Pseudopallene constricta
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Familia: Callipallenidae
Genus: Pseudopallene
Name
Pseudopallene constricta Arango, Claudia P., 2013 – Wikispecies link – Pensoft Profile
- Pseudopallene constricta Arango, Claudia P., 2013, Zootaxa 3616: 422-424.
Materials Examined
Material examined: Holotype (J 4519): 1 male (PSE 2), Nov- 2009, Eaglehawk Neck, Tasmania, 5–20 m depth, on Orthoscuticella spp. Paratypes (S 92223): 4 males (including PSE 2 a), 3 females (including PSE 2 b), 2 postembryonic stages (PSE 10, PSE 10 a); all from the same location as holotype.
Diagnosis
Diagnosis: Medium-sized species; uniformly yellow when live; marked constriction of proboscis at mid-point, chela fingers straight, tips weakly or distinctly crossing when closed, leaving a narrow proximal gap in between, femora curved, legs slender, with no constrictions, with rows of nodulose, short spines giving ‘prickly’ appearance to legs under high magnification; prominent propodal heel with four stout heel spines. Sequence divergence ranges from 10 to 13 % in COI and 6 to 23 % in ITS.
Description
Description of male: Leg span 32 mm, live colouration uniform bright yellow on body and legs. Body (Fig. 12 A,C) fully segmented; neck about 0.5 mm long, parallel sides in between the ovigers insertion and the constriction between the neck and a laterally expanded cephalon; cephalon without conspicuous pre-ocular middorsal mound, or longitudinal cuticular division line. Ocular tubercle (Fig. 12 A,C) as wide as tall, with only weakly protruding dorsal papillae; four small, darkly pigmented eyes, all of equal size. Lateral processes (Fig. 12 C) 1.25 as long as wide, glabrous, separated by about one-quarter of their basal diameter. Abdomen (Fig. 12 C) straight, overreaching the distal margin of the fourth lateral processes. Proboscis (Fig. 12 A,B) directed ventrally, with conspicuous mid-point constriction, somewhat inflated in distal part, tapering to oral tip, mamilliform, no tuft of setae visible.
Cheliphore (Fig. 12 A,B) scape one-articled, indistinct proximal constriction, as long as proboscis. Chelae robust, outer surface of palm inflated, spare minute spinules; fingers subequal in length, 80 % of palm length, finger tips cross when closed, leaving proximal gap, immovable finger with straight cutting edge, movable finger slightly curved. Oviger (Fig. 12 F) fifth article longest, with distinct apophysis distally; strigilis articles subequal, spine formula 12: 6: 6: 6; terminal claw ~ 70 % of tenth article length, acute, endal margin denticulate, only distal half of ectal margin denticulate. Legs (Fig. 12 D,E) 4.3 times as long as body, with minute spines arranged in longitudinal rows. Second coxa 2.5 as long as subequal first and third; femur curved; tibia 1 distally swollen, shorter than femur; tibia 2 straight, longest article; tarsus typical, with one main distal spine, covered in tiny setae; propodus curved, prominent heel with row of four stout spines, two middle ones larger; sole with median row of 14–15 small spines. Main claw long, nearly 70 % of propodus length. Genital pores on second coxae of third and fourth leg pairs. Measurements of male holotype in mm: body length = 3.32; body width = 1.96; abdomen length = 0.53; ocular tubercle height = 0.32; proboscis length = 1.18; scape = 1.19; chela fingers = 0.57; oviger 5 th article = 1.16, 10 th article = 0.27, claw = 0.13; 3 rd leg coxa 1 = 0.58, coxa 2 = 1.72, coxa 3 = 0.67, femur = 3.13, tibia 1 = 2.73, tibia 2 = 3.42, tarsus = 0.23, propodus = 1.03, claw = 0.68.
Etymology
Etymology: The species name refers to the characteristic constriction of the proboscis, which serves to readily distinguish this species from similarly coloured, sympatric congeners.
Discussion
Remarks: Previously, Stevenson (2003) in his MSc thesis investigated specimens of this form, which had been collected at the same sampling site. In accordance with the present study, he found morphological as well as molecular evidence (16 S rDNA and COI fragments) in support of its valid species status, without, however, presenting a formal species description. Recent studies (Brenneis et al.2011 a, b) have focussed on the development of the yellow Pseudopallene species from Tasmania. The investigation of post-embryonic development was conducted on the transparent-yellowish post-embryonic stages that have been clearly assigned by the molecular data to P. constricta sp. nov. (see Brenneis et al.2011 b for morphological description of postembryonic stages). During the collection period (second half of November), all yellow Pseudopallene species encountered in the study area did carry eggs. Yet, in P. constricta, they were observed to be generally in later developmental stages, males often bearing already hatched post-embryonic stages 1 and 2. This might be indicative of a slight shift in the reproductive periods of the sympatric Pseudopallene species.
Taxon Treatment
- Arango, Claudia P.; Brenneis, Georg; 2013: New species of Australian Pseudopallene (Pycnogonida: Callipallenidae) based on live colouration, morphology and DNA, Zootaxa 3616: 422-424. doi
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