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Evolutionary Step (evolutionary + step)
Selected AbstractsThe evolutionary ecology of vegetative dormancy in mature herbaceous perennial plantsJOURNAL OF ECOLOGY, Issue 5 2009Richard P. Shefferson Summary 1.,I present an evolutionary ecology interpretation of vegetative dormancy in mature herbaceous perennials. This kind of vegetative dormancy has been noted for at least 40 years, but has only recently become a topic of study. 2.,Vegetative dormancy may be considered in a life-history context. Both vegetative dormancy and mortality typically decrease with increasing size. Vegetative dormancy's relationship to reproduction is more complex, because some species increase flowering and fruiting after dormancy while others do the opposite. 3.,If vegetative dormancy is adaptive, then it is most likely a bet-hedging trait. Dormancy-prone plants are often long-lived, and in such organisms, bet-hedging traits should counter the effects of environmental stochasticity on adult survival. This adaptive context may vary by life span, because in shorter-lived plants, fitness is most sensitive to changes in reproduction rather than survival. 4.,Vegetative dormancy could evolve if the costs of sprouting ever outweigh the benefits. The benefits of sprouting include: (i) photosynthesis and (ii) the opportunity to flower and reproduce. The costs include: (i) greater chance of herbivory, (ii) greater need for limiting nutrients, and (iii) greater maintenance costs. The many losses of photosynthesis among plants suggest that these benefits may not always outweigh the costs. 5.,Vegetative dormancy may be an evolutionary step towards the loss of photosynthesis. Many non-photosynthetic plants acquire carbon from their mycorrhizal fungi. Many autotrophic, dormancy-prone plants also acquire some carbon from their mycorrhizal fungi. Further, non-photosynthetic plants often become dormant to an even greater extent than autotrophic, dormancy-prone plants. 6.Synthesis,Vegetative dormancy often occurs in clades with non-photosynthetic, myco-heterotrophic plants, with implications for the evolution of traits involved in carbon nutrition. The links between vegetative dormancy, other life-history traits, mycorrhizas and the loss of photosynthesis should provide exciting directions for further research in plant evolutionary ecology. Particularly needed is an assessment of the physiology of vegetative dormancy, including whether the mycorrhiza is a carbon source in all dormancy-prone plant species. Equally important is a better understanding of the genetic relationships among photosynthesis, myco-heterotrophy and dormancy. [source] Spatial repartition and genetic relationship of green and albino individuals in mixed populations of Cephalanthera orchidsPLANT BIOLOGY, Issue 4 2010V. Tranchida-Lombardo Abstract Several green orchids of the Neottieae tribe acquire organic carbon both from their mycorrhizal fungi and from photosynthesis. This strategy may represent an intermediate evolutionary step towards mycoheterotrophy of some non-photosynthetic (albino) orchids. Mixed populations of green and albino individuals possibly represent a transient evolutionary stage offering opportunities to understand the evolution of mycoheterotrophy. In order to understand the emergence of albinos, we investigated patterns of spatial and genetic relationships among green and albino individuals in three mixed populations of Cephalanthera damasonium and one of C. longifolia using spatial repartition and Amplified fragment length polymorphism (AFLP) markers. Two of these populations were monitored over two consecutive flowering seasons. In spatial repartition analyses, albino individuals did not aggregate more than green individuals. Genetic analyses revealed that, in all sampled populations, albino individuals did not represent a unique lineage, and that albinos were often closer related to green individuals than to other albinos from the same population. Genetic and spatial comparison of genets from the 2-year monitoring revealed that: (i) albinos had lower survival than green individuals; (ii) accordingly, albinos detected in the first year did not correspond to the those sampled in the second year; and (iii) with one possible exception, all examined albinos did not belong to any green genet from the same and/or from the previous year, and vice versa. Our results support a scenario of repeated insurgence of the albino phenotypes within the populations, but unsuccessful transition between the two contrasting phenotypes. Future studies should try to unravel the genetic and ecological basis of the two phenotypes. [source] Six major steps in animal evolution: are we derived sponge larvae?EVOLUTION AND DEVELOPMENT, Issue 2 2008Claus Nielsen SUMMARY A review of the old and new literature on animal morphology/embryology and molecular studies has led me to the following scenario for the early evolution of the metazoans. The metazoan ancestor, "choanoblastaea," was a pelagic sphere consisting of choanocytes. The evolution of multicellularity enabled division of labor between cells, and an "advanced choanoblastaea" consisted of choanocytes and nonfeeding cells. Polarity became established, and an adult, sessile stage developed. Choanocytes of the upper side became arranged in a groove with the cilia pumping water along the groove. Cells overarched the groove so that a choanocyte chamber was formed, establishing the body plan of an adult sponge; the pelagic larval stage was retained but became lecithotrophic. The sponges radiated into monophyletic Silicea, Calcarea, and Homoscleromorpha. Homoscleromorph larvae show cell layers resembling true, sealed epithelia. A homoscleromorph-like larva developed an archenteron, and the sealed epithelium made extracellular digestion possible in this isolated space. This larva became sexually mature, and the adult sponge-stage was abandoned in an extreme progenesis. This eumetazoan ancestor, "gastraea," corresponds to Haeckel's gastraea. Trichoplax represents this stage, but with the blastopore spread out so that the endoderm has become the underside of the creeping animal. Another lineage developed a nervous system; this "neurogastraea" is the ancestor of the Neuralia. Cnidarians have retained this organization, whereas the Triploblastica (Ctenophora+Bilateria), have developed the mesoderm. The bilaterians developed bilaterality in a primitive form in the Acoelomorpha and in an advanced form with tubular gut and long Hox cluster in the Eubilateria (Protostomia+Deuterostomia). It is indicated that the major evolutionary steps are the result of suites of existing genes becoming co-opted into new networks that specify new structures. The evolution of the eumetazoan ancestor from a progenetic homoscleromorph larva implies that we, as well as all the other eumetazoans, are derived sponge larvae. [source] Opisthonotal glands in the Camisiidae (Acari, Oribatida): evidence for a regressive evolutionary trendJOURNAL OF ZOOLOGICAL SYSTEMATICS AND EVOLUTIONARY RESEARCH, Issue 1 2009G. Raspotnig Abstract Paired, sac-like and typically large opisthonotal glands (syn. oil glands), mainly considered for chemical protection and communication, characterize the so-called ,glandulate Oribatida' which include the Parhyposomata, Mixonomata, Desmonomata and Brachypylina but also the Astigmata. Among these groups distinct evolutionary trends affect the morphology of glands and their secretion profiles, thereby rendering them highly informative characters with phylogenetic significance. One striking tendency, convergently occurring in a few glandulate groups, leads to the degeneration or even complete regression of opisthonotal glands. In this study, a first example of coherent evolutionary steps towards opisthonotal gland degeneration is described by using desmonomatan Camisiidae as a model: Opisthonotal glands in representatives of genus Platynothrus still show morphologically and chemically ancient conditions with fairly-well developed glandular reservoirs. Secretion patterns mainly consist of a characteristic set of terpenes and aromatics (,astigmatid compounds') as found in outgroups such as desmonomatan Trhypochthoniidae. Progressive states of regression of opisthonotal glands, along with a reduction of component-richness and amounts of secretions, occur in representatives of Heminothrus and, more conspicuously, in species of Camisia, most likely indicating a consistent evolutionary trend. This trend towards opisthonotal gland atrophy may be due to novel alternative and cheap strategies of passive defense in more-derivative camisiids , such as mechanical protection by encrustation of the cuticle , that possibly compensate for the lack of chemical defenses. Zusammenfassung Paarige, sackförmige und typischerweise große opisthosomatische Drüsen (syn. Öldrüsen), deren Sekrete hauptsächlich zum chemischen Schutz und zur Kommunikation dienen sollen, kennzeichnen die sogenannten glandulaten Hornmilben. Innerhalb dieser Hornmilbengruppe, die die Parhyposomata, Mixonomata, Desmonomata, Brachypylina, aber auch die astigmaten Milben umfasst, waren die Öldrüsen offensichtlich in morphologischer und chemischer Hinsicht deutlich unterschiedlichen evolutiven Trends unterworfen; damit sind Öldrüsen ein phylogenetisch außerordentlich wichtiger Merkmalskomplex in der Oribatiden-Systematik geworden. Eine auffällige Tendenz allerdings, die offensichtlich mehrmals konvergent auftritt, führt zur Rückbildung der Drüsen in bestimmten glandulaten Gruppen. In der vorliegenden Arbeit wird zum ersten Mal eine zusammenhängende Linie solcher Rückbildungsstadien am Beispiel der Camisiidae (Desmonomata) beschrieben: die weitgehend noch gut ausgebildeten Öldrüsen von Vertretern der Gattung Platynothrus zeigen morphologisch und chemisch ursprüngliche Merkmale. Sekretprofile bestehen hauptsächlich aus einem charakteristischen Set von Terpenen und Aromaten ("astigmatid compounds'), das auch in Außengruppen wie z.B. bei Trhypochthoniiden auftritt. Fortschreitende Stadien der Rückbildung von Öldrüsen, verbunden mit einer Verarmung der Sekretprofile und einer Verringerung an Sekretmengen, treten in Vertretern von Heminothrus und, noch auffälliger, bei verschiedenen Arten von Camisia auf: dieses Phänomen, übereinstimmend mit einem auf morphologischen Daten basierenden Systemvorschlag, wird als evolutiver Trend innerhalb der Camisiidae gedeutet. Dieser Trend zur Öldrüsenrückbildung ist möglicherweise mit einer alternativen Strategie passiver Verteidigung bei weiter abgeleiteten Camisiiden zu erklären, die Krustenbildungen aus Cerotegument und Bodenpartikeln auf der Körperöberfläche als mechanischen Schutz gegen Prädatoren nützen. Diese möglicherweise energetisch billige Variante könnte den Verlust chemischer Verteidigung über Öldrüsensekretion kompensieren. [source] | ||||||||||