What have exotic plant invasions taught us over the past 20 years?

Invasive organisms have become a focal interest in ecology, owing not only to the tremendous destruction that they can cause, but also because we do not yet understand fully how they change from being minor components of their native communities to dominant components of invaded communities. Here, we discuss our perceptions of how the study of exotic plant species has contributed to the changing face of ecology over the past 20 years. Research on invasive organisms has promoted synthetic efforts between fields that have historically operated in isolation. Most importantly, the study of invasions has resulted in significant intellectual shifts in the way that old paradigms are perceived by ecologists and have led us into new and uncharted territory.     

What can Caenorhabditis elegans tell us about the nuclear envelope?

The nuclear envelope (NE) of the eukaryotic cell provides an essential barrier that separates the nuclear compartment from the cytoplasm. In addition, the NE is involved in essential functions such as nuclear stability, regulation of gene expression, centrosome separation and nuclear migration and positioning. In metazoa the NE breaks down and re-assembles around the segregated chromatids during each cell division. In this review we discuss the molecular constituents of the Caenorhabditis elegans NE and describe their role in post-mitotic NE re-formation, as well as the usefulness of C. elegans as an in vivo system for analyzing NE dynamics.     

What stories can the Frankia genomes start to tell us?

Among the Actinobacteria, the genus Frankia is well known for its facultative lifestyle as a plant symbiont of dicotyledonous plants and as a free-living soil dweller. Frankia sp. strains are generally classified into one of four major phylogenetic groups that have distinctive plant host ranges. Our understanding of these bacteria has been greatly facilitated by the availability of the first three complete genome sequences, which suggested a correlation between genome size and plant host range. Since that first report, eight more Frankia genomes have been sequenced. Representatives from all four lineages have been sequenced to provide vital baseline information for genomic approaches toward understanding these novel bacteria. An overview of the Frankia genomes will be presented to stimulate discussion on the potential of these organisms and a greater understanding of their physiology and evolution.     

What can whole genome expression data tell us about the ecology and evolution of personality?

Consistent individual differences in behaviour, aka personality, pose several evolutionary questions. For example, it is difficult to explain within-individual consistency in behaviour because behavioural plasticity is often advantageous. In addition, selection erodes heritable behavioural variation that is related to fitness, therefore we wish to know the mechanisms that can maintain between-individual variation in behaviour. In this paper, we argue that whole genome expression data can reveal new insights into the proximate mechanisms underlying personality, as well as its evolutionary consequences. After introducing the basics of whole genome expression analysis, we show how whole genome expression data can be used to understand whether behaviours in different contexts are affected by the same molecular mechanisms. We suggest strategies for using the power of genomics to understand what maintains behavioural variation, to study the evolution of behavioural correlations and to compare personality traits across diverse organisms.     

What can aquatic gastropods tell us about phenotypic plasticity? A review and meta-analysis

There have been few attempts to synthesise the growing body of literature on phenotypic plasticity to reveal patterns and generalities about the extent and magnitude of plastic responses. Here, we conduct a review and meta-analysis of published literature on phenotypic plasticity in aquatic (marine and freshwater) gastropods, a common system for studying plasticity. We identified 96 studies, using pre-determined search terms, published between 1985 and November 2013. The literature was dominated by studies of predator-induced shell form, snail growth rates and life history parameters of a few model taxa, accounting for 67% of all studies reviewed. Meta-analyses indicated average plastic responses in shell thickness, shell shape, and growth and fecundity of freshwater species was at least three times larger than in marine species. Within marine gastropods, species with planktonic development had similar average plastic responses to species with benthic development. We discuss these findings in the context of the role of costs and limits of phenotypic plasticity and environmental heterogeneity as important constraints on the evolution of plasticity. We also consider potential publication biases and discuss areas for future research, indicating well-studied areas and important knowledge gaps.     

What can the hippocampal representation of environmental geometry tell us about Hebbian learning?

 The importance of the hippocampus in spatial representation is well established. It is suggested that the rodent hippocampal network should provide an optimal substrate for the study of unsupervised Hebbian learning. We focus on the firing characteristics of hippocampal place cells in morphologically different environments. A hard-wired quantitative geometric model of individual place fields is reviewed and presented as the framework in which to understand the additional effects of synaptic plasticity. Existent models employing Hebbian learning are also reviewed. New information is presented regarding the dynamics of place field plasticity over short and long time scales in experiments using barriers and differently shaped walled environments. It is argued that aspects of the temporal dynamics of stability and plasticity in the hippocampal place cell representation both indicate modifications to, and inform the nature of, the synaptic plasticity in place cell models. Our results identify a potential neural basis for long-term incidental learning of environments and provide strong constraints for the way the unsupervised learning in cell assemblies envisaged by Hebb might occur within the hippocampus. Received: 8 March 2002 / Accepted: 13 June 2002 Acknowledgements. This work was supported by the Medical Research Council of the United Kingdom. Correspondence to: C. Lever or N. Burgess (e-mail: colin.lever@ucl.ac.uk; n.burgess@ucl.ac.uk, Tel.: +44-20-76793388 or 1147, Fax: +44-20-76791306 or 1145)     

What can phylogenetics tell us about speciation in the Cape flora?

The spectacular diversity of the Cape flora has promoted wide speculation on the evolutionary processes behind its origins, but until recently these ideas could not be tested rigorously due to the almost complete absence of a fossil record for the region. Now, molecular phylogenetic approaches, combined with analyses of ecological and biogeographical information, offer the potential to test key hypotheses about speciation of so-called Cape clades of flowering plants. We outline the main theories and how they might be tested by phylogenetic approaches. One conclusion is that population level studies of particular species complexes are now needed to complement the growing volume of phylogenetic information for Cape clades and to provide better understanding of mechanisms of population divergence in the Cape. Another is that comparisons between Cape and non-Cape clades are needed to confirm whether speciation is indeed faster in the Cape region. An alternative possibility, that extinction rates are lower, should also be considered in these comparisons. By virtue of the ongoing, coordinated efforts by a global team of botanists, the Cape is now uniquely placed for exploring the origins and assembly of a regional assemblage or biome.     

Reconstruction of paleoclimates by isotopic analysis: What can the fossil isotopic record tell us about the plant life of past environments?

The last two decades of scientific research have seen a pronounced increase in studies of abrupt climatic change. Understanding past shifts in climate becomes a priority as we examine reasons for climatic change and the interrelationship between the biosphere and the atmosphere-ocean-cryosphere. The realisation that modern climate appears to be changing at a rapid rate has challenged scientists to look at past records of abrupt climate change. How rapidly can vegetation respond to climate shifts? What magnitude of vegetation change has been seen in the past? How widespread were these changes and how do they compare with shifts in the polar ice cores and the ocean? A selection of vegetation records, for which the isotopic signatures reflect environmental changes, are examined here. This paper focuses on the type of paleoclimatic interpretation that can be made: qualitative information with or without temporal constraint or even, in the best instances, the possibility of reaching a quantitative reconstruction.     

What can the structures of enzyme-inhibitor complexes tell us about the structures of enzyme substrate complexes?

Proteinases perform many beneficial functions that are essential to life, but they are also dangerous and must be controlled. Here we focus on one of the control mechanisms: the ubiquitous presence of protein proteinase inhibitors. We deal only with a subset of these: the standard mechanism, canonical protein inhibitors of serine proteinases. Each of the inhibitory domains of such inhibitors has one reactive site peptide bond, which serves all the cognate enzymes as a substrate. The reactive site peptide bond is in a combining loop which has an identical conformation in all inhibitors and in all enzyme-inhibitor complexes. There are at least 18 families of such inhibitors. They all share the conformation of the combining loops but each has its own global three-dimensional structure. Many three-dimensional structures of enzyme-inhibitor complexes were determined. They are frequently used to predict the conformation of substrates in very short-lived enzyme-substrate transition state complexes. Turkey ovomucoid third domain and eglin c have a Leu residue at P(1). In complexes with chymotrypsin, these P(1) Leu residues assume the same conformation. The relative free energies of binding of P(1) Leu (relative to either P(1) Gly or P(1) Ala) are within experimental error, the same for complexes of turkey ovomucoid third domain, eglin c, P(1) Leu variant of bovine pancreatic trypsin inhibitor and of a substrate with chymotrypsin. Therefore, the P(1) Leu conformation in transition state complexes is predictable. In contrast, the conformation of P(1) Lys(+) is strikingly different in the complexes of Lys(18) turkey ovomucoid third domain and of bovine pancreatic trypsin inhibitor with chymotrypsin. The relative free energies of binding are also quite different. Yet, the relative free energies of binding are nearly identical for Lys(+) in turkey ovomucoid third domain and in a substrate, thus allowing us to know the structure of the latter. Similar reasoning is applied to a few other systems.     

What can venom phospholipases A(2) tell us about the functional diversity of mammalian secreted phospholipases A(2)?

Most venomous animals including snakes, bees and scorpions contain a variety of venom phospholipases A(2) (vPLA(2)s) which participate in both digestion of prey and venom toxicity. So far, more than 150 vPLA(2)s have been characterized. They all have a conserved fold with several disulfide bridges, can be catalytically active or not, and several of them can display a tremendous array of toxic effects including neurotoxicity and myotoxicity. Furthermore, the molecular diversity of vPLA(2)s found within a single snake venom can result from positive Darwinian selection. Over the last decade, receptors and binding proteins for vPLA(2)s have been identified in mammals, suggesting that vPLA(2)s can exert their toxicities through specific protein-protein interactions, besides their catalytic activity. The brain N-type receptors are involved in the neurotoxicity of vPLA(2)s, but are not yet cloned. The M-type receptor has been cloned from skeletal muscle, belongs to the superfamily of C-type lectins, and interestingly, has homology with vPLA(2) inhibitors purified from snake blood. The molecular diversity of vPLA(2)s and the presence of receptors for vPLA(2)s in mammals raises the possibility that there is also a diversity of mammalian secreted PLA(2)s (msPLA(2)s) which are the normal endogenous ligands of the vPLA(2) receptors. This view led us to clone five novel msPLA(2)s (IID, IIE, IIF, III, and X msPLA(2)s), which together with the previously cloned msPLA(2)s (IB, IIA, IIC, and V), indicate that mammals also express a large diversity of sPLA(2)s. M-type receptors can have IB and IIA msPLA(2)s as natural endogenous ligands, suggesting that msPLA(2)s, like vPLA(2)s, can function as both enzymes and ligands. msPLA(2)s were first implicated in lipid digestion, and more recently in host defense mechanisms including inflammation and antibacterial defense. The growing molecular diversity of msPLA(2)s, which all have a specific tissue distribution, and the presence of receptors suggest that msPLA(2)s, like vPLA(2)s, are endowed with a wide array of biological effects which remain to be discovered.     

What can Drosophila tell us about serpins,thrombosis and dementia?

The validity of the fruit-fly as a model of human disease has been confirmed in a striking way by Green and colleagues.1 They show that the mutations causing a necrotic disease phenotype in Drosophila, precisely mirror those resulting in a group of well-studied but perplexing diseases in the human. These diseases, ranging from thrombosis to dementia, arise from mutations causing a conformational instability of serpin protease inhibitors. The findings provide clues as to the unusual severity and variable onset of such conformational diseases and demonstrate the potential of Drosophila as a model for their future study.     

What can population genetics tell us about dispersal and biogeographic history of coral-reef fishes?

Abstract Coral-reef fishes, like many other marine organisms, generally possess a benthic adult stage and pelagic larval stage. What can population genetics studies tell us about the demographic, evolutionary and biogeographic consequences of this life cycle? Ten studies of geographical patterns of intraspecific genetic differentiation in reef fishes have been published. These studies have included 2t > species/species complexes (14 in the family Pomacentridae, the remaining 12 in 9 different families) and have been about equally divided between the tropical Pacific and the tropical western Atlantic. A survey of these studies shows the following: (i) the existence of the pelagic larval stage appears to have led to high levels of gene flow even among populations separated by thousands of kilometres of open ocean; (ii) an apparent pattern of increased gene flow among populations connected by intermediate 'stepping stones’; (iii) very tentative evidence for a relationship between length of pelagic larval life and gene flow; (iv) no clear relationship between egg type (pelagic rs non-pelagic) and gene flow; and (v) suggestive evidence that damselfishes (family Pomacentridae) may have more restricted dispersal (less gene flow) than other reef fishes. The application of current and future molecular tools has the strong potential to clarify some of these relationships, particularly by using relatively neutral genetic markers. Additionally, discoveries of DNA markers having very high rates of mutation may allow tracking of demographically relevant levels of larval dispersal. Molecular tools are becoming especially valuable in uncovering the biogeographic and phylogenetic history of reef fishes. The one molecular study to date has suggested that at least some speciation events may have occurred during the climate changes and sea-level regressions associated with Pleistocene glacial episodes. Molecular tools need to be used to further explore the means by which high species diversity can be generated in the face of the apparently high gene flow observed in most coral-reef fishes.     

What can patterns of differentiation across plant genomes tell us about adaptation and speciation?

Genome scans have become a common approach to identify genomic signatures of natural selection and reproductive isolation, as well as the genomic bases of ecologically relevant phenotypes, based on patterns of polymorphism and differentiation among populations or species. Here, we review the results of studies taking genome scan approaches in plants, consider the patterns of genomic differentiation documented and their possible causes, discuss the results in light of recent models of genomic differentiation during divergent adaptation and speciation, and consider assumptions and caveats in their interpretation. We find that genomic regions of high divergence generally appear quite small in comparisons of both closely and more distantly related populations, and for the most part, these differentiated regions are spread throughout the genome rather than strongly clustered. Thus, the genome scan approach appears well-suited for identifying genomic regions or even candidate genes that underlie adaptive divergence and/or reproductive barriers. We consider other methodologies that may be used in conjunction with genome scan approaches, and suggest further developments that would be valuable. These include broader use of sequence-based markers of known genomic location, greater attention to sampling strategies to make use of parallel environmental or phenotypic transitions, more integration with approaches such as quantitative trait loci mapping and measures of gene flow across the genome, and additional theoretical and simulation work on processes related to divergent adaptation and speciation.     

What can vicariance biogeographic models tell us about the distributional history of subterranean amphipods?

Because of taxonomic diversity, geographic isolation, and other considerations, subterranean groundwater amphipods would appear to make excellent candidates for biogeographic studies. Limted dispersal ability in combination with local endemism makes it likely that vicariance models will generally offer better explanations for present distribution patterns of subterranean amphipods than scenarios based on centers of origin and dispersal. Vicariance biogeography demands a knowledge of both phylogeny and area relationships, which are typically shown on biological area cladograms. To date most biogeographic studies on subterranean amphipods have been limited to cladograms of single taxonomic groups. Although useful in showing possible relationships between areas and nested subsets of taxa, these single taxon studies do not consider covariant patterns among different groups. However, in order to be fully effective, future biogeographic research will have to focus on analyses of congruence between biological area cladograms of amphipod taxa and other subterranean crustacean groups, such as isopods. To date many covariant distributions among groups of subterranean crustaceans have been recognized but not yet analyzed for congruence.     

What can morphology and isozymes tell us about the history of the Dryas integrifolia–octopetala complex?

An earlier study of the morphological variation in the circumpolar genus Dryas in Greenland revealed that populations in east Greenland are highly variable and this variation was interpreted as a hybrid zone between D. octopetala and D. integrifolia. It was proposed that populations of Dryas in east Greenland immigrated postglacially from Svalbard. The purpose of our study was to investigate the population structure of the Dryas integrifolia-octopetala complex using a combination of morphological and genetic characters. Populations of Dryas were sampled in Greenland, Svalbard, Iceland and north Scandinavia (Sweden). The morphological traits clearly separated west Greenland from Svalbard, Iceland and north Scandinavia. A large number of individuals from east Greenland and some from north Greenland could be interpreted as hybrids between the morphs. The genetic pattern was, however, partly different as the greatest amount of differentiation among regions was found between west and north Greenland (FRT = 0.65). The highest degree of genetic variation appeared within east Greenland. This was in accordance with the putative hybrid origin of the populations, as concluded based on the morphological results. The total amount of genetic differentiation found among the six regions (FRT = 0.61) was larger than between the two species (FRT = 0.44). The genetic pattern matched the proposed postglacial migration routes.     

What can yeast tell us about N-linked glycosylation in the Golgi apparatus?

The N-glycans found on eukaryotic glycoproteins occur in a vast range of different structures. A universal N-glycan core is attached to proteins during synthesis in the endoplasmic reticulum, and then diversity is generated as the proteins pass through the Golgi apparatus. Many of the Golgi-localised glycosyltransferases have now been identified in both yeast and mammalian cells, but it is still unclear how these enzymes are integrated into the Golgi and the rest of the cell so as to ensure efficient and specific processing of passing substrates. This review discusses the potential of the yeast system to address these issues.