Caridina lobocensis Cai, Choy & Ng, 2009
publication ID |
https://doi.org/10.3390/d16040200 |
DOI |
https://doi.org/10.5281/zenodo.15091684 |
persistent identifier |
https://treatment.plazi.org/id/D477D357-D222-A52E-7E93-C0D9FADC0037 |
treatment provided by |
Carolina (2025-03-26 18:54:20, last updated 2025-03-26 19:58:48) |
scientific name |
Caridina lobocensis Cai, Choy & Ng, 2009 |
status |
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Caridina lobocensis Cai, Choy & Ng, 2009 View in CoL
Figures 3D View Figure 3 and 6 View Figure 6 .
- Caridina lobocensis Cai, Choy, and Ng, 2009: 68 , Figures 2–4 View Figure 2 View Figure 3 View Figure 4 [type locality: Tributary of Loboc River, Loboc (approx. 9 ◦ 38.206 ′ N, 124 ◦ 1.807 ′ E), Bohol Island, Philippines];
-? Caridina lobocensis —de Mazancourt et al., 2019 [47]: 166, Figures 2–5 View Figure 2 View Figure 3 View Figure 4 View Figure 5 .
Material examined
PALAU: Babeldaob Island . MNHN-IU-2024-455 (DNA: CA1552 ): 1 ♀ ovig. cl 4.6 mm and MNHN-IU-2024-456 (DNA: CA1553 ): 1 ♀ ovig. cl 4.2 mm, Ngerchokl river ( Station 2), 07 ◦ 36.527 ′ N, 134 ◦ 36.958 ′ E, 27 February 2011, coll. M. Castelin, P. Keith, P. Gerbeaux, G. Marquet, and L. Taillebois. GoogleMaps MNHN-IU-2024-457 (DNA: CA1056 ): 1 ♀ ovig. cl 4.2 mm and MNHN-IU-2024-458 (DNA: CA1554 ): 1 ♀ ovig. cl 4.3 mm, Tireloich river ( Station 3 ), 07 ◦ 41.417 ′ N, 134 ◦ 37.754 ′ E, 28 February 2011, coll. M. Castelin, P. Keith, P. Gerbeaux, G. Marquet, and L. Taillebois. GoogleMaps MNHN-IU-2024-459 (DNA: CA1555 ): 1 ♀ ovig. cl 4.3 mm, West Coast stream Northern Tip ( Station 4 ), 07 ◦ 43.056 ′ N, 134 ◦ 36.924 ′ E, 28 February 2011, coll. M. Castelin, P. Keith, P. Gerbeaux, G. Marquet, and L. Taillebois. GoogleMaps MNHN-IU-2024- 460 (DNA: CA1556 ): 1 ♀ ovig. cl 4.4 mm, Ngermeskang river ( Station 6 ), 75 m a.s.l., 07 ◦ 32.484 ′ N, 134 ◦ 34.670 ′ E, 1 March 2011, coll. M. Castelin, P. Keith, P. Gerbeaux, G. Marquet, and L. Taillebois. GoogleMaps USNM 105446 : 2 ♀, cl 4.3–4.8 mm and 1 juv. cl 2.3 mm, Station 122 , 7 ◦ 42.885 ′ N, 134 ◦ 37.386 ′ E, 23 August 1955, Coll. F.M. Bayer. GoogleMaps USNM 105447 : 2 ♀ ovig., cl 4.4–5.0 mm and a juv. cl 3.0 mm, Station 241 , 7 ◦ 32.833 ′ N, 134 ◦ 35.766 ′ E, 18 October 1955, coll. H.A. Fehlmann. GoogleMaps USNM 105448 : 1 ♀ ovig., cl 3.0 mm and 2 ♀, cl 3.0– 3.9 mm, Arakitaoch river , cascade zone , 7 ◦ 31.557 ′ N, 134 ◦ 34.202 ′ E, 4 November 1956, coll. H.A. Fehlmann. GoogleMaps Koror Island: USNM 105445 : 2 ♀, 4.5–4.9 mm, Station 194 , 7 ◦ 20.421 ′ N, 134 ◦ 29.642 ′ E, 30 September 1955, coll. H.A. Fehlmann. GoogleMaps
THE PHILIPPINES. RMNH.CRUS.D.54659 : 1 ♀ ovig., cl 7.1 mm, Barrio Mainit , Tayabas , Quezon Province, Luzon , 2 November 1986, coll. D.S. Bale.
Description
Cephalothorax. Suborbital angle indistinguishably fused with antennal spine. Pterygostomian margin rounded. Rostrum ( Figure 6k View Figure 6 ): straight, short, 0.4–0.5 times length of cl, reaching middle of the third segment of antennular peduncle, armed with 12–17 teeth on dorsal margin, 1–3 of them situated on carapace behind orbital margin, ventral margin with 2–3 teeth.
Eyes well-developed, anterior end reaching to 0.7 times length of basal segment of antennular peduncle. Antennular peduncle 0.54 times as long as carapace. Anterolateral angle reaching 0.28 times length of the second segment, second segment slightly shorter than third segment. Stylocerite reaching to the basal segment of antennular peduncle.
Pereiopods. Epipods on first four pereiopods. P1 ( Figure 6a View Figure 6 ): chela about 1.3–1.6 times as long as wide, movable finger 1.9–2.4 times as long as wide, 0.5–0.7 times length of palm; carpus 1.3–1.6 times as longas wide. P2 ( Figure 6b View Figure 6 ) more slender and longer than first pereiopod with chela 2.2–2.8 times as long as wide: movable finger 3.5–5.0 times as long as wide, 1.3–1.7 times length of palm; carpus slender 4.3–5.5 times as longas wide. P3 ( Figure 6c View Figure 6 ): stout, dactylus ( Figure 6e View Figure 6 ) 3.7–4.4 times as longas wide (terminal spiniform seta included) terminating in two very strong claws with four-five spiniform setae on flexor margin; propodus 7.3–9.9 times as longas wide, 3.7–4.4 times as longas dactylus. P5 ( Figure 6d View Figure 6 ): dactylus ( Figure 6f View Figure 6 ) with two strong claws, 2.5–3.7 as long as wide with 31–33 spiniform setae on flexor margin; propodus 11.7–14.3 times as long as wide, 4.3–7.4 times as long as dactylus.
Abdomen. Third abdominal somite with moderately convex dorsal profile. Sixth abdominal somite 0.45 times as long as carapace, 1.3 times as long as fifth somite, and 0.77 times as long as telson.
Telson ( Figure 6g View Figure 6 ) two times as long as wide, with four pairs of dorsal spinules and one pair of dorsolateral spinules; posterior margin without a median process, rounded with from seven to nine very long intermediate plumose setae longer than lateral ones.
Pl1 and Pl2: no males in our collected specimens. According to Cai et al. [50], “Endopod of male first pleopod subtriangular, half-length of exopod, appendix interna stout, exceeding end of endopod. Appendix masculina of male second pleopod 2/3 length of endopod, with appendix interna reaching base of distal one-third of appendix masculina”.
Uropodal diaeresis ( Figure 6i View Figure 6 ) with 16–21 spinules.
Pre-anal carina ( Figure 6j View Figure 6 ) elevated, without spine but with a few stiff setae.
Ovigerous females with eggs sized 0.37–0.43 mm × 0.22–0. 27 mm ( Figure 6h View Figure 6 ).
Habitat
This species is largely rheophile and prefers waters that are fresh and fast-flowing waters the lower to the higher courses.
Colour pattern
Unknown.
Distribution
This species has been found in Palau and the Philippines.
Remarks
Our specimens agree well with those described from Bohol Island (Philippines) by Cai et al. [50] in relation to their long stylocerite, their stout first pereiopod, their short fingers, their third to fifth pereiopods ending in two claws, and their egg size. The rostrum in our specimens seems shorter: reaching the middle of the third segment of antennular peduncle (vs. reaching slightly beyond end of antennular peduncle) and its pterygostomian margin is rounded (vs. pterygostomian margin subrectangular), but we consider these differences to be within intra-specific variability. This species is closely related to C. buehleri and C. gueryi, both recently re-described by de Mazancourt et al. [43], but they are clearly separated in our molecular analyses and they can be distinguished by its P1 chela 1.3–1.6 times as long as wide (vs. 2.2–2.3 for C. buehleri and 1.9–2.4 for C. gueryi), and by its P5 dactylus with two strong claws (vs. one strong claw for C. buehleri and C. gueryi). Its P2 carpus is 4.3–5.5 times as long as wide and its P5 propodus is 4.3–7.4 times as long as its dactylus (vs., respectively, 5.5–6.2 and 3.8–4.1 for C. buehleri). Its rostrum is armed with dorsal teeth, one–three of them situated on carapace behind orbital margin (vs. three–five for C. gueryi) and its P5 dactylus has 31–33 spiniform setae on its flexor margin (vs. 26–31 for C. gueryi).
Figure 3. Phylogenetic tree of the atyid species from Micronesia obtained by Bayesian inference from the 16S rRNA. Numbers above branches indicate Bayesian posterior probabilities, numbers under branches indicate maximum likelihood bootstraps. Letters A–K for the clades refer to the species listed in the taxonomic account.
Figure 4. Atyoida chacei sp. nov. (a) first pereiopod of female; (b) first pereiopod of male; (c) second pereiopod of female; (d) second pereiopod of male; (e) third pereiopod; (f) dactylus of third pereiopod; (g) fifth pereiopod; (h) dactylus of fifth pereiopod; (i) uropodal diaeresis; (j) pre-anal carina; (k) telson; (l) male first pleopod, endopod; (m) male second pleopod; (n) undeveloped eggs; (o) cephalothorax; (p,q) rostrum variations. Holotype MNHN-IU-2024-439 (DNA: 1858): i, l, m, and p. Paratypes: MNHN-IU-2024-440 (DNA: CA1859): b, d, and q; MNHN-IU-2024-442 (DNA: CA1860): e, f, j, k, and o; MNHN-IU-2024-446 (DNA: CA1871): a, c, g, h, and n.
Figure 5. Caridina ponapensis sp. nov. (a) first pereiopod; (b) second pereiopod; (c) third pereiopod; (d) fifth pereiopod; (e) dactylus of third pereiopod; (f) dactylus of fifth pereiopod; (g) pre-anal carina; (h) uropodal diaeresis; (i) telson; (j) undeveloped eggs; (k) male first pleopod; (l) male second pleopod; (m) rostrum; (n) cephalothorax. Holotype: MNHN-IU-2024-447: h, k, l, and m. Paratypes: MNHN-IU-2024-451 (DNA: CA1391): a–f, i, j, and n; MNHN-IU-2024-452 (DNA: CA1388): g.
Figure 6. Caridina lobocensis. (a) first pereiopod; (b) second pereiopod; (c) third pereiopod; (d) fifth pereiopod; (e) dactylus of third pereiopod; (f) dactylus of fifth pereiopod; (g) telson; (h) undeveloped eggs; (i) uropodal diaeresis; (j) pre-anal carina; (k) cephalothorax. MNHN-IU-2024-459 (DNA: CA1555): a, b, j, and k; MNHN-IU-2024-455 (DNA: CA1552): d and f; MNHN-IU-2024-456 (DNA: CA1553): g, h, and i; MNHN-IU-2024-460 (DNA: CA1556): c and e.
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 |
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InfraOrder |
Caridea |
Family |
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Genus |
Caridina lobocensis Cai, Choy & Ng, 2009
Mazancourt, Valentin de, Marquet, Gérard & Keith, Philippe 2024 |
Caridina lobocensis
Cai, Choy, and Ng 2009: 68 |
Caridina lobocensis
Cai, Choy, and Ng 2009 |