Limnodrilus paraclaparedianus Zhou & Peng & Wang & Ers��us & Cui 2021, n. sp

Autor: Zhou, Tingting, Peng, Yu, Wang, Hongzhu, Ers��us, Christer, Cui, Yongde
Rok vydání: 2021
Předmět:
ISSN: 1966-0510
DOI: 10.5281/zenodo.5793888
Popis: Limnodrilus paraclaparedianus Zhou & Cui n. sp. (Figures 4���6) Limnodrilus ��� claparedianus-cervix ���. Liu et al. 2017a: p. 483f., Fig. 3, Supplementary document S1, Suppl. Table S1, Suppl. Fig. S2, S 3, S 5. Liu et al. 2017b: Table 1, p. 251f. Holotype. IHB HB20171202 a (CW0008), whole-mounted specimen, mature, stored at Institute of Hydrobiology, Chinese Academy of Sciences. Collected in the bottom sludge of Donghu Lake, Wuhan, Hubei (GPS: 114.352˚ E/30.535˚ N). COI barcode: GenBank MT 460105. Paratype. IHB HB20171202 b, whole-mounted specimen, mature, from type locality. Other material. 1 specimen for SEM (Fig. 4), from type locality; IHB AH20171211 a���b (CW0009���CW0010), 2 mature specimens from Longganhu Lake, Anhui; IHB AH20171123 a (CW0011), 1 mature specimen from Huaihe River, Anhui; IHB JS20181130 a (CW0018), 1 mature specimen from Taihu Lake, Jiangsu. For more details see Table 1. Etymology. Named ��� paraclaparedianus ��� for the resemblance with ��� Limnodrilus claparedianus Ratzel, 1868 ��� in terms of the male genitalia. Description. Length 18.00��� 19.25 mm (fixed worms), first XII segments 2.85���3.30 mm (Holotype 2.85 mm), width at clitellum 0.42���0.54 mm (Holotype 0.42 mm), segments 80���95 (Holotype 80). Prostomium conical (Fig. 4A). Clitellum inconspicuous. All chaetae bifid (Figs. 4C���F, 5A���D). Anterior bundles with 4���7 chaetae, length 80���125 ��m, width 2.5���3.7 ��m, nodulus 1/3 from the distal end. 3���4 chaetae per bundle in mid-body, 1���2 per bundle in posterior segments. Upper tooth slightly longer than lower in anterior chaetae, thereafter progressively equal-to-shorter than lower towards the posterior part of body. No modified spermathecal chaetae. Spermathecal pores (Fig. 4B) paired ventrally in middle of X; male pores paired ventrally in middle of XI. Chloragogen cells from VI. No coelomocytes. Male genitalia (Fig. 6B) paired. Sperm funnel (Fig. 6B, sf) 90 ��m long. Vas deferens (Fig. 6B, vd) long and coiled, 25���30 ��m wide, entering atrium apically.Atrium (Fig. 6B, at) long, fusiform, 270���300 ��m long, 75���80 ��m wide. Prostate gland (Fig. 6B, pr) large, with irregular lobes, connected to middle of atrium. Ejaculatory duct (Fig. 6B, ed) leading to penis. Penis sheath (Figs. 5E, 6B, ps) long, cylindrical, slender, narrowing from base to head, tapering abruptly with a constriction near the top; the latter bent with a teardrop-shaped plate placed in oblique position; sheath walls not abruptly reduced in thickness at constriction. Penis sheath 620���1030 ��m long, 40���50 ��m wide at base, 15 ��m wide at top, 15���27 times longer than broad. Spermathecal duct (Fig. 6A, sd) 50���56 ��m wide, ampulla (Fig. 6A, sa) difficult to observe but about 340 ��m long, 215 ��m wide in one specimen. Spermatozeugmata (Fig. 6A, sz) about 300 ��m long, 35���60 ��m wide. Distribution and habitat: Species here reported from Provinces Hubei, Anhui, Jiangsu, Shanxi and Heilongjiang in China; also known (as ��� L. claparedianus-cervix ���) from Europe (Germany, Romania) and USA (Liu et al. 2017a). Freshwater. Remarks: This species has the character combination diagnostic of Limnodrilus (Brinkhurst 1971; Liu et al. 2017a, b): no coelomocytes, bifid chaetae only, long vasa deferentia, small atria, large prostates connected to the middle of atria, long ejaculatory ducts, conspicuous cuticular penis sheaths, and presence of spermatozeugmata. Elongate penis sheaths similar to the ones in L. paraclaparedianus are also present in L. maumeensis, L. cervix, L. claparedianus, and in a species of L. hoffmeisteri s.l. (species "III" in Liu et al. 2017a, Fig. 6). Differences of these species to the new one are as follows: In L. maumeensis, the walls of the penis sheaths are conspicuously thickened on one side near the end, causing a bend in the shaft. In L. cervix, the walls of the penis sheaths are conspicuously thickened and abruptly thinner near the end, furthermore, the head has a triangular downward projection. In L. claparedianus, the upper tooth of the anterior chaetae is distinctly longer than the lower. Further subtle differences are the usually larger length/width ratio of the penis sheath (28 and more) and its rounded-triangular (vs. tear-dropshaped) head. In species III of L. hoffmeisteri, the upper tooth of anterior chaetae is much thicker and almost three times longer than the lower; furthermore, the head of the penis sheath is shaped like a plate-top, perpendicular to the long axis of the shaft (comp. Liu et al. 2017a, Fig. 3). The morphological and molecular characteristics of L. paraclaparedianus are identical with those of " L. claparedianus - cervix " described by Liu et al. (2017a), and therefore, we consider them as the same species. With the inclusion of the records in Liu et al. (2017a), it is clear that this new species is Holarctic in distribution.
Published as part of Zhou, Tingting, Peng, Yu, Wang, Hongzhu, Ers��us, Christer & Cui, Yongde, 2021, Molecular taxonomy and description of a new species of Limnodrilus (Naididae, Clitellata, Annelida) in China, pp. 301-321 in Zootaxa 5082 (4) on pages 313-316, DOI: 10.11646/zootaxa.5082.4.1, http://zenodo.org/record/5792737
{"references":["Liu, Y. K., Fend, S. V. Martinsson, S. & Erseus, C. (2017 a) Extensive cryptic diversity in the cosmopolitan sludge worm Limnodrilus hoffmeisteri (Clitellata, Naididae). Organisms Diversity & Evolution, 17, 477 - 495. https: // doi. org / 10.1007 / s 13127 - 016 - 0317 - z","Liu, Y. K., Fend, S. V., Martinsson, S., Luo, X., Ohtaka, A. & Erseus, C. (2017 b) Multi-locus phylogenetic analysis of the genus Limnodrilus (Annelida: Clitellata: Naididae). Molecular Phylogenetics & Evolution, 112, 244 - 257. https: // doi. org / 10.1016 / j. ympev. 2017.04.019","Ratzel, V. F. (1868) Beitrage zur anatomischen und systematischen Kenntniss der Oligochaeten. Zeitschrift fur wissenschaftliche Zoologie, 18, 563 - 591, pl. 42.","Brinkhurst, R. O. (1971) Family Tubificidae. In: Brinkhurst, R. O. & Jamieson, B. G. M. (Eds.), Aquatic Oligochaeta of the World. Oliver & Boyd, Edinburgh, pp. 444 - 625.","Brinkhurst, R. O. (1963) Taxonomical studies on the Tubificidae (Annelida, Oligochaeta). Internationale Revue der gesamten Hydrobiologie, Systematische Beihefte, 2, 1 - 89. https: // doi. org / 10.1002 / iroh. 19660510504","Brinkhurst, R. O. & Cook, D. G. (1966) Studies on the North American aquatic Oligochaeta III: Lumbriculidae and additional notes and records of other families. Proceedings of the Academy of Natural Sciences of Philadelphia, 118 (1), 1 - 33."]}
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