Manayunkia occidentalis Atkinson & Bartholomew & Rouse 2020, sp. nov.

• Main Authors: Atkinson, Stephen D., Bartholomew, Jerri L., Rouse, Greg W.
• Format: Text
• Language: unknown
• Published: Zenodo 2020
• Subjects: Biodiversity; Taxonomy; Animalia; Annelida; Polychaeta; Sabellida; Fabriciidae; Manayunkia; Manayunkia occidentalis; Atkinson; Hallett; Fang; Diaz; Morales; Rouse; Bjork; Beaver Creek
• Online Access: https://dx.doi.org/10.5281/zenodo.3718188; https://zenodo.org/record/3718188

Manayunkia occidentalis sp. nov. Figures 2–4 Manayunkia speciosa : Hazel, 1966; Bartholomew et al . 1997; 2006; 2007; Alexander et al. 2014; Stocking and Bartholomew, 2007; Bjork & Bartholomew 2009; Willson et al . 2010; Atkinson et al ., 2011; Malakauskas et al ., 2013; 2015. Holotype (in 70% ethanol, initially fixed in 10% formalin). Adult male from Klamath River mainstem near confluence with Beaver Creek, California, USA. 41.867240°N, - 122.809763°E, collected by Julie Alexander (OSU), 25 April 2014 (SIO-BIC A12115) Paratypes (in 70% ethanol, fixed in 10% formalin); One specimen, adult female, same locality, collector and date as holotype (SIO A12116); One specimen, adult male, same locality, collector and date as holotype (SIO A12117). Etymology. The specific epithet is derived from the Latin word for “west”, to contrast with M. speciosa , which occurs in eastern and central North American drainages. Description. Holotype (SIO-BIC A12115) a male with eight thoracic segments and three abdominal segments. Total length (unfixed) 3.0 mm, crown 0.3 mm. Body cylindrical with tapering, dorso-ventrally flattened abdomen. Body wall translucent grey with minor brown pigmentation on peristomium and pygidium, and green pigmentation on chaetiger 6. Branchial crown ~10% of total body length. Two pairs of radioles, each with six pinnules. One ventral pinnule on radiole with 4–5 yellow-white spots in life (Fig. 2 B–C). One pair of vascularised, unbranched ventral filamentous appendages present, extending for about two-thirds length of radiolar crown, approximately same width as pinnules (Fig. 2 B–C). Anterior peristomial ring with membranous collar, followed by posterior peristomial ring (Fig. 4 A–B,D). Collar margin smooth, higher ventrally, separated by a narrow dorsal gap that corresponds with ciliated faecal groove (Fig. 4D). Peristomial eyes, black rounded spots (Fig. 2E). Pygidial eyes absent. Superior thoracic notochaetae elongate, narrowly hooded; 5–7 per fascicle (chaetigers 1–5), 4–5 per fascicle (chaetigers 6–8) (Figs 3A; 4 A–C). Inferior thoracic notochaetae on chaetigers 1–8 short; 3–4 per fascicle except chaetiger 2, which has 6 per fascicle. Thoracic neuropodia each with 4–7 uncini in chaetigers 2–8 (Fig. 3B). Thoracic uncini with rows of evenly small teeth gradually decreasing in size away from main fang (Figs 3B; 4E). Position of chaetae and uncini reversed in abdominal segments; number of abdominal uncini per fascicle decreasing posteriorly from 22 to 9. Abdominal uncini each with multiple rows of teeth that are uniform in size (Figs 3C; 4H); manubrium at least five times longer than dentate region, with base about two thirds the width of the dentate region. Abdominal neuropodia are elongate, narrowly hooded, decreasing posteriorly from 4–6 to 2 per fascicle (Fig. 4G). Variation. Paratypes are similar to the holotype. However, females have oocytes in thoracic chaetigers 4–5 (Fig. 2C) and a pair of pigmented spermathecae in the base of the radiolar crown. Females differ from males in having thoracic neuropodia with uncini in chaetigers 2–5 followed by 3–6 elongate hooded chaetae in neuropodia of chaetigers 6–8 (Fig. 3E,G). Remarks. Manayunkia occidentalis sp. nov. is the sister group to M. speciosa based on COI sequence data with a minimum pairwise distance (simple distance) to our M. speciosa samples of 11.0%, clearly supporting that they can be regarded as a separate taxon, although phylogenetic support for this relationship was weak (bootstrap 28%). Manayunkia occidentalis sp. nov. and M. speciosa are the only species of Manayunkia, and in fact of any Fabriciidae (see Huang et al . 2011), to show sexual dimorphism with regards to thoracic chaetal complement. Males of M. occidentalis sp. nov. , and M. speciosa (Rouse pers. obs.) on specimens from near the type locality (SIO-BIC A12106), show the typical arrangement of thoracic uncini in each of chaetigers 2–8, while females have thoracic uncini in chaetigers 2–5 only (Fig. 3H). The neuropodia of chaetigers 6–8 instead have elongate hooded chaetae (Fig. 3G). These elongate hooded chaetae were seen in all females examined. Larval development would be worth studying to see if there is a loss of thoracic uncini or if they never develop in chaetigers 6–8. It is somewhat surprising that this major difference in chaetal complement was never noted previous in observations on M. speciosa. Manayunkia occidentalis sp. nov. differs markedly from descriptions of M. speciosa by Leidy (1883) and Pettibone (1953) in that it has far fewer pinnules on the radioles. In this regard Manayunkia occidentalis sp. nov. is similar to other Manayunkia species that have relatively few pinnules (see Rouse 1996). : Published as part of Atkinson, Stephen D., Bartholomew, Jerri L. & Rouse, Greg W., 2020, The invertebrate host of salmonid fish parasites Ceratonova shasta and Parvicapsula minibicornis (Cnidaria: Myxozoa), is a novel fabriciid annelid, Manayunkia occidentalis sp. nov. (Sabellida: Fabriciidae), pp. 310-320 in Zootaxa 4751 (2) on pages 313-315, DOI: 10.11646/zootaxa.4751.2.6, http://zenodo.org/record/3713128 : {"references": ["Hazel, C. R. (1966) A note on the freshwater polychaete Manayunkia speciosa Leidy, from California and Oregon. Ohio Journal of Science, 66 (5), 533 - 535.", "Bartholomew, J. L., Whipple, M. J., Stevens, D. G. & Fryer, J. L. (1997) The life cycle of Ceratomyxa shasta, a myxosporean parasite of salmonids, requires a freshwater polychaete as an alternate host. Journal of Parasitology, 83, 859 - 868. https: // doi. org / 10.2307 / 3284281", "Alexander, J. D., Hallett, S. L., Stocking, R., Xue, L. & Bartholomew, J. L. (2014) Host and parasite populations after a flood. Northwest Science, 88, 219 - 233. https: // doi. org / 10.3955 / 046.088.0305", "Stocking, R. W. & Bartholomew, J. L. (2007) Distribution and habitat characteristics of Manayunkia speciosa and infection prevalence with the parasite Ceratomyxa shasta in the Klamath River, Oregon-California. Journal of Parasitology, 93, 78 - 88. https: // doi. org / 10.1645 / GE- 939 R. 1", "Bjork, S. J. & Bartholomew, J. L. (2009) Effects of Ceratomyxa shasta dose on a susceptible strain of rainbow trout and comparatively resistant Chinook and coho salmon. Diseases of Aquatic Organisms, 86, 29 - 37. https: // doi. org / 10.3354 / dao 02092", "Willson, S. J., Wilzbach, M. A., Malakauskas, D. M. & Cummins, K. W. (2010) Lab Rearing of a Freshwater Polychaete (Manayunkia speciosa, Sabellidae) Host for Salmon Pathogens. Northwest Science, 84 (1), 183 - 191. https: // doi. org / 10.3955 / 046.084.0207", "Atkinson, S. D., Jones, S. R. M., Adlard, R. & Bartholomew, J. L. (2011) Geographical and host distribution patterns of Parvicapsula minibicornis (Myxozoa) small subunit ribosomal RNA genetic types. Parasitology, 138 (8), 960 - 968. https: // doi. org / 10.1017 / S 0031182011000734", "Malakauskas, D. M., Willson, S. J., Wilzbach, M. A. & Som, N. A. (2013) Flow variation and substrate type affect dislodgement of the freshwater polychaete, Manayunkia speciosa. Freshwater Science, 32, 862 - 873. https: // doi. org / 10.1899 / 12 - 140.1", "Malakauskas, D. M., Altman, E. C., Malakauskas, S. J., Thiem, S. M. & Schloesser, D. W. (2015) Ribosomal DNA identification of Nosema / Vairimorpha in freshwater polychaete, Manayunkia speciosa, from Oregon / California and the Laurentian Great Lakes. Journal of Invertebrate Pathology, 132, 101 - 104. https: // doi. org / 10.1016 / j. jip. 2015.09.004", "Atkinson, S. D., Hallett, S. L., Diaz Morales, D., Bartholomew, J. L. & de Buron, I. (2019) First myxozoan infection (Cnidaria: Myxosporea) in a marine polychaete from North America, and erection of actinospore collective group Saccimyxon. Journal of Parasitology, 105 (2), 252 - 262. https: // doi. org / 10.1645 / 18 - 183.", "Huang, D., Fitzhugh, K. & Rouse, G. W. (2011) Inference of phylogenetic relationships within Fabriciidae Annelida) using molecular and morphological data. Cladistics, 27 (4), 256 - 379. https: // doi. org / 10.1111 / j. 1096 - 0031.2010.00343. x", "Pettibone, M. H. (1953) Fresh-Water Polychaetous Annelid, Manayunkia speciosa Leidy, from Lake Erie. The Biological Bulletin, 105 (1), 149 - 153. https: // doi. org / 10.2307 / 1538563", "Rouse, G. W. (1996) New Fabriciola and Manayunkia species (Fabriciinae: Sabellidae: Polychaeta) from Papua New Guinea. Journal of Natural History, 30, 1761 - 1778. https: // doi. org / 10.1080 / 00222939600771031"]}