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Truth After cinema: The explosion of facts in the documentary films of Jia Zhangke
Get PDFThis is the author's accepted manuscript. The final published article is available from the link below. Copyright @ 2013 Intellect Books.This article identifies and elaborates on two models of resistance evident in JiaZhangke’s film corpus. The deployment of different cinematic strategies produces an experimental calling into question of the value of truth and of truth as value. In the films here analysed Jia moves from resistance through organic observation to a model of resistance structured around a series of fabulations. If the first regime addresses the truth of ideology, then the target of the second is the ideology of truth. It is in this passage that Jia enters political cinema, collapsing the distinction between factual and fictional and opening up a space that belongs to no collectivity
Cymbiodyta lishizheni Jia & Lin, sp. nov.
No full textCymbiodyta lishizheni Jia & Lin sp. nov. (Figs. 1 –11, 15, 18) Type material: Holotype ♂ (SYSU), CHINA: Jiangxi Province, Jing’an County, Guanyinyan, 20.vii. 2014, 29.04 °N, 115.14 °E, 690 m, Ren-Chao Lin lgt. (Labeled in both Chinese and English). Paratypes (49): 41 specs. (SYSU, SEMC, NMPC) same data as holotype; 8 specs., CHINA: Jiangxi Province, Jing’an County, Sanzhaolun town, Baishuidong (translation: labeled in Chinese), 22.vii. 2014, 29.04 °N, 115.11 °E, 660 m, Ren-Chao Lin lgt. Diagnosis. The species is easily distinguished from C. marginella (Fabricius), the only Old World known species outside of China, bythe coarsely punctate striae on the elytra (Figs. 1, 2, 6). It can be separated from the other known Chinese species of the genus, C. orientalis Jia & Short, 2010, by (1) its smaller size (3.2–3.3 mm), (2) its broader and more extensive paler elytral margins (Figs. 1–2), (3) the more extensive femoral pubescence, and (4) the aedeagus with median lobe bottle-shaped, more strongly narrowed towards apex (Fig. 15); in C. orientalis Jia & Short, the median lobe is not so strongly narrowed towards the apex (Figs. 16–17). Description. Body length 3.2–3.3 mm, body width 2.3 mm. Dorsum blackish brown, with margins of pronotum and elytra broadly paler (Figs. 1–2), occasionally dark brown; anterior margin of pronotum usually with narrow paler band (Fig. 2), sometimes without such paler band (Fig. 5); posterior quarter of elytra paler (Figs. 1–2) or dark brown (Fig. 6). Body oval, convex. Head black with narrow reddish yellow clypeal spots in front of eyes (Fig. 2) or completely black. Maxillary palpomeres reddish yellow, not darkened apically (Fig. 4). Ventral surface generally light brown to dark brown to brown; legs light brown to rufous, tarsi light brown to rufotestaceous. Head. Labrum with fine punctures, slightly emarginate anteriorly. Clypeus subtruncate anteriorly, frontoclypeal suture clearly detectable, punctures on posterior part somewhat stronger than those on anterior part. Eyes separated by ca. 4.5 x the width of one eye. Maxillary palps ca. 3 / 4 x as long as width of head, second palpomere slightly swollen, apical palpomere almost symmetrical, apical palpomere shorter than penultimate (Fig. 4). Mentum depressed anteriorly, with strong scattered punctures. Thorax. Pronotum ca. 3.5 x as wide as long, rather strongly narrowed in front, posterior corner broadly round (Fig. 2); anterior margin smooth, with a very fine transverse groove, posterior margin without such groove; size and density of ground punctation similar to that of the head, lateral punctures a little finer than on disc, surface between punctures smooth, without microsculpture; systematic punctures present but indistinct. Elytra with ground punctation denser than on pronotum; sutural stria present in posterior half, continuing anteriorly as a row of punctures to the base of elytra (Figs. 1, 6); with nine punctate striae, which become gradually more impressed posteriorly; strial punctures becoming coarser laterally, the outer ones very coarse; distinct scutellar stria between sutural and first stria consisting of only 5 to 7 strong punctures (Fig. 6), systematic punctures on 3, 5, 7, 9 intervals present but indistinct, only slightly larger than surrounding ground punctation. Prosternum weakly convex, not carinate. Mesoventrite with a low transverse ridge medially, which does not bear an elevated tooth or projection (Fig. 7). Metaventrite with somewhat raised, more convex middle portion, which does not project anteriorly between mesocoxae; with hydrofuge pubescence except for a posteromedian glabrous area on raised middle portion.Profemora pubescent on basal two-thirds, hairline somewhat oblique (Fig. 9); meso- and metafemora with hairline not oblique, pubescent on basal third-fourths (Figs. 10–11) Abdomen. Abdomen with five exposed ventrites, covered in dense uniform pubescence; first abdominal ventrite without carina, fifth ventrite arcuate, not emarginate apically (Fig. 8). Aedeagus. Total length of aedeagus 0.45–0.48 mm. Length of parameres/length of phallobase 0.66–0.67 mm. Median lobe bottle-shaped, strongly narrowed towards apex, broader and shorter than parameres. Parameres much narrower basally, slightly bent externally (Fig. 15). Etymology. Named after Shizhen Li, a biologist and pharmaceutical scientist during the Ming Dynasty, 430 years ago, in honor of his contribution to the Chinese biological taxonomy. Habitat. This species occurs on wet rock seepages, similar to the habitat of C. orientalis Jia & Short (Jia, 2014). At the same locality, a few specimens of Oocyclus fikaceki Short & Jia were also collected. Distribution. Known only from the type locality. Remarks. When C. orientalis Jia & Short was described, only six females were known from a small temporary pool with some grass, fallen leaves and decomposed grass and branches (Jia & Short 2010). This temporary pool was formed by water flowing from a cliff not far away from the pool. From 2010 to 2013, many specimens of C. orientalis Jia & Short were collected on the wet cliff. It seems likely that the type specimens were washed down from the cliff and arrived at the temporary pond with water flow. Most New World species of the genus for which we have ecological information are known to occur in water (both lentic and lotic), wet leaf litter, at the edge of water and debris etc. and this is also true of the Palaearctic C. marginella (Fabricius) (Smetana 1974). The habitats of the two species occurring in China, C. orientalis Jia & Short and C. lishizheni sp. nov., are apparently wet rock, with specimens occasionally moved to running or stagnant water. Populations of the two species were rather dense on the wet rock, but specimens are only rarely collected in stagnant and running water. The following key adapted from Jia & Short (2010) that allows identification of all species of genus Cymbiodyta occurring in Old World. 1. Elytra with 10 rows of punctate striae (e.g. Figs. 1–2). Southern China...................................................................... 2 - Elytra without rows of punctate striae (except sutural stria). Palearctic species ........................ marginella (Fabricius) 2. Size 3.2–3.3 mm. Elytra with very broad pale lateral margin and posterior third paler in color. Anterior femora pubescent on basal two-thirds, hairline oblique; meso- and metafemora with hairline not oblique and pubescent on basal third-fourths. Aedeagus with median lobe more strongly narrowed towards apex (Fig. 15)................................ ......................................................................................................................................................... lishizheni Jia & Lin - Size 3.4–3.7 mm. Elytra with narrow pale lateral and posterior margins. Anterior femora with slightly rounded hairline, pubescence extending to just over basal half, mesofemora moderately oblique, pubescent on basal two-thirds along anterior margin and only the basal half along the posterior margin; metafemora hairline strongly oblique, with almost basal two-thirds pubescent on anterior margin and only basal third on posterior margin. Aedeagus with median lobe not so narrowed towards apex as above (Fig. 16–17) ............................................. orientalis Jia & ShortPublished as part of Jia, Fenglong & Lin, Renchao, 2015, Cymbiodyta lishizheni sp. nov., the second species of the genus from China, pp. 446-450 in Zootaxa 3985 (3) on pages 446-447, DOI: 10.11646/zootaxa.3985.3.9, http://zenodo.org/record/24166
Chaetarthria chenjuni Jia & Yang 2020, sp. nov.
No full textChaetarthria chenjuni Jia & Yang, sp. nov. (Figs 1–7) Type material. Holotype. male (SYSU), China, Hainan, Wuzhishan Mt., Guanshandian, 18˚53´N, 109˚41´E, elev. 650 m, 21.IV.2012, Yin Ziwei leg. Paratypes (3 spec. IZCAS; 2 spec. NMPC; 2 spec. SHNU; 6 spec. SYSU). 5 spec. same data as holotype; 1 male, 1 female, China, Hainan, Lingshui County, Diaoluoshan Mt., Winding Road, 18˚42´N, 109˚52´E, elev. 600–1000 m, 28.IV.2012, Peng & Dai leg.; 2 females (IZCAS: IOZ(E)20022538, IOZ(E)20022533), China, Guangxi, Napo, Defu, elev. 1440 m, 3.IV.1998, Wenzhu Li leg. (transcribed from Chinese); 1 female (IZCAS: IOZ(E)20022536), locality as above, elev. 1300 m, 14.VIII.1998, Tongli He leg. (transcribed from Chinese); 3 females, China, Guangdong, Shenzhen, Dapeng Peninsula, Getian Village, 22.48157°N, 114.62643°E, 2.VIII.2019, Jia & Mai leg. (transcribed from Chinese). Diagnosis. This new species may be close to C. indica d'Orchymont, 1920. It can be distinguished from C. indica by its labrum black, elytra uniformly black, maxillary palps piceous, ventral surface black, legs black with tarsomeres dark brown, elytra with distinct punctures as well as the systematic punctures, an arrangement otherwise only known from C. saundersi d'Orchymont in the Oriental Region; aedeagus with median lobe broadly rounded apically, without a flagellum arising out of the middle of anterior margin, gonopore oval (Fig. 7). General description. Labrum same colour as clypeus, maxillary palps uniformly dark reddish brown, pronotum with posterior angles dark brown, only slightly lighter than disc, elytra uniformly black. Ventral surface black; legs black, with tarsomeres dark brown. Head and pronotum without punctures. Pronotum without distinct anterior angles, posterior angles acute. Elytra with 4 distinct regular series of punctures, between regular series of punctures with 2 distinct irregular series of punctures, lightly finer than systematic punctures, lateral portion with irregular punctures, coarser than those on disc. Aedeagus with phallobase ca. 1.6× as long as parameres, median lobe broadly rounded apically, without a flagellum, gonopore situated apically. Description. Size and Form. 2.4–2.6 mm. Broadly oval, strongly convex (Fig. 1). Elytra slightly longer than wide. Colour. Dorsum black. Labrum same colour as clypeus or slightly lighter, without lighter anterior margin. Maxillary palps uniformly dark reddish brown. Pronotum with posterior angles dark brown (Jia et al., 2018: fig. 3a), only slightly lighter than disc. Elytra uniformly black (Figs 1, 3). Ventral surface black. Mentum dark brown. Legs black with slightly lighter tarsomeres; epipleura dark brown. Head. Ground punctation on labrum, clypeus and frons undetectable (Fig. 4). Systematic punctures on labrum, frons and clypeus very fine but detectable. Labrum not emarginate anteriorly. Eyes small, slightly protruding, separated by ca. 5.5 × width of one eye. Maxillary palps about a half as long as width of head, apical palpomere almost symmetrical and longer than penultimate (Jia et al., 2018: fig. 3d). Labial palps about one-third as long as width of mentum, apical palpomere conical, shorter than 2nd, 2nd palpomere with numerous long setae on inner and outer face. Antennae 8-segmented, scape almost as long as following antennomeres combined, club loosely segmented. Mentum (Jia et al., 2018: fig. 3d) longer than wide, quadrate, entire anteriorly; with very fine and scattered punctures anteriorly, not punctate medially. Thorax. Pronotum shinning, without distinct anterior angles, lateral margin of anterolateral angle dilated, posterior angles acute (Fig. 6); lateral stria present along entire lateral margin, terminating posteriorly at hind angle. Pronotal ground punctation undetectable, systematic punctures very fine but detectable. Elytra smooth and shining, with 4 distinct regular series of punctures (Fig. 5) between regular series of punctures with a few irregular series of punctures (Fig. 3), lateral portion with irregular punctures that are coarser than those on disc. Sutural stria reaching half of elytral length (Jia et al., 2018: fig. 3c), no series of punctures before sutural stria. Prosternum extremely short, only slightly convex, not carinate. Mesosternum glabrous, slightly concave, with a median, transverse and lightly arcuate ridge at level of anterior mesocoxal margin. Metasternum slightly raised, a little more convex and sparsely pubescent medially. Metepisterna about 4.3× as long as wide, more densely pubescent than metasternum, almost parallel sided except posteriorly, where inner margin bends smoothly towards outer margin. Procoxae densely pubescent, meso- and metacoxae glabrous. Femora with sharply defined tibial grooves on inner face; Femora stout. Pro- and meso-femora densely pubescent except on apical extremity; anterior half of metafemora densely pubescent, posterior half glabrous with some coarse punctures (Jia et al., 2018: fig. 3b), posterodorsal margin densely pubescent. Tibiae slender, hardly flattened. Tarsi with 5 tarsomeres, first metatarsomere shorter than second. Abdomen. Ventrites 1–2 with a large cavity on each side, filled with a hyaline mass supported and covered by a fringe of long stiff yellow setae rising from anterior margin of basal ventrite (Fig. 2); first two ventrites carinate medially. Aedeagus. Aedeagus with phallobase ca. 1.6× as long as parameres; parameres narrowly rounded apically; median lobe distinctly broader than parameres medially, broadly rounded apically, without a flagellum, gonopore situated apically (Fig. 7). Etymology. The species is named after Dr. Jun Chen, a specialist of mites from Institute of Zoology, Chinese Academy of Sciences, Beijing, China, who kindly invited the senior author to examine the specimens in IZCAS. Distribution. China (Hainan, Guangxi, Guangdong).Published as part of Jia, Fenglong, Yang, Zhenming, Jiang, Lu, Chen, Kai & Jiang, Shujiao, 2020, Chaetarthria chenjuni Jia & Yang, sp. nov. (Coleoptera: Hydrophilidae), a new species from China and additional faunistic records, pp. 146-149 in Zoological Systematics 45 (2) on pages 147-149, DOI: 10.11865/zs.202019, http://zenodo.org/record/461721
Coelostoma (Lachnocoelostoma) huangi Jia, Aston & Fikacek 2014
No full textCoelostoma (Lachnocoelostoma) huangi Jia, Aston & Fikáček, 2014 (Fig. 9) Material examined. THAILAND: 14 spec. (ASHC, NMPC): Phang-nga province, Lamri district, 6 km NE Lam Khan (white banana waterfall), 8°37.324ʹN 88°18.362ʹE, 75 m a.s.l., 13.viii.2012, A. Skale lgt.; 13 spec. (AWWC, NME, NMPC): same data, but A. Weigel lgt. Distribution. Described recently from Chinese provinces Guangxi and Jiangxi (Jia et al. 2014). First record for Thailand. Remarks. The inspection of type specimens deposited in Orchymont collection in IRSNB and of the additional specimens of C. huangi listed above revealed that C. huangi is extremely similar to C. coomani diversum from Sumatra in morphology of genitalia (compare Fig. 9 for C. huangi with Fig. 10 for C. diversum) and in external characters. All examined specimens of C. huangi have wide apices of parameres, in contrast to the examined paratype of C. coomani diversum Orchymont, 1932; for that reason, we consider both species as separate ones at the moment. However, studies of additional specimens from Malay archipelago would be necessary to corroborate the status of both taxa. In addition, the genitalia of C. coomani diversum differ from those of C. coomani Orchymont, 1932 (see Fig. 24 in Jia et al. 2014) in many aspects including the shape and position of the gonopore, shape of the internal sclerite of the median lobe and shape of parameres, and clearly indicate a separate species status of this taxon. For this reason, and in agreement with species concept adopted here and by Jia et al. (2014), we are elevating the taxon to species rank, as C. diversum stat. nov.Published as part of Jia, Fenglong, Lin, Renchao, Chan, Eric, Skale, Andre & Fikáček, Martin, 2017, Two new species of Coelostoma Brullé, 1835 from China and additional faunistic records of the genus from the Oriental Region (Coleoptera: Hydrophilidae: Sphaeridiinae: Coelostomatini), pp. 113-122 in Zootaxa 4232 (1) on page 120, DOI: 10.11646/zootaxa.4232.1.8, http://zenodo.org/record/29285
sj-docx-1-jia-10.1177_23259582241235779 - Supplemental material for Providing Trauma-Informed Care During a Pandemic: How Health Care Workers at Ryan White-Funded Clinics in the Southeastern United States Responded to COVID-19 and Its Effects on Their Well-Being
No full textSupplemental material, sj-docx-1-jia-10.1177_23259582241235779 for Providing Trauma-Informed Care During a Pandemic: How Health Care Workers at Ryan White-Funded Clinics in the Southeastern United States Responded to COVID-19 and Its Effects on Their Well-Being by Caroline W. Kokubun, Katherine M. Anderson, Olivia C. Manders, Ameeta S. Kalokhe and Jessica M. Sales in Journal of the International Association of Providers of AIDS Care (JIAPAC)</p
sj-docx-2-jia-10.1177_23259582241235779 - Supplemental material for Providing Trauma-Informed Care During a Pandemic: How Health Care Workers at Ryan White-Funded Clinics in the Southeastern United States Responded to COVID-19 and Its Effects on Their Well-Being
No full textSupplemental material, sj-docx-2-jia-10.1177_23259582241235779 for Providing Trauma-Informed Care During a Pandemic: How Health Care Workers at Ryan White-Funded Clinics in the Southeastern United States Responded to COVID-19 and Its Effects on Their Well-Being by Caroline W. Kokubun, Katherine M. Anderson, Olivia C. Manders, Ameeta S. Kalokhe and Jessica M. Sales in Journal of the International Association of Providers of AIDS Care (JIAPAC)</p
Daily 10-m wind speed observation dataset CN05.1 over China
No full textThe daily 10-m wind speed observation dataset CN05.1, which covers the period from 1961 to 2020, with horizontal resolution of 0.25° × 0.25° (latitude × longitude). This dataset was developed by Jia Wu from National Climate Center, China Meteorological Administration.
References: Jia Wu, Xue-Jie Gao. A grided daily observation dataset over China region and comparison with the other datasets. Chinese J. Geophys. (in Chinese), 2013, 56(4): 1102-1111, doi: 10.6038/cjg20130406
POS0166 POLYARTICULAR JIA HAS A DISTINCT CO-INHIBITOR RECEPTOR PROFILE AMONG OTHER JIA SUBTYPES
No full textBackgroundJuvenile idiopathic arthritis (JIA) is the most common inflammatory joint disease in children, driven by continuous T-cell activation.[1] T cell activation is counter-balanced by signals generated by co-inhibitory receptors (co-IRs) such CTLA-4, PD-1, LAG-3, and TIM-3.[2]ObjectivesWe aimed to identify the role of co-IRs in the pathogenesis of different subtypes of JIA.MethodsIn total, we included 107 patients with oligoarticular JIA (n=67), polyarticular JIA (n=12), enthesitis related arthritis (n=17), systemic JIA (n=11) and healthy controls (HC, n=10). We collected plasma samples from the patients during the active phase of their disease. We measured the soluble plasma levels of co-IRs by commercial pre-defined cytometric bead array kits and their cellular expression by flow cytometry in blood mononuclear cells. We compared the plasma levels and cellular expressions of different coIRs within different JIA subgroups.ResultsIL-2 levels were lower than HC in all JIA subgroups. The polyarticular JIA group distinguished from the four different JIA subgroups, by having different co-IR pattern. In this specific subgroup, CTLA4, PD-1 and 4-1BB levels were higher than other groups. Polyarticular JIA is the more chronic and severe form of JIA, especially when compared to oligoarticular JIA. (Figure 1).Figure 1.We investigated the correlations between disease activity markers and plasma co-IRs. Plasma TIM3 levels correlated with erythrocyte sedimentation rate, C-reactive proteins and JADAS in the polyarticular JIA group. In oligoarticular JIA group, JADASs correlated with plasma PD-1 levels, C-reactive protein with PD-L1 plasma levels. Erythrocyte sedimentation rates correlated with IL-2, CD86, PD-L1 and PD-1 plasma levels. There was no correlation between disease activity markers and co-IRs levels in the systemic JIA group and enthesitis related arthritis group.Finally, we analysed the cellular surface expression of different co-IRs on the PBMCs of different JIA subtypes. Similar to plasma levels, both the percentage and the MFI (mean fluorescence intensity) of CTLA4 expression was higher in polyarticular JIA subgroup.ConclusionThis is the first report studying the effects of different co-IRs in different subtypes of JIA. Polyarticular JIA patients had a different coIR profile, having more CTLA-4, PD-1 and 4-1BB in their plasma than the other subtypes of JIAReferences[1]Wedderburn, L.R., et al., Int Immunol, 2001. 13(12): p. 1541-50.[2]Wherry, E.J. and M. Kurachi, Nat Rev Immunol, 2015. 15(8): p. 486-99.AcknowledgementsThis work was supported by a research grant from FOREUM Foundation for Research in RheumatologyDisclosure of InterestsNone declared</jats:sec
Patrus coomani Liang & Angus & Jia 2021, comb. nov.
No full textPatrus coomani (Peschet, 1925) comb. nov. Fig. 12 Orectochilus coomani Peschet, 1925: 253 (original description). Material examined CHINA – Guangdong • 1 ♂, 2 ♀♀; 深圳市大鹏半岛坪头岭 [Shenzhen, Dapeng Peninsula, Pingtouling Mt.]; 22°39′48″ N, 114°25′11″ E; alt. 259 m; 25 Jul. 2019; 梁祖龙, 杨圳铭, 姜卓寅, 郭光宇, 纪新元采 [Liang Zulong, Yang Zhenming, Jiang Zuoyin, Guo Guangyu and Ji Xinyuan leg.]; SYSU • 1 ♀; 广东省 深圳市大鹏半岛田头山 [Shenzhen, Dapeng Peninsula, Tiantoushan Mt.]; 22°40′12″ N, 114°24′44″ E; alt. 208.4 m; 30 Jul. 2019; 杨圳铭, 姜卓寅, 郭光宇, 纪新元采 [Yang Zhenming, Jiang Zuoyin, Guo Guangyu, Ji Xinyuan leg.]; SYSU • 7 ♂♂, 5 ♀♀; 广东省台山市上川岛猕猴省级保护区 [Guangdong Prov., Taishan City, Shangchuan Island Macaque Provincial Nature Reserve]; 21°44′36″ N, 112°50′33″ E; alt. 10 m; 18 Jan. 2019; 贾凤龙, 梁祖龙采 [Jia Fenglong and Liang Zulong leg.]; SYSU • 2 ♂♂, 1 ♀; 广东省台山市上川岛猕猴省级保护区 [Guangdong Prov., Taishan City, Shangchuan Island Macaque Provincial Nature Reserve]; 21°44′51″ N, 112°49′36″ E; alt. 50 m; 17 Jan. 2019; 贾凤龙, 梁祖龙采 [Jia Fenglong and Liang Zulong leg.]; SYSU • 1 ♀; 广东省台山市上川岛猕猴省级保护区石背潭 [Guangdong Prov., Taishan City, Shangchuan Island Macaque Provincial Nature Reserve, Shibeitang]; 21°46′1″ N, 112°49′2″ E; alt. 20 m; 19 Jan. 2019; 贾凤龙, 梁祖龙采 [Jia Fenglong and Liang Zulong leg.]; SYSU • 1 ♂; 广东肇庆鼎湖山 [Guangdong, Zhaoqing, Dinghushan Mt.]; 19 Jun. 1958; 利翠英 采 [Li Cuiying leg.]; SYSU • 1 ♂, 4 ♀♀; 广东肇庆鼎湖山 [Guangdong, Zhaoqing, Dinghushan Mt.]; 13 Oct. 1958; SYSU • 1 ♂, 3 ♀♀; 广东鼎湖山 [Guangdong, Dinghushan Mt.]; 8 Jul. 1964; 吴思添采 [Wu Sitian leg.]; SYSU • 1 ♀; 肇庆鼎湖山 [Zhaoqing, Dinghushan Mt.]; 3 Nov. 1974; 春强采 [Chun Qiang leg.]; SYSU • 1 ♀; 广东高要县鼎湖山 [Guangdong, Gaoyao County, Dinghushan Mt.]; 15 Jul. 1964; 何目秀采 [He Muxiu leg.]; SYSU • 1 ♀; 和平县九连山 [Heping County, Jiulianshan Mt.]; 26 Aug. 1986; 陈振耀采 [Chen Zhenyao leg.]; SYSU • 1 ♀; 广东连县大东山 [Guangdong, Lianxian County, Dadongshan Mt.]; 4 Sep. 1994; 彭红采 [Peng Hong leg.]; SYSU • 1 ♂, 2 ♀♀; 广东高明鹿田 [Guangdong Gaoming, Lutian]; 14 May 2004; 贾凤龙, 方小端采 [Jia Fenglong and Fang Xiaoduan leg.]; SYSU. Distribution Known from Vietnam. New for China.Published as part of Liang, Zulong, Angus, Robert B. & Jia, Fenglong, 2021, Three new species of Patrus Aubé with additional records of Gyrinidae from China (Coleoptera, Gyrinidae), pp. 1-39 in European Journal of Taxonomy 767 on page 25, DOI: 10.5852/ejt.2021.767.1481, http://zenodo.org/record/571552
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