242,352 research outputs found
Pareuchiloglanis tianquanensis Ding & Fang 1997
No full textPareuchiloglanis tianquanensis Ding & Fang 1997 Pareuchiloglanis tianquanensis Ding & Fang 1997: 17, fig. 1. Type locality: Tianquan County [Yangtze drainage], Shichuan, China. Holotype: Mus. Sichuan Inst. Nat. Res. 920185. Paratypes: Mus. Sichuan Inst. Nat. Res. 920177-184 (8), 920186-205 (20). Distribution: Yangtze drainage, China (Ding & Fang, 1997).Published as part of Alfred W. Thomson & Lawrence M. Page, 2006, Genera of the Asian Catfish Families Sisoridae and Erethistidae (Teleostei: Siluriformes)., pp. 1-96 in Zootaxa 1345 on page 8
Miridiba (Miridiba) xingkei Gao & Bai & Fang & Yu 2018, new species
No full textMiridiba (Miridiba) xingkei Gao & Fang, new species (Figs. 3, 6) Type locality. CHINA: Yunnan Province: Xishuangbanna City. Type material examined. Holotype, male, labelled: “ Menga, Xishuangbanna, Yunnan / 1050–1180 m / Chinese Academy of Sciences [typeset, Chinese] // 1958. V. 13 / Collector Pu Fuji [typeset, Chinese] // Holotrichia (P.) ciliatipennis Moser ♂ / Designed by You-wei Zhang [handwritten, Chinese] // HOLOTYPE ♂ / Miridiba xingkei sp. nov. / Chuanbu Gao & Hong Fang / det. 2018 [typeset, red label]”, deposited in IZCAS; paratype, female: “Jingdong, Yunnan 1200 m / 1957. IV. 29 / A. Monchadsky [typeset, Chinese and Russian] // PARATYPE ♀ / Miridiba xingkei sp. nov. / Chuanbu Gao & Hong Fang / det. 2018 [typeset, yellow label]”, deposited in IZCAS; paratype, male: “Jingdong 1170 m / 1956. V. 26 / Zagulyaev lamp [typeset, Chinese and Russian] // PARATYPE ♂ / Miridiba xingkei sp. nov. / Chuanbu Gao & Hong Fang / det. 2018 [typeset, yellow label]”, deposited in IZCAS; paratype, female: “Xiaomengyang, Yunnan 850 m / 1957. V. 3 / Qiuzhen Liang [typeset, Chinese and Russian] // Holotrichia (P.) ciliatipennis Moser ♀ / Identified by Youwei Zhang 1981. VI [handwritten, Chinese] // PARATYPE ♀ / Miridiba xingkei sp. nov. / Chuanbu Gao & Hong Fang / det. 2018 [typeset, yellow label]”, deposited in IZCAS; paratype, male: “Yun Jinghong, Xishuangbanna, Yunnan / 650 m / Chinese Academic of Sciences [typeset, Chinese] // 1959-?-5 / Collector Xuezhong Zhang [typeset] // H. ciliatipennis Moser / genitalia / 62.3.19 [handwritten] // Holotrichia ciliatipennis Moser / Identified by Youwei Zhang [handwritten, Chinese] // IOZ(E)1967842 [typeset] // PARATYPE ♂ / Miridiba xingkei sp. nov. / Chuanbu Gao & Hong Fang / det. 2018 [typeset, yellow label]”, deposited in IZCAS; paratype, male: “Yun Jinghong, Xishuangbanna, Yunnan / 650 m / Chinese Academic of Sciences [typeset, Chinese] // 1958-V-11 / Collector Xuewu Meng [typeset] // Holotrichia ciliatipennis Moser / Identified by Youwei Zhang [handwritten, Chinese] // IOZ(E)1967836 [typeset] // PARATYPE ♂ / Miridiba xingkei sp. nov. / Chuanbu Gao & Hong Fang / det. 2018 [typeset, yellow label]”, deposited in IZCAS; paratype, female: “Yunpenghun, Xishuangbanna, Yunnan / 1200- 1400 m / Chinese Academic of Sciences [typeset, Chinese] // 1958-V-11 / Collector Xuewu Meng [typeset] // PARATYPE ♀ / Miridiba xingkei sp. nov. / Chuanbu Gao & Hong Fang / det. 2018 [typeset, yellow label]”, deposited in IZCAS; paratypes, 3 females: “Jingdong, Yunnan 1200 m / 1957. IV. 25 / A. Monchadsky [typeset, Chinese and Russian] // PARATYPE ♀ / Miridiba xingkei sp. nov. / Chuanbu Gao & Hong Fang / det. 2018 [typeset, yellow label]”, deposited in IZCAS; paratype, female: “Simao, Yunnan 1300 m / 1957. V. 9 / Fuji Pu [typeset, Chinese and Russian] // PARATYPE / Miridiba xingkei sp. nov. / Chuanbu Gao & Hong Fang / det. 2018 [typeset, yellow label]”, deposited in IZCAS; paratype, male: “Jingdong 1170 m / 1956.?. 1 / Zagulyaev lamp [typeset, Chinese and Russian] // PARATYPE ♂ / Miridiba xingkei sp. nov. / Chuanbu Gao & Hong Fang / det. 2018 [typeset, yellow label]”, deposited in IZCAS; paratype, female: “ Yunnan Xishuangbanna Menghai / 1982-?- 16 / Wang Sumei, Zhou Jingruo [handwritten, Chinese] // C586 [handwritten] // PARATYPE ♀ / Miridiba xingkei sp. nov. / Chuanbu Gao & Hong Fang / det. 2018 [typeset, yellow label]”, deposited in NWAUF; paratypes, 2 females: “ Yunnan, Xishuangbanna, Menglong / Miridiba xingkei sp. nov. / Chuanbu Gao & Hong Fang / det. 2018 [typeset, yellow label]”, deposited in NWAUF Description of holotype (male). Body length 22.8 mm; width across humeri 9.8 mm, oval-elongate, strongly convex, dorsal surface glabrous. Colour: head, pronotum, scutellum and legs dark reddish brown; antennae, elytra and abdomen brown (Figs. 3a, b). Head: Frons densely punctate and glabrous; clypeus arcuate shaped, apex weakly emarginate medially; anterior margin moderately reflexed; fronto-clypeal suture wave-shaped; frontal carina distinctly raised and nearly straight; clypeus shorter than frons, length ratio between clypeus and frons before carina 0.60; distance between eyes nearly four times wider than eye (Fig. 3c). Antenna with 9 antennomeres; club with 3 antennomeres, slightly longer than antennomeres 2-6 combined (Fig. 3d). Thorax: Dorsal surface of pronotum densely punctate and glabrous, widest at basal 2/5; anterior margin smooth and flanged; lateral margin smooth and broadly reflexed; posterior margin smooth; anterolateral angles obtuse, posterior angles obtuse and round. Prosternal process basiconic shaped. Scutellum triangular, dorsal surface densely punctate and glabrous, 1.58 times wider than long. Dorsal surface of elytra glabrous, sutural costae developed; epipleuron with long, dense cilia (Figs. 3a, b). Legs: Protibia tridentate, denticle 2 sharp; dorsal carina forking to denticle 2; apical spur of protibia sharp, apical spur reaching basal one half of protarsomere 1. Metafemora moderately covered with long soft hairs near anterior margin and rough setae near posterior margin (Fig. 3b); outside of metatibia with 1 completed carina at distal 2/5, carina arc-shaped; dorsolateral margin with 2 thorns; dorsomedial margin with 5 pubescent thorns small to large; metatibia with two apical spurs of different sizes, the big spur acinaciform, 1.72 times longer than the small spur (Fig. 3e); metatarsomere 1 equal in length to metatarsomere 2. Abdomen: Lateral sides of abdominal sternites densely punctate and setiferous, setae short; posterior sternites 5 and 6 covered with long soft hairs. Pygidium: Fan-shaped pygidium densely punctate and setiferous, 1.37 times wider than long, apical pygidium at a right angle; middle area weakly convex. Male genitalia. Phallobase: Phallobase 1.2 times longer than parameres; dorsal surface with a depressed longitudinal sulcus at middle; anterior 1/5 of phallobase weakly constricted. Parameres: Parameres with two pairs of branches: two thick long dorsal branches and two short ventral branches; each dorsal branch with a thick protuberance on dorsum; tip of each dorsal branch with a notch in the ventral side; ventral branch with a big coneshaped hook ventrally before the apex (Figs. 3 g–i). Endophallus: Dorsal endophallus with temones tapered; medial endophallus with small hooks; distal end of endophallus with a round seminal vesicle (Fig. 3j). Female. Body slightly longer and broader than in male. Antenna with 9 antennomeres; club with 3 antennomeres, shorter than antennomeres 2–6 combined. Metafemora and apex of metatibia broader than in male. The big spur of apical metatibia broader and blunter than male, 1.3 times longer than the smaller spur (Fig. 3f). Variability. All the paratypes slightly differ in size (total body length 21.7–25.6 mm, width across humeri 9.5– 11.6 mm). Diagnosis. Miridiba (M.) xingkei new species and Miridiba (M.) ciliatipennis (Moser, 1913) are similar in the elytral epipleuron bearing dense, long cilia. The two species can be separated by following characters: the presence or absence of the midline on the posterior of the pronotum (absent in M. (M.) xingkei new species; present in M. (M.) ciliatipennis), the form of setae near the posterior margin of the metafemora (few large setae in M. (M.) xingkei new species, dense small setae in M. (M.) ciliatipennis), the shape of the spurs of the apical metatibia (arcshaped in M. (M.) xingkei new species, straight in M. (M.) ciliatipennis), the form of the parameres (each dorsal branch with a developed protuberance in M. (M.) xingkei new species, the dorsal branches without protuberances in M. (M.) ciliatipennis). Distribution. China (Yunnan: Puer, Xishuangbanna) (Fig. 6). Etymology. This new species is dedicated to Dr Xingke Yang, a respected researcher, who has devoted himself into taxonomy and systematics study of Chinese Coleoptera for more than thirty years. He will retire from the Institute of Zoology, Chinese Academy of Sciences in 2018. Chinese name. 杨脊鳃金龟 Remarks. Chang (1964) listed M. (M.) ciliatipennis from China. However, we examined all specimens in IZCAS identified as M. (M.) ciliatipennis by Chang himself and they all belong to the new species M. (M.) xingkei. Based on this, we have excluded M. (M.) ciliatipennis from the Chinese fauna.Published as part of Gao, Chuan-Bu, Bai, Ming, Fang, Hong & Yu, Zhi-Guo, 2018, Four new species of the genus Miridiba Reitter (Coleoptera: Scarabaeidae: Melolonthinae) from China, pp. 1-20 in Zootaxa 4527 (1) on pages 6-9, DOI: 10.11646/zootaxa.4527.1.1, http://zenodo.org/record/261188
Transmitter-preprocessing-assisted cooperative downlink transmission in DS-CDMA systems experiencing propagation path loss and Nakagami-<i>m</i> fading
No full textIn this contribution we propose and investigate a relay diversity transmission scheme for the direct-sequence code-division multiple-access (DS-CDMA) downlink, where each (destination) mobile terminal (MT) is aided by a cluster of relays for achieving the relay diversity. In the considered system downlink multiuser interference (MUI) is suppressed with the aid of transmitter preprocessing operated at the base-station (BS). Two transmitter preprocessing schemes are considered, which are operated in the principles of transmitter zero-forcing (TZF) and transmitter minimum mean-square error (TMMSE). At the MTs, signals received from the BS and relays are combined based on the principles of maximal ratio combining (MRC) or of maximum signal-to-interference-plus-noise ratio (MSINR). In this contribution the bit error rate (BER) performance of the relay-assisted DS-CDMA downlink is investigated, when the communications channels are assumed to experience both propagation pathloss and generalized Nakagami-m fading. Our study and simulation results show that the transmitter preprocessing can help to achieve the relay diversity by efficiently mitigating the MUI presenting at the relays and MTs. Furthermore, in our proposed relay diversity scheme the relays only require lowcomplexity signal processing for forwarding information to their served MTs
Pareuchiloglanis anteanalis Fang, Xu & Cui 1984
No full textPareuchiloglanis anteanalis Fang, Xu & Cui 1984 Pareuchiloglanis anteanalis Fang, Xu & Cui 1984: 209 (English p. 211), fig. 1. Type locality: Wudu Co. [Yangtze drainage], Gansu Prov., China. Holotype: Shaanxi Inst. Zool. 82VI9565. Paratypes: KIZ 82VI-9567 (1), 9651 (1), 9652 (1), 82X-1479 (1), 1480 (1), 1481 (1); Shaanxi Inst. Zool. 82VI-1420 (1), 9645 (1), 9649-50 (1, 1), 9653 (1), 9566 (1). Distribution: Yangtze drainage, China (Fang et al., 1984; Chu et al., 1999; Fu et. al., 2003).Published as part of Alfred W. Thomson & Lawrence M. Page, 2006, Genera of the Asian Catfish Families Sisoridae and Erethistidae (Teleostei: Siluriformes)., pp. 1-96 in Zootaxa 1345 on page 7
Performance of DS-CDMA downlink using transmitter preprocessing and relay diversity over Nakagami-m fading channels
No full textSigmaboilus Fang, Zhang & Wang 2007
No full textGenus Sigmaboilus Fang, Zhang & Wang, 2007 Type species: Sigmaboilus gorochovi Fang, Zhang & Wang, 2007 Revised diagnosis: Forewing: Base of tegmen constricted; ScA long, mildly undulate, reaching anterior wing margin beyond midlength; ScP long with numerous branches ending in stem ScA; Cross-veins at the base of area between CuA+M and CuP sigmoidal; CuA and CuP 1 a remaining united as CuA+CuP 1 a for a short and appreciable distance. Hindwing: ScP and R with basal common stem, basal free part of R slightly curved; R diverging nearer wing base than in forewing, RP branched before first branch of RA; M bowed toward R and diverging before origin of RP. Species included: S. gorochovi Fang, Zhang & Wang, 2007, S. sinensis Fang, Zhang & Wang, 2007, S. fuscus sp. nov. S. peregrinus sp. nov. Remarks: The genus Sigmaboilus Fang, Zhang & Wang, 2007 was erected based on only a single forewing from the Middle Jurassic of Daohugou, Inner Mongolia, China. The diagnostic characteristics of the hind wing can be seen clearly from the material described here: ScP fused with R at base, separated before the point of origin MA.Published as part of Gu, Junjie, Zhao, Yun-Yun & Ren, Dong, 2009, New fossil Prophalangopsidae (Orthoptera, Hagloidea) from the Middle Jurassic of Inner Mongolia, China, pp. 16-24 in Zootaxa 2004 on page 17, DOI: 10.5281/zenodo.18563
Closure to "Developing a Model of Construction Safety Culture" by Rafiq M. Choudhry, Dongping Fang, and Sherif Mohamed
No full textM. S. Eno Belinga, Découverte des chantefables beti-bulu-fang du Cameroun
No full textGörög-Karady Veronika. M. S. Eno Belinga, Découverte des chantefables beti-bulu-fang du Cameroun. In: L'Homme, 1971, tome 11 n°4. pp. 122-123
Leptotrombidium (Leptotrombidium) biluoxueshanense Yu, Hu and Fang 1982
No full textLeptotrombidium (Leptotrombidium) biluoxueshanense Yu, Hu and Fang, 1982: PAL Leptotrombidium (Leptotrombidium) biluoxueshanensis Yu, Hu and Fang, 1982; Li et al. 1997 Leptotrombidium biluoxueshanense, Stekolnikov 2013 [1 group]Published as part of Nielsen, David H., Robbins, Richard G. & Rueda, Leopoldo M., 2021, Annotated world checklist of the Trombiculidae and Leeuwenhoekiidae (1758 - 2021) (Acari: Trombiculoidea), with notes on nomenclature, taxonomy, and distribution, pp. 1-243 in Zootaxa 4967 (1) on page 126, DOI: 10.11646/zootaxa.4967.1.1, http://zenodo.org/record/474551
Devario xyrops Fang & Kullander, 2009, new species
No full text<i>Devario xyrops,</i> new species <p>(Fig. 1)</p> <p> <b>Holotype.</b> NRM 45658, adult female, 60.6 mm SL; Myanmar: Rakhine State: Thandwe: Thade River drainage: Taunggok, Yan Khaw Chaung, <i>ca</i> 4 km on logging road from Gwetauk village, 23 km on road Taunggok–Pyay; 21 Mar 1998, S. O. Kullander & R. Britz (SOK-98-010).</p> <p> <b>Paratypes.</b> All from Myanmar, Rakhine State. NRM 40843, 21, 44.8–76.9 mm SL; NRM 41674, 1, 55.2 mm SL; NRM 45596, 10, 9.5–21.9 mm SL. Same data as holotype. — NRM 40835, 6: 33.3–49.7 mm SL; NRM 41673, 1, 41.8 mm SL; Kananmae Chaung, near Leldee village, by foot 45 min from Gwechaung village at km 18 on road Thandwe–Taunggok. 20 Mar 1998. S. O. Kullander & R. Britz (SOK-98-007). — BMNH 2009.5.5.20–24, 5, 36.8–74.0 mm SL; Kyeintali Chaung; 15 Oct 2008, Thein Naing.</p> <p> <b>Diagnosis.</b> Distinguished from all other species of <i>Devario</i> except <i>D. anomalus</i> Conway <i>et al.</i> (2009) by the colour pattern, with a dark blotch anteriorly on the side composed of 4–5 short partly confluent vertical bars which may also be confluent to form a homogeneous blotch, and a wide dark horizontal band (P stripe) posteriorly on the side. Distinguished from <i>D. anomalus</i> by proportional measurements and meristics, most important by deeper body (29.9–35.,8% SL, vs. 25.0–26.8 % SL) and fewer lateral line scales (31–33, modally 32 vs. 33–35, modally 34). Distinguished from all barred species of <i>Devario</i> also by presence of an infraorbital process.</p> <p> <b>Description</b>. Measurements and counts were taken from 10 specimens, 59.5–76.9 mm SL (Table 1), representing the largest adults available, supplemented by counts from 13 additional X-radiographed specimens. All measured specimens were examined for gonads, and all have ripe ovaries and testes. The two largest specimens, 74.6 and 76.9 mm SL, are female, and male, respectively.</p> <p>Body laterally compressed, elongate, females slightly more deep-bodied than males (31.4–35.8 % SL vs. 29.9–31.0 %), and with deeper (16.5–18.7 % SL vs. 15.8–16.9 %) and wider (13.5–14.6 % SL vs. 12.9–13.5 %) head. Predorsal contour straight, ascending, sloping posteriorly from dorsal-fin insertion. Prepelvic contour strongly curved, more so in females; chest conspicuously more compressed below pectoral fin, but not keeled. Snout short, rounded in dorsal aspect, subtriangular in lateral aspect, about as long as eye diameter. Infraorbital process broader than high, with truncate distal margin which usually slightly irregular. Danionine notch caudally margined by well developed anteromediad projecting laminar dentary process. Skin cover absent from distal part of infraorbital process, dentary process, and anterior margin of supraorbital. Mouth terminal, obliquely directed upwards. Small bony knob at dentary symphysis. Maxilla reaching to below anterior margin of orbit. Jaws equal anteriorly; lower jaw ending anteriorly at horizontal through middle of eye. Lower jaw with 2–3 rows of minute conical tubercles concentrated on lateral surface, and additional scattered tubercles anteriorly, occasionally absent (Fig. 2) or only a few tubercles close to lower lip; tuberculation variably developed from hardly visible to well developed without correlation with sex. In all males two rows of strong, densely arranged sharp-tipped conical tubercles on the unbranched, and following 6–7 rays of pectoral fin; pectoral-fin tubercles absent in females. Rostral barbels short, length of infraorbital 1 or to base of maxillary barbels; maxillary barbels much shorter, at most half length of rostral barbels.</p> <p>Lateral line complete, along 31 (1), 32 (7), 33 (1) scales, and 2 scales on caudal-fin base; comprising one tubed scale followed by a canal running steeply caudoventrad under unperforated scales to slightly posterior to pectoral-fin base, where curved caudad and represented by scales with indistinct or absent perforation anteriorly, becoming distinctly perforated posterior to adpressed pectoral fin; running in a curve parallel to the ventral body outline and ending low on caudal peduncle and caudal-fin base; vertical section represented by about six scales, horizontal section by 25 or 26 scales, continued by two scales on caudal- fin base. Median predorsal scales 13 (2), 14 (7), 15 (1). Lateral scale rows passing between dorsal and pelvic fins ½7+1+2 (10). Circumpeduncular scale rows 12 (5), 13 (1), 14 (4). A row of scales along anal-fin base. About ¼ of caudalfin length scaled basally.</p> <p>Dorsal-fin rays iii.10½ (10), iii.11½ (11), iii.12½ (2). Anal-fin rays iii.13½ (8), iii.14½ (14), iii.15½ (1). Pectoral-fin rays i.11 (4), i.12 (4), i.13 (2). Pelvic-fin rays i.6 (2), i.7 (18). Dorsal fin inserted at highest point of dorsum, little posterior to middle of body. Anal fin inserted below anterior rays of dorsal fin. Pectoral-fin insertion at about vertical through posterior margin of osseous opercle; extending to pelvic-fin origin, slightly longer in females than in males (22.8–24.9 % SL vs. 20.9–22.4 %). Pectoral-fin axial lobe well developed. Pelvic fin inserted slightly anterior to midbody, not reaching to anal-fin origin. Pelvic axillary scale present. Caudal fin forked, lobes of about equal length.</p> <p>Vertebrae 16+18=34 (7), 17+17=34 (12), 17+18=35 (4). Pharyngeal teeth 5,4,2/2,4,5 (one specimen dissected).</p> <p> <b>Colouration in preservative</b>. Dorsum pale brownish, sides whitish. Opercle brownish dorsally, silvery ventrally. Narrow dark brown predorsal midline. Dark brown vertically oriented cleithral spot covering part of first lateral-line scale and scale above. On middle of side anterior to vertical from dorsal-fin origin a series of 4–5 brown short vertical bars, partly confluent, in many specimens dark brown and confluent to form elongate dark blotch. Dark brown horizontal band, margined by narrower light bands above and below, starting slightly posterior to vertical from anal-fin origin, terminating at end of caudal peduncle. Area between anterior and posterior lateral markings either without markings or with indistinct short vertical bars; dorsally, between posterior part of anterior lateral marking and anterior part of posterior lateral band, usually a short light brown horizontal stripe or row of small spots. Dorsal and anal fins pigmented basally and with a greyish stripe from anterior margin of fin to tips of posterior rays; hyaline distal to dark stripe. Caudal fin lightly pigmented, horizontal dark band on caudal peduncle continuing faintly on middle rays. Pectoral and pelvic fins hyaline. Juvenile 21.9 mm SL (Fig. 3), with dark brown band posteriorly as in adults, but vertical bars only indicated in anterior pigmentation. Smaller juveniles with lateral band indistinct and anterior pigmentation diffuse.</p> <p> <b>Molecular data</b>. Nucleotide sequences of the mitochondrial cytochrome <i>b</i> gene and a fragment of the nuclear rhodopsin gene were obtained from a single specimen from the type locality (NRM 41674) and reported by Fang <i>et al.</i> (2009), with GenBank accession numbers EU241374 and EU241439 (as <i>Danio</i> sp “TwoSpot”).</p> <p> <b>Etymology.</b> The specific epithet refers to the sharp, exposed bony margin of the supraorbital and the wide infraorbital process, and is combined from the Greek <i>xyron</i> (DρOv), razor, and <i>ops</i> (ωΨ) eye. It stands as a noun in apposition.</p> <p> <b>Geographical distribution and habitat</b>. Known only from small streams on the western slope of the Rakhine Yoma, north and south of Thandwe (Fig. 4). The type locality (Fig. 5) is the same as for <i>Garra vittatula</i> (Kullander & Fang, 2004: 265). It was a small forest river, at the time of sampling in the low water season reduced to a series of connected pools, up to 2 m wide, and nowhere more than 1 m deep. The water was clear, colourless, and slow-flowing or stagnant. The stream bottom consisted of stones, gravel and rock. <i>Devario xyrops</i> was the dominant species. Other species included the cyprinids <i>Garra rakhinica</i> Kullander & Fang, <i>G. vittatula</i> Kullander & Fang, <i>Danio feegradei</i> Hora, also endemic to the western Rakhine State, and <i>Xenentodon cancila</i> (Hamilton) (Belonidae), <i>Channa</i> sp. (Channidae), <i>Lepidocephalichthys</i> sp. (Cobitidae), and <i>Sicyopterus fasciatus</i> (Day) (Gobiidae). <i>Puntius binduchitra</i> (Hora) (Cyprinidae); another endemic cyprinid easily identified by its colour pattern, was observed but could not be collected, and also one larger cyprinid specimen could not be sampled. The second locality, the Kananmae Chaung, is the type locality of <i>Danio aesculapii</i> Kullander & Fang, and is described by Kullander & Fang (2004:265; 2009: fig. 3). It is also a small forest stream with stony bottom. Habitat information is not available for the BMNH specimens.</p>Published as part of <i>Fang, Fang & Kullander, Sven O., 2009, Devario xyrops, a new species of danionine fish from south-western Myanmar (Teleostei: Cyprinidae), pp. 33-40 in Zootaxa 2164 (1)</i> on pages 35-38, DOI: 10.11646/zootaxa.2164.1.3, <a href="http://zenodo.org/record/5323423">http://zenodo.org/record/5323423</a>
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