Current problems of environmental gradients and species response curves in relation to continuum theory

Abstract. Comparisons of the positions of species on Grimes'C-S-R triangular ordination model with their responses to individual environmental gradients indicates that the C-S-R model does not necessarily predict species ecological behaviour. The importance of the stress, productivity and disturbance gradients relative to other environmental gradients needs to be determined. In studies of species behaviour along a biomass/productivity gradient the collective vegetation property, biomass, has been confused with the environmental factor, fertility. Patterns of responses to biomass gradients e.g. Keddy's centrifugal model, should be examined in a two-dimensional environmental space to avoid such confounding effects. Assumptions regarding the shapes of species responses to environmental gradients remain untested. A recent model of species response functions to environmental gradients suggested that skewed responses curves show a pattern in the direction of the skew, always with the tail towards the presumed most mesic position on the gradient. Further evidence is presented to support this model for a temperature gradient in eucalypt forest in south-eastern Australia. 21 out of 24 species tested conform to the model.     

Assessing the scale-specific importance of niches and other spatial processes on beta diversity: a case study from a temperate forest

Niche processes and other spatial processes, such as dispersal, may simultaneously control beta diversity, yet their relative importance may shift across spatial and temporal scales. Although disentangling the relative importance of these processes has been a continuing methodological challenge, recent developments in multi-scale spatial and temporal modeling can now help ecologists estimate their scale-specific contributions. Here we present a statistical approach to (1) detect the presence of a space–time interaction on community composition and (2) estimate the scale-specific importance of environmental and spatial factors on beta diversity. To illustrate the applicability of this approach, we use a case study from a temperate forest understory where tree seedling abundances were monitored during a 9-year period at 40 permanent plots. We found no significant space–time interaction on tree seedling composition, which means that the spatial abundance patterns did not vary over the study period. However, for a given year the relative importance of niche processes and other spatial processes was found to be scale-specific. Tree seedling abundances were primarily controlled by a broad-scale environmental gradient, but within the confines of this gradient the finer scale patchiness was largely due to other spatial processes. This case study illustrates that these two sets of processes are not mutually exclusive and can affect abundance patterns in a scale-dependent manner. More importantly, the use of our methodology for future empirical studies should help in the merging of niche and neutral perspectives on beta diversity, an obvious next step for community ecology. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

A new model for the continuum concept

A reformulation of the continuum concept is presented after considering the implications of the community/continuum controversy and current niche theory. Community is a spatial concept dependent on landscape pattern while the continuum is an environmental concept referring to an abstract space. When applying niche theory to plants, the mechanisms of competition are ill-defined and the assumption of bell-shaped response curves for species unrealistic.Eight testable propositions on the pattern of response of vegetation to environmental gradients are presented 1. Environmental gradients are of two types. a) resource gradients or b) direct physiological gradients. 2. The fundamental niche response of species to resource gradients is a series of similar nested response curves. 3. The fundamental niche response of species to direct gradients is a series of separate, independent, overlapping response curves. 4. Species fundamental response curves are such that they have a relative performance advantage in some part of the environmental space. 5. The shape of the realized niche is variable even bimodal but predictable from the fundamental response given the other species present. Propositions 6–8 describe the response shapes of emergent community properties to environmental gradient; species richness is bimodal, dominance trimodal and standing crop unimodal. Detailed comparisons of these propositions are made with the alternative theories of Ellenberg, Gauch and Whittaker, Grime, and Tilman. These theories are incomplete lacking several generally accepted properties of plants and vegetation.     

Growth rate and basal area response curves of four Eucalyptus species on Mt. Wellington,Tasmania

Abstract. The heights, diameters and regrowth basal areas of 22-yr old fire-initiated regeneration of Eucalyptus delegatensis ssp. tasmaniensis, E. urnigera, E. coccifera and E. johnstonii were measured over altitudinal, solar radiation and drainage gradients on Mt. Wellington, Tasmania. The growth rate responses to the altitude gradient-complex vary from linear to curved depending on the performance measure, the species and the gradient. Much of the variation in growth rate appears to be a direct response to the physical environment. However, disparities between trends in growth rate and trends in re-growth basal area are consistent with the hypothesis that competition (sensu Grime 1979) is more important in productive environments and less important in stressful environments. A glasshouse trial with Eucalyptus seedlings indicated that potential growth rates decline with increasing altitude of seed source.     

Growth-climate responses indicate shifts in the competitive ability of European beech and Norway spruce under recent climate warming in East-Central Europe

Long-term changes in climate substantially affect the tree growth and species distribution in Europe. In the presented study, the radial growth of Fagus sylvatica (L.) and Picea abies ((L.) Karst.) has been studied along an altitudinal gradient covering six vegetation formations characteristic for sub-montane, montane and high-montane conditions of the western Carpathians. Tree growth responses to temperature and precipitation changes have been analysed based on the sample of increment cores and standard dendroclimatic methods in two time periods, the reference period 1961–1990 and the recent period 1991–2012. The growth responses of spruce and beech to recent changes in climate were similar up to high-montane zones, where the beech shows significantly larger improvements of radial increments in comparison to spruce. The growth responses were mainly temperature driven. In the sub-montane area, the increased effect of precipitation in the recent period was overridden by the negative effects of warming, and the alleviated temperature limitation had an evidently supportive effect on tree growth in montane and high-montane areas. In the near future, the warming will likely cause decline in radial increments of beech and spruce in sub-montane areas due to expected landscape drying. At the same time, the improved competitive ability of beech in the high-montane zones suggests a shift in the leading edge of beech distribution into higher altitudes in East-Central Europe.     

Elevated CO2 differentially alters the responses of coocurring birch and maple seedlings to a moisture gradient

Summary To determine the effects of elevated CO₂ and soil moisture status on growth and niche characteristics of birch and maple seedlings, gray birch (Betula populifolia) and red maple (Acer rubrum) were experimentally raised along a soil moisture gradient ranging from extreme drought to flooded conditions at both ambient and elevated atmospheric CO₂ levels. The magnitude of growth enhancement due to CO₂ was largely contingent on soil moisture conditions, but differently so for maple than for birch seedlings. Red maple showed greatest CO₂ enhancements under moderately moist soil conditions, whereas gray birch showed greatest enhancements under moderately dry soil conditions. Additionally, CO₂ had a relatively greater ameliorating effect in flooded conditions for red maple than for gray birch, whereas the reverse pattern was true for these species under extreme drought conditions. For both species, elevated CO₂ resulted in a reduction in niche breadths on the moisture gradient; 5% for gray birch and 23% for red maple. Species niche overlap (proportional overall) was also lower at elevated CO₂ (0.98 to: 0.88: 11%). This study highlights the utility of of experiments crossing CO₂ levels with gradients of other resources as effective tools for elucidating the potential consequences of elevated CO₂ on species distributions and potential interactions in natural communities.     

不同密度条件下芨芨草空间格局对环境胁迫的响应

基于小尺度上植物间相互作用与空间格局的高度相关性,选用可避免环境异质性影响的K2点格局函数,研究了沙枣-芨芨草群落中63个芨芨草样方(3密度条件×3生境条件×7重复)中芨芨草种群在小尺度下(0—0.5 m)的空间格局,探讨了在3种密度条件(高、中、低)及3种生境条件下(冠盖区、过渡区、空旷区),芨芨草种群空间格局对土壤理化性质胁迫(盐分、有机质及容重)程度的响应。研究结果表明,就土壤盐分,养分含量及土壤容重而言,土壤理化性质胁迫程度沿冠盖区、过渡区和空旷区增加的趋势。相应地,芨芨草种群呈聚集分布的样方比例在沿冠盖区(6/21)较低,而在过渡区(11/21)和空旷区(11/21)较高。然而,在不同密度条件下,芨芨草种群空间格局对土壤性质胁迫的响应不同。在低密度条件下,芨芨草种群在冠盖区多数为聚集分布(4/7),在过渡区和空旷区全部为聚集分布;中密度条件下,芨芨草聚集分布样方比例沿冠盖区-过渡区-空旷区梯度增加(分别为2/7,3/7,4/7),但低于同等胁迫条件下低密度样方中聚集分布数量;高密度条件下,在各胁迫条件下,除了一个过渡区高密度样方,其余芨芨草种群均为随机分布。总体上,随着环境胁迫增强,在中低密度下,芨芨草种群趋向于聚集分布;但在高密度下,芨芨草种群均以随机分布为主。此外,芨芨草种群空间格局随密度变化趋势比随土壤理化性质胁迫梯度变化趋势更加明显,可能表明相对于土壤理化性质胁迫程度,芨芨草种群密度对其空间格局影响更大。因此,在考虑芨芨草种群空间格局对环境胁迫的响应时,应当考虑种群密度因素。     

Simulated morphogenesis of developmental folds due to proliferative pressure

We present a simulation that models individual cells as spherical particles that can migrate, interact, divide and differentiate. We simulate the evolution of a progenitor layer of cells that reproduce, leading either to more progenitors or to differentiated daughters. We find that this simplified model produces spontaneous folds whose lengths depend linearly on the ratio of rates of production of progenitors to differentiated daughters. We also find that folds grow approximately exponentially in time, and that larger folds can be placed via patterning events that perturb the positions of selected progenitor cells early in the developmental process.     

Annual plant–shrub interactions along an aridity gradient

Annual plants in semi-arid and arid areas are often closely associated with shrubs. The degree of association largely depends on the balance of negative and positive effects between these contrasting plant life-forms, ranging from interference to facilitation. Since positive interactions are predicted to become less important with increasing rainfall, the interaction balance is expected to shift along aridity gradients. However, this prediction has not been tested on a community level and for different life-history stages across large geographical gradients. Here, we show such changes for annual plant populations and communities in four contrasting sites along a steep climatic gradient, ranging from the arid desert to mesic Mediterranean regions in Israel. Above-ground productivity, richness, seedling density, and seed bank density of the annual plant community, as well as fecundity of annual plant populations, were generally higher under shrubs than in areas between shrubs at the arid end of the gradient, but significantly lower at the humid end. Net effects of shrubs on annuals expressed as relative interaction intensity indicated a steady and consistent shift from net positive or neutral effects in the desert to net negative effects in the mesic part of the gradient. These findings emphasize the usefulness of studies along large-scale gradients encompassing a wide range of environmental conditions for understanding community level interactions among coexisting species.     

A comparative approach to examine competitive response of 48 wetland plant species

Abstract. Competitive ability can be separated into competitive effect (ability to suppress neighbours) and competitive response (ability to tolerate suppressive effect from neighbours), but little is known about the competitive response of plants. A screening trial was conducted in outdoor plant pots where competitive response was measured for 48 wetland species during four months grown with seven established sward species: Acorus calamus, Carex crinita, Eleocharis smallii, Lythrum salicaria, Penthorum sedoides, Scirpus acutus and Typha angustifolia. Competitive response was calculated as 100 (x₁–x₂)/x₁, where x₁ is the weight of the target plant grown alone and x₂ the weight of the target plant grown in the swards. Despite significant differences in biomass and survivorship of the target plants between the sward species, the correspondence, W, of the rank order of the competitive response of target plants grown in the seven sward species was 0.70 (P < 0.001). The competitive response values were not significantly correlated with independent measures of competitive effect, relative growth rate or functional classification. Published competitive effect values, however, were significantly positively correlated with RGR. The results suggest a different approach towards the study of competitive response, with a conceptual model including three different response types: (1) escape; (2) foraging; and (3) persistence.