江苏省直立穗型粳稻品种主要农艺性状和品质性状分析

通过对江苏省淮北稻区种植的主要粳稻品种品质状况和近十年来育成的直立穗型粳稻品种(系)主要品质和农艺性状的分析,发现前期育成直立穗型粳稻品种相时半直立穗型粳稻品种加工品质低,垩白率高和垩白度大,蛋白质含量高;而近期育成直立穗型粳稻品种在上述品质指标上有了较大改进,食味品质也有了显著提高.在主要农艺性状中,近期育成品种呈现每穗总粒数上升、穗长变长、着粒密度下降趋势,产量水平的提高与每穗粒数的增加有着紧密相关.     

杂交水稻加工、外观品质性状间接选择的数学模型研究

利用19个优质杂交水稻品种（组合）,采用双向逐步筛选,求出加工和外观品质性状与产量性状的最优相关子集,建立了品质性状的回归方程,并对子集作了广义相关分析。结果表明千粒重、穗长与糙米率、整精米率、垩白粒率的相关已反映了品质性状与产量性状相关的主要信息（90％以上）,千粒重在21.96～27.64g、穗长在21.18～26.07cm范围内,增大千粒重可提高糙米率,但整米率下降、垩白粒率上升,适当缩短穗长可提高糙米率和整精米率,降低垩白粒率。     

粳稻品质性状间及其与植株性状和产量性状间的遗传相关

利用朱军等提出的种子性状遗传模型,采用 3×3 NCⅡ正反交设计的亲本和部分组合F2代种子,分析了品质性状糙米率、垩白粒率、垩白面积和AC间及上述品质性状与株高、穗部性状等的遗传相关,以期为粳稻育种后代选择提供指导。结果表明,精米重与糙米率存在极显著的母体加性相关;虽然控制品质性状的主要遗传效应分量与植株性状相应遗传效应分量遗传协方差不显著,但在其他相应遗传效应分量方面存在着复杂的关系。     

粳稻穗角与稻米品质的相关性及稻米品质遗传分析

测定了粳稻直立穗品种丙8979与弯曲穗品种C堡杂交组合的P1、P2及其重组自交系349个株系的穗角和10个稻米品质性状, 分析了穗角与稻米品质性状之间的相关性, 并运用主基因+多基因混合遗传模型, 对稻米品质10个性状进行了遗传分析。结果表明,穗角与糙米率、整精米率、垩白粒率、垩白度、糊化温度、胶稠度和直链淀粉含量均无显著相关; 与精米率呈显著正相关(r=0.124*); 与粒长和长宽比均呈极显著正相关(相关系数分别为0.470**和0.241**)。糙米率、精米率和直链淀粉含量均受2对主基因+多基因控制, 2对主基因具有累加作用和加性×加性的上位性作用; 整精米率、粒长、长宽比和胶稠度受2对加性-上位性主基因+多基因控制;垩白粒率、垩白度和糊化温度均受3对加性-上位性主基因+多基因控制。糙米率、精米率、整精米率、垩白粒率、垩白度和糊化温度6个品质性状以主基因遗传为主,粒长、长宽比、胶稠度和直链淀粉含量4个性状以多基因遗传为主。     

水稻外观品质的数量性状基因位点分析

利用由98个家系组成的Nipponbare(粳)／Kasalath(秒)∥Nipponbare回交重组自交系(backcross inbred lines,BILs)群体(BC1F9)及其分子连锁图谱,采用复合区间作图的方法,在2个不同年份对粒长、粒宽、粒形、垩白率、垩白大小、垩白度和透明度等7个稻米外观品质性状的数量性状基因位点(Quantiative trait loci,QTL)进行了定位分析。共定位到33个四QTLs,单个性状QTL数目在4-7个之间,以垩白率最多,为7个;粒长和垩白大小次之,为5个;其他性状均为4个,表明该组合外观品质是由多基因控制的数量性状。单个QTL对性状变异解释率粒长为6．2％-15．2％,粒宽为8．3％-32．5％,长宽比为6．8％-19．8％,垩白率为6．4％-28．5％,垩白大小为6．1％-16．9％,垩白度为9．3％-17．2％,透明度为5．6％-25．2％．QTL在染色体上成集中分布的特点,第3染色体C1488-C563、第5染色体R830-R3166和R1436-R2289、第6染色体R2147-R2171均有3个以上的QTLs分布。比较2年的检测结果表明,外观品质性状的QTL定位都受环境影响,但不同性状受影响的程度差异很大。粒长和粒形的QTL定位受环境影响很小,垩白率、垩白大小和垩白度的QTL定位受环境影响很大。     

不同穗型粳稻品种产量和品质性状的比较分析

利用不同穗型粳稻品种,在不同氮肥水平下对产量性状和品质性状进行了比较.试验结果表明,随着施氮水平的提高,直立穗型品种产量增加幅度大于半直立和弯曲穗型品种,但产量构成因素的变化趋势,在各种穗型品种间变化基本一致.随着施氮量的增加,3种穗型品种的糙米率、精米率和整精米率均增加,而垩白率的变化在不同穗型品种间不相一致.直立穗型品种较半直立和弯曲穗型品种,胶稠度相对较硬,蛋白质含量较高,并且对氮素的反应较敏感.     

云南高原粳稻品质特性分析

采用表型主成分及聚类分析法,对76个云南高原粳稻的11个品质性状进行了分析。结果表明,（1）直链淀粉含量的平均值达食用稻品种品质1级标准,糙米率、透明度、碱消值和胶稠度达2级标准,精米率达3级标准,其余品质性状的平均值均在3级以下。品种间变异最小的品质性状是糙米率和碱消值,变异最大的是垩白度,其次是垩白粒率。（2）稻米品质性状间存在复杂的相关关系。（3）在选出的6个影响云南稻米品质的主因子中,精米率、垩白粒率和垩白度因子对稻米品质的累积贡献率为49.6%。（4）76个云南粳稻聚为4类,其中第一类包括52个品种,表明遗传距离近,遗传基础狭窄。在今后的云南粳稻品质育种中,应降低垩白粒率和垩白度,提高精米率和整精米率,同时拓宽遗传基础。     

黑龙江省水稻品种跨积温区种植的产量和品质变化

采用在不同积温区布置田间试验的方法,比较研究了黑龙江省5个水稻主栽品种产量和品质随积温的变化.结果表明： 水稻产量随积温呈二次曲线变化,其相关程度因水稻品种而异;水稻穗数、穗粒数与积温呈极显著二次曲线关系,而千粒重与积温之间相关关系不显著;水稻籽实空瘪率从适宜积温区到低积温区显著增加,而从适宜积温区到高积温区变化不明显;水稻垩白率、整精米率与积温均呈极显著二次曲线关系,即垩白率和整精米率在适宜积温区分别有最小值和最大值存在;稻米蛋白质、直链淀粉含量和食味随积温变化不明显.根据对温度敏感程度的不同,可将水稻品种划分为温敏型、中间型、温钝型3类,其适宜栽培积温带宽度和允许栽培积温带宽度分别为300 ℃和420 ℃、360 ℃和440 ℃、380 ℃和520 ℃.根据积温因地制宜地选种水稻品种对于提高水稻产量、改善稻米品质十分重要.     

太湖流域晚粳稻地方种资源的表型遗传多样性

对368份太湖地区晚粳稻地方种材料的植株及品质性状进行分析与测定,结果表明种质问的性状均有极显著差异。植株形态及穗粒特性中,株高的变化从120．5～160．5cm,每穗总粒数变化在69．9～144．0粒／穗,千粒重的极差达10．7g。在品质性状上,整精米率变化在50．05％～77．05％间,垩白率、垩白度平均48．31％、5．36％,直链淀粉含量、蛋白质含量分别变化在12．8％～25．8％、7．55％～14．55％,平均分别为17．5％、9．42％,总体加工、蒸煮品质较优,外观品质较差。不同级分的种质资源数量的分布总体上亦呈正态分布的特征,如株高主要集中在137cm左右,占41．7％,每穗总粒数主要分布在92．3～110．0粒／穗间,占57．2％,千粒重主要在27．0～28．0g间,占41．7％。种质材料的植株及品质性状均具有较高的遗传多样性,穗粒性状、品质性状、植株形态性状的遗传多样性指数分别为2．02、1．87、1．54。种质资源材料中共有15个大穗型种质,穗粒数超过了140粒／穗,如天下第一种、千斤稻、晚慢种等,还有一些穗粒数低于70粒／穗的小穗型品种,如白叠谷、硬头颈、绿种等,直链淀粉含量≤15％的种质有22个,如来自吴江的田鸡青、野凤凰,也有一些高直链淀粉含量的种质材料,如矮土种、红芒种、木樨球和野稻。优质加工、外观品质的种质资源数量较少,吴江的晚洋稻、野凤凰两个材料属于低直链淀粉含量并且加工、外观品质为优质的种质资源。     

杂交粳稻及其亲本千粒重与产量、品质的相关性

为了探明杂交粳稻及其亲本千粒重与产量、品质的关系,以4个千粒重介于23.1~28.0 g之间的BT型不育系和24个千粒重介于18.1~32.0 g之间的三系粳稻恢复系,采用p×q不完全双列杂交(NCⅡ)设计,配制96个杂交组合为试验材料,对F1千粒重优势表现、F1千粒重与亲本千粒重及其与产量、品质性状间的相关性进行分析,确定高产优质兼顾的杂交粳稻的千粒重范围。结果表明:(1)56.3%的杂交组合千粒重超过其双亲平均值,19.8%的杂交组合千粒重表现正向超亲优势;(2)F1千粒重与母本千粒重、父本千粒重、双亲千粒重平均值的相关性均达极显著水平(r=0.33**、0.71**、0.78**),且恢复系千粒重对杂种的影响大于不育系;(3)F1千粒重、父本千粒重及双亲千粒重平均值与组合单株产量的相关性均达极显著水平(r=0.55**、0.47**、0.51**),母本千粒重与组合单株产量相关不显著;(4)F1千粒重、父本千粒重与糙米率、精米率、整精米率、垩白粒率、粒长、粒宽均呈极显著正相关,与透明度呈显著正相关,母本千粒重与垩白粒率、垩白度、粒长均呈极显著正相关,与粒宽呈显著正相关;(5)杂交粳稻育种中具有高产优质兼顾的F1千粒重范围应在25.1~27.0 g之间。     

Recent advances in the study of Kaposi's sarcoma-associated herpesvirus replication and pathogenesis

It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis.     

The structure, reproduction and taxonomy of Vidalia and Osmundaria (Rhodophyta, Rhodomelaceae)

Comprises species occurring mostly in subtidal habitats in tropical, subtropical and warm-temperate areas of the world. An analysis of the type species, V. spiralis (Sonder) Lamouroux ex J. Agardh, a species from Australia, establishes basic characters for distinguishing species in the genus. These characters are (1) branching patterns of thalli, (2) flat blades that may be spiralled on their axis, (3) width of the blade, (4) primary or secondary derivation of sterile and fertile branchlets and (5) position of sterile and fertile branchlets on the thalli. Application of the latter two characters provides an important basic method for separation of species into three major groups. Osmundaria , a genus known only in southern Australia, was studied in relation to Vidalia , and its separation from the Vidalia assemblage is not accepted. Species of Vidalia therefore are transferred to the older genus name, Osmundaria. Two new species, Osmundaria papenfussii and Osmundaria oliveae are described from Natal. Confusion in the usage of the epithet, Vidalia fimbriala Brown ex Turner has been clarified, and Vidalia gregaria Falkenberg, described as an epiphyte on Osmundaria pro/ifera Lamouroux, is revealed to be young branches of the host, Osmundaria prolifera.     

New or rare chromosome counts in Artemisia L. (Asteraceae, Anthemideae) and related genera from Kazakhstan

Fifteen chromosome counts of six Artemisia taxa and one species of each of the genera Brachanthemum, Hippolytia, Kaschgaria, Lepidolopsis and Turaniphytum are reported from Kazakhstan. Three of them are new reports, two are not consistent with previous counts and the remainder are confirmations of very scarce (one to four) earlier records. All the populations studied have the same basic chromosome number, x = 9, with ploidy levels ranging from 2x to 6x. Some correlations between ploidy level, morphological characters and distribution are noted.     

肝癌中HBV和HCV基因和抗原的分布及意义

采用原位分子杂交方法检测HCV RNA及HBV X基因;采用免疫组织化学方法研究HCV核心抗原,非结构区C33c抗原及HBxAg在肝细胞肝癌中的定位及分布.结果表明(1)HCV RNA、HBV X基因在肝细胞肝癌组织检出率分别为40%(55/136)和82%(112/136).HCV RNA定位于癌细胞的胞浆内,阳性细胞呈散在、灶状及弥漫分布三种形式;HBV X基因在肝癌细胞中的分布呈胞浆型、核型及核浆型,阳性细胞也呈上述三种分布形式;(2)HCV C33c抗原、核心抗原在肝细胞肝癌中的阳性率为81%(133/164)及86%(141/164).C33c抗原定位于癌细胞及肝细胞的胞浆内;核心抗原既定位于癌细胞核中,又可定位于胞浆中.C33c抗原阳性细胞以灶状分布为主;而核心抗原阳性细     

Selection with two alleles and complete dominance

For a plant selection model with frequency-independent viabilities, fertilities and selfing rates, it is shown that apart from global fixation, for certain parameter combinations a protected polymorphism and facultative fixation (either allele may become fixed according to initial frequencies) may both occur. Facultative fixation requires different selling rates for the dominant and recessive type. Protection of the polymorphism requires resource allocation for male and female function. In this connection the problem of purely genetically caused population extinction is discussed.
For general frequency dependence and regular segregation, the chances for establishment of a completely recessive gene are compared to those of a completely dominant gene. It is proven that the process of establishment of the recessive gene, despite a fitness advantage, may be considerably endangered by drift effects if random mating prevails. The recessive gene may reach the same effectivity in establishment as a dominant gene, only if the recessive homozygote mates exclusively with its own type during the period of establishment.