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Asexual Lineages (asexual + lineage)
Selected AbstractsGenetic processes in arbuscular mycorrhizal fungiFEMS MICROBIOLOGY LETTERS, Issue 2 2005Teresa E. Pawlowska Abstract Arbuscular mycorrhizal (AM) fungi (Glomeromycota) colonize roots of the majority of land plants and facilitate their mineral nutrient uptake. Consequently, AM fungi play an important role in terrestrial ecosystems and are becoming a component of sustainable land management practices. The absence of sexual reproductive structures in modern Glomeromycota combined with their long evolutionary history suggest that these fungi may represent an ancient asexual lineage of great potential interest to evolutionary biology. However, many aspects of basic AM fungal biology, including genome structure, within-individual genetic variation, and reproductive mode are poorly understood. These knowledge gaps hinder research on the mechanisms of AM fungal interactions with individual plants and plant communities, and utilization of AM fungi in agricultural practices. I present here the current state of research on the reproduction in AM fungi and indicate what new findings can be expected in the future. [source] EVALUATION OF ELEVATED PLOIDY AND ASEXUAL REPRODUCTION AS ALTERNATIVE EXPLANATIONS FOR GEOGRAPHIC PARTHENOGENESIS IN EUCYPRIS VIRENS OSTRACODSEVOLUTION, Issue 4 2010Sofia Adolfsson Transitions from sexual to asexual reproduction are often coupled with elevations in ploidy. As a consequence, the importance of ploidy per se for the maintenance and spread of asexual populations is unclear. To examine the effects of ploidy and asexual reproduction as independent determinants of the success of asexual lineages, we sampled diploid sexual, diploid asexual, and triploid asexual Eucypris virens ostracods across a European wide range. Applying nuclear and mitochondrial markers, we found that E. virens consists of genetically highly differentiated diploid sexual populations, to the extent that these sexual clades could be considered as cryptic species. All sexual populations were found in southern Europe and North Africa and we found that both diploid asexual and triploid asexual lineages have originated multiple times from several sexual lineages. Therefore, the asexual lineages show a wide variety of genetic backgrounds and very strong population genetic structure across the wide geographic range. Finally, we found that triploid, but not diploid, asexual clones dominate habitats in northern Europe. The limited distribution of diploid asexual lineages, despite their shared ancestry with triploid asexual lineages, strongly suggests that the wider geographic distribution of triploids is due to elevated ploidy rather than to asexuality. [source] Obligate asex in a rotifer and the role of sexual signalsJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 1 2008C.-P. STELZER Abstract Transitions to asexuality have occurred in many animals and plants, yet the biological mechanisms causing such transitions have often remained unclear. Cyclical parthenogens, such as cladocerans, rotifers or aphids often give rise to obligate asexual lineages. In many rotifers, chemical signals that accumulate during population crowding trigger the induction of sexual stages. In this study, I tested two hypotheses on the origin of obligate parthenogenesis in the rotifer Brachionus calyciflorus: (i) that obligate parthenogens have lost the responsiveness to the sexual signal; and (ii) that obligate parthenogens have lost the ability to produce the sexual signal. Pairwise cross-induction assays among three obligate parthenogenetic strains and two cyclically parthenogenetic (sexual) strains were used to test these hypotheses. I found that obligate parthenogens can induce sexual reproduction in sexual strains, but not vice versa. This demonstrates that obligate parthenogens do still produce the sexual signal, but have lost responsiveness to that signal. [source] The nature and reality of the aphid clone: genetic variation, adaptation and evolutionAGRICULTURAL AND FOREST ENTOMOLOGY, Issue 2 2008Hugh D. Loxdale Abstract 1,When aphid clones and clonality are discussed, it is still often said that they are ,genetically identical', a statement for which there is no direct evidence, and certainly not for the entire genome. By contrast, there is a growing body of empirical data from the application of high resolution molecular (DNA) markers that aphid asexual lineages rapidly mutate and that, in some documented cases, this variation is selectable, either positively or negatively. 2,Although it is true that, in enclosed conditions (e.g. laboratory or field cage), a so-called clone as defined as the asexual progeny of a single foundress may be traceable, this is rarely if ever possible in the field without the use of genetic markers, and even then, usually only at a relatively few loci (multilocus genotypes, ,MLGs'). 3,The continued use of the term clone without qualification of its true nature and the reality of its interesting biology is likely to hamper a proper understanding of the ecology and evolution of these insects (which are interesting in their own right because of their complex life histories, but also because they are important as major pests globally, both by causing direct feeding damage and by transmitting pathogenic plant viruses and thereby leading to huge economic losses in the agricultural, horticultural and forestry industries). 4,In this short review, I provide evidence of what is now known about aphid clonality after the widespread use of molecular markers, comprising information mainly gained within the last 15 years or so. 5,The data demonstrate widespread adaptation and evolution, sometimes involving introgression and hybridization. Because of this new knowledge, our ideas of what constitutes a clone are in need of serious re-evaluation. [source] The ecological differentiation of asexual lineages of cotton aphids: alate behaviour, sensory physiology, and differential host associationsBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 3 2009ADRIANA J. NAJAR-RODRÍGUEZ The cotton aphid (Aphis gossypii Glover) is a cosmopolitan pest species consisting of various host plant-associated lineages that appear to have different patterns of insecticide resistance, electrophoretic banding, and reproductive output across alternative host species. Debate continues as to whether these differences represent intraspecific variation or indicate a complex of cryptic or sibling species. We studied the host plant-related ecology of two asexual lineages of A. gossypii associated with the families Malvaceae and Cucurbitaceae, respectively, in particular the host plant finding and acceptance processes of the alate forms. The two lineages proved to be differentiated across host plants in terms of: (1) their landing and settling behaviour, nymphal production rate, and subsequent colony establishment (i.e. nymphal survival and development) and (2) their sensory abilities in relation to host plant-derived odours. Furthermore, genetic structuring according to host plant type was detected using the gene for elongation factor 1-,. The magnitude of the genetic differentiation across lineages was low, perhaps indicating a relatively recent divergence. The results demonstrate: (1) the presence of (at least) two cryptic species within the current definition of A. gossypii, as anticipated in previous studies, and (2) the practicalities of using a multidisciplinary approach to understanding the ,limits' of asexual species. If sexuals can be generated from each of these lineages, this conclusion will be open to further testing. © 2009 The Linnean Society of London, Biological Journal of the Linnean Society, 2009, 97, 503,519. [source] Heritable genetic variation and potential for adaptive evolution in asexual aphids (Aphidoidea)BIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 1 2003ALEX C. C. WILSON Aphid life cycles can encompass cyclical parthenogenesis, obligate parthenogenesis, obligate parthenogenesis with male production and an intermediate ,bet-hedging' strategy where an aphid genotype will over-winter by continuing to reproduce by parthenogenesis and by investment in sexually produced eggs. In this paper, we focus on aphid lineages that reproduce entirely parthenogenetically (asexual aphids), in contrast to those that have any sexual forms in the annual cycle. Using modern molecular techniques, aphid biologists have made many empirical observations showing that asexual lineages are widespread both geographically and temporally. Indeed, we are collectively beginning to gather data on the evolution and persistence of these lineages through time. Here we review aphid karyology and parthenogenesis, both essential for interpretation of the molecular and ecological evolution of aphid asexual lineages. We describe the growing list of studies that have identified aphid genotypes that are both temporally and geographically widespread. We then collate examples of molecular and chromosomal evolution in asexual aphids and review the literature pertaining to phenotypic evolution and ecological diversification of asexual aphid lineages. In addition, we briefly discuss the potential of bacterial endosymbionts and epigenetic effects to influence the evolution of asexual aphid lineages. Lastly we provide a list of aphid taxa believed to be obligately asexual. This will be a useful resource for those seeking parthenogenetic animals as study systems. In conclusion, we present guidelines for the use of the term clone in aphid biology and stress the need for well-designed and well-executed studies examining the potential of asexual aphid lineages for adaptive evolution. © 2003 The Linnean Society of London. Biological Journal of the Linnean Society, 2003, 79, 115,135. [source] | ||||||||||