Biologists have conclusively failed to arrive at a generally acceptable definition of sexual reproduction. Because of this, several reproductive processes are seen as sexual by some authors but as asexual by others. Included among these are automictic methods of reproduction. Automixis describes several reproductive processes whereby a new individual derives from a product or products of a single meiotically dividing cell. Several forms involve an episode of nuclear fusion and it is argued that, because of this, they should be seen as sexual processes irrespective of whether the fusing bodies are differentiated as gametes or are simply meiotic tetrad nuclei. Other forms involve no episode of nuclear fusion and it is argued that, because of this, they should be seen as asexual processes. These latter forms involve the generation of diploid eggs either by restitutional meioses, or by an endomitotic event preceding or following a reductional meiosis, or involve the generation of a diploid embryo by the fusion of cleavage division nuclei in a haploid embryo; in each case the egg develops parthenogenetically. In addition to the disagreement that exists over the reproductive status of automixis, considerable confusion exists over its taxonomic distribution. It is often described as being restricted to a few species of insects, where it is parthenogenetic, but in factde range of taxa, including both isogamous and anisogamous plants and fungi, where it may be either parthenogenetic or non‐parthenogenetic. This confusion results both from a failure of many biologists writing on this subject to adequately consider the variation in life‐cycles existing between major taxa and from a general failure by botanists and mycologists to distinguish between automixis and autogamous forms of self‐fertilization (in which the fusing nuclei derive from different meioses). It is further compounded by a proliferation of synonyms for automictic processes. Thus in a number of publications automictic processes are variously described as being matromorphic, thelytokous, parthenogamic, autogamic or apomictic rather than as being automictic.
Swarm raiding army ants, with hundreds of thousands or millions of workers per colony, have evolved convergently in the Old World and New World tropics. Here we demonstrate for the ¢rst time, to our knowledge, supere¤cient foraging teams in Old World army ants and we compare them quantitatively with such teams in New World army ants. Colonies of Dorylus wilverthi in the Old World and Eciton burchelli in the New World retrieve almost identical sizes of prey item and the overall size range of their workers is very similar. However, 98% of D. wilverthi workers are within the size range of the smallest 25% of E. burchelli workers. In E. burchelli larger workers specialize in prey retrieval, whereas in D. wilverthi workers form many more teams than in E. burchelli. Such teams compensate for the relative rarity of larger workers in Dorylus. The proportions of prey items retrieved by teams in Dorylus and Eciton are 39% and 5%, respectively. The percentages of all prey biomass retrieved by teams in Dorylus and Eciton are 64% and 13%, respectively. Working either as single porters or teams, Dorylus carry more per unit ant weight than do Eciton, but Eciton are swifter. However, these di¡erent ergonomic factors counterbalance one another, so that performance at the colony level is remarkably, although by no means completely, similar between the Old and New World species. The remaining di¡erences are attributable to adaptations in worker and colony tempo associated with the recovery dynamics of their prey populations. Our comparative analysis provides a unique perspective on worker-level and colony-level adaptations and is a special test of the theory of worker caste distributions.
The genus Taraxucum is a widely dispersed, ecologically variable taxon of some 2000 sexual and apomictic (agarnospermous) species. Data from numerous studies are used to examine the influences sexuality and apomixis have had on its evolution, geographical distribution and rrological diversification. A new explanation is given of the geographiral distribution of sexual and apomirtic forms, and the role of polyploidy in buffering apomicts against the effects of a n accumulation of deleterious mutations is examined.
A model is presented for the evolution and control of generative apomixis—a collective term for apomixis in animals and diplosporous apomixis in flowering plants. Its development takes into account data obtained from studies of apomictic‐like processes in sexual organisms and in non‐apomictic parthenogens, as well as data obtained from studies of generative apomicts. This approach provides insights into the evolution and control of generative apomixis that cannot be obtained from studies of generative apomicts alone. It is argued that the control of the avoidance of meiotic reduction during egg production in generative apomicts resides at a single locus, the identity of which can vary between lineages. This variation accounts for the observed variation between taxa in the pattern of avoidance of meiotic reduction. The affected locus contains a wild‐type allele that codes for meiotic reduction and excess copies of a mutant allele that codes for its avoidance. The dominance relationship between these is determined by their ratio and by the environment. Environmental differences between female generative cells and somatic cells are such that the phenotypic expression of the mutant allele is favoured in the former, while that of the wild‐type allele is favoured in the latter. This is important, for the locus is also involved in the control of mitosis which would be disrupted by the expression of the mutant allele in somatic cells. The requirement to maintain a viable pattern of growth and development explains why the wild‐type allele is retained by generative apomicts, and this in turn explains why the ability to produce meiotically reduced eggs is retained by facultative forms and why it appears to be suppressed in, rather than absent from, obligate forms. The requirement for excess copies of the mutant allele in generative cells explains why generative apomicts are typically polyploid, as this condition provides a simple and effective means of generating the correct balance of mutant and wild‐type alleles. Environmental effects can also lead to the dominance relationship between wild‐type and mutant alleles varying between generative cells. In plants, this can lead to the apomixis gene being expressed, and thus to meiotic reduction being avoided, in only some ovules. Meiotically reduced, as well as meiotically unreduced, eggs are produced when this occurs. If compatible and viable pollen is available the meiotically reduced eggs may be fertilized, resulting in these organisms reproducing as facultative apomicts. It is argued that the control and evolution of parthenogenesis in generative apomicts varies between taxa. In some, the parthenogenetic initiation of embryos may result from the acquisition of a parthenogenesis gene or genes; but there is no reason to believe that this is either a general or a common requirement. Indeed, in some it may be an ancestral trait, these apomicts differing from their sexual ancestors in the ability to mature, rather than in the ability to initiate, embryos from unfertilized eggs; ...
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