利用腊叶标本初探豹子花属植物的性表达及其与个体大小的关系

植物性系统进化过程中很少有植物通过雌性败育的方式实现性系统由联合走向分离,然而雄花在百合科植物中大量存在,引起了研究者的关注。本研究利用百合科豹子花属植物的腊叶标本,获取它们的花性别表型、花大小、株高以及分布海拔等信息探讨豹子花属植物的性表达样式,并对样本量较多的开瓣豹子花、云南豹子花、多斑豹子花和豹子花四个种的性表达及其与个体大小的关系进行分析。研究结果表明:1)六种豹子花属植物标本中都有雄花存在;根据雄性花和两性花的不同组合,形成雄性个体、两性花个体,和雄花两性花同株个体三种植株类型;2)个体大小(株高)和分布海拔之间不存在相关关系,和植株性别类型相关,即雄性个体一般显著小于具有雌性功能的两性花个体和雄花两性花同株个体;3)个体大小与花大小、每个个体开花总数和雌花数量成显著的正相关关系,而与每个个体的雄花数量无显著的相关关系。本研究更正了一直以来对豹子花属植物性系统的错误认识,首次报道雄花在豹子花属植物中普遍存在,并指出雄花和雄性个体的出现是大小依赖性分配的结果。同时,以研究实例证明了利用腊叶标本开展植物性系统多样性的可行性。     

湿地植物大花百合种群的性系统特征

开花植物性系统特征是植物在长期适应进化过程中逐渐形成的繁殖策略, 它在一定程度上影响了物种的种群结构及其在生境中的分布格局, 因此性系统特征一直是植物进化与生态学领域的研究热点。本研究于2012年和2020年在吉林省金川泥炭沼泽湿地, 通过样地调查取样的方法, 研究了湿地植物大花百合(Lilium concolor var. megalanthum)的性系统特征以及不同性别表型植株的比例、密度及空间分布格局, 并探究了大花百合植株个体大小和其性别表达的联系, 比较了不同性别表型的花粉实际可育性和来源不同的花粉授粉处理结实后的种子活力。结果显示, 个体水平上, 大花百合具有雄花植株、两性花植株和雄花两性花同株(即雄全同株) 3种性表型; 种群水平上, 具有雄花的个体充当父本, 通过花粉向下一代传递基因, 而具有两性花的个体主要充当母本, 通过胚珠实现基因的传递。2020年大花百合雄花植株占种群内开花植株的39.14%, 相比2012年雄花植株比例增加了22.80%; 大花百合种群分布密度为0.06株/m², 较2012年下降了0.09株/m²。从2012年到2020年, 总体表现为种群密度降低, 雄花植株相对比例增加的趋势。两性花植株和雄花植株在小尺度范围主要呈聚集分布, 随着尺度增大, 趋于随机分布。雄花植株显著小于两性花植株, 但鳞茎资源分配显著高于两性花植株。大花百合植株的性表达遵循大小依赖的性分配假说: 个体较小的植株表达为雄花植株, 而个体较大的植株则为两性花植株或雄全同株。在不同授粉处理下的结籽率和种子萌发结果表明, 大花百合自花授粉结籽率和坐果率显著低于异花授粉, 雄花植株和两性花植株花粉可育性以及对两性花植株授粉后所获得种子活力无显著差异。大花百合雄花植株的出现可能是对有限环境资源条件适应的结果, 反映了湿地条件下该植物在生长和繁殖资源之间的权衡策略, 在长期的湿地演变过程中, 这种性系统特征的出现具有一定的适应性意义。     

Polyploidization and sexual dimorphism of floral traits in a subdioecious population of Dasiphora glabra

银露梅亚雌雄异株种群的多倍化和花特征性二态 性二态是性别分离植物的常见性状,对植物的雌性和雄性功能可能产生不同的影响。本文以青藏高原特有植物银露梅(Dasiphora glabra)为研究对象,利用银露梅同时存在两性、雌性和雄性植株的种群,探讨银露梅与传粉相关的花特征性二态现象及其对传粉者访问、花粉流和结实的影响。另外,本文还利用流式细胞仪检查了两性植株、雄性植株和雌性植株之间基因组大小的差异。研究结果表明：银露梅雌性植株和雄性植株数量约占种群中植株总数量的40%,表明银露梅两性植株数量多于雄性和雌性的植株数量。两性植株的花数量显著多于雄性和雌性植株的花数量。雄花的花大小显著大于雌花和两性花的花大小。雄花的花粉数量与两性花的花粉数量没有差异,但是雌花的胚珠数量显著高于两性花的胚珠数量。双翅目的蝇类是银露梅最主要的访花者,尽管访花者偏好访问更大的花,但是在花间连续访问对大花没有表现出偏好。模拟花粉流实验表明,两性植株和雄性植株的有效花粉转移都很低,从而导致较低的结实率。雌性植株和雄性植株的DNA含量约为两性植株的4倍,并且单性植株和两性植株之间相互授粉不能结实。以上结果表明,与两性花相比,雌花和雄花在与传粉相关的花特征二态性上分别在雌性和雄性功能上表现出优势,但这种优势在很大程度上被低效的花粉转移所掩盖。银露梅的雌性植株和雄性植株经历了多倍化事件,导致与两性植株之间存在繁殖隔离,从而维持了3种性别植株的共存。     

新疆郁金香一居群个体性别7年的动态变化

在雌雄同株植物中, 花性别被认为是两性资源分配对环境条件的响应, 了解个体性别随时间的变化对探讨植物性系统的变异有重要意义。早春短命植物新疆郁金香(Tulipa sinkiangensis)多为两性花居群, 前期调查显示一些居群由雄花和两性花构成。为了探讨新疆郁金香雄花的发生与变化, 我们连续7年对一个居群的花性别及其变化动态进行了跟踪。结果显示: (1)该居群主要是由一朵花植株和两朵花植株构成, 分别占居群植株总数的74.5%和23.0%。两种性别的花随机分布在不同类型的单株上, 形成了以两性花植株为主, 含有雄株、雄花与两性花同株(andromonoecy)的居群结构。(2)雄花相对较小, 子房退化, 无胚珠发育, 在植株或居群中花期较晚出现。与相同大小的两性花相比, 雄花在单花花粉量、花粉败育率、花粉粒大小及形态、雄性功能等方面没有差异。(3) 7年间, 雄花在居群中的比例经历了2011-2014年间的显著下降(23.4-3.1%)和2015-2017年间相对稳定的零星分布(1.5-1.0%)两个阶段。居群中一朵花植株数量和两朵花植株数量在年份间呈波动性变化。(4)雄花的出现可能是植株受自身资源状况及环境条件等因素的影响在花性别选择上作出的可塑性反应。     

雄全同株植物簇花芹花期性别分配与开花式样

簇花芹(Soranthus meyeri)是古尔班通古特沙漠中常见的、具雄全同株性系统的伞形科多年生早春短命植物。该文对簇花芹花期性比(两性花数/总花数)与植株大小的关系及其开花式样进行了研究, 重点对花期大小依赖的性别资源分配进行了讨论。结果表明: 2006-2008年簇花芹群体水平的性比分别为0.69 ± 0.03、0.62 ± 0.03和0.69 ± 0.02, 彼此间无显著差异( p > 0.05), 表明其性比是相对稳定的, 可能受遗传因素的控制。雄花生物量与花粉量均比两性花的小, 说明产生雄花比产生两性花所需资源少。一级复伞形花序比二级复伞形花序具有较多的两性花, 说明前者易从植株上获得资源用于增加雌性适合度; 而后者产生较多的雄花以避免在雌性功能上资源投入的浪费, 增大花展示以吸引更多传粉者来增加花粉输出总量, 提高其整体适合度。植株水平的性比与地上营养器官的生物量间呈正相关关系, 说明较大个体对雌性功能的投资较大, 雌性繁殖成功受资源限制。复伞形花序内各伞形花序几乎同时向心开放, 且所有两性花及花序均为雄性先熟, 雌雄阶段完全分离, 但一级复伞形花序比二级复伞形花序早开放约5天, 彼此开花重叠期约为1天。这些特征对于一级复伞形花序进行异株异花授粉以及植株内不同级别花序间的同株异花传粉、避免雌雄功能间的干扰具有重要意义。     

细枝柃性别表达特性及资源分配

已有的资料将柃木属(Eurya)描述为严格的雌雄异株植物, 性别变异现象极为少见。目前仅在柃木(E. japonica)和钝叶柃(E. obtusifolia)等少数种类中报道过两性花的存在。近几年笔者发现细枝柃(E. loquaiana)存在性别变异现象, 性别变异株上具有不同性别类型的花。该文从单花和植株水平分析了细枝柃的性别表达特性, 并对不同类型花的花部构件生物量分配进行比较分析。结果表明, 细枝柃具有6种类型的花, 从单花水平上看, 细枝柃性别有雌性、雄性及两性3种类型; 细枝柃性别在植株水平上体现较为复杂, 有雌株, 雄株, 雌花和两性花同株, 雄花和两性花同株, 雌雄异花同株及雌花、雄花、两性花同株6种类型; 在细枝柃花部构件生物量分配中, 雄花(包括雄株花和变异株雄花)花部构件生物量分配中雄蕊生物量的分配低于雌花(包括雌株花和变异株雌花)中雌蕊生物量的分配; 两性花中, 雄蕊生物量分配低于雌蕊, 这是其优化资源分配的手段, 进而获取最大适合度收益。     

雌全同株植物三脉紫菀花期偏雄的个体大小依赖的性别分配

经典的虫媒传粉植物个体大小依赖的性别分配模型通常预期:分配给雌性功能的资源比例将随着个体大小的增大而增加;但一些研究表明,花期个体大小依赖的性别分配模式表现出随个体大小增大而偏雄的趋势.我们以植株高度衡量个体大小,从花和花序两个水平上研究了雌花、两性花同株植物三脉紫菀(Aster ageratoides)花期个体大小依赖的性别分配策略.随着植株高度的增大,植株产生的头状花序数量增加,表明三脉紫菀投入到繁殖的资源不是固定不变的,而是随个体大小增大而增加的.在花和花序水平上,繁殖资源在雌雄性别功能之间的分配均表现为随个体大小的增大而更偏雄的模式,即花粉/胚珠比增加,产生花粉的两性花占两性花和雌花总花数的比例升高.这些结果与花期个体越大、性别分配越偏雄的预期一致.花期更偏雄的性别分配可能有助于植物在花期通过输出花粉提高雄性适合度,从而实现个体适合度的最大化.     

高寒退化草地不同海拔狼毒种群花大小与叶大小、叶数量的关系

植物花大小与叶大小、叶数量的关系反映了植物长期与环境相互作用形成的外在形态方面的适应对策,不同生境中其生长关系的变异体现了植物对异质环境的适应方式。本文研究了祁连山北坡高寒退化草地4个不同海拔狼毒(Stellera chamaejasme)种群花大小与叶大小、叶数量的关系。结果表明:随着海拔的升高,草地群落的高度、密度和地上生物量均呈先升高后降低的倒U型分布;狼毒的地上生物量、株高和叶大小均呈减小趋势,而繁殖分配、花大小和叶数量均呈增大的变化趋势;在海拔梯度上,狼毒花大小与叶数量呈极显著正相关(P0.01),与叶大小呈不显著负相关(P0.05),说明狼毒种群花大小与叶数量具有显著的依赖关系;生境对狼毒花大小与叶数量之间的依赖关系产生显著影响,高海拔的环境胁迫导致狼毒个体减小,植株通过增加花大小和叶数量、减小叶大小的资源分配策略来保证物种的繁衍。     

茂兰喀斯特森林木本植物性系统数量特征及其与环境因子的关系

植物性系统在群落更新、适应性和未来发展中起着重要作用。为了明确喀斯特森林性系统数量特征及其与环境因子的关系, 本研究采用相邻格子法从茂兰白鹇山山脚到山顶连续设置11个垂直样地, 同时采用该方法从山体中部沿同一等高线连续设置21个水平样地, 分析了研究区样地内胸径大于1 cm的木本植物性系统数量特征, 采用独立样本t检验分析了垂直样地与水平样地植物数量与性系统的差异, 采用冗余分析(RDA)探究了性系统数量特征与环境因子的相关性。结果表明: (1)样地内共有木本植物286种14,622株, 其中两性花植物156种(54.5%) 8,235株; 雌雄同株异花植物57种(20.0%) 3,838株; 雌雄异株植物73种(25.5%) 2,549株。垂直方向上, 随着海拔升高雌雄同株异花植物的植株数量显著增加, 两性花植物的物种比例显著下降; 坡位上表现为中坡位植物性系统多样性较低; 水平方向上, 两性花、雌雄同株异花与雌雄异株植物的植株数量、物种比例、性系统多样性指数都无明显规律。(2)雌雄同株异花植物的植株数量和物种比例在垂直样地与水平样地间有显著差异(P < 0.05); 雌雄异株与两性花植物的植株数量与物种比例无显著差异。(3)环境因子对木本植物的性系统数量特征有一定影响, 其中海拔的影响达到极显著水平(P < 0.01), 坡位的影响达到显著水平(P < 0.05)。总体上, 茂兰喀斯特森林木本植物性系统表现出与其他地区不同的丰富性、多样性和复杂性, 但大部分物种种群较小, 其数量分布特征可能是对喀斯特生境异质性适应的结果。     

不同海拔藜芦种群繁殖特征的初步研究

 在北京东灵山地区,沿一定海拔梯度,对藜芦（Veratrum nigrum）这一雄花两性花同株的多年生草本植物的繁殖特征进行了初步研究。结果表明：藜芦开花植株的生物量显著大于未开花植株的生物量。藜芦开花植株大小存在最小临界值,总种群的最小临界值为2.61 g,不同种群的繁殖临界值存在一定的差异。根据花粉/胚珠比（Pollen / ovule ratio,P/O比）推测,藜芦应属于以异交为主的混合交配系统。雄花的大小与生物量都比两性花小,而且其开放时间也晚于两性花,但二者的花粉生产量却没有显著差异。这种现象与人们针对雄花两性花同株植物的雄花功能所提出的最优资源分配假说（Optimal resource allocation hypothesis）是一致的。     

Maternal investment in reproduction and its consequences in leatherback turtles

Maternal investment in reproduction by oviparous non-avian reptiles is usually limited to pre-ovipositional allocations to the number and size of eggs and clutches, thus making these species good subjects for testing hypotheses of reproductive optimality models. Because leatherback turtles (Dermochelys coriacea) stand out among oviparous amniotes by having the highest clutch frequency and producing the largest mass of eggs per reproductive season, we quantified maternal investment of 146 female leatherbacks over four nesting seasons (2001–2004) and found high inter- and intra-female variation in several reproductive characteristics. Estimated clutch frequency [coefficient of variation (CV) = 31%] and clutch size (CV = 26%) varied more among females than did egg mass (CV = 9%) and hatchling mass (CV = 7%). Moreover, clutch size had an approximately threefold higher effect on clutch mass than did egg mass. These results generally support predictions of reproductive optimality models in which species that lay several, large clutches per reproductive season should exhibit low variation in egg size and instead maximize egg number (clutch frequency and/or size). The number of hatchlings emerging per nest was positively correlated with clutch size, but fraction of eggs in a clutch yielding hatchlings (emergence success) was not correlated with clutch size and varied highly among females. In addition, seasonal fecundity and seasonal hatchling production increased with the frequency and the size of clutches (in order of effect size). Our results demonstrate that female leatherbacks exhibit high phenotypic variation in reproductive traits, possibly in response to environmental variability and/or resulting from genotypic variability within the population. Furthermore, high seasonal and lifetime fecundity of leatherbacks probably reflect compensation for high and unpredictable mortality during early life history stages in this species.     

Body size and fecundity in the waterstrider Aquarius remigis: a test of Darwin's fecundity advantage hypothesis

The general female bias in body size of animals is usually attributed to fecundity selection. While many studies have demonstrated a positive relationship between body size and fecundity, the most common interpretation of fecundity selection is that larger females have larger abdomens and can hold more eggs, yet the relationship between abdomen size and fecundity has rarely been examined. For the waterstrider, Aquarius remigis, we find a significant relationship between body size and fecundity and demonstrate that the target of fecundity selection is abdomen size. Thus, larger females have higher fecundities because they have larger abdomens and not because of their total size per se. The rate at which fecundity increases with increasing abdomen size exceeds that which would be expected due to a simple volume constraint and suggests that other factors, such as increased ability to obtain resources, may contribute to the increase in fecundity with body size. Selection intensities estimated from our data indicate that fecundity selection could be a significant selective force on both total and abdomen lengths. Previous studies have found that abdomen size increased faster than body size and thus, larger females had relatively larger abdomens. The relationship of abdomen length and thorax length in A. remigis is hypoallometric and indicates that larger females have relatively smaller abdomens. We hypothesize that this may reflect conservation of abdomen size in females developing under poor conditions. Finally, while egg size is not directly related to body size, we find a trade-off between egg size and number when female abdomen length is held constant, suggesting that selection on egg size may influence abdomen length only indirectly through its effects on fecundity.     

Leaf size and inflorescence size may be allometrically related traits

Summary Corner's rules for plant form relate the degree of branching to branch diameter, and branch diameter to leaf or inflorescence size. We report the first interspecific test of these rules for inflorescence size and branch diameter. We derived a simple corollary of Corner's rules; since leaf size and inflorescence size are both correlated to branch thickness, they may be correlated to each other. This corollary holds for Leucadendron and Protea (Proteaceae), and in certain other taxa in the Asteraceae, Bruniaceae and Pinaceae which also have leaves and reproductive structures on the same shoot. For such taxa this implies that selection for aspects of floral display (inflorescence size, pollination type) may also be expressed at the level of leaf size and vice versa. This has implications for many aspects of botany and also points to the importance of the co-ordinating role of plant architecture for aspects of plant form.     

The “Good Enough” Body Size as Judged by People of Varying Age and Weight

Objective: To examine the concept of the “good enough” body size acceptability across a wide range of ages and weight status. Research Methods and Procedures: Subjects were 303 children, 427 adolescents, 261 young adults, and 326 middle‐age adults who selected acceptable body sizes from an array of drawings representing their own age and gender. They also selected body sizes representing their own actual and ideal size. Results: A large majority (87%) of subjects considered their own body size socially acceptable. This finding applied to both genders in all age groups and to underweight, normal weight, and overweight subjects. Even among obese subjects, 48% considered their own body size socially acceptable. For the large percentage of subjects who reported a discrepancy between their actual and ideal body sizes, most considered their own body size acceptable. This finding also applied to both genders in all age groups and to underweight, normal weight, and overweight subjects. Discussion: Most male and female subjects across a wide range of ages and status considered their own body size to be within the range of socially acceptable body sizes even though, for many, it did not match their ideal. The implications of expanding body size research to include the conceptual framework of body size acceptability is discussed in terms of contributing to a paradigm of positive psychology.     

Grid map analysis and its application for detecting vegetation changes in Japan

Abstract. Grid maps are used as a basic vegetation data base in Japan; they are simplified from vector-based vegetation maps. We estimated the frequency error or lack of information corresponding to reduced resolution and examined the reliable limits of this data base. We produced 10 grid maps on five different scales from 50 m to 1000 m using two different methods using both the whole cell (W-method) and only the central circle (C-method) from a vegetation map at scale 1: 25 000. We found that patches larger than the area of a cell on a vector-based map could be kept almost certainly on any map, but many patches of less than the cell size were lost. The number of missing patches with the C-method is fewer at every scale than those with the W-method. Though the value of Morisita's Cλ (p) index showed that the similarity with the original map was high - from the 50-m to the 200-m resolution - it was increasingly lower on the 400-m and 1000-m grid maps. The values of the Shannon index on the original map, 50-m and 100-m grid maps were not different, but they decreased from the 200-m to 1000-m grid maps. Because the vegetation data base of the Japanese Environment Agency used a 1000-m C-method grid map, we found that much information on patches less than 100 ha had disappeared. Information about dominant vegetation or large patches is almost accurate in this data base.     

Body size and sexual size dimorphism in calanoid copepods

Patterns of sexual size dimorphism and body size in calanoid copepods are examined. We hypothesize that favorable conditions for development will result in large body size and high sexual size dimorphism among populations of a given species and that differences in this allometric relationship among species is governed by the male's role in insemination. We confirm that there is a greater advantage to large female size, normally the larger sex, when compared to males, hence leading to selection for developmental patterns favoring high size dimorphism. Individuals from populations of four centropagid copepod species were measured; other sizes were obtained from published sources. In the four species we examined, the relationships between prosome length and both clutch size and the ability to produce multiple clutches with one insemination were determined. Results show a trend toward hyperallometry in all centropagid species examined: sexual size dimorphism increases with increasing size. Large females produce larger clutches and more additional clutches on one insemination. That hyperallometry is not observed in diaptomid copepods may result from the greater role the male plays in reproduction. Males are needed for each clutch produced, hence the selective pressure to be larger is greater than that in the centropagidae.     

Effect of female size on fecundity and egg size in white-spotted charr: comparison between sea-run and resident forms

The relationships between fecundity, egg size and female size of sea-run form were compared with resident form, using white-spotted charr, Salvelinus leucomaenis. Both fecundity and egg size increase with female size. However, the relationship between egg size and female size differed significantly between the resident and sea-run forms. Egg sizes of sea-run and resident were similar even though sea-run fish were much larger. ? 1998 The Fisheries Society of the British Isles     

Correlation of tooth size and body size in living hominoid primates, with a note on relative brain size in Aegyptopithecus and Proconsul.

Second molar length and body weight are used to test the correlation between tooth size and body size in living Hominoidea. These variates are highly correlated (r= 0.942, p less than 0.001), indicating that tooth size can be used in dentally unspecialized fossil hominoids as one method of predicting the average body weight of species. Based on tooth size, the average body weight of Aegyptopithecus zeuxis is estimated to have been beteen 4.5 and 7.5 kg, which is corroborated by known cranial and postcranial elements. Using Radinsky's estimates of brain size, the encephalization quotient (EQ) for Aegyptopithecus was between 0.65 and 1.04. A similar analysis for Proconsul africanus yields a body weight between 16 and 34 kg, and an EQ between 1.19 and 1.96.     

The cellular basis of wing size modification in Drosophila: The effects of the miniature gene,crowding, and temperature

To elucidate the mechanisms whereby genes and environment influence wing size, we investigated the effects of various rearing temperatures and larval crowding conditions on the wings of the mutant miniature and wild-type fruit flies. In adults we monitored wing size, cell number, wing thickness, cell density; in larval imaginal discs we looked for cell death. Cell density was inversely proportional to wing size. Of particular interest was the finding that smaller wings tend to be thicker. Electron microscope studies showed that the miniature wing layers are grossly abnormal. We hypothesize that these abnormalities are due to abnormal cell flattening of the wing epithelial cells, and we conclude that gene and environmental effects on cell flattening may be an important component in determining cell density and hence organ size.     

A comparative study of the relationship between host size and brood size in Apanteles spp. (Hymenoptera: Braconidae)

ABSTRACT. 1. Current models of insect oviposition predict that clutch size in parasitoids should correlate with host size, with a continuum from solitary species at one end to large gregarious broods at the other. This prediction is tested for the genus Apanteles (sensu lato).
2. The distribution of brood sizes in Apanteles is bimodal, with peaks at one (solitary species) and at about twenty (gregarious species).
3. Brood size of gregarious species correlates with host size, but when a measure of the total volume of a parasitoid brood is plotted against host size, solitary species do not lie on the same regression slope as gregarious species.
4. There is a relative shortage of gregarious species on small hosts, and a relative excess of solitary species on large hosts. Solitary species on large hosts do not fully consume the host resource.
5. The possible role of evolutionary constraints to adaptive progeny allocation in Apanteles is discussed.