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Evolutionary Ecology of Mountain Birch in Subarctic Stress Gradients: Interplay of Biotic and Abiotic Factors in Plant-Plant Interactions and Evolutionary Processes

机译:亚北极胁迫梯度下山桦的进化生态学:植物与植物相互作用和进化过程中生物和非生物因素的相互作用

摘要

In nature, variation for example in herbivory, wind exposure, moisture and pollution impact often creates variation in physiological stress and plant productivity. This variation is seldom clear-cut, but rather results in clines of decreasing growth and productivity towards the high-stress end. These clines of unidirectionally changing stress are generally known as ‘stress gradients’. Through its effect on plant performance, stress has the capacity to fundamentally alter the ecological relationships between individuals, and through variation in survival and reproduction it also causes evolutionary change, i.e. local adaptations to stress and eventually speciation. In certain conditions local adaptations to environmental stress have been documented in a matter of just a few generations.In plant-plant interactions, intensities of both negative interactions (competition) and positive ones (facilitation) are expected to vary along stress gradients. The stress-gradient hypothesis (SGH) suggests that net facilitation will be strongest in conditions of high biotic and abiotic stress, while a more recent ‘humpback’ model predicts strongest net facilitation at intermediate levels of stress. Plant interactions on stress gradients, however, are affected by a multitude of confounding factors, making studies of facilitation-related theories challenging. Among these factors are plant ontogeny, spatial scale, and local adaptation to stress. The last of these has very rarely been included in facilitation studies, despite the potential co-occurrence of local adaptations and changes in net facilitation in stress gradients. Current theory would predict both competitive effects and facilitative responses to be weakest in populations locally adapted to withstand high abiotic stress.This thesis is based on six experiments, conducted both in greenhouses and in the field in Russia, Norway and Finland, with mountain birch ( subsp. as the model species. The aims were to study potential local adaptations in multiple stress gradients (both natural and anthropogenic), changes in plant-plant interactions under conditions of varying stress (as predicted by SGH), potential mechanisms behind intraspecific facilitation, and factors confounding plant-plant facilitation, such as spatiotemporal, ontogenetic, and genetic differences.I found rapid evolutionary adaptations (occurring within a time-span of 60 to 70 years) towards heavy-metal resistance around two copper-nickel smelters, a phenomenon that has resulted in a trade-off of decreased performance in pristine conditions. Heavy-metal-adapted individuals had lowered nickel uptake, indicating a possible mechanism behind the detected resistance. Seedlings adapted to heavy-metal toxicity were not co-resistant to others forms of abiotic stress, but showed co-resistance to biotic stress by being consumed to a lesser extent by insect herbivores. Conversely, populations from conditions of high natural stress (wind, drought etc.) showed no local adaptations, despite much longer evolutionary time scales.Due to decreasing emissions, I was unable to test SGH in the pollution gradients. In natural stress gradients, however, plant performance was in accordance with SGH, with the strongest host-seedling facilitation found at the high-stress sites in two different stress gradients. Factors confounding this pattern included (1) plant size / ontogenetic status, with seedling-seedling interactions being competition dominated and host-seedling interactions potentially switching towards competition with seedling growth, and (2) spatial distance, with competition dominating at very short planting distances, and facilitation being strongest at a distance of circa ¼ benefactor height. I found no evidence for changes in facilitation with respect to the evolutionary histories of plant populations. Despite the support for SGH, it may be that the ‘humpback’ model is more relevant when the main stressor is resource-related, while what I studied were the effects of ‘non-resource’ stressors (i.e. heavy-metal pollution and wind).The results have potential practical applications: the utilisation of locally adapted seedlings and plant facilitation may increase the success of future restoration efforts in industrial barrens as well as in other wind-exposed sites. The findings also have implications with regard to the effects of global change in subarctic environments: the documented potential by mountain birch for rapid evolutionary change, together with the general lack of evolutionary ‘dead ends’, due to not (over)specialising to current natural conditions, increase the chances of this crucial forest-forming tree persisting even under the anticipated climate change.
机译:在自然界中,例如食草,风,水分和污染影响等方面的变化通常会造成生理胁迫和植物生产力的变化。这种变化很少是明确的,而是导致向高压力端下降的增长和生产率下降的趋势。这些单向变化的应力线通常称为“应力梯度”。通过其对植物生长的影响,胁迫具有从根本上改变个体之间生态关系的能力,并且通过生存和繁殖的变化,它还引起进化变化,即局部适应胁迫并最终形成物种。在某些情况下,已经证明了对环境压力的局部适应仅需几代之久。在植物与植物的相互作用中,预计负向相互作用(竞争)和正向相互作用(促进)的强度均会随应力梯度而变化。压力梯度假设(SGH)表明,在高生物和非生物压力下,净促进作用最强,而最新的“座头鲸”模型预测,在中等压力水平下,净促进作用最强。然而,植物在应力梯度上的相互作用受到多种混杂因素的影响,这使得与便利相关的理论的研究具有挑战性。这些因素包括植物的个体发育,空间尺度以及对胁迫的局部适应性。尽管局部适应和应力梯度中的净便利化可能同时发生,但最后一项很少包含在促进研究中。当前的理论认为,在当地适应高非生物胁迫的人群中,竞争效应和促进反应最弱。本论文基于六个实验,分别在俄罗斯,挪威和芬兰的温室和田间进行,山桦木(目的是研究多种应力梯度(自然和人为)中的潜在局部适应性,在变化胁迫条件下植物与植物相互作用的变化(如SGH预测),种内促进作用的潜在机制,我发现了两个铜镍冶炼厂周围对重金属抗性的快速进化适应(发生在60到70年的时间范围内),这是一个现象。这导致了在原始条件下性能下降的权衡。适应重金属的个体降低了镍ckel吸收,表明检测到的阻力背后的可能机制。适应重金属毒性的幼苗对其他形式的非生物胁迫并不具有抗性,但由于被昆虫食草动物的消费较少,因此对生物胁迫具有抗性。相反,尽管进化时间尺度更长,但来自高自然压力条件下的种群(风,干旱等)并未表现出局部适应性。由于排放量减少,我无法在污染梯度中测试SGH。然而,在自然胁迫梯度下,植物表现与SGH一致,在两个不同胁迫梯度下的高胁迫部位发现最强的寄主苗生长。造成这种模式混淆的因素包括:(1)植株大小/个体发育状态,其中幼苗与幼苗之间的相互作用以竞争为主,宿主与幼苗之间的相互作用有可能转向与幼苗生长的竞争;(2)空间距离,其中竞争在很短的种植距离上即为主导,并且在大约1/4恩人高度的距离处促进作用最强。在植物种群的进化史方面,我没有发现便利化发生变化的证据。尽管支持SGH,但当主要压力源与资源相关时,“座头鲸”模型可能更相关,而我研究的是“非资源”压力源(即重金属污染和风)的影响研究结果具有潜在的实际应用价值:利用当地适应的幼苗和促进植物生长可以增加工业贫瘠地区以及其他受风暴露地点未来修复工作的成功率。这些发现还对全球变化在亚北极环境中的影响产生了影响:由于没有特别针对当前自然环境,山桦树记录了快速进化变化的潜力,以及普遍缺乏进化的“死胡同”。情况下,即使在预期的气候变化下,这种至关重要的森林形成树的生存机会也会增加。

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    Eränen Janne;

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  • 年度 2009
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