Tritodynamia serratipes Anker & Ng, 2014
publication ID |
https://doi.org/ 10.26107/RBZ-2023-0007 |
publication LSID |
lsid:zoobank.org:pub:F0603729-62D0-46E4-A383-627C27337732 |
persistent identifier |
https://treatment.plazi.org/id/03FE082C-FFD7-526A-FC5B-ECCCFB539FAF |
treatment provided by |
Felipe |
scientific name |
Tritodynamia serratipes Anker & Ng, 2014 |
status |
|
Tritodynamia serratipes Anker & Ng, 2014 View in CoL
( Figs. 1 View Fig , 2 View Fig )
Tritodynamia serratipes Anker & Ng, 2014: 370 View in CoL View Cited Treatment , figs. 1–3; Rahayu & Ng, 2021: 1188, 1197.
Material examined. Holotype: female (8.2 × 4.5 mm) ( ZRC 2014.0229 View Materials ), Straits of Singapore, off Marina East, 1°17′199″– 1°17′185″N 103°53′830″–103°53′575″E, Singapore, 6.3–6.5 m, soft mud, rectangular dredge, R. V. Galaxea , coll. C.K. Chim et al., 26 March 2014. Other: 1 male (9.5 × 4.9 mm)
( NHM 2022.154), littoral zone, Siglap, southern Singapore, coll. M.W.F. Tweedie, June 1933 .
Diagnosis. (Modified from Anker & Ng, 2014) Carapace transversely elongated, male carapace width-to-length ratio 1.9 (female 1.8); front about 0.2 times CW, margin entire, cristate, about 0.4 times width between external orbital angles; anterolateral margin cristate. Mxp3 with ischium slightly shorter than merus; propodus with projecting, foliaceous, distodorsal lobe; dactylus elongate-elliptical, inserted at ventral submedian part of propodus, reaching far beyond propodus. P1 symmetrical; lower part of manus with 2 granulated cristae, lower crista of manus with prominent concavity on subventral inner face adjacent to pollex base; cutting edge of pollex with 3 prominent teeth in proximal third, proximal tooth subtriangular, distal tooth subquadrate; dactylus with 2 strong teeth in proximal half, subtriangular to subquadrate in form. P2 of both sexes with merus about 3.9 times as long as wide, with row of granules distally on anterodorsal surface, numerous granules on posterior surface, including rows of strong granules along posterodorsal, ventral margins. Male P3 elongated, length (from merus to dactylus) about 2.0 times carapace width (1.7 in female); ischium with granules on dorsal, ventral surfaces; posterior margin with strong projecting tooth; merus with anterior, posterior surfaces bearing numerous rounded, conical granules; posterodorsal, ventral margins lined with strong conical granules; male propodus about 1.5 times as long as dactylus (1.5 times in female), 3.9 times as long as wide (1.9 in female); rows of strong granules present on anterior, ventral margin, median part of dorsal surface; posterodorsal margin with uneven row of conical or slightly arched, adjacent teeth, 7–10 of them conspicuously strong. Male P4 merus stout, 3.1 times as long as wide (2.2 in female), anterior, posterior surfaces with numerous granules, especially on dorsal, ventral margins; propodus about 1.3 times as long as dactylus (same in female), about 2.5 times as long as wide (2.2 in female), surface without granules. P5 of both sexes with dactylus directed slightly dorsally. Thoracic sternites 1 and 2 fused, forming subtriangular structure, medially depressed, separated from third sternite by distinctly concave suture. Male pleon relatively broad, 6 free somites and telson; somite 6 wide with strongly convex lateral margins; telson partially sunken into distal margin of somite 6. G1 relatively slender, gently curved, distal part prominently bent at almost 90º angle, distalmost part chitinous, base relatively wide, tapering to form beak-like structure.
Remarks. The holotype female of T. serratipes was described and figured in great detail so there is no need to repeat the data here. The present male of T. serratipes differs from the holotype female in having the carapace relatively wider (width-to-length ratio 1.9 vs. 1.8) ( Fig. 1B View Fig ; cf. Anker & Ng, 2014: fig. 1A); the P3 propodus is distinctly longer in proportions (length-to-width ratio 3.9 vs. 1.9) ( Fig. 1A, D View Fig ; cf. Anker & Ng, 2014: fig. 1J); and the P4 merus is proportionately longer (length-to-width ratio 3.1 vs. 2.2) ( Fig. 1E View Fig ; cf. Anker & Ng, 2014: fig. 1L). Otherwise, most of the non-sexual characters, including the structures of the third maxilliped and chela ( Figs. 1C View Fig , 2A View Fig ), closely agree.
The species most similar in morphology to T. serratipes is T. bengalensis Trivedi, Mitra & Ng, 2021 , described from a male from the eastern Indian Ocean. Tritodynamia bengalensis appears to be closest to T. serratipes in having the ventral margins of the P3 merus and propodus prominently serrated. Trivedi et al. (2021) noted that T. serratipes can be separated from T. bengalensis by the following morphological features: the dactylus of the third maxilliped is much longer than the propodus ( Anker & Ng, 2014: fig. 1E) (vs. dactylus of the third maxilliped is relatively shorter, being only slightly longer than the propodus, in T. bengalensis ; Trivedi et al., 2021: fig. 2C); there are two distinct teeth present in the proximal half of the cheliped pollex ( Anker & Ng, 2014: figs. 1F, 3C) (vs. there is one strong and one low tooth at the base of pollex in T. bengalensis ; Trivedi et al., 2021: fig. 2E); and the P3 propodus is proportionately shorter and strongly serrated, with 15 large teeth, along the ventral margin ( Anker & Ng, 2014: figs. 1J, K, 3A) (vs. P3 propodus is proportionately longer and is relatively less strongly serrated with 18 small teeth on the ventral margin in T. bengalensis ; Trivedi et al., 2021: fig. 3B). The present discovery of a male T. serratipes shows that the P3 leg character it is not a suitable distinguishing character as it seems to be associated with sexual dimorphism. Although the morphology of the present male of T. serratipes ( Fig. 1A, D View Fig ) is similar to that of T. bengalensis (cf. Trivedi et al., 2021: fig. 3B), four additional characters can still separate the two taxa: the chela is proportionately longer in both sexes of T. serratipes ( Fig. 1C View Fig ; Anker & Ng, 2014: fig. 1F) (vs. the chela being proportionately shorter in T. bengalensis ; Trivedi et al., 2021: fig. 2E); the proximal part of the pollex has two or three teeth on the cutting edge ( Fig. 1C View Fig ; Anker & Ng, 2014: fig. 1F) (vs. with only one tooth; Trivedi et al., 2021: fig. 2E); the male telson is less sunken into the distal margin of somite 6 ( Figs. 1G View Fig , 2B View Fig ) (vs. prominently sunken in into the distal margin of somite 6; Trivedi et al., 2021: fig. 2D); and the G1 has the terminal chitinous process proportionately broader at the base ( Fig. 2C–E View Fig ) (vs. the G1 has the terminal chitinous process basally narrower base in T. bengalensis ; Trivedi et al., 2021: fig. 3E, F).
No author has discussed possible sexual dimorphism in Tritodynamia species. This is despite the fact that most authors use carapace proportions and leg proportions (especially those of P3) to separate species, and the several keys and tabular comparisons between species mainly use these characters (cf. Shen, 1932, 1935; Yang & Tang, 2005; Rahayu & Ng, 2021). Two species T. fujianensis Chen, 1979 , T. longipropoda Dai , in Dai, Feng, Song & Chen, 1980, and T. yeoi Naruse & Ng, 2010 , are known only from males ( Chen, 1979; Dai et al., 1980; Naruse & Ng, 2010); while the types of T. fani Shen, 1932 , are almost certainly juveniles. Shen (1932: 127) reported that he probably had five males and four females in his type series of the species but noted that the female pleons are still narrow like those of the male and he did not figure the first gonopod and pleon like he did with the other species. His figure of the dorsal habitus ( Shen, 1932: text-fig. 73) and the small size reported (the largest male is only 7.5 × 5.0 mm) suggest that all the types of T. fani are immature.
For the other species, Shen (1932: 120 text fig. 69b, c) commented that the male chela of T. rathbuni was relatively larger compared to other congeners; as did Yang & Tang (2005: 782, fig. 1C, D) for T. bidentata . The figures of T. dilatata by Yang & Sun (1996: fig. 1B, C) showed that the male chela is likewise larger than the female chela. Dai et al. (1980: 138) recorded two males and two females of T. hainanensis Dai , in Dai, Feng, Song & Chen, 1980, but did not comment on any sexual dimorphism. In his overview of Chinese species, Shen (1935) did not comment on sexual dimorphism but his table of measurements ( Shen, 1935: 24) is interesting. For T. intermedia , the male and female carapace width-to-length ratios are 1.5 and 1.8, respectively, i.e., the female carapaces are proportionately wider; while the P3 merus has the following length-to-width ratios: male 2.1, female 1.8; i.e., the males have longer legs. For T. horvathi Nobili, 1905 , Shen (1935) reported male and female carapace width-to-length ratios as 1.4 and 1.5 respectively, i.e., females were only slightly wider; while the P3 merus length-to-width ratios were the same (2.0) for both sexes ( Shen, 1935: 24). In T. serratipes , the male P3 and P4 meri (and propodi) are proportionately longer than in the female, like T. intermedia . Rahayu & Ng (2021) had one male and one female of T. nontjii , with carapace width-to-length ratios of 2.2 and 2.1, respectively; no ambulatory leg differences were recorded.
The prominently serrated P3 merus and propodus, and the relatively slender G1 with the strongly bent, sharp and elongate chitinous distal part are characters unique to T. serratipes and T. bengalensis . In all other congeners, the P3 merus and propodus are at most uneven or granular, never serrate; and the G1 is stout, with the distal part rounded, bilobed to varying degrees, sometimes gently curved, but never with a chitinous extension. Once all the members of the genus can be reviewed, it may be necessary to recognise a separate genus for these two species.
R |
Departamento de Geologia, Universidad de Chile |
V |
Royal British Columbia Museum - Herbarium |
NHM |
University of Nottingham |
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
Kingdom |
|
Phylum |
|
Class |
|
Order |
|
Family |
|
Genus |
Tritodynamia serratipes Anker & Ng, 2014
Ng, Peter K. L. & Clark, Paul F. 2023 |