scholarly journals Zooplankton biodiversity and community structure vary along spatiotemporal environmental gradients in restored peridunal ponds

Author(s):  
Maria Anton-Pardo ◽  
Xavier Armengol ◽  
Raquel Ortells

<p>Zooplankton assemblages in neighboring ponds can show important spatial and temporal heterogeneity. Disentangling the influence of regional versus local factors, and of deterministic versus stochastic processes has been recently highlighted in the context of the metacommunity theory. In this study, we determined patterns of temporal and spatial variation in zooplankton diversity along one hydrological year in restored ponds of different hydroperiod and age. The following hypotheses regarding the assembling of species over time were tested: i) dispersal is not limited in our study system due to its small area and high exposure to dispersal vectors; ii) community dissimilarity among ponds increases with restoration age due to an increase in environmental heterogeneity and stronger niche-based assemblages;and iii) similarity increases with decreasing hydroperiod because hydroperiod is a strong selective force filtering out organisms with long life cycles. Our results confirmed dispersal as a homogenizing force and local factors as gaining importance with time of restoration. However, short hydroperiod ponds were highly dissimilar, maybe due to the environmental differences among these ponds, or to high stochasticity followed by priority effects under a weak selection pressure. By adding a temporal dimension to the study of zooplankton structuring, we could identify the first months after flooding as being crucial for species richness, especially in short hydroperiod ponds; and we detected differences in seasonal species richness related to hydroperiod and pond age.</p>

2021 ◽  
Vol 53 (1) ◽  
pp. 149-158
Author(s):  
Robert J. Smith ◽  
Sarah Jovan ◽  
Susan Will-Wolf

AbstractLichens occupy diverse substrates across tremendous ranges of environmental variation. In boreal forests, lichen communities co-occur in ‘strata’ defined by terrestrial or arboreal substrates, but these strata may or may not be interchangeable as bioindicators. Do co-occurring lichen strata have similar community structures and environmental responses? Could one stratum serve as a proxy for the other? We assessed variation in species richness and community compositions between ground-layer versus epiphyte-layer lichen strata in boreal forests and peatlands of interior Alaska. Species richness was lower and more spatially structured in the ground layer than the epiphyte layer. Richness of strata was not correlated. The most compositionally unique ground-layer communities were species-poor but contained regionally rare species not common in other plots. Variation in community compositions (ordination scores) were not congruent between strata (Procrustes congruence < 0.16 on 0–1 scale); the largest departures from congruence occurred where ground layers were species-poor. The best predictors of ground-layer community compositions were hydrological and topographic, whereas epiphytes were most associated with macroclimate and tree abundances. We conclude that lichens on different substrates ‘move in different circles’: compositional gradients did not agree and the environmental gradients most important to each lichen stratum were not the same. The conditions which strongly influence one vegetation stratum may have little bearing upon another. As global changes modify habitats, an incremental change in environment may lead community trajectories to diverge among lichen strata.


2015 ◽  
Vol 200 ◽  
pp. 120-125 ◽  
Author(s):  
Thomas M.W.J. van Goethem ◽  
Mark A.J. Huijbregts ◽  
G.W. Wieger Wamelink ◽  
Aafke M. Schipper

2020 ◽  
Vol 2 (4) ◽  
pp. 352-376
Author(s):  
Lindsay Hollingsworth ◽  
Marcus Collier

Despite the fact that field boundary (dry) stone walls are globally common in rural landscapes, very little research has been carried out regarding them. Dry stone walls may act as refuges for a range of plants and animals, especially in areas where conditions do not favour a high biodiversity or areas of high exposure. They may also provide connectivity via habitat corridors and may even serve as a habitat in their own right. This paper reports on a case study survey of the forb assemblages of field boundary dry stone walls in terms of species richness, biodiversity, and composition in comparison to the surrounding landscape, and aims to provide some insight into the floral ecology characteristics of dry stone walls. To accomplish this, the forbs growing in and immediately adjacent to 18 segments of dry stone wall in the Burren region of western Ireland, were surveyed. The forb assemblages growing within the walls were compared with those growing in the 0.5 m closest to the walls and those growing the areas 0.5-1.0 m on either side of the walls. The wall assemblages were shown to have lower species richness and each category of assemblage was shown to have significantly different species composition. This research indicates that the dry stone walls of the Burren may be associated with a distinct floral ecology, and therefore may act as habitat corridors in an otherwise exposed landscape.


Forests ◽  
2018 ◽  
Vol 9 (9) ◽  
pp. 511 ◽  
Author(s):  
Ji-Hua Wang ◽  
Yan-Fei Cai ◽  
Lu Zhang ◽  
Chuan-Kun Xu ◽  
Shi-Bao Zhang

Knowledge about how species richness varies along spatial and environmental gradients is important for the conservation and use of biodiversity. The Ericaceae is a major component of alpine and subalpine vegetation globally. However, little is known about the spatial pattern of species richness and the factors that drive that richness in Ericaceae. We investigated variation in species richness of Ericaceae along an elevational gradient in Yunnan, China, and used a variation partitioning analysis based on redundancy analysis ordination to examine how those changes might be influenced by the mid-domain effect, the species-area relationship, and climatic variables. Species richness varied significantly with elevation, peaking in the upper third of the elevational gradient. Of the factors examined, climate explained a larger proportion of the variance in species richness along the elevational gradient than either land area or geometric constraints. Species richness showed a unimodal relationship with mean annual temperature and mean annual precipitation. The elevational pattern of species richness for Ericaceae was shaped by the combined effects of climate and competition. Our findings contribute to a better understanding of the potential effects of climate change on species richness for Ericaceae.


The Auk ◽  
2021 ◽  
Author(s):  
Flavia A Montaño-Centellas ◽  
Harrison H Jones

Abstract Mixed-species flocks constitute community modules that can help test mechanisms driving changes to community composition across environmental gradients. Here, we examined elevational patterns of flock diversity (species richness, taxonomic diversity, species, and guild composition) and asked if these patterns were reflections of the full bird community at a given elevation (open-membership hypothesis), or if they were instead structured by environmental variables. We surveyed both the overall avian community and mixed-species flocks across an undisturbed elevational gradient (~1,350–3,550 m) in the Bolivian Andes. We then tested for the role of temperature (a surrogate for abiotic stress), resource diversity (arthropods, fruits), and foraging niche diversity (vegetation vertical complexity) in structuring these patterns. Patterns for the overall and flocking communities were similar, supporting our open-membership hypothesis that Andean flocks represent dynamic, unstructured aggregations. Membership openness and the resulting flock composition, however, also varied with elevation in response to temperature and vegetation complexity. We found a mid-elevation peak in flock species richness, size, and Shannon’s diversity at ~2,300 m. The transition of flocking behavior toward a more open-membership system at this elevation may explain a similar peak in the proportion of insectivores joining flocks. At high elevations, increasing abiotic stress and decreasing fruit diversity led more generalist, gregarious tanagers (Thraupidae) to join flocks, resulting in larger yet more even flocks alongside a loss of vegetation structure. At lower elevations, flock species richness increased with greater vegetation complexity, but a greater diversity of foraging niches resulted in flocks that were more segregated into separate canopy and understory sub-types. This segregation likely results from increased costs of interspecific competition and activity matching (i.e., constraints on movement and foraging rate) for insectivores. Mid-elevation flocks (~2,300 m) seemed, therefore, to benefit from both the open-membership composition of high-elevation flocks and the high vegetation complexity of mid- and low-elevation forests.


<i>Abstract.</i>—Linking landscape features, both natural and human-altered, to aquatic ecosystem structure and function is a fundamental objective in landscape ecology and freshwater science, but this process is data- and resource-intensive. Quantifying how landscape stressors influence aquatic communities requires balancing logistic and financial constraints with effectively sampling the landscape to capture gradients of interest. There are a variety of ways to balance these constraints, such as using existing data, handpicked site selection, or a statistical site-selection scheme. Poor sampling design reduces statistical power; however, we do not know how differences in site-selection designs influence our ability to measure ecological responses to landscape gradients. We quantified how the distribution of sample sites across landscape gradients affected the measured responses of stream fish assemblages to these gradients at different sample sizes. Specifically, we used randomization tests to compare the variability in the responses of fish assemblage structure (species richness and composition) to catchment area and land use (agricultural land) with manipulated distributions (random, highly skewed, and uniform) of sites across these landscape gradients. Assemblage composition was more sensitive than species richness to sampling design, and we observed less variability in the detected response of assemblage composition when samples were distributed uniformly across landscape gradients, especially when sample sizes were small. Although strong responses to environmental gradients, such as species richness to catchment area, are robust to sampling distributions, large sample size and a uniform distribution of samples might help elucidate more subtle responses to environmental gradients.


2019 ◽  
Vol 15 (10) ◽  
pp. 20190493 ◽  
Author(s):  
T. Edward Roberts ◽  
Sally A. Keith ◽  
Carsten Rahbek ◽  
Tom C. L. Bridge ◽  
M. Julian Caley ◽  
...  

Natural environmental gradients encompass systematic variation in abiotic factors that can be exploited to test competing explanations of biodiversity patterns. The species–energy (SE) hypothesis attempts to explain species richness gradients as a function of energy availability. However, limited empirical support for SE is often attributed to idiosyncratic, local-scale processes distorting the underlying SE relationship. Meanwhile, studies are also often confounded by factors such as sampling biases, dispersal boundaries and unclear definitions of energy availability. Here, we used spatially structured observations of 8460 colonies of photo-symbiotic reef-building corals and a null-model to test whether energy can explain observed coral species richness over depth. Species richness was left-skewed, hump-shaped and unrelated to energy availability. While local-scale processes were evident, their influence on species richness was insufficient to reconcile observations with model predictions. Therefore, energy availability, either in isolation or in combination with local deterministic processes, was unable to explain coral species richness across depth. Our results demonstrate that local-scale processes do not necessarily explain deviations in species richness from theoretical models, and that the use of idiosyncratic small-scale factors to explain large-scale ecological patterns requires the utmost caution.


Koedoe ◽  
1997 ◽  
Vol 40 (1) ◽  
Author(s):  
H.C. Eckhardt ◽  
N. Van Rooyen ◽  
G.J. Bredenkamp

An analysis of the woody vegetation of northern KwaZulu-Natal is presented. Releves were compiled in 102 stratified random sample plots. A TWINSPAN classification, refined by Braun-Blanquet procedures, revealed 24 plant communities, also referred to as vegetation units. For each of these vegetation units, the species richness was determined. Four associations were identified which have a conservation importance. An ordination (DECORANA), based on floristic data, revealed the position of the syntaxa on environmental gradients.


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Tomás A. Altamirano ◽  
Devin R. de Zwaan ◽  
José Tomás Ibarra ◽  
Scott Wilson ◽  
Kathy Martin

Abstract Mountains produce distinct environmental gradients that may constrain or facilitate both the presence of avian species and/or specific combinations of functional traits. We addressed species richness and functional diversity to understand the relative importance of habitat structure and elevation in shaping avian diversity patterns in the south temperate Andes, Chile. During 2010–2018, we conducted 2202 point-counts in four mountain habitats (successional montane forest, old-growth montane forest, subalpine, and alpine) from 211 to 1,768 m in elevation and assembled trait data associated with resource use for each species to estimate species richness and functional diversity and turnover. We detected 74 species. Alpine specialists included 16 species (22%) occurring only above treeline with a mean elevational range of 298 m, while bird communities below treeline (78%) occupied a mean elevational range of 1,081 m. Treeline was an inflection line, above which species composition changed by 91% and there was a greater turnover in functional traits (2–3 times greater than communities below treeline). Alpine birds were almost exclusively migratory, inhabiting a restricted elevational range, and breeding in rock cavities. We conclude that elevation and habitat heterogeneity structure avian trait distributions and community composition, with a diverse ecotonal sub-alpine and a distinct alpine community.


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