1,721,983 research outputs found

    Metaphire dorsomultitheca Nguyen & Nguyen 2015

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    Metaphire dorsomultitheca Nguyen & Nguyen, 2015 Pheretima dorsomultitheca Nguyen & Nguyen, 2015 (in Nguyen et al. 2015b): 465, Fig.2. Type locality. Vietnam (An Giang: Chau Doc). Type material. CTU (EW.025), Vietnam. Examined material. 1 C (CTU-EW.025.h01) and 8 C (CTU-EW.025.p02) natural forest, Sam Mountain (10 0 40' 06,8N; 105 0 04' 50,2E), Chau Doc Distr., An Giang Prov., Vietnam, 06/11/2010, coll. Nguyen Thanh Tung; 3C (CTU-EW.025.p03) natural forest, To Mountain (10 0 23' 09.2N; 105 0 00' 22.8E), Tri Ton Distr., An Giang Prov., Vietnam, 09/11/2010, coll. Nguyen Thanh Tung. Records from Vietnam. An Giang (Chau Doc) (Nguyen et al. 2015b). Distribution. Only known from Vietnam.Published as part of Nguyen, Tung T., Nguyen, Anh D., Tran, Binh T. T. & Blakemore, Robert J., 2016, A comprehensive checklist of earthworm species and subspecies from Vietnam (Annelida: Clitellata: Oligochaeta: Almidae, Eudrilidae, Glossoscolecidae, Lumbricidae, Megascolecidae, Moniligastridae, Ocnerodrilidae, Octochaetidae), pp. 1-92 in Zootaxa 4140 (1) on page 56, DOI: 10.11646/zootaxa.4140.1.1, http://zenodo.org/record/25650

    Amynthas erroneous Nguyen & Nguyen 2015

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    Amynthas erroneous Nguyen & Nguyen, 2015 Amynthas erroneous Nguyen D. A. & Nguyen, 2015: 129, Fig. 1. Pheretima multitheca multitheca— Nguyen 1994: 53; Pham 1995c: 68; Thai 2000a: 309; Huynh 2005a: 89; Huynh 2005b: 20; Nguyen V.T. & Tran 2008: 185; Pham 2010: 63. Type locality. Vietnam (Quang Ngai: Duc Pho). Type material. CTU, Vietnam. Examined material. 8 C (SORC-V.153.01), and 13 C (CTU-EW.071.02) garden, Duc Pho town, Pho Minh, Quang Ngai, 15/4/1995, coll. Huynh Thi Kim Hoi. Records from Vietnam. Quang Tri (Quang Tri town); Thua Thien Hue (Huong Tra; Hue; Nam Dong; Phu Loc); Da Nang; Quang Nam (Que Son); Quang Ngai (Quang Ngai city; Duc Pho); Binh Dinh; Dak Nong (Ta Dung Mts) (Nguyen 1994; Pham 1995c, 2010; Huynh 2005a, b; Nguyen & Tran 2008). Distribution. Only known from Vietnam. Remarks. The species had been erroneously identified as Pheretima multitheca multitheca Chen, 1938. It was corrected by Nguyen D. A. & Nguyen (2015).Published as part of Nguyen, Tung T., Nguyen, Anh D., Tran, Binh T. T. & Blakemore, Robert J., 2016, A comprehensive checklist of earthworm species and subspecies from Vietnam (Annelida: Clitellata: Oligochaeta: Almidae, Eudrilidae, Glossoscolecidae, Lumbricidae, Megascolecidae, Moniligastridae, Ocnerodrilidae, Octochaetidae), pp. 1-92 in Zootaxa 4140 (1) on page 27, DOI: 10.11646/zootaxa.4140.1.1, http://zenodo.org/record/25650

    HUCM Student Sight Savers 2018-2019

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    SSSP is a collaborative volunteer effort by ophthalmology physician attendings, residents, and medical students of Howard University College of Medicine. Volunteers obtained participants’ ocular health history and medical risk factors at screenings. Participants then underwent visual acuity, visual field, and intraocular pressure tests. Ophthalmologists reviewed the results to determine recommendations

    First record of Scincella fansipanensis Okabe, Motokawa, Koizumi, Nguyen, Nguyen & Bui, 2024 (Squamata, Scincidae) from China

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    The Fansipan ground skink, Scincella fansipanensis Okabe, Motokawa, Koizumi, Nguyen, Nguyen & Bui, was recently described from Fansipan Mountain, Lao Cai Province, northern Vietnam. Herein, we report the first national record of this species from China, based on four specimens collected from Ailao Mountain, Jingdong Yi Autonomous County, Yunnan Province.Morphologically, the Chinese specimens are consistent with the type series, but differ slightly in possessing a higher number of ventral scales (including gulars) and relatively shorter fore-limbs. Phylogenetic analyses, based on CO1 sequences, place the Chinese specimens within the S. fansipanensis clade; however, uncorrected p-distances of 6.5–7.3% between the Chinese and Vietnamese populations suggest moderate genetic divergence. This level of differentiation may reflect historical isolation by the Red River Basin's complex topography and the low dispersal ability of Scincella species. This record raises the number of the genus Scincella species known from China to 15

    Metaphire peguana subsp. laisonensis Nguyen & Nguyen 2017

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    Metaphire peguana laisonensis Nguyen & Nguyen, 2017 (Figures 5–6, Table 3) Metaphire peguana laisonensis Nguyen et al. 2017b: 900, fig. 12; Nguyen et al. 2021c: 105. Pheretima sp. 11 – Nguyen 2013: 78, 2014: 111. Type locality. Viet Nam (Kien Giang: Lai Son island) (Nguyen et al. 2017b) Type material. Laboratory of Zoology, Department of Biology, Can Tho University (EW.087.01), Vietnam. Diagnosis. Body cylindrical, length 62–114 mm, diameter 2.7–4.4 mm, segments 62–111. Prostomium epilobous. First dorsal pore at 12/13. Three pairs of spermathecal pores in lateral intersegments 6/7/8/9, bithecate. Two pairs of ellipsoid genital markings in xvii and xix, each genital marking with a small opening at the center. Male pores located inside copulatory pouches in xviii. Septum 10/11 only present ventrally. Intestinal caeca simple. Holandric, testis sacs separated. Accessory glands coelomic, strongly covered by muscular-walled bursae in 17/18 and 18/19. Habitat. The subspecies were found numerously in leaf litters in natural forest (Nguyen 2014; Nguyen et al. 2017b). Distribution. Only known in Vietnam (Kien Giang: Lai Son island; An Giang: Cam mountain) (Nguyen 2014; Nguyen et al. 2017b) (Fig. 3). Remarks. Nguyen et al. (2017b) described a new subspecies, M. peguana laisonensis found in Lai Son Island (Kien Giang Province, Vietnam) based on the location of genital markings, spermathecal pores, and the attachment of the spermathecal diverticulum (Fig. 5) (Nguyen et al. 2017b). Previously, Nguyen (2013) identified samples collected from the Cam Mountain (An Giang Province) as M. bahli (Fig. 6), and observed that these samples have intermediate characters between M. bahli and M. peguana, for example, slit-shaped genital markings in xvii and xix, and the much laterally wider spermathecal pores (Nguyen 2013). The re-examination confirmed that specimens were definitely M. peguana laisonensis. There was a minor difference in the ending of the spermathecal diverticulum between the type specimens from Lai Son Island and samples collected from the Cam Mountain (An Giang Province) (attached directly to the base of the ampulla duct vs. attached to the middle of the ampulla duct). Genetic distance of M. peguana laisonensis in Cam Mountain and M. peguana peguana was 12.2%±1.4%, and that distance with other Metaphire species was 12.9%±1.5% (with M. bahli (type I)) to 22.3%±2.1% (with M. grandiverticulata) (Table 4). Notes: Intraspecific distances are in bold; na = no dataPublished as part of Nguyen, Tung T., Lam, Dang H. & Nguyen, Anh D., 2023, A revision of the Metaphire peguana species-group (Oligochaeta: Megascolecidae) from Vietnam, pp. 113-135 in Zootaxa 5255 (1) on pages 123-125, DOI: 10.11646/zootaxa.5255.1.15, http://zenodo.org/record/774455

    Replication Data for: Associations between lean mass and leptin in men with chronic spinal cord injury: results from the FRASCI-muscle study

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    Contains dataset for: Park, A.J., Battaglino, R.A., Nguyen, N., Morse, L.R. Associations between lean mass and leptin in men with chronic spinal cord injury: results from the FRASCI-muscle study. We assessed body composition, leptin, adiponectin, and IL-6 levels in 205 men with chronic spinal cord injury

    Replication Data for: Associations between lean mass and leptin in men with chronic spinal cord injury: results from the FRASCI-muscle study

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    Contains dataset for: Park, A.J., Battaglino, R.A., Nguyen, N., Morse, L.R. Associations between lean mass and leptin in men with chronic spinal cord injury: results from the FRASCI-muscle study. We assessed body composition, leptin, adiponectin, and IL-6 levels in 205 men with chronic spinal cord injury

    Replication Data for: MicroRNA-148a-3p is a Candidate Mediator of Increased Bone Marrow Adiposity and Bone Loss Following Spinal Cord Injury

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    Contains dataset for: Lincoln S, Morse LR, Troy K, Mattson N, Nguyen N, Battaglino RA MicroRNA-148a-3p is a candidate mediator of increased bone marrow adiposity and bone loss following spinal cord injury. We assessed bone marrow adipose tissue volume, body composition, and microRNA expression in subjects with acute SCI, chronic SCI, and controls with no SCI

    Sphenomorphus yersini Nguyen & Nguyen & Nguyen & Orlov & Murphy 2018, sp. nov.

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    Sphenomorphus yersini sp. nov. (Figs. 1–4) Holotype. ITBCZ 5685, adult male, collected from Hon Ba NR., Khanh Hoa Province, Vietnam; coordinates 12°8’13”N, 108°57’39”E; elevation 1162 m a.s.l. by L.T. Nguyen, V.D.H. Nguyen, and S.N. Nguyen on 16 October 2016 (Fig. 1). Paratypes. Two specimens, also collected from Hon Ba NR by L.T. Nguyen, V.D.H. Nguyen, and S.N. Nguyen: ITBCZ 5686, adult female (Fig. 2C&D), and ITBCZ 5684, adult male (Figs. 2A&B and 3), collected on 14 October 2016, coordinates 12°8’22”N, 108°58’06”E; elevation 932 m a.s.l. Referred specimen. HBA 44 (released, Fig. 4), adult female, collected on 19 October 2016, coordinates 12°8’22”N, 108°58’06”E; elevation 932 m a.s.l. Diagnosis. Sphenomorphus yersini sp. nov. is distinguished from all of its congeners by a combination of the following morphological characters: size in adults (SVL) up to 56 mm; TaL/SVL ratio 1.81; toes reach to fingers when limbs adpressed; 32–34 smooth midbody scale rows; 61–69 paravertebral scales; 58–67 ventral scale rows; 112 subcaudal scales; four, rarely five, supraoculars; prefrontals in broad contact with one another; two loreal scales; tympanum deeply sunk; smooth lamellae beneath Finger IV and Toe IV 10–12 and 18 –20, respectively; two enlarged precloacal scales; hemipenis smooth, deeply forked, asymmetrical with a long lobe and another short; black and interruptive dorsolateral line; lateral side and lower part of head, neck, and tail orange to red in male. Description of holotype. Adult male; head small and elongate (HW/HL = 0.7); SVL 54 mm; tail long (TaL/ SVL = 1.81), 98 mm in length; lower eyelid scaly; tympanum deeply sunk with a prominent oblique edge; limbs pentadactyl, toes reach to fingers when limbs adpressed. Head scalation smooth; rostral convex, distinctly visible from above, in broad contact with frontonasal, which is broader than long; no supranasals; prefrontals in broad contact with one another; 5 supraoculars on left side and 4 on right side; a pair of frontoparietals, shorter than frontal; frontal narrowing posteriorly, longer than wide, bordered laterally by first two supraoculars, anteriorly by prefrontals, and posteriorly by frontoparietals; frontoparietals in contact with the second to fifth supraoculars on left side and the second to fourth supraoculars on right side; parietals in contact posteriorly, behind the interparietal; no nuchal; 7 supralabials on both sides, the fifth and sixth below the eye; 2 loreals, posterior loreal larger than anterior; nostril in center of nasal, which is in contact with the first supralabial, rostral, anterior loreal, and frontonasal; 8 supraciliaries, first largest; 1 anterior temporal, in contact with sixth and seventh supralabials; 2 secondary temporals, lower temporal overlapping upper one and in contact with seventh supralabial, upper temporal larger, in contact with parietal; lower eyelid scaly, 2 scales in center larger than scales in posterior and anterior areas; 6 infralabials, first pair medially in contact with each other; 1 anterior and 2 postmentals. Dorsal scales smooth, not larger than lateral and ventral scales; 34 midbody scale rows; 61 paravertebral scales; ventral scales smooth, in 60 rows; 112 subcaudal scales, slightly enlarged posteriorly; 11 and 20 smooth lamellae beneath finger IV and toe IV, respectively; 2 enlarged precloacal scales. Hemipenes. Each hemipenis deeply forked and asymmetrical with two smooth lobes. In fully everted position, the inner lobe is shorter and the outer lobe is much longer. Clear sulcus spermaticus starts from the base, divides into two branches at the fork and extends to the tips of the two lobes; body of the long lobe forming regular transversal shallow grooves and ending with terminal papillae. Short lobe obtuse, not forming regular transversal shallow grooves (Fig. 1F). Coloration. In life, overall dorsal coloration black (Hex #000000) to dark brown (Hex #654321) with two interrupted copper (Hex # B87333) dorsal lines in margins of dorsum extending from neck to base of tail; black and interrupted lateral lines under the copper ones; dorsum with irregular black spots; lateral side and lower part of head, neck, and tail orange (Hex #FF6600) to red (Hex #FE2712); venter from chest to tail base yellow (Hex #FFD300) to cream (Hex # FFFDD 0); upper side of limbs black with bright dots. Lateral margins of supralabials and infralabials with black blotches. Free margin of upper eyelid orange and the margin of lower eyelid yellow (Hex #FFD300). Eyes black. In preservation, color fades; orange and yellow disappear; overall dorsal coloration black with two interrupted brighter lines in margins of dorsum extending from neck to base of tail; venter zebra white (Hex #F5F5F5). Variation. Table 2 summarizes variation in size and scalation of the holotype, paratypes, and referred specimen. Supraoculars four in all specimens except for the left side of the holotype which bears 5 scales. Midbody scale rows vary from 32 to 34. Paravertebral and ventral scale rows range from 61 to 69 and from 58 to 67, respectively. Hemipenes of the second paratype ITBCZ 5684 (Fig. 3) similar to those of the holotype in being deeply forked and asymmetrical. Natural history. All specimens were collected at night and under rotting leaf layer in evergreen forest (Fig. 5), elevations 932 m and 1162 m a.s.l., between 19:00–23:30. However, the species was observed being active in the daytime and it may be diurnal. Sphenomorphus yersini sp. nov. was observed to be sympatric with other congener, S. indicus. Sexual dimorphism. Males are larger than females (SVL 56 mm vs. 52 mm, n=4) and have orange (Hex #FF6600) or red (Hex #FE2712) color on lateral sides and lower part of head, neck, and tail. The color on the lateral side in females faded to yellow (Hex #FFD300) or brown (Hex #964B00) with bright spots; lower part of head, limbs, and tail white (Hex #FFFFFF) to zebra white (Hex #F5F5F5); venter from neck to vent yellow (Hex #FCE883). Distribution. The new species is currently known only from Hon Ba NR, Khanh Hoa Province, southern Vietnam (Fig. 5). Etymology. We name this new species in honor of the famous physician and bacteriologist, Alexandre Yersin (1863–1943), who discovered the bacterium responsible for bubonic plague. Hon Ba NR associates with the name of Alexandre Yersin who built a research station on the top of the mountain and worked there. Currently, the research station has been reconstructed and opened to visitors. We recommend Yersin’s Forest Skink as the common name of this new species. Comparisons. Sphenomorphus yersini sp. nov. differs from its congeners in Indochina (Vietnam, Laos, Cambodia, Thailand, Myanmar, Peninsular Malaysia, and southern China [Yunnan]) as follows: from S. anomalopus (Boulenger) by having a smaller size (SVL 50–56 mm vs. 70 mm), fewer midbody scale rows (32–34 vs. 38) and more lamellae beneath toe IV (18–20 vs. 14); from S. bacboensis by having one (vs. two) anterior temporal, more midbody scale rows (32–34 vs. 30–32), and more supralabials (7 vs. 6); from S. cameronicus Smith by having a smaller size (SVL 50–56 mm vs. 70 mm) and fewer midbody scale rows (32–34 vs. 38); from S. cophias Boulenger by having a larger size (SVL 50–56 mm vs. 37 mm), more midbody scale rows (32–34 vs. 24), more lamellae under fourth toe (18–20 vs. 9) and prefrontals in broad contact (vs. separated); from S. cryptotis by having a smaller size (SVL 50–56 mm vs. 58–79 mm), fewer midbody scale rows (32–34 vs. 36–39) and tympanum deeply sunk (vs. superficial); from S. grandisonae Taylor by having a larger size (SVL 50–56 mm vs. 30 mm), one (vs. two) anterior temporal, more supralabials (7 vs. 6) and lamellae under toe IV (18–20 vs. 12), and adpressed limbs overlapping (vs. failing to touch); from S. helenae Cochran by having more midbody scale rows (32–34 vs. 30), prefrontals in broad contact (vs. separated), and presence of an interrupted (vs. uninterrupted) lateral stripe; from S. incognitus by having a smaller size (SVL 50–56 mm vs. 80–103 mm), fewer midbody scale rows (32–34 vs. 36–40), and one (vs. two) anterior temporal; from S. indicus by having a smaller size (SVL 50–56 mm vs. 90 mm), prefrontals in broad contact (vs. separated), and asymmetrical and deeply forked hemipenis (vs. symmetrical); from S. lineopunctulatus Taylor by having a smaller size (SVL 50–56 mm vs. 84 mm), fewer midbody scale rows (32–34 vs. 38), fewer paravertebral scale rows (61–69 vs. 76), and prefrontals in broad contact (vs. separated); from S. maculatus by having a smaller size (SVL 50–56 mm vs. 62 mm), fewer midbody scale rows (32–34 vs. 38–42), and prefrontals in broad contact (vs. separated); from S. malayanum by having fewer ventral scales (32–34 vs. 74), fewer paravertebral scales (61–69 vs. 76–80), more lamellae under fourth toe (18–20 vs. 15), and deeply sunk (vs. shallow) tympanum; from S. mimicus by having a larger size (SVL 50–56 mm vs. 36 mm), more midbody scale rows (32–34 vs. 30) and more lamellae under fourth toe (18–20 vs. 16); from S. orientale (Shreve) by having more midbody scale rows (32–34 vs. 24–26) and fewer paravertebral scale rows (61– 69 vs. 69–71); and from S. praesignis (Boulenger) by having a smaller size (SVL 50–56 mm vs. 109 mm) and more midbody scale rows (32–34 vs. 28). Sphenomorphus yersini sp. nov. differs from S. sanctus (Duméril & Bibron) by having a larger size (SVL 50–56 mm vs. 40–45 mm), fewer paravertebral scales (61–69 vs. 71), fewer supraoculars (4[5] vs. 5), and fewer lamellae under toe IV (18–20 vs. 26–27); from S. scotophilus (Boulenger) by having more midbody scale rows (32–34 vs. 28–31), fewer supraoculars (4 vs. 5), and fewer lamellae under fourth toe (18–20 vs. 22–23); from S. senja Grismer & Quah by having a smaller size (SVL 50–56 mm vs. 60–65 mm), fewer paravertebral scales (61–69 vs. 72–73), fewer ventral scale rows (60–67 vs. 68), one (vs. two) anterior temporal, more lamellae under toe IV (18–20 vs. 13–17) and prefrontals in broad contact with each other (vs. narrow in contact or slightly separated); from S. sheai by having a larger size (SVL 50–56 mm vs. 35 mm), more midbody scale rows (32–34 vs. 20), more paravertebral scales (61–69 vs. 53), more supralabials (7 vs. 6), more lamellae under fourth toe (18–20 vs. 6), and adpressed limbs overlapping (vs. separated); from S. shelfordi (Boulenger 1900) by having a smaller size (SVL 50–56 mm vs. 67 mm), fewer lamellae under toe IV (18–20 vs. 28–29) and the absence of nuchals (vs. presence of a single pair of nuchals); from S. stellatus by having a smaller size (SVL 50–56 mm vs. 80 mm), more midbody scale rows (32–34 vs. 24) and absence (vs. presence) of two enlarged, broader than long, vertebral scale rows; from S. sungaicolus Sumarli, Grismer, Wood, Ahmad, Rizal, Ismail, Izam, Ahmad & Linkem by having a smaller size (SVL 50–56 mm vs. 67–90 mm), fewer midbody scale rows (32–34 vs. 39–44), fewer paravertebral scales (61–69 vs. 72–81) and fewer ventral scale rows (32–34 vs. 74–86); from S. tarsus (Smith) by having a smaller size (SVL 50–56 mm vs. 90–92 mm) and two loreals (vs. three); from S. tetradactylus by having more midbody scale rows (32–34 vs. 20), absence (vs. presence) of external ear opening, and forelimb with five digits (vs. four digits); from S. tonkinensis by having a larger size (SVL 50–56 mm vs. 36–49 mm), TaL/ SVL ratio 1.80 (vs. 1.32), and one (vs. two) anterior temporal; from S. tridigitus by having a larger size (SVL 50– 56 vs. 35), more midbody scale rows (32–34 vs. 20), absence (vs. presence) of external ear opening and forelimb with five digits (vs. three digits); and from S. tritaeniatus by having a larger size (SVL 50–56 vs. 47), fewer midbody scale rows (32–34 vs. 38) and paravertebral scales (61–69 vs. 81), more lamellae under toe IV (18–20 vs. 15) and one anterior temporal (vs. two). Sphenomorphus yersini sp. nov. is similar to S. buenloicus in many aspects (size, midbody scale rows, number of anterior temporals, lamellae under fourth toe, etc.). However, the new species can be distinguished from S. buenloicus by having a relatively longer tail (TaL/SVL ratio 1.8 vs. 1.2), usually more ventral scale rows (58–67 vs. 55–58) and deeply forked hemipenis with two asymmetrical lobes and the outer lobe is much longer than the inner one (vs. hemipenis forked at the middle point of its length with two developing lobes and the outer lobe is slightly longer than the inner one [Figs. 6 & 7]).Published as part of Nguyen, Sang Ngoc, Nguyen, Luan Thanh, Nguyen, Vu Dang Hoang, Orlov, Nikolai L. & Murphy, Robert W., 2018, A new skink of the genus Sphenomorphus Fitzinger, 1843 (Squamata: Scincidae) from Hon Ba Nature Reserve, southern Vietnam, pp. 313-326 in Zootaxa 4438 (2) on pages 315-323, DOI: 10.11646/zootaxa.4438.2.6, http://zenodo.org/record/129477
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