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Li han lin quan ji: si shi er juan, mu lu si juan, nian pu. v.1
No full text[李白].綫裝, 1函.框20.3x14.8公分, 9行18字, 小字雙行同. 白口, 左右雙邊, 單白魚尾. 版心中鐫"李集"及卷次, 下鐫葉次.書根印有"李翰林集"前有王樨登序, 李陽冰《李翰林詩序》, 樂史《別集序》, 宋敏求後序, 曾鞏後序, 毛漸題跋.書中樂史《別集序》載"李翰林歌詩李陽冰纂為草堂集十卷史又別收歌詩十卷與草堂集互有得失因校勘排為二十卷號曰李翰林集"With: 李翰林年譜 / 薛仲邕編 ; 舊唐書列傳 ; 新唐書列傳 ; 李翰林墓誌銘 / 李華 ; 碣記 / 劉全 ; 碑陰記 / 蘇軾.Xian zhuang, 1 han.Kuang 20.3 x 14.8 gong fen, 9 hang 18 zi, xiao zi shuang hang tong. Bai kou, zuo you shuang bian, dan bai yu wei. Ban xin zhong juan "Li ji"ji juan ci, xia juan ye ci.Shu gen yin you "Li han lin ji"Qian you Wang Xideng xu, Li Yangbing "Li han lin shi xu", Yue Shi "Bie ji xu", Song Minqiu hou xu, Zeng Gong hou xu, Mao Jian ti ba.Shu zhong Yue Shi "Bie ji xu" zai "Li han lin ge shi Li Yangbing zuan wei Cao tang ji shi juan shi you bie shou ge shi shi juan yu Cao tang ji hu you de shi yin jiao kan pai wei er shi juan hao yue Li han lin ji"[Li Bai].With: Li han lin nian pu / Xue Zhongyong bian ; Jiu Tang shu lie zhuan ; Xin Tang shu lie zhuan ; Li han lin mu zhi ming / Li Hua ; Jie ji / Liu Quan ; Bei yin ji / Su Shi
Eutetrapha lini Chou, Chung & Lin 2010
No full textEutetrapha lini Chou, Chung & Lin, 2010 Figs. 122, 153 f & 153g Eutetrapha lini Chou, Chung & Lin, 2010: 313, figs. 1–16. Type locality: China, Taiwan, Taitung County, Soca. Type depository: NMNST. Eutetrapha lini; Lin, 2015: 276, figs. 1859432–434. Description. Male: length: 13.2–14.0 mm, humeral width: 4.2–4.4 mm. Female: length: 13.8–16.0 mm, humeral width: 4.7–5.3 mm. Details refer to Chou et al. (2010). Diagnosis. This species differs from Paraglenea spp. by male with only anterior claws of pro- and mesotarsi appendiculate, remainders all simple (all male claws in Paraglenea appendiculate). It is similar to Eutetrapha chrysochloris (Bates, 1879), but can be distinguished by metallic blue to purple blue scales, larger and sparser elytral punctures, almost rounded black arc on apical half of elytra, hardly visible elytral apical tooth at the outer angle, etc., and on genitalia distinguished by stouter lateral lobes of tegmen, nearly rounded apex of ventral plate etc. Remarks. Eutetrapha lini is a nocturnal species, being attracted by light trap. We believe it is probably monophagous (Chou et al. 2010). Distribution. China: Taiwan. Type specimens: Holotype male, Taiwan, Taitung county, Soca, 22°15′N, 120°50′E, 2009. V.16, leg. Yi-Ting Chung (NMNST). Paratypes: 1 female, Taitung county, Soca, 1999. VII.7, leg. Wenhsin Lin (NMNST, ex CWSL); 1 female, Taitung county, Soca, Da-Ren Hsiang (township), alt. 500 m, 2006. VI.30, leg. WenI Chou (CWIC); 3 males 3 females, Taitung county, Soca, 2009. V.16, leg. Yiting Chung (1 female in CYTC, 1 male 2 females in IZAS, 1 male in CWIC, 1 male in CWSL); 2 females, same data but 2009. IV.29 (1 female in CCCC, 1 female in NMNST); 1 male, same data but 2009. IV.23 (CCCC); 1 male, same data but 2009. IV.2 (CYTC).Published as part of Lin, Mei-Ying, Bi, Wen-Xuan & Yang, Xing-Ke, 2017, A revision of the genus Eutetrapha Bates (Coleoptera: Cerambycidae: Lamiinae: Saperdini), pp. 151-202 in Zootaxa 4238 (2) on pages 188-189, DOI: 10.11646/zootaxa.4238.2.1, http://zenodo.org/record/34519
Han lin shuo chang zhuan ji dai
No full textLive recording.Possibly reproduced from other commercial recording or radio broadcast (Pending for review)Electronic reproduction from Rulan Chao Pian Betamax collection.Performing group: 漢霖民俗說唱藝術團.Sung in Chinese.Performing group: han lin min su shuo chang yi shu tuan
Molecular phylogeny and morphological revision of Myotis bats (Chiroptera: Vespertilionidae) from Taiwan and adjacent China
No full textRuedi, Manuel, Csorba, Gábor, Lin, Liang- Kong, Chou, Cheng-Han (2015): Molecular phylogeny and morphological revision of Myotis bats (Chiroptera: Vespertilionidae) from Taiwan and adjacent China. Zootaxa 3920 (1): 301-342, DOI: 10.11646/zootaxa.3920.2.
Teng Yen-lin, Tchong-wen ts'an-k'ao-chou kiu-yao
No full textStein Rolf Alfred. Teng Yen-lin, Tchong-wen ts'an-k'ao-chou kiu-yao. In: Bulletin de l'Ecole française d'Extrême-Orient. Tome 41, 1941. pp. 393-394
Myotis soror Ruedi, Csorba, Lin & Chou, 2015, sp. n.
No full textMyotis soror sp. n. Figures 2, 3, 5, 8 a, and 9 a Holotype. Adult female collected by G. Csorba, C.-C. Huang and H.-C. Kuo on 5 September 2003 (field number # CSOTA 141). The dry skin and skull are deposited in the collections of the Hungarian Natural History Museum (HNHM) under accession number 2003.36. 20. Part of the mitochondrial Cyt b (413 bp) was sequenced from tissue extracts taken from the holotype; this sequence is deposited in GenBank under accession number KP 187901. The Cyt b gene was used in the phylogenetic analyses presented herein (Fig. 3). Type locality. The holotype and only known specimen was caught along the “water pipe road”, near the Highland Experimental Farm of National Taiwan University, Nantou County, Taiwan ROC (approximate coordinates: 24 °05’ N, 121 °09’ E), at an altitude of 2100 m above sea level (location 9 in figure 1). Distribution. The only known specimen of M. soror sp. n. is an adult female caught in a mist-net placed across a small road at Meifong, Nantou County, in the slopes of Mt Hehuan, in central Taiwan (location 9 in figure 1). The evergreen, temperate forests surrounding this area is the typical vegetation found at this elevation (2100 m). Other species of bat caught in the same area during our survey include an unknown species of Pipistrellus, Harpiola isodon, M. frater, M. laniger, M. secundus sp. n., S. latirostris, Murina gracilis, Plecotus taivanus, Miniopterus fuliginosus, Barbastella leucomelas, Rhinolophus monoceros and R. formosae. As none of the previous, intensive surveys of the bat fauna of Taiwan evidenced this species elsewhere (Chou 2004; Lin et al. 2004), M. soror sp. n. might indeed be a very rare forest species. Nothing is known about its natural history besides that the female was in a post-lactating stage (with teats still enlarged and devoid of hairs) when it was collected, and thus must have been breeding recently in the area. Etymology. We name it soror (meaning sister in Latin) as it is clearly related to Myotis frater, its sister species in phylogenetic reconstructions (see Clade III in figure 3). Owing to its peculiar coloration, we suggest Reddish Myotis as an appropriate vernacular name. Measurements of the holotype. Measurements are in mm and, unlike in other species, were taken on the prepared specimen. Head and body length, 48; tail length, 41; forearm length, 42.1; hind foot length (including claw), 7.6; tibia length, 17.2; thumb length, 5.1 and claw 2.5; ear length, 11; tragus length, 6; greatest skull length, including incisors, 13.8; greatest zygomatic breadth, 8.9; postorbital breadth, 4.1; mastoid breadth, 7.8; greatest braincase width, 7.2; upper canine-molar toothrow, 5.2; width across upper canines, 4.2; width across 3 rd upper molars, 5.7 (Table 4). Diagnosis. Medium-sized Myotis with striking pelage color, rich cinnamon-brown with lighter, golden hair tips dorsally (Fig. 7 a) and only slightly lighter ventrally. Color of face brownish and other bare parts dark brown. Wing membranes attached close to base of outer toe, on the distal part of the metatarsus (Fig. 7 b). Feet nearly half tibia length. Tail notably shorter than head and body length. Ears relatively short and broad with a distinct notch on the middle of the rear edge of conch (Fig. 7 c). The inner and outer sides of the conch are covered with sparse, cinnamon-rufous hairs. Skull angular, with short rostrum and abruptly raised frontal part of braincase (as seen in profile, Fig. 8 a). Teeth relatively robust with second upper premolars small and moderately displaced inside from toothrow, but not visible in side view. Upper canines strong, with a marked groove along the labial edge. Description. The pelage is dense, soft and relatively long on the dorsum (about 6 mm); dorsal hairs cinnamon brown on the base and becoming progressively lighter towards the tips, the last 2 mm being golden yellow, giving a frosted appearance to the dorsal fur. Ventral parts appear slightly paler, with hairs brown to the middle, becoming lighter, almost creamy towards the tip. Bare parts, including ears and patagium, reddish-brown, with face lighter, flesh colored. Ears short and broad, not reaching the nose tip when laid forward; conspicuous notch at two-thirds of its height on the rear edge (Fig. 7 c). Long (up to 1.6 mm), sparse cinnamon hairs are present on both inner and outer sides of the conch. Tragus relatively short, but reaching the ear notch; the anterior edge is slightly convex but the exterior margin has a small lobe at the base (hidden into the conch), and a larger one along half of its length; the tragus is convergent and tapers medially forming a slightly rounded head at the tip (Fig. 7 c). Wing membranes are essentially naked (except the underparts, close to the body), and attached to the distal parts of the metacarpus, near the base of the outer toe (Fig. 7 b). Feet are robust, with strong curved claws, and about half the size of tibia length. Uropatagium broad with tail almost fully included in the membrane. The calcar is short (about one-third uropatagium edge length), and bears an indistinct, unkeeled lobe. The tail is notably shorter than head and body length. When viewed in profile, the skull has a relatively short rostrum, and an abruptly raising frontal part of the braincase (Fig. 9 a). The occipital part looks like a square in profile or when viewed from above (Fig. 8 a). Lambdoid crests are visible laterally, but no notable sagittal crest is present. Dental formula I 2 / 3 C 1 / 1 PM 3 / 3 M 3 / 3, comprising the adult dentition of 38 teeth. Teeth are robust, with upper canines longer than third premolars, but the lower canines are much weaker, barely reaching the height of lower premolars (Fig. 8 a). The two upper incisive are nearly as high as wide, short, of comparable size and both are visible in side view. The upper canines have a distinct groove along the labial edge. The first upper premolar is small and aligned in toothrow, but the second is minute and displaced inwards and barely visible in side view. The third premolar is large, but bears an inconspicuous paraconule in its front margin. Molars are robust, but low, with ill-defined paraconules. The three lower premolars are in a row, not particularly crowded. All lower molars are myotodont. Comparisons. Owing to its short rostrum, raised frontal parts of braincase, angular skull shape (Figs. 8 a, 9 a) and inwards displaced second upper premolars, Myotis soror sp. n. is clearly related to the M. frater species complex (sensu Tsytsulina & Strelkov 2001). However, it differs genetically from sympatric specimens of M. frater by at least 11 % (K 2 P divergence at the Cyt b gene; Table 5). Its rich cinnamon pelage (Fig. 7 a) with golden frosted appearance of the dorsal fur is also unique in this group, all other taxa living in temperate regions being darker brown (sometimes lighter brown in juvenile specimens, Yoshiyuki 1989). The desert form M. bucharensis is decidedly much paler and slightly larger. With a forearm length of 42.1 mm, M. soror sp. n. is also larger than the Far Eastern taxa (longicaudatus, kaguyae and eniseensis) and slightly larger than sympatric M. frater s. s. (FA barely reaching 41 mm; Table 4). The tail of M. soror sp. n. is shorter than head and body length, and thus is considerably shorter than in other taxa in this group (Table 4). Compared to M. frater s.s. the shape and pilosity of ears differ notably, the notch on the rear edge being less visible in the later species, with pilosity confined to inner side (hairy on both sides in M. soror sp. n., Fig. 7 c). Due to an absolute shorter tibia length (about 17 mm) compared to other taxa in the frater s. l. group (about 20 mm or more), the feet (about 8 mm) appear relatively large, almost half the tibia length, whereas they are much shorter than 50 % tibia length in the other related taxa. Other, unrelated Asian species of Myotis with inwards displaced second upper premolars, such as M. davidii, are either much smaller (FA about 31 mm) and have a darker, blackish pelage color, or are much larger (FA about 50 mm) and have particolored wings (see M. formosus s.l. group, Csorba et al. 2014). Phylogenetic relationships. The partial (413 bp) Cyt b gene of the holotype of M. soror sp. n. diverges by at least 11 % K 2 P distance from any other homologous sequences, including from its sympatric, sister taxon M. f. frater (Fig. 2; Table 5).Published as part of Ruedi, Manuel, Csorba, Gábor, Lin, Liang- Kong & Chou, Cheng-Han, 2015, Molecular phylogeny and morphological revision of Myotis bats (Chiroptera: Vespertilionidae) from Taiwan and adjacent China, pp. 301-342 in Zootaxa 3920 (1) on pages 327-329, DOI: 10.11646/zootaxa.3920.2.6, http://zenodo.org/record/28792
Myotis secundus Ruedi, Csorba, Lin & Chou, 2015, sp. n.
No full text<i>Myotis secundus</i> sp. n. <p>Figures 2, 3, 4d, and 6a</p> <p> <b>Synonymy.</b> <i>Myotis</i> sp. 2: Lin <i>et al.</i> 2004. Vernacular, unavailable name. <i>Myotis</i> sp. 2: Cheng <i>et al.</i> 2010. Vernacular, unavailable name.</p> <p> <i>Myotis</i> sp. 2: Ruedi <i>et al.</i> 2013. Vernacular, unavailable name.</p> <p> <b>Holotype.</b> Adult male collected by C.H. Chou on 8 July 2003 (field number #B030018). The dry skin and skull are deposited in the collections of the Department of Biology, Tunghai University under accession number THUMB 30018. The complete mitochondrial Cyt <i>b</i> gene was sequenced from tissue extracts taken from the holotype and deposited in GenBank under accession number KP187896 and was used in the phylogenetic analyses presented herein (Clade VIII in figure 3).</p> <p> <b>Paratypes.</b> The identity of all six paratypes listed hereafter was confirmed by both the multivariate morphological (Fig. 2) and genetic analyses (Fig. 3). These paratypes are 5 adult males and 1 adult female from near Kaohsiung City in Taoyuan District collected between 2002 and 2004 (TESRI B0271, THUMB 92, 30017, 30020, 30051–2). The following GenBank accession numbers correspond to the complete mitochondrial Cyt <i>b</i> gene sequenced in these paratypes: KP187889, KP187895 –97, KP187899 –00 (Table 1).</p> <p> <b>Other referred material.</b> 3 adult males from near Datong Township, Yilan County (TESRI B0273–5); 1 adult female from Fuxing Township, Taoyuan County (TESRI B0272); 3 adult males from near Wufeng Township, Hsinchu County (TESRI B0265, B0267, B0268); 2 adult male and 1 adult female from near Taichung City, Heping District (NMNS t-3474, TESRI B0270, THUMB 30013); 1 adult male and 1 adult female from near Yuli Township, Hualian County (THUMB 30023, 30031); 2 adult females and 1 adult male from Taoyuan District, Kaohsiung City (THUMB 30053, 30016, 30019); 1 adult male from Yuli Township, Hualian County (THUMB 30055); 1 adult male from Donghe Township, Taitung County (TESRI B0269).</p> <p> <b>Type locality.</b> The designated type series originate from the forest areas near Kaohsiung City (Taoyuan District) in south-central Taiwan ROC (approximate coordinates: 23°08’ N, 120°48’ E).</p> <p> <b>Distribution.</b> <i>M. secundus</i> <b>sp. n.</b> has so far only been recorded in Taiwan, where it is relatively common and widespread in forested habitats across most of the central regions. It was found near locations 1- 4, 7, 15, 17, 19, 21 and 21 (Fig. 1).</p> <p> <b>Etymology.</b> We name it <i>secundus</i> (meaning second in Latin), as it was the second unnamed taxon found in Taiwan and initially mentioned under the name <i>Myotis</i> sp. 2 (Chou 2004; Lin <i>et al.</i> 2004; Cheng <i>et al.</i> 2010; Ruedi <i>et al.</i> 2013). In the photographic guide to the bats of Taiwan (Cheng <i>et al.</i> 2010), it was illustrated under the vernacular name of Long-toed Myotis, although this attribute is not particularly developed in this species.</p> <p> <b>Measurements of the holotype.</b> Measurements are in mm. Head and body length, 37; tail length, 41; forearm length, 35.7; hind foot length (including claw), 7.1; tibia length, 17.5; thumb length, 6.6; ear length, 12.8; tragus length, 6.2; greatest skull length, including incisors, 14.1; greatest zygomatic breadth, 8.4; postorbital breadth, 3.3; mastoid breadth, 6.7; greatest braincase width, 6.3; upper canine-molar toothrow, 5.4; width across upper canines, 3.4; width across 3rd upper molars, 5.6.</p> <p> <b>Diagnosis.</b> Small-sized <i>Myotis</i> (weight 3–5 g) with dark brown pelage color, slightly lighter ventrally, without demarcation between dorsal and ventral sides. Face and ears dark brown becoming more flesh-colored near the base of ears and above the eyes. Wing membranes attached to base of outer toe. Feet about half tibia length. Tail approximately same length as head and body length. Ears relatively long and narrow with a slight notch on the proximal third of the rear edge of conch. Tragus elongated and narrow, reaching the ear notch. Skull profile slender and relatively angular, with nearly flat braincase apex and abruptly falling posterior parts (Fig. 6 a); frontal part of braincase gently rising from rostrum to the top. Anterior part of the rostrum narrow and convergent. Teeth relatively robust with upper premolars aligned in toothrow and all visible in side view (Figs. 4d, 6a). The second upper and lower premolars are distinctly smaller than corresponding first premolars. Canines relatively strong, slightly larger than premolars. All lower molars are myotodont.</p> <p> <b>Description.</b> This small <i>Myotis</i> has a long, shaggy and very dark brown pelage, with a tinge of lighter brown color at hair tips, giving a frosted appearance to its fur (unlike e.g., <i>M. yanbarensis</i>). The underparts are lighter, buffier, also with pale brown hair tips. The face is densely haired, with a small bare part located above the eyes (Cheng <i>et al.</i> 2010). The patagium is essentially naked and dark brown, with wing membrane attaching to the base of outer toe. The ears are relatively long and narrow, with a small but distinct notch. The tragus is narrow, straight, slightly bent forward close to the tip; it extends to about a third of the distance to the tip of ear. Feet (about 7–9 mm, including claw) and thumbs are slender, both with sparse guard hairs and slender claws. The tibia is long (16–17.7 mm). Tail (about 40 mm) is as long as head and body length.</p> <p> When viewed in profile (Figs. 4d, 6a), the braincase of the skull has gently rising frontal parts, and is nearly flat on its summit; the occipital region is rounded, smooth with no visible crests. The frontal part of the rostrum is narrow and, in front of the canines, is convergent. Mean and range of external and skull measurements of <i>M. secundus</i> <b>sp. n.</b> from Taiwan are given in Table 4.</p> <p>Dental formula I 2 /3 C 1/1 PM 3/3 M 3/3, comprising the adult dentition of 38 teeth. The teeth are not particularly weak, although the canines (both upper and lower) are only slightly higher than the corresponding last premolars (Figs. 4d, 6a). The second incisor is clearly smaller than the first (in lateral view), although in occlusal view both are of similar basal dimensions. All premolars are in the toothrow and visible in lateral view, but the second one (both upper and lower) is much smaller than the first one (Fig. 4d). The third upper premolar has a distinct paraconule. Lower molars are all myotodont.</p> <p> <b>Comparisons.</b> In recent taxonomic accounts (e.g., Corbet & Hill 1992, Simmons 2005), a single small species of Myotinae was found on Taiwan and was called <i>Myotis muricola latirostris</i> (see above for its current taxonomic position). However, since 2004, bat surveys showed that a second small (weight 3–5 g), relatively common <i>Myotis</i> species, that was not fitting the characteristics of <i>latirostris,</i> was living in various habitats of the island. It was referred subsequently as <i>Myotis</i> sp. 2, and hence named here <i>M. secundus</i> <b>sp. n.</b> Although both species are indeed small and have a dark, almost black dorsal pelage, the new species is easily distinguished from <i>S. latirostris</i> by its larger external dimensions such as thumb or tibia length, or by mostly larger skull dimensions as well (Table 4). <i>M. secundus</i> <b>sp. n.</b> has myotodont lower molars, whereas they are nyctalodont in <i>S. latirostris</i>. This character also distinguishes the new species from other small, blackish <i>Myotis</i> from continental Asia pertaining to the <i>siligorensis</i> group, such as <i>M. siligorensis</i>, <i>M. badius</i>, <i>M. alticraniatus</i>, etc. (see Tiunov <i>et al.</i> 2011). Another small <i>Myotis</i> living in south-east China and described originally as <i>M. sowerbyi</i> (Howell 1926), is also very similar to <i>M. secundus</i> <b>sp. n.</b> (similar external dimensions, wing insertion to the base of the toes, myotodont lower molars), but is clove-brown, not blackish, has much more slender upper (Fig. 8 b) and lower canines, has a first lower premolar nearly as large as the canine (it is only half its size in <i>M. secundus</i> <b>sp. n.</b>, Fig. 4d), and in skull profile it has a more inflated and elevated braincase and rostrum (Fig. 6 b). <i>M. davidii</i> is also a small myotodont species, but has the upper premolars crowded, the second being completely displaced lingually from toothrow and is now considered as belonging to the <i>mystacinus</i> morpho-group (see illustrations in Benda <i>et al.</i> 2012). Compared to the closest relatives of <i>M. secundus</i> <b>sp. n.</b> in phylogenetic analyses (Clade VIII in figure 3), <i>M. pruinosus</i> has a less elevated frontal part of skull and relatively flat braincase (Fig. 6 c), whereas the skull of <i>M. yanbarensis</i> (known from Okinawa, Japan) is characterized by a longer rostrum, more globose braincase (Fig. 6 d) and is larger (e.g., CBL over 14 mm,) than <i>M. secundus</i> <b>sp. n.</b> (CBL about 13 mm). Furthermore, the tibia is particularly long in <i>M. secundus</i> <b>sp. n.</b> (about 17 mm), unlike in related <i>M. pruinosus</i> from Japan (13 mm). The tail of <i>M. secundus</i> <b>sp. n.</b> is nearly as long as head and body length, whereas it is distinctly longer in <i>M. yanbarensis</i>.</p> <p> <b>Phylogenetic relationships.</b> The complete (1140 bp) Cyt <i>b</i> gene of the holotype and paratypes of <i>M. secundus</i> <b>sp. n.</b> are all similar (with less than 1% K2P distance) and diverge by at least 10.5% K2P distance from their closest relative, <i>M. yanbarensis</i> (Fig. 3) and by at least 20% for any other sympatric <i>Myotis</i> from Taiwan (Table 5). In a more general phylogenetic context, <i>M. secundus</i> <b>sp. n.</b> (named <i>Myotis</i> sp. 2 in Ruedi <i>et al.</i> 2013) is part of the strongly supported Clade VIII within the Myotinae radiation, together with <i>M. yanbarensis</i>, <i>M. pruinosus</i>, and representatives of the <i>M. montivagus</i> species complex. It also differs notably from species of the <i>mystacinus</i> morpho-group that appear in Clade VI (Fig. 3 and Ruedi <i>et al.</i> 2013).</p> <p> <b>Natural history.</b> <i>M. secundus</i> <b>sp. n.</b> is essentially a forest-dwelling species, but we observed breeding females also occupying small holes or chinks in caves. It is common both in the lowlands and higher mountains, suggesting that this species may have a relatively broad ecological niche. It was found in sympatry with <i>S. latirostris</i> in the higher elevations. Lactating females were observed from May to July, while males with enlarged testis were recorded from August to March.</p>Published as part of <i>Ruedi, Manuel, Csorba, Gábor, Lin, Liang- Kong & Chou, Cheng-Han, 2015, Molecular phylogeny and morphological revision of Myotis bats (Chiroptera: Vespertilionidae) from Taiwan and adjacent China, pp. 301-342 in Zootaxa 3920 (1)</i> on pages 324-327, DOI: 10.11646/zootaxa.3920.2.6, <a href="http://zenodo.org/record/287922">http://zenodo.org/record/287922</a>
sj-pdf-1-imr-10.1177_03000605221115161 - Supplemental material for Elevated alanine aminotransferase is associated with biphasic insulin secretion in the healthy elderly Han Chinese population
No full textSupplemental material, sj-pdf-1-imr-10.1177_03000605221115161 for Elevated alanine aminotransferase is associated with biphasic insulin secretion in the healthy elderly Han Chinese population by Tzong-Yow Wu, En-Chih Liao, Yen-Lin Chen, Yung-Feng Lin, Shu-Hsiang Liu, Hua-Ching Lin, Yi-Chou Chiu, Chung-Ze Wu, Jiunn-Diann Lin, Dee Pei and Chun-Hsien Hsu in Journal of International Medical Research</p
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