CULTURE AND HYBRIDIZATION STUDIES ON GIGARTINA PAPILLATA (RHODOPHYTA)1

The foliose red alga Gigartina papillata (C. Ag.) J. Ag. was studied in culture to determine its life history and possible relationship to the life history of Petrocelis middendorffii (Ruprecht) Kjellman. Carpospores cultured from individual female plants gave rise to either crustose Petrocelis-like plants that reproduced by tetraspores, or to another generation of foliose female (cystocarpic) plants that reproduced by carpospores. Apices cultured from blades of individual field-collected female plants produced either papillae with many procarps that developed cystocarps only when crossed with male plants, or papillae with few procarps that produced cystocarps in the absence of male plants. The results are interpreted to demonstrate that two types of life history occur in G. papillata: one, a sexual life history involving a crustose tetrasporophyte; the other, a possibly apomictic life history involving only cystocarpic plants. Hybridization experiments demonstrated, that G. papillata is interfertile with Gigartina-phase gametophytes cultured from tetraspores of P. middendorffii. Sexual plants of G. papillata are postulated to represent the naturally-occurring gametophyte of P. middendorffii in California. The possible relationships of the sexual and apomictic plants of G. papillata are discussed.     

Theory of nucleus breeding schemes with overlapping generations

Summary Explicit methods are derived for estimating steady-state genetic responses and genetic differences between nucleus and base progeny crops in open nucleus breeding schemes which utilize genetic differences between progeny groups with parents of different ages or between age groups. Explicit methods are also given for estimating proportions which should be selected from the different nucleus and base selection groups so as to maximise genetic responses under each of a range of selection methods. Some basic differences between selection programmes utilizing genetic differences between progeny groups with parents of different ages and those utilizing genetic differences between age groups in nucleus breeding schemes are summarized.     

桉树枝瘿姬小蜂连续世代种群生命表

桉树枝瘿姬小蜂在广州地区一年发生4-5代,且世代重叠,其越冬期为11月中旬到翌年3月底,越冬虫态为大龄幼虫和蛹.在广州自然条件下,通过人工接种和自然接种相结合的方法,桉树枝瘿姬小蜂在2010年3月至2011年3月间共完成4个世代.利用生命表的方法分析桉树枝瘿姬小蜂连续世代可知,第1代的净增值率R0最大,而第2代的最小;第3代的内禀增长率rm和周限增长率λ最大,其世代平均历期T最小;第4代的rm和λ最小,其T最大.这说明第3代桉树枝瘿姬小蜂的种群增长能力最大,对桉树的危害最强.该代害虫的发生时间为7-9月,因此在防治上要注意该阶段的防控和监测.     

中国自然保护地空间重叠分析与保护地体系优化整合对策

自然保护地体系的构建是国际社会高度重视的生物多样性保护策略。近年来, 中国已关注到自然保护地空间重叠交叉的问题, 并出台了《关于建立以国家公园为主体的自然保护地体系的指导意见》。为落实这一战略, 需要对现有保护地的彼此关系与空间分布进行系统研究。为此, 本研究收集了8,572个不同类型和级别自然保护地的坐标、生态系统类型、行政区域及边界等信息, 筛选出1,532个具有空间重叠、管理部门交叉的自然保护地, 计算地理集中指数并采用ArcGIS软件进行了核密度分析, 得出空间重叠保护地分布的生态地理区、生态系统类型、交叉管理部门、所在省份等空间分布特点。研究结果显示: (1)鲁中山区、太行山、大别山、天目山-怀玉山、皖江等生态功能区的自然保护地重叠最为严重(核密度Mean > 6, Max > 8), 其中太行山区、大别山区、天目山-怀玉山区为重叠保护地密度高的生物多样性优先保护区, 目前10个国家公园试点区域中仅大熊猫国家公园体制试点区、湖南南山国家公园体制试点区、钱江源国家公园体制试点区三处位于保护地重叠高密度区; (2)原主管部门中, 原国家林业局与住房和城乡建设部的交叉管理保护地数量最多, 为294个; (3)黑龙江、安徽、山东、河南、湖北、湖南等省范围内的自然保护地空间重叠状况明显高于其他省区, 而晋冀豫与皖鄂赣这两处三省交界处重叠程度更高, 其他多处三省交界区域也存在保护地的中度重叠。故上述生态地理区、原主管部门与行政区应作为中国自然保护地体系优先普查区域与优化整合重点对象。基于重叠保护地核密度热点区、生物多样性保护优先区与生态系统文化服务的分析框架, 本研究按照国家公园、自然保护区、自然公园三类, 对不同生态功能区自然保护地优化整合优先性与类型提出了初步建议, 以期为当前中国自然保护地体系改革的紧迫需求提供参考。     

Mating system shifts a species’ range

Understanding the ecological and evolutionary mechanisms that shape a species’ range is an important goal in evolutionary biology. Evidence indicates that mating system is an effective predictor of the global range of native species or naturalized alien plants, but the mechanisms underlying this predictability are not elaborated. Here, we develop a theoretical model to account for the ranges of plants under different mating systems based on migration‐selection processes (an idea proposed by Haldane). The model includes alternation of gametophyte and sporophyte generations in one life cycle and the dispersal of haploid pollen and diploid seeds as vectors for gene flow. We show that the interaction between selfing rates and gametophytic selection determines the role of mating system in shaping a species’ range. Selfing restricts the species’ range under gametophytic selection in nonrandom mating systems, but expands the species’ range under the absence of gametophytic selection in any mating system. Gametophytic selection slightly restricts the species’ range in random mating. Both logarithmic and logistic models of population demography yield similar conclusions in the case of fixed or evolving genetic variance. The theory also helps to explain a broader relationship between mating system and range size following biological invasion or plant naturalization.     

New insights on ChlD1 function in Photosystem II from site-directed mutants of D1/T179 in Thermosynechococcus elongatus

The monomeric chlorophyll, Chl_D1, which is located between the P_D1P_D2 chlorophyll pair and the pheophytin, Pheo_D1, is the longest wavelength chlorophyll in the heart of Photosystem II and is thought to be the primary electron donor. Its central Mg²⁺ is liganded to a water molecule that is H-bonded to D1/T179. Here, two site-directed mutants, D1/T179H and D1/T179V, were made in the thermophilic cyanobacterium, Thermosynechococcus elongatus, and characterized by a range of biophysical techniques. The Mn₄CaO₅ cluster in the water-splitting site is fully active in both mutants. Changes in thermoluminescence indicate that i) radiative recombination occurs via the repopulation of *Chl_D1 itself; ii) non-radiative charge recombination reactions appeared to be faster in the T179H-PSII; and iii) the properties of P_D1P_D2 were unaffected by this mutation, and consequently iv) the immediate precursor state of the radiative excited state is the Chl_D1⁺Pheo_D1^? radical pair. Chlorophyll bleaching due to high intensity illumination correlated with the amount of ¹O₂ generated. Comparison of the bleaching spectra with the electrochromic shifts attributed to Chl_D1 upon Q_A^? formation, indicates that in the T179H-PSII and in the WT*3-PSII, the Chl_D1 itself is the chlorophyll that is first damaged by ¹O₂, whereas in the T179V-PSII a more red chlorophyll is damaged, the identity of which is discussed. Thus, Chl_D1 appears to be one of the primary damage site in recombination-mediated photoinhibition. Finally, changes in the absorption of Chl_D1 very likely contribute to the well-known electrochromic shifts observed at ~430?nm during the S-state cycle.     

Phytochrome regulation of nuclear gene expression in plants

The photoregulation of gene expression in higher plants was extensively studied during the 1980s, in particular the light-responsive cis -acting elements and trans -acting factors of the Lhcb and rbcS genes. However, little has been discovered about: (1) which plant genes are regulated by light, and (2) which photoreceptors control the expression of these genes. In the 1990s, the functional analysis of the various photoreceptors has progressed rapidly using photoreceptor-deficient mutants, including those of the phytochrome gene family. More recently however, advanced techniques for gene expression analysis, such as fluorescent differential display and DNA microarray technology, have become available enabling the global identification of genes that are regulated by particular photoreceptors. In this paper we describe distinct and overlapping effects of individual phytochromes on gene expression in Arabidopsis thaliana.     

How to compute the effective size of spatiotemporally structured populations using separation of time scales

Calculations to derive effective population size become highly complicated when complex population structure is considered. We provide an easy method of computing the effective size of a subdivided population with overlapping generations (a spatiotemporally structured population) using an approximation based on separation of time scales. We also numerically compute the effective size to verify the accuracy of the derived formula. Various interesting quantities, including moments of coalescent time, are readily derived using this approach.