Ecological and evolutionary aspects of isoprene emission from plants

Isoprene (2-methyl-1,3,-butadiene), produced by many woody and a few herbaceous plant species, is the dominant volatile organic compound released from vegetation. It represents a non-trivial carbon loss to the plant (typically 0.5–2%, but much higher as temperatures exceed 30°C), and plays a major role in tropospheric chemistry of forested regions, contributing to ozone formation. This review summarizes current knowledge concerning the occurrence of isoprene production within the plant kingdom, and discusses other aspects of isoprene biology which may be of interest to the ecological community. The ability to produce significant amounts of isoprene may or may not be shared by members of the same plant family or genus, but emitting species have been found among bryophytes, ferns, conifers and Ephedra and in approximately one-third of the 122 angiosperm families examined. No phylogenetic pattern is obvious among the angiosperms, with the trait widely scattered and present (and absent) in both primitive and derived taxa, although confined largely to woody species. Isoprene is not stored within the leaf, and plays no known ecological role as, for example, an anti-herbivore or allelopathic agent. The primary short-term controls over isoprene production are light and temperature. Growth in high light stimulates isoprene production, and growth in cool conditions apparently inhibits isoprene, production of which may be induced upon transfer to warmer temperatures. The stimulation of isoprene production by high irradiance and warm temperatures suggests a possible role in ameliorating stresses associated with warm, high-light environments, a role consistent with physiological evidence indicating a role in thermal protection. Received: 1 April 1998 / Accepted: 9 November 1998     

Ecological and evolutionary aspects of photothermal regulation of diapause in trichogrammatidae

Facultative winter diapause in the genus of Trichogramma Westw. (Hymenoptera, Trichogrammatidae), like in most other insect species, is regulated by photoperiod and temperature. Their prepupae are diapausing, but sensitivity to temperature and day length (environmental cue factors inducing diapause) is characteristic of all stages of development from embryo to the egglaying female. The environmental cues can affect not only the current, but also the next generations. Under the natural conditions, the photothermal regulation provides the timely diapause induction coordinated both with the astronomical season (the photoperiodic response) and with the peculiarity of the given year (the thermal response). The special experiments revealed “rudimentary responses” that had lost their adaptive role. The results of these studies have proved once more that the specificity of photoperiodic and thermal diapause-regulating responses, their relative importance, and association with sensitive stages of development are determined not only by the ecological peculiarities of different insect taxa, but also by their previous evolution.     

Ecological and evolutionary aspects of photothermal regulation of diapause in Trichogramma

Facultative winter diapause in species of the genus Trichogramma Westw. (Hymenoptera, Trichogrammatidae) is regulated, like in the majority of other insects, by photoperiod and temperature. In trichograms, prepupae are diapausing, but sensitivity to length of the light day and to temperature as to the cue factors inducing diapause is characteristic of all stages of development from embryo to the egg-laying female. The action of the cue factors affects not only the current, but also the subsequent generations. Under natural conditions the photothermal regulation provides the timely induction of the diapause coordinated both with astronomical year time (the photoperiodic reaction) and with specificity of this season (the temperature reaction). In the course of special experiments in trichograms there are also revealed the "rudimentary" reactions that have lost their adaptive role. Results of these studies prove once more that specificity of photoperiodic and temperature reactions inducing diapause and their relative importance and confinement to certain sensitive stages are determined not only by peculiarities of ecology of different insect taxa, but also by the course of their previous evolution.     

Gut-islet endocrinology-some evolutionary aspects

Immunological and biological studies have shown that many of the mammalian gastroenteropancreatic (GEP) hormones have counterparts in lower vertebrates. Hormonal localization in cyclostomes and fishes suggests that insulin was phylogenetically the first islet hormone, followed by somatostatin, glucagon and, last, pancreatic polypeptide (PP). Some of the GEP peptides are present in the central and peripheral nervous system of lower vertebrates as well as mammals. GEP hormone-like substances resembling insulin, somatostatin, glucagon, PP, gastrin, secretin, VIP, substance P and enkephalin also occur in protostomian invertebrates (Annelida, Arthropoda, Mollusca), particularly in their nervous system. These findings indicate that the vertebrate hormones may have originated in neural tissue before the development of the vertebrate line of evolution.     

Experimental analyses of the evolutionary processes inTrillium

In the Japanese species ofTrillium examined here, every interspecific cross produced healthy F₁ progeny at the rate of about 50 to 60 per cent of the total inborn ovules except forT. hagae. These figures were not appreciably different from those of self-pollinated or sib-mated examples of these species.Trillium hagae, a putative natural hybrid betweenT. kamtschaticum (2n=10) andT. tschonoskii (2n=20), accepted all foreign sources of pollen grains in manual pollination. These and other crossing experiments suggest that no appreciable barrier has developed that might cause interspecific crossability and that they are habitual inbreeders. Despite theri crossability, a very low rate of actual pollen flow was detected by examining electrophoretic phenotypes of seeds taken from sympatric populations of these species.     

Quantitative aspects of the estimation of evolutionary trees

Various approaches to the estimation of evolutionary trees are reviewed, with emphasis on recent developments. It is argued that no approach is 'model-free', that is, without some assumptions about the processes of evolutionary change. A statistical approach provides a general framework and it is accepted that cladistic methodology represents a special case within this framework. The idea of evolutionary convergence is examined in the light of recent discussion of the existence of convergence in molecular evolution. It is concluded that attempts to estimate evolutionary trees are justifiable at least on the grounds that, despite present shortcomings, they are the most appropriate way to analyse comparative data. There are good prospects for further progress.     

Handicapped individua in evolutionary processes

Usually, when considering an evolutionary development, the fittest individua and their succesfull mutations recive most attention. The less fit ones, existing due to selection-mutation equilibria, are regarded, as an inevitable waste. It appears that these handicaped individua play an important role in evolution, as they make escapes from evolutionary traps possible. It is concluded that crucial improvements come from mutations of mutants. The implications seem to account to some extent for the observed speed and mode of evolution. An appropriate stochastic model is introduced, numerical experiments reported and results discussed.     

Inferring evolutionary processes from phylogenies

Evolutionary processes shape the regular trends of evolution and are responsible for the diversity and distribution of contemporary species. They include correlated evolutionary change and trajectories of trait evolution, convergent and parallel evolution, differential rates of evolution, speciation and extinction, the order and direction of change in characters, and the nature of the evolutionary process itself—does change accumulate gradually, episodically, or in punctuational bursts. Phylogenies, in combination with information on species, contain the imprint of these historical evolutionary processes. By applying comparative methods based upon statistical models of evolution to well resolved phylogenies, it is possible to infer the historical evolutionary processes that must have existed in the past, given the patterns of diversity seen in the present. I describe a set of maximum likelihood statistical methods for inferring such processes. The methods estimate parameters of statistical models for inferring correlated evolutionary change in continuously varying characters, for detecting correlated evolution in discrete characters, for estimating rates of evolution, and for investigating the nature of the evolutionary process itself. They also anticipate the wealth of information becoming available to biological scientists from genetic studies that pin down relationships among organisms with unprecedented accuracy.     

The evolutionary aspects of aquaporin family

Aquaporins (AQPs) were originally identified as channels facilitating water transport across the plasma membrane. They have a pair of highly conserved signature sequences, asparagine-proline-alanine (NPA) boxes, to form a pore. However, some have little conserved amino acid sequences around the NPA boxes unclassifiable to two previous AQP subfamilies, classical AQPs and aquaglyceroporins. These will be called unorthodox AQPs in this review. Interestingly, these unorthodox AQPs have a highly conserved cysteine residue downstream of the second NPA box. AQPs also have a diversity of functions: some related to water transport such as fluid secretion, fluid absorption, and cell volume regulation, and the others not directly related to water transport such as cell adhesion, cell migration, cell proliferation, and cell differentiation. Some AQPs even permeate nonionic small molecules, ions, metals, and possibly gasses. AQP gene disruption studies have revealed their physiological roles: water transport in the kidney and exocrine glands, glycerol transport in fat metabolism and in skin moisture, and nutrient uptakes in plants. Furthermore, AQPs are also present at intracellular organelles, including tonoplasts, mitochondria, and the endoplasmic reticulum. This review focuses on the evolutionary aspects of AQPs from bacteria to humans in view of the structural and functional diversities of AQPs.     

Considering evolutionary processes in conservation biology

Conservation biologists assign population distinctiveness by classifying populations as evolutionarily significant units (ESUs). Historically, this classification has included ecological and genetic data. However, recent ESU concepts, coupled with increasing availability of data on neutral genetic variation, have led to criteria based exclusively on molecular phylogenies. We argue that the earlier definitions of ESUs, which incorporated ecological data and genetic variation of adaptive significance, are more relevant for conservation. Furthermore, this dichotomous summary (ESU or not) of a continuum of population differentiation is not adequate for determining appropriate management actions. We argue for a broader categorization of population distinctiveness based on concepts of ecological and genetic exchangeability (sensu Templeton).     

Computational modeling of evolutionary learning processes in the brain

The evolutionary selection circuits model of learning has been specified algorithmically. The basic structural components of the selection circuits model are enzymatic neurons, that is, neurons whose firing behavior is controlled by membrane-bound macromolecules called excitases. Learning involves changes in the excitase contents of neurons through a process of variation and selection. In this paper we report on the behavior of a basic version of the learning algorithm which has been developed through extensive interactive experiments with the model. This algorithm is effective in that it enables single neurons or networks of neurons to learn simple pattern classification tasks in a number of time steps which appears experimentally to be a linear function of problem size, as measured by the number of patterns of presynaptic input. The experimental behavior of the algorithm establishes that evolutionary mechanisms of learning are competent to serve as major mechanisms of neuronal adaptation. As an example, we show how the evolutionary learning algorithm can contribute to adaptive motor control processes in which the learning system develops the ability to reach a target in the presence of randomly imposed disturbances.     

Fundamental processes in the evolutionary ecology of Lyme borreliosis

The evolutionary ecology of many emerging infectious diseases, particularly vector-borne zoonoses, is poorly understood. Here, we aim to develop a biological, process-based framework for vector-borne zoonoses, using Borrelia burgdorferi sensu lato (s.l.), the causative agent of Lyme borreliosis in humans, as an example. We explore the fundamental biological processes that operate in this zoonosis and put forward hypotheses on how extrinsic cues and intrinsic dynamics shape B. burgdorferi s.l. populations. Additionally, we highlight possible epidemiological parallels between B. burgdorferi s.l. and other vector-borne zoonotic pathogens, including West Nile virus.     

Genetic and evolutionary aspects of aging.

Four questions of fundamental importance to gerontology are considered. 1) The number of genes involved in aging--in the case of man, an analysis of the phenotypes of relevant spontaneous mutants indicates that aging is highly polygenic. 2) General categories of genes--regulator genes may be more relevant than structural genes: a) three aneuploid disorders, Down's, Turner's and Klinefelter's syndromes, ranked among the top 10 candidates as "segmental progeroid syndromes" when compared with 162 single gene disorders of relevance to the pathobiology of aging; b) the rates at which maximum life spans have been increasing, especially among hominids, have probably been too rapid to be accounted for by changes in the amino acid sequences of proteins; c) a preliminary analysis of the variance of maximum life spans among a few orders of mammals is suggestive of a linear correlation with the indexes of rates of chromosomal evolution, as estimated by Bush et al. (Proc. Natl. Acad. Sci. USA 74: 3942-3946, 1977). 3) Nature of gene action--although there are reasons for invoking genes that modulate the rates of accumulation of somatic mutations, differential regulation of development is likely to be a major setting for gene action. 4) New approaches to formal genetic analysis of aging--advances in experimental embryology and somatic cell genetics offer such opportunities.     

Community convergence: Ecological and evolutionary

Ecologists have often compared ecological communities in different areas, for example on different continents. The main interest is that the communities might be more similar in the characters of their species than expected under a null model of random species assortment. We suggest that such a null model should be based only on the species observed across the samples. Species-level convergence and community-level convergence must be distinguished. Physical filters (limitation to growth by the physical environment) can give species-level convergence, but only biotic filtering (based on species interactions) can give community-level convergence. Matching to species and species mutual matching must also be distinguished; the process is different, but the same tests work for both.     

Nonheritable cellular variability accelerates the evolutionary processes of cancer

Recent cancer studies emphasize that genetic and heritable epigenetic changes drive the evolutionary rate of cancer progression and drug resistance. We discuss the ways in which nonheritable aspects of cellular variability may significantly increase evolutionary rate. Nonheritable variability arises by stochastic fluctuations in cells and by physiological responses of cells to the environment. New approaches to drug design may be required to control nonheritable variability and the evolution of resistance to chemotherapy.