13 results on '"Zhang, Shengli"'
Search Results
2. Species-specific and general allometric equations for estimating tree biomass components of subtropical forests in southern China.
- Author
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Xiang, Wenhua, Zhou, Jing, Ouyang, Shuai, Zhang, Shengli, Lei, Pifeng, Li, Jiaxiang, Deng, Xiangwen, Fang, Xi, and Forrester, David
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TROPICAL forests ,ALLOMETRIC equations ,FUNCTIONAL groups ,REGRESSION analysis - Abstract
Chinese subtropical forests contain a diversity of tree species and exhibit a high carbon (C) sequestration capacity, but biomass and C stock assessments in subtropical secondary forests remain uncertain because of a limited availability of allometric equations and an uncertain applicability of existing allometric equations that have not been tested for these forests. We developed allometric equations for important coniferous ( Pinus massoniana), deciduous broadleaved ( Alniphyllum fortunei, Choerospondias axillaris, Liquidambar formosana) and evergreen broadleaved ( Cyclobalanopsis glauca, Litsea rotundifolia, Schima superba) species. A total of 70 trees (10 trees for each species) with diameters at breast height ( D) ranging from 2.6 to 50.9 cm were destructively harvested and dissected into tree components (stem, branch, leaf and coarse root). Species-specific equations using D alone as the predictor variable fitted the data well ( p < 0.0053 and R > 0.72) for each tree component. Including height ( H) in the form of D H only improved the regression fit for A. fortunei and L. rotundifolia. The relationships of branch, leaf and root biomass against D varied among tree species. General equations for functional groups and all species combined showed comparable bias for stem, aboveground and total tree biomass to species-specific equations. We recommend the general equations of multiple species to estimate forest biomass at regional scales and also to estimate stem, aboveground and total tree biomass for each species when species-specific allometric equations are not available at a given site. For branch, leaf and root biomass, species-specific equations are preferred, even though this requires biomass data for additional tree species. [ABSTRACT FROM AUTHOR]
- Published
- 2016
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- View/download PDF
3. Molecular tracing of white muscardine of the silkworm, Bombyx mori I: genetic structure analysis of Beauveria bassiana populations as the causal agents in China.
- Author
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Chen, Xue, Zhang, Shengli, He, Lingmin, and Li, Zengzhi
- Subjects
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BIOLOGICAL pest control , *SILKWORMS , *ENTOMOPATHOGENIC fungi , *BEAUVERIA bassiana - Abstract
Beauveria bassianais a ubiquitous entomopathogenic fungus, which causes white muscardine in the silkworm,Bombyx mori, and is an important limiting factor in global silk production. Knowledge of the genetic structure ofB. bassianapopulations as the causal agents in China will aid in tracing the origins of muscardine and in developing effective control strategies. In the present study, a total of 489B. bassianaisolates were obtained from silkworm cadavers in 12 different provinces of China. An analysis of the genetic structure of the causal agent populations using the internal simple sequence repeat technique to trace their origins revealed a high level (100%) of DNA polymorphism. An unweighted pair group method with arithmetic mean dendrogram revealed that the 489B. bassianaisolates were heterogenic and polyphyletic and displayed typical regional distribution, although the genetic differentiations were not associated with geographic distance. The genetic differentiation (Gst) among populations reached 0.406, with the maximumGstbetween populations reaching 0.647. The general gene flow (Nm) was low at 0.366, with the lowest at only 0.137, suggesting that the low gene flow maintained a high degree of differentiation. These data indicated that the white muscardine in each local silkworm population was predominantly caused by a native group ofB. bassiana, rather than by any exotic strain as in the case of biological control based onB. bassianainsecticides. [ABSTRACT FROM AUTHOR]
- Published
- 2016
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4. Genome-wide association study for pigmentation traits in Chinese Holstein population.
- Author
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Fan, Yipeng, Wang, Peng, Fu, Weixuan, Dong, Tian, Qi, Chao, Liu, Lin, Guo, Gang, Li, Cong, Cui, Xiaogang, Zhang, Shengli, Zhang, Qin, Zhang, Yi, and Sun, Dongxiao
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HOLSTEIN-Friesian cattle ,ANIMAL coloration ,CATTLE genetics ,GENOMES - Abstract
With the Illumina Bovine SNP50K BeadChip, we performed a genome-wide association study ( GWAS) for two pigmentation traits in a Chinese Holstein population: proportion of black ( PB) and teat colour ( TC). A case-control design was used. Cases were the cows with PB <0.30 ( n = 129) and TC <2 points ( n = 140); controls were those with PB >0.90 ( n = 58) and TC >4 points ( n = 281). The RM test of roadtrips (version 1.2) was applied to detect SNPs for the two traits with 42 883 and 42 741 SNPs respectively. A total of nine and 12 genome-wide significant ( P < 0.05) SNPs associated with PB and TC respectively were identified. Of these, two SNPs for PB were located within the KIT and IGFBP7 genes, and the other four SNPs were 23~212 kb away from the PDGFRA gene on BTA6; nine SNPs associated with TC were located within or 21~78.8 kb away from known genes on chromosomes 4, 11, 22, 23 and 24. By combing through our GWAS results and the biological functions of the genes, we suggest that the KIT, IGFBP7, PDGFRA, MITF, ING3 and WNT16 genes are promising candidates for PB and TC in Holstein cattle, providing a basis for further investigation on the genetic mechanism of pigmentation formation. [ABSTRACT FROM AUTHOR]
- Published
- 2014
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5. Determinants affecting residents' waste classification intention and behavior: A study based on TPB and A-B-C methodology.
- Author
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Zhang, Shengli, Hu, Daiyan, Lin, Tong, Li, Wei, Zhao, Rui, Yang, Hongwei, Pei, Yanbo, and Jiang, Lei
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PLANNED behavior theory , *STRUCTURAL equation modeling , *INTENTION , *WASTE management - Abstract
Waste classification is regarded as one of the most important strategies for waste management, and its success depends on the active participation of the public. Based on the theory of planned behavior (TPB) and attitude-behavior-condition (A-B-C) theory, this research investigated the key factors affecting residents' domestic waste classification intention (WCI) and waste classification behavior (WCB), and explored the moderating effects of three external factors including infrastructure (INF), government publicity (GP), and incentive measures (IM) on the intention-behavior relationship. The valid data were collected from 584 residents via conducting a face-to-face interview in Chengdu, a pilot city of waste classification in China, and analyzed by using the structural equation model (SEM). Results showed that residents' WCI and WCB had a significant discrepancy with the average values of 4.07 and 2.81, respectively. Attitude (AT), perceived behavior control (PBC) and classification knowledge (CK) were significantly related to residents' WCI, with AT (β = 0.65, P < 0.001) having the greatest direct impact. Meanwhile, CK and INF had a stronger impact on the WCB than WCI. GP indirectly affected WCB through the intermediary effect of CK. In addition, INF and GP had a positively moderating effect on residents' waste classification intention-behavior relationship and can facilitate the intention-behavior conversion. By contrast, IM failed to promote the conversion of residents' classification intention into behavior, and had no direct significant influence on residents' WCB. Finally, some relevant policy suggestions were put forward for the new pilot cities of waste classification in China. • Key factors affecting residents' WCI and WCB were investigated. • Moderating effects of external factors on intention-behavior relation was explored. • Attitude had the greatest direct influence on residents' WCI. • CK and Infrastructure had a stronger impact on WCB than WCI. • Infrastructure and GP can strengthen the intention-behavior conversion. [ABSTRACT FROM AUTHOR]
- Published
- 2021
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6. Molecular tracing of white muscardine in the silkworm, Bombyx mori (Linn.) II. Silkworm white muscardine is not caused by artificial release or natural epizootic of Beauveria bassiana in China.
- Author
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Chen, Xue, Huang, Cui, He, Lingmin, Zhang, Shengli, and Li, Zengzhi
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SILKWORM diseases , *COMMUNICABLE diseases in animals , *BEAUVERIA bassiana , *SERICULTURE , *INSECTICIDES , *INSECT population genetics , *ECONOMICS - Abstract
The fungal pathogen Beauveria bassiana causes serious economic losses in sericulture. Its origin is usually attributed to the release of B. bassiana insecticides against pine caterpillars ( Dendrolimus punctuatus ). In the present study, 488 B. bassiana isolates obtained from silkworm ( Bombyx mori ) collected from 13 Chinese provinces, and 327 B. bassiana isolates obtained from D. punctatus collected from 9 provinces, were analyzed for population genetic structure using the ISSR technique based on genetic distance. A UPGMA dendrogram clustered them into three independent clades: two B. mori clades and one D. punctatus clade. A 3-D principal component analysis further divided them into two completely independent host groups, revealing high host-specificity. This suggested that white muscardine occurring in B. mori populations throughout southern China was not caused by any B. bassiana strain either naturally prevailing in D. punctatus populations or by any strain artificially released as a fungal insecticide against D. punctatus . We further investigated the genetic differentiation coefficient G st and gene flow between B. mori -pathogenic and D. punctatus -pathogenic B. bassiana isolates from across China and from five provinces inhabited by both B. mori and D. punctatus . The G st value across China was computed as 0.410, while the values of the five provinces ranged from 0.508 to 0.689; all above 0.25, which is the threshold for significant genetic differentiation. This suggests that B. bassiana strains isolated from the two different hosts maintained their respective heredity without a convergent homogenization trend, and reduces the possibility that the host range of the caterpillar isolates could expand and enhance their virulence in B. mori . These findings indicate that the use of B. bassiana does not threaten the safety of sericulture. [ABSTRACT FROM AUTHOR]
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- 2015
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7. The role of construction of healthcare consortium on the allocation of human resources for primary care resources and its equity in China: A quantitative study.
- Author
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Li S, Liao C, and Zhang S
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- China, Humans, Primary Health Care, Resource Allocation
- Abstract
Objectives: This study aims to measure the effect of Construction of Healthcare Consortium (CHC) on the allocation and equity of human resources (HR) for primary health care (PHC) in China, at the same time, it provides some data to support the government's policies improvement in the next stage., Methods: Changes in the equity of allocation of HR for PHC by population are demonstrated through a three-stage approach to inequality analysis that includes the Gini coefficient (G), the Theil index (T), the Concentration index (CI) and Concentration curves. Trends in resource allocation from 2021 to 2030 were projected using the GM (1, 1) model., Results: The average rate of growth in volume of HR for PHC accelerates following the release of CHC in the 2016. Whilst some regions have seen their G and T rise between 2012 and 2016, their levels of inequality of allocation for resource shave gradually declined in the years following 2016, but there are exceptions, with the regions of northeast and northwest seeing the opposite. Eastern and northern region accounted for a larger contribution to intra-regional inequality. Concentration index and concentration curves indicate HR for PHC is related to economic income levels. GM (1, 1) projects a growing trend in allocation of resources from 2021 to 2030, but different regions differ in the average rate of growth of resources., Conclusions: The inequality of HR for PHC in China is low, however, the inequality between regions has not been eliminated. We still need to take a long-term view to monitor the impact of CHC on the allocation of HR for PHC and its equity in China., Competing Interests: The authors have declared that no competing interests exist., (Copyright: © 2024 Li et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
- Published
- 2024
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8. Genome-wide association studies for immunoglobulin concentrations in colostrum and serum in Chinese Holstein.
- Author
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Lin S, Ke C, Liu L, Gao Y, Xu L, Han B, Zhao Y, Zhang S, and Sun D
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- Animals, Animals, Newborn, Cattle, China, Dairying, Female, Immunoglobulin G, Pregnancy, Colostrum, Genetic Association Studies veterinary
- Abstract
Background: The early death and health problems of calves caused substantial economic losses in the dairy industry. As the immune system of neonates has not been fully developed, the absorption of maternal immunoglobulin (Ig) from colostrum is essential in protecting newborn calves against common disease organisms in their early life. The overwhelming majority of Ig in bovine whey is transported from the serum. Therefore, Ig concentration in the colostrum and serum of dairy cows are critical traits when estimating the potential disease resistance of its offspring., Results: Colostrum, blood, and hair follicle samples were collected from 588 Chinese Holstein cows within 24 h after calving. The concentration of total IgG, IgG1, IgG2, IgA and IgM in both colostrum and serum were detected via ELISA methods. With GCTA software, genome-wide association studies (GWASs) were performed with 91,620 SNPs genotyped by GeneSeek 150 K (140,668 SNPs) chips. As a result, 1, 5, 1 and 29 significant SNPs were detected associated with the concentrations of colostrum IgG1, IgG2, IgA IgM, and serum IgG2 at the genome-wide level (P < 3.08E-6); 11, 2, 13, 2, 12, 8, 2, 27, 1 and 4 SNPs were found significantly associated with total IgG, IgG1, IgG2, IgA and IgM in colostrum and serum at the suggestive level (P < 6.15E-5). Such SNPs located in or proximate to (±1 Mb) 423 genes, which were functionally implicated in biological processes and pathways, such as immune response, B cell activation, inflammatory response and NF-kappaB signaling pathways. By combining the biological functions and the known QTL data for immune traits in bovine, 14 promising candidate functional genes were identified for immunoglobulin concentrations in colostrum and serum in dairy cattle, they were FGFR4, FGFR2, NCF1, IKBKG, SORBS3, IGHV1S18, KIT, PTGS2, BAX, GRB2, TAOK1, ICAM1, TGFB1 and RAC3., Conclusions: In this study, we identified 14 candidate genes related to concentrations of immunoglobulins in colostrum and serum in dairy cattle by performing GWASs. Our findings provide a groundwork for unraveling the key genes and causal mutations affecting immunoglobulin concentrations in colostrum and important information for genetic improvement of such traits in dairy cattle., (© 2022. The Author(s).)
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- 2022
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9. Prevalence of nine genetic defects in Chinese Holstein cattle.
- Author
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Khan MYA, Omar AI, He Y, Chen S, Zhang S, Xiao W, and Zhang Y
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- Animals, China epidemiology, Female, Haplotypes, Prevalence, Cattle genetics, Cattle Diseases epidemiology, Cattle Diseases genetics, Leukocyte-Adhesion Deficiency Syndrome epidemiology, Leukocyte-Adhesion Deficiency Syndrome genetics, Leukocyte-Adhesion Deficiency Syndrome veterinary
- Abstract
Worldwide use of elite sires has caused inbreeding accumulation and high frequencies of genetic defects in dairy cattle populations. In recent years, several genetic defect genes or haplotypes have been identified in Holstein cattle. A rapid and reliable microfluidic chip with Kompetitive allele-specific PCR (KASP) assay was developed in our previous study for the detection of heterozygotes at eight genetic defect loci of bovine leukocyte adhesion deficiency (BLAD), Brachyspina syndrome (BS), complex vertebral malformation (CVM), Holstein haplotype 1 (HH1), Holstein haplotype 3 (HH3), Holstein haplotype 4 (HH4), Holstein haplotype 5 (HH5) and haplotype for cholesterol deficiency (HCD). This study aimed to extend that assay to include a newly identified genetic defect of Holstein haplotype 6 (HH6) and to estimate the frequencies of carriers for each of the nine genetic defects in six Chinese Holstein herds. Of the 1633 cows, carrier frequencies of the genetic defects were 6.92%, 5.76%, 4.46%, 4.30%, 3.62%, 2.94%, 1.86% and 0.37% for HH1, HH3, CVM, HH5, HCD, BS, HH6 and BLAD, respectively. No carrier was found for HH4. Notably, 27.43% of cows carried at least one genetic defect, while 2.27% and 0.12% of cows carried double and triple genetic defect alleles, respectively. The existence of genetic defects calls for routine molecular testing and effective management of genetic defects by avoiding carrier-to-carrier mating in production herds and eliminating or at least reducing the frequency of the defective alleles through marker-assisted selection in breeding herds., (© 2021 The Authors Veterinary Medicine and Science Published by John Wiley & Sons Ltd.)
- Published
- 2021
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10. Relationship between osteonecrosis and antiphospholipid antibodies in patients with systemic lupus erythematosus: a systematic review protocol.
- Author
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Wei Q, Zhou M, Liu J, Zhang S, Gao F, Lin H, and Chen Z
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- Antibodies, Antiphospholipid, Case-Control Studies, China, Humans, Meta-Analysis as Topic, Research Design, Systematic Reviews as Topic, Lupus Erythematosus, Systemic complications, Osteonecrosis etiology
- Abstract
Introduction: Osteonecrosis (ON) is characterised by the destruction of the normal blood supply to the bone tissue. ON is the main cause of disability in patients with systemic lupus erythematosus (SLE). Studies have reported the existence of many risk factors for SLE complicated by ON, including the use of high-dose glucocorticoids and high disease activity. The correlation between antiphospholipid antibodies (aPLs) and ON in SLE has been controversial. We aim to conduct a systematic review of the literature related to SLE, aseptic ON and aPLs, to provide a reference for the clinical screening of high-risk patients and for early prevention., Methods and Analysis: The following six databases will be searched: MEDLINE/PubMed, Embase, Web of Science, Chinese Biomedical Literature Database, Wan-Fang Database and China National Knowledge Infrastructure. The database searches will not be restricted by date. Case-control studies, cohort studies or observational studies that compare aPLs between SLE patients with and without ON will be considered eligible. Articles published in English and Chinese will be included. Two researchers will independently perform the processes of study selection, data extraction and study quality assessment. The Newcastle-Ottawa Quality Assessment Scale will be used to assess the quality of the retrieved studies. A meta-analysis will be performed after screening the studies. Data will be analysed using ORs for dichotomous data., Ethics and Dissemination: Ethical approval is not required because this systematic review will use published data. The systematic review will be electronically disseminated through a peer-reviewed publication or conference presentations., Prospero Registration Number: CRD42020209637., Competing Interests: Competing interests: None declared., (© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.)
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- 2021
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11. Genetic diversity and population structure of the Chinese Fungus Metarhizium rileyi causing green muscardine in silkworm.
- Author
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Zhang S, Chen X, Luan F, He L, Pu S, and Li Z
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- Animals, China, Genetic Variation, Polymerase Chain Reaction, Species Specificity, Bombyx parasitology, Metarhizium genetics, Mycoses veterinary
- Abstract
Green muscardine caused by Metarhizium rileyi affects sericulture, and is typically enzootic and occurs frequently at low incidence. We collected 152 M. rileyi isolates from silkworm cadavers in eight sericulture areas in seven provinces of China, and four strains from other Lepidoptera larvae in Qianshan(QS) County, Anhui province. Nine microsatellite inter-simple sequence repeat (ISSR) primers produced 91 distinct and reproducible bands, revealing a high level (90.11%) of DNA polymorphism. Unweighted Pair Group Method with Arithmetic Mean (UPGMA) cluster analysis divided the populations into four groups, with isolates from Qianshan County forming a single branch. All the 156 M. rileyi isolates were heterogenic and polyphyletic and did not displayed typical regional distribution except strains from Qianshan country. PCA analysis of the nine populations of M. rileyi revealed similar phylogenies among accessions. Genetic differentiation index (G
st ) among eight enzootic populations was 0.3789 and gene flow (Nm ) was 0.4098, suggesting the low gene flow maintained a high degree of differentiation. Gst between the enzootic population of Qianshan County and other seven populations exceeded the threshold of severe differentiation, with moderate differentiation between the remaining seven enzootic populations. Analysis of molecular variance (AMOVA) showed most ISSR variation (61%) among isolates occurred within populations. No significant correlation was observed between geographical and genetic distance. According to cluster analysis based on single enzootic population, every enzootic population showed dominance, namely mainly constituted of strains with high genetic similarity. These data indicated that the green muscardine in each local silkworm population was predominantly caused by a native group of M. rileyi. Furthermore, Gst and Nm of M. rileyi from silkworm and other Lepidoptera larvae in Qianshan County were 0.1174 and 1.8791, respectively, suggesting strains isolated from different hosts in Qianshan County do not show obvious host specificity. This demonstrated that host transfer may take place in silkworm and other insects., (Copyright © 2016 Elsevier Inc. All rights reserved.)- Published
- 2016
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12. Screening for JH1 genetic defect carriers in Jersey cattle by a polymerase chain reaction and restriction fragment length polymorphism assay.
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Zhang Y, Guo G, Huang H, Lu L, Wang L, Fang L, Liu L, Wang Y, and Zhang S
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- Abortion, Veterinary genetics, Animals, Cattle, Cattle Diseases genetics, China, Female, Mutation, Pedigree, Polymorphism, Restriction Fragment Length, Polymorphism, Single Nucleotide, Pregnancy, Sequence Analysis, DNA veterinary, Abortion, Veterinary diagnosis, Cattle Diseases diagnosis, Dairying, Polymerase Chain Reaction veterinary, Protein Subunits genetics
- Abstract
An autosomal recessive genetic defect termed JH1 has been associated with early embryonic loss in the Jersey cattle breed. The genetic basis has been identified as a cytosine to thymine mutation in the CWC15 gene that changes an amino acid from arginine to a stop code. To screen for JH1 carriers in an imported Jersey population in China, a method based on a polymerase chain reaction amplification followed by a restriction fragment length polymorphism assay (PCR-RFLP) was developed for the accurate diagnosis of the JH1 allele. A total of 449 randomly chosen cows were examined with the PCR-RFLP assay, and 31 were identified as JH1 carriers, corresponding to a carrier frequency of 6.9%. The PCR-RFLP method was validated by DNA sequencing of 8 positive and 13 negative samples, with all 21 samples giving the expected DNA sequence. In addition, 3 negative and 3 positive samples were confirmed by a commercial microarray-based single nucleotide polymorphism assay. Finally, samples from 9 bulls in the United States of known status were correctly identified as carriers (5 bulls) or noncarriers (4 bulls). As the JH1 defect has most likely spread worldwide, implementing routine screening is necessary to avoid the risk of carrier-to-carrier matings and to gradually eradicate the deleterious gene., (© 2015 The Author(s).)
- Published
- 2015
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13. Associations between variants of the HAL gene and milk production traits in Chinese Holstein cows.
- Author
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Wang H, Jiang L, Wang W, Zhang S, Yin Z, Zhang Q, and Liu JF
- Subjects
- 3' Untranslated Regions, Animals, Base Sequence, Binding Sites, China, Female, Gene Expression, Gene Frequency, Genetic Association Studies, Haplotypes, Histidine Ammonia-Lyase metabolism, Kruppel-Like Transcription Factors metabolism, Linkage Disequilibrium, Polymorphism, Single Nucleotide, Cattle genetics, Histidine Ammonia-Lyase genetics, Milk metabolism
- Abstract
Background: The histidine ammonia-lyse gene (HAL) encodes the histidine ammonia-lyase, which catalyzes the first reaction of histidine catabolism. In our previous genome-wide association study in Chinese Holstein cows to identify genetic variants affecting milk production traits, a SNP (rs41647754) located 357 bp upstream of HAL, was found to be significantly associated with milk yield and milk protein yield. In addition, the HAL gene resides within the reported QTLs for milk production traits. The aims of this study were to identify genetic variants in HAL and to test the association between these variants and milk production traits., Results: Fifteen SNPs were identified within the regions under study of the HAL gene, including three coding mutations, seven intronic mutations, one promoter region mutation, and four 3'UTR mutations. Nine of these identified SNPs were chosen for subsequent genotyping and association analyses. Our results showed that five SNP markers (ss974768522, ss974768525, ss974768531, ss974768533 and ss974768534) were significantly associated with one or more milk production traits. Haplotype analysis showed that two haplotype blocks were significantly associated with milk yield and milk protein yield, providing additional support for the association between HAL variants and milk production traits in dairy cows (P < 0.05)., Conclusion: Our study shows evidence of significant associations between SNPs within the HAL gene and milk production traits in Chinese Holstein cows, indicating the potential role of HAL variants in these traits. These identified SNPs may serve as genetic markers used in genomic selection schemes to accelerate the genetic gains of milk production traits in dairy cattle.
- Published
- 2014
- Full Text
- View/download PDF
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