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ClinicalTrials.gov36/100

Effects of Integrative Neuromuscular Traning on Physical Fitness and Dribbling Performance Among High School Male Football Players in Shandong, China

ClinicalTrials.gov study NCT07017049. IPD Sharing: NO. Countries: 1. Publications: 2.

closedIPD-NOFeb 2026View details →
dryad36/100

Data from: First record of organic-walled microfossils from the Tonian Shiwangzhuang Formation of the Tumen Group in western Shandong, North China

Open the record for dataset details and reuse information.

publicJun 2021View details →
zenodo32/100

FIGURE 3 in A new mesopterous species of the genus Phryganogryllacris (Orthoptera Gryllacrididae: Hyperbaeninae) from Shandong, China

FIGURE 3. Tegmina of Phryganogryllacris laoshanica sp. nov. A. left tegmen of holotype; B. right tegmen of paratype.

opennotspecifiedJan 2021View details →
zenodo32/100

FIGURE 5 in A new mesopterous species of the genus Phryganogryllacris (Orthoptera Gryllacrididae: Hyperbaeninae) from Shandong, China

FIGURE 5. Map of Shandong Peninsula. Showing the type locality and habitat for Phryganogryllacris laoshanica sp. nov.

opennotspecifiedJan 2021View details →
zenodo32/100

FIGURE 1 in A new mesopterous species of the genus Phryganogryllacris (Orthoptera Gryllacrididae: Hyperbaeninae) from Shandong, China

FIGURE 1. Body of holotype of Phryganogryllacris laoshanica sp. nov. A. dorsal view; B. lateral view.

opennotspecifiedJan 2021View details →
zenodo32/100

FIGURE 2 in A new mesopterous species of the genus Phryganogryllacris (Orthoptera Gryllacrididae: Hyperbaeninae) from Shandong, China

FIGURE 2. Features of Phryganogryllacris laoshanica sp. nov. A. face; B. dorsal view of head and pronotum; C. left hind wing; D. stridulatory pegs on second and third abdominal tergites, left lateral view; E. internal apical spur on dorsal right mid tibia (black arrow); F. dorsal view of right hind tibia.

opennotspecifiedJan 2021View details →
zenodo32/100

FIGURE 4 in A new mesopterous species of the genus Phryganogryllacris (Orthoptera Gryllacrididae: Hyperbaeninae) from Shandong, China

FIGURE 4. Male abdominal apex of Phryganogryllacris laoshanica sp. nov. A. dorsal view; B. lateral view; C. ventral view; D. rear view. Abbreviations: 8th eighth abdominal tergite, 9th ninth abdominal tergite, 10th tenth abdominal tergite, ce cercus, rc rim around cercus base, sg subgenital plate, st stylus.

opennotspecifiedJan 2021View details →
dryad32/100

Data from: Incidence and fatality of serious suicide attempts in a predominantly rural population in Shandong, China: a public health surveillance study

Objectives: To estimate the incidence of serious suicide attempts (SSAs, defined as suicide attempts resulting in either death or hospitalisation) and to examine factors associated with fatality among these attempters. Design: A surveillance study of incidence and mortality. Linked data from two public health surveillance systems were analysed. Setting: Three selected counties in Shandong, China. Participants: All residents in the three selected counties. Outcome: measures Incidence rate (per 100 000 person-years) and case fatality rate (%). Methods: Records of suicide deaths and hospitalisations that occurred among residents in selected counties during 2009–2011 (5 623 323 person-years) were extracted from electronic databases of the Disease Surveillance Points (DSP) system and the Injury Surveillance System (ISS) and were linked by name, sex, residence and time of suicide attempt. A multiple logistic regression model was developed to examine the factors associated with a higher or lower fatality rate. Results: The incidence of SSAs was estimated to be 46 (95% CI 44 to 48) per 100 000 person-years, which was 1.5 times higher in rural versus urban areas, slightly higher among females, and increased with age. Among all SSAs, 51% were hospitalised and survived, 9% were hospitalised but later died and 40% died with no hospitalisation. Most suicide deaths (81%) were not hospitalised and most hospitalised SSAs (85%) survived. The fatality rate was 49% overall, but was significantly higher among attempters living in rural areas, who were male, older, with lower education or with a farming occupation. With regard to the method of suicide, fatality was lowest for non-pesticide poisons (7%) and highest for hanging (97%). Conclusions: The incidence of serious suicide attempts is substantially higher in rural areas than in urban areas of China. The risk of death is influenced by the attempter's sex, age, education level, occupation, method used and season of year.

opencc-zeroDec 2013View details →
zenodo32/100

FIGURE 3 in A new species, Microphysogobio wulonghensis (Teleostei: Cypriniformes: Cyprinidae), from Shandong Province, China

FIGURE 3. Distribution of Microphysogobio wulonghensis sp. nov. and similar species. Hollow cross, M. hsinglungshanensis; solid square M. anudarini; solid circle, M. chinssuensis; solid star, M. wulonghensis sp. nov.; solid triangle, M. linghensis; hollow square, M. rapidus; hollow circle, M. yaluensis; asterisk M. amurensis.

opennotspecifiedDec 2011View details →
zenodo32/100

FIGURE 2 in A new species, Microphysogobio wulonghensis (Teleostei: Cypriniformes: Cyprinidae), from Shandong Province, China

FIGURE 2. Lateral and ventral views of Microphysogobio wulonghensis sp. nov. Holotype, ASIZB 176476, 41.2 mm SL: a, lateral and ventral views; b1, photograph of upper and lower lips; b2, illustration of upper and lower lips.

opennotspecifiedDec 2011View details →
zenodo32/100

FIGURE 1 in A new species, Microphysogobio wulonghensis (Teleostei: Cypriniformes: Cyprinidae), from Shandong Province, China

FIGURE 1. Principal measurements taken on Microphysogobio species. The picture is based on the type species of Microphysogobio, M. hsinglungshanensis. Standard length (SL), from tip of snout to last half-centrum (point A to point H); body depth, from insertion of dorsal-fin vertically to ventral midline (D–T); pre-dorsal length, from tip of snout to origin of dorsal fin (A– D); head to dorsal-fin origin, from nape (point between head and body, dorsal scales start here) to dorsal-fin origin (C–D); dorsal-fin length, from origin of dorsal fin to tip of longest ray (D–F); dorsal-fin base length, from anterior to posterior end of dorsal-fin base (D–E); pre-anal length, from tip of snout to origin of anal fin (A–K); anal-fin length, from origin of anal fin to tip of longest ray (K–L); anal-fin base length, from anterior to posterior end of anal-fin base (K–J); pre-pectoral length, from tip of snout to base of anterior pectoral-fin ray (A–Q); pectoral-fin length, from base of anterior pectoral-fin ray to tip of the longest ray (Q-R); pectoral-fin base length, from anterior to posterior end of pectoral-fin base (Q–P); pre-pelvic length, from tip of snout to base of anterior pelvic-fin ray (A–N); pelvic-fin length, from base of anterior pelvic-fin ray to tip of longest ray (N–O); pelvic-fin base length, from anterior to posterior end of pelvic-fin base (N–M); caudal peduncle length, from end of anal-fin base to last half-centrum (J–H); caudal peduncle depth, at approximately middle of caudal peduncle (G–I); head length, from tip of snout to most posterior point of operculum (including skin flap, 1; A–S); head depth, from nape vertically to the venter (C–B); head width, distance between most posterior margins of opercles; snout length, from tip of snout to anterior margin of circumorbital series (2); eye diameter, from anterior to posterior margins of circumorbital series (3), pressing tips of calipers to firm points (bony rim); rictal barbel length, from anterior to posterior end of rictal barbel.

opennotspecifiedDec 2011View details →
zenodo32/100

FIGURE 4 in A new species, Microphysogobio wulonghensis (Teleostei: Cypriniformes: Cyprinidae), from Shandong Province, China

FIGURE 4. Comparison of lip shapes of species in the "incompletely scaled" group. a, M. linghensis, ASIZB 184871, 42.7 mm SL; b, M. chinssuensis, ASIZB 168078, 45.9 mm SL; c, M. yaluensis, ASIZB 184660, 40.7 mm SL; d, M. amurensis, printed in the light of IBH 12208735-0382, 44.8 mm SL; e, M. rapidus, CUNC 37898, 56.2 mm SL; f1, f2: M. wulonghensis sp. nov., ASIZB 176476, 41.2 mm SL.

opennotspecifiedDec 2011View details →
zenodo32/100

Subspecies and Distribution. M.f.fimbriatusPeters,1871—E&SEChina(Shandong,Jiangsu,Anhui,Zhejiang,Jiangxi,Fujian,andGuangdong). M. f. taiwanensis Arnback-Christie-Linde, 1908 — Taiwan. Specimens from Yunnan, SC China and possibly specimens from Sichuan and Guizhou represent an undescribed species. in Vespertilionidae

Subspecies and Distribution. M.f.fimbriatusPeters,1871—E&SEChina(Shandong,Jiangsu,Anhui,Zhejiang,Jiangxi,Fujian,andGuangdong). M. f. taiwanensis Arnback-Christie-Linde, 1908 — Taiwan. Specimens from Yunnan, SC China and possibly specimens from Sichuan and Guizhou represent an undescribed species.

opennotspecifiedOct 2019View details →
zenodo32/100

Subspecies and Distribution. E.p.pachyomusTomes,1857—SEIran,NEAfghanistan,NPakistan,extremeSWChina(Tibet[=Xizang]),NIndia(JammuandKashmirEtoNagaland),Nepal,andBhutan. E.p.andersoniDobson,1871—EMyanmar,C,SC&SEChina(Sichuan,Yunnan,Guizhou,Hunan,Jiangxi,Anhui,Jiangsu,Shanghai,Zhejiang,andFujian),NThailand,NLaos,andNVietnam. E.p.horikawaiKishida,1924—TaiwanI. E. p. pallens G. S. Miller, 1911 — S Mongolia, NC, NE, C & E China (Gansu, Inner Mongolia [= Nei Mongol], Heilongjiang, Jilin, Liaoning, Sichuan, Ningxia, Shaanxi, Shanxi, Hebei, Beijing, Tianjin, Shandong, Henan, Hubei, Anhui, andJiangsu), and Korean Peninsula. in Vespertilionidae

Subspecies and Distribution. E.p.pachyomusTomes,1857—SEIran,NEAfghanistan,NPakistan,extremeSWChina(Tibet[=Xizang]),NIndia(JammuandKashmirEtoNagaland),Nepal,andBhutan. E.p.andersoniDobson,1871—EMyanmar,C,SC&SEChina(Sichuan,Yunnan,Guizhou,Hunan,Jiangxi,Anhui,Jiangsu,Shanghai,Zhejiang,andFujian),NThailand,NLaos,andNVietnam. E.p.horikawaiKishida,1924—TaiwanI. E. p. pallens G. S. Miller, 1911 — S Mongolia, NC, NE, C & E China (Gansu, Inner Mongolia [= Nei Mongol], Heilongjiang, Jilin, Liaoning, Sichuan, Ningxia, Shaanxi, Shanxi, Hebei, Beijing, Tianjin, Shandong, Henan, Hubei, Anhui, andJiangsu), and Korean Peninsula.

opennotspecifiedOct 2019View details →
zenodo32/100

Distribution. SE Mongolia, NE, E & C China (Gansu, Ningxia, Inner Mongolia [= Nei Mongol], Heilongjiang, Jilin, Liaoning, Sichuan, Henan, Shandong, and Anhui), S Russian Far East, Korean Peninsula (includingJeju I), andJapan (S Hokkaido, N Honshu, and Tsushima Is). in Vespertilionidae

Distribution. SE Mongolia, NE, E & C China (Gansu, Ningxia, Inner Mongolia [= Nei Mongol], Heilongjiang, Jilin, Liaoning, Sichuan, Henan, Shandong, and Anhui), S Russian Far East, Korean Peninsula (includingJeju I), andJapan (S Hokkaido, N Honshu, and Tsushima Is).

opennotspecifiedOct 2019View details →
zenodo32/100

Subspecies and Distribution. N.p.plancyiGerbe,1880—NE&ECChina(Gansu,Shaanxi,Shanxi,Henan,Beijing,Shandong,Liaoning,andJilin). N.p.labiatusHodgson,1835—HimalayasfromNPakistan,NIndia,Nepal,SCChina,andNMyanmaralongwithNW&SVietnam;mayoccurinThailand,NLaos,NEVietnam,andPeninsularMalaysia,buttherearenoconfirmedrecordsfromtheseregions. N. p. velutinus G. M. Allen, 1923 — C & SE China (Sichuan, Yunnan, Hubei, Anhui, Jiangsu, Shanghai, Zhejiang, Guizhou, Guangxi, Hunan, Jiangxi, Fujian, Guangdong, and Hong Kong) and Taiwan I. The subspecific status of recently collected specimens from the Central Cordillera of Luzon I in the Philippines is uncertain, although they may represent velutinus. Another specimen recently collected from Hainan I may also represent velutinus. in Vespertilionidae

Subspecies and Distribution. N.p.plancyiGerbe,1880—NE&ECChina(Gansu,Shaanxi,Shanxi,Henan,Beijing,Shandong,Liaoning,andJilin). N.p.labiatusHodgson,1835—HimalayasfromNPakistan,NIndia,Nepal,SCChina,andNMyanmaralongwithNW&SVietnam;mayoccurinThailand,NLaos,NEVietnam,andPeninsularMalaysia,buttherearenoconfirmedrecordsfromtheseregions. N. p. velutinus G. M. Allen, 1923 — C & SE China (Sichuan, Yunnan, Hubei, Anhui, Jiangsu, Shanghai, Zhejiang, Guizhou, Guangxi, Hunan, Jiangxi, Fujian, Guangdong, and Hong Kong) and Taiwan I. The subspecific status of recently collected specimens from the Central Cordillera of Luzon I in the Philippines is uncertain, although they may represent velutinus. Another specimen recently collected from Hainan I may also represent velutinus.

opennotspecifiedOct 2019View details →
zenodo32/100

FIGURES 1–12 in A new species of the genus Mongolotettix Rehn, 1928 from Shandong, China (Acrididae, Acridoidea, Orthoptera)

FIGURES 1–12. Mongolotettix shandongensis sp. nov. 1. body in lateral view ♂; 2. epiphallus, ♂; 3. head and pronotum in dorsal view ♂; 4. head Frontal view; 5. stridulatory pegs, ♂; 6. end of abdomen ♂; 7. mesosternum ♂; 8. tegmen ♂; 9. body in lateral view ♀; 10. end of abdomen in lateral view ♀; 11. mesosternum ♀; 12. end of abdomen ventral view ♀. 13–16 Mongolotettix hubeiensis Zheng, et al, 2017 13. tegmen ♂; 14. Epiphallus; 15. Tegmen; 16. end of abdomen in lateral view ♀ (figs. 13–15 after Zheng, et al, 2017).

opennotspecifiedApr 2022View details →
zenodo32/100

Subspecies and Distribution. C.n.nipponTemminck,1838—SJapan(SHonshu,Shikoku,Kiushu,NRyukyu,andseveralsmallerassociatedIs). C.n.centralisKishida,1936—CJapan(N&CHonshu). C.n.grassianusHeude,1884—NChina(Shanxi);possiblyextinctinthewild. C.n.kopschiSwinhoe,1873—SEChina. C.n.mandarinusMilne-Edwards,1871—NChina(Hebei&Shandong);possiblyextinctinthewild. C.n.mantschuricusSwinhoe,1864—Ussuriland(RussianFarEast),NEChina(Heilongjiang),andpossiblyNorthKorea. C.n.pseudaxisGervais,1841—NVietnam;probablyextinctinthewild. C.n.sichuanicusGuo,Cheng&Wang,1978—SWChina(Sichuan&Gansu). C.n.taiouanusBlyth,1860—Taiwan. C. n. yesoensis Heude, 1884 — N Japan (Hokkaido). It was anciently introduced to Solo I (Philippines) and in 17" century to Kerama Is (Ryukyu Is, Japan). Also introduced in 19" and 20" centuries into British Is, mainland Europe (Austria, Czech Republic, Denmark, Finland, France, Germany, Poland, western Russia, and Ukraine), Armenia, Azerbaijan, Madagascar, New Zealand, and USA. in Cervidae

Subspecies and Distribution. C.n.nipponTemminck,1838—SJapan(SHonshu,Shikoku,Kiushu,NRyukyu,andseveralsmallerassociatedIs). C.n.centralisKishida,1936—CJapan(N&CHonshu). C.n.grassianusHeude,1884—NChina(Shanxi);possiblyextinctinthewild. C.n.kopschiSwinhoe,1873—SEChina. C.n.mandarinusMilne-Edwards,1871—NChina(Hebei&Shandong);possiblyextinctinthewild. C.n.mantschuricusSwinhoe,1864—Ussuriland(RussianFarEast),NEChina(Heilongjiang),andpossiblyNorthKorea. C.n.pseudaxisGervais,1841—NVietnam;probablyextinctinthewild. C.n.sichuanicusGuo,Cheng&Wang,1978—SWChina(Sichuan&Gansu). C.n.taiouanusBlyth,1860—Taiwan. C. n. yesoensis Heude, 1884 — N Japan (Hokkaido). It was anciently introduced to Solo I (Philippines) and in 17" century to Kerama Is (Ryukyu Is, Japan). Also introduced in 19" and 20" centuries into British Is, mainland Europe (Austria, Czech Republic, Denmark, Finland, France, Germany, Poland, western Russia, and Ukraine), Armenia, Azerbaijan, Madagascar, New Zealand, and USA.

opennotspecifiedAug 2011View details →
zenodo32/100

Distribution. Disjunct locations in NE China (Liaoning, Inner Mongolia [= Nei Mongol], Hebei, Beijing, and Shandong), N & C Laos, and NE Thailand (Loei Province). There are three vagrant records in Japan, on Amami-Oshima, Kuchinoerabujima, and Yoronjima Is. in Molossidae

Distribution. Disjunct locations in NE China (Liaoning, Inner Mongolia [= Nei Mongol], Hebei, Beijing, and Shandong), N & C Laos, and NE Thailand (Loei Province). There are three vagrant records in Japan, on Amami-Oshima, Kuchinoerabujima, and Yoronjima Is.

opennotspecifiedOct 2019View details →
zenodo32/100

Subspecies and Distribution. L.t.tolaiPallas,1778—InnerMongolia(=NeiMongol),andGansu(NCChina). L.t.buchariensisOgnev,1922—TajikistanandNEAfghanistan. L.t.cheybaniBaloutch,1978—SWIran(ZagrosMts). L.t.cinnamomeusShamel,1940—SWSichuan,andNYunnan(SCChina). L.t.filchneriMatschie,1908—Shaanxi(CChina). L.t.lehmanniSevertzov,1873—SKazakhstan,Turkmenistan,andextremeN&NEIran,EtoSSiberia,Mongolia,andXinjiang(NWChina). L. t. swinhoei Thomas, 1894 — from Heilongjiang, Jilin, Liaoning, Inner Mongolia S to Hebei, Beijing, Henan, Shaanxi, Shanxi, and Shandong (NE & E China). in Leporidae

Subspecies and Distribution. L.t.tolaiPallas,1778—InnerMongolia(=NeiMongol),andGansu(NCChina). L.t.buchariensisOgnev,1922—TajikistanandNEAfghanistan. L.t.cheybaniBaloutch,1978—SWIran(ZagrosMts). L.t.cinnamomeusShamel,1940—SWSichuan,andNYunnan(SCChina). L.t.filchneriMatschie,1908—Shaanxi(CChina). L.t.lehmanniSevertzov,1873—SKazakhstan,Turkmenistan,andextremeN&NEIran,EtoSSiberia,Mongolia,andXinjiang(NWChina). L. t. swinhoei Thomas, 1894 — from Heilongjiang, Jilin, Liaoning, Inner Mongolia S to Hebei, Beijing, Henan, Shaanxi, Shanxi, and Shandong (NE & E China).

opennotspecifiedJul 2016View details →

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