Box 9E. 1 Continued FIGURE 2. The C–S–R triangle model (Grime 1979). The strategies at the three corners are C, competiti- winning species; S, stress-tolerating s- cies; R,ruderalspecies. Particular species can engage in any mixture of these three primary strategies, and the m- ture is described by their position within the triangle. comment briefly on some other dimensions that Grime’s (1977) triangle (Fig. 2) (see also Sects. 6. 1 are not yet so well understood. and 6. 3 of Chapter 7 on growth and allocation) is a two-dimensional scheme. A C—S axis (Com- tition-winning species to Stress-tolerating spe- Leaf Economics Spectrum cies) reflects adaptation to favorable vs. unfavorable sites for plant growth, and an R- Five traits that are coordinated across species are axis (Ruderal species) reflects adaptation to leaf mass per area (LMA), leaf life-span, leaf N disturbance. concentration, and potential photosynthesis and dark respiration on a mass basis. In the five-trait Trait-Dimensions space,79%ofallvariation worldwideliesalonga single main axis (Fig. 33 of Chapter 2A on photo- A recent trend in plant strategy thinking has synthesis; Wright et al. 2004). Species with low been trait-dimensions, that is, spectra of varia- LMA tend to have short leaf life-spans, high leaf tion with respect to measurable traits. Compared nutrient concentrations, and high potential rates of mass-based photosynthesis. These species with category schemes, such as Raunkiaer’s, trait occur at the ‘‘quick-return’’ end of the leaf e- dimensions have the merit of capturing cont- nomics spectrum.

This textbook is remarkable for emphasising that the mechanisms underlying plant physiological ecology can be found at the levels of biochemistry, biophysics, molecular biology and whole-plant physiology. The authors begin with the primary processes of carbon metabolism and transport, plant-water relations, and energy balance. After considering individual leaves and whole plants, these physiological processes are then scaled up to the level of the canopy. Subsequent chapters discuss mineral nutrition and the ways in which plants cope with nutrient-deficient or toxic soils. The book then looks at patterns of growth and allocation, life-history traits, and interactions between plants and other organisms. Later chapters deal with traits that affect decomposition of plant material and with plant physiological ecology at the level of ecosystems and global environmental processes.

capable of providing at least a relative measure of stomatal aperture were first used shortly thereafter (Darwin and Pertz, 1911). The Carnegie Institution of Washington's Desert Research Laboratory in Tucson from 1905 to 1927 was the first effort by plant physiologists and ecologists to conduct team research on the water relations of desert plants. Measurements by Stocker in the North African deserts and Indonesia (Stocker, 1928, 1935) and by Lundegardh (1922) in forest understories were pioneering attempts to understand the environmental controls on photosynthesis in the field. While these early physiological ecologists were keen observers and often posed hypotheses still relevant today they were strongly limited by the methods and technologies available to them. Their measurements provided only rough approximations of the actual plant responses. The available laboratory equip ment was either unsuited or much more difficult to operate under field than laboratory conditions. Laboratory physiologists distrusted the results and ecologists were largely not persuaded of its relevance. Consequently, it was not until the 1950s and 1960s that physiological ecology began its current resurgence. While the reasons for this are complicated, the development and application of more sophisticated instruments such as the infrared gas analyzer played a major role. In addition, the development of micrometeorology led to new methods of characterizing the plant environments.

Although, as W.D. Billings notes in his chapter in this book. the development of physiological ecology can be traced back to the very beginnings of the study of ecology it is clear that the modern development of this field in North America is due in the large part to the efforts of Billings alone. The foundation that Billings laid in the late 1950s came from his own studies on deserts and subsequently arctic and alpine plants, and also from his enormous success in instilling enthusiasm for the field in the numerous students attracted to the plant ecology program at Duke University. Billings' own studies provided the model for subsequent work in this field. Physiological techniques. normally confined to the laboratory. were brought into the field to examine processes under natural environmental conditions. These field studies were accompanied by experiments under controlled conditions where the relative impact of various factors could be assessed and further where genetic as opposed to environmental influences could be separated. This blending of field and laboratory approaches promoted the design of experiments which were of direct relevance to understanding the distribution and abundance of plants in nature. Physiological mechanisms were studied and assessed in the context of the functioning of plants under natural conditions rather than as an end in itself.

This richly illustrated text covers the ecophysiology of plants of all major tropical ecosystems, from tropical rain forests, epiphytic habitats, mangroves and savannas to salinas, inselbergs and paramos and their ecophysiological adaptation to these different tropical environments. The physiognomy of biotopes and characteristic life forms of plants are depicted with photographs.

O.L. LANGE, P.S. NOBEL, C.B. OSMOND, and H. ZIEGLER Growth, development and reproductive success of individual plants depend on the interaction, within tolerance limits, of the factors in the physical, chemical and biological environment. The first two volumes of this series addressed fea tures of the physical environment (Vol. 12A) and the special responses of land plants as they relate to water use and carbon dioxide assimilation (Vol. 12B). In this volume we consider specific aspects of the chemical and biological envi ronment, and whereas the previous volumes were primarily concerned with the atmospheric interactions, our emphasis here shifts very much to the soil. This complex medium for plant growth was briefly reviewed in Chapter 17, Volume 12A. Since it is difficult to determine the precise physical and chemical interactions in the soil, it is even more difficult to determine the important biological interactions among organisms. Nevertheless there is growing aware ness of the significance of these interactions and their effects on physiological processes in the individual plant.

In the spring of 1969 a small meeting was convened at the CSIRO Riverina Laboratory, Deniliquin, New South Wales, to discuss the biology of the genus Atriplex, a group of plants considered by those who attended to be of profound importance both in relation to range management in the region and as a tool in physiological research. The brief report of this meeting (Jones, 1970) now serves as a marker for the subsequent remarkable increase in research on this genus, and served then to interest the editors of the Ecological Studies Series in the present volume. This was an exciting time in plant physiology, particularly in the areas of ion absorption and photosynthesis, and unknowingly several laboratories were engaged in parallel studies of these processes using the genus Atriplex. It was also a time at which it seemed that numerical methods in plant ecology could be used to delineate significant processes in arid shrubland ecosystems. Nevertheless, to presume to illustrate and integrate plant physiology and ecology using examples from a single genus was to presume much. The deficiencies which became increasingly apparent during the preparation of the present book were responsible for much new research described in these pages.

Part 2=Volume 12B.

Unlocking the puzzle of how animals behave and how they interact with their environments is impossible without understanding the physiological processes that determine their use of food resources. But long overdue is a user-friendly introduction to the subject that systematically bridges the gap between physiology and ecology. Ecologists--for whom such knowledge can help clarify the consequences of global climate change, the biodiversity crisis, and pollution--often find themselves wading through an unwieldy, technically top-heavy literature. Here, William Karasov and Carlos Martínez del Rio present the first accessible and authoritative one-volume overview of the physiological and biochemical principles that shape how animals procure energy and nutrients and free themselves of toxins--and how this relates to broader ecological phenomena. After introducing primary concepts, the authors review the chemical ecology of food, and then discuss how animals digest and process food. Their broad view includes symbioses and extends even to ecosystem phenomena such as ecological stochiometry and toxicant biomagnification. They introduce key methods and illustrate principles with wide-ranging vertebrate and invertebrate examples. Uniquely, they also link the physiological mechanisms of resource use with ecological phenomena such as how and why animals choose what they eat and how they participate in the exchange of energy and materials in their biological communities. Thoroughly up-to-date and pointing the way to future research, Physiological Ecology is an essential new source for upper-level undergraduate and graduate students-and an ideal synthesis for professionals. The most accessible introduction to the physiological and biochemical principles that shape how animals use resources Unique in linking the physiological mechanisms of resource use with ecological phenomena An essential resource for upper-level undergraduate and graduate students An ideal overview for researchers