Secular changes in growth and obesity in perinatal population

The survey was conducted during the last 25 years and included 2414 healthy women who delivered in "Sestre milosrdnice" University Hospital Center in Zagreb, Croatia and their newborns. The aim was to establish the secular trend of some anthropological factors through two generations. Anthropological features such as pre-pregnancy weight, body mass index before pregnancy, height, age, place of residence, educational level, parity and the newborn weight were registered. The study was randomized. The mothers from the city of Zagreb and the surrounding villages, rural areas are examined. The women age was different and also different levels of education and socioeconomic status. The study included women who had not given birth yet, who had delivered once, twice, and three or more times. Maternal height in 25 years increased by 3.1cm. and increases with education. The pre-pregnancy weight increased 2.8 kg and increases with age, parity and rural life. The body mass index (BMI) which the women had before pregnancy was calculated, and according to its value the participants were divided in three groups: with normal weight, overweight and fat. Among the studied periods BMI does not differ significantly, but does differ significantly with respect to the ordinal number of births, parity, age and living environment. Higher BMI was associated with deliveries to heavier children.     

Temporal changes in pollen flow and neighbourhood structure in a population of Saxifraga hirculus L.

Summary The population are of flowering shoots of the perennial herb, Saxifraga hirculus, reaches a max. of 134 m² and an overall density of flowers/m² of 11.4. The flower is mainly visited by a syrphid sp., Eurimyia lineata, and to a lesser extent by another syrphid Neoscia tenur, a moth, Zygaena trifolii, and a fungus gnat, Asindulum nigrum. The distribution of the interfloral flight distance is leptokurtic. The mean flight distance of the visitors is 101 cm. 10% of the flights are much longer (2–8 m: cross-flower patch, and about 20 m: cross-population flights). If they are not included, the mean of flights (<1.7 m) becomes 28 cm. These flights become shorter with increasing flower density. The visitors do not have a nearest-neighbour foraging pattern. They visit on average the 8th nearest neighbour. The distribution of flight directions is uniform. Seed dispersal distances have a leptokurtic distribution and a mean dispersal distance of 13 cm. The ecological neighbourhood area is 66.4 m² and 64.9 m² assuming normality and allowing for leptokurtosis. Z. trifolii with its large proportion of long flights increases the size of the neighbourhood area considerably. The mean flight distance (<1.7 m) is correlated with neighbourhood area. The evolutionary impact of moths and butterflies to plant population structure is stressed.     

Glucocorticoid receptors in WI-38 fibroblasts: characterization and changes with population doubling in culture.

A high-affinity dexamethasone binding macromolecule was identified in WI-38 human fetal lung fibroblasts. High specificity of binding for glucocorticoids was shown by competition studies in which binding of dexamethasone was inhibited by cortisol and corticosterone but not by testosterone or 17 beta-estradiol. WI-38 cells exposed to [3H]dexamethasone at 30 degrees C were able to transfer the 3H-labeled steroid-receptor complex to the nuclear materal. A reduction of 30--50% was observed in the number of [3H]dexamethasone-receptor binding sites per cell as well as in the nuclear fraction of the cells as a function of age (passage levels 27 and 54). However, in the same cells no significant changes in affinity of receptor for [3H]dexamethasone as a function of the two passage levels were detected.     

Microbial population changes during bioremediation of an experimental oil spill.

Three crude oil bioremediation techniques were applied in a randomized block field experiment simulating a coastal oil spill. Four treatments (no oil control, oil alone, oil plus nutrients, and oil plus nutrients plus an indigenous inoculum) were applied. In situ microbial community structures were monitored by phospholipid fatty acid (PLFA) analysis and 16S rDNA PCR-denaturing gradient gel electrophoresis (DGGE) to (i) identify the bacterial community members responsible for the decontamination of the site and (ii) define an end point for the removal of the hydrocarbon substrate. The results of PLFA analysis demonstrated a community shift in all plots from primarily eukaryotic biomass to gram-negative bacterial biomass with time. PLFA profiles from the oiled plots suggested increased gram-negative biomass and adaptation to metabolic stress compared to unoiled controls. DGGE analysis of untreated control plots revealed a simple, dynamic dominant population structure throughout the experiment. This banding pattern disappeared in all oiled plots, indicating that the structure and diversity of the dominant bacterial community changed substantially. No consistent differences were detected between nutrient-amended and indigenous inoculum-treated plots, but both differed from the oil-only plots. Prominent bands were excised for sequence analysis and indicated that oil treatment encouraged the growth of gram-negative microorganisms within the alpha-proteobacteria and Flexibacter-Cytophaga-Bacteroides phylum. alpha-Proteobacteria were never detected in unoiled controls. PLFA analysis indicated that by week 14 the microbial community structures of the oiled plots were becoming similar to those of the unoiled controls from the same time point, but DGGE analysis suggested that major differences in the bacterial communities remained.     

Dynamics of numerical changes in human population in terms of animal population ecology

The author uses data concerning the natural regulation of population size and growth among animals to consider possible future scenarios for human population growth. Four possible variants are considered: "numerical stabilization and its consequences connected with density effect; sharp slump caused by a global ecological catastrophe; limited slump brought about by exhaustion of resources and environmental pollution; numerical decrease through birth regulation. It has been shown that only the last variant can, in [the] case of the human population being 1.2-1.5 billion people, ensure restoration of [the] biosphere with keeping [the] existing tempo of scientific-technological progress." (SUMMARY IN ENG)     

The extent of complex population changes in nature

Summary Many models of animal populations show complex yet predictable patterns of density changes under simple and plausible assumptions. Yet one previous attempt to determine the extent and importance of complex dynamics concluded that they were likely only in some laboratory populations, but not in field populations. Ecologists have treated changes more complex than a return to a simple equilibrium, such as the cyclical changes in populations of lynx and voles in the arctic, as special cases. Highly variable populations, such as insects, are usually thought to be driven by unpredictable changes in the weather. Here, we assemble 71 populations counted for over 50 years, and suggest that complex yet predictable population changes are more common than previously thought.     

Disequilibrium among several linked neutral genes in finite population I. Mean changes in disequilibrium

Formulae are developed for computing changes in expected values in a finite population of linkage disequilibrium among neutral genes from more than two loci, although the exact analysis is taken up to only six loci. An essentially haploid model is used. As with two loci, the three-locus disequilibrium declines exponentially at all generations, but for m > 3 loci a matrix has to be constructed to give joint changes in the m-locus disequilibrium and products of disequilibria with fewer loci, for example of two m/2-locus disequilibria. The asymptotic rates of change in multilocus disequilibria depend on the arrangement of genes on the chromosome as well as its total length, but the initial rate of breakdown of disequilibrium from a line cross base is less dependent on the arrangement. With equally spaced loci the asymptotic rate of breakdown of m locus disequilibrium is roughly proportional to m. Although mutation and interference are excluded from the main analysis, it is shown how they can be incorporated.     

Disequilibrium among several linked neutral genes in finite population 1. mean changes in disequilibrium

Formulae are developed for computing changes in expected values in a finite population of linkage disequilibrium among neutral genes from more than two loci, although the exact analysis is taken up to only six loci. An essentially haploid model is used. As with two loci, the three-locus disequilibrium declines exponentially at all generations, but for m > 3 loci a matrix has to be constructed to give joint changes in the m-locus disequilibrium and products of disequilibria with fewer loci, for example of two $\text{m}\text{2}\text{-}\text{locus}$ disequilibria. The asymptotic rates of change in multilocus disequilibria depend on the arrangement of genes on the chromosome as well as its total length, but the initial rate of breakdown of disequilibrium from a line cross base is less dependent on the arrangement. With equally spaced loci the asymptotic rate of breakdown of m locus disequilibrium is roughly proportional to m. Although mutation and interference are excluded from the main analysis, it is shown how they can be incorporated.     

Using maximum likelihood to estimate population size from temporal changes in allele frequencies.

We develop a maximum-likelihood framework for using temporal changes in allele frequencies to estimate the number of breeding individuals in a population. We use simulations to compare the performance of this estimator to an F-statistic estimator of variance effective population size. The maximum-likelihood estimator had a lower variance and smaller bias. Taking advantage of the likelihood framework, we extend the model to include exponential growth and show that temporal allele frequency data from three or more sampling events can be used to test for population growth.     

Algal-periphyton population and community changes from zinc stress in stream mesocosms

Three treatments of zinc (0.05, 0.5, 1.0 mg Zn l⁻¹) and a control could be identified by different algal communities in outdoor, flow-through, stream mesocosms. Established communities were continuously exposed to Zn, and samples were collected on days 0, 2, 5, 10, 20 and 30 after treatment began. Experiments were conducted in spring, summer, and fall 1984. Control stream mesocosms could be identified by diatoms in all seasons. The 0.05 mg Zn l⁻¹ treatment could be identified by certain diatom taxa being more abundant than in the control in all seasons and by a filamentous green alga in summer and fall. The 0.5 mg Zn l⁻¹ treatment could be identified by a filamentous green alga in fall. The 1.0 mg Zn l⁻¹ treatment was dominated by unicellular green algae in all seasons and by a filamentous blue-green alga in summer. A similarity index (SIMI) indicated that Zn-stressed samples generally became less similar to control samples as Zn concentration increased from 0.05 to 1.0 mg Zn l⁻¹. Total biovolume-density of all taxa responded slower than individual taxa in spring and failed to distinguish between Zn treatments in summer and fall. Zinc bound to periphyton was much better than total Zn in water for identifying Zn treatments. Zinc treatments as low as 0.05 mg Zn l⁻¹ changed algal species composition despite 0.047 mg Zn l⁻¹ being the Criterion of the US Environmental Protection Agency for the 24-h average of total recoverable Zn.     

Geographical variation in species' population responses to changes in temperature and precipitation

Despite increasing concerns about the vulnerability of species'' populations to climate change, there has been little overall synthesis of how individual population responses to variation in climate differ between taxa, with trophic level or geographically. To address this, we extracted data from 132 long-term (greater than or equal to 20 years) studies of population responses to temperature and precipitation covering 236 animal and plant species across terrestrial and freshwater habitats. Our results identify likely geographical differences in the effects of climate change on populations and communities in line with macroecological theory. Temperature tended to have a greater overall impact on populations than precipitation, although the effects of increased precipitation varied strongly with latitude, being most positive at low latitudes. Population responses to increased temperature were generally positive, but did not vary significantly with latitude. Studies reporting significant climatic trends through time tended to show more negative effects of temperature and more positive effects of precipitation upon populations than other studies, indicating climate change has already impacted many populations. Most studies of climate change impacts on biodiversity have focused on temperature and are from middle to high northern latitudes. Our results suggest their findings may be less applicable to low latitudes.     

Effect of changes in population size on genetic microdifferentiation

Changes in local population size are expected to have an effect on the degree of genetic microdifferentiation. A decrease in population size is expected to lead to an increase in microdifferentiation, and an increase in population size to a decrease in microdifferentiation. These expectations are routinely used with historical and/or demographic data to evaluate changes in estimates of microdifferentiation obtained over time for human populations. Here I look more closely at these expectations by using simple mathematical models that relate a change in average effective population size to the degree of microdifferentiation. The direction of change in microdifferentiation is influenced by the migration structure of the populations and the proximity of the region to an equilibrium state. A change in population size always leads to a new equilibrium, but the speed at which this new equilibrium is reached depends on migration and time depth. A decline in population size in one generation always leads to an immediate increase in the degree of microdifferentiation. An increase in population size in one generation could lead to an initial decrease or increase in the degree of microdifferentiation or to no change at all. Consideration of the parameters of the models shows under what conditions such changes occur. The relevance of these models is explored using summary data from a number of human populations.