种皮和环境温度对橡胶树种子萌发的影响

在人工气候箱控制的条件下,研究了种皮和环境温度对橡胶树(Hevea brasiliensis)种子萌发的影响.结果表明,种皮对橡胶树种子的吸水和萌发具有明显的机械限制作用;去除种皮后种子萌发速率加快,萌发指数增大,但萌发率从83.8%下降到47.8%,幼苗活力指数从332.3下降到187.9.15℃以下的温度明显推迟种子萌发,且萌发率下降.去除种皮后的种仁萌发率、萌发指数和幼苗活力指数均随着温度的升高而增大;有种皮种子的萌发率、萌发指数和幼苗活力指数分别在20℃(94.7%)、30℃(1.86)和25℃(374.4)时最大,而萌发速率系数随着温度的升高先增大后减小.在橡胶树栽培和胶园建设中,可利用种皮对种仁水分散失的限制作用以及对低温的不敏感性,有效延长橡胶树种子的贮藏时间,提高萌发率和籽苗质量.     

‘勐海大叶茶’种子萌发特性

以大叶茶品种‘勐海大叶茶’ （Camellia sinensis var. assamica cv. Menghai Dayecha） 种子为材料,进行种子萌发特性的初步研究。研究发现,种皮对‘勐海大叶茶’种子的萌发存在一定的作用,含水量较高时,人为破除种皮有助于种子的萌发,随着含水量的降低,人为破除种皮反而降低了种子的萌发率。‘勐海大叶茶’种子的最适萌发温度为30℃,15℃以下时萌发率较低,容易发生低温伤害,变温处理对提高种子萌发率的效果不明显。基质对大叶茶种子萌发的影响不明显,四种不同种植基质条件下,种子的萌发率趋于相同水平,证明基质类型并非影响种子萌发的关键因子。     

顽拗性竹柏种子的贮藏特性?

文章对竹柏( Podocarpus nagi)种子的脱水耐性和贮藏特性进行了研究,结果表明：竹柏种子成熟时初始含水量约为(35±0?7)％,种子对脱水敏感,其最低安全含水量约为(16?86±0?73)％,具有顽拗性种子的典型特征;湿藏和半干藏都可以作为短期保存竹柏种子的方法,且以4℃保存优于15℃保存,但不管种子含水量如何,零下低温保存对竹柏种子都是致命的;半干藏法保存实验中,未进行脱水处理的种子(对照)在4℃贮藏6个月,种子萌发率没有发生明显下降,但贮藏期延长到9个月时,临界含水量的种子萌发力保存最高;不管贮藏介质的含水量高低,也无论贮藏在4℃还是15℃,湿藏种子在9个月的贮藏期内萌发率均没有明显的降低,但当贮藏到12个月时,15℃湿藏种子的萌发率显著高于4℃贮藏的种子,但15℃湿藏的种子在贮藏到3个月时即发现种子在贮藏期间萌发,且随着贮藏介质含水量的升高和贮藏期的延长,萌发的种子增多;竹柏的离体胚经过2h硅胶快速脱水至含水量7％后再冷冻即可获得90％以上的融后存活率,且超低温保存1年的离体胚解冻后,与只保存1周的存活率没有明显差异,表明超低温长期保存竹柏种子是可行的。本研究可以为进一步探究顽拗性种子的短期贮藏和长期保存提供理论基础和基础资料。     

狼毒种子萌发特性与种群更新机制的研究

研究了采集于植株上的和收集于土壤种子库的狼毒(Stellera chamaejasme)种子在不同温度、光照和5种预处理(即破裂种皮、去除种皮、98％H2SO4浸种5min、0．2％KNO3浸种24h、10℃低温保存1周)条件下的萌发力。结果表明,狼毒种子萌发率较低,25℃恒温、黑暗条件下萌发率为13％,较适宜的萌发温度为30℃恒温或10～30℃变温,破裂种皮和去除种皮萌发率显著提高,25℃恒温、光暗交替条件下萌发率分别为49％和47％,浓硫酸浸种5min处理萌发率可达到32％,KON3浸种和10℃低温保存两个处理对促进狼毒种子萌发效果不明显,狼毒种子萌发对光照条件不敏感,种子硬实性是导致狼毒种子萌发率较低的主要原因,取自土壤种子库内的狼毒种子萌发率高于当年采集的种子,在自然条件下,并非每年都有狼毒种子萌发长成幼苗,种群更新时机是随机的或周期性的。     

温度、土壤水分和NaCl对黄顶菊种子萌发的影响

光照和黑暗条件下的黄顶菊种子萌发无显著差异;种子萌发的适宜温度为25—35℃;种子萌发率随着NaCl浓度的升高而下降;种子萌发的最佳土壤含水量为35％-45％。在最适温度下,种子萌发耐受NaCl的临界值为89．919mmol·L^-1极限值为218．92mmol·L^-1;不同温度和NaCl以及二者共同作用使黄顶菊种子萌发受到的抑制都极显著。     

顽拗性竹柏种子的贮藏特性

文章对竹柏(Podocarpus nagi)种子的脱水耐性和贮藏特性进行了研究,结果表明:竹柏种子成熟时初始含水量约为(35±0.7)%,种子对脱水敏感,其最低安全含水量约为(16.86±0.73)%,具有顽拗性种子的典型特征;湿藏和半干藏都可以作为短期保存竹柏种子的方法,且以4℃保存优于15℃保存,但不管种子含水量如何,零下低温保存对竹柏种子都是致命的;半干藏法保存实验中,未进行脱水处理的种子(对照)在4℃贮藏6个月,种子萌发率没有发生明显下降,但贮藏期延长到9个月时,临界含水量的种子萌发力保存最高;不管贮藏介质的含水量高低,也无论贮藏在4℃还是15℃,湿藏种子在9个月的贮藏期内萌发率均没有明显的降低,但当贮藏到12个月时,15℃湿藏种子的萌发率显著高于4℃贮藏的种子,但15℃湿藏的种子在贮藏到3个月时即发现种子在贮藏期间萌发,且随着贮藏介质含水量的升高和贮藏期的延长,萌发的种子增多;竹柏的离体胚经过2 h硅胶快速脱水至含水量7%后再冷冻即可获得90%以上的融后存活率,且超低温保存1年的离体胚解冻后,与只保存1周的存活率没有明显差异,表明超低温长期保存竹柏种子是可行的。本研究可以为进一步探究顽拗性种子的短期贮藏和长期保存提供理论基础和基础资料。     

白木香种子脱水耐性的发育变化及贮藏特性

研究白木香种子发育进程中种子性状、萌发能力和脱水耐性的变化,以及不同光温条件对种子萌发的影响和种子的贮藏特性。结果表明：白木香种子在花后78d获得最大干重,进入生理成熟期,此时萌发率接近最大值;胚在花后57～85d,脱水耐性逐渐增强,并在花后85d获得最大脱水耐性。种子萌发的适宜温度范围为25℃-35℃,光照对种子萌发有一定的抑制作用。新鲜自木香种子（含水量27．45％）在4℃低温条件下贮藏1个月后萌发率仅为30％左右,而含水量7．38％的干燥种子在4℃低温条件下贮藏120d,萌发率仍有53．33％,因此,4℃低温和适度脱水有利于种子短期贮藏。白木香种子能忍耐一定程度的脱水,但干燥至含水量7．50％以下时种子会发生损伤,因此推测白木香种子是一种中间性种子。     

温度、土壤水分和NaCl对黄顶菊种子萌以的影响

光照和黑暗条件下的黄顶菊种子萌发无显著差异;种子萌发的适宜温度为25～35℃:种子萌发率随着NaCl浓度的升高而下降;种子萌发的最佳土壤含水量为35%～45%.在最适温度下,种子萌发耐受NaCI的临界值为89.919 mmol·L-1,极限值为218.92 mm01.L-1;不同温度和NaCl以及二者共同作用使黄顶菊种子萌发受到的抑制都极显著.     

温度和硬实对金花菜种子萌发的影响

为科学指导金花菜的田间生产,以不同来源的5份金花菜(Medicago polymorpha L.)种子为试验材料,研究其在不同温度(5、10、15、20、25、30、35、40℃)下和破除种皮后的萌发情况。结果表明:海门、扬中、江都金花菜种子萌发率在20℃左右达到最大值,分别是43%、60%、59%。海安金花菜种子在25℃下萌发率最高,为24%;温岭金花菜种子则在15℃和25℃下萌发率达最高,均为22%。40℃时金花菜种子均无法萌发。金花菜的种皮硬实是限制其萌发的重要因素。不同来源金花菜种子的硬实情况差异较大,海安、海门、扬中、江都、温岭等金花菜种子硬实率分别为84.67%、50.83%、40.50%、37.67%、67.67%。破除种皮硬实可明显提高金花菜种子的萌发率。     

温度和土壤含水量对青冈栎种子萌发的影响

运用直播法,研究应用人工气候箱控制温度和土壤含水量对野生青冈栎种子萌发和幼苗生长的影响。结果表明:在12h光照条件下,青冈栎种子在变温为10℃/15℃时,萌发率很低,仅为(12±12.29)%;变温为30℃/35℃时,萌发率达最大,为(81±13.7)%。土壤含水量为30%～40%时,萌发率为(79±15.9)%;土壤含水量为90%～100%时,萌发率为(56.67±19.36)%。青冈栎种子萌发呈现出迅速萌发和推迟萌发的特点;温度对青冈栎幼苗的苗高、叶长和叶宽影响显著,对幼苗的地径、叶片数量影响不显著。恒温下,不同梯度土壤含水量处理对幼苗的苗高、地径、叶长、宽影响不显著。     

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.