记述隐脉叶蝉族Nirvanini 1新属1新种,即:长索叶蝉属,新属Longiconnecta gen.nov.和斑缘长索叶蝉,新种L.marginalspota sp.nov.,新属以Nirvana basimaculata Wang et Li,1997作为模式种,同时建立3新组合,即:基斑长索叶蝉,新组合,L.basim...记述隐脉叶蝉族Nirvanini 1新属1新种,即:长索叶蝉属,新属Longiconnecta gen.nov.和斑缘长索叶蝉,新种L.marginalspota sp.nov.,新属以Nirvana basimaculata Wang et Li,1997作为模式种,同时建立3新组合,即:基斑长索叶蝉,新组合,L.basimaculata(Wang et Li)comb.nov.、白翅长索叶蝉,新组合L.albula(Cai et Shen)comb.nov.和黄色长索叶蝉,新组合L.flava(Cai et He)comb.nov.。新种模式标本保存于贵州大学昆虫研究所(GUGC)。展开更多
In 2008 and 2009,we made continuous and repeated breeding surveys of the Scaly-sided Merganser(Mergus squamatus)in the Changbai Mountain range(China side),using a combination of rubber-boat drifting and walking.Each s...In 2008 and 2009,we made continuous and repeated breeding surveys of the Scaly-sided Merganser(Mergus squamatus)in the Changbai Mountain range(China side),using a combination of rubber-boat drifting and walking.Each survey consisted of a census of breeding pairs in the spring and broods in the summer.A total of 1553 km in length of 17 river stretches were surveyed in four different river systems of the Yalujiang,Songhuajiang,Tumenjiang and Mudanjiang rivers.A total of 1354 individuals of the Scaly-sided Merganser were recorded during the both surveys.The breeding density for all the stretches surveyed over both years averaged 0.26 ± 0.30 pairs per km;the population density in the spring averaged 0.75 ± 0.88 individuals per km.According to our survey results,we estimated that the breeding population in the Changbai Mountain range was about 170 breeding pairs of the Scaly-sided Merganser.Three major breeding sites of this bird were found in the Changbai Mountain range in these surveys.展开更多
A new cecidomyiid species,Rhizomyia acroleptosipha sp.nov.collected from Ning’an in Heilongjiang Province of China,is described and illustrated as the first record of the mycophagous genus Rhizomyia Kieffer,1898 from...A new cecidomyiid species,Rhizomyia acroleptosipha sp.nov.collected from Ning’an in Heilongjiang Province of China,is described and illustrated as the first record of the mycophagous genus Rhizomyia Kieffer,1898 from Northeast China.This new species is characterized by the unique bell-jar-shaped aedeagus with the basal 3/4 extremely broadened and the distal 1/4 constricted to be inverted-funnel-shaped.A new revised generic description is given to include this new species,and a key to all known species in China is provided.展开更多
Objective To examine the relationship between apolipoprotein E (Apo E) gene polymorphism and risk of coronary artery disease (CAD), analyzing association of polymorphism with classical risk factors. Methods A total of...Objective To examine the relationship between apolipoprotein E (Apo E) gene polymorphism and risk of coronary artery disease (CAD), analyzing association of polymorphism with classical risk factors. Methods A total of 124 patients (including 84 Han population and 40 Uygur population) with angiographically verified CAD or myocardial infarction were prospectively evaluated. Data referring to hypertension, diabetes, and tobacco consump-tion were recorded. The levels of total cholesterol (TC), high density lipoprotein (HDL) cholesterol, Apo A1 and B, and triglycerides (TG) were determined. DNA was obtained from 124 patients and 70 controls. In order to determine Apo E genotypes, DNA was PCR amplified and digested with HhaI. The genetic polymorphism of Apo E is due to three common alleles, epsilon(ε) 2, ε3, ε4, at a single autosomal gene locus. These alleles determine the six phenotypes E2/2, E3/3, E4/4, E4/2, E4/3, and E3/2. Results In Uygur population, the frequency of the ε2, ε3, and ε4 was 0.155, 0.648, and 0.197 respectively. In Han po-pulation, the frequency of the ε2, ε3, and ε4 was 0.081, 0.772, and 0.146 respectively. In the patient group, the frequency of the ε2, ε3, and ε4was 0.060, 0.758, and 0.182 respectively. In the control group, the frequency of the ε2, ε3, and ε4 was 0.193, 0.671, and 0.136 respectively. ε2 frequency of Uygur’ patients and controls was 0.050 and 0.290 respectively. Serum low density lipoprotein (LDL) cholesterol, TC, and TG values tended to decrease from the Apo E-4 phenotypes to Apo E-2 phenotypes. When deletion polymorphism of ε2 was compared with the common risk factors for CAD, its risk ratio (RR) is 4.38. Conclusions These studies confirm and find that Apo E phenotype distribution in Uygur population differs significantly from that in Han population in Xinjiang. CAD patients have significantly lower ε2 allele and slightly higher ε3 or ε4 allele frequency than controls, especially in Uygur population. It shows protective effects of ε2 on CAD.展开更多
Hereditary hemorrhagic telangiectasia(HHT)is a rare autosomal-dominantly inherited disease that occurs in approximately one in 5000 to 8000 people.Clinical diagnosis of HHT is made when a person presents three of the ...Hereditary hemorrhagic telangiectasia(HHT)is a rare autosomal-dominantly inherited disease that occurs in approximately one in 5000 to 8000 people.Clinical diagnosis of HHT is made when a person presents three of the following four criteria:family history,recurrent nosebleeds,mucocutaneous telangiectasis,and arteriovenous malformations(AVM)in the brain,lung,liver and gastrointestinal(GI)tract.Although epistaxis is themost common presenting symptom,AVMs affecting the lungs,brain and GI tract provoke a more serious outcome.Heterozygous mutations in endoglin,activin receptor-like kinase 1(ACVRL1;ALK1),and SMAD4,the genes involved in the transforming growth factor-βfamily signaling cascade,cause HHT.We report here the case of a 63 year-old male patient who presented melena and GI bleeding episodes,proven to be caused by bleeding from multiple gastric angiodysplasia.Esophagogastroduodenoscopy revealed multiple angiodysplasia throughout the stomach.Endoscopic argon plasma coagulation was performed to control bleeding from a gastric angiodysplasia.The patient has been admitted several times with episodes of hemoptysis and hematochezia.One year ago,the patient was hospitalized due to right-sided weakness,which was caused by left basal ganglia hemorrhage as the part of HHT presentation.In family history,the patient's mother and elder sister had died,due to intracranial hemorrhage,and his eldest son has been suffered from recurrent epistaxis for 20 years.A genetic study revealed a mutation in exon 3 of ALK1(c.199C>T;p.Arg67Trp)in the proband and his eldest son presenting epistaxis.展开更多
Objectives To study the association of single nucleotide polymorphism （SNP） rs2076185 in chromosome 6p24.1 with the premature coronary artery diseases （PCAD） in Chinese Hun population. Methods A total of 1382 pati...Objectives To study the association of single nucleotide polymorphism （SNP） rs2076185 in chromosome 6p24.1 with the premature coronary artery diseases （PCAD） in Chinese Hun population. Methods A total of 1382 patients were divided into the PCAD group and the control group based on their coronary arteriography （CAG） results. Their SNP rs2076185 were analyzed by the mass-spectrometry. Their allele and genotype frequency in Hardy-Weinberg equilibrium were calculated for assessment. Logistic regression was employed to remove confounding factors and correlate SNP rs2076185 with PCAD. Results The allele and genotype frequencies of the control group were in Hardy-Weinberg equilibrium （P 〉 0.05）. The frequencies of allele G of rs2076185 were 54.2% in the PCAD group and 49.5% in the control group. The difference was significant （P = 0.042）. The genotype distribution ofrs2076185 of the two groups was also significantly different. The univariate analysis showed that the rs2076185 polymorphisms were associated with the PCAD only in the additive model （OR： 0.828, 95% CI： 0.711-0.964, P = 0.014）, and in the dominant model （OR： 0.753, 95% CI： 0.591-0.958, P = 0.021）. After removing the confound- ing variables, the rs2076185 polymorphisms was associated with PCAD in the additive model （OR： 0.775, 95% CI： 0.648-0.928, P = 0.005）, in the dominant model （OR： 0.698, 95% CI： 0.527-0.925, P = 0.012）, and in the recessive model （OR： 0.804, 95% CI： 0.538-0.983, P - 0.038）. Conclusion Allele G of rs2076185 reduces the PCAD risks in Chinese Hun population, therefore it could be a coronary artery diseases protective factor in Chinese Hun population.展开更多
Nature's greatest splendors are often secreted in the remotest of spots. This is certainly true of Kanas Lake, deep in the Altay Mountains of northern Xinjiang Uygur Autonomous Region. This area of sublime, and as...Nature's greatest splendors are often secreted in the remotest of spots. This is certainly true of Kanas Lake, deep in the Altay Mountains of northern Xinjiang Uygur Autonomous Region. This area of sublime, and as yet unsullied, natural beauty is home to 2,000 people of the Tuwa ethnic minority. The ancestry of these herder-hunters is unclear. Certain anthropologists believe that they are descended from Genghis Khan's "Mongol hordes" that swept through on their 13th century rampage of Central Asia and Europe. Others argue that they are the posterity of Siberian migrants, and cousins to the Tuvan people of Russia.展开更多
文摘记述隐脉叶蝉族Nirvanini 1新属1新种,即:长索叶蝉属,新属Longiconnecta gen.nov.和斑缘长索叶蝉,新种L.marginalspota sp.nov.,新属以Nirvana basimaculata Wang et Li,1997作为模式种,同时建立3新组合,即:基斑长索叶蝉,新组合,L.basimaculata(Wang et Li)comb.nov.、白翅长索叶蝉,新组合L.albula(Cai et Shen)comb.nov.和黄色长索叶蝉,新组合L.flava(Cai et He)comb.nov.。新种模式标本保存于贵州大学昆虫研究所(GUGC)。
基金supported by the National Natural Science Foundation of China(3207047831372233+2 种基金31420103911)the Ministry of Science and Technology of the People’s Republic of China(2015FY210300)the National Animal Collection Resource Center,China。
基金sponsored by the Rufford Small Grant of the Rufford Foundation
文摘In 2008 and 2009,we made continuous and repeated breeding surveys of the Scaly-sided Merganser(Mergus squamatus)in the Changbai Mountain range(China side),using a combination of rubber-boat drifting and walking.Each survey consisted of a census of breeding pairs in the spring and broods in the summer.A total of 1553 km in length of 17 river stretches were surveyed in four different river systems of the Yalujiang,Songhuajiang,Tumenjiang and Mudanjiang rivers.A total of 1354 individuals of the Scaly-sided Merganser were recorded during the both surveys.The breeding density for all the stretches surveyed over both years averaged 0.26 ± 0.30 pairs per km;the population density in the spring averaged 0.75 ± 0.88 individuals per km.According to our survey results,we estimated that the breeding population in the Changbai Mountain range was about 170 breeding pairs of the Scaly-sided Merganser.Three major breeding sites of this bird were found in the Changbai Mountain range in these surveys.
基金The ZooBank Life Science Identifier(LSID)for this publication is:http://zoobank.org/urn:lsid:zoobank.org:pub:428AA291-11A9-44BD-B99B-F142BE93457D.
文摘A new cecidomyiid species,Rhizomyia acroleptosipha sp.nov.collected from Ning’an in Heilongjiang Province of China,is described and illustrated as the first record of the mycophagous genus Rhizomyia Kieffer,1898 from Northeast China.This new species is characterized by the unique bell-jar-shaped aedeagus with the basal 3/4 extremely broadened and the distal 1/4 constricted to be inverted-funnel-shaped.A new revised generic description is given to include this new species,and a key to all known species in China is provided.
文摘Objective To examine the relationship between apolipoprotein E (Apo E) gene polymorphism and risk of coronary artery disease (CAD), analyzing association of polymorphism with classical risk factors. Methods A total of 124 patients (including 84 Han population and 40 Uygur population) with angiographically verified CAD or myocardial infarction were prospectively evaluated. Data referring to hypertension, diabetes, and tobacco consump-tion were recorded. The levels of total cholesterol (TC), high density lipoprotein (HDL) cholesterol, Apo A1 and B, and triglycerides (TG) were determined. DNA was obtained from 124 patients and 70 controls. In order to determine Apo E genotypes, DNA was PCR amplified and digested with HhaI. The genetic polymorphism of Apo E is due to three common alleles, epsilon(ε) 2, ε3, ε4, at a single autosomal gene locus. These alleles determine the six phenotypes E2/2, E3/3, E4/4, E4/2, E4/3, and E3/2. Results In Uygur population, the frequency of the ε2, ε3, and ε4 was 0.155, 0.648, and 0.197 respectively. In Han po-pulation, the frequency of the ε2, ε3, and ε4 was 0.081, 0.772, and 0.146 respectively. In the patient group, the frequency of the ε2, ε3, and ε4was 0.060, 0.758, and 0.182 respectively. In the control group, the frequency of the ε2, ε3, and ε4 was 0.193, 0.671, and 0.136 respectively. ε2 frequency of Uygur’ patients and controls was 0.050 and 0.290 respectively. Serum low density lipoprotein (LDL) cholesterol, TC, and TG values tended to decrease from the Apo E-4 phenotypes to Apo E-2 phenotypes. When deletion polymorphism of ε2 was compared with the common risk factors for CAD, its risk ratio (RR) is 4.38. Conclusions These studies confirm and find that Apo E phenotype distribution in Uygur population differs significantly from that in Han population in Xinjiang. CAD patients have significantly lower ε2 allele and slightly higher ε3 or ε4 allele frequency than controls, especially in Uygur population. It shows protective effects of ε2 on CAD.
基金Supported by A grant of the South Korea Healthcare technology R and D Project,Ministry for Health,Welfare and Family Affairs,South Korea,No.A080588-23in part by a grant from the World Class University(WCU by Korean Ministry of Education,Science and Technology)(to Oh SP)
文摘Hereditary hemorrhagic telangiectasia(HHT)is a rare autosomal-dominantly inherited disease that occurs in approximately one in 5000 to 8000 people.Clinical diagnosis of HHT is made when a person presents three of the following four criteria:family history,recurrent nosebleeds,mucocutaneous telangiectasis,and arteriovenous malformations(AVM)in the brain,lung,liver and gastrointestinal(GI)tract.Although epistaxis is themost common presenting symptom,AVMs affecting the lungs,brain and GI tract provoke a more serious outcome.Heterozygous mutations in endoglin,activin receptor-like kinase 1(ACVRL1;ALK1),and SMAD4,the genes involved in the transforming growth factor-βfamily signaling cascade,cause HHT.We report here the case of a 63 year-old male patient who presented melena and GI bleeding episodes,proven to be caused by bleeding from multiple gastric angiodysplasia.Esophagogastroduodenoscopy revealed multiple angiodysplasia throughout the stomach.Endoscopic argon plasma coagulation was performed to control bleeding from a gastric angiodysplasia.The patient has been admitted several times with episodes of hemoptysis and hematochezia.One year ago,the patient was hospitalized due to right-sided weakness,which was caused by left basal ganglia hemorrhage as the part of HHT presentation.In family history,the patient's mother and elder sister had died,due to intracranial hemorrhage,and his eldest son has been suffered from recurrent epistaxis for 20 years.A genetic study revealed a mutation in exon 3 of ALK1(c.199C>T;p.Arg67Trp)in the proband and his eldest son presenting epistaxis.
文摘Objectives To study the association of single nucleotide polymorphism （SNP） rs2076185 in chromosome 6p24.1 with the premature coronary artery diseases （PCAD） in Chinese Hun population. Methods A total of 1382 patients were divided into the PCAD group and the control group based on their coronary arteriography （CAG） results. Their SNP rs2076185 were analyzed by the mass-spectrometry. Their allele and genotype frequency in Hardy-Weinberg equilibrium were calculated for assessment. Logistic regression was employed to remove confounding factors and correlate SNP rs2076185 with PCAD. Results The allele and genotype frequencies of the control group were in Hardy-Weinberg equilibrium （P 〉 0.05）. The frequencies of allele G of rs2076185 were 54.2% in the PCAD group and 49.5% in the control group. The difference was significant （P = 0.042）. The genotype distribution ofrs2076185 of the two groups was also significantly different. The univariate analysis showed that the rs2076185 polymorphisms were associated with the PCAD only in the additive model （OR： 0.828, 95% CI： 0.711-0.964, P = 0.014）, and in the dominant model （OR： 0.753, 95% CI： 0.591-0.958, P = 0.021）. After removing the confound- ing variables, the rs2076185 polymorphisms was associated with PCAD in the additive model （OR： 0.775, 95% CI： 0.648-0.928, P = 0.005）, in the dominant model （OR： 0.698, 95% CI： 0.527-0.925, P = 0.012）, and in the recessive model （OR： 0.804, 95% CI： 0.538-0.983, P - 0.038）. Conclusion Allele G of rs2076185 reduces the PCAD risks in Chinese Hun population, therefore it could be a coronary artery diseases protective factor in Chinese Hun population.
文摘Nature's greatest splendors are often secreted in the remotest of spots. This is certainly true of Kanas Lake, deep in the Altay Mountains of northern Xinjiang Uygur Autonomous Region. This area of sublime, and as yet unsullied, natural beauty is home to 2,000 people of the Tuwa ethnic minority. The ancestry of these herder-hunters is unclear. Certain anthropologists believe that they are descended from Genghis Khan's "Mongol hordes" that swept through on their 13th century rampage of Central Asia and Europe. Others argue that they are the posterity of Siberian migrants, and cousins to the Tuvan people of Russia.
