Nested Faunas and Extinction in Fragmented Habitats

Abstract: The faunas of habitat islands, such as those produced by fragmentation of formerly continuous habitats, are commonly made up of nonrandom subsets of the total available species pool. Faunas within an archipelago may form a nested series, with depauperate faunas made up of subsets of more species-rich faunas. The pattern is seldom perfect: widespread species may be absent from otherwise rich faunas (holes), and uncommon species may occur in depauperate faunas (outliers). The "nestedness" of an assemblage of faunas (its fit to the "nested subset model"; Patterson & Atmar 1986) can be measured by summing the holes and outliers.
The distributions of boreal mammals and birds among mountain ranges in the Great Basin of western North America were analyzed by this method Despite differences in their derivation (mammalian faunas are thought to be relicts, isolated since the Pleistocene; bird faunas have probably experienced recurrent colonization throughout their history] both groups show an approximately equal (and highly significant) fit to the nested subset model. They differ, however, in the relative numbers of holes and outliers in their patterns. The mammalian pattern is hole-rich; the bird pattern is outlier-rich.
The present-day composition of the mammalian faunas is the result of selective extinction of species of originally richer faunas. The existence of nested subsets in these faunas suggests that extinction is a highly deterministic process: extinctions occurred in approximately the same sequence throughout the region, despite wide variation in extinction rates Extinction sequence has, in fact, been less variable than extinction rates.     

Extinction Rates in Archipelagoes: Implications for Populations in Fragmented Habitats

To study the effect of habitat fragmentation on population viability, I used extinction rates on islands in archipelagoes and estimated the relative probability of extinction per species on single large islands and sets of smaller islands with the same total area. Data on lizards, birds, and mammals on oceanic islands and mammals on mountaintops and in nature reserves yield similar results. Species are likely to go extinct on all the small islands before they go extinct on the single, large island. In the short term, the analysis indicates that extinction probabilities may be lower on a set of small islands. This is perhaps an artifact due to underestimation of extinction rates on small islands and/or the necessity of pooling species in a focal taxon to obtain estimates of extinction rates (which may obscure area thresholds and underestimate the slope and curvature of extinction rates as a function of area). Ultimately, cumulative extinction probabilities are higher for a set of small islands than for single large islands. Mean and median times to extinction tend to be shorter in the fragmented systems, in some cases much shorter. Thus, to minimize extinction rates in isolated habitat remnants and nature reserve systems, the degree of fragmentation should be minimized     

Bird Species' Tolerance of Secondary Forest Habitats and Its Effects on Extinction

Abstract:  Intense deforestation causes massive species losses. These losses occur because the habitats supplanting primary forest are inadequate to sustain viable populations of forest-dependent species. Despite this, certain species do seem to persist within the secondary habitats that replace original forest. This implies that there is a special class of species that might survive the loss of primary forest. Such a result would significantly influence conservation plans and extinction predictions. We tested whether species that tolerate secondary habitats survive extensive habitat loss and whether the same degree of loss threatens species that are forest obligates. To identify purported "survivors," we compared the remaining range sizes of endemic birds, their abundances, and their degree of extinction threat. We did this within the remaining Atlantic Forest of Brazil, a region extremely rich in endemics but with only approximately 10% of its forest remaining. We found no survivors. Habitat loss threatens forest-obligate birds and those using secondary habitats equally.     

Extinction times in experimental populations

Predicting population extinctions is a key element of quantitative conservation biology and population ecology. Although stochastic population theories have long been used to obtain theoretical distributions of population extinction times, model-based predictions have rarely been tested. Here I report results from a quantitative analysis of extinction time in 281 experimental populations of water fleas (Daphnia magna) in variable environments. To my knowledge, this is the first quantitative estimate of the shape of the distribution of population extinction times based on extinction data for any species. The finding that the distribution of population extinction times was extraordinarily peaked is consistent with theoretical predictions for density-independent populations, but inconsistent with predictions for density-dependent populations. The tail of the extinction time distribution was not exponential. These results imply that our current theories of extinction are inadequate. Future work should focus on how demographic stochasticity scales with population size and effects of nonrandom variable environments on population growth and decline.     

Armageddon Versus Extinction

Note from the Editor : Some readers may feel that topics such as politics and religion are inappropriate for a scientific journal. Our "Conservation in Context" column, however, is intended to cover the entire spectrum of the context within which the science of conservation biology must operate. Thus, we freely and openly explore topics in this column that ordinarily are not addressed in scientific journals, to better understand the real-world constraints and opportunities that define how conservation science is applied in a complex world.     

Strategic Habitats for Biodiversity Conservation in Florida

Abstract: Privately owned lands support a large portion of the biodiversity in some areas, but procedures for identifying those private lands critical to the maintenance of biodiversity vary tremendously. We used habitat-based distribution maps in combination with population conservation goals to help identify strategic habitats on private lands in Florida. We used a vegetation map, occurrence data, and published life-history information to create habitat-based distribution maps for 179 rare taxa. We estimated the security of 130 of the taxa by overlaying public land boundaries on habitat maps and then estimating whether conservation lands satisfied a population goal of supporting at least 10 populations of approximately 200 breeding adults. The remaining taxa were evaluated in terms of number of occurrence records on conservation lands. Of the 179 taxa evaluated, existing conservation lands did not adequately protect 56. We then identified habitats on private lands that could best satisfy the minimum conservation goal or else significantly enhance the survival potential of inadequately protected taxa. Strategic habitats included a mix of large and small sites, incorporated some corridor or stepping-stone connections among habitat patches, and protected multiple species. Additional strategic habitats were identified for shorebirds, four natural plant communities, and 105 globally rare plants. The strategic habitats identified in Florida cover 1.65 million ha (12% of the land area) and would cost $8.2 billion (about 15% of Florida's annual state budget) to purchase and $122 million per year to manage. Existing conservation lands account for 3.07 million ha (22% of the land area).     

Fragmentation of Phragmites Habitats, Minimum Viable Population Size, Habitat Suitability, and Local Extinction of Moths, Midges, Flies, Aphids, and Birds

Results from populations of insects and birds inhabiting Phragmites habitats were used to analyze effects of fragmentation. Flush-crash cycles of the stem-boring moth Archanara geminipuncta (Lepidoptera, Noctuidae) showed regionally concurrent, local extinctions despite an originally enormous population size (more than 180,000 adults), emphasizing the importance of metapopulation dynamics. Further, A. geminipuncta could be considered a keystone species, since shoot damage facilitated more than twenty species of herbivores, saprovores (of the caterpillars' feces), and their parasitoids. The gall midge Lasioptera arundinis could survive only in side shoots induced by shoot damage of A. geminipuncta .
Small Phragmites stands had thinner shoots (due to a water or nutrient deficiency) and shoots with more leaves (due to a better light supply) than large stands, thereby influencing species-specific demands for habitat suitability and nutritiousness of reed tissue. In other words significance of habitat fragmentation could not be assessed by area alone. For example, two chloropid flies depending on thin, yellowish shoots survived only in small habitats or in the unmown edges of large habitats.
Local persistence of Phragmites herbivores depended on much larger population sizes than could be expected from a population size sufficient to maintain genetic variation. At least 11,000 adults of the gall midge Giraudiella inclusa (or more than 84,000 galls) were necessary to avoid local extinction.
With regard to conservation management of reed habitats, nature reserves should consist of old and unmown reeds, have fewer disturbed (particularly, fewer mown) habitat edges, measure more than two hectares (priority should go to the largest remaining fragments), and be surrounded by nearby reed habitats providing reservoir populations and diverse shoot types.     

城市中不同生境下鸟类群落特征研究

2004年1月至2004年12月,对内蒙古自治区呼和浩特市市区7种不同生态环境类型中的鸟类进行了调查研究。研究结果显示:商业区和交通占地中的鸟类群落最为相似,苗圃和公园中的鸟类群落较为相似。景观水平和干扰因素(样带至市中心的距离、噪音、建筑指标)对鸟类的分布、密度、多样性和丰富度具有不同程度的影响。分析表明,人为干扰影响鸟类多样性、群落结构和生态分布。