antennular peduncle by entire length of propo- merus, unarmed; propodus about 1.5 times as long as carpus, dus; merus about 1.6 times as long as ischium, unarmed; car- with single spiniform setae on ventral margin, with a pair of pus about 0.6 as long as merus, unarmed; propodus about 1.2 stout spiniform setae on distoventral flexor margin; dactylus 324 Anim. Syst. Evol. Divers. 36(4), 319-329 First Records of Anchistioides compressus from Korea A, B C, D E C D E A B Fig. 6. Anchistioides compressus Paulson, 1875, female pocl 3.3 mm (A, B) (MADBK 120531_002), male pocl 3.9 mm (C-E) (NI- BRIV0000837766): A, C, First pleopod; B, D, Second pleopod; E, Appendices interna and masculina. Scale bars: A-D 1.0 mm, E 0.3 mm. = = about 0.2 as long as propodus, biunguiculate, with dorsal un- maximal width, with plumose setae. guis larger than ventral one, flexor margin entire. Second pleopod of male (Fig. 6D, E) with basipodite as Fifth pereiopod (Figs. 5H, I, 7B) with merus about 1.6 long as endopod, about 1.6 times longer than wide, medi- times as long as ischium, unarmed; carpus about 0.6 as long ally with plumose setae; endopod with appendix masculina as merus, unarmed; propodus about 1.5 times as long as car- slightly shorter than appendix interna, distally with 2 long pus, with or without two spiniform setae on ventral margin, setae. with one stout spiniform setae on distoventral flexor margin, Uropod (Fig. 3C) overreaching distal end of telson; exopod a row of poor developed setae (six simple setae per row) slightly longer than endopod, outer margin entire, with one present on distolateral margin; dactylus about 0.3 as long as small spiniform setae, distolateral tooth well-developed. propodus, biunguiculate, with dorsal unguis larger than ven- Colour in life. Body and appendages transparent, with yel- tral one, flexor margin entire. low and red chromatophores along anterior appendages and First pleopod of female (Figs. 6A, 7D) with basipodite as pereiopods (Fig. 8B, C). long as exopod, about 2.5 times longer than wide, medial- Ecological information. All Korean specimens were collect- ly with plumose setae; endopod about 2.5 times longer than ed inside the unidentified orange coloured sponges below 35 wide, tapering distally, with plumose setae; exopod about 3.9 m. times longer than maximal width, with plumose setae. Geographical distribution. The species is widespread in Second pleopod of female (Fig. 6B) with basipodite as long tropical to temperate waters in Indo-Pacific Ocean (Fig. 1): as endopod, about 1.8 times longer than wide; appendix inter- Red Sea (type locality, no further details), East Africa (Zan- na reaching to middle of endopod. zibar, Kenya), Maldives (Magoodhoo Atoll), Andaman Is- First pleopod of male (Figs. 6C, 7C) with basipodite as lands, Western Australia (Dampier Archipelago), Eastern long as exopod, about 2.2 times longer than wide, medial- Australia (Heron Island; Capricorn Island; Wilson Island; ly with plumose setae; endopod about 2.3 times longer than Moreton Bay), Vanuatu (Aoré Island). French Polynesia (Tu- wide, tapering distally; appendix interna slightly overreaching amotu-Gambier Islands), Indonesia (Spermonde Archipelago; distal margin of endopod; exopod about 3.5 times longer than Bali), Philippines (Bohol), South China Sea (Xisha (Paracel) Anim. Syst. Evol. Divers. 36(4), 319-329 325 Jin-Ho Park, Damin Lee, Sang-Hui Lee, Sammy De Grave A B C D Fig. 7. Anchistioides compressus Paulson, 1875, male pocl 4.0 mm (A-C) (MADBK 120531_001), female pocl 4.2 mm (D) (MADBK 120531_003): A, Second, pereiopod, coxa and basis, lateral; B, Fifth pereiopod, dactylus and distal propodus, mesial; C, D, First pleopod, endopod. Scale bars: A-D 3.0 mm = Archipelago, Nansha (Spartly) Archipelago), U.S.A (Hawaiian descriptions of Anchistioides compressus (Paulson, 1875; Islands), Japan (Amakusa Island; Yakabi Island) and Korea Kemp, 1925; Miyake and Fujino, 1967; Fransen, in press). (Jejudo Island) (Paulson, 1875; Nobili, 1906; Kemp, 1925; Notably in the shape of the rostrum, the posterolateral teeth Miyake and Fujino, 1967; Bruce, 1974, 1979, 1981, 2007; of the sixth somite, the anterior margin of the scaphocerite Nomura et al., 1996; present study; Fransen, in press). sharply produced, the biunguiculate dactyli of the ambula- tory pereiopods, as well as the proportions of the fingers of the second pereiopods. A few minor differences are however DISCUSSION apparent when comparing the Korean specimens to previous descriptions. The length of telson of the holotype was de- The material examined herein agree well with the previous scribed as “telson is three times as long as the sixth segment”, 326 Anim. Syst. Evol. Divers. 36(4), 319-329 First Records of Anchistioides compressus from Korea A B C Fig. 8. Anchistioides compressus Paulson, 1875, female pocl 4.2 mm (MADBK 120531_003) and host sponges: A, Preserved speci- men, lateral view; B, Specimen on the host sponge; C, Specimen inside the host sponge. Photographs by JH Park. whilst in the Korean specimens, the telson less than 1.5 times paired stout spiniform setae on distoventral flexor margin on as long as the sixth segment (Fig. 3C). The molar process of fourth pereiopod; and two spiniform setae on the ventral mar- the mandible was described as terminating in five large cusps gin, with one spiniform setae on distoventral flexor margin by Kemp (1925), but in the present specimens it is armed on fifth pereiopod (Fig. 5G, I). The upper antennular flagel- with four distal teeth (Fig 4A). The propodi of the fourth and lum was described as “the third fused segment, the shorter of fifth pereiopods were described as “fifth pair the propodus which consists of four joints” in Miyake and Fujino (1967), without spinule on the posterior border” and “fourth and fifth while in the present specimens the upper flagellum has the pereiopods lack this spine”, respectively in Kemp (1925) and proximal 4-5 segments fused, and the short ramus with 5-6 Miyake and Fujino (1967), while in the present specimens a segments. Fransen (in press) also reported on the presence of single spiniform seta is present on the ventral border, with a rudimentary exopods on the third maxilliped and all ambula- Anim. Syst. Evol. Divers. 36(4), 319-329 327 Jin-Ho Park, Damin Lee, Sang-Hui Lee, Sammy De Grave tory pereiopods. These are, however, absent in all specimens REFERENCES in Korea (Fig. 7A). These are all considered to be natural vari- ation within the species and the current specimens largely fall Borradaile LA, 1900. On the Stomatopoda and Macrura brought well within the variation noted on a larger series of specimens by Dr. Willey from the South Seas. In: Zoological results (Fransen, in press). A more substantial difference lies howev- based on material from New Britain, New Guinea, Loyalty er in the appendix interna on the first pleopod in both sexes, Islands and elsewhere, collected during the years 1895, 1896, and 1897 (Ed., Willey A). Cambridge University Press, Lon- with its presence having been considered to be a unique char- acter for Anchistioides within Palaemonidea (Gordon, 1935; don, pp. 395-428. https://doi.org/10.5962/bhl.title.27080 Bruce AJ, 1967. The results of the re-examination of the type Holthuis, 1952; Chow et al., 2020; Fransen, in press). All specimens of some pontoniid shrimps in the collection of three female specimens from Korea, however, have the en- the Muséum National d’Histoire Naturelle, Paris. Bulletin dopod of the first pleopod without an appendix interna, only du Muséum National d’Histoire Naturelle (2), 39:564-572. male specimens having an appendix interna on first pleopod Bruce AJ, 1974. A synopsis of the pontoniinid shrimp fauna of (Figs. 6A, B, 7C, D). Miyake and Fujino (1967) also reported central East Africa. Journal of the Marine Biological Asso- on the absence of appendix interna in their female specimens ciation of India, 16:462-490. (see fig. 3C in Miyake and Fujino, 1967). Hawaiian speci- Bruce AJ, 1979. Records of some pontoniine shrimps from the mens have a developed appendix interna in small non-oviger- South China Sea. Cahiers de l’Indo-Pacifique, 1:215-248. ous female specimen (pocl 1.95) (see Fransen, in press). The Bruce AJ, 1981. Pontoniine shrimps of Heron Island. Atoll Re- postorbital carapace length (pocl) of mature female specimens search Bulletin, 245:1-33. from Korea is however larger (3.2-4.2 mm). The presence of Bruce AJ, 1984. The pontoniine shrimp fauna of Australia. Australian Museum Memoir, 18:195-218. https://doi. the morphological variations within A. compressus should be org/10.3853/j.0067-1967.18.1984.385 analyzed through molecular approach. Bruce AJ, 2007. Palaemonoid shrimps from the Dampier Archi- pelago (Crustacea: Decapoda), with a review of the Western Australian pontoniine shrimp fauna. Records of the Western ORCID Australian Museum, 73:97-129. https://doi.org/10.18195/ issn.0313-122x.73.2007.097-129 Jin-Ho Park: https://orcid.org/0000-0001-6522-744X Chow LH, De Grave S, Tsang LM, 2020. The family Anchisti- Damin Lee: https://orcid.org/0000-0002-7805-6050 oididae Borradaile, 1915 (Decapoda: Caridea) is a synonym Sang-Hui Lee: https://orcid.org/0000-0002-8724-9292 of Palaemonidae Rafinesque, 1815 based on molecular and Sammy De Grave: https://orcid.org/0000-0002-2437-2445 morphological evidence. Journal of Crustacean Biology, 40:277-287. https://doi.org/10.1093/jcbiol/ruaa012 Coleman CO, 2006. Substituting time-consuming pencil draw- CONFLICTS OF INTEREST ings in arthropod taxonomy using stacks of digital photo- graphs. Zootaxa, 1360:61-68. https://doi.org/10.11646/zoo- taxa.1360.1.4 No potential conflict of interest relevant to this article was re- Davie PJF, 2002. Crustacea: Malacostraca Phyllocarida, Hoplo- ported. carida, Eucarida (Part 1). In: Zoological catalogue of Aus- tralia (Eds., Wells A, Houston WWK). CSIRO Publishing, Melbourne, pp. 1-551. ACKNOWLEDGMENTS De Grave S, Anker A, 2017. An annotated checklist of ma- rine caridean and stenopodidean shrimps (Malacostraca: JHP is grateful to Prof. Won Kim (Seoul National Universi- Decapoda) of the Caribbean coast of Panama. Nauplius, ty, Korea) for supporting the fieldwork for caridean shrimp 25:e2017015. https://doi.org/10.1590/2358-2936e2017015 research throughout the world. The authors are grateful to De Grave S, Fransen CHJM, 2011. Carideorum catalogus: the Charles Fransen (Naturalis Biodiversity Center, Leiden) to recent species of the Dendrobranchiate, Stenopodidean, Pro- provide us for valuable manuscript for comparing the mor- carididean and Caridean shrimps (Crustacea: Decapoda). Zo- ologische Mededelingen, 85:195-588. phological variation between his material and Korean spec- Fransen CHJM, in press. New records of the sponge-symbiot- imens. This study was supported by grants of the National ic shrimp genus Anchistioides from the Indo-West Pacific Institute of Biological Resources (NIBR202002110 and (Decapoda, Caridea). Crustaceana. NIBR201801102), and the Marine Biotechnology Program Gordon I, 1935. On new or imperfectly known species of Crus- of Marine Biotechnology Program (No. 20170431) of Korean tacea Macrura. Zoological Journal of the Linnean Society, Government. 39:307-351. https://doi.org/10.1111/j.1096-3642.1935. 328 Anim. Syst. Evol. Divers. 36(4), 319-329

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