Amblyops tattersalli Zimmer, 1914

Wittmann, Karl J., 2024, The Mysidae (Crustacea, Mysida) of the ANDEEP I-III expeditions to the Antarctic deep sea with the description of twelve new species, establishment of four new genera and with world-wide keys to the species of Erythropinae and Mysidellinae, European Journal of Taxonomy 940, pp. 1-180 : 27-32

publication ID

https://doi.org/ 10.5852/ejt.2024.940.2577

publication LSID

lsid:zoobank.org:pub:19DE5E4F-3A2C-41FF-A593-A4C74F7A9ABD

DOI

https://doi.org/10.5281/zenodo.12206499

persistent identifier

https://treatment.plazi.org/id/EF7B8639-FFCA-FFAE-FDF1-056EFB4B2032

treatment provided by

Plazi

scientific name

Amblyops tattersalli Zimmer, 1914
status

 

Amblyops tattersalli Zimmer, 1914 View in CoL

Figs 11–13 View Fig View Fig View Fig

Amblyops tattersalli Zimmer, 1914: 390–391 View in CoL , pl. xxiii figs 13–16 (coast of E Antarctica ).

Amblyops tattersalli View in CoL – W.M. Tattersall 1923: 275, 277, 285 (short description, record, Ross Sea). — O.S. Tattersall 1965: 15–16, figs 1–4 (description, record, Ross Sea). — Birstein & Tchindonova 1970: 284–285 (in species list). — Ariani et al. 1993: table 1 (mineral composition of statoliths). — Wittmann 1995: fig. 1 (reproductive adaptations). — Brandt et al. 1998: table 1 (biogeography, endemism). — Petryashov 2006: 1409, fig. 5 (distribution, in key). — San Vicente et al. 2006: table 2 (biodiversity, new records, Southern Ocean). — San Vicente 2010: 42, table 4, fig. 35 (distribution, diagnosis, in key). — Murano 2012: 84 (in key). — Petryashov 2014a: 150, map 10 (biogeography). — Wittmann & Ariani 2019: suppl. (fluorite statoliths, biogeography). — Mees & Meland 2024: Aphia-ID 227029 (accepted).

Diagnosis

Based on adults of both sexes. All features within limits of generic diagnosis. Carapace with rounded, obtusely angled anterior margin. Eye rudiments without visual elements, roughly trapeziform with widely rounded lateral margin and with roughly linear, oblique anterior margin. Ocular papilla with ¼–⅓ of antero-posterior extension of eye rudiments. Disto-lateral edge of antennal sympod with only one large tooth. Antennal scale length 2.6–3.2 times maximum width. Scale extends 0.4–0.6 times its length beyond antennular trunk. Scale with small apical segment; bare portion of lateral margin ending at 9/10 of scale length in a large tooth, mesially tightly accompanied by 2–3 small spines. Setose terminal lobe of scale well projecting beyond large tooth. Mouthparts normal, labrum rostrally rounded. Thoracic exopod 1 with 9-segmented flagellum, exopods 2–8 with 10-segmented flagellum. Endopods 3–8 with unsegmented carpus separated from propodus by a strongly oblique articulation, two segments of propodus separated by a less oblique articulation. Female with three pairs of oostegites contributing to wall of marsupium. Male pleopods 1–5 biramous; endopods with 1, 18, 16–17, 16 and 15–16 segments, exopods with 17, 17, 17–18, 18 and 18 segments, respectively. Pleopods of both sexes with normal setae only. Both rami of uropods undivided, setose all around, endopod with one spine on mesial margin below statocyst. Telson linguiform, distal ⅔ with weakly converging, slightly sigmoid lateral margins and with broad, slightly flattened, convex terminal margin, disto-lateral edges rounded; length 1.7–1.9 times maximum width. Proximal ⅖ of telson with bare lateral margins, distal ⅗ of each lateral margin with dense series of 18–23 normal-shaped spines discontinuously increasing in length distally. Terminal margin with pair of paramedian setae tightly flanked by a pair of small spines, in turn flanked by 2–3 pairs of large spines, the latter forming a continuous series and gradually changing in length with proximally adjoining lateral spines; innermost large spine ⅑–⅙ of telson length. Telson with total of 42–54 spines plus two barbed setae.

Material examined

SE ATLANTIC • 1 ♂ subad. (BL = 16.4 mm); Cape Basin, ANDEEP-III station 016-10; 41°07.06ʹ S, 9°54.88ʹ E to 41°06.99ʹ S, 9°54.75ʹ E; depth 4687– 4669 m; 26 Jan. 2005; EBS epinet.

SOUTHERN OCEAN • 1 juv. (BL = 7.7 mm); NW Weddell Sea, ANDEEP-II station 131-3; 65°19.83ʹ S, 51°31.62ʹ W to 65°19.95ʹ S, 51°31.41ʹ W; depth 3049–3050 m; 5 Mar. 2002; EBS supranet 1 ♀ ad. (fragmented, BL ≈ 27.3 mm, bearing nauplioid larvae), 1 ♂ ad. (BL = 22.7 mm), 3 juv.; NW Weddell Sea, ANDEEP-II station 133-3; 65°20.15ʹ S, 54°14.35ʹ W to 65°20.06ʹ S, 54°14.51ʹ W; depth 1122– 1119 m; 7 Mar. 2002; EBS epinet 1 imm. (BL = 8.7 mm); Weddell Abyssal Plain, ANDEEP-III station 088-8; 68°03.66ʹ S, 20°27.90ʹ W to 68°03.61ʹ S, 20°27.52ʹ W; depth 4929–4931 m; 27 Feb. 2005; EBS supranet 1 juv. (BL = 6.2 mm); Weddell Abyssal Plain, ANDEEP-III station 102-13; 65°34.32ʹ S, 36°31.32ʹ W to 65°34.40ʹ S, 36°31.07ʹ W; depth 4805– 4803 m; 6 Mar. 2005; EBS supranet 2 ♂♂ ad. (BL = 24.6, 27.7 mm), 1 ♀ subad. (BL = 17.4 mm); Powell Basin, ANDEEP-III station 133-2; 62°46.49ʹ S, 53°03.50ʹ W to 62°46.38ʹ S, 53°03.98ʹ W; depth 1584– 1579 m; 16 Mar. 2005; EBS epinet 1 ♂ ad. (BL = 22.8 mm, on slides); same collection data as for preceding 1 ♀ subad. (BL = 11.1 mm); Powell Basin, SW continental slope of South Orkney Islands, ANDEEP-III station 151-7; 61°45.52ʹ S, 47°07.68ʹ W to 61°45.42ʹ S, 47°08.04ʹ W; depth 1182–1185 m; 21 Mar. 2005; EBS epinet GoogleMaps 1 imm. (BL = 6.5 mm); Drake Passage, N of South Shetland Islands, ANDEEP-I station 114-4; 61°43.54ʹ S, 60°44.20ʹ W to 61°43.54ʹ S, 60°44.55ʹ W; depth 2914–2920 m; 18 Feb. 2002; EBS epinet GoogleMaps 1 ♀ ad. (BL = 20.9 mm), 1 imm., 1 juv.; same collection data as for preceding except for occurrence in supranet GoogleMaps 1 juv. (BL = 4.6 mm); South Sandwich Trench , E of Montagu Island, ANDEEP-II station 141-10; 58°25.08ʹ S, 25°00.77ʹ W to 58°24.93ʹ S, 25°00.95ʹ W; depth 2313– 2281 m; 23 Mar. 2002; EBS supranet GoogleMaps .

Supplementary description

All features within the limits of the above diagnosis.

CARAPACE ( Figs 11A–B View Fig , 13B View Fig ). Anterior margin convex, posterior margin weakly concave. Median pore group 6% of carapace length in front of posterior margin. This group is constituted by eight (2 ×4) pores flanking a larger pore-like structure, together in M-like arrangement ( Fig. 13B View Fig ).

EYES ( Fig. 11A–E View Fig ). Eye rudiments dorsoventrally compressed by a factor of 1.5–1.9 measured near center. Eye surface mostly hispid by minute, slender triangular scales ( Fig. 11C–D View Fig ); on average largest scales ( Fig. 11C View Fig ) in median portions of anterior margin. Dorsal face covered only partly by somewhat shorter scales ( Fig. 11D View Fig ) scattered over surface, for methodological reasons best visible along accidental folds produced by forcing eye rudiments into a plane. Each eye with large, distally broadly rounded ocular papilla ( Fig. 11B, E View Fig ) closely behind anterior margin at ⅓ of eye width from mesial margin. Papilla ends in a toroid with central pore. Organ of Bellonci near papilla.

ANTENNAE S. LAT. ( Figs 11F–G View Fig , 13A View Fig ). Basal segment of antennula dorsally with striated sensory cushion well visible at bottom of an almost empty antennular bursa ( Fig. 11F View Fig ); such striation not visible in a bursa filled with extraneous material ( Fig. 11G View Fig ). Terminal segment of antennular trunk without female lobe. Disto-median lobe of trunk armed with four teeth increasing in size laterally, lobe disto-laterally with four barbed setae. The 2–3 tooth-like structures mesially adjoining disto-lateral tooth of antennal scale show a clear basal articulation ( Fig. 13A View Fig ) and thus represent true spines (or spiniform setae), as already concluded by W.M. Tattersall (1923), but not representing the “secondary denticles” [translation] indicated by Zimmer (1914) in the original description of this species.

MANDIBLES. Compared with left mandible (as in Fig. 21C–D View Fig ), right mandible (as in Fig. 21E View Fig ) bears smaller, serrate digitus mobilis and more strongly tooth-like spines of pars centralis.

GUT ( Fig. 12 View Fig ). Similar to that of A. bipapillatus sp. nov. ( Fig. 22 View Fig ). Dissected adult male of A. tattersalli differs from this species by presence of small denticles on distal fourth of apically coronate spines ( Fig. 12B View Fig ), posterior part of lateralia on each side with cluster of fewer (eight vs eleven) unilaterally serrated spines rather than with stiff bristles ( Fig. 12D View Fig ), and by dorsolateral infoldings on each side with cluster of fewer (five vs six) spines, more homogeneous in length ( Fig. 12E View Fig ). Lateral setae of superomedianum are basally much thicker ( Fig. 12F View Fig ) than slender normal setae in caudal position. All setae of superomedianum distally microserrated. Storage volume poorly filled with crustacean remains (mainly setae), a few very large mineral particles and very little masticated material. Midgut almost empty. Anal lobe distinct, weakly cuticularized (dashed line in Fig. 13C View Fig ).

THORAX. Basal plate of exopods 1–8 with minute knob at subrectangular disto-lateral edge. Dactylus of endopod 2 not reflexed; oriented about perpendicular to carpopropodus. Endopods 3–8 long and slender. Endopod 8 when stretched reaches anteriorly to tip of antennal scale, posteriorly to end of pleomere 6. Penes with ⅘ length of ischium 8.

PLEON. Length of pleomeres 1–5 is 0.6–0.7, 0.6, 0.5, 0.5–0.7 and 0.5–0.6 times length of pleomere 6, respectively, telson 1.1–1.2 times length of pleomere 6. Pleomere 6 shorter than combined pleomeres 4–5. Female pleopods increasing in length caudally. Exopods of male pleopods 1–5 subequal in length. Scutellum paracaudale triangular with narrowly blunt apex.

TAIL FAN ( Fig. 13C–F View Fig ). Exopod of uropods 1.5 times endopod length and 1.5–1.7 that of telson; endopod 0.9–1.0 length of telson. Exopod extends 0.3–0.4 times its length beyond endopod and 0.4–0.6 beyond telson. Statoliths composed of fluorite, diameter 0.18–0.29 mm (n = 5). Telson dissected in two specimens: both spines flanking pair of paramedian setae minute (0.05 mm) in adult male with BL 22.8 mm ( Fig. 13F View Fig ); only right paramedian spine that small in adult female with BL 27.8 mm, left spine five times that size, i.e., one third of adjacent large spine. Telson with a pair of paramedian subbasal fields (visualized as shadowed areas in Fig. 13C View Fig ) with 68–83 pores (n = 4; not all pores in focus in Fig. 13D View Fig ). Telson with 2–3 µm long triangular scales organized in groups of up to twenty, mostly about ten scales ( Fig. 13E View Fig ); groups together forming narrow longitudinal ribbon proceeding close to each lateral margin between ⅕ and ⅘ telson length from basis (visualized as shadowed lateral areas in Fig. 13C View Fig ).

NAUPLIOID LARVAE ( Fig. 13G–I View Fig ). Female with BL 27.3 mm carried 15 nauplioid larvae at substage N3. Body length of larvae 4.0– 4.6 mm. Nauplioid abdomen ends in furcal appendages, each armed with a fan of 18–22 spine-setae increasing in length distally (n = 5; Fig. 13I View Fig ). Tip of larval antennula with 9–12 mostly shorter spine-setae, not arranged in series (n = 5; Fig. 13H View Fig ). Remaining parts of body with smooth cuticle. Remaining features in Fig. 13G–I View Fig typical of stage of development.

Type locality and distribution

The type locality is the winter station (= Gauss Station) of the Deutsche Südpolar-Expedition 1901– 1903, coast of East Antarctica, 66°02ʹ S, 89°38ʹ E, depth 385 m. This circum-Antarctic species was reported by Petryashov (2006, 2014a) from 55– 78° S, depth 510–860 m and by San Vicente (2010) from 66– 75° S, depth 385– 547 m. The ANDEEP records are from Cape Basin, Weddell Abyssal Plain, NW Weddell Sea, Powell Basin, South Sandwich Trench and Drake Passage in the range of 41– 68° S, 10° E – 61° W, depth 1119–4931 m, thus representing strong latitudinal and bathymetric range extensions. Resulting total ranges 41– 78° S, 90° E anticlockwise to 61° W, depth 385–4931 m.

Kingdom

Animalia

Phylum

Arthropoda

Class

Malacostraca

Order

Mysida

Family

Mysidae

Genus

Amblyops

Loc

Amblyops tattersalli Zimmer, 1914

Wittmann, Karl J. 2024
2024
Loc

Amblyops tattersalli

Zimmer C. 1914: 391
1914
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