克隆植物矮嵩草对放牧的等级性反应

对高寒草甸克隆植物矮嵩草（Kobresio humilis）基株、分株片断和分株3个层次构件单元的数量、生物量性状及其变异系数在不同放牧强度处理间以及构件等级间的变化进行了研究。研究工作于1999年至2001年在中国科学院海北高寒草甸生态系统定位站矮嵩草草甸内进行。家畜放牧实验设4个放牧强度水平。研究结果显示,3a中矮嵩草克隆等级基株层次只有分株数和叶数在放牧处理间表现出显著差异（F（3.56）〉F0.05,P〈0．05）,而死亡分株百分数、死亡叶片百分数、基株大小以及繁殖分配4个性状在3a中未表现出显著差异（F（3.56）〈F0.05,P〉0．05）,占被测性状的57．1％;与此同时,分株片断和分株两个层次在第1年就有50％以上的性状达到显著差异,到第3年时全部被测性状都表现出显著差异（F（3.56）〉F0.05,P〈0．05）。放牧第3年时,基株、分株片断和分株层次达到显著差异的性状数分别为42％、100％和100％。性状的变异系数在等级间的变化均表现为分株〉分株片断〉基株层次或分株〉分株片断的顺序。被测性状的变异系数在放牧强度间无显著差异,在放牧第1、第2和第3年,变异系数在等级间有显著差异的性状比例分别为42％、71％和85％。这说明克隆植物矮嵩草基株、分株片断和分株各层次被测性状在放牧强度处理问表现出的差异性不同,具有显著差异的性状比例在基株层次少,在分株片断和分株层次高,相同性状在处理间的差异可能先出现在分株和分株片断层次,后出现在基株层次。放牧强度不影响性状的相对变异,但长期持续的放牧扰动使性状在等级间变异性逐渐增大。这些结果说明矮嵩草构件等级对放牧扰动具有明显的等级性反应,并可概括为“分株层次〉分株片断层次〉基株层次”的等级反应模式。研究结果证实我们关于克隆植物等级选择模式的推断。     

植物的表型可塑性、异速生长及其入侵能力

表型可塑性是指同一个基因型对不同环境响应产生不同表型的特性,特定性状的可塑性本身可以遗传,也可以接受选择而发生进化。植物个体的异速生长是指生物体某一特征的相对生长速率不等于第二种特征的相对生长速率的特性,该特性是由物种的遗传性决定的一种固定特征,植物往往朝着最佳的异速生长曲线进化。植物特定基因型在不同环境下,诸如生物量分配和种群几何学上的一些表型差异,既可由异速生长造成,也可由表型可塑性造成。植物本身的异速生长是一种"外观可塑性",而异速生长曲线的改变才是真正的可塑性。植物的表型可塑性、异速生长对于入侵植物的适应具有重要意义。干扰等异质性生境下表型可塑性成为物种生存扩散的有利性状,表型可塑性强的物种更有可能成为广布种。植物本身的异速生长特性或其异速生长曲线的改变都能影响其入侵能力。     

竹类植物对异质生境的适应——表型可塑性

竹类植物是一类以木本为主的克隆植物,凭借表型可塑性的优势,对异质生境具有很强适应能力。然而,目前对竹类植物表型可塑性的实现方式及其异质生境适应对策未见系统总结,从而在一定程度上限制了竹类生态学的发展。从形态可塑性、选择性放置、克隆整合和克隆分工等4个方面对竹类植物的表型可塑性研究进行分析和梳理,结果表明:竹类植物在异质生境中具有明显的表型可塑反应,主要采用形态可塑性、选择性放置和克隆整合来适应异质生境,而克隆分工的普遍性仍有待验证;目前侧重于研究构件形态和生物量分配格局,而很少深入探讨形态、生理和行为等可塑性机理。今后竹类植物表型可塑性研究重点在于:1)克隆整合的格局与机理;2)克隆整合对生态系统的影响;3)克隆分工的形成及其与环境关系;4)表型可塑性的等级性及环境影响;5)不同克隆构型的表型可塑性特征及其内在机制。     

匍匐茎草本金戴戴对盐分梯度的表型可塑性

研究了匍匐茎型克隆草本金戴戴(Halerpestes ruthenica) 4种基株（基因型）对不同盐分处理（0,85.5, 171.0, 256.5和342.0 mM NaCl）的表型可塑性。随着盐分浓度的增加,实验植物与生长相关的性状指标 (如植株干重、总叶面积、分株数和总匍匐茎长度) 显著减小。植株干重、总叶面积和总匍匐茎长度具有显著的基株间差异。实验植物与形态相关的性状指标 (如平均叶柄长和根冠比) 对盐分梯度具有可塑性并具有显著的基株间差异;而其它形态指标 (如平均节间长、比节间长和比叶柄长)     

匍匐茎草本金戴戴对盐分梯度的表型可塑性

 研究了匍匐茎型克隆草本金戴戴(Halerpestes ruthenica) 4种基株（基因型）对不同盐分处理（0,85.5, 171.0, 256.5和342.0 mM NaCl）的表型可塑性。随着盐分浓度的增加,实验植物与生长相关的性状指标 (如植株干重、总叶面积、分株数和总匍匐茎长度) 显著减小。植株干重、总叶面积和总匍匐茎长度具有显著的基株间差异。实验植物与形态相关的性状指标 (如平均叶柄长和根冠比) 对盐分梯度具有可塑性并具有显著的基株间差异;而其它形态指标 (如平均节间长、比节间长和比叶柄长)     

克隆植物矮嵩草在刈割条件下的等级反应研究

对刈割处理下高寒矮嵩草草甸建群种矮嵩草（Kobresia humilis）构件等级中基株、分株和分蘖3个层次构件单元的数量、生物量及其变异系数的变化进行了研究。结果表明．矮嵩草株丛刈割部分和未刈割部分被测性状在处理间的差异显著性以及作构件等级间变异系数的大小均为分蘖层次〉分株层次〉基株层次。刈割后相同时期内,分蘖层次对相同处理的反应发叶生得最快,基株则最为迟缓。这说明在刈割后的相同时期内,构件等级中较外层次（分蘖层次）会发生更大的表型变异．对相同强度的刈割扰动发生反应也最快。由此证实矮嵩草在刈割条件下也同样会发生等级性反应。     

林下和林窗内绢毛匍匐委陵菜的克隆生长和克隆形态

 为了验证绢毛匍匐委陵菜(Potentilla reptans var. sericophylla)林窗和林下种群间的行为差异是完全由表型可塑性引起,还是局部分化的结果,将生长在北京东灵山油松（Pinus tabulaeformis）林林窗和林下的绢毛匍匐委陵菜,进行生境间的交互移植-重植野外生态实验。研究结果表明,实验植物的叶片长度、叶片宽度、叶柄长度和匍匐茎节间长度等克隆形态特征在两生境间无差异。两个来源的植株,其基株生物量、基株分株数和基株匍匐茎总长度等克隆生长特征在林下生境中都比在林窗生境中小,表现出显著的可塑性。所研究的克隆形态特征和克隆生长特征及其可塑性在不同生境来源的实验植物间没有差异。绢毛匍匐委陵菜克隆形态特征和克隆生长特征及其可塑性在林下和林窗生境间没有发生局部分化,林窗为其较适生境,克隆生长特征的可塑性对绢毛匍匐委陵菜利用生境异质性可能具有重要意义     

表型可塑性变异的生态-发育机制及其进化意义

表型可塑性赋予生物个体在不同环境条件下通过产生不同表型来维持其适合度的能力.研究结果显示多数可塑性变异的产生是基于对环境变异信号的响应、改变基因表达式样并调整发育轨迹的结果,表观遗传调控体系在基因选择性表达和可塑性变异的跨世代传递过程中发挥了重要作用.不同物种和种群对环境变化的敏感性、发生可塑性变异的能力以及可塑性反应模式不尽相同,预示着控制可塑性能力并独立于控制性状的可塑性基凶的存在,这些基因是直接响应环境信号并控制表型表达的调控基因.表型可塑性不仅是物种适应性进化的一个重要方面,也是选择进化的产物,物种的表型可塑性变异对其生态适应和进化模式有深远的影响.     

克隆植物的无性与有性繁殖对策

许多植物同时具有克隆生长与有性繁殖,两种繁殖方式间的平衡在不同物种间以及同一物种内不同种群间变化很大。旺盛的克隆生长可能会从多方面影响生活史进化。首先,许多克隆植物的有性繁殖与更新程度都很低,甚至有一些植物由于克隆生长而几乎完全放弃了有性过程,从而影响到克隆植物对局域环境的适应和地理范围进化。其次,克隆生长增大花展示进而增加了对传粉者的吸引,同时也增加了同株异花授粉的风险,而同株异花授粉往往会导致植物雄性和雌性适合度的下降。因此,克隆植物的空间结构与交配方式间可能存在着协同进化关系。最后,克隆生长与有性繁殖间可能存在着权衡关系:对克隆生长的资源投入将会减少对有性繁殖的资源投入。这种权衡关系可能是由环境条件、竞争力度、植物寿命和遗传等因素决定的。如果不同的繁殖方式是植物在不同环境下采取的适应性对策,那么我们可以预期:在波动和竞争力度大的生境中,植物应将大部分的繁殖资源分配给有性繁殖;而在相对稳定的环境中,克隆繁殖应该占据优势地位。但是自然选择对两种繁殖方式的选择结果是什么,以及控制这两种方式间平衡的生态和遗传因子究竟有哪些,到底是克隆生长单向地影响了植物的有性繁殖,还是与有性过程相伴随的选择压力同时塑造了植物的克隆习性?目前尚不清楚。同时从无性与有性繁殖两个方面综合考察克隆植物的繁殖对策是今后亟待加强的工作。     

喜旱莲子草对同基因型邻体根系的表型可塑性: 入侵地和原产地的比较

植物对邻体根系的表型可塑性是指与无邻体对照相比, 即使个体平均可获取土壤资源相同, 在有邻体根系存在时植物也会改变根系生物量分配, 并影响其他功能性状和适合度。表型可塑性进化假说(evolution of plasticity hypothesis)认为外来植物在入侵地进化出了更强的表型可塑性。对该假说的验证多集中于外来植物对光照、水分、养分以及天敌等的可塑性进化, 但对邻体根系的可塑性在入侵植物中是否发生进化尚未见报道。我们采用同质园实验比较了喜旱莲子草(Alternanthera philoxeroides)入侵地(美国)和原产地(阿根廷)各5个基因型的适合度与功能性状对同基因型邻体根系的可塑性。结果表明: 喜旱莲子草的根冠比(P = 0.088)和比叶面积(P = 0.007)对同基因型邻体根系的可塑性在入侵地和原产地基因型间存在差异: 入侵地基因型在有邻体根系时根冠比和比叶面积增加, 而原产地基因型则相反。但是, 总生物量、贮藏根生物量、比茎长和分枝强度对邻体根系的可塑性在入侵地和原产地间没有显著差异。此外, 与分隔邻体根系相比, 同基因型邻体根系存在时总生物量(+9.9%)和贮藏根生物量(+13.9%)显著增加, 比茎长(-9.5%)显著降低。最后, 与原产地基因型相比, 总体上入侵地基因型的总生物量(+62.0%)和贮藏根生物量(+58.9%)增加, 比茎长(-28.5%)和分枝强度(-42.8%)降低。这些结果表明喜旱莲子草入侵地基因型与资源利用相关功能性状(如根冠比和比叶面积)对邻体根系的可塑性方向与原产地基因型相反; 但适合度和株型相关性状(如比茎长和分枝强度)对同基因型邻体根系的可塑性与原产地没有差异。     

Fitness and evolution in clonal plants: the impact of clonal growth

Seeds have often been emphasized in estimates of plant fitness because they are the units that carry genes to the next generation, disperse, and found new populations. We contend that clonal growth also needs to be considered when estimating fitness in clonal plants, regardless of whether fitness is measured from a genet or ramet perspective. Clonal growth affects genet fitness through both genet persistence and seed production. It affects ramet fitness through new ramet production, because both seeds and clonal propagants are considered offspring. The differential production of clonal propagants will contribute to fitness differences among individuals which may result in population-level changes in allele frequencies (i.e. microevolution). We describe a form of selection unique to clonal organisms, genotypic selection, that can result in evolution. Genotypic selection occurs when genotypically based traits are associated with differences in the rate of ramet production. It can lead to evolutionary change in quantitative trait means both directly and indirectly. It leads directly to change in the ramet population by increasing the proportion of ramets with more advantageous trait values. From the genet perspective, it leads indirectly to evolution within and among populations whenever significant portions of the genetic effect on a trait are inherited through seed. We argue that under most conditions, clonal growth will play a major role in the microevolution of clonal plants.     

Dynamics of distribution and performance of ramets constructing genets: a demographic�Cgenetic study in a clonal plant, Convallaria keiskei

Background and Aims

In clonal plants producing vegetative offspring, performance at the genet level as well as at the ramet level should be investigated in order to understand the entire picture of the population dynamics and the life history characteristics. In this study, demography, including reproduction and survival, the growth patterns and the spatial distributions of ramets within genets of the clonal herb Convallaria keiskei were explored.

Methods

Vegetative growth, flowering and survival of shoots whose genets were identified using microsatellite markers were monitored in four study plots for 3 years (2003–2005). The size structures of ramets in genets and their temporal shifts were then analysed. Their spatial distributions were also examined.

Key Results

During the census, 274 and 149 ramets were mapped in two 1 × 2 m plots, and 83 and 94 ramets in two 2 × 2 m quadrats. Thirty-eight genotypes were identified from 580 samples. Each plot included 5–18 genets, and most ramets belonged to the predominant genet(s) in each plot. Shoots foliated yearly for several years, but flowering ramets did not have an inflorescence the next year. A considerable number of new clonal offspring persistently appeared, forming a bell-shaped curve of the size structure of ramets in each genet. Comparing the structures modelled by the normal distributions suggested variation among ramets belonging to a single genet and variation among genets. Furthermore, spatial analyses revealed clumped and distant distributions of ramet pairs in a genet, in which the distant patterns corresponded to the linearly elongating clonal growth pattern of this species.

Conclusion

Characteristics of ramet performances such as flowering and recruitment of clonal offspring, in addition to growth, played a large part in the regulation of genet dynamics and distribution, which were different among the studied genets. These might be characteristics particularly relevant to clonal life histories.Key words: Clonal plant, Convallaria keiskei, demography, genet, genetic identification, growth pattern, life history, ramet, spatial distribution     

Clonal Diversity in Differently-Aged Populations of the Pseudo-Annual Clonal Plant Circaea lutetiana L.

Abstract: In many clonal plant species seedling recruitment is restricted to short colonization episodes early in the development of the population, and clonal diversity (i.e., genet diversity) in the population is expected to decrease with increasing population age. In established populations of the pseudo-annual Circaea lutetiana seedling recruitment has previously not been observed. Therefore, we expected established populations to have low clonal diversities. We analysed number and frequency of genets and spatial distribution of genets in six differently-aged C. lutetiana populations with the use of four informative RAPD primers. We found relatively low clonal diversities in young populations but very high clonal diversities in established populations. Therefore, the hypothesis was rejected that seedling recruitment does not occur in established populations. Moreover, we did not find large genet size asymmetries in established populations. Genet size differences can be caused by stochastic processes or by fitness related traits, such as differences in vegetative reproduction. Because vegetative propagation of ramets is dependent on ramet size, and the number of ramets and the size of each ramet determine genet size, we expected that large genets produced, on average, large ramets. However, this was not the case, suggesting that stochastic processes caused genet size differences. Genet size may also be bounded if spatial distribution of genets is affected by micro-habitat differences. For this we expected to find a clumped spatial distribution of ramets of the same genet. However, ramets of large genets were always found intermingled with ramets belonging to other genets.     

Species-specific sprouting pattern in two dioecious Lindera shrubs: The role of physiological integration

Sprouting is recognized as an important genet persistence strategy for clonal woody plants, but the role of sprouting may differ between species and between sexes, depending on physiological integration. We tested the effect of physiological integration on the mortality, recruitment and growth of the sprouting male and female ramets of two closely related dioecious shrubs of Lindera, in a field experiment using girdling manipulation. Although between-sex differences observed were obscure, we found between-species differences in the sprouting patterns. The rates of ramet mortality and recruitment were significantly lower for L. praecox than L. triloba. In L. praecox genets, the ramet production was low, and the main ramets might actively translocate assimilates towards the small sprouted ramets, which then facilitates high ramet growth and survival (sprout-nursing strategy). Meanwhile, in L. triloba genets, although many ramets were recruited, assimilate translocation from the main ramets to the sprouted ramets might be less abundant, which causes high ramet mortality (sprout-turnover strategy). For a more general knowledge of the various sprouting strategies in clonal plants, our study demonstrated that inter-specific comparisons using girdling experiments at the whole-plant level could reveal the role of physiological integration on the link between the sprouting pattern and above-ground structures of clonal plants.     

Sexual reproduction and clonal growth in Reinhardtia gracilis (Palmae), an understory tropical palm

Patterns of sexual reproduction and clonal growth were investigated in the understory palm Reinhardtia gracilis var. gracilior over a 3-yr period. R. gracilis is a very abundant clonal palm in the tropical rain forest of Los Tuxtlas, Veracruz, México. Because ramets form clumps, genets are easily identified in the field. Genets were monitored in a 0.5-ha area, and classified by size according to the number of ramets they possessed. In contrast to clonal growth, sexual reproduction was highly dependent on genet size. The probability of reproduction, the number of inflorescences, and the number of fruits produced were positively correlated with genet size. However, neither the probability of producing a ramet, nor the number of ramets produced per genet were correlated with genet size. Over the 3 yr of study, 55% of the genet population had at least one ramet with reproductive structures, while <1% (a single genet in one year) had six ramets with flowers. Thirty-two percent of the mature genets reproduced during each of three consecutive years. In contrast, 58% of the genets produced no new ramets during these 3 yr. No evidence was found of a trade-off between clonal growth and sexual reproduction. Ramet production increases genet size and this in turn increases genet reproductive performance. Clonal growth in this species may be viewed as a growth strategy that tends to maximize genet fitness.     

Demography of the clonal palm Geonoma brevispatha in a Neotropical swamp forest

Abstract We expected that in clonal plants with the phalanx growth form, prereproductive ramets function as a meristem bank that helps buffer ramet demography against environmental fluctuations. Specifically, we evaluated four expectations for the forest understorey clonal palm Geonoma brevispatha in a swamp forest in south‐eastern Brazil. Our expectations were are follows: (i) the vital rates of prereproductive ramets are more responsive to genet‐related characteristics (genet size, distance and size of the nearest genet neighbour, and reproductive ramet survivorship) than to environmental variables (canopy openness, basal area of small trees, flooding, and distance and size of the nearest large tree neighbour), whose effects are expected to affect ramet dynamics indirectly through physiological integration; (ii) the progress of prereproductive ramets to later stages is dependent on the death of reproductive ramets; (iii) the population dynamics of G. brevispatha is resistant to significant interannual changes in the vital rates of ramets, (i.e. the occurrence of good and bad years); and (iv) there are large negative covariances among demographic transitions within a given year, as well as between years, reflecting the flexibility of G. brevispatha to adjust to environmental variability. Expectations 1, 2 and 4 were confirmed, while expectation 3 was only partially confirmed. Matrix models predicted that the growth rate of the overall ramet population was significantly greater than unity in the first study year, but it was significantly smaller than 1.0 in the second study year. Ramet population growth rates at the level of individual genets were greater than unity in the majority of genets in the first year, but in the second year genets with growth rates smaller than unity prevailed. Ramet population dynamics seems to be resistant to the succession of good and bad years; in effect, the presence of a meristem bank of ramets helps stabilize λ.     

The oldest known clones of Salix herbacea growing in the Northern Apennines,Italy are at least 2000 years old

Premise

Dominant in many ecosystems around the world, clonal plants can reach considerable ages and sizes. Due to their modular growth patterns, individual clonal plants (genets) can consist of many subunits (ramets). Since single ramets do not reflect the actual age of genets, the ratio between genet size (radius) and longitudinal annual growth rate (LAGR) of living ramets is often used to approximate the age of clonal plants. However, information on how the LAGR changes along ramets and how LAGR variability may affect age estimates of genets is still limited.

Methods

We assessed the variability of LAGR based on wood-section position along the ramets and on the duration of the growing season on three genetically distinct genets of Salix herbacea growing in the Northern Apennines (Italy). We compared genet ages estimated by dividing genet radius by the LAGRs of its ramets.

Results

LAGR increased significantly from the stem apex to the root collar; indicating that ramet growth rate decreased with time. Furthermore, a difference of ca. 2 weeks in the onset of the growing period did not impact LAGR. Considering the high LAGR variability, we estimated that the three genets started to grow between ~2100 and ~7000 years ago, which makes them the oldest known clones of S. herbacea even considering the most conservative age estimate.

Conclusions

Our findings indicate that analyzing ramets at the root collar provides an integrative measurement of their overall LAGR, which is crucial for estimating the age of genets.     

Simulations of clonal species genotypic diversity – trembling aspen (Populus tremuloïdes) as a case study

We built two models to follow clonal species genotypic diversity (G/N) over long periods of time at the stand and landscape levels. The models were then validated with empirical data from trembling aspen (Populus tremuloides) populations in Quebec’s boreal forest. Data was collected using a chronosequence approach in seven sites that burned in 1717, 1760, 1797, 1823, 1847, 1944, and 1916. Genetic identification was done by using four microsatellite loci. At the stand scale, simulations were repeated for a genet size of 5, 25, 50 and 100 ramets each. At the landscape level, we simulated the cumulative genet survival rate under different fire cycles (5–500 years) for 500 years after fire. Stand simulations indicated that ramet mortality within genets rather than genet mortality accounts for the increase in G/N with time since fire. Both the initial genet size and the recurrent suckering of some genets (or ramet recruitment) play an important role in maintaining high G/N levels for long periods of time. In general, the larger the number of ramets per genet, the longer the genet survives under a gap disturbance regime and a minimum of 100 ramets per genet is required to maintain aspen genet survival for 500 years. At the landscape level, genet loss increases as the fire cycle gets longer. In Quebec’s boreal forest, short rotation even-aged management practices seem to maintain a genet survival rate similar to that produced by the natural succession regime.