中国4种蝗虫不同种群的遗传分化

采用水平淀粉凝胶电泳技术,应用等位酶分析方法对采自我国山西、江苏、河北等地不同蝗区优势蝗虫种类3科4种8个种群的12种酶18个酶位点进行了检测,比较了4种蝗虫种群水平的等位基因频率变化和它们之间的遗传距离。等位基因频率分析表明：中华稻蝗和笨蝗各位点等位基因丰富,而长翅素木蝗和短额负蝗各位点等位基因较少。在所研究的4种蝗虫8个种群中,多态位点百分率普遍较高(P＝53．3％—100．0％),由于杂合子数目较少而使每个位点的平均杂合度观察值偏低(H。＝0．034—0．139)。受迁飞能力、繁殖方式和活动范围的限制,4种蝗虫的平均杂合度观察值表现出一定的差异：笨蝗较高(H。＝0．089—0．139),其次是中华稻蝗(H。＝0．073—0．090),而长翅素木蝗(H。＝0．0488—0．068)和短额负蝗(H。＝0．034—0．050)相对较低。除Adk-1、Ao-1、Idh-1、Ldh-1、Ldh-2和Me-1在部分蝗虫种群符合Hardy-Weinberg平衡外,其余绝大多数位点的基因型频率显著偏离H—W平衡,但短额负蝗的多个位点符合或接近H—W平衡,表明该种蝗虫在自然种群结构方面明显有别于其他种类。从4种蝗虫的F—统计量(Fst)看,笨蝗种群间基因分化程度最高(Fst＝0．32),其次是短额负蝗(Fst＝0．31),而中华稻蝗相对较低(Fsl＝0．20),长翅素木蝗种群间基因分化程度最低(Fsl＝0．18),利用非加权算术平均法(UPGMA)对I值和D值进行聚类,所得聚类树也证实了这种遗传分化差异,上述结果反映了迁飞能力、适应性和环境因子对不同蝗虫遗传分化的影响。Nei的遗传距离(D)和遗传一致度(I)进行的聚类分析基本符合传统形态学、细胞学等研究结果：即同属于斑腿蝗科的中华稻蝗和长翅素木蝗遗传距离最小(D＝0．559),遗传一致度最高(I＝0．576)。在3个科中,癞蝗科和锥头蝗科之间呈现较小的遗传距离(D＝0．776)和较高的遗传一致度(I＝0．776),而这两科与斑腿蝗科之间的遗传距离相对较大(D＝0．908),遗传一致度相对较低(I＝0．406)。等位酶分析能较好地反映蝗虫不同物种的亲缘关系和种内不同种群之间的遗传分化程度。     

中华稻蝗四个种群的遗传分化

采用水平淀粉凝胶电泳技术研究中华稻蝗(Oxya chinensis)四个种群的12个基因座位,探讨其遗传分化.这四个种群分别采自内蒙古呼和浩特、山西代县、山西太原和陕西西安.Ck和Mdh-2在四个种群中均为单态,其余的基因座位至少在一个种群内有两个以上的等位基因;在Ldh和Mdh-1的等位基因频率呈现梯度分布趋势.多态基因座位百分率(P)和平均每个基因座位的等位基因数目(A)分别为58.3%-66.7%和2.2-2.8,平均杂合度为Ho=0.173-0.240.除Gpi,Hk-2,Idh,Ldh和Mdh-1在部分蝗虫种群符合Hardy-Weinberg平衡外,其余绝大多数基因座位的基因型频率显著偏离Hardy-Weinberg平衡.四个种群间FST平均值不存在显著差异(FST=0.0510,P＞0.05),结合高的Nei's遗传一致度(I＞0.97)可知,种群之间遗传分化不明显.我们认为人类的农业活动可能促进了种群间的基因交流,从而降低了分化程度[动物学报50(2)187-192,2004].     

宽翅曲背蝗两个地理种群等位酶的比较

采用水平淀粉凝胶电泳技术及应用等位酶分析方法,研究我国河北黄骅、辽宁葫芦岛宽翅曲背蝗两个自然种群的遗传多样性和遗传分化。在检测的11种酶15个酶基因座位中,Adk-I、Fbp-I、Mdh-2和G3pd-I基因座位的等位基因少,而Fbp-2、Mdh-I和Me-I基因座位的等位基因多。对每个基因座位的各基因型进行χ^2检验,除Mdh-I在辽宁葫芦岛种群、Adk-I在河北黄骅种群分别符合Hardy-Weinberg平衡外,其余绝大多数基因座位的基因型频率显著偏离Hardy-Weinberg平衡。两个种群之间存在明显的遗传多样性和分化：多态位点百分率分别为100％和93．3％,等位基因平均数分别为3．1和2．5,平均杂合度观测值分别为0．086和0．061。与其他非迁飞性蝗虫如中华稻蝗(Oxya chinensis)比较,这种蝗虫种群的平均杂合度较低但遗传多态性较高。结果表明：该蝗虫较强的跳跃能力可使个体暴露于各种不同环境,有利于维持种内遗传多态性的动态平衡,而种群保持较高的遗传多态性能增强该物种在不同栖息地的生存和繁殖能力。F-统计量表明两个种群之间的遗传分化相对较小,但这种分化显著高于迁飞性蝗虫如东亚飞蝗(Locusta migratoria manilensis)。Nei的遗传一致度(I)和Roger的遗传距离(D)的结果分析揭示了两个种群之间较高的遗传一致度(I=0．904)和较小的遗传距离(D=0．256)。然而,在一些酶基因座位如Aep-I(Fst=0．462)和Pgi-I(Fst=0．182),F-统计值相对较大,遗传分化比较明显。     

短额负蝗与中华蚱蜢精子比较：直翅目：蝗总科

短额负蝗与中华蚱蜢精子比较（直翅目：蝗总科）奚耕思,郑哲民（陕西师范大学动物研究所陕西省西安市７１００６２）短额负蝗Ａｔｒａｃｔｏｍｏｒｐｈａｓｉｎｅｎｓｉｓ与中华蚱蜢Ａｃｒｉｄａｃｉｎｅｒｅａ为中国两种常见的蝗虫。由于头顶细纵沟,后足股节外侧花纹及...     

不同地理种群短额负蝗对环境温度的适应性

[目的]本研究旨在探明短额负蝗Atractomorpha sinensis不同地理种群对环境温度响应的适应性差异.[方法]以大豆叶片为食物饲养,在恒温16,20,24,28和32℃,相对湿度70％,光周期16L:8D条件下,系统观测陕西延安、河南郑州、四川成都、云南曲靖和广东广州5个短额负蝗地理种群的生长发育过程,比较...     

华北2蝗区东亚飞蝗种群遗传结构的比较研究

利用水平淀粉凝胶电泳对采自天津北大港和河北黄骅两个相临蝗区的东亚飞蝗（Locusta migratoria manilensis)种群进行等位酶基因频率分析,比较了这两个种群的遗传结构,等位酶酶谱分析表明,19个基因座中4个基因座（Mdh-l,Pgm,Adk,G3pd)的等位基因频率变化很小,常见等位基因的频率均高于0．95,其他基因座有2－4个等位基因,但是两个种群的等位基因频率除两个基因座（Fbp,Got-2)外都很相似,多态位点的27个χ2检验表明,由于常见等位基因纯合子的高频率的和相应杂合子的缺乏,仅有北大港种群的2个基因座（Pgi,Got-1)符合Hardy-Weinberg平衡,在每个种群内的蝗虫存在明显的遗传变异,但在种群间遗传结构极为相似,多态位点的百分数P分别为73．7％和78．9％,每个基因座的平均等位基因数A为2．9和3．1,平均每个基因座的实际杂合度几乎相等（约为0．138）,F－统计量（FST＝0．053）也表明了两个种群间的遗传 一致性,遗传相似性系数（I）高达0．938,这些结果提示,这两个种群可能属于1 个大种群,在两个种群的一定位点上的遗传多态性和分化可能都与迁飞因素有关,因为东亚飞蝗的高度扩散能力有利于遗传结构的连续分布,高度的迁飞能力也导致个体暴露于各种不同的环境,而在种群水平上的遗传为异能增强种群在各种生态条件生存和繁殖能力,因此,迁飞有利于维持东亚飞蝗种群的遗传多态性的动态平衡。     

中国东亚飞蝗两个种群遗传分化的研究

采用水平淀粉凝胶电泳技术,分析了我国河北平山、辽宁葫芦岛两个蝗区东亚飞蝗自然种群的遗传结构。在酶谱分析的19个位点中,多数位点的等位基因数目较少,而位点Aat—l、Pgi和Mdh—2的等位基因数目相对较多。由于杂合子数目较少而使每个基因位点的平均杂合度降低(Ho=0．024和0．028)。对每个位点的各基因型进行x^2检验,绝大多数位点的基因型频率偏离Hardy—Weinberg平衡。较低的Fst值(Fst=0．021)表明两个种群的遗传分化程度不高。两个种群间较高的遗传一致度(I=0．991)和较小的遗传距离(D=0．092)也证实了上述结果。由此推测,该蝗虫较强的迁飞能力有可能增强种群间的基因交流,降低种群间的遗传分化。然而,在一些等位酶指标如位点Ao-2、Fbp—l、Mdh—2的等位基因频率分布、每个位点的平均等位基因数(A=2．5和2．7)和多态位点百分率(P=52．6％和57．9％)等,两个种群之间呈现出明显的差异。这也许与两个种群之间不同的生态环境条件和较远的地理距离有关。     

亚洲小车蝗不同地理种群遗传多样性的等位酶分析

采用等位酶电泳技术对亚洲小车蝗8个地理种群遗传多样性和遗传分化进行了研究,并对8种等位酶系统:苹果酸脱氢酶(MDH)、苹果酸酶(ME)、乙醇脱氢酶(ADH)、谷氨酸脱氢酶(GDH)、谷氨酸-草酰乙酸转氨酶(GOT)、异柠檬酸脱氢酶(IDH)、腺苷酸激酶(AK)和己糖激酶(HK)进行聚丙烯酰胺凝胶电泳分析。结果表明:在亚洲小车蝗8个地理种群中共检测到14个基因位点,其中7个位点为多态位点,检测到25个等位基因;种群总体水平多态位点比率P=42.86%,平均有效基因数A=1.786,平均期望杂合度He=0.072,种群平均遗传距离为0.069～0.235。聚类分析表明,遗传距离与地理距离存在一定相关性。亚洲小车蝗8个种群的遗传分化系数Fst=0.086,基因流Nm=3.142,表明亚洲小车蝗种群间有一定程度的遗传分化及基因交流。     

三种蝗虫消化道贲门瓣形态比较

采用扫描仪和扫描电镜观察的方法对太原地区中华稻蝗、短额负蝗和东亚飞蝗的贲门瓣的形态结构进行了观察,并对其结构和功能进行了描述和分析.     

短额负蝗精子发生过程中SBA受体的动态分布

用常规组织学方法观察短额负蝗Atractomorpha sinensis Bolivar精子发生过程中生精细胞的显微结构,并以大豆凝集素(soybean agglutinin,SBA)为探针利用凝集素细胞化学方法研究该过程中N-乙酰半乳糖复合物的分布变化。结果表明,短额负蝗精子发生经历了精原细胞增殖期、初级精母细胞期、次级精母细胞期、精子细胞形成期和精子成熟期5个时期,在这5个时期中各期生精细胞的大小、形态、核染色体等变化明显。在整个精子发生过程中,N-乙酰半乳糖复合物出现于精原细胞期,并于精母细胞期发生明显的修饰和变化,精子形成期和成熟期没有N-乙酰半乳糖复合物的表达。提示,N-乙酰半乳糖复合物的修饰和变化与短额负蝗生精细胞的生长和分化密切相关。     

Genetic diversity of six populations of Atractomorpha sinensis and Atractomorpha peregrina in Shanxi Province, China

Ten enzymes (AAT,CK,G3PDH,HEX,IDH,LDH,MDH,ME,PGI,PGM)were examined using horizontal starch gel electrophoresis to estimate the levels of genetic variation within and among six natural populations of two grasshopper species Atractomorpha sinensis and A.peregrina from Shanxi,China.The collecting sites were geographically distant from each other from south to north:Quwo district,Linfen city;Xiangyuan county,Changzhi;Jinyuan district,Taiyuan city;Yuanping county,Xinzhou city and Fanshi county of Xinzhou.A.sinensis showed 43 alleles at 16 loci but A.peregrine showed 39 alleles at 15 loci (ldh-1 was deficient).The zymograms showed that some common alleles were shared at several loci in these two species (Aat-1-b,Aat-2-b,G3pdh-a,Ck-1-b and Ldh-b).However,Hex-1-a,Hex-2-a,Hex-3-a,Idh-2-b,Mdh-2-b,Mdh-1-f Pgi-b,Pgm-b had common alleles in A.sinensis and Hex-1-b,Hex-2-b,Hex-3-b,Idh-2-a,Mdh-2-a,Mdh-1-d,Pgi-a,Pgm-c were of high frequency in A.peregrine instead.Most of the observed genotype frequencies were found to significantly deviate from the Hardy-Weinberg expectations in both species.A tendency of clinal distribution of allele frequency was observed at three loci.The frequency of the moderately migrating allele Me-c (0.318-0.740)in A.peregrina,Hex-1-a (0.800-1.000)and Ldh-b (0.487-0.750)in A.sinensis demonstrated increased frequency from north to south.Such tendency suggests that the allele frequency in these three loci may be correlated with the species'geographic distributions.A.sinensis showed higher genetic diversity than A.peregrina as indicated by higher mean number of alleles per locus (A=1.9-2.3 in A.sinensis and 1.7-2.2 in A.peregrina),percentage of polymorphic loci (56.3%-68.8%in A.sinensis and 43.8%-56.3%in A.peregrina),and the observed heterozygosities (Ho=0.072-0.096 in A.sinensis and 0.070-0.107 in A.peregrina).The observed heterozygosities of the six populations were all noticeably lower than the Hardy-Weinberg expectations,mostly due to heterozygote deficiency in the populations of both species.The overall mean Fsr were small (FST=0.045,P＞0.05 in A.sinensis populations and 0.087,P＞0.05 in A.peregrina populations).Nei's genetic identity (I)estimates indicate low intraspecific (＞0.95)but higher interspecific (0.377-0.447)genetic diversity.The cluster analysis based on modified Roger's genetic distance (D)showed that the two species were divided into two branches.Both species are of limited dispersal capacity and a moderate geographical barrier might significantly restrict the gene exchange among populations,resulting in accumulation of local genetic differentiations.The A.sinensis populations used in this study were separated from each other by 155.2 to 271.4 km and the A.peregrina populations were separated from each other by 78.8 to 174.9 km with observable physical barriers.The aUozyme data showed only minimal genetic differentiation at population level,most likely as a result of gene exchange.It is reasoned that natural factors and human agricultural activities might have facilitated migration and dispersal for the two species.     

Genetic diversity of six populations of Atractomorpha sinensis and Atractomorpha peregrina in Shanxi Province, China

Ten enzymes (AAT, CK, G3PDH, HEX, IDH, LDH, MDH, ME, PGI, PGM) were examined using horizontal starch gel electrophoresis to estimate the levels of genetic variation within and among six natural populations of two grasshopper species Atractomorpha sinensis and A. peregrina from Shanxi, China. The collecting sites were geographically distant from each other from south to north: Quwo district, Linfen city; Xiangyuan county, Changzhi; Jinyuan district, Taiyuan city; Yuanping county, Xinzhou city and Fanshi county of Xinzhou.A. sinensis showed 43 alleles at 16 loci but A. peregrine showed 39 alleles at 15 loci (Idh-1 was deficient). The zymograms showed that some common alleles were shared at several loci in these two species (Aat-1-b, Aat-2-b, G3pdh-a, Ck-1-b and Ldh-b). However, Hex-1-a, Hex-2-a, Hex-3-a, Idh-2-b, Mdh-2-b, Mdh-1-f, Pgi-b, Pgm-b had common alles in A. sinensis and Hex-1-b, Hex-2-b, Hex-3-b, Idh-2-a, Mdh-2-a, Mdh-1-d, Pgi-a, Pgm-c were of high frequency in A. peregrine instead. Most of the observed genotype frequencies were found to significantly deviate from the Hardy-Weinberg expectations in both species. A tendency of clinal distribution of allele frequency was observed at three loci. The frequency of the moderately migrating allele Me-c (0.318–0.740) in A. peregrina, Hex-1-a (0.800–1.000) and Ldh-b (0.487–0.750) in A. sinensis demonstrated increased frequency from north to south. Such tendency suggests that the allele frequency in these three loci may be correlated with the species’ geographic distributions. A. sinensis showed higher genetic diversity than A. peregrina as indicated by higher mean number of alleles per locus (A = 1.9–2.3 in A. sinensis and 1.7–2.2 in A. peregrina), percentage of polymorphic loci (56.3%–68.8% in A. sinensis and 43.8%–56.3% in A. peregrina), and the observed heterozygosities (H _o = 0.072–0.096 in A. sinensis and 0.70–0.107 in A. peregrina). The observed heterozygosities of the six populations were all noticeably lower than the Hardy-Weinberg expectations, mostly due to heterozygote deficiency in the populations of both species. The overall mean F _ST were small (F _ST = 0.045, P > 0.05 in A. sinensis populations and 0.087, P > 0.05 in A. peregrina populations). Nei’s genetic identity (I) estimates indicate low intraspecific (>0.95) but higher interspecific (0.377–0.447) genetic diversity. The cluster analysis based on modified Roger’s genetic distance (D) showed that the two species were divided into two branches. Both species are of limited dispersal capacity and a moderate geographical barrier might significantly restrict the gene exchange among populations, resulting in accumulation of local genetic differentiations. The A. sinensis populations used in this study were separated from each other by 155.2 to 271.4 km and the A. peregrina populations were separated from each other by 78.8 to 174.9 km with observable physical barriers. The allozyme data showed only minimal genetic differentiation at population level, most likely as a result of gene exchange. It is reasoned that natural factors and human agricultural activities might have facilitated migration and dispersal for the two species. __________ Translated from Acta Ecologica Sinica, 2005, 25(10): 2574–2481 [译自: 生态学报]     

短额负蝗的营养成分与利用评价

本文分析了短额负蝗AtractomorphasinensisBolivar的营养成分 ,包括蛋白质、氨基酸、总糖、粗脂肪、脂肪酸及维生素B1,B2 ,C和E。此种昆虫粗蛋白含量为 2 2 4 5 %～ 32 5 9% ,粗脂肪含量为 2 87%～4 91 % ,总糖为 0 0 95 %。在分析其营养价值的基础上 ,进行了开发利用评价。     

黄脸油葫芦与短额负蝗马氏管组织结构比较

采用组织学方法对直翅目剑尾亚目和锥尾亚目的两个物种--黄脸油葫芦Teleogryllus emma和短额负蝗Atractomorpha sinensis成虫的马氏管进行了观察,发现两者在着生位置、方式和细胞结构上存在明显不同.着生位置上,黄脸油葫芦的马氏管着生在后肠前端与后肠后端的交界处,短额负蝗的马氏管着生在中肠与后肠的交界处.着生方式上,黄脸油葫芦的马氏管是通过一根无色透明的公共管与肠道相通的,而短额负蝗的马氏管分为12丛,每一丛直接与肠道相连.细胞结构上,黄脸油葫芦的管壁由8个细胞构成,且集中在管的中央,与管壁有空隙;而短额负蝗的管壁由3～4个细胞组成,分散在管壁外围,有马氏管凸.     

短额负蝗卵子发生过程中糖复合物的动态分布

以生物素标记的凝集素(UEA-I、SBA、PNA)为探针,利用凝集素组织化学方法对短额负蝗(Atracto-morphasinensis)卵子发生过程中滤泡细胞和卵母细胞内糖复合物的分布进行了定位研究。结果表明,在卵子发生的各期滤泡细胞和卵母细胞中没有UEA-I受体的表达,SBA和PNA受体以不同的分布模式呈阶段性表达。两者首次出现于卵母细胞生长期,随后PNA受体消失,SBA受体大量表达;在卵黄形成期前期SBA受体和重新出现的PNA受体表达于卵黄颗粒形成部位,卵黄形成期后期两者均为阴性表达;成熟卵子中两种受体又以不同程度重新出现于卵黄膜。两种受体在滤泡细胞内均大量表达。提示,N-乙酰半乳糖胺和半乳糖-β-(1,3)半乳糖胺复合物的修饰和变化与卵母细胞的发育、卵黄物质的形成及滤泡细胞的增殖分化密切相关,卵黄膜上的糖复合物可能与精卵识别有关。     

短额负蝗线粒体基因组及其lrRNA和srRNA二级结构分析

采用长距PCR扩增及保守引物步移法测定并注释了短额负蝗的线粒体基因组全序列。结果表明,短额负蝗的线粒体基因组全长15558bp,A T含量为74.3%,37个基因位置与飞蝗的一致,基因间隔序列共计11处64bp,间隔长度从1～16bp不等;有15对基因间存在51bp重叠,重叠碱基数在1～8bp之间。13个蛋白质编码基因中找到6种可能的起始密码子,有12个基因在基因3'端能找到完全的TAA或TAG终止密码子,只有ND5基因终止密码子为不完整的TA。除tRNASer(AGN)外,其余21个tRNA基因的二级结构均属典型的三叶草结构。tRNASer(AGN)的DHU臂缺失,在相应的位置上只形成一个环。预测的lrRNA二级结构总共有6个结构域(结构域Ⅲ缺失),49个茎环结构。预测的srRNA的二级结构包含3个结构域,33个茎环结构。A T丰富区中存在一个被认为与复制及转录起始有关的Ploy(T)(T-stretch)结构。     

异翅负蝗配子发生过程中c-kit蛋白表达动态

应用免疫组织化学和生物统计分析相结合的方法,对异翅负蝗Atractomorp haheteroptera Bei Bienko配子发生过程中c-kit特异表达特点和动态进行研究。结果表明,(1)精子发生过程中,精原细胞、初级精母细胞、次级精母细胞和成熟精子中均有不同程度的c-kit蛋白表达,精巢末端还有较粗大的阳性颗粒分布;(2)卵子发生过程中,第1~6阶段卵母细胞中有不同程度的c-kit蛋白特异性表达,但随着卵黄发生的开始逐渐消失;(3)此外,滤泡细胞、输卵管和受精囊的腺细胞中有c-kit蛋白颗粒的存在;(4)从c-kit蛋白季节动态变化看,精子发生和卵子发生中的阳性表达都随着时间的延续出现下降的态势。因此,c-kit蛋白的特异性表达提示该蛋白参与配子发生过程的阶段性调控,具有重要的生理作用。     

中华水韭(Isoetes sinensis)等位酶分析的初步研究

采用超薄平板聚丙烯酰胺等电聚焦技术对珍稀涉危植物中华水韭（Isoetes sinensis Palmer）72个样品的等位酶遗传变异进行了初步研究。从24种酶筛选,得到了13种酶系统可用于该植物的遗传变异分析,其中7种酶系统在中华水韭的迁地保护区群中检测出16个位点,共27个等位基因,12个位点表现出多态性。遗传多样性初步分析表明：中华水韭具较低的等位酶遗传多样性。研究结果为中华水韭的综合保育及居群恢复、重建提供了初步的依据。中华水韭遗传变异的全面研究将在进一步改善等位酶方法的基础上,采用其它更为灵敏的分子标记方法做深入检测。