Polycystidinae Schockaert and Karling 1970

Subfamily POLYCYSTIDINAE Schockaert and Karling, 1970 Genus Austrorhynchus Karling, 1952 Austrorhynchus wennersgaardi Volonterio and Ponce de León, sp. nov. (Figures 1–4) Diagnosis Austrorhynchus species with eyes and white to greyish parenchyma. Type II prostate stylet, double-walled; funnel about...

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Main Authors: Volonterio, Odile, Ponce de León, Rodrigo
Format: Text
Language:unknown
Published: Zenodo 2018
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Online Access:https://dx.doi.org/10.5281/zenodo.5187221
https://zenodo.org/record/5187221
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Summary:Subfamily POLYCYSTIDINAE Schockaert and Karling, 1970 Genus Austrorhynchus Karling, 1952 Austrorhynchus wennersgaardi Volonterio and Ponce de León, sp. nov. (Figures 1–4) Diagnosis Austrorhynchus species with eyes and white to greyish parenchyma. Type II prostate stylet, double-walled; funnel about 20–25% of total stylet length, with the proximal rim rolled upon itself to a varying degree; tube of the outer stylet slightly bent, with the inner stylet extending throughout its length; a strongly bent hook arises at the level of the junction between the funnel and the tube; hook and tube of about the same size. Type III stylet with a foot and a shorter style connected by a long bridge, defining a broad window; style expands to a thin comb-bearing plate with large teeth, decreasing in size and thickness towards the base of the flagellum; in general, the third to seventh teeth from the free end of the plate are the larger ones, and their bases are frequently placed at a higher level than those of the rest; foot continues into a sinuous to straight, narrow flagellum, bearing a distal expansion; a row of progressively shorter, fine teeth extends from the base of the flagellum to the proximal part of the expansion. Oviparous. Description General organization. Preserved specimens are 431–1044 µm (mean 711.0, SD 191.5) long, white to greyish, rather opaque and bear two eyes (Figure 1). Proboscis about 10–20% of body length. Pharynx 68–158 µm (mean 123.7, SD 30.9) in diameter. Testes paired. Seminal vesicle tapers into an ejaculatory duct opening into proximal end of male genital canal, between bases of type II and III prostate stylets. Prostate vesicle of type II associated with type II stylet. Compact muscle sheet connects wall of prostate vesicle to base of type III stylet. Paired ovaries and vitellaria. Ovo-vitelloducts of each side join into a common ovovitelloduct. Female bursa connected to a female duct type I, which opens into posterior wall of genital atrium. Common ovo-vitelloduct and insemination ducts open into bursal stalk. Uterus opens into anterior wall of distalmost portion of atrium. Sclerotized parts of copulatory organ. The double-walled type II prostate stylet (Figure 2 (a,b)) is 40–49 µm (mean 44.5, SD 2.2) long and consists of a funnel, a distal tube and a hook. The funnel is 8–14 µm (mean 10.4, SD 1.6) long (about 20–25% of the total stylet length) and 22–33 µm (mean 28.9, SD 2.8) wide proximally; its proximal rim is broad and rolled upon itself to a varying degree. Tube of outer stylet slightly bent, 27–34 µm (mean 31.1, SD 2.0) long, 11–17 µm (mean 13.8, SD 1.6) wide proximally and 5–8 µm (mean 6.4, SD 1.1) wide distally; inner stylet extends throughout its length. In a few specimens, distal portion of tube of outer stylet is dilated (Figure 2 (b)). A large, 28–34 µm (mean 31.0, SD 2.1) long, strongly bent hook arises at the level of the junction between the funnel and the tube. Type III prostate stylet (Figure 2 (c,d)) has a foot and style connected by a long bridge, defining a broad window. Style expands to a thin comb-bearing plate carrying 22–27 µm (mean 24, SD 1.9) large teeth. In general, third to seventh teeth from free end of plate are the larger ones, measuring 10–15 µm (mean 12.1, SD 1.6) in length; their bases are frequently placed at a higher level than those of the rest (Figure 2 (d)). Remaining teeth on comb decrease in size and thickness towards base of flagellum. Flagellum, 29–37 µm (mean 32, SD 2.6) in length, is sinuous to straight and has a distal expansion; a row of progressively shorter, fine teeth extends up to proximal part of latter. Distance from proximal end of foot to tip of flagellum is 59–77 µm (mean 71.5, SD 4.7). Histology. At the histological level, the overall characteristics of the new species are in agreement with the previous histological descriptions of Austrorhynchus (Karling 1952; Brunet 1965); the relevant differences are described below. The genital canal can be divided into three sections based on the histology of its wall (Figure 3 (a)): (i) the proximal portion of the male genital canal, with an epithelium bearing pseudo-cilia surrounded by an internal layer of thin circular muscle fibres and two external layers composed of thick, oblique fibres; (ii) the distal portion of the male genital canal, where the internal oblique fibres adopt a longitudinal direction and the external ones are replaced by a sphincter; (iii) the atrium inferius sensu Karling 1952, with an epithelium bearing long pseudo-cilia and a mono-layer of thin circular muscle fibres surrounded by scarce longitudinal fibres. Most of the longitudinal fibres present in the distal portion of the male genital canal leave the wall of the canal immediately below the sphincter and attach to the ventral body wall close to the gonopore. In a few specimens (for example, NHMUK 2017.11.3.11), the anterior wall of the genital canal is dilated at the level of the sphincter, forming a pouch (Figure 3 (a,b), indicated with an arrowhead). Sperm cells seen in the male genital canal were always located in the vicinity or at the level of the sphincter, either in the main cavity of the canal or inside the pouch. Gland cells open into the dorsal wall of the bursal stalk, just posteriorly to the opening of the common ovo-vitelloduct. In a few specimens, the ventral wall of the bursal stalk presents an expansion filled with sperm cells (Figure 3 (a,c), indicated with an asterisk). Material examined Holotype. One whole mount of a specimen from Balvino Point, King George Island, South Shetland Islands (62.188889ºS, 58.903889ºW), Antarctica, collected by Odile Volonterio and Rodrigo Ponce de León on 22 January 2009, deposited in the Natural History Museum (NHM), London (accession number: NHMUK 2017.11.3.1). Paratypes. Eight slides with whole mounts of specimens from Balvino Point, Maxwell Bay, King George Island, South Shetland Islands (62.188889ºS, 58.903889ºW), Antarctica, collected by Odile Volonterio and Rodrigo Ponce de León on 19 December 2006 (two slides), 5 January 2008 (one slide), 6 January 2009 (one slide), 24 January 2009 (two slides) and 6 February 2009 (two slides with gravid specimens); one slide with a whole mount of a specimen from Pata de Perro Point, Maxwell Bay, King George Island, South Shetland Islands (62.185278°S, 58.878889°W), Antarctica, collected by Odile Volonterio and Rodrigo Ponce de León on 29 January 2010. Deposited in the Natural History Museum (NHM), London (accession numbers: NHMUK 2017.11.3.2–9 and 2017.11.3.10 respectively). Additional material. Two slides with sagittal sections of two specimens from Balvino Point, King George Island, South Shetland Islands (62.188889ºS, 58.903889ºW), Antarctica, collected by Odile Volonterio and Rodrigo Ponce de León on 22 January 2009, deposited in the Natural History Museum (NHM), London (accession number: NHMUK 2017.11.3.11–12). Biology The species is oviparous. In February 2009 two gravid specimens, each carrying a single egg, were found; eggs are oval, 282–299 µm (mean 290.5, SD 12.0, n = 2) long, 231–243 µm (mean 237.0, SD 8.5, n = 2) wide and present a short adhesive peduncle (Figure 4). Distribution King George Island, South Shetland Islands, Maritime Antarctic. Etymology Specific name in honour of the Norwegian sailor Ole Wennersgaard, a crew member of the Swedish Antarctic Expedition who died during the extreme Antarctic winter of 1903, when part of the expedition was forced to remain in Poulet Island until rescued by the vessel Uruguay (Ekelof 1904). : Published as part of Volonterio, Odile & Ponce de León, Rodrigo, 2018, A new species of Austrorhynchus (Platyhelminthes: Kalyptorhynchia) from King George Island (Maritime Antarctic), pp. 739-750 in Journal of Natural History (J. Nat. Hist.) (J. Nat. Hist.) 52 (11 - 12) on pages 741-746, DOI: 10.1080/00222933.2018.1444212, http://zenodo.org/record/5174376 : {"references": ["Schockaert ER, Karling TG. 1970. Three new anatomically remarkable Turbellaria Eukalyptorhynchia from the North American Pacific coast. Arkiv Zool. 23: 237 - 253.", "Karling TG. 1952. Kalyptorhynchia (Turbellaria). In: Odhner NHJ, editor. Further Zoological results of the Swedish Antarctic Expedition 1901 - 1903. Vol. 4 (9). Stockholm: Norstedt & Soner; p. 1 - 54.", "Brunet M. 1965. Turbellaries calyptorhynques de substrats meubles de la region de Marseille [Kalyptorhynch turbellarians from mobile substrates of the Marseille region]. Recl Trav Stn mar Endoume. 39: 127 - 219. French. [COMNAP / SCAR] Council of Managers of National Antarctic Programs and Scientific Committee on Antarctic Research. 2000. Antarctic Environmental Monitoring Handbook, Standard techniques for monitoring in Antarctica. Hobart: COMNAP / SCAR Publication.", "Ekelof E. 1904. Medical aspects of the Swedish Antarctic Expedition, October 1901 - January 1904. J Hyg (Lond). 4: 511 - 540."]}