Growth patterns of a stream vertebrate differ between urban and forested catchments

1. Urban development results in the decline of amphibian density and species richness. A logical next step towards understanding why urbanisation negatively impacts amphibians is to track species‐specific demographic responses to urbanisation. 2. We monitored growth of two‐lined salamander (Eurycea cirrigera Green) larvae over two complete cohorts (2006 and 2007) in nine western Georgia, U.S.A. streams. 3. We found that salamanders in streams surrounded by urbanised and developing catchments hatched at the same size as their reference‐stream counterparts, but achieved larger sizes within the first few months of growth. We evaluated the effect of four variables that correlate with the urban‐forest gradient and found that elevated temperatures in the urban environment, coupled with decreased intraspecific competition because of lower survivorship in these same habitats, were two of the most likely explanations for increased growth rates. 4. Such an increase in growth of surviving larvae may maintain population viability in urban areas where it has been shown survival is difficult because of increased in‐channel flow during flood events. Because larvae that do survive in urban streams undergo metamorphosis at large sizes, they may recoup a component of fitness (i.e. increased adult survivorship and reproduction) through growth.     

A test of three hypotheses for ovariole number determination in the grasshopper Romalea microptera

Ovariole number in insects determines potential fecundity and can be influenced by genes, environmental conditions during development and parental effects. In the present study, three hypotheses are tested for ovariole number determination in the grasshopper Romalea microptera (Beauvois), which exhibits both intra‐ and interpopulation variation in ovariole number. In hypothesis 1, variation in ovariole number is a result of genetic variation. In hypothesis 2, ovariole number is influenced by nutrition during development. In hypothesis 3, ovariole number is influenced by maternal nutritional status. Females from four treatments are compared: low‐food, high‐food, daughters of low‐food, and daughters of high‐food. There is a relationship between parent and offspring ovariole number despite different environments, supporting hypothesis 1. Also, ovariole numbers are slightly, but significantly lower in individuals fed a low‐food diet compared with a high‐food diet, supporting hypothesis 2. Hypothesis 3 is not supported: starved and well‐fed females produce eggs of similar mass, as well as offspring with similar numbers of ovarioles, suggesting that the nutritional status of mothers does not influence offspring mass or offspring ovariole number. The results imply that genetic variation and developmental conditions determine ovariole number in this species but maternal environment does not. These results conflict with previous studies of ovariole determination in grasshoppers and locusts.     

Infusing considerations of trophic dependencies into species distribution modelling

Community ecology involves studying the interdependence of species with each other and their environment to predict their geographical distribution and abundance. Modern species distribution analyses characterise species‐environment dependency well, but offer only crude approximations of species interdependency. Typically, the dependency between focal species and other species is characterised using other species’ point occurrences as spatial covariates to constrain the focal species’ predicted range. This implicitly assumes that the strength of interdependency is homogeneous across space, which is not generally supported by analyses of species interactions. This discrepancy has an important bearing on the accuracy of inferences about habitat suitability for species. We introduce a framework that integrates principles from consumer–resource analyses, resource selection theory and species distribution modelling to enhance quantitative prediction of species geographical distributions. We show how to apply the framework using a case study of lynx and snowshoe hare interactions with each other and their environment. The analysis shows how the framework offers a spatially refined understanding of species distribution that is sensitive to nuances in biophysical attributes of the environment that determine the location and strength of species interactions.     

Sex differences in the social behavior of wild spider monkeys (Ateles geoffroyi yucatanensis)

Competition for resources and the need for cooperation are reported to affect patterns of social interactions and thus the quality of social relationships in primates. Relationships may be described as high quality when both individuals behave in a way that benefits their partner. We investigated the distribution of a wide range of social behaviors across sex partner combinations of adult spider monkeys with specific reference to contested resources. Data were collected from two communities of wild spider monkeys (Ateles geoffroyi yucatanensis) in the Otoch Ma'ax Yetel Kooh reserve in Yucatan, Mexico. Affiliative behavior was exchanged most frequently between males, and as male-male aggression was rare, male-male social relationships were characterized as high quality. Female-female social relationships were best described as low quality as females showed no preference to be in proximity with other females and female-female affiliative behavior was rare. Relationships between the sexes generally were characterized by high rates of female-directed male aggression, although additional investigation into the effects of kinship and female reproductive state on male-female relationships is required before further conclusions can be drawn. Dyadic and coalitionary female-female aggression was significantly higher than expected in a feeding context, confirming that female spider monkeys primarily compete for access to food. Male-male aggression did not increase significantly when in the presence of females, but males embraced at higher rates when in mixed-sex subgroups. As embraces serve to reduce the likelihood of aggression during tense situations, high rates of male-male embraces in mixed-sex subgroups may mitigate male conflicts over access to females.     

基于GIS支持下的土地资源空间格局生态优化

以防治水土流失和维护景观整体生态优化为目标,选择我国滇西南地区亚热带山地为典型案例,利用遥感数据和GIS的空间信息处理技术,采用适宜性评价与土地资源利用格局整体优化相结合的方法,用最小累积阻力模型(MCR)确定土地利用的功能分区和生态格局组分,探讨山地土地资源空间格局生态优化途径.结果表明:(1)基于GIS空间分析技术和"成本距离加权"制图分析工具,采用最小累积阻力模型(MCR)的土地资源空间格局生态优化方法是可行的;(2)将水平生态过程作为一种对景观的控制过程来对待,以常绿阔叶林和思茅松林为保护源,基于最小累积阻力面(MCR)模型,构建了对土地资源整体生态功能起维护作用,对源内物种的迁移或扩散过程具有关键作用的廊道、辐射道和战略点等生态格局组分;(3)基于MCR阻力值建立的频率序列及拐点图,拐点两侧的土地利用类型异质性较大,可以作为划分土地功能分区的临界点,以此划分出有利于生态安全的核心源保护区、生态缓冲区、生态过渡区、生态边缘区、农业耕作区和居民生活区等6类土地功能区,并提出各功能区的管理措施.     

Frequency-dependent conspecific attraction to food patches

In many ecological situations, resources are difficult to find but become more apparent to nearby searchers after one of their numbers discovers and begins to exploit them. If the discoverer cannot monopolize the resources, then others may benefit from joining the discoverer and sharing their discovery. Existing theories for this type of conspecific attraction have often used very simple rules for how the decision to join a discovered resource patch should be influenced by the number of individuals already exploiting that patch. We use a mechanistic, spatially explicit model to demonstrate that individuals should not necessarily simply join patches more often as the number of individuals exploiting the patch increases, because those patches are likely to be exhausted soon or joining them will intensify future local competition. Furthermore, we show that this decision should be sensitive to the nature of the resource patches, with individuals being more responsive to discoveries in general and more tolerant of larger numbers of existing exploiters on a patch when patches are resource-rich and challenging to locate alone. As such, we argue that this greater focus on underlying joining mechanisms suggests that conspecific attraction is a more sophisticated and flexible tactic than currently appreciated.     

白颈环毛蚓(Pheritima catifornica)与壮伟环毛蚓(Amynthas robusto)的PTC-氨基酸分析

对白颈环毛蚓与壮伟环毛蚓的体壁及内脏器官ＰＴＣ—氨基酸的含量进行了初步分析,结果表明：两种蚯蚓具有１５种氨基酸,８种必需氨基酸含量均较高。而壮伟环毛蚓的必需氨基酸总量均超过白颈环毛蚓,也大大超过国产或进口鱼粉氨基酸总含量;加上壮伟环毛蚓个体大,分布广,又耐污染,抗病能力强,所以这是一种值得开发的动物蛋白的新资源。     

Predation on primates: Ecological patterns and evolutionary consequences

It has long been thought that predation has had important ecological and evolutionary effects on primates as prey. Predation has been theorized to have been a major selective force in the evolution of hominids.¹ In modern primates, behaviors such as active defense, concealment, vigilance, flight, and alarm calls have been attributed to the selective pressures of predation, as has group living itself. It is clear that primates, like other animals, have evolved ways to minimize their risk of predation. However, the extent to which they have been able to do so, given other constraints of living such as their own need to acquire food, has not yet been resolved. Perhaps most hotly debated is whether predation has been the primary selective force favoring the evolution of group living in primates. Part of the difficulty in resolving the debate lies in a paucity of direct evidence of predation. This is regrettable yet understandable since primatologists, by definition, focus on the study of primates, not predators of primates (unless these are also primates). Systematic direct evidence of the effects of predation can best be obtained by studying predators that are as habituated to observers as are their primate prey. Until this is done, we must continue to rely on opportunistic accounts of predation and predation attempts, and on systematically obtained indirect evidence. Such data reveal several interesting patterns: (1) although smaller primates may have greater predation rates than larger primates, even the largest primates are not invulnerable to predation; (2) the use by primates of unfamiliar areas can result in higher predation rates, which might be one pressure favoring philopatry, or site fidelity; (3) arboreal primates are at greater risk of predation when they are more exposed (at forest edges and tops of canopies) than in more concealed locations; (4) predation by mammalian carnivores may often be episodic; and (5) terrestrial primates may not experience greater predation than arboreal primates.