Article(id=1309573296849515193, tenantId=1146029695717560320, journalId=1308397196074385509, issueId=1309573278520406630, articleNumber=null, orderNo=null, doi=10.11733/j.issn.1007-0435.2026.05.021, pmid=null, cstr=null, oa=null, hot=0, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1766592000000, receivedDateStr=2025-12-25, revisedDate=1769529600000, revisedDateStr=2026-01-28, acceptedDate=null, acceptedDateStr=null, onlineDate=1790156204664, onlineDateStr=2026-09-23, pubDate=null, pubDateStr=null, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1790156204664, onlineIssueDateStr=2026-09-23, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1790156204664, creator=13701087609, updateTime=1790156204664, updator=13701087609, issue=Issue{id=1309573278520406630, tenantId=1146029695717560320, journalId=1308397196074385509, year='2026', volume='34', issue='5', pageStart='1557', pageEnd='1962', issueExtLink='null', onlineDate='null', pubDate='1778774400000', pubDateStr='2026-05-15', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=null, createTime=1790156200293, creator='13701087609', updateTime=1790156821973, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1309575886110814336, tenantId=1146029695717560320, journalId=1308397196074385509, issueId=1309573278520406630, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1309575886115008641, tenantId=1146029695717560320, journalId=1308397196074385509, issueId=1309573278520406630, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=1798, endPage=1806, ext={EN=ArticleExt(id=1309573297168282299, articleId=1309573296849515193, tenantId=1146029695717560320, journalId=1308397196074385509, language=EN, title=Effects of Alkaline Salt Stress on AsA-GSH Cycle of Mitochondria in the Radicle and Plumule of Bothriochloa ischaemum, columnId=null, journalTitle=Acta Agrestia Sinica, columnName=null, runingTitle=null, highlight=null, articleAbstract=In order to explore the effects of alkaline salt stress on the ascorbic acid-glutathione cycle(AsA-GSH) of mitochondria in the radicle and plumule of Bothriochloa ischaemum, this experiment used ‘Taihang’ Bothriochloa ischaemum as material, which was germinated in NaHCO3 and Na2CO3 solutions with Na+ concentration of 0(CK), 10 and 30 mmol·L-1, and then changes in the activities of AsA-GSH enzymes and lipid peroxidation in their mitochondria of radicle and plumule were analyzed. The results showed that the activities of superoxide dismutase, catalase, glutathione peroxidase and monodehydroascorbate reductase in the mitochondria of radicle increased with the increase of Na+ concentration (0-30 mmol·L-1), but the opposite phenomenon was observed in the activities of glutathione sulfur transferase, ascorbate peroxidase and glutathione reductase. With the increase of Na+ concentration (0-30 mmol·L-1), the activities of superoxide dismutase, catalase and glutathione peroxidase in the mitochondria of plumule increased significantly (P<0.05), but the activities of glutathione sulfur transferase, glutathione reductase and monodehydroascorbate reductase decreased significantly (P<0.05). There were differences in the effects of type and concentration under alkaline salt on the AsA-GSH in radicle and plumule of Bothriochloa ischaemum, and the sensitivity of mitochondrial AsA-GSH in radicle of Bothriochloa ischaemum to alkaline salt stress was higher than that in plumule., authors=DONG Qiu-li1,2, ZHAO Chen-yang1, CHAI Ling1, CHEN Yi-lin1, LI Yin-lin1, XIA Fang-shan1, authorsList=DONG Qiu-li, ZHAO Chen-yang, CHAI Ling, CHEN Yi-lin, LI Yin-lin, XIA Fang-shan, authorCompany=1 College of Grassland Science, Shanxi Agricultural University, Taigu, Shanxi Province 030801, China;
2 College of Forestry, Shanxi Agricultural University, Taigu, Shanxi Province 030801, China, correspAuthors=null, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1309573297105367738, articleId=1309573296849515193, tenantId=1146029695717560320, journalId=1308397196074385509, language=CN, title=碱性盐胁迫对白羊草胚根和胚芽线粒体AsA-GSH循环的影响, columnId=1309565024058835950, journalTitle=草地学报, columnName=研究论文, runingTitle=null, highlight=null, articleAbstract=为探究碱性盐胁迫对白羊草(Bothriochloa ischaemum)胚根和胚芽线粒体抗坏血酸-谷胱甘肽(AsA-GSH)循环的影响,本试验以‘太行’白羊草为材料,在Na⁺浓度为0(CK),10和30 mmol·L⁻¹的NaHCO₃和Na₂CO₃溶液中进行萌发试验,分析其胚根和胚芽线粒体AsA-GSH循环酶活性及脂质过氧化变化规律。结果表明:白羊草胚根线粒体中超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶和单脱氢抗坏血酸还原酶活性随Na⁺浓度(0~30 mmol·L⁻¹)的增加均呈上升趋势,而其谷胱甘肽硫转移酶、抗坏血酸过氧化物酶和谷胱甘肽还原酶活性则相反;白羊草胚芽线粒体中超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶活性随Na⁺浓度(0~30 mmol·L⁻¹)的增加均显著上升(P<0.05),而其谷胱甘肽硫转移酶、谷胱甘肽还原酶和单脱氢抗坏血酸还原酶活性则显著下降(P<0.05)。碱性盐种类和浓度对白羊草胚根和胚芽AsA-GSH循环的影响存在差异,且胚根线粒体AsA-GSH循环响应碱性盐胁迫的敏感性要高于胚芽。, authors=董秋丽1,2, 赵晨洋1, 柴玲1, 陈奕霖1, 李尹琳1, 夏方山1, authorsList=董秋丽, 赵晨洋, 柴玲, 陈奕霖, 李尹琳, 夏方山, authorCompany=1 山西农业大学草业学院, 山西 太谷 030801;
2 山西农业大学林学院, 山西 太谷 030801, correspAuthors=null, authorNote=董秋丽(1985-),女,实验师,硕士,主要从事草种科学研究工作,E-mail:sxaudql@163.com, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=aMfUpVSSeG7CHdZ1LpEwXw==, pdfFileSize=3007377, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=山西农业大学“十四五”生物育种工程项目“乡土草种质资源挖掘与新品种选育 (YZGC134))}, authors=[Author(id=1320569854290153767, tenantId=1146029695717560320, journalId=null, articleId=1309573296849515193, orderNo=null, firstName=null, middleName=null, lastName=null, nameCn=null, orcid=null, stid=null, country=null, authorPic=null, dead=null, email=null, emailSecond=null, emailThird=null, correspondingAuthor=null, authorType=null, ext={}, companyList=null)], 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LYU Y Z, YAO X J, ZHANG Z, et al. Evaluation of alkali tolerance and key indicators screening during seed germination of different alfalfa cultivars[J]. Acta Agrestia Sinica, 2025, 33(6):1852-1861 吕艳贞, 姚兴洁, 张昭, 等. 不同品种紫花苜蓿种子萌发期耐碱性评价与关键指标筛选[J]. 草地学报, 2025, 33(6):1852-1861
YU C, ZHANG Y L, LI Q Y, et al. Effects of saline-alkali stresses on seed germination and seedling physiological and biochemical characteristics of Origanum vulgare[J]. Acta Agrestia Sinica, 2024, 32(6):1882-1892 于婵, 张依琳, 李秋莹, 等. 盐碱胁迫对牛至种子萌发和幼苗生理生化特性的影响[J]. 草地学报, 2024, 32(6):1882-1892
WANG Y J, ZHAO Y R, WEI Y Q. Effects of salt, alkali and drought stress on seed germination of quinoa under different temperature conditions[J]. Molecular Plant Breeding, 2025, 23(2):543-553 王悦娟, 赵延蓉, 魏玉清. 不同温度条件下盐、碱和干旱胁迫对藜麦种子萌发过程的影响[J]. 分子植物育种, 2025, 23(2):543-553
GUO K W, XU Z S, HUO Y Z, et al. Effects of salt concentration, pH, and their interaction on plant growth, nutrient uptake, and photochemistry of alfalfa (Medicago sativa) leaves[J]. Plant Signaling & Behavior, 2020, 15(12):1832373
CHEN Y L. Effects of saline-alkali stress and AsA priming on the AsA-GSH cycle of embryonic mitochondrial in Bothriochloa ischaemum[D]. Taigu:Shanxi Agricultural University, 2022:3-62 陈奕霖. 盐碱胁迫及AsA引发对白羊草种胚线粒体AsA-GSH循环的影响[D]. 太谷:山西农业大学, 2022:3-62
MAURYA A K. Oxidative stress in crop plants[M]//Agronomic crops. Singapore:Springer Singapore, 2020:349-380
XIA F S, CHANG H, CHEN L L, et al. Influence of exogenous ascorbic acid and glutathione priming on mitochondrial structural and functional systems to alleviate aging damage in oat seeds[J]. BMC Plant Biology, 2020, (1):104
LI Y P. Effects of copper stress on Γ-aminobutyric acid metabolism during wheat seed germination[D]. Lanzhou:Northwest Normal University, 2023:1-61 李亚萍. 铜胁迫对小麦种子萌发过程中γ-氨基丁酸代谢的影响[D]. 兰州:西北师范大学, 2023:1-61
LI Y L, CHEN Y L, XIA F S, et al. Effects of salt stress on mitochondrial antioxidant resistance of Bothriochloa ischaemum seedlings[J]. Acta Agrestia Sinica, 2024, 32(8):2498-2504 李尹琳, 陈奕霖, 夏方山, 等. 盐胁迫对白羊草幼苗线粒体抗氧化性能的影响[J]. 草地学报, 2024, 32(8):2498-2504
ZHANG J M, ZHANG J C, LI J J, et al. Effect of ascorbic acid priming on mitochondrial oxidation resistance of oat seedlings under salt stress[J]. Acta Agrestia Sinica, 2025, 33(2):481-488 张杰敏, 张金成, 李嘉俊, 等. 抗坏血酸引发对盐胁迫下燕麦幼苗线粒体抗氧化性能的影响[J]. 草地学报, 2025, 33(2):481-488
LI H Y, WANG C C, XIA F S, et al. Effect of AsA priming on the oxidation resistance of embryonic cells of aged oat seeds[J]. Acta Agrestia Sinica, 2023, 31(8):2392-2398 李红玉, 王聪聪, 夏方山, 等. 抗坏血酸引发对燕麦老化种子胚细胞抗氧化性能的影响[J]. 草地学报, 2023, 31(8):2392-2398
MI C J, HONG L, SUN S J, et al. Ascorbic acid priming restores the seed vigor by enhancing the mitochondrial AsA-GSH cycle and related gene expression in the aged oat seeds[J]. Physiologia Plantarum, 2025, 177(2):e70190
ZHAO A R, ZENG J, XIA F S, et al. Effects of storage years on antioxidant properties of embryonic cells of Bothriochloa ischaemum seeds from different population[J]. Pratacultural Science, 2024, 41(9):2046-2053 赵奥然, 曾佳, 夏方山, 等. 贮藏年限对不同居群白羊草种胚细胞抗氧化特性的影响[J]. 草业科学, 2024, 41(9):2046-2053
LI Y Y, DONG K H, WANG R M, et al. Establishment and optimization of ISSR-PCR reaction system for Bothriochloa ischaemum[J]. Chinese Journal of Grassland, 2012, 34(4):15-20 李钰莹, 董宽虎, 王若梦, 等. 白羊草ISSR-PCR反应体系的建立与优化[J]. 中国草地学报, 2012, 34(4):15-20
FANG Z H, LIU J N, ZHANG Y, et al. Bioinformatics analysis of NAC gene family in Bothriochloa ischaemum[J]. Acta Agrestia Sinica, 2020, 28(5):1266-1274 方志红, 刘建宁, 张燕, 等. 白羊草NAC转录因子家族生物信息学分析[J]. 草地学报, 2020, 28(5):1266-1274
QI Q, DONG Y Y, LIANG Y L, et al. Overexpression of SlMDHAR in transgenic tobacco increased salt stress tolerance involving S-nitrosylation regulation[J]. Plant Science, 2020, 299:110609
LIU Y, LI P, WANG Y X, et al. Quantification of carbon-water dynamics in soil-perennial grass (Bothriochloa ischaemum) feedbacks under drought stress following a double isotope-labelled pulse experiment[J]. Agricultural and Forest Meteorology, 2023, 329:109270
YNI N G K, SUN H M, XIN X, et al. Mitochondrial damage in the soybean seed axis during imbibition at chilling temperatures[J]. Plant & Cell Physiology, 2009, 50(7):1305-1318
AEBI H.Catalase[M]//Methods of enzymatic analysis. 2nd ed. Academic press, 1974:673-684
BEYER W F, FRIDOVICH I. Assaying for superoxide dismutase activity: some large consequences of minor changes in conditions[J]. Analytical Biochemistry, 1987, 161(2):559-566
FIOHÉ L, GÜNZLER W A. Assays of glutathione peroxidase[M]//Methods in enzymology. New York:Academic Press, 1984, 105:114-120
MADAMANCHI N R, AISCHER R G. Metabolic bases for differences in sensitivity of two pea cultivars to sulfur dioxide[J]. Plant Physiology, 1991, 97(1):88-93
NAKANO Y, ASADA K. Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts[J]. Plant and Cell Physiology, 1981, 22(5):867-880
NAGALAKSHMI N, PRASAD M N V. Responses of glutathione cycle enzymes and glutathione metabolism to copper stress in Scenedesmus bijugatus[J]. Plant Science, 2001, 160(2):291-299
ARRIGONI O, DIPIERRO S, BORRACCINO G. Ascorbate free radical reductase, a key enzyme of the ascorbic acid system[J]. FEBS Letters, 1981, 125(2):242-244
BAILLY C, BENAMAR A, CORBINEAU F, et al. Changes in malondialdehyde content and in superoxide dismutase, catalase and glutathione reductase activities in sunflower seeds as related to deterioration during accelerated aging[J]. Physiologia Plantarum, 1996, 97(1):104-110
DONG L, ZHAO M, HOU K B, et al. Does folcisteine (NATCA) play a role in facilitating seed germination, root development, and elevating root AsA-GSH cycle efficiency under combined copper–cadmium stress in maize?[J]. International Journal of Molecular Sciences, 2025, 26(22):11220
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HUO Q P. Physiological and molecular mechanisms of coordinated adaptation of barley roots and leaves to alkaline stress[D]. Tongliao:Inner Mongolia University for the Nationalities, 2024:3-54 霍庆平. 大麦根、叶协同适应碱胁迫的生理与分子机制[D]. 通辽:内蒙古民族大学, 2024:3-54)
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碱性盐胁迫对白羊草胚根和胚芽线粒体AsA-GSH循环的影响
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草地学报 | 研究论文 2026,34(5): 1798-1806
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草地学报 |研究论文 2026 , 34 (5) : 1798 -1806
碱性盐胁迫对白羊草胚根和胚芽线粒体AsA-GSH循环的影响
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作者信息
作者简介:
董秋丽(1985-),女,实验师,硕士,主要从事草种科学研究工作,E-mail:sxaudql@163.com
Effects of Alkaline Salt Stress on AsA-GSH Cycle of Mitochondria in the Radicle and Plumule of Bothriochloa ischaemum
Affiliations
    1 College of Grassland Science, Shanxi Agricultural University, Taigu, Shanxi Province 030801, China;
    2 College of Forestry, Shanxi Agricultural University, Taigu, Shanxi Province 030801, China
doi: 10.11733/j.issn.1007-0435.2026.05.021
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为探究碱性盐胁迫对白羊草(Bothriochloa ischaemum)胚根和胚芽线粒体抗坏血酸-谷胱甘肽(AsA-GSH)循环的影响,本试验以‘太行’白羊草为材料,在Na⁺浓度为0(CK),10和30 mmol·L⁻¹的NaHCO₃和Na₂CO₃溶液中进行萌发试验,分析其胚根和胚芽线粒体AsA-GSH循环酶活性及脂质过氧化变化规律。结果表明:白羊草胚根线粒体中超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶和单脱氢抗坏血酸还原酶活性随Na⁺浓度(0~30 mmol·L⁻¹)的增加均呈上升趋势,而其谷胱甘肽硫转移酶、抗坏血酸过氧化物酶和谷胱甘肽还原酶活性则相反;白羊草胚芽线粒体中超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶活性随Na⁺浓度(0~30 mmol·L⁻¹)的增加均显著上升(P<0.05),而其谷胱甘肽硫转移酶、谷胱甘肽还原酶和单脱氢抗坏血酸还原酶活性则显著下降(P<0.05)。碱性盐种类和浓度对白羊草胚根和胚芽AsA-GSH循环的影响存在差异,且胚根线粒体AsA-GSH循环响应碱性盐胁迫的敏感性要高于胚芽。
碱性盐胁迫  /  白羊草  /  线粒体  /  抗坏血酸-谷胱甘肽循环  /  胚根  /  胚芽
In order to explore the effects of alkaline salt stress on the ascorbic acid-glutathione cycle(AsA-GSH) of mitochondria in the radicle and plumule of Bothriochloa ischaemum, this experiment used ‘Taihang’ Bothriochloa ischaemum as material, which was germinated in NaHCO3 and Na2CO3 solutions with Na+ concentration of 0(CK), 10 and 30 mmol·L-1, and then changes in the activities of AsA-GSH enzymes and lipid peroxidation in their mitochondria of radicle and plumule were analyzed. The results showed that the activities of superoxide dismutase, catalase, glutathione peroxidase and monodehydroascorbate reductase in the mitochondria of radicle increased with the increase of Na+ concentration (0-30 mmol·L-1), but the opposite phenomenon was observed in the activities of glutathione sulfur transferase, ascorbate peroxidase and glutathione reductase. With the increase of Na+ concentration (0-30 mmol·L-1), the activities of superoxide dismutase, catalase and glutathione peroxidase in the mitochondria of plumule increased significantly (P<0.05), but the activities of glutathione sulfur transferase, glutathione reductase and monodehydroascorbate reductase decreased significantly (P<0.05). There were differences in the effects of type and concentration under alkaline salt on the AsA-GSH in radicle and plumule of Bothriochloa ischaemum, and the sensitivity of mitochondrial AsA-GSH in radicle of Bothriochloa ischaemum to alkaline salt stress was higher than that in plumule.
Alkaline salt stress  /  Bothriochloa ischaemum  /  Mitochondria  /  Ascorbic acid-glutathione cycle  /  Radicle  /  Plumule
董秋丽, 赵晨洋, 柴玲, 陈奕霖, 李尹琳, 夏方山. 碱性盐胁迫对白羊草胚根和胚芽线粒体AsA-GSH循环的影响. 草地学报, 2026 , 34 (5) : 1798 -1806 . DOI: 10.11733/j.issn.1007-0435.2026.05.021
DONG Qiu-li, ZHAO Chen-yang, CHAI Ling, CHEN Yi-lin, LI Yin-lin, XIA Fang-shan. Effects of Alkaline Salt Stress on AsA-GSH Cycle of Mitochondria in the Radicle and Plumule of Bothriochloa ischaemum[J]. Acta Agrestia Sinica, 2026 , 34 (5) : 1798 -1806 . DOI: 10.11733/j.issn.1007-0435.2026.05.021

    山西农业大学“十四五”生物育种工程项目“乡土草种质资源挖掘与新品种选育 (YZGC134)

参考文献 引证文献
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YU C, ZHANG Y L, LI Q Y, et al. Effects of saline-alkali stresses on seed germination and seedling physiological and biochemical characteristics of Origanum vulgare[J]. Acta Agrestia Sinica, 2024, 32(6):1882-1892 于婵, 张依琳, 李秋莹, 等. 盐碱胁迫对牛至种子萌发和幼苗生理生化特性的影响[J]. 草地学报, 2024, 32(6):1882-1892
WANG Y J, ZHAO Y R, WEI Y Q. Effects of salt, alkali and drought stress on seed germination of quinoa under different temperature conditions[J]. Molecular Plant Breeding, 2025, 23(2):543-553 王悦娟, 赵延蓉, 魏玉清. 不同温度条件下盐、碱和干旱胁迫对藜麦种子萌发过程的影响[J]. 分子植物育种, 2025, 23(2):543-553
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MAURYA A K. Oxidative stress in crop plants[M]//Agronomic crops. Singapore:Springer Singapore, 2020:349-380
XIA F S, CHANG H, CHEN L L, et al. Influence of exogenous ascorbic acid and glutathione priming on mitochondrial structural and functional systems to alleviate aging damage in oat seeds[J]. BMC Plant Biology, 2020, (1):104
LI Y P. Effects of copper stress on Γ-aminobutyric acid metabolism during wheat seed germination[D]. Lanzhou:Northwest Normal University, 2023:1-61 李亚萍. 铜胁迫对小麦种子萌发过程中γ-氨基丁酸代谢的影响[D]. 兰州:西北师范大学, 2023:1-61
LI Y L, CHEN Y L, XIA F S, et al. Effects of salt stress on mitochondrial antioxidant resistance of Bothriochloa ischaemum seedlings[J]. Acta Agrestia Sinica, 2024, 32(8):2498-2504 李尹琳, 陈奕霖, 夏方山, 等. 盐胁迫对白羊草幼苗线粒体抗氧化性能的影响[J]. 草地学报, 2024, 32(8):2498-2504
ZHANG J M, ZHANG J C, LI J J, et al. Effect of ascorbic acid priming on mitochondrial oxidation resistance of oat seedlings under salt stress[J]. Acta Agrestia Sinica, 2025, 33(2):481-488 张杰敏, 张金成, 李嘉俊, 等. 抗坏血酸引发对盐胁迫下燕麦幼苗线粒体抗氧化性能的影响[J]. 草地学报, 2025, 33(2):481-488
LI H Y, WANG C C, XIA F S, et al. Effect of AsA priming on the oxidation resistance of embryonic cells of aged oat seeds[J]. Acta Agrestia Sinica, 2023, 31(8):2392-2398 李红玉, 王聪聪, 夏方山, 等. 抗坏血酸引发对燕麦老化种子胚细胞抗氧化性能的影响[J]. 草地学报, 2023, 31(8):2392-2398
MI C J, HONG L, SUN S J, et al. Ascorbic acid priming restores the seed vigor by enhancing the mitochondrial AsA-GSH cycle and related gene expression in the aged oat seeds[J]. Physiologia Plantarum, 2025, 177(2):e70190
ZHAO A R, ZENG J, XIA F S, et al. Effects of storage years on antioxidant properties of embryonic cells of Bothriochloa ischaemum seeds from different population[J]. Pratacultural Science, 2024, 41(9):2046-2053 赵奥然, 曾佳, 夏方山, 等. 贮藏年限对不同居群白羊草种胚细胞抗氧化特性的影响[J]. 草业科学, 2024, 41(9):2046-2053
LI Y Y, DONG K H, WANG R M, et al. Establishment and optimization of ISSR-PCR reaction system for Bothriochloa ischaemum[J]. Chinese Journal of Grassland, 2012, 34(4):15-20 李钰莹, 董宽虎, 王若梦, 等. 白羊草ISSR-PCR反应体系的建立与优化[J]. 中国草地学报, 2012, 34(4):15-20
FANG Z H, LIU J N, ZHANG Y, et al. Bioinformatics analysis of NAC gene family in Bothriochloa ischaemum[J]. Acta Agrestia Sinica, 2020, 28(5):1266-1274 方志红, 刘建宁, 张燕, 等. 白羊草NAC转录因子家族生物信息学分析[J]. 草地学报, 2020, 28(5):1266-1274
QI Q, DONG Y Y, LIANG Y L, et al. Overexpression of SlMDHAR in transgenic tobacco increased salt stress tolerance involving S-nitrosylation regulation[J]. Plant Science, 2020, 299:110609
LIU Y, LI P, WANG Y X, et al. Quantification of carbon-water dynamics in soil-perennial grass (Bothriochloa ischaemum) feedbacks under drought stress following a double isotope-labelled pulse experiment[J]. Agricultural and Forest Meteorology, 2023, 329:109270
YNI N G K, SUN H M, XIN X, et al. Mitochondrial damage in the soybean seed axis during imbibition at chilling temperatures[J]. Plant & Cell Physiology, 2009, 50(7):1305-1318
AEBI H.Catalase[M]//Methods of enzymatic analysis. 2nd ed. Academic press, 1974:673-684
BEYER W F, FRIDOVICH I. Assaying for superoxide dismutase activity: some large consequences of minor changes in conditions[J]. Analytical Biochemistry, 1987, 161(2):559-566
FIOHÉ L, GÜNZLER W A. Assays of glutathione peroxidase[M]//Methods in enzymology. New York:Academic Press, 1984, 105:114-120
MADAMANCHI N R, AISCHER R G. Metabolic bases for differences in sensitivity of two pea cultivars to sulfur dioxide[J]. Plant Physiology, 1991, 97(1):88-93
NAKANO Y, ASADA K. Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts[J]. Plant and Cell Physiology, 1981, 22(5):867-880
NAGALAKSHMI N, PRASAD M N V. Responses of glutathione cycle enzymes and glutathione metabolism to copper stress in Scenedesmus bijugatus[J]. Plant Science, 2001, 160(2):291-299
ARRIGONI O, DIPIERRO S, BORRACCINO G. Ascorbate free radical reductase, a key enzyme of the ascorbic acid system[J]. FEBS Letters, 1981, 125(2):242-244
BAILLY C, BENAMAR A, CORBINEAU F, et al. Changes in malondialdehyde content and in superoxide dismutase, catalase and glutathione reductase activities in sunflower seeds as related to deterioration during accelerated aging[J]. Physiologia Plantarum, 1996, 97(1):104-110
DONG L, ZHAO M, HOU K B, et al. Does folcisteine (NATCA) play a role in facilitating seed germination, root development, and elevating root AsA-GSH cycle efficiency under combined copper–cadmium stress in maize?[J]. International Journal of Molecular Sciences, 2025, 26(22):11220
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2026年第34卷第5期
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doi: 10.11733/j.issn.1007-0435.2026.05.021
  • 接收时间:2025-12-25
  • 首发时间:2026-09-23
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  • 收稿日期:2025-12-25
  • 修回日期:2026-01-28
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2种不同金属材料的力学参数
科
Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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