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At least 19 recordsLinked to original sources
PubMed1977

Food webs and the dimensionality of trophic niche space.

If the trophic niche of a kind of organism is a connected region in niche space, then it is possible for trophic niche overlaps to be described in a one-dimensional niche space if and only if the trophic niche overlap graph is an interval graph. An analysis of 30 food webs, using the combinatorial theory of interval graphs, suggests that a niche space of dimension 1 suffices, with unexpectedly high frequency and perhaps always, to describe the trophic niche overlaps implied by real food webs in single habitats. Consequently, real food webs fall in a small subset of the set of mathematically possible food webs. That real food webs are compatible with one-dimensional trophic niche spaces, more often than can be explained by chance alone, has not been noticed previously.

Journal Article↗
PubMed2026

Quantifying niche overlap and transgression in allopolyploid hybrids: Case study of Sorbus subgenus Aria.

BACKGROUND AND AIMS: Apomixis, the formation of seeds without recombination, facilitates adaptation and persistence under environmental change. By preserving hybrid genotypes over long time periods, apomixis may conserve adaptive trait combinations from parental niche margins. We tested whether apomictic entities occupy intermediate, marginal, or transgressive niche space relative to their parents and whether differentiation is associated with ploidy. METHODS: We studied polyploid Sorbus subgenus Aria in the Franconian Jura (Germany), comprising two progenitors Sorbus aria and S. collina, seven triploid entities, and a pool of genetically heterogenous individuals (single genotypes). Genetic structure was assessed using MIG-seq. Overall niche differentiation between parental taxa and hybrids was evaluated using Sørensen similarity of two-dimensional hypervolumes derived from principal component analysis (PCA) axes. Niche shifts were further analyzed using hypervolumes based on the three strongest PCA variables. Across 762 occurrences, observations ranged from 11 to 453 individuals per entity. KEY RESULTS: Environmental niche space was transgressive in three, significantly allocated towards the margins of parental niche space in one, while remaining intermediate in the other entities. Niche transgression occurred towards milder temperatures and drier conditions. Genetic analyses confirmed morphologically defined entities, although one morphotype was polyphyletic. Tetraploid S. collina significantly occupied warmer and wetter environments compared to other cytotypes. Triploids differed from S. aria along microtopographic gradients represented by the second PCA axis. CONCLUSIONS: Apomictic Sorbus entities show diverse strategies in niche occupation and can occupy environmental niche space at and beyond the limits of their parental taxa. Apomicts may conserve evolutionary adaptations at the edges of parental niche space that may otherwise be lost from, or fail to emerge in, the parental gene pool. Over long timescales these trait combinations may re-enter the parental gene pool through introgression, thereby reintroducing adaptations critical for survival under changing conditions.

Aria↗
PubMed2005

Dietary ecospace and the diversity of euprimates during the Early and Middle Eocene.

This study examined adapoid and omomyoid euprimate dietary and body size diversity from the Eocene of North America and Europe. Estimates of body weights and shearing quotients calculated from lower molars were plotted on a coordinate graph as a representation of dietary niche space (dietary ecospace) occupied by extinct species. By computing the areas, average intertaxon distances, and average distances from the centroid of the resulting polygons, comparisons of Eocene euprimate dietary and body size diversity were made. Results indicate that euprimate dietary niche space expanded significantly in North America from the Early to Middle Eocene, and at all times during the Early and Middle Eocene, the niche space occupied by North American euprimates exceeded that of corresponding European euprimates. These results confirm that fossil euprimate diversity, as measured by diet and body size, significantly differed across biogeographic areas. There are many possible explanations as to why North American euprimates were significantly more diverse in terms of diet and body size than their European counterparts. The explanation advocated here as most responsible for the increased diversity during the Early and Middle Eocene relates to the existence and increased sampling of more ecologically diverse environments, such as basin margins in the western interior of North America. These diverse environments could have promoted biological processes that led to the generation of increased diversity in North America compared to the isolated island refugia of Western Europe during this time.

Animals↗
PubMed1970

Ecological consequences of island colonization by southwest Pacific birds. II. The effect of species diversity on total population density.

Among southwest Pacific birds colonizing a species-poor island from a species-rich island, spatial expansion of the niche to include a wider range of altitudes, habitats, or vertical strata is often an immediate response, while changes in foraging techniques and diet usually occur more slowly and require genotypic change. Despite occupation of spatially broader niches by some colonizing species and increases in abundance by others, the total population density of the whole avifauna is up to nine times lower on a species-poor island than in a comparable habitat on a species-rich island. Total population density varies among islands approximately linearly with the number of species in the lowlands, supralinearly at higher elevations. Part of the explanation is that many birds on small islands expand into niche space which is suboptimal for them and from which they would be excluded by species utilizing this niche space optimally on a species-rich island. The other suggested explanation is an intrinsic inefficiency or loss of fitness among populations on small Pacific islands compared to large-island populations, due to impoverished gene pools, reduced selection pressure, and low degree of endemism.

Animals↗
PubMed2006

Population characteristics predict responses in moose body mass to temporal variation in the environment.

1. A general problem in population ecology is to predict under which conditions stochastic variation in the environment has the stronger effect on ecological processes. By analysing temporal variation in a fitness-related trait, body mass, in 21 Norwegian moose Alces alces (L.) populations, we examined whether the influence of temporal variation in different environmental variables were related to different parameters that were assumed to reflect important characteristics of the fundamental niche space of the moose. 2. Body mass during autumn was positively related to early access to fresh vegetation in spring, and to variables reflecting slow phenological development (low June temperature, a long spring with a slow plant progression during spring). In contrast, variables related to food quantity and winter conditions had only a minor influence on temporal variation in body mass. 3. The magnitude of the effects of environmental variation on body mass was larger in populations with small mean body mass or living at higher densities than in populations with large-sized individuals or living at lower densities. 4. These results indicate that the strongest influence of environmental stochasticity on moose body mass occurs towards the borders of the fundamental niche space, and suggests that populations living under good environmental conditions are partly buffered against fluctuations in environmental conditions.

Animals↗
PubMed2004

Echolocation signals reflect niche differentiation in five sympatric congeneric bat species.

Echolocating bats can be divided into guilds according to their preferred habitat and foraging behaviour, which coincide with distinct adaptations in wing morphology and structure of echolocation signals. Although coarse structuring of niche space between different guilds is generally accepted, it is not clear how niches differ within guilds, or whether there is fine-grained niche differentiation reflected in echolocation signal structure. Using a standardized performance test, here we show clutter-dependent differences in prey-capture success for bats from five species of European Myotis. These species are morphologically similar, sympatric, and all belong to the guild labelled "edge space aerial/trawling foragers". We further demonstrate a strong correlation between the prey-detection ability of the species and the respective search-call bandwidth. Our findings indicate that differences in echolocation signals contribute to within-guild niche differentiation. This is the first study relating sensory abilities of a set of potentially competing animal species to a direct measure of their respective foraging performance, suggesting an important role of sensory ecology in the structuring of animal communities.

Acoustics↗
PubMed2003

Contrasting flowering phenology and species richness in abiotically and biotically pollinated angiosperms.

Biotic pollination is thought to correlate with increased interspecific competition for pollination among plants and a higher speciation rate. In this study we compared patterns of flowering phenology and species richness between abiotically (wind) and biotically pollinated plants, using phylogenetically independent contrasts. We compiled phenological data from eight local seasonal floras, in which we found geographically overlapping sister clades. Of 65 documented origins of wind pollination, we were able to use up to 17 independent contrasts. In contrast to previous studies we found no difference in global species richness between wind- and biotically pollinated sister clades. Regarding phenology, we found wider phenological spread in biotically pollinated clades, earlier flowering onset in wind-pollinated trees, but no difference in duration of flowering between pollination modes. These results corroborate previous views that niche space is more constrained for wind-pollinated species, and that niche partitioning is less important between wind-pollinated plants compared to plants pollinated by animals.

Biodiversity↗
PubMed2006

Potential effects of climate change on ecosystem and tree species distribution in British Columbia.

A new ecosystem-based climate envelope modeling approach was applied to assess potential climate change impacts on forest communities and tree species. Four orthogonal canonical discriminant functions were used to describe the realized climate space for British Columbia's ecosystems and to model portions of the realized niche space for tree species under current and predicted future climates. This conceptually simple model is capable of predicting species ranges at high spatial resolutions far beyond the study area, including outlying populations and southern range limits for many species. We analyzed how the realized climate space of current ecosystems changes in extent, elevation, and spatial distribution under climate change scenarios and evaluated the implications for potential tree species habitat. Tree species with their northern range limit in British Columbia gain potential habitat at a pace of at least 100 km per decade, common hardwoods appear to be generally unaffected by climate change, and some of the most important conifer species in British Columbia are expected to lose a large portion of their suitable habitat. The extent of spatial redistribution of realized climate space for ecosystems is considerable, with currently important sub-boreal and montane climate regions rapidly disappearing. Local predictions of changes to tree species frequencies were generated as a basis for systematic surveys of biological response to climate change.

British Columbia↗
PubMed2006

Testing the niche apportionment hypothesis with parasite communities: is random assortment always the rule?

Niche apportionment models have only been applied once to parasite communities. Only the random assortment model (RA), which indicates that species abundances are independent from each other and that interspecific competition is unimportant, provided a good fit to 3 out of 6 parasite communities investigated. The generality of this result needs to be validated, however. In this study we apply 5 niche apportionment models to the parasite communities of 14 fish species from the Great Barrier Reef. We determined which model fitted the data when using either numerical abundance or biomass as an estimate of parasite abundance, and whether the fit of niche apportionment models depends on how the parasite community is defined (e.g. ecto, endoparasites or all parasites considered together). The RA model provided a good fit for the whole community of parasites in 7 fish species when using biovolume (as a surrogate of biomass) as a measure of species abundance. The RA model also fitted observed data when ecto- and endoparasites were considered separately, using abundance or biovolume, but less frequently. Variation in fish sizes among species was not associated with the probability of a model fitting the data. Total numerical abundance and biovolume of parasites were not related across host species, suggesting that they capture different aspects of abundance. Biovolume is not only a better measurement to use with niche-orientated models, it should also be the preferred descriptor to analyse parasite community structure in other contexts. Most of the biological assumptions behind the RA model, i.e. randomness in apportioning niche space, lack of interspecific competition, independence of abundance among different species, and species with variable niches in changeable environments, are in accordance with some previous findings on parasite communities. Thus, parasite communities may generally be unsaturated with species, with empty niches, and interspecific interactions may generally be unimportant in determining parasite community structure.

Animals↗
PubMed2006

Experimental verification of ecological niche modeling in a heterogeneous environment.

The current range of ecological habitats occupied by a species reflects a combination of the ecological tolerance of the species, dispersal limitation, and competition. Whether the current distribution of a species accurately reflects its niche has important consequences for the role of ecological niche modeling in predicting changes in species ranges as the result of biological invasions and climate change. We employed a detailed data set of species occurrence and spatial variation in biotic and abiotic attributes to model the niche of a native California annual plant, Collinsia sparsiflora. We tested the robustness of our model for both the realized and fundamental niche by planting seeds collected from four populations, representing two ecotypes, into plots that fully represented the five-dimensional niche space described by our model. The model successfully predicted which habitats allowed for C. sparsiflora persistence, but only for one of the two source ecotypes. Our results show that substantial niche divergence has occurred in our sample of four study populations, illustrating the importance of adequately sampling and describing within-species variation in niche modeling.

California↗
PubMed1976

Genetic variation in heterogeneous environments.

A model of population structure in heterogeneous environments is described and conditions sufficient for maintaining a polymorphism are derived. The absolute fitness of any genotype is regarded as a function of location in the niche space and the population density at that location. Two modes of habitat selection are examined: (1) organisms are distributed uniformly over the environment; and (2) each organism selects to occupy that habitat in which it is most fit ("optimal habitant selection"). Sufficient conditions for maintenance of genetic polymorphisms are derived for both models. In populations which do not practice habitat selection heterozygote superiority averaged over the environment is sufficient to guarantee the existence of polymorphisms. Comparable conditions for populations which practice optimal habitat selction are much less restrictive. If the heterozygotes are superior to one homozygote in any one part of the niche and to the other homozygote in any other part of the niche then a polymorphism will be defined. A positive correlation between genetic and environmental variation follows from the model with habitat selection, but not from the other. The adaptive significance of polymorphisms thus depends on how animals behave.

Environment↗
PubMed2006

[Growth patterns of Leymus chinensis clones under different habitat conditions in Songnen Plain of China].

A tracking investigation was conducted in the Songnen Plain of China on the experimental clones of Leymus chinensis under cultivation, and the natural clones of this grass in the succession process of vegetation restoration after meadow flooding. The results showed that on aeolian sandy soil where existed enough growth space but no interspecific competition, there was a month interval between the transplanting of two experimental clones, and the sizes of these clones had a one-fold difference by the end of next growth season. During the whole growth season, the vegetative reproduction of the two experimental clones followed the same exponential pattern. After 6 years restoration succession on flooded meadow, the vegetative reproduction of clonal populations in L. chinensis + Carex duriuscula and L. chinensis + weed communities were all accorded with power function. On flooded alkaline meadow where existed interspecific competition, the natural clones could still increase their offspring numbers exponentially, and quickly expand their niche space at the same time.

China↗
PubMed1994

Superinfection, metapopulation dynamics, and the evolution of diversity.

Using both analytic and numerical methods, we elucidate the dynamical properties of a class of metapopulation models in which many different species/strains contend for persistence, with local extinction of subpopulations being balanced by colonization of other patches. The species/strains have a strict competitive hierarchy with a given species/strain "taking over" any patch occupied by a lower-ranking species/strain; competitively inferior species/strains compensate by having higher colonization rates and/or lower patch death rates. New species/strains keep appearing, so that we can follow the evolution of the system. Such models may be metaphors for multispecies metapopulations, or for the evolution of virulence (where the patches are hosts, who are infected with various strains of a pathogen, and then die or recover at strain-dependent rates). Our emphasis is on a set of questions relating to the evolution of diversity. How many species/strains are present after a long time, t? Asymptotically, this number continues to increase very slowly, as ln t. What are the relative abundances of the species/strains? Under a broad range of assumptions about the mutations which produce new species/strains, the rank-abundance distribution is roughly geometric (as is commonly observed in early succession and other "ecologically one-dimensional" situations); some of our analysis here is based in part on an interesting but unproved mathematical conjecture about a new kind of probabilistic/combinatorial problem. If the number of patches/hosts is permanently reduced--by habitat destruction or vaccination--what happens? Characteristically, there is an initial sharp loss of species/strains (with selective removal of the competitive dominants), with subsequent slow recovery as new mutants continue to partition the now-diminished "niche space" (but the pristine levels of virulence are not regained).

Animals↗
PubMed2004

Habitat structural complexity and morphological diversity of fish assemblages in a Neotropical floodplain river.

High species richness and evenness in structurally complex habitats has been hypothesized to be associated with niche partitioning. To test this idea, relationships between habitat structural complexity in river littoral-zone habitats and morphological diversity of tropical fishes were examined in the Cinaruco River, Venezuela. Six habitat attributes were quantified in 45 sites spanning a range of structural complexity. Fishes were collected during day and night to estimate species density and relative abundances at each site. Twenty-two morphological variables were measured for each species. Principal components analysis (PCA) of physical habitat data yielded two axes that modeled >80% of variation across sites. The first two axes from PCA of fish morphological variables modeled >70% of variation. Species density during both day and night was negatively associated with flow velocity and positively associated with habitat complexity. Similarity of day and night samples from the same site was significantly greater for sites with high habitat complexity and low flow. In general, mean local assemblage morphological PC scores were not significantly associated with habitat PC scores. Average, maximum, and standard deviation of morphological Euclidean distances of local assemblages revealed positive associations with structural complexity and negative associations with flow. These relationships held even when the positive relationship of species density was statistically removed from assemblage morphological patterns. Findings suggest that both species niche compression and assemblage niche space increase when habitat complexity is greater and flow velocity is lower in this tropical lowland river.

Animals↗
PubMed2004

Comparative methods based on species mean values.

Comparative methods that use simple linear regression based on species mean values introduce three difficulties with respect to the standard regression model. First, species values may not be independent because they form part of a hierarchically structured phylogeny. Second, variation about the regression line includes two sources of error: 'biological error' due to deviations of the true species mean values from the regression line and sampling error associated with the estimation of these mean values [B. Riska, Am. Natural. 138 (1991) 283]. Third, sampling error in the independent variable results in an attenuated estimate of the regression slope. We consider estimation and hypothesis testing using two statistical models which explicitly justify the use of the species mean values, without the need to account for phylogenetic relationships. The first (random-effects) is based on an evolutionary model whereby species evolve to fill a bivariate normal niche space, and the second (fixed-effects) is concerned with describing a relationship among the particular species included in a study, where the only source of error is in the estimation of species mean values. We use a modification of the maximum-likelihood method to obtain an unbiased estimate of the regression slope. For three real datasets we find a close correspondence between this slope and that obtained by simply regressing the species mean values on each other. In the random effects model, the P-value also approximates that based on the regression of species mean values. In the fixed effects model, the P-value is typically much lower. Simulated examples illustrate that the maximum-likelihood approach is useful when the accuracy in estimating the species mean values is low, but the traditional method based on a regression of the species mean values may often be justified provided that the evolutionary model can be justified.

Acer↗
PubMed2002

Ecology and biogeography of marine parasites.

A review is given of (mainly recent) work on the biodiversity, ecology, biogeography and practical importance of marine parasites. Problems in estimating species numbers have been thoroughly discussed for free-living species, and the main points of these discussions are reviewed here. Even rough estimates of the richness of most parasite groups in the oceans are premature for the following reasons: species numbers of host groups, in particular in the deep sea and the meiofauna, are not known; most host groups have been examined only insufficiently for parasites or not at all; even in some of the best known groups, latitudinal, longitudinal and depth gradients in species richness are only poorly understood or not known at all; effects of hosts on parasite morphology and geographical variation have been studied only in a few cases; there are few studies using techniques of molecular biology to distinguish sibling species. Estimates of species richness in the best known groups, trematodes, monogeneans and copepods of marine fishes, are given. Parasites are found in almost all taxa of eukaryotes, but most parasitic species are concentrated in a few taxa. Important aspects of the ecology of marine parasites are discussed. It is emphasized that host specificity and host ranges should be distinguished, and an index that permits calculation of host specificity is discussed. The same index can be applied to measure site specificity. Central problems in ecology are the importance of interspecific competition and whether equilibrium or non-equilibrium conditions prevail. Marine parasites are among the few groups of organisms that have been extensively examined in this regard. A holistic approach, i.e. application of many methods, has unambiguously shown that metazoan ecto- (and probably endo-) parasites of marine fish live in largely non-saturated niche space under non-equilibrium conditions, i.e. they live in assemblages rather than in communities structured by competition. Nestedness occurs in such assemblages, but it can be explained by characteristics of the species themselves. There is little agreement on which other factors are involved in "structuring" parasite assemblages. Few studies on metapopulations of marine parasites have been made. A new approach, that of fuzzy chaos modelling, is discussed. It is likely that marine parasites are commonly found in metapopulations consisting of many subpopulations, and they are ideally suited to test the predictions of fuzzy chaos. Some recent studies on functional ecology and morphology--especially with regard to host, site and mate finding--are discussed, and attention is drawn to the amazing variety of sensory receptors in some marine parasites. Effects of parasites on hosts, and some studies on the evolution and speciation of marine parasites are discussed as well. A detailed overview of biogeographical studies is given, with respect to latitudinal gradients in species diversity, reproductive strategies and host ranges/specificity. Studies of marine parasites have contributed significantly to giving a non-equilibrium explanation for latitudinal diversity gradients. Recent studies on longitudinal and depth gradients are discussed, as well as parasites in brackish water, parasites as indicators of zoogeographical regions and barriers, and parasites as biological tags. The practical importance of marine parasites in mariculture, as monitors of pollution, agents of human disease, the use of parasites for controlling introduced marine pests, and some related aspects, are also discussed.

Animals↗
PubMed2001

Interactions between species and the structure of helminth communities.

The role of interspecific interactions in the structure of gastrointestinal helminth communities has been at the core of most research in parasite community ecology, yet there is no consensus regarding their general importance. There have been two different approaches to the study of species interactions in helminths. The first one consists of measuring the responses of helminth species in concomitant infections, preferably in laboratory experiments. Any change in numbers of parasite individuals or in their use of niche space, compared with what is observed in single infections, provides solid evidence that the species are interacting. The second approach can only provide indirect, circumstantial evidence. It consists in contrasting observed patterns either in the distribution of species richness of infracommunities from wild hosts, in their species composition, or in pairwise associations between helminth species among infracommunities, with the random patterns predicted by appropriate null models. In many cases, observed patterns do not depart from predicted ones; when they do, alternative explanations are usually as plausible as invoking the effect of interactions among helminth species. The present evidence suggests that the role of species interactions in helminth community structure is often negligible, but that it must always be evaluated on a case-by-case basis.

Animals↗