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Fangliang He

Publications and source records attributed to Fangliang He.

10 recordsLinked to original sources
PubMed2006

Nonrandom processes maintain diversity in tropical forests.

An ecological community's species diversity tends to erode through time as a result of stochastic extinction, competitive exclusion, and unstable host-enemy dynamics. This erosion of diversity can be prevented over the short term if recruits are highly diverse as a result of preferential recruitment of rare species or, alternatively, if rare species survive preferentially, which increases diversity as the ages of the individuals increase. Here, we present census data from seven New and Old World tropical forest dynamics plots that all show the latter pattern. Within local areas, the trees that survived were as a group more diverse than those that were recruited or those that died. The larger (and therefore on average older) survivors were more diverse within local areas than the smaller survivors. When species were rare in a local area, they had a higher survival rate than when they were common, resulting in enrichment for rare species and increasing diversity with age and size class in these complex ecosystems.

Biodiversity↗
PubMed2006

Abundance, spatial variance and occupancy: arthropod species distribution in the Azores.

1. The positive abundance-occupancy and abundance-variance relationships are two of the most widely documented patterns in population and community ecology. 2. Recently, a general model has been proposed linking the mean abundance, the spatial variance in abundance, and the occupancy of species. A striking feature of this model is that it consists explicitly of the three variables abundance, variance and occupancy, and no extra parameters are involved. However, little is known about how well the model performs. 3. Here, we show that the abundance-variance-occupancy model fits extremely well to data on the abundance, variance and occupancy of a large number of arthropod species in natural forest patches in the Azores, at three spatial extents, and distinguishing between species of different colonization status. Indeed, virtually all variation about the bivariate abundance-occupancy and abundance-variance relationships is effectively explained by the third missing variable (variance in abundance in the case of the abundance-occupancy relationship, and occupancy in the case of the abundance-variance relationship). 4. Introduced species tend to exhibit lower densities, less spatial variance in these densities, and occupy fewer sites than native and endemic species. None the less, they all lie on the same bivariate abundance-occupancy and abundance-variance, and trivariate abundance-variance-occupancy, relationships. 5. Density, spatial variance in density, and occupancy appear to be all the things one needs to know to describe much of the spatial distribution of species.

Animals↗
PubMed2006

Comparing tropical forest tree size distributions with the predictions of metabolic ecology and equilibrium models.

Tropical forests vary substantially in the densities of trees of different sizes and thus in above-ground biomass and carbon stores. However, these tree size distributions show fundamental similarities suggestive of underlying general principles. The theory of metabolic ecology predicts that tree abundances will scale as the -2 power of diameter. Demographic equilibrium theory explains tree abundances in terms of the scaling of growth and mortality. We use demographic equilibrium theory to derive analytic predictions for tree size distributions corresponding to different growth and mortality functions. We test both sets of predictions using data from 14 large-scale tropical forest plots encompassing censuses of 473 ha and > 2 million trees. The data are uniformly inconsistent with the predictions of metabolic ecology. In most forests, size distributions are much closer to the predictions of demographic equilibrium, and thus, intersite variation in size distributions is explained partly by intersite variation in growth and mortality.

Biomass↗
PubMed2005

Seed and pollen flow in expanding a species' range.

The distinct processes of gene flow via seeds and pollen in hermaphrodite plants provide a biological basis for interpreting their different roles in expanding a species' range. A species' range is primarily expanded through the colonization process by seed dispersal and followed by the joint effects of both seed and pollen flow. Here we examined the effects of seed and pollen flow on shaping a species' distribution in one-dimensional space. Our results demonstrate that pollen flow can enhance range expansion when immigrating genes are adaptive to recipient populations, but can shrink a species' range when immigrating genes are maladaptive. The incompletely purging of maladaptive genes from immigrating pollen grains at the gametophyte stage can reinforce the biological barrier to range expansion. The linkage disequilibria attained by immigrating seeds and pollen grains indirectly amplify the effects of the reaction component and further limit a species' range. The cumulative effect from multiple loci each with a small effect can be substantial on altering a species' range when these genes are maladaptive. These theoretical predictions can help understand the role of pollen flow that is incapable of colonizing new habitats in range expansion.

Gene Flow↗
PubMed2005

Density dependence explains tree species abundance and diversity in tropical forests.

The recurrent patterns in the commonness and rarity of species in ecological communities--the relative species abundance--have puzzled ecologists for more than half a century. Here we show that the framework of the current neutral theory in ecology can easily be generalized to incorporate symmetric density dependence. We can calculate precisely the strength of the rare-species advantage that is needed to explain a given RSA distribution. Previously, we demonstrated that a mechanism of dispersal limitation also fits RSA data well. Here we compare fits of the dispersal and density-dependence mechanisms for empirical RSA data on tree species in six New and Old World tropical forests and show that both mechanisms offer sufficient and independent explanations. We suggest that RSA data cannot by themselves be used to discriminate among these explanations of RSA patterns--empirical studies will be required to determine whether RSA patterns are due to one or the other mechanism, or to some combination of both.

Biodiversity↗
PubMed2005

Background selection and population differentiation.

A general analytical formula is derived, which predicts the effects of background selection on population differentiation at a neutral locus as a result of its linkage with selected loci of deleterious mutations. The theory is based on the assumptions of random mating, multiplicative fitness, and weak selection in hermaphrodite plants in the island model of population structure. The analytical results show that Fst at the neutral locus increases as a result of the effects of background selection, regardless of the dependence or independence among linked background selective loci. The increment in Fst is closely related to the magnitude of linkage disequilibria between the neutral locus and selected loci, and can be estimated by the ratio of Fst with background selection to Fst without background selection minus one. The steady-state linkage disequilibrium between a neutral locus and a selected locus in subpopulations, primarily attained by gene flow, decreases with the recombination rate, and can be enhanced when there are dependence among linked selected loci. Monte Carlo computer simulations with two- and three-locus models show that the analytical formulae perform well under general conditions. Application of the present theory may aid in analyzing the genome-wide mapping of the effect of background selection in terms of Fst.

Computer Simulation↗
PubMed2003

Percolation theory for the distribution and abundance of species.

We develop and test new models that unify the mathematical relationships among the abundance of a species, the spatial dispersion of the species, the number of patches occupied by the species, the edge length of the occupied patches, and the scale on which the distribution of species is mapped. The models predict that species distributions will exhibit percolation critical thresholds, i.e., critical population abundances at which the fragmented patches (as measured by the number of patches and edge length) start to coalesce to form large patches.

Croton↗
PubMed2002

The distribution of species range size: a stochastic process.

The major role played by environmental factors in determining the geographical range sizes of species raises the possibility of describing their long-term dynamics in relatively simple terms, a goal which has hitherto proved elusive. Here we develop a stochastic differential equation to describe the dynamics of the range size of an individual species based on the relationship between abundance and range size, derive a limiting stationary probability model to quantify the stochastic nature of the range size for that species at steady state, and then generalize this model to the species-range size distribution for an assemblage. The model fits well to several empirical datasets of the geographical range sizes of species in taxonomic assemblages, and provides the simplest explanation of species-range size distributions to date.

Animals↗
PubMed1998

Histological response of resistant and susceptible white spruce to simulated white pine weevil damage.

The traumatic wound response of families of white spruce, Picea glauca (Moench) Voss, resistant or susceptible to the white pine weevil, Pissodes strobi (Peck), were compared after simulated weevil damage. Leaders from 331 trees were wounded just below the apical bud in the spring, coinciding with the natural time of weevil oviposition. A portable 1-mm diameter drill was used to drill 24 holes per leader. Leaders were removed in the fall and examined for evidence of traumatic resin canal formation. Drilled trees had a traumatic wound response 8 times greater than that of undrilled trees; however, undrilled trees also formed some resin canals in response to unknown causes. In the drilled trees, the traumatic wound response extended into the lower part of the leader, where it could possibly affect older larvae. Trees from resistant families responded with greater intensity than trees from susceptible families, by producing multiple rings of traumatic resin canals. Trees from resistant families also responded more rapidly than trees from susceptible families based on number of cells to the first ring of traumatic resin canals. Trees from some resistant families exhibited no traumatic resin canal formation, showing considerable within-family variation and suggesting that other resistance mechanisms might be important. In the year after drilling, there was a reduction in tree diameter growth and trees suffered a reduction in constitutive resin canals in the bark, which suggests some energetic cost of traumatic resin production. There was no indication that the extent of constitutive defenses, as measured by density of cortical resin canals before wounding, was related to the ability to produce traumatic resin canals. Screening trees based on their capacity to produce traumatic resin canals may be useful in selecting genotypes resistant to white pine weevil.

Journal Article↗