不同频次刈割对羊草草原主要植物种群能量现存量的影响

对内蒙古羊草草原主要植物种群能量现存量对刈割频次响应的研究表明,在17年不同频次刈割干扰影响下,植物种群能量现存量随刈割频次的变化表现出不同的变化趋势,据此可以划分出3个不同的刈割响应类群：受抑种、耐刈种和受益种。受抑种包括羊草、羽茅、黄囊苔草、葱属植物和直根型杂类草; 耐刈种包括大针茅和冰草; 受益种包括洽草和糙隐子草。对于种群相对能量现存量而言,除羊草随刈割频次的增加呈显著下降趋势外,其他受抑种均随刈割频次的增加保持相对稳定,而受益种和耐刈种的相对值则随刈割频次的增加而呈增加趋势。同时,刈割对植物能量现存量的影响还表现在植物热值变化上,但变化幅度小于10%。     

刈割干扰下内蒙古草原两种丛生禾草繁殖策略的适应性调节

刈割是内蒙古草原的主要利用方式之一。当植物面对刈割干扰时, 可以通过繁殖策略的调节适应变化的环境。研究刈割干扰下植物繁殖策略的调节对于揭示植物的适应与进化机制具有重要意义。为此, 选择内蒙古典型草原的大针茅(Stipa grandis)和糙隐子草(Cleistogenes squarrosa), 在1979年围封的羊草(Leymus chinensis)样地(对照)和毗邻的长期刈割区对其繁殖策略进行了研究。结果显示: 1)长期刈割干扰下, 大针茅的种群生物量与对照区无显著差异, 由于其株丛生物量显著降低, 大针茅种群生物量的维持得益于种群密度的显著增加。糙隐子草的种群生物量比对照区显著提高, 由于其株丛生物量与对照区无显著差异, 糙隐子草种群生物量的增加也是因为密度的显著提高。因此, 密度调节是两种植物应对长期刈割干扰的重要的调节机制。2)长期刈割干扰下, 两种植物在无性繁殖和有性繁殖过程所采取的密度调节策略并不相同。大针茅种群生殖株丛的密度无显著变化, 非生殖株丛的密度显著提高, 导致其非生殖株丛的相对密度显著增加, 而生殖株丛的相对密度显著降低。因此刈割干扰下大针茅种群在密度调节上采取了保持有性繁殖株丛密度, 增加无性繁殖株丛密度的策略。糙隐子草种群非生殖株丛的密度显著增加, 但生殖株丛的密度增加幅度更大, 导致其非生殖株丛的相对密度显著降低, 而生殖株丛的相对密度显著提高。因此刈割干扰下糙隐子草种群在密度调节上采取了增加无性繁殖株丛密度的同时, 更大幅度地增加有性繁殖株丛密度的策略。3)长期刈割干扰下, 两种植物对生物量生殖分配的调节采取了不同的策略。大针茅株丛生物量向生殖枝分配的比例无显著变化, 通过降低生殖枝向穗的生物量分配比例, 降低了对有性生殖过程的生物量分配的投入; 而糙隐子草则通过增加株丛生物量向生殖枝分配的比例, 维持生殖枝向穗的生物量分配比例, 从而增加了对有性繁殖过程生物量分配的投入。4)长期刈割干扰下, 大针茅的株丛面积和株丛分蘖数与对照区无显著差异。糙隐子草株丛面积降低, 但是株丛分蘖数无显著变化。本实验说明, 植物种群有性繁殖和无性繁殖之间的密度调节和资源分配调节是草原植物应对刈割干扰下的重要调节机制, 不同的响应策略影响着植物种群的消长动态。     

刈割频次对白三叶能量分配及构型的影响

4～ 10月 ,在亚热带高山人工草地 ,通过生长季割 2、4和 7次的刈割试验后发现 ,不同刈割频次对翌年白三叶能量分配、构件密度、分枝数量及分枝角度影响显著 .随刈割频次的增加 ,白三叶匍匐茎的能量分配递增 ,分别为 42 .8%、44 .9%、47.7% ,而单位长度茎所含能量递减 ,分别为 13 .0、12 .2和 11.1kJ·m-1;叶密度、茎密度、分枝数量及节间长度出现低→高→低的变化趋势 .提高刈割频次后 ,白三叶的分枝强度由 15分枝·m-1递增到 2 3 .7分枝·m-1;分枝角度由 49.5°递增到 60 .2° ,从而提高了白三叶种群在刈割干扰下对土壤微生境资源的利用率     

香港山坡地草本、灌木群落的植物能量生产

利用收获法和植物热值分析,在研究香港桃金娘灌木群落、芒萁群落和鸭嘴草+野古草+金茅草地植物的生物量和净生产量的基础上,探讨群落各组分的干重热值以及植物能量现存量、净固定量和现存净增量.结果表明,芒萁具有较高的热值,而禾草植物的干重热值较低.草地、芒萁、灌木群落植物的能量现存量分别为18683、38436和65632kJ·m^-2;能量净固定量为13286、20354和18784kJ·m^-2·a^-1;能量现存净增量为3437、9626和6695kJ·m^-2·a^-1.与地带性植被南亚热带常绿阔叶林相比,草地、芒萁、灌木群落的能量现存量、能量净固定量和能量现存净增量都较低.刈割实验也表明,随着人类干扰活动强度加大,植物能量净固定量明显下降.     

高原鼠兔刈割行为与栖息地植物群落的关系

采用观察法和样条法对不同栖息地高原鼠兔刈割植物的行为、相对频次、生物量百分比以及刈割植物与鼠兔冬季食物组成之间的关系进行了分析,并阐述了高原鼠兔刈割植物的生物学意义。结果表明:高原鼠兔刈割植物始于每年的6 月下旬,早于其它草原小型哺乳动物贮草时间。不同栖息地鼠兔对植物的刈割频次和生物量比例并非完全一致。在矮嵩草草甸,鼠兔刈割频次较高的为垂穗披碱草、二柱头藨草、甘肃棘豆、短穗兔耳草、铺散亚菊和鹅绒萎陵菜;这些植物生物量所占比例亦较高,仅短穗兔耳草比例较低;在垂穗披碱草草甸,鼠兔刈割频次较高的为垂穗披碱草和早熟禾;垂穗披碱草生物量较高;而在杂类草草甸,鼠兔主要刈割植物为铺散亚菊、大籽蒿、黄帚橐吾、长茎藁本和圆齿狗娃花,生物量比例较高的主要为铺散亚菊。相似性分析结果表明,不同栖息地间鼠兔刈割植物频次和生物量比例差异较大,相似性系数最大分别为0. 7862 和0. 6100, 最小仅为0.1422 和0. 1035,而同一栖息地间鼠兔刈割植物频次和生物量差异相对较小,相似性系数最高达0. 9203 和0. 8490,最小亦达到0. 6662 和0. 4440,表明栖息地变化对鼠兔刈割植物频次和比例有明显的影响作用。鼠兔刈割主要植物频次和生物量比例与冬季主要食物组成的相关分析结果表明,生物量比例与主要食物组成呈显著的正相关(r =0.8412,df = 6, P <0. 05),而刈割植物频次与主要食物相关不显著。     

刈割留茬高度对大针茅草原群落结构及稳定性的影响

2014—2018年8月在内蒙古锡林郭勒盟毛登牧场大针茅典型草原,以围封为对照,设置2、5和8 cm 3个刈割留茬高度,研究刈割留茬高度对群落结构及稳定性的影响。结果表明: 群落中共出现15科23属27种植物;优势种为大针茅、知母、羊草及糙隐子草,累计相对重要值为76.1%。多年生杂类草15种,一、二年生植物5种,多年生丛生禾草和灌木半灌木植物各有3种,多年生根茎禾草有1种。大针茅等处于群落上层;知母、羊草等植物处于群落中层;糙隐子草、刺穗藜、猪毛菜等植物处于群落底层。刈割造成大针茅及多年生丛生禾草相对重要值降低,使得糙隐子草、刺穗藜、猪毛菜及一、二年生植物相对重要值增加。留茬2 cm降低羊草相对重要值,而留茬5、8 cm使其增加;留茬5 cm增加知母相对重要值,而留茬2、8 cm使其降低;留茬8 cm降低杂类草相对重要值,而留茬2、5 cm使其增加。物种及功能群多样性年度间差异显著。总体上,刈割对物种丰富度无显著影响,对其物种多样性影响较小,但对功能群多样性存在一定影响。表明在刈割过程中,群落各功能群存在一定的补偿作用,使得群落保持相对稳定。刈割使群落稳定性增加,留茬5和8 cm时群落稳定性较大;留茬5 cm时群落变异性较大,而留茬8 cm时最小。留茬8 cm时群落稳定性高且变异性小,能促进群落长期稳定。     

水分梯度上放牧对内蒙古主要草原群落功能群多样性与生产力关系的影响

应用样线法对放牧对内蒙古草原沿水分梯度分布的主要植物群落:小针茅(Stipaklemenzii)群落、大针茅(Stipagrandis)群落、羊草(Leymuschinensis)群落和羊草杂类草群落多样性、生产力以及两者关系的影响进行了研究,结果表明,除羊草杂类草群落外,物种多样性、生活型多样性和水分生态类型多样性随放牧强度的加大而降低,但适度放牧增加了羊草杂类草群落的上述多样性指标。群落地上现存量一般随放牧强度的增大而下降,但小针茅群落反之,主要与1年生植物猪毛菜(Salsolacollina)的生物量迅速增加有关。除羊草群落外,其他群落0～10cm地下生物量随放牧强度的变化不显著;放牧显著降低羊草群落和羊草杂类草群落0～30cm地下生物量。多样性和生产力间的关系在群落水平上的趋势是不同的,但放牧影响下内蒙古草原4种群落多样性与生产力总体而言呈线性增加关系;同时两者之间的关系还和采用哪种多样性指标和生产力指标有关,用水分生态类型多样性比物种多样性更能反映与地上地下总生产力间的关系,得到放牧影响下内蒙古草原植物群落地上地下总生物量与水分生态类型多样性的回归方程。     

割一年休一年割草制度下羊草群落植物多样性动态变化

利用1982—2002年样方观测资料,对典型草原区羊草草原群落割一年休一年刈割处理过程中的植物多样性变化规律及引起这些变化的主要植物种群进行了研究。结果表明:建群种羊草的个体数量先下降然后略有上升,但总体呈下降趋势;偶见种和伴生种增加,但组成有所不同。就群落多样性而言,多样性指数和均匀性指数均呈现一个明显高峰值的单峰曲线,物种分布的均匀度是影响多样性指数变化的主要因子。群落主要植物种群密度、生物量与多样性指数存在显著的相关关系,这与它们在群落中的作用有关。     

高寒矮嵩草草甸两种主要植物耐牧性的比较

通过野外控制实验,研究了刈割(留茬3 cm、留茬1 cm及不刈割)、施肥(施肥、不施肥)和浇水(浇水、不浇水)处理对高寒草甸矮嵩草(Kobresia humilis)和垂穗披碱草(Elymus nutans)补偿高度、株高相对生长率、比叶面积、叶片净光合速率和地上总生物量的影响.结果表明:2物种的株高和地上总生物量在刈割后均为低补偿响应,但其株高相对生长率显著提高,并均随年份而增加;垂穗披碱草比叶面积、叶片净光合速率和地上总生物量对刈割损伤更加敏感;尽管施肥能显著提高2物种上述各项指标,但在不同处理条件下矮嵩草的耐牧性指数均小于垂穗披碱草;浇水的作用不显著.说明2物种的耐牧性依赖于土壤养分资源获得性,矮嵩草的耐牧性强于垂穗披碱草.     

刈割、施肥和浇水对垂穗披碱草补偿生长的影响

植物的补偿生长特性受放牧强度和生境资源获得性的影响。通过为期2年的野外控制实验,研究了刈割高度(留茬1cm、3cm及不刈割)、施肥(施、不施)和浇水(浇、不浇)处理对垂穗披碱草(Elymus natans)补偿生长的影响,并结合对各处理分株密度、比叶面积、净光合速率和相对生长率的变化研究,探讨了其补偿生长机制。结果表明:刈割后垂穗披碱草分株种群密度显著增加,补偿生长高度显著降低,比叶面积和相对生长率随刈割强度增加而呈上升趋势,叶片净光合速率变化不显著;施肥能显著增加垂穗披碱草的补偿生长高度、比叶面积、叶片净光合速率和相对生长率;浇水处理以及刈割、浇水、施肥处理之间的交互作用均不显著。可见,在刈割条件下,垂穗披碱草具有一定的密度补偿机制,但由于刈割抑制补偿性高生长,导致分株高度出现低补偿。因此,即使刈割后比叶面积和株高相对生长率显著增加,也不一定必然引起株高的超补偿;但施肥可显著提高垂穗披碱草的补偿能力,增加耐牧性,证实了改进后的限制资源模型的预测。     

Seasonality of standing crop of a Sargassum (Fucales,Phaeophyta) bed in Bolinao,Pangasinan, Philippines

The seasonality of standing crop of a Sargassum bed was investigated by conducting monthly sampling from February 1988 to July 1989. Environmental parameters of water movement, salinity, number of daytime minus tides, and water temperature were also measured. An intra-annual pattern of variation in standing crop of Sargassum crassifolium, S. cristaefolium, S. oligocystum, and S. polycystum was observed. Standing crop was generally lowest in February, March, April, or May, and highest in November through January. Sargassum accounted for about 35 to 85% of the monthly algal standing crop of the bed, and the observed variation in overall standing crop of the bed generally reflected the standing crop of Sargassum. The seasonality of the standing crops of the associated algal divisions also followed an annual cycle, but their maximum and minimum standing crops did not coincide with those of Sargassum. Individually, as well as collectively, the standing crops of the Sargassum spp. were poorly correlated with the environmental factors observed.     

Soil, biomass, and management of semi-natural vegetation – Part II. Factors controlling species diversity

Using a wide range of conditions and plant community types, species diversity was investigated in relation to edaphic and non-edaphic site conditions, management, and biomass characteristics. Both standing biomass and aboveground production were investigated, and their effects compared. Three taxonomic assemblages were studied: (1) vascular plants only, (2) bryophytes also included, (3) terrestrial lichens included as well. Using a multivariate approach, both species richness and evenness could best be explained when only vascular plants were considered, emphasizing the role of taxonomic restrictions. The models best explaining species richness merely required abiotic conditions. This supports recent theories emphasizing the importance of an environmental regulation of the pool of (adapted) species from which the actual species are recruited. Explanatory soil properties were moisture and pH (both unimodal), and the soil available N:P ratio. Plots with large perimeter:area ratios had significantly more species than those with low ratios, indicating the importance of consistency in quadrat shape. Hump-shaped species richness relationships could be identified for both standing biomass and productivity, but they explained only a small part of the variation and were apparent only if soil and management effects were not accounted for. Unimodality (and notably the decreasing phase) was most pronounced when using maximum standing biomass, suggesting that the key factor is competition for light. At intermediate levels of standing biomass, the positive effects of habitat productivity and the negative effects of standing biomass itself are in balance, and high species numbers may be expected. When soil or management variables were allowed in the models, hump-shaped biomass relationships were no longer confirmed, suggesting that such relationships may arise from the covariation of biomass with other factors. Management explained a much larger part of the variation than the hump-shaped biomass relationship, suggesting that mowing and hay removal (both showing independent positive effects) regulate species richness in ways other than solely through the control of maximum standing biomass. Significantly higher evenness values were obtained at sites with low maximum biomass values, but only for the vascular plants. In addition, species evenness was positively related to the frequency of mowing. The numbers of both rare and endangered species were strongly curtailed by high standing biomass values, suggesting that these species are more susceptible to competitive exclusion than others. Through direct as well as indirect effects, management is confirmed to be beneficial not only for general species richness, but also for the occurrence of rare and endangered species.     

Adaptive introgression in animals: examples and comparison to new mutation and standing variation as sources of adaptive variation

Adaptive genetic variation has been thought to originate primarily from either new mutation or standing variation. Another potential source of adaptive variation is adaptive variants from other (donor) species that are introgressed into the (recipient) species, termed adaptive introgression. Here, the various attributes of these three potential sources of adaptive variation are compared. For example, the rate of adaptive change is generally thought to be faster from standing variation, slower from mutation and potentially intermediate from adaptive introgression. Additionally, the higher initial frequency of adaptive variation from standing variation and lower initial frequency from mutation might result in a higher probability of fixation of the adaptive variants for standing variation. Adaptive variation from introgression might have higher initial frequency than new adaptive mutations but lower than that from standing variation, again making the impact of adaptive introgression variation potentially intermediate. Adaptive introgressive variants might have multiple changes within a gene and affect multiple loci, an advantage also potentially found for adaptive standing variation but not for new adaptive mutants. The processes that might produce a common variant in two taxa, convergence, trans‐species polymorphism from incomplete lineage sorting or from balancing selection and adaptive introgression, are also compared. Finally, potential examples of adaptive introgression in animals, including balancing selection for multiple alleles for major histocompatibility complex (MHC), S and csd genes, pesticide resistance in mice, black colour in wolves and white colour in coyotes, Neanderthal or Denisovan ancestry in humans, mimicry genes in Heliconius butterflies, beak traits in Darwin's finches, yellow skin in chickens and non‐native ancestry in an endangered native salamander, are examined.     

Relationships between culture density and the composition of three floating aquatic macrophytes

Eichhornia crassipes (Mart.) Solms, Pistia stratiotes (L.), and Lemna minor (L.) were cultured at four different densities each and analyzed for cell-wall fraction, crude protein, total available carbohydrate and ash. Cell-wall fraction increased and crude protein content decreased as density increased in Eichhornia and Pistia cultures. The cell-wall and crude protein content of Lemna did not change with increasing culture density. Differences in the trends of cell-wall and crude protein content of the three plants at increasing culture densities appear to be related to differences in growth form. There was no difference in the total available carbohydrate or ash content of the three species at different culture densities.     

Molecular diagnosis for a Tamarix species from two reclaimed lands along the Yellow Sea in Korea inferred from genome wide SNP markers

The taxonomy and phylogenetic relationships of related taxa are important for understanding the biology of a species. Also, spatial distribution of genetic variation may offer insights into history of range shifts and demographic changes. The genus Tamarix L. from the Old World is a taxonomically challenging group that has widely expanded its range in the recent past. We examined genomic diversity patterns and the taxonomic identities of Korean Tamarix species whose taxonomy has remained unresolved. We used a total of 1773 SNP data from genotyping by sequencing for 37 Tamarix plants representing two species; T. chinensis and T. ramosissima to infer species delimitation and the geographic distribution of genomic diversity. Clustering (STRUCTURE; PCA, neighbor joining) and phylogenetic tree results indicated that the two morphologically similar species T. chinensis and T. ramosissima are genetically distinct and the two Korean populations (Sihwa & Songdo) are clustered closely with T. chinensis. Approximate Bayesian Computation based hypothesis testing results suggested that one of the two Korean populations, Songdo might have primarily been derived from the native area, China, followed by range expansion to Sihwa with a secondary admixture event between an established population, Songdo, and a native population, Beijing.     

Standing geographic variation in eclosion time and the genomics of host race formation in Rhagoletis pomonella fruit flies

Taxa harboring high levels of standing variation may be more likely to adapt to rapid environmental shifts and experience ecological speciation. Here, we characterize geographic and host‐related differentiation for 10,241 single nucleotide polymorphisms in Rhagoletis pomonella fruit flies to infer whether standing genetic variation in adult eclosion time in the ancestral hawthorn (Crataegus spp.)‐infesting host race, as opposed to new mutations, contributed substantially to its recent shift to earlier fruiting apple (Malus domestica). Allele frequency differences associated with early vs. late eclosion time within each host race were significantly related to geographic genetic variation and host race differentiation across four sites, arrayed from north to south along a 430‐km transect, where the host races co‐occur in sympatry in the Midwest United States. Host fruiting phenology is clinal, with both apple and hawthorn trees fruiting earlier in the North and later in the South. Thus, we expected alleles associated with earlier eclosion to be at higher frequencies in northern populations. This pattern was observed in the hawthorn race across all four populations; however, allele frequency patterns in the apple race were more complex. Despite the generally earlier eclosion timing of apple flies and corresponding apple fruiting phenology, alleles on chromosomes 2 and 3 associated with earlier emergence were paradoxically at lower frequency in the apple than hawthorn host race across all four sympatric sites. However, loci on chromosome 1 did show higher frequencies of early eclosion‐associated alleles in the apple than hawthorn host race at the two southern sites, potentially accounting for their earlier eclosion phenotype. Thus, although extensive clinal genetic variation in the ancestral hawthorn race exists and contributed to the host shift to apple, further study is needed to resolve details of how this standing variation was selected to generate earlier eclosing apple fly populations in the North.     

Admixture facilitates adaptation from standing variation in the European aspen (Populus tremula L.), a widespread forest tree

Adaptation to new environments can start from new mutations or from standing variation already present in natural populations. Whether admixture constrains or facilitates adaptation from standing variation is largely unknown, especially in ecological keystone or foundation species. We examined patterns of neutral and adaptive population divergence in Populus tremula L., a widespread forest tree, using mapped molecular genetic markers. We detected the genetic signature of postglacial admixture between a Western and an Eastern lineage of P. tremula in Scandinavia, an area suspected to represent a zone of postglacial contact for many species of animals and plants. Stringent divergence‐based neutrality tests provided clear indications for locally varying selection at the European scale. Six of 12 polymorphisms under selection were located less than 1 kb away from the nearest gene predicted by the Populus trichocarpa genome sequence. Few of these loci exhibited a signature of ‘selective sweeps’ in diversity‐based tests, which is to be expected if adaptation occurs primarily from standing variation. In Scandinavia, admixture explained genomic patterns of ancestry and the nature of clinal variation and strength of selection for bud set, a phenological trait of great adaptive significance in temperate trees, measured in a common garden trial. Our data provide a hitherto missing direct link between past range shifts because of climatic oscillations, and levels of standing variation currently available for selection and adaptation in a terrestrial foundation species.     

羊草种群生物量分配动态模拟

基于4种密度羊草种群的温室模拟试验,分析了羊草种群地上生物量与地下生物量的动态变化．结果表明：羊草种群的地上生物量与地下生物量随生长期呈增加的趋势,且随密度的增加而增加,但不同密度间羊草地上生物量与地下生物量的相对生长速率没有显著差异;不同密度羊草种群的根冠比随生长进程而增加,但差异不显著,表明环境因子是影响羊草种群根冠比变化的主导因素;单株羊草及羊草种群的地上生物量和地下生物量间存在显著的幂函数关系,但幂函数指数与系数随羊草密度的变化而变化,表明资源竞争引起的微环境差异导致了羊草种群根冠比的动态变化,可为定量研究光合产物分配提供参考．