Search results for "phylogenetic diversity"
showing 10 items of 19 documents
SELECTING HERB-RICH FOREST NETWORKS TO PROTECT DIFFERENT MEASURES OF BIODIVERSITY
2001
Data on vascular plants of herb-rich forests in Finland were used to compare the efficiency of reserve selection methods in representing three measures of biodiversity: species richness, phylogenetic diversity, and restricted-range diversity. Comparisons of reserve selection methods were carried out both with and without consideration of the existing reserve system. Our results showed that the success of a reserve network of forests in representing different measures of biodiversity depends on the selection procedure, selection criteria, and data set used. Ad hoc selection was the worst option. A scoring procedure was generally more efficient than maximum random selection. Heuristic methods…
Plant-animal interactions in fire-prone ecosystems
2018
SÍNTESIS Estudiar cómo responden las interacciones ecológicas a las perturbaciones es clave para abordar la creciente pérdida de biodiversidad en diferentes ecosistemas. En la Tierra existen especies que han evolucionado ante la presencia recurrente de perturbaciones naturales, como ocurre en ecosistemas con incendios frecuentes. En ellos el fuego se originó poco después de la aparición de las primeras plantas terrestres y también algunos de los patrones de incendios característicos que todavía permanecen. Sin embargo, las actividades humanas están alterando los patrones naturales de incendios, lo que puede suponer una amenaza incluso para las especies que presentan una rápida recuperación …
Selecting networks of nature reserves: methods do affect the long-term outcome
1999
Data on vascular plants of boreal lakes in Finland were used to compare the efficiency of reserve selection methods in representing four aspects of biodiversity over a 63 year period. These aspects included species richness, phylogenetic diversity, restricted range diversity and threatened species. Our results show that the efficiency of reserve selection methods depends on the selection criteria used and on the aspect of biodiversity under consideration. Heuristic methods and optimizing algorithms were nearly equally efficient in selecting lake networks over a small geographical range. In addition, a scoring procedure was observed to be efficient in maintaining different aspects of biodive…
Formally described species woefully underrepresent phylogenetic diversity in the common lichen photobiont genus Trebouxia (Trebouxiophyceae, Chloroph…
2020
Lichens provide valuable systems for studying symbiotic interactions. In lichens, these interactions are frequently described in terms of availability, selectivity and specificity of the mycobionts and photobionts towards one another. The lichen-forming, green algal genus Trebouxia Puymaly is among the most widespread photobiont, associating with a broad range of lichen-forming fungi. To date, 29 species have been described, but studies consistently indicate that the vast majority of species-level lineages still lack formal description, and new, previously unrecognized lineages are frequently reported. To reappraise the diversity and the evolutionary relationships of species-level lineages …
Assembly rules of helminth parasite communities in grey mullets: combining components of diversity.
2020
Abstract Organisms aggregate in ecological communities. It has been widely debated whether these associations are explained by deterministic or, in contrast, random processes. The answer may vary, depending on the level of an organisational scale (α, β and γ) and the facet of diversity considered: taxonomic, functional and phylogenetic. Diversity at the level of a sampling unit (i.e. host individual) is the α diversity; β diversity represents the extent of dissimilarity in diversity among sampling units (within a level of an organisational scale, β1; between levels of an organisational scale, β2); and the total diversity of a system is γ diversity. Thus, the combination of facets and levels…
Microbial communities of polluted sub-surface marine sediments
2018
Abstract Microbial communities of coastal marine sediment play a key role in degradation of petroleum contaminants. Here the bacterial and archaeal communities of sub-surface sediments (5–10 cm) of the chronically polluted Priolo Bay (eastern coast of Sicily, Italy), contaminated mainly by n-alkanes and biodegraded/weathered oils, were characterized by cultural and molecular approaches. 16S-PCR-DGGE analysis at six stations, revealed that bacterial communities are highly divergent and display lower phylogenetic diversity than the surface sediment; sub-surface communities respond to oil supplementation in microcosms with a significant reduction in biodiversity and a shift in composition; the…
Degradation in landscape matrix has diverse impacts on diversity in protected areas.
2017
Introduction: A main goal of protected areas is to maintain species diversity and the integrity of biological assemblages. Intensifying land use in the matrix surrounding protected areas creates a challenge for biodiversity conservation. Earlier studies have mainly focused on taxonomic diversity within protected areas. However, functional and especially phylogenetic diversities are less studied phenomena, especially with respect to the impacts of the matrix that surrounds protected areas. Phylogenetic diversity refers to the range of evolutionary lineages, the maintenance of which ensures that future evolutionary potential is safeguarded. Functional diversity refers to the range of ecologic…
New Algorithms for Computing Phylogenetic Biodiversity
2014
A common problem that appears in many case studies in ecology is the following: given a rooted phylogenetic tree \(\mathcal{T}\) and a subset R of its leaf nodes, we want to compute the distance between the elements in R. A very popular distance measure that can be used for this reason is the Phylogenetic Diversity (PD), which is defined as the cost of the minimum weight Steiner tree in \(\mathcal{T}\) that spans the nodes in R. To analyse the value of the PD for a given set R it is important also to calculate the variance of this measure. However, the best algorithm known so far for computing the variance of the PD is inefficient; for any input tree \(\mathcal{T}\) that consists of n nodes…
Plant facilitation and phylogenetics
2013
The relationship between facilitation and evolutionary ecology is poorly understood. We review five issues elucidating how the phylogenetic relatedness of species provides insight into the role of facilitation in community assembly: (a) Are the facilitative interactions more common between species that differ in a regeneration niche? (b) Are facilitative interactions more common between distantly related species? (c) Do communities governed by facilitation (rather than competition) have higher phylogenetic diversity? (d) As facilitated juvenile plants mature, do they compete with their nurses more often if they are closely related to them? (e) How does the phylogenetic signature in a commun…
Ammonoid recovery after the Permian-Triassic mass extinction: a re-exploration of morphological and phylogenetic diversity patterns.
2013
The explosive ammonoid rediversification after the Permian–Triassic mass extinction is now well understood in terms of taxonomic richness and biogeography. Using an updated dataset of Early Triassic ammonoids, we compare morphological disparity and taxonomic richness patterns at the regional and global scales. Disparity evolved similarly at both scales, suggesting a global influence of abiotic factors. Morphological diversification occurred early in the Smithian and a marked contraction of the morphospace took place during the end-Smithian extinction. We confirm that trends in disparity and richness were decoupled during the Griesbachian and Dienerian. Three macroevolutionary processes may …