George W. Uetz

Abstract: Behavioral ecologists might often benefit by the ability to directly measure an animal's body condition as an estimate of foraging success, and ultimately fitness. Here we compare the reliability and effectiveness of three indices of body condition that have been heavily used in the morphometrics literature. We examined the ratio index (body mass/body size), the slope-adjusted ratio index (based on regression slopes generated from a reference population), and the residual index (the residuals of a regression of body mass on body size). We present the results of tests performed in the field and laboratory on two ecologically and evolutionarily divergent spider species : the vagrant wolf spider Pardosa milvina (Araneae, Lycosidae), and the colonial orb-weaver Metepeira incrassata (Araneae, Araneidae). The ratio index correlated with body size, which weakened the strength of conclusions that could be drawn. The slope-adjusted ratio index requires an independent and large data set with which to generate the expected values, and was likewise sensitive to body size. The residual index, with appropriate transformations to achieve homoscedasticity, was the most reliable index because it did not vary with body size, and we recommend its general use in behavioral studies that require a condition estimate.

Abstract: Spiders are extremely common inhabitants of most terrestrial communities, yet, compared to other animal taxa, they have only recently become the subject of ecological research (Turnbull, 1973; Witt and Rovner, 1982; Wise, 1984; Shear, 1986; Nentwig, 1987, for reviews). From the earliest studies, it has been clear that the physiognomy or physical structure of environments has an important influence on the habitat preferences of spider species, and ultimately on the composition of spider communities. This is certainly no coincidental observation for two important reasons: 1. Many spiders build webs for prey capture, and the attachment of these webs to surrounding structures often requires the presence of specific architectural features or arrangements (Riechert and Gillespie, 1986). 2. The nature of both web-building and non-web-building spiders’ primary sensory modalities (they perceive vibration through mechanoreceptors) dictates that they perceive their environment using tactile and vibratory cues (Barth, 1985).

Abstract: The ecological guild concept has been of great interest to arachnologists, and the different manner in which spiders forage for a common resource—prey arthropods—has led to numerous attempts to classify them into guilds. However, questions have been raised about the validity of guilds and the taxon-centered basis of their definition. Here, we propose an alternative approach to guild classification, using quantitative analysis of ecological characteristics of spider families. While generalizations may not apply to all species within a taxon, results from this approach suggest eight major spider guilds similar to earlier guild assignments by some authors and provide a reasonable framework for future studies. We used this classification in a comparison of spider guild composition across several major crops (from published studies). While total species richness varied widely among crops, the proportion of the total species within each guild was remarkably even across crops. The relative abundance of guilds (based on numbers of individuals) varied greatly, which may reflect availability of resources within a crop type. Patterns of similarity in guild composition suggest the possibility of plant habitat structure as an influence on the spider community. Further detailed analyses of spider guilds in various crops have been constrained by both a lack of comparable quantitative data and the paucity of behavioral and natural history infor- mation available for many taxa. As recent studies have shown that assemblages of spiders can impact pest populations and reduce crop damage, a better understanding of spider guild composition and variation in spider community structure among crops is essential in future studies of the arthropod fauna in agroeco- systems.

Abstract: Spider communities were sampled over an artificial gradient of litter depth (created by raking) and compared to those of two other forests exhibiting natural variation in litter depth. More species of spiders were present in areas of greater depth and/or complexity in all sites. Relative abundance of Lycosidae decreased, while relative abundance of Clubionidae, Thomisidae and Gnaphosidae increased over gradients of increasing depth and complexity. Similarity of species composition between areas within a forest was related to site differences in litter depth and structure.

Abstract: Spiders perceive the world using multiple sensory modes, including vibration, vision, and chemical senses, for prey detection and communication. These sensory modes are used in many communication contexts, either individually or in multimodal signaling. Selection for effective signaler-receiver communication and species discrimination is especially strong for these predatory and potentially cannibalistic arthropods, resulting in the evolution of considerable diversity in signaling behaviors. In this paper, we review sensory mechanisms involved in spider signaling and present an overview of recent work done on wolf spiders (Lycosidae) that use multimodal communication (simultaneous visual and vibratory signals) in sexual signals during courtship. The relative importance of visual and vibratory signaling modes, and the use of multiple modes varies among closely related species in the genus Schizocosa, providing a model system for investigating multisensory guidance of complex behavior. Here we examine previous and current research on responses of female spiders to components of male courtship behavior, using several experimental techniques including cue isolation (single sensory modes), video/audio digitization and playback, and cue-conflict (mixed conspecific/heterospecific components) to tease apart elements of multimodal signaling.

Abstract: Preface to the Princeton Landmarks in Biology Edition vii Preface xi Symbols Used xiii 1. The Importance of Islands 3 2. Area and Number of Speicies 8 3. Further Explanations of the Area-Diversity Pattern 19 4. The Strategy of Colonization 68 5. Invasibility and the Variable Niche 94 6. Stepping Stones and Biotic Exchange 123 7. Evolutionary Changes Following Colonization 145 8. Prospect 181 Glossary 185 References 193 Index 201

Abstract: Beginning with Emlen (1966) and MacArthur and Pianka (1966) and extending through the last ten years, several authors have sought to predict the foraging behavior of animals by means of mathematical models. These models are very similar,in that they all assume that the fitness of a foraging animal is a function of the efficiency of foraging measured in terms of some "currency" (Schoener, 1971) -usually energy- and that natural selection has resulted in animals that forage so as to maximize this fitness. As a result of these similarities, the models have become known as "optimal foraging models"; and the theory that embodies them, "optimal foraging theory." The situations to which optimal foraging theory has been applied, with the exception of a few recent studies, can be divided into the following four categories: (1) choice by an animal of which food types to eat (i.e., optimal diet); (2) choice of which patch type to feed in (i.e., optimal patch choice); (3) optimal allocation of time to different patches; and (4) optimal patterns and speed of movements. In this review we discuss each of these categories separately, dealing with both the theoretical developments and the data that permit tests of the predictions. The review is selective in the sense that we emphasize studies that either develop testable predictions or that attempt to test predictions in a precise quantitative manner. We also discuss what we see to be some of the future developments in the area of optimal foraging theory and how this theory can be related to other areas of biology. Our general conclusion is that the simple models so far formulated are supported are supported reasonably well by available data and that we are optimistic about the value both now and in the future of optimal foraging theory. We argue, however, that these simple models will requre much modification, espicially to deal with situations that either cannot easily be put into one or another of the above four categories or entail currencies more complicated that just energy.

Abstract: Aim In a selected literature survey we reviewed studies on the habitat heterogeneity–animal species diversity relationship and evaluated whether there are uncertainties and biases in its empirical support. Location World-wide. Methods We reviewed 85 publications for the period 1960–2003. We screened each publication for terms that were used to define habitat heterogeneity, the animal species group and ecosystem studied, the definition of the structural variable, the measurement of vegetation structure and the temporal and spatial scale of the study. Main conclusions The majority of studies found a positive correlation between habitat heterogeneity/diversity and animal species diversity. However, empirical support for this relationship is drastically biased towards studies of vertebrates and habitats under anthropogenic influence. In this paper, we show that ecological effects of habitat heterogeneity may vary considerably between species groups depending on whether structural attributes are perceived as heterogeneity or fragmentation. Possible effects may also vary relative to the structural variable measured. Based upon this, we introduce a classification framework that may be used for across-studies comparisons. Moreover, the effect of habitat heterogeneity for one species group may differ in relation to the spatial scale. In several studies, however, different species groups are closely linked to ‘keystone structures’ that determine animal species diversity by their presence. Detecting crucial keystone structures of the vegetation has profound implications for nature conservation and biodiversity management.

Abstract: theoretical framework, the concept of the mixed strategy has not been realized in nature, and alternative strategies are very rare. Recent findings suggest that almost all alternative reproductive phenotypes within the sexes are due to alternative tactics within a conditional strategy, and, as such, while the average fitnesses of the alternative phenotypes are unequal, the strategy is favoured in evolution. Proximate mechanisms that underlie alternative phenotypes may have many similarities with those operating between the sexes.

Abstract: ION, GENERAL CONCEPTIONS, SELF-CONSCIOUSNESS, MENTAL INDIVIDUALITY. It would be very difficult for any one with even much more knowledge than I possess, to determine how far animals exhibit any traces of these high mental powers. This difficulty arises from the impossibility of judging what passes through the mind of an animal; and again, the fact that writers differ to a great extent in the meaning which they attribute to the above terms, causes a further difficulty. If one may judge from various articles which have been published lately, the greatest stress seems to be laid on the supposed entire absence in animals of the power of abstraction, or of forming general concepts. But when a dog sees another dog at a distance, it is often clear that he perceives that it is a dog in the abstract; for when he gets nearer his whole manner suddenly changes, if the other dog be a friend. A recent writer remarks, that in all such cases it is a pure assumption to assert that the mental act is not essentially of the same nature in the animal as in man. If either refers what he perceives with his senses to a mental concept, then so do both. (44. Mr. Hookham, in a letter to Prof. Max Muller, in the 'Birmingham News,' May, 1873.) When I say to my terrier, in an eager voice (and I have made the trial many times), "Hi, hi, where is it?" she at once takes it as a sign that something is to be hunted, and generally first looks quickly all around, and then rushes into the nearest thicket, to scent for any game, but finding nothing, she looks up into any neighbouring tree for a squirrel. Now do not these actions clearly shew that she had in her mind a general idea or concept that some animal is to be discovered and hunted? It may be freely admitted that no animal is self-conscious, if by this term it is implied, that he reflects on such points, as whence he comes or whither he will go, or what is life and death, and so forth. But how can we feel sure that an old dog with an excellent memory and some power of imagination, as shewn by his dreams, never reflects on his past pleasures or pains in the chase? And this would be a form of self-consciousness. On the other hand, as Buchner (45. 'Conferences sur la Theorie Darwinienne,' French translat. 1869, p. 132.) has remarked, how little can the hardworked wife of a degraded Australian savage, who uses very few abstract words, and cannot count above four, exert her self-consciousness, or reflect on the nature of her own existence. It is generally admitted, that the higher animals possess memory, attention, association, and even some imagination and reason. If these powers, which differ much in different animals, are capable of improvement, there seems no great improbability in more complex faculties, such as the higher forms of abstraction, and selfconsciousness, etc., having been evolved through the development and combination of the simpler ones. It has been urged against the views here maintained that it is impossible to say at what point in the ascending scale animals become capable of abstraction, etc.; but who can say at what age this occurs in our young children? We see at least that such powers