Körner and Hoch's (2023) definition of “treeline” to include only forest edges that are arctic or alpine, globally distributed and thermally limited is reconsidered for the alpine, with attention to ...the alpine treeline ecotone. They characterize the alpine treeline and the ecotone as a single phenomenon at a single fundamental niche limit, with all other montane forest edges at realized niche limits. The framework restricts treeline and the treeline ecotone to narrow but interesting ecophysiological questions but leaves other fundamentally limited edges, those in disequilibrium with a changed temperature regime, and the extensive zone of krummholz and tree‐species seedlings now often referred to as the treeline ecotone, without terminology. Recognizing other fundamental niche limited edges as treelines, if not alpine, and defining “alpine treeline” as a zone or line within the broader “alpine treeline ecotone”, are proposed to promote synergies in research in these related systems.
Research resource review Malanson, George P.
Progress in Physical Geography: Earth and Environment,
12/2020, Letnik:
44, Številka:
6
Book Review, Journal Article
Aim
Alpine ecosystems differ in area, macroenvironment and biogeographical history across the Earth, but the relationship between these factors and plant species richness is still unexplored. Here, ...we assess the global patterns of plant species richness in alpine ecosystems and their association with environmental, geographical and historical factors at regional and community scales.
Location
Global.
Time period
Data collected between 1923 and 2019.
Major taxa studied
Vascular plants.
Methods
We used a dataset representative of global alpine vegetation, consisting of 8,928 plots sampled within 26 ecoregions and six biogeographical realms, to estimate regional richness using sample‐based rarefaction and extrapolation. Then, we evaluated latitudinal patterns of regional and community richness with generalized additive models. Using environmental, geographical and historical predictors from global raster layers, we modelled regional and community richness in a mixed‐effect modelling framework.
Results
The latitudinal pattern of regional richness peaked around the equator and at mid‐latitudes, in response to current and past alpine area, isolation and the variation in soil pH among regions. At the community level, species richness peaked at mid‐latitudes of the Northern Hemisphere, despite a considerable within‐region variation. Community richness was related to macroclimate and historical predictors, with strong effects of other spatially structured factors.
Main conclusions
In contrast to the well‐known latitudinal diversity gradient, the alpine plant species richness of some temperate regions in Eurasia was comparable to that of hyperdiverse tropical ecosystems, such as the páramo. The species richness of these putative hotspot regions is explained mainly by the extent of alpine area and their glacial history, whereas community richness depends on local environmental factors. Our results highlight hotspots of species richness at mid‐latitudes, indicating that the diversity of alpine plants is linked to regional idiosyncrasies and to the historical prevalence of alpine ecosystems, rather than current macroclimatic gradients.
By addressing several key features overlooked in previous studies, i.e. human disturbance, integration of ecosystem- and species-level conservation features, and principles of complementarity and ...representativeness, we present the first national-scale systematic conservation planning for China to determine the optimized spatial priorities for biodiversity conservation. We compiled a spatial database on the distributions of ecosystem- and species-level conservation features, and modeled a human disturbance index (HDI) by aggregating information using several socioeconomic proxies. We ran Marxan with two scenarios (HDI-ignored and HDI-considered) to investigate the effects of human disturbance, and explored the geographic patterns of the optimized spatial conservation priorities. Compared to when HDI was ignored, the HDI-considered scenario resulted in (1) a marked reduction (∼9%) in the total HDI score and a slight increase (∼7%) in the total area of the portfolio of priority units, (2) a significant increase (∼43%) in the total irreplaceable area and (3) more irreplaceable units being identified in almost all environmental zones and highly-disturbed provinces. Thus the inclusion of human disturbance is essential for cost-effective priority-setting. Attention should be targeted to the areas that are characterized as moderately-disturbed, <2,000 m in altitude, and/or intermediately- to extremely-rugged in terrain to identify potentially important regions for implementing cost-effective conservation. We delineated 23 primary large-scale priority areas that are significant for conserving China's biodiversity, but those isolated priority units in disturbed regions are in more urgent need of conservation actions so as to prevent immediate and severe biodiversity loss. This study presents a spatially optimized national-scale portfolio of conservation priorities--effectively representing the overall biodiversity of China while minimizing conflicts with economic development. Our results offer critical insights for current conservation and strategic land-use planning in China. The approach is transferable and easy to implement by end-users, and applicable for national- and local-scale systematic conservation prioritization practices.
Increasing environmental variability could exacerbate the effects of climate change on ecological processes such as population dynamics, or positive and negative effects (favorable or unfavorable ...weather) could balance. Such a balance could depend on constraints of the processes. Biological and spatial constraints are represented in a spatially explicit individual based simulation of an ecotone reduced to two species on a single environmental gradient. The effects of climate amelioration are simulated from a plant's-eye-view by increasing the establishment and decreasing the mortality rates. Variability is introduced as a random multiplier of these rates, and the strength of the variation is increased through the period of climate change. The biological constraints limit change in the rates, and the extent of the simulation grid represents a spatial constraint. A small increase in environmental variation, multiplied through time with climate change, increases extinction rates. The biological and spatial constraints have little effect on the response of populations. Instead, competition, based on the form of the species response functions to the environmental gradient at the point where they intersect, determines differences in population responses. Positive and negative variations in the environment do not balance because the responses are hierarchical and asymmetric. Differences persist because extinction during a negative anomaly cannot be reversed by a later positive one.
•Increased volatility with climate change is simulated in a grid-based 2-species model.•Hierarchical niche responses on environmental gradients are represented.•Effects of volatility on coexistence are confined to a narrow ecotone.•Biological constraints (responses) and spatial constraints (grid) have low effect.•With extinctions, negative anomalies cannot be balanced by positive ones.
How does the stress-gradient hypothesis affect coexistence in relation to established theory? For two orthogonal stress gradients, a spatially explicit agent based simulation is used to project ...diversity for simple competitive and facilitative interactions and for three variations of the stress-gradient hypothesis: intraspecific and interspecific competitive and facilitative interactions are a function of the abiotic environment; interactions are relative to species-specific fitness along gradients; or interaction is fixed by species regardless of the abiotic environment. Simulations are run with two orthogonal environmental gradients for two representations of niche. Facilitation can increase diversity by maintaining larger source populations and thus higher establishment rates and sink populations. With species hierarchically related in niche space, the simulations show that positive interactions and changing interactions along a stress gradient maintain greater diversity through intraspecific competition that is effective where dominance would occur and through facilitation where stress is high. A changing environment that favors some species and harms others decreases diversity in the hierarchical cases, where poor competitors most likely subject to interspecific interaction respond most strongly. Diversity outcomes differ among the three stress gradient variations because the intensity of interactions differs across the environmental gradients, not because of change in the environment.
•3 modes of interaction for the stress gradient hypothesis (SGH) are simulated.•Hierarchical and separated niche responses on environmental gradients are represented.•Positive interactions increase coexistence through greater source-sink dynamics.•SGH effects increase coexistence by the separation of facilitation and competition.•Among the 3 SGH modes coexistence decreases variably with environmental change.
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