ecological gradients
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Plants ◽  
2021 ◽  
Vol 10 (11) ◽  
pp. 2372
Author(s):  
Inayat Ur Rahman ◽  
Aftab Afzal ◽  
Zafar Iqbal ◽  
Abeer Hashem ◽  
Al-Bandari Fahad Al-Arjani ◽  
...  

The ecotonal zones support populations that are acclimated to changing, fluctuating, and unstable conditions, and as a result, these populations are better equipped to adjust to expected change. In this context, a hypothesis was tested that there must be vegetation dominated by unique indicator plant species under the influence of ecological gradients in the ecotonal zone of Manoor Valley (northwestern Himalaya), Pakistan. Keeping the aforementioned hypothesis in mind, detailed field studies were conducted during different seasons in 2015-18. Line transect sampling and phytosociological characteristics (density, frequency, cover, and their relative values and Importance Value) were implemented as ecological methods. This investigation documented 97 plant species recorded from seven sampling sites. The community distribution modelling revealed that the ecological variables separate the seven sampling sites into two major plant communities (Indigofera-Parrotiopsis-Bistorta and Ziziphus-Leptopus-Quercus) recognized by TWINSPAN. The IBP communities showed a positive and significant correlation with altitude (1789.6–1896.3 m), sandy soil texture with a slightly acidic pH (6.4–6.5), and higher phosphorous (9–13 mg kg−1). In contrast with this, the ZLQ community was recognized on the southern slope under the strong influence of high electrical conductivity (2.82–5.4 dsm−1), organic matter (1.08–1.25%), calcium carbonate (5.8–7.6 mg kg−1), potassium (202–220 mg kg−1), and temperature (28.8–31.8 °C). Hence, both communities were found on opposite axes with clear differences based on the ecological gradients. NMDS clustered different species with similar habitats and different stands with common species, showing that plant species and stands were in a linear combination with ecological gradients. The IPB community has the maximum number of plant species (87 species), Shannon value (H’ = 4), Simpson value (0.98), and Pielou’s evenness value (0.96). Thus, the multivariate approaches revealed unique vegetation with sharp boundaries between communities which might be due to abrupt environmental changes.


Paleobiology ◽  
2021 ◽  
pp. 1-18
Author(s):  
Daniel G. Dick ◽  
Marc Laflamme

Abstract Classic similarity indices measure community resemblance in terms of incidence (the number of shared species) and abundance (the extent to which the shared species are an equivalently large component of the ecosystem). Here we describe a general method for increasing the amount of information contained in the output of these indices and describe a new “soft” ecological similarity measure (here called “soft Chao-Jaccard similarity”). The new measure quantifies community resemblance in terms of shared species, while accounting for intraspecific variation in abundance and morphology between samples. We demonstrate how our proposed measure can reconstruct short ecological gradients using random samples of taxa, recognizing patterns that are completely missed by classic measures of similarity. To demonstrate the utility of our new index, we reconstruct a morphological gradient driven by river flow velocity using random samples drawn from simulated and real-world data. Results suggest that the new index can be used to recognize complex short ecological gradients in settings where only information about specimens is available. We include open-source R code for calculating the proposed index.


2021 ◽  
Author(s):  
Bert van der Veen ◽  
Francis K.C. Hui ◽  
Knut A. Hovstad ◽  
Robert B. O’Hara

SummaryIn community ecology, unconstrained ordination can be used to predict latent variables from a multivariate dataset, which generated the observed species composition.Latent variables can be understood as ecological gradients, which are represented as a function of measured predictors in constrained ordination, so that ecologists can better relate species composition to the environment while reducing dimensionality of the predictors and the response data.However, existing constrained ordination methods do not explicitly account for information provided by species responses, so that they have the potential to misrepresent community structure if not all predictors are measured.We propose a new method for model-based ordination with constrained latent variables in the Generalized Linear Latent Variable Model framework, which incorporates both measured predictors and residual covariation to optimally represent ecological gradients. Simulations of unconstrained and constrained ordination show that the proposed method outperforms CCA and RDA.


2021 ◽  
pp. 125891
Author(s):  
J. Julio Camarero ◽  
Michele Colangelo ◽  
Patricia M. Rodríguez-González ◽  
Ángela Sánchez-Miranda ◽  
Raúl Sánchez-Salguero ◽  
...  

2021 ◽  
Author(s):  
Eleanor K O'Brien ◽  
Megan Higgie ◽  
Andrew D Saxon ◽  
Ary A. Hoffmann ◽  
Jon R Bridle

Evolutionary responses to environmental change require heritable variation in traits under selection. Both heritability and selection vary with the environment, and may also covary, meaning that environmental variation can be an important source of evolutionary constraint. However, estimates of heritability and selection along environmental gradients in the field are rare. We estimated environmental variation in selection on three traits (cold tolerance, heat tolerance and wing size) of the rainforest fly Drosophila birchii by transplanting flies in cages along two elevational gradients in north-east Queensland, Australia, and calculating the genetic covariance of trait values with cage productivity at each elevation. We estimated heritability of each trait from laboratory crosses, and environmental variation in heritability of wing size from the correlation of mothers and daughters in cages at each elevation. We then used estimates of selection and heritability to predict selection responses along the elevation gradients. Laboratory assays revealed low-moderate genetic variation in all traits and low covariation among traits, suggesting the potential for a strong response to selection. Estimated selection responses predicted divergence of cold tolerance with elevation at one gradient. However, this was not observed at either gradient, with no difference between high and low elevation populations for this trait. Despite substantial variation in heritability (and predicted selection response) of wing size, this appeared random with respect to elevation, preventing overall divergence and suggesting that local environmental variation constrains evolutionary responses along natural ecological gradients. Such an effect, if widespread, may significantly slow evolutionary responses to environmental change.


2021 ◽  
Author(s):  
Manfredo A. Turcios-Casco ◽  
Roberto Cazzolla Gatti ◽  
Gabriela Franzoi Dri ◽  
Niltón Cáceres ◽  
Richard Stevens ◽  
...  
Keyword(s):  

Author(s):  
Maria Papadopoulou ◽  
Ioannis Tsiripidis ◽  
Sampson Panajiotidis ◽  
Georgios Fotiadis ◽  
Daniel Veres ◽  
...  

AbstractDue to the complex relationship between pollen and vegetation, it is not yet clear how pollen diagrams may be interpreted with respect to changes in floristic diversity and only a few studies have hitherto investigated this problem. We compare pollen assemblages from moss samples in two southeastern European forests with the surrounding vegetation to investigate (a) their compositional similarity, (b) the association between their diversity characteristics in both terms of richness and evenness, and (c) the correspondence of the main ecological gradients that can be revealed by them. Two biogeographical regions with different vegetation characteristics, the Pieria mountains (north central Greece) and the slopes of Ciomadul volcano (eastern Romania), were chosen as divergent examples of floristic regions, vegetation structure and landscape openness. Pollen assemblages are efficient in capturing the presence or absence, rather than the abundance in distribution of plants in the surrounding area and this bias increases along with landscape openness and vegetation diversity, which is higher in the Pieria mountains. Pollen assemblages and vegetation correlate better in terms of richness, that is, low order diversity indices. Relatively high correlation, in terms of evenness, could be potentially found in homogenous and species poor ecosystems as for Ciomadul. Composition and diversity of woody, rather than herb, vegetation is better reflected in pollen assemblages of both areas, especially for Pieria where a direct comparison of the two components was feasible, although this depends on the species-specific pollen production and dispersal, the openness of landscape and the overall diversity of vegetation. Gradients revealed by pollen assemblages are highly and significantly correlated with those existing in vegetation. Pollen assemblages may represent the vegetation well in terms of composition, diversity (mainly richness) and ecological gradients, but this potential depends on land use, vegetation structure, biogeographical factors and plant life forms.


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