109,706 research outputs found
Kwangtung 1:50,000 [cartographic material] /
No full textVarious eds. Relief shown by contours and spot heights.; Sheets individually titled at top margin, e.g. Tang Cun = Tang-tsun.; Sheets individually numbered at top margin, e.g. Sheet 7621-II.; Original published: Beijing? : Jun shi wei yuan hui jun ling bu lu di ce liang zong ju, surveyed in 1927, published 1938.; Includes index map to adjoining sheets.; Some of National Library of Australia's copies mounted on linen.Alternate title: Guangdong 1:50,000Title on index map: Guangdong wu wan fen yi di xing tuAlternate title: Series L78
mechanization of lily microbulb
No full textmechanization of lily microbulb multiplication operations. ta-te lin & ching-lu hsieh. department of agricultural machinery engineering.. national taiwan university.. taipei. taiwan. roc. mechanization of lily microbul
Guineapona Lu & Zhang 2023, gen. nov.
No full textGuineapona gen. nov. Type species: Guineapona monolophos sp. nov., here designated.Published as part of Lu, Lin & Zhang, Yalin, 2023, New genera and species of Paraboloponina (Hemiptera: Cicadellidae: Drabescini) from Indonesia, pp. 588-594 in Zootaxa 5244 (6) on page 589, DOI: 10.11646/zootaxa.5244.6.4, http://zenodo.org/record/767310
Canopyana apicospina Lu & Zhang 2023, sp. nov.
No full textCanopyana apicospina sp. nov. (Figs. 2A–W)Published as part of Lu, Lin & Zhang, Yalin, 2023, New genera and species of Paraboloponina (Hemiptera: Cicadellidae: Drabescini) from Indonesia, pp. 588-594 in Zootaxa 5244 (6) on page 591, DOI: 10.11646/zootaxa.5244.6.4, http://zenodo.org/record/767310
Streptomyces reniochalinae Li & Wang & Zhou & Lin & Lu 2019, SP. NOV.
No full textDESCRIPTION OF STREPTOMYCES RENIOCHALINAE SP. NOV. Streptomyces reniochalinae (re.ni.o.cha′ li.nae. N.L. gen. n. reniochalinae of the marine sponge Reniochalina stalagmitis). Aerobic, Gram-stain-positive, non-motile, non-acid–alcohol-fast actinomycete that forms extensively branched substrate mycelia and white aerial hyphae which differentiated into chains of smooth-surfaced spores. Growths occurs at 20–40 Ǫ C and at pH 6.0–11.0 with 0–15% NaCl. Gelatin, and Tweens 40 and 60 are degraded, but CMC, aesculin and Tween 80 are not. Degradation of Tween 20 and starch are weakly positive. Milk coagulation, peptonization and nitrate reduction are positive. Utilizes L- arabinose, D- arabinose, cellobiose, D- fructose, D- galactose, D- glucose, glycerol, lactose, maltose, D- mannitol, D- mannose, melibiose, L- rhamnose, D-ribose, trehalose, D- xylose, sodium acetate, sodium pyruvate and sodium citrate as sole carbon sources; weakly utilizes inositol and raffinose, but not dulcitol, D- sorbitol, sucrose or D- xylitol. Utilizes L- glutamine, L- lysine, L- proline, L- serine and L- threoninexanthine as sole nitrogen sources; weakly utilizes L- alanine, L- arginine, L- asparagine, glycine, L- histidine, hypoxanthine, L- hydroxyproline and L- leucine, but not adenine, L- aspartic acid, L- cystenine, L- glutamic acid, L-methionine, L- phenylalanine, L- tryptophan, L- tyrosine or L-valine. The cell wall contains LL- diaminopimelic acid and the whole-cell sugars are galactose, glucose and ribose. Diphosphatidylglycerol, phosphatidylethanolamine and phosphatidylinositol are the predominant polar lipids. The menaquinone system contains MK-9(H 6) as a major component, and MK-9(H 4) and MK-9(H 8) as minorities. The major fatty acids are iso-C 16: 0, anteiso-C 15: 0 and anteiso-C 17: 0. The G+C content is 71.9 mol% of the 7.6 Mb draft genome. The type strain, LHW50302 T (=DSM 106194 T =CCTCC AA 2018013 T), was isolated from a Reniochalina stalagmitis marine sponge collected in the South China Sea. The GenBank accession number for the 16S rRNA gene sequence and the draft genome sequence of the type strain are KX347891 and QOIM00000000, respectively.Published as part of Li, Lei, Wang, Jie, Zhou, Yong-jun, Lin, Hou-wen & Lu, Yan-hua, 2019, Streptomyces reniochalinae sp. nov. and Streptomyces diacarni sp. nov., from marine sponges, pp. 99-104 in International Journal of Systematic and Evolutionary Microbiology 69 (1) on pages 102-103, DOI: 10.1099/ijsem.0.003109, http://zenodo.org/record/604864
Streptomyces diacarni Li & Wang & Zhou & Lin & Lu 2019, SP. NOV.
No full textDESCRIPTION OF STREPTOMYCES DIACARNI SP. NOV. Streptomyces diacarni (di.a.car′ ni. N.L. gen. n. diacarni of the marine sponge Diacarnus megaspinorhabdosa). Aerobic, Gram-stain-positive, non-motile, non-acid–alcohol-fast actinomycete that forms extensively branched substrate mycelia and white aerial hyphae which differentiated into chains of smooth-surfaced spores. Growths occurs at 20–40 Ǫ C and at pH 6.0–11.0 with 0–15 % NaCl. Growths occurs at 20–40 Ǫ C and at pH 6.0–11.0 with 0–15 % NaCl. Gelatin, and Tweens 20, 40 and 60 are degraded, but CMC and Tween 80 are not. Degradation of aesculin and starch are weakly positive. Milk coagulation, peptonization and nitrate reduction are positive. Utilizes L- arabinose, D- arabinose, cellobiose, D- fructose, D- galactose, D- glucose, glycerol, lactose, maltose, D- mannitol, D- mannose, melibiose, L-rhamnose, D- ribose, sodium acetate, sodium pyruvate, sodium citrate, trehalose and D- xylose as sole carbon sources; weakly utilizes inositol and raffinose, but not dulcitol, D- sorbitol, sucrose or D- xylitol. Utilizes L- alanine, L- arginine, L- asparagine, L- glutamine, glycine, L- histidine, L-hydroxyproline, L- lysine, L- proline, L- serine, L- threonine and xanthine as sole nitrogen sources; and weakly utilizes hypoxanthine, L- leucine and L- valine, but not adenine, L-aspartic acid, L- cystenine, L- glutamic acid, L- methionine, L-phenylalanine, L- tryptophan or L- tyrosine. The cell wall contains LL- diaminopimelic acid and whole-cell sugars are glucose, galactose and ribose. Diphosphatidylglycerol, phosphatidylethanolamine and phosphatidylinositol are the predominant polar lipids. The menaquinone system contains MK-9(H 6) as a major component, and MK-9(H 4) and MK-9(H 8) as minorities. The major fatty acids are iso-C 16: 0, anteiso-C 15: 0 and anteiso-C 17: 0. The G+C content is 72.1 mol% of the 7.6 Mb draft genome. The type strain, LHW51701 T (=DSM 106126 T =CCTCC AA 2018017 T), was isolated from a Diacarnus megaspinorhabdosa marine sponge collected in the South China Sea. The GenBank accession number for the 16S rRNA gene sequence and the draft genome sequence of the type strain are KX347890 and QOIN00000000, respectively.Published as part of Li, Lei, Wang, Jie, Zhou, Yong-jun, Lin, Hou-wen & Lu, Yan-hua, 2019, Streptomyces reniochalinae sp. nov. and Streptomyces diacarni sp. nov., from marine sponges, pp. 99-104 in International Journal of Systematic and Evolutionary Microbiology 69 (1) on page 103, DOI: 10.1099/ijsem.0.003109, http://zenodo.org/record/604864
AIM912248_Supplemental_material – Supplemental material for Manual acupuncture relieves microglia-mediated neuroinflammation in a rat model of traumatic brain injury by inhibiting the RhoA/ROCK2 pathway
No full textSupplemental material, AIM912248_Supplemental_material for Manual acupuncture relieves microglia-mediated neuroinflammation in a rat model of traumatic brain injury by inhibiting the RhoA/ROCK2 pathway by Ming-min Zhu, Ji-huan Lin, Peng Qing, Liu Pu, Shu-lian Chen, Shu-jun Lin, Cheng-lu Li, Lu-xi Cao and Yi-min Zhang in Acupuncture in Medicine</p
Bombus (Pyrobombus) taiwanensis Williams, Sung, Lin & Lu 2022
No full textBombus (Pyrobombus) taiwanensis Williams, Sung, Lin & Lu, 2022 Figs 1‒4 [Bombus sp. non descripta Chiu 1948: 71.] [Bombus (Pyrobombus) nr. hypnorum Starr, 1992: 149.] Bombus (Pyrobombus) taiwanensis Williams et al., 2022: 438. Holotype by original designation: ♀, Mt Hehuan, Taiwan (TFRI). Examined. Diagnosis Female Distinguished by: clypeus in the central area smooth and shining with only a few large punctures, mostly spaced by much more than their own widths; ocello-ocular area with the inner eye margin mostly shining with few small punctures and the few larger, medium punctures forming a single row parallel to the eye margin; front, middle and hind leg basitarsi all with the exoskeleton lighter brown than for the tibiae; hair predominantly black but with metasomal T4‒6 a dull sandy-brown or pale orange. Male Distinguished by: front, middle and hind leg basitarsi all with the integument lighter brown than the tibiae; genitalia with the gonostylus inner anterior (basal) projection separated from the gonocoxa by less than the breadth of the recurved hook of the penis-valve head. Material examined Material sequenced or examined CHINA – Taiwan • 1 ♀ (worker); Nantou Hsien, Tsuifeng [Cuifeng]; 24.1060° N, 121.1988° E; alt. 2300 m; 23‒25 Jun. 1983; K.S. Lin and C. Lin leg.; BOLD-1550A06-TWN; PW • 1 ♂; Hualien Hsien, Tayuling; 23.9767° N, 121.5206° E; alt. 2560 m; 9‒16 Jun. 1980; K.S. Lin and B.H. Chen leg.; BOLD- 1550A07-TWN; PW. Other material sequenced GenBank: MZ831884, MZ831885, MZ831886, MZ831887, MZ831891, MZ831892. Distribution Endemic to the mountains of Taiwan, where it is extremely rare, at elevations of 2300‒3100 m (Williams et al. 2022).Published as part of Williams, Paul H., Dorji, Phurpa, Ren, Zongxin, Xie, Zhenghua & Orr, Michael, 2022, Bumblebees of the hypnorum-complex world-wide including two new near-cryptic species (Hymenoptera: Apidae), pp. 46-72 in European Journal of Taxonomy 847 on page 56, DOI: 10.5852/ejt.2022.847.1981, http://zenodo.org/record/735916
Bombus (Pyrobombus) taiwanensis Williams, Sung, Lin and Lu 2022, sp. nov.
No full textBombus (Pyrobombus) taiwanensis Williams, Sung, Lin and Lu sp. nov. (Figures 1, 2) urn:lsid:zoobank.org:act: 726E8A64-28A2-4DD9-8801-651DED8BD495 [Bombus sp. non descripta Chiu 1948: 71, 1♀ (worker) (TARI)] [Bombus (Pyrobombus) nr. hypnorum Starr, 1992: 149, 3♀ (workers) 2♂ (TARI)] +Inference of being conspecific supported by published (Huang et al. 2015; Williams et al. 2020) or ++unpublished (Thanoosing, in prep.) GMYC- or PTP-coalescent analyses for COI barcodes. *Inference of being separate species supported by PTP-coalescent analyses for COI barcodes (Williams et al. 2020) or **by morphology (Williams et al. 2009). Bombus (Megabombus) trifasciatus Smith, 1852 Bombus wilemani Cockerell, 1911 Bombus (Megabombus) bicoloratus Smith, 1879 Bombus (Psithyrus) turneri (Richards, 1929 [Psithyrus]) Psithyrus monozonus (Friese, 1931) not of Friese 1909 [= B. lucorum (Linnaeus)] Bombus (Pyrobombus) taiwanensis sp. nov. * Bombus (Pyrobombus) flavescens Smith, 1852 Bombus (Pyrobombus) sonani (Frison, 1934 [Bremus])* Bombus (Alpigenobombus) angustus Chiu, 1948 * [Bombus (Bombus) terrestris (Linnaeus, 1758) – introduced from Europe only in glass houses] Bombus (Melanobombus) eximius Smith, 1852 Bombus latissimus Friese, 1910 Bombus (Melanobombus) formosellus (Frison, 1934 [Bremus])* Material examined. Holotype: 1♀ (queen), labels (1): white, printed in black ‘ Mt. Hehuan, South peak/(3100 m), Nantou Co.,/ Taiwan, VI-15-2019,/ I. H. Sung’; (2) white, printed in black ‘ Bombus taiwanensis /Williams, Sung, Lin & Lu sp. nov./det. Paul H. Williams’; (3) red, printed in black ‘ HOLOTYPE / ♀ / Bombus taiwanensis /Williams, Sung, Lin & Lu’; (4) white, printed in black ‘[barcode]/00214314’ (TFRI). Paratypes: 1♀ (worker), labels: (1) white, printed in black ‘Mt. Hehuan, South peak/ (3100 m), Nantou Co,/ Taiwan, VI-15-2019,/I. H. Sung’; (2) white, printed in black ‘ Bombus taiwanensis /Williams, Sung, Lin & Lu sp. nov./det. Paul H. Williams’; (3) red, printed in black ‘ PARATYPE / ♀ / Bombus taiwanensis / Williams, Sung, Lin & Lu’; (4) white, printed in black ‘[barcode]/00214315’ (TFRI). 1♀ (worker), labels (1): white, printed in black ‘ Mt. Hehuan, South peak/(3100 m), Nantou Co.,/ Taiwan, VI-15-2019 /I. H. Sung’; (2) white, printed in black ‘ Bombus taiwanensis /Williams, Sung, Lin & Lu sp. nov./det. Paul H. Williams’; (3) red, printed in black ‘ PARATYPE / ♀ / Bombus taiwanensis / Williams, Sung, Lin & Lu’; (4) white, printed in black ‘[barcode]/00214316’ (TFRI). 1♀ (worker), labels (1): white, printed in black ‘Mt. Hehuan, South peak/(3100 m), NantouCo.,/ Taiwan, VI-15-2019,/I. H. Sung’; (2) white, printed in black ‘ Bombus taiwanensis / Williams, Sung, Lin & Lu sp. nov./det. Paul H. Williams’; (3) red, printed in black ‘ PARATYPE / ♀ / Bombus taiwanensis / Williams, Sung, Lin & Lu’; (4) white, printed in black ‘[barcode]/00214317’ (TFRI). 1♀ (worker), labels (1): white, printed in black ‘ Mt. Hehuan, South peak/(3100 m), Nantou Co.,/ Taiwan, VI-15- 2019,/I. H. Sung’; (2) white, printed in black ‘ Bombus taiwanensis /Williams, Sung, Lin & Lu sp. nov./det. Paul H. Williams’; (3) red, printed in black ‘ PARATYPE / ♀ / Bombus taiwanensis / Williams, Sung, Lin & Lu’; (4) white, printed in black ‘[barcode]/00214318’ (TFRI). Compared material. 1♀ (worker), labels: (1) orange, printed in black ‘C. TAIWAN: Tsuifeng/ 2300 m. Nantou Hsien / 23‒25.VI.1983 /K.S. Lin & S.C. Lin’; (2) white, handwritten ‘nr. ardens ’; (3) white, handwritten ‘[worker] Bombus /(Pyrobombus)/ hypnorum /(Linnaeus)/ det. P.H. Williams /1991’; (4) green, printed in black ‘BOLD# (BEE-BOL /BBW/ PHW)/ 1550A06-TWN’; (5) white, printed in black ‘[worker] Bombus /(Pyrobombus)/ taiwanensis / det. P.H. Williams /2021’ (PHW). 1♂, labels: (1) orange, printed in black ‘C. TAIWAN: Tayuling/ 2560 m. Hualien Hsien / 9‒16.VI.1980 /K.S. Lin & B.H. Chen’; (2) white, handwritten ‘ ♂ Bombus /(Pyrobombus)/ hypnorum /(Linnaeus)/det. P.H. Williams /1991’; (3) green, printed in black ‘BOLD# (BEE-BOL /BBW/ PHW)/1550A07-TWN’; (4) white, printed in black ‘ ♂ Bombus /(Pyrobombus)/ taiwanensis /det. P.H. Williams /2021’ (PHW). Etymology Named for its occurrence in Taiwan, avoiding homonymy with earlier names in Bombus of formosanus, formosellus, formosulus and formosus. Diagnosis A predominantly black, orange-tailed bumblebee from Taiwan (Figure 1). Within the hypnorum complex distinguished by (Figure 1): female and male with the front, middle and hind leg basitarsi all with the integument lighter brown than the tibiae (vs darker like the rest of the body for B. hypnorum); hair (pubescence) of the metasoma with all of terga 4‒6 a pale but dull sandy brown or very pale orange (vs white for B. hypnorum). Female clypeus in the half nearest to the labrum smooth and shining with only a few large punctures, mostly spaced by much more than their own widths (Figure 2) (vs large punctures often separated by only their own widths for B. hypnorum). Male genitalia with the gonostylus inner anterior (basal) projection separated from the gonocoxa by less than the breadth of the recurved hook of the penis-valve head (vs separated by much more than the breadth of the recurved hook of the penis-valve head for B. hypnorum). Description Female habitus illustrated in Figure 1, body size small (worker body length 10‒12 mm), hair (pubescence) moderately long, wings nearly clear. Mandible with the distal notch anterior to the posterior tooth (incisura) very shallow and hardly marked. Oculo-malar area (‘cheek’ sensu Williams et al. 2014; not the gena) of medium length, 1.0× longer (length measured between the ventral edge of the compound eye and the edge of the malar area at the articulation of the mandible midway between the mandibular condyles) than the breadth of the mandible at its base (breadth between and including the mandibular condyles). Clypeus weakly swollen (Figure 2), its raised area nearly flat, the central area with few widely scattered large and medium punctures, few punctures especially medially and ventrally adjacent to the labrum. The area between the inner edge of the compound eye and the outer edge of the lateral ocellus occupied in just over its outer third by a broad band with a few mostly large punctures, spaced by more than their own widths, the smaller punctures between the larger punctures very few. Mid basitarsus with the distal posterior corner broadly rounded; hind tibia outer surface with a corbicula, the surface sculpturing weakly reticulate so that the surface appears slightly matt; hind basitarsus in the distal three-quarters covered with short branched decumbent and weakly overlapping hairs with golden reflections; tergum 6 posteriorly rounded and not divided medially, with a small subapical dorsal boss. Colour pattern of the hair of the body predominantly brownish black. Head entirely black except for orange hairs anteriorly on the labrum and laterally on the mandibles. Thoracic dorsum anterior to the wing bases with paler but dark sandy brown hair intermixed, this paler hair extending down the side of the thorax anteriorly, and on the scutellum posteriorly; the front, middle and hind leg tibiae all with some hairs orange, the basitarsi all with the integument lighter brown than the tibiae and with more orange hairs. Hair of the metasoma with tergum 3 posteriorly and all of terga 4‒6 a pale but dull sandy brown or very pale orange. Male body size small (body length 12 mm), hair (pubescence) moderately long, wings nearly clear. Colour pattern of the hair of the body predominantly dark brownish, almost black. Head and the thoracic dorsum anterior to the wing bases with paler but dull sandy brown hair intermixed, this pale hair covering the side of the thorax (mesepisternum), and on most of the scutellum; the front, middle and hind leg tibiae all with the long hairs orange, the basitarsi all with the integument lighter brown than the tibiae and with the long hairs orange. Hair of the metasoma with tergum 1 and all of terga 4‒7 a pale but dull sandy-brown or very pale orange. Male genitalia with the gonostylus nearly triangular, the inner anterior (basal) projection separated from the gonocoxa by less than the breadth of the recurved hook of the penis-valve head; the volsella scarcely projecting beyond the gonostylus; the penis valve with the head recurved as a flattened sickle-shaped hook that is not strongly tapered. Distribution Endemic to the mountains of Hsinchu, Nantou and Hualien counties, central Taiwan, at elevations of 2300‒3100 m.Published as part of Williams, Paul H., Sung, I-Hsin, Lin, Yi-Jing & Lu, Sheng-Shan, 2022, Discovering endemic species among the bumblebees of Taiwan (Apidae, genus Bombus), pp. 435-447 in Journal of Natural History 56 (5 - 8) on pages 438-442, DOI: 10.1080/00222933.2022.2052991, http://zenodo.org/record/680972
sj-pdf-1-imr-10.1177_03000605221096161 - Supplemental material for Does Waldenstrom’s macroglobulinemia also cause bone destruction? A rare case report
No full textSupplemental material, sj-pdf-1-imr-10.1177_03000605221096161 for Does Waldenstrom’s macroglobulinemia also cause bone destruction? A rare case report by Jun-Ming Lin, Xiao-Jun Yuan, Lu Zhang, Guang Li, Xin-rong Gan and Wen-Hua Xu in Journal of International Medical Research</p
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