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Research Article
Mysidella hoshinoi, a new species from Izu-Oshima Island, Japan (Crustacea, Mysidae, Mysidellinae)
expand article infoMichitaka Shimomura
‡ Kitakyushu Museum of Natural History and Human History, Kitakyushu, Japan
Open Access

Abstract

A new mysid, Mysidella hoshinoi sp. n. is described from Izu-Oshima Island, Sagami Sea, central Japan. This species differs from its congeners in having a posterodorsal finger-like papilla on the eyestalk, five peculiar spines terminating in plumed seta on outer margin of carpopropodus of endopod of first thoracopod, and uropodal endopod bearing 27 spines on inner margin.

Keywords

Izu-Oshima Island, Mysidae , Mysidella , Sagami Sea

Introduction

Mysidella G. O. Sars, 1872, is the only genus of the subfamily Mysidellinae Czerniavsky, 1882 and includes 16 species (WoRMS 2016), ranging in depth from 3 m to 738 m worldwide (Murano 2002). Among these, four species have so far been reported from Japan:

Mysidella nana Murano, 1970 at 18–80 m, Oomura Bay, Tateyama Bay, and Suruga Bay (Murano 1970a, 1970b, 2002),

M. orientalis Murano, 2002 at 347–369 m, eastern East China Sea (Murano 2002),

M. tanakai Ii, 1964 at 220–660 m, Suruga Bay, Tateyama Bay and Sagami Bays (Ii 1964; Murano 1970b, 2002), and

M. truncata Murano, 2002 at 138–141 m, Amami-Oshima Island (Murano 2002).

Our recent investigations yielded an undescribed species Mysidella from a marine benthic habitat of Izu-Oshima, Sagami Sea. Based on this material, a new species Mysidella hoshinoi sp. n. is described, and an updated identification key is provided to the known species of Mysidella.

Material and methods

Mysids were collected with sealable plastic bags (20 cm × 20 cm) by scooping seawater on a sea anemone beloninging to the family Haloclavidae by a local SCUBA diver. All specimens obtained were fixed and preserved in 80% ethanol. Each individual was dissected and prepared for observation by a light microscope (Nikon E600). The total length of individuals was measured from the end of the rostrum to the end of the telson excluding spines.

The terminology follows Murano (2002). The type specimens are deposited in the Kitakyushu Museum of Natural History and Human History, Japan (KMNH).

Systematics

Mysidella G. O. Sars, 1872

Mysidella G. O. Sars, 1872: 266; G. O. Sars 1879: 84–86; Zimmer 1909: 169; Illig 1930: 600; Banner 1948: 108–109; Tattersall and Tattersall 1951: 427; Ii 1964: 574; Kathman et al. 1986: 191; Fenton 1990: 437; Murano 2002: 66.

Type species

Mysidella typica G. O. Sars, 1879 (by original designation and monotypy).

Mysidella hoshinoi sp. n.

Figs 2, 3, 4, 5

Material examined

Holotype. Adult ♂ (4.0 mm) (KMNH IvR 500893), 34°47'N, 139°24'E, Akino-hama, Izu-Oshima Island, Sagami Sea, Japan, 23 August 2014, 35 m.

Paratypes. Adult ♀ (4.0 mm) (KMNH IvR 500894), immature ♀ (3.0 mm) (KMNH IvR 500895), immature ♂ (3.1 mm) (KMNH IvR500896), data same as holotype; adult ♀ (3.4 mm) (KMNH IvR 500897), immature ♀ (3.0 mm) (KMNH IvR 500898), immature ♂ (2.7 mm) (KMNH IvR 500899), 34°47'N, 139°24'E,Akino-hama, Izu-Oshima Island, Tokyo, Japan, 16 August 2014, 35 m.

Diagnosis

Eyestalk with posterodorsal finger-like papilla; carpopropodus of endopod of first thoracopod with five peculiar spines terminating in plumed seta on outer margin; terminal claw of carpopropodus of endopod of first thoracopod with one short seta and suture distinct; uropodal endopod with 27 spines on inner margin.

Description of the holotype

Carapace (Fig. 2A): anterior margin produced into short rounded rostral plate and covering basal part of eyestalks; anterolateral corner produced; posterior margin emarginated, leaving last thoracic somite exposed. Eye (Fig. 2A, C) developed; cornea well-pigmented, globular, wider than eyestalk, occupying nearly half of eye; eyestalk with posterodorsal finger-like papilla.

Figure 1. 

Mysidella hoshinoi sp. n., sex unknown, on a tentacle of a sea anemone (family Haloclavidae), Akino-hama, Izu-Oshima Island, Sagami Sea, Japan, 25 March 2016, 35 m depth, habitus in situ, photographed by O. Hoshino.

Figure 2. 

Mysidella hoshinoi sp. n., A, C, D, G, H, J holotype male B, E, I paratype female (KMNH IvR 500894) F paratype female (KMNH IvR 500895): A, B anterior part of head, dorsal C right eye, dorsal D–F telson, dorsal G telson and left uropod, ventral H, I basal part of right antennula, dorsal J basal part of right antenna, dorsal. Scale bars: 500 µm.

Antennula (Fig. 2A, H): first segment of antennular peduncle longest, 1.3 times as long as third article, with anterolateral corner produced laterally and tipped with three plumose setae, and with two short projections anterodorsally bearing some plumose setae apically; second article shortest, with short projection anterodorsally bearing four plumose setae apically and one simple seta distomedially; third article slightly wider than long, small appendix masculina on ventral side, with short projection anterodorsally bearing some short stout setae and two plumose setae apically, and with six simple setae distomedially.

Antenna (Fig. 2A, J): antennal scale setose all round, extending beyond distal margin of antennular peduncle for 0.3 of its length, 3.2 times as long as width, distal suture distinct; outer margin slightly concave; inner margin convex. Antenna peduncle 3-articlulate: first segment shortest; second and third segments subequal in length.

Labrum (Fig. 3A) rounded apically, produced posteriorly into two unequal lobes; right lobe broadly rounded posteriorly, with fine teeth on margin; left lobe smaller; both lobes with fine teeth on posterior margin.

Figure 3. 

Mysidella hoshinoi sp. n., holotype male: A labrum ventral B left mandible, dorsal C right mandible, ventral D left maxillula, dorsal E left maxilla, dorsal F right first thoracopod, dorsal G peculiar spines on outer margin of carpopropodus of endopod of first thoracopod H right second thoracopod, lateral. Scale bars: 500 µm.

Left mandible (Fig. 3B) without teeth; molar portion trapezoidal; first article of mandibular palp shortest; second article longest, with seven setulate setae distally; third article slightly curved, with several setae. Right mandible (Fig. 3C) without teeth and molar portion, slightly curved medially, mandibular palp similar in shape than the left one.

Maxillula (Fig. 3D): inner lobe broad, 2.6 times as wide as outer lobe, with three plumose and one simple setae; outer lobe with 12 stout setae distally.

Maxilla (Fig. 3E): exopod with nine plumose setae on margin; first article of endopod with two plumose setae distally; second article with many plumose and some simple setae on margin; bilobulate basal endites each with ten plumose setae distally; coxal endite with six plumose setae distally and four plumose setae medially.

Endopod of first thoracopod (Fig. 3F) robust: basis with two plumose setae; preischium triangular, with four plumose setae distally; ischium 1.1 times as long as basis, with five plumose setae distally; merus 0.6 times as long as ischium, with two plumose setae and one simple seta; carpopropodus 1.4 times as long as merus, twice as long as width, with five peculiar spines (Fig. 3G) terminating in plumed seta on outer margin; terminal claw nearly straight, 1.1 times as long as carpopropodus, with one short setae, suture distinct.

Endopod of second thoracopod (Fig. 3H): ischium 0.8 times as long as basis; merus longest, 1.6 times as long as ischium; carpopropodus 0.7 times as long as merus, with two rows of setae distally; dactylus small, with one long, setulate seta apically and several short setae. Endopod of third thoracopod (Fig. 4A): preischium trapezoidal; ischium 3.0 times as long as preischium; merus 1.1 times as long as ischium; carpopropodus divided into two subsegments, 0.8 times as long as merus; dactylus small, with strong terminal claw. Endopod of fourth thoracopod (Fig. 4B): preischium trapezoidal; ischium 3.0 times as long as preischium; merus 0.9 times as long as ischium; carpopropodus divided into two subsegments, 0.7 times as long as merus; dactylus small, with strong terminal claw. Endopod of fifth thoracopod (Fig. 4C): preischium triangular; ischium 6.1 times as long as preischium; merus half as long as ischium; carpopropodus divided into three subsegments, 0.8 times as long as merus; dactylus small, with strong terminal claw. Endopod of sixth thoracopod (Fig. 4D): preischium triangular; ischium 5.7 times as long as preischium; merus half as long as ischium; carpopropodus divided into three subsegments, 0.8 times as long as merus; dactylus small, with strong terminal claw. Endopod of seventh thoracopod (Fig. 4E): preischium triangular; ischium 4.2 times as long as preischium; merus 0.7 as long as ischium; carpopropodus divided into three subsegments, 0.8 times as long as merus; dactylus small, with strong terminal claw. Endopod of eighth thoracopod (Fig. 4F): preischium triangular; ischium 3.9 times as long as preischium; merus 0.7 as long as ischium; carpopropodus divided into three subsegments, 0.8 times as long as merus; dactylus small, with strong terminal claw.

Figure 4. 

Mysidella hoshinoi sp. n., holotype male: A left third thoracopod, lateral B left fourth thoracopod C left fifth thoracopod, lateral D left sixth thoracopod, lateral E left seventh thoracopod, lateral F left eighth thoracopod, lateral G left penis, ventral. Scale bar: 500 µm.

Exopod of first thoracopod with 8-segmented flagellum. Exopods of second to seventh thoracopods (Figs 3H, 4A–E) similar in shape and size, with 7-segmeted flagellum; basal plate with rounded outer corner. Exopod of eighth thoracopod (Fig. 4F) with 7-segmented flagellum; basal plate narrower than those of anterior six thoracopods.

Penis (Fig. 4G) cylindrical, 6.2 times as long as width, without setae.

Abdomen: first four somites decreasing in length posteriorly; second and fifth segments subequal in length; sixth somite 1.3 times as long as fifth somite.

All pleopods (Fig. 5A–E) reduced to unsegmented lobe, not modified. First pleopod as long as second pleopod; second pleopod to fifth pleopod increasing in length; fifth pleopod 1.3 times as long as fourth pleopod.

Figure 5. 

Mysidella hoshinoi sp. n., A–E holotype male F paratype female (KMNH IvR 500894): A left first pleopod, ventral B left second pleopod, ventral C left third pleopod, ventral D left fourth pleopod, ventral E left fifth pleopod, ventral F left first pleopod, ventral. Scale bar 100 µm.

Uropod (Fig. 2G): endopod of uropod extending to apex of apical spines of telson, 2.1 times as long as width, with large statolith and 27 spines on inner margin; exopod of uropod 3.9 times as long as width.

Telson (Fig. 2D) tapering posteriorly, 1.3 as long as maximum width; lateral margins each with three pairs of anterior spiniform setae, seven posterior spiniform setae on left side and six posterior spiniform setae on right side, and three pairs of terminal spiniform setae; cleft shallow and narrow, 0.08 times as deep as telson length, with six short spines on margin.

Description of the paratype female

(KMNH IvR 500894).Antennula (Fig. 2B, I): first segment of antennular peduncle as long as third article, with anterolateral corner produced laterally and tipped with three plumose setae, and with two short projections anterodorsally bearing some plumose setae apically; second article shortest, with short projection anterodorsally bearing four plumose setae apically and one plumose and one simple setae distomedially; third article slightly wider than long, with short projection anterodorsally bearing some short stout setae and two plumose setae apically, and with two plumose setae medially and six simple setae distomedially.

All thoracopods and pleopods (Fig. 5F) similar to holotype male in morphology and chaetotaxy.

Telson (Fig. 2E): lateral margins each with two pairs of anterior, six pairs of posterior and three pairs of terminal spiniform setae; cleft with four spines on margin.

Marsupium composed of two pairs of developed oostegites on seventh and eighth thoracopods.

Variation

Some variations (N = 7: holotype and 6 paratypes) were recognized in the number of spiniform setae on telson (Fig. 2F). Lateral margins each with two or three pairs of anterior, four to seven pairs of posterior spiniform setae; cleft with one to four spines on margin.

Color in life

Body (Fig. 1) dark to light read, with or without light brownish marbled pattern. Cornea of eye light orange; posterodorsal finger-like papilla on the eyestalk white. Antennular flagella transparent with white and red stripes.

Distribution and habitat

The new species has so far been found only the type locality, 35 m depth, Akino-hama, Izu-Oshima Island, Sagami Sea, central Japan. According to the sampling notes by Mr. O. Hoshino, a number of individuals hovered above and around oral disc and tentacles of Haloclavidae sp. at the bottom. The mysids sometimes perched on the tentacles of the sea anemone. The new species live in ectocommensal association with sea anemones of the family.

Remarks

Mysidella hoshinoi sp. n. differs from all the congeners in having a posterodorsal finger-like papilla on the eyestalk.

The arrangement of the spines of the telson links the new species to Mysidella incisa Wang, 1998, from the northern area of the South China Sea (Wang, 1998) and the Timor Sea (Murano, 2002). Mysidella hoshinoi is distinguished from M. incisa by the following characters (those of M. incisa in parentheses): cornea occupying nearly half of eye (nearly one third); eyestalk with posterodorsal finger-like papilla (without papilla); uropodal endopod 2.1 times as long as width (2.5–2.7 times as long as width), with 27 spines on inner margin (with 22–24 spines).

Etymology

This species is named after Mr. O. Hoshino, who gave me the present material for taxonomic study. The specific name thus is a noun in the genitive singular.

Key to the species of Mysidella, with the depth ranges and distributions (modified from Brattegard 1973 and Murano 2002)

1 Eye well developed, with cornea 2
Eye rudimentary, without cornea. 375 m depth, Norway M. typhlops
2 Posterodorsal finger-like papilla on the eyestalk absent 3
Posterodorsal finger-like papilla on the eyestalk present. 35 m depth, Izu-Oshima Island, Japan M. hoshinoi sp. n.
3 Distal cleft / total length in telson less than 5% 4
Distal cleft / total length in telson more than 5% 5
4 Two or three spines on distal cleft of telson. 20–115 m depth, northern South China Sea, Timor Sea M. incisa
Six spines on distal cleft of telson. 33–79 m depth, Bass Strait M. australiana
5 Distal cleft / total length in telson less than 10% 6
Distal cleft / total length in telson more than 10% 8
6 Telson 1.3 times as long as width; two to four spines on distal cleft of telson 7
Telson about twice as long as width; eight spines on distal cleft of telson. 25.5–260 m depth, northern South China Sea M. rotundincisa
7 Three peculiar spines on outer margin of carpopropodus of endopod of first thoracopod; 16 spines on inner margin of uropodal endopod; seven to nine spiniform setae along whole length of lateral margin of telson. 3 m depth, Rottnest Island, West Australia M. mukaii
Five peculiar spines on outer margin of carpopropodus of endopod of first thoracopod; 25 spines on inner margin of uropodal endopod; eight spiniform setae on distal half of lateral margin of telson. 138–141 m depth, Amami-Oshima Island, southwestern Japan M. truncata
8 Distal cleft / total length in telson less than 19% 9
Distal cleft / total length in telson more than 19% 13
9 Distal cleft / total length in telson 17%. 500–600 m depth, British Columbia to S. California M. americana
Distal cleft / total length in telson less than 15%. 10
10 46 spines on inner margin of uropodal endopod 11
24–32 spines on inner margin of uropodal endopod 12
11 Telson 2.4 times as long as width. 300–720 m depth, Bay of Biscay M. biscayensis
Telson less than twice as long as width. 415–437 m depth, northern South China Sea M. macrophthalma
12 Six or seven spiniform setae on distal half of lateral margin of telson; 24 or 25 spines on inner margin of uropodal endopod. 40 m depth, Caribbean coast of Colombia M. minuta
16–18 spiniform setae on distal half of lateral margin of telson; 30–32 spines on inner margin of uropodal endopod. 90–540 m depth, Norway to Bay of Biscay, Mediterranean M. typica
13 Five peculiar spines on outer margin of carpopropodus of endopod of first thoracopod; 12–20 spines on distal cleft of telson 14
Three peculiar spines on outer margin of carpopropodus of endopod of first thoracopod; 24–36 spines on distal cleft of telson 15
14 20 spiniform setae on distal half of lateral margin of telson; 35 spines on inner margin of uropodal endopod. 80 m depth, Suruga bay, Japan M. nana
Eleven or 12 spiniform setae on distal half of lateral margin of telson; 29 spines on inner margin of uropodal endopod. 78 m depth, northern South China Sea M. tenuicauda
15 16 spiniform setae on distal half of lateral margin of telson; 30 spines on inner margin of uropodal endopod. 347–369 m depth, eastern East China Sea M. orientalis
25–27 spiniform setae on lateral margin of telson; 47 or 48 spines on inner margin of uropodal endopod 16
16 Deep transverse groove on rostrum present; telson 2.6 times as long as width. 535–738 m depth, Timor Sea, Sulu Sea M. sulcata
Deep transverse groove on rostrum absent; telson 2.3 times as long as width. 220–660 m depth, Suruga Bay, Sagami Bay, Japan M. tanakai

Acknowledgements

I am deeply grateful to Mr. Osamu Hoshino (Diving Service Chap, Izu-Oshima, Tokyo) for providing the material for this taxonomic study and Dr. Kensuke Yanagi (Coastal Branch of Natural History Museum and Institute, Chiba) for help to identify the sea anemone. Also, many thanks are given to Dr. Alan A. Myers (University College Cork), Dr. Carlos San Vicente (Tarragona, Spain), and an anonymous reviewer, for their valuable comments and suggestions on the manuscript. This research was supported in part by KAKENHI (No. 15K14596).

References

  • Banner AH (1948) A taxonomic study of the Mysidacea and Euphausiacea (Crustacea) of the northeastern Pacific, Part II, Mysidacea from Tribe Mysini through subfamily Mysidellinae. Transactions of the Royal Canadian Institute 27: 65–125.
  • Fenton GE (1990) Mysidella australiana sp. nov. from Bass Strait, Australia (Crustacea: Mysidae: Mysidellinae). Memoirs of the Museum of Victoria 50(2): 437–441.
  • Ii N (1964) Fauna Japonica, Mysidae (Crustacea). Biogeographical Society of Japan, Tokyo, 610 pp.
  • Lagardère JP, Nouvel H (1980) Les Mysidacés du talus continental du golfe de Gascogne. II. Familles des Lophogastridae, Eucopiidae et Mysidae (Tribu des Erythropini exceptée). Bulletin du Muséum National d´Histoire Naturelle, sér. 4, Section A, No. 3: 845–887.
  • Murano M (1970a) A small collection of benthic Mysidacea from coastal waters in Suruga Bay, Japan. Crustaceana 18: 251–268. doi: 10.1163/156854070X00202
  • Murano M (1970b) Systematic and ecological studies on Mysidacea collected by the bottom-net. Journal of the Oceanographical Society of Japan 26: 137–150. doi: 10.1007/BF02753888
  • Murano M (2002) The genus Mysidella (Crustacea, Mysidacea, Mysidae), with descriptions of five new species. Bulletin of the National Science Museum. Series A: Zoology 28(2): 65–90.
  • Sars GO (1872) Undersøgelser over Hardangerfjordens fauna Forh. Videnskabsselsk. Kristiania 1871: 246–286.
  • Wang S (1998) On new and rare species of Mysidacea (Crustacea) from the Northern South China Sea. Studia Marina Sinica 40: 199–244.
  • Zimmer C (1909) Die nordischen Schizopoden. In: Brandt K, Apstein C (Eds) Nordisches Plankton. Lipsius und Tischler, Kiel & Leipzig, 178 pp. doi: 10.5962/bhl.title.10255
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