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Resprouting of herbs in disturbed habitats: is it adequately described by Bellingham-Sparrow's model?

机译:在受干扰的栖息地中重新种植草药:贝灵汉·斯派洛(Bellingham-Sparrow)的模型是否充分描述了这种草药?

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Severe disturbances may result in a partial or complete removal of above-ground parts of plants. This is usually followed by establishment of new populations from seeds, either persisting in the seed bank or imported from the outside. Alternatively, vegetative resprouting from plant organs surviving the disturbance may ensure development of the plant cover. The later process has received relatively little attention so far. However, its role in re-establishment of severely disturbed vegetation has been recently considered by several authors (Noble and Slatyer 1980, Walker and Chapin 1987. Fahrig ct al. 1994, Bond and Midgley 2001. Dietz et al. 2002). The dominant role of resprouting ( = vegetative regeneration) in vegetation establishment on severely disturbed sites has been appreciated by authors dealing with a single life form (woody plants; Bell 2001. Del Tredici 2001) or studying response of vegetation to disturbance within a plant community (weeds on arable land, water plants communities: Wehsarg 1954. Barrat-Segretain el al. 1998, Combroux et al. 2001). A broader concept covering plant regeneration across several environments and plant groups is so far missing. A promising step forward was made by Bellingham and Sparrow (2000; referred to henceforth as B&S) who developed a graphic model showing frequency distribution of resprouting plants along gradients of disturbance frequency and severity. They found that this distribution is unimodal. According to their model species with a resprouting strategy (i.e. preferentially investing their resources into storage of assimilates and into a bud bank and resprouting after a disturbance) are more abundant at intermediate severity and frequency of disturbance than plants with a seeding strategy (i.e. preferentially investing into seed production). The latter arc favoured when disturbance is moderate and rare (trees) or strong and frequent (annuals). B&S discussed in their paper only woody plants and virtually all examples given concerned trees and shrubs. This resulted in a misunderstanding of their model by Pausas (2001) who applied it to woody plants only. However, the model by B&S does not preclude herbaceous plants (sec their Fig. 3).
机译:严重的干扰可能会导致植物的地上部分被部分或全部清除。通常,随后是从种子建立新种群,这些种群要么留在种子库中,要么从外部输入。或者,从遭受干扰的植物器官中再生出的营养可以确保植物覆盖的发展。到目前为止,后期的过程很少受到关注。但是,最近有几位作者考虑了它在重建受严重干扰的植被中的作用(Noble和Slatyer 1980,Walker和Chapin1987。Fahrig等,1994; Bond和Midgley,2001; Dietz等,2002)。处理单一生命形式(木本植物; Bell 2001; Del Tredici 2001)的作者或研究植物对植物群落内干扰的响应的作者都赞赏转基因(=营养再生)在严重受干扰地点的植被建立中的主要作用。 (在耕地上的杂草,水生植物群落:Wehsarg1954。Barrat-Segretain等1998,Combroux等2001)。到目前为止,还缺少涵盖多个环境和植物组中植物再生的更广泛概念。贝林汉姆和斯派洛(Bellingham and Sparrow,2000;以后简称B&S)向前迈出了令人鼓舞的一步,他们开发了一个图形模型,显示了沿着干扰频率和严重性梯度的重生植物的频率分布。他们发现这种分布是单峰的。根据其具有重生策略(即优先将其资源投入同化物和芽库并在发生干扰后重新萌发并在发生干扰后进行重生)的模型物种,在中等严重程度和干扰频率下比具有播种策略(即优先进行投资)的植物更为丰富进入种子生产)。当扰动为中度和罕见(树木)或强而频繁的(年度)时,后者受到青睐。 B&S在他们的论文中只讨论了木本植物,并且几乎所有有关树木和灌木的例子都讨论过。这导致Pausas(2001)仅将其应用于木本植物而误解了他们的模型。但是,B&S的模型并不排除草本植物(参见图3)。

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