Synalpheus pinkfloydi, Anker, Arthur, Hultgren, Kristin M. & Grave, Sammy De, 2017

Anker, Arthur, Hultgren, Kristin M. & Grave, Sammy De, 2017, Synalpheus pinkfloydi sp. nov., a new pistol shrimp from the tropical eastern Pacific (Decapoda: Alpheidae), Zootaxa 4254 (1), pp. 111-119 : 112-118

publication ID	https://doi.org/ 10.11646/zootaxa.4254.1.7
publication LSID	lsid:zoobank.org:pub:38E37727-9EDC-4412-98FF-8A7718182E5E
DOI	https://doi.org/10.5281/zenodo.6049802
persistent identifier	https://treatment.plazi.org/id/C11487B2-123C-FFFE-0387-FAABFBFDC550
treatment provided by	Plazi
scientific name	Synalpheus pinkfloydi
status	sp. nov.

Treatment

Synalpheus pinkfloydi View in CoL sp. nov.

( Figs. 1–3 View FIGURE 1 View FIGURE 2 View FIGURE 3 )

Synalpheus aff. antillensis — Hultgren et al. 2014: Suppl. Data 1; Suppl. figs. 2, 3, 5; fig. 3 (cladogram).

Type material. Holotype: male (cl 5.5 mm), MZUSP 33778 View Materials , Panama, Pacific coast, Las Perlas Archipelago, Isla Bartolomé (near Isla Contadora), intertidal and shallow subtidal rocky bottom, in crevices of rocks and living and dead corals, low tide, leg. A. Anker et al., 18.iv.2015 . Paratypes: 1 ovig. female (cl 6.6 mm), MZUSP 34615 View Materials , same collection data as for holotype ; 1 female (cl 5.3 mm), MZUSP 33779 View Materials , Panama, Pacific coast, Las Perlas Archipelago , Isla Contadora, eastern end of Playa Galeon, in crevices of rocks and coral rubble, low tide, leg. A. Anker et al., 16.iv.2015 ; 1 female (cl 4.9 mm), OUMNH.ZC. 2013.03.0 44, Panama, Pacific coast, Las Perlas Archipelago, Isla Saboga, intertidal, in crevices of rock and coral rubble, leg. A. Anker et al., 15.xi.2005 (fcn 05- 074).

Additional material examined. 1 ovig. female (cl 4.7 mm), OUMNH.ZC. 2013.03.0 46, Panama, Pacific coast, Taboga Archipelago , Isla Taboga, channel between Isla Taboga and Isla Taboguilla, rocky intertidal with partly exposed corals, coral rubble and large rocks, leg. A. Anker et al., 21.ii.2007 (fcn 07-066); 1 immature specimen (cl 3.5 mm), OUMNH 2013.03 .0 45, same collection data (fcn 07-061); 1 male (cl 5.2 mm), 1 ovig. female (cl 5.2 mm), OUMNH. 2013.03.0 47, same collection data (fcn 07-065).

Description. Small-sized species of Synalpheus brevicarpus group (maximum cl 6.6 mm in females), with subcylindrical, non-compressed body. Carapace and abdomen smooth, with few scattered setae. Rostrum subtriangular in dorsal view, rounded or subacute distally, slightly longer than wide, equal in length to orbital teeth, of equal width or slightly narrower than orbital teeth ( Fig. 1 View FIGURE 1 A), occasionally reduced. Orbital hoods feebly inflated; orbital teeth broadly triangular, as wide as long or slightly wider, blunt distally; margin between rostrum and orbital teeth forming deep rounded V-shaped sinus ( Fig. 1 View FIGURE 1 A); orbito-rostral process feebly developed. Pterygostomial angle anteriorly produced, blunt ( Fig. 1 View FIGURE 1 B). Posterior margin of carapace with small cardiac notch.

Males with relatively slender pleon; first pleuron with posteroventral margin produced into triangular, slightly ventrally directed tooth; second to fourth pleura truncate ventrally, with blunt angle posteroventrally; fifth pleuron more rounded posteroventrally. Females with bulkier pleon and all pleura rounded ventrally. Telson broad, gradually and slightly tapering distally, posterior margin about 0.6 length of anterior margin; dorsal surface with slight median longitudinal depression and two pairs of spiniform setae, situated approximately at mid-length and 0.7 length of telson, respectively; posterior margin broadly rounded, with two spiniform setae at each posterolateral corner, mesial distinctly longer than lateral; posterolateral corners slightly projecting ( Fig. 1 View FIGURE 1 C).

Antennular peduncle with first article by far longest; stylocerite well developed, with sharp tip and slightly convex lateral margin, reaching 0.7 length of second article; second article slightly longer than wide; third article shortest, wider than long; lateral flagellum with distinct accessory branch ( Fig. 1 View FIGURE 1 A, B). Antenna with basicerite armed with strong, very long distoventral tooth, latter exceeding distal margin of first article of antennular peduncle, but not reaching to stylocerite tip, reaching mid-length of carpocerite; dorsal margin of basicerite bluntly projecting, without acute tooth; scaphocerite with well-developed blade exceeded by strong distolateral tooth, latter not exceeding distal margin of antennular peduncle; carpocerite robust, reaching well beyond end of antennular peduncle ( Fig. 1 View FIGURE 1 A, B).

Mouthparts typical for genus. Third maxilliped with coxa bearing small blunt lateral plate; antepenultimate article as long as ultimate, more robust; penultimate article short, widening distally; ultimate article distally tapering, with distal circlet of at least five, relatively slender, spiniform setae; exopod not overreaching distal margin of antepenultimate article ( Fig. 1 View FIGURE 1 E); arthrobranch well developed (not drawn in Fig. 1 View FIGURE 1 E).

Major cheliped with very short ischium; merus robust, about 2.2 times as long as wide, with strongly convex dorsal margin and flattened ventral surface, distodorsal margin unarmed; carpus very short, cup-shaped; chela ovoid, inflated, subcylindrical; palm smooth, with distodorsal protuberance ending in acute tooth, latter directed somewhat ventrally (downwards); fingers slightly less than half-length of palm; pollex subequal to dactylus; dactylus with relatively short, distally truncate plunger ( Fig. 2 View FIGURE 2 A–E). Minor cheliped with short ischium; merus about 2.5 times as long as maximal width, with convex ventral margin; carpus cup-shaped, constricted ventrally; palm subcylindrical, slightly compressed laterally; fingers shorter than palm; dactylus with setae isolated or organised in tufts, without setal rows; finger tips sharp, simple ( Fig. 2 View FIGURE 2 F, G).

Second pereiopod (fig. 1F) with ischium slightly shorter than merus; carpus consisting of five articles, latter with ratio more or less equal to 4: 1: 1: 1: 2; chela simple, longer than distal-most carpal article, with dense groups of setae ventrally and acute finger tips. Third pereiopod relatively stout; ischium widening distally, unarmed; merus about 3.6 times as long as wide, not particularly inflated; carpus distinctly more slender than merus, about 0.4 length of merus, distoventral margin with small spiniform seta; propodus shorter than merus, armed with several (three to five) spiniform setae on ventral margin, in addition to one distal pair of stronger spiniform setae adjacent to dactylus; dactylus biunguiculate, with accessory (flexor) unguis much shorter than terminal (extensor) unguis ( Fig. 1 View FIGURE 1 G, H). Fourth pereiopod similar to third, more slender. Fifth pereiopod more slender than third and fourth, with much shorter merus; carpus unarmed distoventrally; propodus with four or five small spiniform setae on ventral margin, two spiniform setae adjacent to dactylus and several (at least six) transverse combs of stiff cleaning setae, distolaterally.

Second to fifth pleopods with appendices internae. Uropod reaching far beyond posterior margin of telson; exopod with slender spiniform seta between stout sharp fixed distolateral tooth on exopodal margin and similarly stout lateral tooth of diaeresis, remaining part of diaeresis sinuous; exopod and endopod subequal in length ( Figs. 1 View FIGURE 1 C, D).

Ovigerous female paratype with 17 eggs (majority of eggs from other ovigerous females were subsampled for DNA analyses): eggs ellipsoid, diameter approximately 1.1 x 0.7 mm.

Colour pattern. Body semitransparent with greenish or yellow-olive tinge; deep-red line present between the eyes (seemingly composed of chromatophores on internal wall of carapace or on eyestalks); third maxilliped pinkish distally; major chela bright pink-red on distal half of palm and fingers (colour usually preserved in alcohol), except for amber-yellow finger tips; distal portion of palm and fingers of minor chela also intensely pink; second pereiopod colourless; third to fifth pereiopods with conspicuous reddish chromatophores on carpus and propodus; tail-fan colourless with slight greenish tinge; eggs or ovaries in females dull-green ( Fig. 3 View FIGURE 3 ).

Etymology. Named after the well-known British rock band Pink Floyd, inspired by the bright pink-red claw of the new species. Suggested vernacular name: Pink Floyd pistol shrimp.

Type locality. Las Perlas Archipelago , Bay of Panama.

Distribution. Presently known only from the type locality on the Pacific side of Panama; likely more widespread in the tropical eastern Pacific, but unlikely to occur on the Dark Side of the Moon due to lack of suitable habitat.

GenBank accession numbers. Synalpheus pinkfloydi sp. nov., Panama, Pacific coast (as S. aff. antillensis ): KJ477706 View Materials , KJ595016 View Materials , KJ595015 View Materials ( COI 5 About COI ’ end) ; KJ625120 View Materials (PEPCK); KJ494388 View Materials , KJ595167 View Materials , KJ595166 View Materials (16S) [ OUMNH.ZC. 2013.03.0 46, 2013.03.047]. Synalpheus antillensis , Tobago : KJ595033 View Materials ( COI 5 About COI ’ end), KJ625121 View Materials ( PEPCK), KJ595175 View Materials (16S) [ FLMNH UF 10944]; Panama, Caribbean coast : KJ595034 View Materials ( COI 5 About COI ’ end), KJ625122 View Materials ( PEPCK), KJ595176 View Materials (16S) [voucher deposited in the crustacean reference collection of the Universidad de Panamá, fcn 07-246, specimen listed in Anker et al. 2012].

Remarks. Within the speciose genus Synalpheus , S. pinkfloydi sp. nov. clearly belongs to the S. brevicarpus group, as first defined by Coutière (1909) and recently confirmed to be small monophyletic clade restricted to the Americas ( Hultgren et al. 2014). The S. brevicarpus group is mainly characterised by the rostrum and orbital teeth being similar in shape and length, and includes the western Atlantic S. minus , S. brevicarpus and S. antillensis , and the eastern Pacific S. digueti Coutière, 1909 and S. pinkfloydi sp. nov. (= S. aff. antillensis in Hultgren et al. 2014 ). According to the results of the molecular analyses in Hultgren et al. (2014), S. minus , S. brevicarpus and S. digueti are genetically heterogeneous and at least the latter two taxa may represent species complexes, which remain to be resolved. As a result, the taxonomic status of Coutière’s (1909) varieties and subspecies currently treated as junior synonyms, such as S. minus bahiensis Coutière, 1909 , S. digueti ecuadorensis Coutière, 1909 and S. brevicarpus guerini Coutière, 1909 , will need a thorough re-assessment. The clade containing S. antillensis and S. pinkfloydi sp. nov. is genetically more distant from the other members of the S. brevicarpus group, forming their sister clade ( Hultgren et al. 2014). They differ morphologically from S. minus , S. brevicarpus and S. digueti by the noticeably stouter antennular peduncles (see illustrations in Coutière 1909) and also by the uniform intense pink-red colour of the distal half of the major and minor cheliped ( Fig. 3 View FIGURE 3 ; see also Anker et al. 2012: fig. 10a–c). In the absence of other species with similar morphology and colour in the region and worldwide, S. antillensis and S. pinkfloydi sp. nov. represent, beyond any shadow of a doubt, a pair of transithmian sister taxa (see also below).

The only noticeable morphological differences between S. pinkfloydi sp. nov. and S. antillensis lie in the relative proportions of the merus of the major and minor chelipeds, the distodorsal armature of the major cheliped merus, and the length of the antennal scaphocerite. In S. pinkfloydi sp. nov., the major cheliped merus appears shorter and stouter, its maximal width being only about 0.5 of its length ( Fig. 2 View FIGURE 2 B), whereas the minor cheliped merus is about 2.2 times as long as wide and with a conspicuously convex ventral margin ( Fig. 2 View FIGURE 2 F). In S. antillensis , the major cheliped merus is relatively more slender, its maximal width being at most 0.4 of its length ( Anker et al. 2012: fig. 9d), whereas the minor cheliped merus is about 2.5 times as long as wide, its ventral margin being only slightly convex (ibid.: fig. 9e). In S. pinkfloydi sp. nov., the distodorsal margin of the major cheliped merus is blunt or bears at most a small blunt projection ( Fig. 2 View FIGURE 2 A, B), although in the majority of specimens the latter is poorly developed to absent. In the majority of specimens of S. antillensis , this margin typically bears a small, but relatively well developed, sometimes sharp and curved tooth ( Anker et al. 2012: fig. 9d). The scaphocerite of S. pinkfloydi sp. nov. is slightly shorter than that of S. antillensis , with its distolateral tooth reaching, but usually not overreaching the distal margin of the antennular peducle ( Fig. 1 View FIGURE 1 A). In S. antillensis , the distolateral tooth of the scaphocerite distinctly overreaches the distal margin of the antennular peduncle ( Anker et al. 2012: fig. 9a; see also Coutière 1909: fig. 27a). In addition, S. pinkfloydi sp. nov. appears to be larger than S. antillensis , with four individuals of the material examined exceeding 5.0 mm in cl, in contrast to only a single individual of S. antillensis in the comparative material reaching 4.5 mm in cl.

The above-listed morphological differences are rather subtle and may be subject to some variation. For instance, the proportions of the cheliped merus may be difficult to evaluate directly on the specimens, especially in the absence of comparative material, and may be limited to adult males. Therefore, S. pinkfloydi sp. nov. and S. antillensis can be considered as cryptic species with little to almost no morphological differentiation, similar or identical colour patterns, but being geographically clearly separated as well as genetically distinct. Other examples of transisthmian cryptic species pairs include the alpheid shrimps Alpheus cylindricus Kingsley, 1878 / A. vanderbilti Boone, 1930 (see Anker et al. 2008), and the sesarmid mangrove crabs Aratus pacificus Thiercelin & Schubart, 2014 / A. pisonii (H. Milne Edwards, 1837) (see Thiercelin & Schubart 2014).

The molecular phylogenetic analysis of Synalpheus , which included most of the members of the S. brevicarpus group clearly corroborate the sister position of S. pinkfloydi sp. nov. relative to S. antillensis , as already indicated by morphology and colouration ( Hultgren et al. 2014: fig. 3, as S. aff. antillensis ). That is, multiple specimens of S. pinkfloydi sp. nov. formed a monophyletic clade—sister to a monophyletic clade formed by specimens of S. antillensis —using individual gene trees of the mtDNA genes COI and 16S ( Hultgren et al. 2014, Suppl. fig. 2, 3), as well as in combined phylogenetic analyses of nuclear and mitochondrial data ( Hultgren et al. 2014: fig. 3). The mean genetic distance between S. pinkfloydi sp. nov. and its sister S. antillensis (COI gene, K2P distance) was 10.2%, which is approximately equal to 10 times the mean intraspecific genetic distance in all studied species of Synalpheus , also exceeding the mean divergence between other sister species pairs in this genus (8.1%, Hultgren et al. 2014).

Based on genetic data (10.2% K2P COI distance) and calibration methods used herein, these two taxa diverged approximately 6.8–7.8 mya, i.e. well before the final closure of the Isthmus of Panama, which created an impenetrable barrier in the Central American Seaway ( Lessios 2008 and references therein). The recently proposed, radically different views of the happening and timing of the closure of the Isthmus of Panama ( Bacon et al. 2015; Montes et al. 2015) would contradict the calculated divergence times and imply that the separation of the two transisthmian sister species happened at least 10 mya (in the case of Bacon et al. 2015 already in the Pliocene, i.e. more than 20 mya), which seems rather unlikely given their morphological similarity (see also criticism by O’Dea et al. 2016).

Verrill (1922), in his taxonomically problematic and difficult-to-use report on the Decapoda of Bermuda, named an eastern Pacific taxon as Synalpheus bradleyi Verrill, 1922 , providing only a very short descriptive paragraph in the remarks under S. minus , as well as one diagrammatic drawing of the major cheliped ( Verrill 1922: pl. XXIV, fig. 1). As it was possible that the herein described new species was S. bradleyi , at our request, Eric A. Lazo-Wasem of the Yale Peabody Museum of Natural History, Yale University, New Haven, USA (YPM), provided high-resolution photographs of two specimens labelled “syntype” of S. bradleyi , viz. YPM IZ 000742CR (cl 7.9 mm) and YPM IZ 006629CR (cl 5.3 mm). However, only the first specimen was listed in Verrill’s original report ( Verrill 1922: p. 108). The very distinctive shape of the frontal margin of the carapace of this specimen (YPM IZ 000742CR) indicates that S. bradleyi is not closely related to S. minus or any other species of the S. brevicarpus group, including S. pinkfloydi sp. nov. and S. antillensis . The frontal region of the other specimen labelled as “syntype” (YPM IZ 006629CR) is very different from that of the syntype of S. bradleyi , suggesting that it belongs to a different taxon, which is also distant from the S. brevicarpus group. Since S. bradleyi has absolutely no affinity to S. pinkfloydi sp. nov., its taxonomic status will be discussed elsewhere.