Reinhardorhynchus soror Diez, Reygel & Artois, 2021

Diez, Yander L., Monnens, Marlies, Aguirre, Rosa Isabel, Yurduseven, Rana, Jouk, Philippe, Van Steenkiste, Niels W. L., Leander, Brian S., Schockaert, Ernest, Reygel, Patrick, Smeets, Karen & Artois, Tom, 2021, Taxonomy and phylogeny of Koinocystididae (Platyhelminthes, Kalyptorhynchia) with the description of three new genera and twelve new species, Zootaxa 4948 (4), pp. 451-500 : 478-479

publication ID

https://doi.org/ 10.11646/zootaxa.4948.4.1

publication LSID

lsid:zoobank.org:pub:44061E80-81B7-46AF-AD51-9B461C2E2B67

DOI

https://doi.org/10.5281/zenodo.4629269

persistent identifier

https://treatment.plazi.org/id/19AA34C8-D7BD-4299-93C0-31856253020B

taxon LSID

lsid:zoobank.org:act:19AA34C8-D7BD-4299-93C0-31856253020B

treatment provided by

Plazi

scientific name

Reinhardorhynchus soror Diez, Reygel & Artois
status

sp. nov.

Reinhardorhynchus soror Diez, Reygel & Artois sp. n.

( Fig. 14 View FIGURE 14 )

urn:lsid:zoobank.org:act:19AA34C8-D7BD-4299-93C0-31856253020B

Material and distribution. Observations on live specimens, whole mounted afterwards. Three whole mounts from Tombolo West (08°48’05”N; 79°33’15”W) (Type Locality), Taboga Island, Panama (December 9, 2011), one of which designated holotype ( USNM 1642508 View Materials ), the others in the USNM (1642509–1642510), from medium-coarse sand with ripple marks close to swash zone, small waves, salinity 28 GoogleMaps ‰.

Etymology. Species name refers to its similarities with R. beatrizae sp. n. Lat. soror : sister.

Diagnosis. Species of Reinhardorhynchus gen. n. with a copulatory bulb encompassing a spiny cirrus and two distal hooks. Cirrus armed with triangular, ±5-μm-long spines. It also has a ±437-μm-long belt of spines, which shows three distinct regions: 1) a proximal part with curved and hook-shaped spines fused at their bases, the largest one ±57 μm long, the others measuring 6–40 μm, 2) a middle part with 3-μm-long spines, and 3) a distal, combshaped part armed with ±39-μm-long and triangular spines. The larger of the distal hooks curved, ±87 μm long and ±68 μm wide at its base; its base provided with a funnel-like, ±70-μm-long hook. Smaller hook ±59 μm long and ±59 μm wide at its base.

Description. The specimens are 1.5–2.2 mm long (x̄ = 1.7 mm; n = 3), translucent, with two rounded eyes ( Fig. 14A View FIGURE 14 : e). The proboscis ( Fig. 14A View FIGURE 14 : pr) is of the typical koinocystidid construction (see Brunet 1972; Karling 1980); it represents 15% of the body length in live specimens. The pharynx ( Fig. 14A View FIGURE 14 : ph) has a diameter of 15% of the body length in live specimens and is located at 40–50%.

The testes ( Fig. 14A View FIGURE 14 : t) are located rostral to the pharynx. The seminal vesicles ( Fig. 14A View FIGURE 14 : sv) fuse just before entering the copulatory bulb. The male copulatory bulb is globular and 320–391 μm long (x̄ = 356 μm; n = 2). The prostate vesicle ( Fig. 14A View FIGURE 14 : pv) opens into the armed cirrus. The cirrus is of the same structure as that of R. beatrizae sp. n. The cirrus ( Fig. 14A View FIGURE 14 : ci) is armed with triangular, 4–5-μm-long spines (x̄ = 5 μm; n = 35) ( Fig. 14F View FIGURE 14 : cis). The cirrus also includes a 437-μm-long belt of spines (n = 1) ( Fig. 14A View FIGURE 14 : cir), which consists of three parts. The proximal part is provided with spines that are curved and hook shaped ( Fig. 14B, 14F View FIGURE 14 : cps, 14G), the largest one 55–60 μm long (x̄ = 57 μm; n = 3) and the other ones 6–40 μm long (x̄ = 18 μm; n = 3). This proximal part forms a continuous 62–72-μm-long row (x̄ = 66 μm; n = 3). The middle part forms a broad surface consisting of 3-μm-long spines ( Fig. 14F View FIGURE 14 : cms) and measuring 109 μm (n = 1). The distal part is 129–135 μm long (x̄ = 132 μm; n = 2) and consists of a continuous comb-shaped row of spines ( Fig. 14C, 14F View FIGURE 14 : cds). The spines in this part are 20–59 μm long (x̄ = 39 μm; n = 44) and increase in size from the most proximal one to the most distal one.

There are two large distal hooks. The larger one ( Fig. 14A & 14F View FIGURE 14 : h 1, 14E) is 84–89 μm long (x̄ = 87 μm; n = 3) and 63–77 μm wide at its base (x̄ = 68 μm; n = 3), curved, and carries a funnel-like and 65–80 μm long (x̄ = 70 μm; n = 3) projection at its base ( Fig. 14E–F View FIGURE 14 : fh). This structure is straight, makes a ±90º angle with the main hook, and ends in a blunt tip. The hook proper is strongly curved and ends in a sharp tip. At its base, there is a small, more or less square and folded projection ( Fig. 14E View FIGURE 14 : fp). The smaller hook ( Fig. 14A & 14F View FIGURE 14 : h2, 14D) is 57–89 μm long (x̄ = 59 μm; n = 3) and 54–62 μm wide (x̄ = 59 μm; n = 3) at its base. The base of this hook is asymmetrical. The hook is slightly curved and ends in a sharp tip.

Vitellaria were not observed. The ovaries are oval shaped ( Fig. 14A View FIGURE 14 : ov), located rostral to the copulatory bulb, with the oocytes organised in a row. The oviducts open into the female duct. The female duct opens into the receptacle bursa (terminology of Karling 1980) ( Fig. 14A View FIGURE 14 : rb) through a strong sphincter. In a live specimen one embryo ( Fig. 14A View FIGURE 14 : em), apparently not surrounded by a shell, was observed, suggesting the species is (ovo-)viviparous. The common gonopore ( Fig. 14A View FIGURE 14 : cg) is located ventrally, at 90%.

USNM

Smithsonian Institution, National Museum of Natural History

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