166,715 research outputs found
Lanlabeo Yao & He & Peng 2018, gen. nov.
No full textLanlabeo, gen. nov. (Figs. 2–3) Type species. Lanlabeo duanensis, sp. nov. Diagnosis. Lanlabeo is diagnosed from all other labeonin genera by the following combination of characters: 1) frenum connecting upper jaw and lower lip at corner of the mouth; 2) papillae densely scattered over ventral margin of rostral cap and regularly arranged; 3) upper lip vestigial; 4) rostral cap overlying upper jaw, with its posterior margin fimbriate; 5) lower lip divided into two small lateral and translucent fleshy lobes and one central plate; 6) median lobe of lower lip large, with papillae regularly arranged in many transverse rows (Fig. 2). Comparison. Among the described genera of Labeonini, the morphology of this new genus appears to most closely resemble that of Rectoris posehensis (Lin 1935). It distinctly differs from this genus, however, in having a pair of well-developed maxillary barbels and in its lower lip being divided into two small lateral and translucent fleshy lobes and one central plate. There are no known cyprinids with mouths of similar structure to that of the fish of this new genus. In the lower jaw of the new genus, the dentary is transversely L-shaped in ventral view, as the anterior part forms a right-angle turn and the transverse branch is anterioposteriorly expanded (Fig. 4B). These unique osteological characters can distinguish it from other known genera. Additionally, molecular analyses indicated that this new genus forms a distinct lineage within the Labeonini (Fig. 5). Etymology. The generic name is made from a combination of the Chinese family name Lan, after Jiahu Lan for his contributions to the discovery of fish diversity in southern China, and the Latin word Labeo, a generic name commonly utilized suffix for the labeonin genera.Published as part of Yao, Min, He, You & Peng, Zuo-Gang, 2018, Lanlabeo duanensis, a new genus and species of labeonin fish (Teleostei: Cyprinidae) from southern China, pp. 556-568 in Zootaxa 4471 (3) on pages 559-560, DOI: 10.11646/zootaxa.4471.3.7, http://zenodo.org/record/143994
Oral Interview with Eng Peng
No full text26 min.Interview with Eng Peng on his experience coming to America, and how he attained the American Dream of hard work and being a homeowner
Thermal-aware SoC test scheduling with test set partitioning and interleaving
No full textHigh temperature has become a major problem for system-on-chip testing. In order to reduce the test application time while keeping the temperatures of the cores under test within safe ranges, a thermal-aware test scheduling technique is required. This paper presents an approach to minimize the test application time and, at the same time, prevent the temperatures of cores under test going beyond given limits. We employ test set partitioning to divide test sets into shorter test sequences, and add cooling periods between test sequences so that overheating can be avoided. Moreover, test sequences from different test sets are interleaved, such that the cooling periods and the bandwidth of the test bus can be utilized for test data transportation, and hence the test application time can be reduced. The test scheduling problem is formulated as a combinatorial optimization problem, and we use the constraint logic programming (CLP) to build the optimization model and find the optimal solution. As the optimization time of the CLP-based approach increases exponentially with the problem size, we also propose a heuristic which generates longer test schedules but requires substantially shorter optimization time. Experimental results have shown the efficiency of the proposed approach
Svistella wuyong Li & Peng & He 2021, sp. nov.
No full textSvistella wuyong He sp. nov. Figs. 1C, 3E&F, 4 Holotype: male, CHINA, Yunnan Prov., Yingjiang, Nabang, E 97.57, N 24.75, 23-viii-2019, coll. He Zhu-Qing. (depository: East China Normal University, China) Paratype: 2 males, same data as holotype. Male: Body large for this genus (Fig 3E). Head: head little wider than anterior margin of pronotum (Fig. 1C, 3E, 4B), vertex not flattened, frontal rostrum as wide as 1st antennal joint (Fig. 4A), 3rd–4th segments of maxillary palpi elongated, 5th segment triangular. Pronotum: pronotum pubescent and posteriorly widened (Fig. 4B), no lateral carina, anterior and posterior margin straight, fore tibia with oval tympanum on outer side (Fig. 4C), but a slit on inner side (Fig. 4D), hind tibia with three pairs of dorsal spurs and five apical spurs, tegmen long and narrow, almost extending to apex of abdomen, mirror large and oval. Genitalia: Epiphallic lateral lobe long with three minute teeth on the apex of each lateral lobe (Fig. 4E&F). Female: unknown. Coloration: Overall color yellow. Frons reddish brown with two red longitudinal bands from head to posterior margin of pronotum; lateral lobes of pronotum red. Two black stripes on the outer pagina of hind femur, and one on the inner side, a black spot on the dorsal and lateral side near hind femur near apical portion, a small black spot on the opposite side of above spot, in the ventral side of hind femur near apical portion. Comparison: This species can be easily distinguished from other species by the combination of red bands on pronotum and black stripes on the hind femur (Fig. 1C). Measurements (in mm): Male: SZ 7.6–7.7, PR 1.2–1.3, FW 5.5–5.6, HF 5.8–5.9. Distribution: China (Yunnan). Etymology: The specific epithet wuyong is for the Chinese phonetic alphabet. It means “improperly use”. Because this new species was misidentified as S. rufonotata for many years. See details in discussion. Song: The song was stereotyped with 78 chirps /minute. Each chirp contained 16.4±0.55 pulses, and continued 0.439±0.015 s (Fig. 6).Published as part of Li, Shi-Yu, Peng, Hui-Ling & He, Zhu-Qing, 2021, Two new species of genus Svistella Gorochov, 1987 from China (Orthoptera Trigonidiidae: Trigonidiinae), pp. 173-183 in Zootaxa 4949 (1) on pages 177-179, DOI: 10.11646/zootaxa.4949.1.10, http://zenodo.org/record/463566
Nais longidentata Cui, He, Peng & Wang, 2015, sp. n.
No full text13. <i>Nais longidentata</i> sp. n. <p>(Figures 4, 5; Table 2)</p> <p> <b>Holotype.</b> IHB NMC 20110702a, mature specimen mounted in Canada balsam, and stained with borax carmine.</p> <p> <b>Type locality.</b> ST57, N 30°47'12.6", E 90°58'43.9", Lake Namco of Tibet, ca. 4,716 m asl, lake shore substrate type coarse gravel and sand; water depth 0.3 m, water temperature 10.0°C, dissolved oxygen 7.48 mg/L, pH 10.42, conductivity 1,783 µS/cm. 2 July 2011, collected by X. B. He, Y. D. Cui.</p> <p>2014).</p> <p> <i>N. longidentata N. bretscheri N. communis N. elinguis N. pardalis N. variabilis N. badia</i></p> <p> Species <b>sp. n.</b> Michaelsen, 1899 Piguet, 1906 Müller, 1774 Piguet, 1906 Piguet, 1906 Peng <i>et al.</i>, 2014 Length (mm) 4.3–5.7 3–7 1.8–12 2.2–12 2.5–7.0 3–10 4.2–9.1 <b>Paratypes.</b> IHB NMC 20110702b–e, 4 specimens from the type locality mounted in Canada balsam, and stained with borax carmine.</p> <p> <b>Other material.</b> More than 50 immature specimens from ST5, ST9, ST31, ST53, ST57, preserved in 10% formalin, collected by X. B. He, Y. D. Cui.</p> <p> <b>Etymology.</b> The specific name " <i>longidentata</i> ” is Latin for "with long teeth”, and refers to the needle with two long teeth.</p> <p> <b>Description.</b> Length 3.3–7.4 mm (holotype 4.3 mm), width at VI 0.3–0.6 mm (holotype 0.5 mm), segments 34–41(holotype 34). Prostomium conical. Eyes present, body pigment absent. Pharynx in II–III. Stomach in VII– VIII, dilatation sudden in VII, no elongate cells. Clitellum inconspicuous. Coelomocytes abundant. No swimming.</p> <p>Dorsal chaetae from VI onwards (Fig. 5 F). Hairs (0)1–2 per bundle, 225–450 Μm long, with faint serration (Fig. 5 C). Needles 1–2 per bundle, 92–112 Μm long, with two long parallel teeth (10.0–13.8 Μm long), distal tooth slightly thinner and shorter than proximal, or subequal; nodulus ca. 2/5 from distal end (Fig. 4 D, Fig. 5 D–E). Ventral chaetae of II–V 3–4 per bundle, 78–84 Μm long, distal tooth longer and thinner than proximal, with median or slightly distal nodulus, hardly longer and thinner than the rest. Ventral chaetae from VI 2–5 per bundle, 68–78 Μm long, distal tooth slightly longer than proximal, with 1–3 fine intermediate teeth, nodulus 2/5 from distal end (Fig. 4 A–C; Fig. 5 A–B). Penial chaetae (Fig. 4 E) 3 per bundle, 70–112 Μm long, 4 Μm thick, simple-pointed. Male pores paired in segment VI. Spermathecal pores paired in segment V.</p> <p>Clitellum in V–VI. Male genitalia paired in V–VI. Vasa deferentia (Fig. 4 F, vd) 90–100 Μm long, 8–9 Μm wide, completely surrounded by abundant prostate gland cells (Fig. 4 F, pr), joining the atria subapically. Atrial ampullae large and round, 120 Μm in length, 45 Μm in diameter, wall 5 Μm thick (Fig. 4 F, at). Spermathecal ampulla pear-shaped, 90 Μm long, 50 Μm wide, with distinct duct 60–70 Μm long, 9–10 Μm wide (Fig. 4 F, sp).</p> <p> <b>Distribution.</b> Known only from Lake Nam Co and Lake Yamzho Yumco of Tibet.</p> <p> <b>Remarks.</b> Considering the characters such as the presence of eyes, coelomocytes abundant, dorsal chaetae from VI with hairs and double-pronged needles, ventral chaetae of II–V longer and thinner than the rest, pharynx in II–III, stomach beginning in VII, spermathecae with distinct ducts, vasa deferentia with prostate gland cells joining the atria subapically, atria without prostate glands, penial chaetae present with a simple hook, we think that the new species fits the definition of <i>Nais</i> Müller, 1773 (Sperber 1948; Brinkhurst & Jamieson 1971; Hrabě 1979; Timm 1999; Envall <i>et al.</i> 2012).</p> <p> About 31 species have been described in <i>Nais</i>, and ten species are distributed in China (Sperber 1948; Liang 1964; Brinkhurst & Jamieson 1971; Semernoy 2004; Envall <i>et al.</i> 2012; Peng <i>et al.</i> 2014). <i>N. longidentata</i> <b>sp. n.</b> is distinguished from congeners in having long and parallel needle teeth, faintly serrated hairs, and pectinate ventral chaetae with 1–2 intermediate teeth.</p> <p> Comparing <i>N. longidentata</i> <b>sp. n.</b> with allied species (Table 2), the new species is similar to <i>N. elinguis</i> by the long and parallel needle teeth. However, the needles of the new species are longer than those of <i>N. elinguis</i> (10.0– 13.8 Μm <i>vs</i>. 3.1–4.6 Μm). <i>N. badia</i> Peng <i>et al</i>., 2014 resembles the new species in serrate hairs and pectinate ventral chaetae, but its large area of reddish brown pigment in I–VIII, wave-like body movements, and vasa deferentia with prostate gland cells only on their posterior parts are significantly different from <i>N. longidentata</i> <b>sp. n.</b>. Among further similar species, <i>N. bretscheri</i> Michaelsen, 1899 differs from the new species in giant chaetae in some anterior ventral segments; <i>N. communis</i> Piguet, 1906 differs in the thick prostate gland cells only on their posterior parts; <i>N. variabilis</i> Piguet, 1906 and <i>N. pardalis</i> Piguet, 1906 swim with spiral body movements and their stomach has elongate cells. In all these species the needle teeth are considerably shorter than in <i>N. longidentata</i> <b>sp. n.</b></p>Published as part of <i>Cui, Yongde, He, Xuebao, Peng, Yu & Wang, Hongzhu, 2015, Records of Naididae and Lumbriculidae (Clitellata) from Tibet, China, with description of a new species of Nais, pp. 513-530 in Zootaxa 3956 (4)</i> on pages 521-524, DOI: 10.11646/zootaxa.3956.4.4, <a href="http://zenodo.org/record/240764">http://zenodo.org/record/240764</a>
Svistella malu Li & Peng & He 2021, sp. nov.
No full textSvistella malu He sp. nov. Figs. 1D, 3G&H, 5 Holotype: male, CHINA, Yunnan Prov., Kunming, E 102.84, N 24.90, altitude 2000 m, 18-viii-2019, coll. He Zhu-Qing. (depository: East China Normal University, China) Paratype: 1 male, same data as holotype; 1 male, 22-ix-2016, other data same as holotype; 2 males & 2 females CHINA, Yunnan Prov., Tengchong, Houqiao, E 98.28, N 25.33, altitude 2000 m, 5-ix-2018, coll. Bi Wen-Xuan. Male: Body medium-sized for this genus (Fig. 3G). Head: head little wider than anterior margin of pronotum (Fig. 1D, 3G, 5B), vertex not flattened, frontal rostrum as wide as 1st antennal joint (Fig. 5A), 3rd–4th segments of maxillary palpi elongated, 5th segment triangular. Pronotum: pronotum pubescent and posteriorly widened (Fig. 5B), no lateral carina, anterior and posterior margin straight, fore tibia with oval tympanum on outer side (Fig. 5C), but concave on inner side (Fig. 5D), hind tibia with three pairs of dorsal spurs and five apical spurs, tegmen elongate and narrow, almost extending to apex of abdomen, mirror large and oval. Genitalia: Epiphallic lateral lobe long with one reverse tooth on outer side, and two minute teeth on the apex of each lateral lobe (Fig. 5E&F). Female: Similar to male, ovipositor straight and little curved. Coloration: Overall color yellow. Frons brown with two red longitudinal bands from head to posterior margin of pronotum, one short red stripe behind each eye; lateral lobes of pronotum red. No mark on hind femur, but a small black spot on the ventral side of hind femur near apex. Variation: Individuals from Kunming is larger than those from Tengchong. Two females were only collected from Tengchong, and they were all long wing type (2.5 times as long as forewing). Comparison: This species can be distinguished from other species by the combination of the lack of black stripes on the hind femur, red bands on the lateral lobes of pronotum, and a small black spot on the ventral side of hind femur near apical part. Measurements (in mm): Male: SZ 7.0–7.3, PR 1.1–1.2, FW 4.5–5.6, HF 4.4–4.9; female: SZ 5.9–6.0, PR 1.0–1.1, FW 5.4–5.5, HF 4.3–4.6, OV 2.0–2.1. Distribution: China (Yunnan). Etymology: The specific epithet malu is for the Chinese phonetic alphabet, which is the abbreviation of. It means “deliberately confuse”. The new species was misidentified as S. dubia previously by He Zhu-Qing. Song: The song was stereotyped with 80 chirps/minute. Each chirp contained 17.4±0.55 pulses, and continued 0.45±0.015 s (Fig. 6).Published as part of Li, Shi-Yu, Peng, Hui-Ling & He, Zhu-Qing, 2021, Two new species of genus Svistella Gorochov, 1987 from China (Orthoptera Trigonidiidae: Trigonidiinae), pp. 173-183 in Zootaxa 4949 (1) on pages 179-181, DOI: 10.11646/zootaxa.4949.1.10, http://zenodo.org/record/463566
Lanlabeo duanensis Yao & He & Peng 2018, sp. nov.
No full textLanlabeo duanensis, sp. nov. (Figs. 2–3) Holotype. SWU 20170110006, 90.3 mm SL, collected from a tributary flowing into the Hongshuihe River in the Xijiang River drainage basin in Longwan, Du’an County, Guangxi Province, southern China (23°53′N 108°15′E); collected by J. Lan, August 2016. Paratypes. SWU 20170110002–4(3), SWU 20170110007–9(3), six specimens, 90.3–142.6 mm SL, same collection data as the holotype. Diagnosis. See generic diagnosis for characters distinguishing the species from all other genera of Labeonini. Description. Whole body and oromandibular structures illustrated in Figs. 2 and 3, respectively. Morphometric data for 7 type specimens presented in Table 2. Body elongate and slightly compressed; breast slightly carinate; highest point of body immediately anterior to the dorsal-fin origin; caudal peduncle slender with smallest depth close to base of caudal fin. Dorsal profile of body gradually ascending from snout tip to dorsal-fin origin; from there to origin of dorsal procurrent caudal-fin rays slightly concave. Ventral profile of body rounded from anterior to anal-fin origin; slightly concave from anal-fin origin to origin of ventral procurrent caudal-fin rays. Head relatively small, longer and deeper than wide, its length accounting for 20.1%¯22.9% of SL. Eye medium-sized, dorsolaterally situated in middle of head, visible from ventral view; interorbital space wide, slightly convex. Snout rounded and blunt, snout length 44.3%¯51.9% of HL. Nostrils closer to anterior margin of eye than to snout tip. Mouth inferior and arched. Ventral margin of rostral cap fringed, not covering base of upper jaw. Rostral cap connected to lower lip at corner of mouth. Postlabial grooves very deep, dividing lower lip into three parts including median portion and two lateral portions. Median lobe of lower lip large, with papillae densely and regularly arranged in many transverse rows. Two lateral fleshy lobes present and devoid of papillae. Two pairs of long barbels, with rostral barbels almost as long as maxillary barbels; maxillary barbels close to corners of mouth. Three rows of pharyngeal teeth, tooth pattern 5,4,2–2,4,5, with compressed and pointed distal tips (Fig. 4C). Gill rakers on outer side of first gill arch 14–16; rakers short and small. Body scales moderate in size. Lateral line complete, horizontal with 36–38 scales; 5 scale rows between lateral line and origin of dorsal fin; 3 scale rows between lateral line and origin of pelvic fin; circumpeduncular scale rows 14–16. Dorsal fin inserted slightly before pelvic fin. Ventral scales between pectoral fins and pelvic fins halfhidden and subcutaneous. Axillary scale present at pelvic-fin base; two scales between vent and anal-fin origin. Dorsal fin with 2 soft unbranched and 8 or 9 branched rays; insertion of dorsal fin nearer to tip of the snout than to caudal-fin base; distal margin slightly concave, its length accounting for 22.2%¯27.3% of SL. Pectoral fin with 1 simple and 12 or 13 branched rays, no longer than HL, reaching two-fifths of distance to pelvic-fin insertion. Pelvic-fin origin roughly at midpoint of body and slightly posterior, with one unbranched and 7 or 8 branched rays, inserted vertically posterior to fourth branched dorsal fin ray base, and extending to anal fin origin. Anal fin with one unbranched and 5 branched rays; distal margin concave; origin nearer pelvic-fin insertion than caudal fin base. Caudal fin with 9+9 branched rays, deeply forked; upper and lower lobes equal in length and similarly shaped, with tapering, rounded tips. Color pattern in formalin. Body dark brown dorsally; dark brown laterally, darker above; yellowish-white ventrally. An indistinct longitudinal black stripe, roughly two scales in depth, originates at upper extremity of gill opening and extends along lateral line on flank ending at middle of caudal-fin base. Fin rays black, membrane hyaline (Fig. 3). Distribution. Lanlabeo duanensis is only known from the Hongshuihe River of the Xijiang River drainage basins in Du’an County, Guangxi Province, China (Fig. 1). Etymology. The specific epithet, used as an adjective, is based on the type locality: Du’an County, in southern China.Published as part of Yao, Min, He, You & Peng, Zuo-Gang, 2018, Lanlabeo duanensis, a new genus and species of labeonin fish (Teleostei: Cyprinidae) from southern China, pp. 556-568 in Zootaxa 4471 (3) on pages 560-563, DOI: 10.11646/zootaxa.4471.3.7, http://zenodo.org/record/143994
Leptonetela latapicalis He & Liu & Xu & Yin & Peng 2019, sp. nov.
No full text<i>Leptonetela latapicalis</i> sp. nov. <p>Figures 5–8, 12</p> <p>http://zoobank.org/NomenclaturalActs/ 9D53BD4D-BCDF-4DA2-9369-6AADA3C89151</p> <p> <b>Type material. Holotype:</b> male (HNU) China, Hunan Province, Shaoyang County, Hebo Town, Chengbei Village, Jigong Cave, 111°17.460'E, 26°45.438'N, 576 m, 23 November, 2011, Xiang Xu, Jinlong Wan, Yi Zhao, Shihong Peng leg. <b>Paratypes</b>: 14 females, 15 males, same data as holotype.</p> <p> <b>Etymology.</b> The specific name is an adjective in apposition and derived from the Latin words “lata” (broad) and “apicalis” (apical), in reference to the presence of broad and peak-shaped median apophysis.</p> <p> <b>Diagnosis.</b> Males resemble those of <i>Leptonetela hexacantha</i> Lin & Li, 2010, <i>L. jinsha</i> Lin & Li, 2010, <i>L. reticulopecta</i> Lin & Li, 2010, <i>L. kanellisi</i> (Deeleman-Reinhold, 1971), and <i>L. tianxingensis</i> Wang & Li, 2011 by having depressed and strongly contracted structure in the middle of the pedipalpal tarsus (Figs 5C, D, 7A, B in the present paper; figs 24A, B, 26A, B, 45A, B in Lin & Li 2010; figs 18A, B, 63A, B in Wang & Li 2011); short distance between apical tarsus and pedipalpal bulb (Figs 5C, D, 7A, B in the present paper; figs 24A, B, 26A, B, 45A, B in Lin & Li 2010; figs 18A, B, 63A, B in Wang & Li 2011), the new species is distinguished from these species by presence of three prolateral, nine retrolateral tibial spines on male pedipalpus; broad and peak-shaped median apophysis; short, wide, translucent conductor on male bulb (Figs 5C, D, 7A, B). The new species resembles <i>L. quinquespinata</i> (Chen & Zhu, 2008) in being eyeless, having membranous embolus, slightly twisted prolaterally (Figs 5A, B, 8B in this present paper; figs 44A, B, 47D in Wang & Li 2011); it can be distinguished by nine strong spines located in retrolateral side of pedipalpal tibia (Figs 5D, 7A in this present paper; figs 44B, 46C in Wang & Li 2011); nine small retromarginal teeth on the chelicerae in the new species (Fig. 8D in this present paper; fig. 47C in Wang & Li 2011), while six strong spines retrolaterally-directed on the pedipalpal tibia; five small retromarginal teeth on the chelicerae in <i>L. quinquespinata</i> (Figs 5D, 7A in this present paper; figs 44D, 46B in Wang & Li 2011). Females resemble those of <i>L. quinquespinata</i> in being eyeless; having highly twisted sperm, but can be distinguished by the distal ends of sperm ducts closer placed to each other in the new species (Figs 6C, 8B), slightly further away from each other in <i>L. quinquespinata</i> (figs 45C, 47B in Wang & Li 2011).</p> <p> <b>Description. Male</b>. Total length 2.69 (Fig. 5A). Carapace 1.26 long, 1.12 wide. Opisthosoma 1.37 long, 1.03 wide. Prosoma reddish brown, with several setae near the anterior margin of carapace. Ocular area with a pair of setae, eyes absolutely absent. Median groove short, cervical grooves and radial furrows light brown. Clypeus 0.24 high. Chelicerae brown, with nine promarginal and eight small retromarginal teeth, promarginal row of teeth gradually becoming smaller and denser from the base to distal end of fang furrow (Fig. 8D). Endites brown. Labium brown and plump, fused with sternum. Sternum and legs yellowish. Leg measurements: I 12.72 (3.53, 0.45, 3.98, 2.97, 1.79); II 10.03 (2.91, 0.41, 3.09, 2.12, 1.50); III 8.66 (2.52, 0.42, 2.41, 2.10, 1.21); IV 10.34 (3.12, 0.36, 2.98, 2.53, 1.35). Leg formula: I–IV–II–III. Opisthosoma pale brown, ovoid, lacking distinctive patterns. Male pedipalpus (Figs5 B–D, 7A, B, 8C): femur covered with long and thin hairs; tibia with three trichobothria dorsally; three slender spines prolaterally and nine strong spines retrolaterally (six spines along the tibia form a longitudinal row and the other three spines along distal margin of the tibia form a transversal row) exist on the pedipalpal tibia (Figs 7A, B). Tarsus rugose and contracted mesially, attaching to an earlobe-shaped process retrolaterally, with long spines distally (Figs 5C, D, 7A, B). Pedipalpal bulb nearly round; embolus membranous, slightly twisted towards the prolateral side; conductor translucent, broad, flat; median apophysis broad, peakshaped (Figs 5B, 8C). Prolateral lobe cuspate (Fig. 7B).</p> <p> <b>Female</b>. Similar to male in coloration of opisthosoma and general features, but larger body size, shorter legs, and prosoma yellowish. Total length 3.06 (Figs 6A, B). Carapace 1.23 long, 1.15 wide. Opisthosoma 1.70 long, 1.24 wide. Clypeus 0.24 high. Leg measurements: I 10.94 (3.06, 0.40, 3.33, 2.42, 1.73); II 9.46 (2.62, 0.41, 2.88, 2.13, 1.42); III 7.93 (2.38, 0.33, 2.21, 1.86, 1.15); IV 10.26 (2.95, 0.36, 2.95, 2.48, 1.52). Leg formula: I–IV–II–III. Genital area densely covered with long hairs (Figs 6B, 8A). Internal genitalia with a pair of spermathecae and sperm ducts: spermathecae dark brown, sclerotized and highly twisted, with the distal ends very close to each other; sperm ducts pale brown, less sclerotized (Figs 6C, 8B). The atrium broad, nearly triangular, slightly procurved at anterior median margin (Fig. 8B).</p> <p> <b>Distribution.</b> Known only from the type locality (Fig. 12).</p>Published as part of <i>He, Ailan, Liu, Jinxin, Xu, Xiang, Yin, Haiqiang & Peng, Xianjin, 2019, Description of three new species of spider genus Leptonetela Kratochvíl, 1978 from caves of Hunan Province, China (Araneae, Leptonetidae), pp. 584-600 in Zootaxa 4554 (2)</i> on pages 590-595, DOI: 10.11646/zootaxa.4554.2.10, <a href="http://zenodo.org/record/2623679">http://zenodo.org/record/2623679</a>
Tubifex conicus He, Cui & Wang 2012
No full text23. Tubifex conicus He, Cui & Wang, 2012 Tubifex conicus He, Cui & Wang, 2012: 160 –162. Material. Lake Yamzhao Yumco: ST 36, 2 spms; ST 37, 17 spms; ST 39, 45 spms; ST 40, 12 spms; ST 41, 24 spms; ST 42, 6 spms; ST 43, 27 spms; ST 44, 2 spms; ST 47, 36 spms; ST 48, 29 spms; ST 49, 21 spms. Remarks. Known only from Lake Yamzhao Yumco.Published as part of Cui, Yongde, He, Xuebao, Peng, Yu & Wang, Hongzhu, 2015, Records of Naididae and Lumbriculidae (Clitellata) from Tibet, China, with description of a new species of Nais, pp. 513-530 in Zootaxa 3956 (4) on page 527, DOI: 10.11646/zootaxa.3956.4.4, http://zenodo.org/record/24076
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