Asexual Animals Research Articles

Early release of eggs and embryos in a brooding ancient asexual ostracod: brood selection or a gambling strategy to increase fecundity?

Asexual lineages lack the means to purge their genomes of (deleterious) mutations through recombination. Evolutionary theory thus predicts that such lineages will be prone to early extinction. In brooding animals, brood selection might provide a mechanism to counter the accumulation of mutations. Of the three putative ancient asexual animal groups, only the darwinulid ostracods are brooders. Here, we test the incidence of egg and juvenile abortion in a darwinulid species, Penthesilenula brasiliensis, under two temperature treatments. Part of the offspring is released without brooding (close to 30% in one treatment). The majority of these aborted eggs hatches and develops. As it is unlikely that females are such bad judges of offspring quality, either the surviving animals will present deficiencies later on in development (brood selection) or early egg release can be a (bet-hedging) strategy to increase fecundity in favourable conditions.

Evolution in the slow lane: molecular rates of evolution in sexual and asexual ostracods (Crustacea: Ostracoda)

Parthenogenetic lineages within non-marine ostracods can occur either in mixed (with sexual and asexual females) or exclusively asexual taxa. The former mode of reproduction is associated with a high intraspecific diversity at all levels (genetic, morphological, ecological) and, at least in the Cypridoidea, with geographical parthenogenesis. Obligate asexuality is restricted to the Darwinuloidea, the strongest candidate for an ancient asexual animal group after the bdelloid rotifers, and is characterized by low diversity. We have compared rates of molecular evolution for the nuclear ITS1 region and the mitochondrial COI gene amongst the three major lineages of non-marine ostracods with sexual, mixed and asexual reproduction. Absolute rates of molecular evolution are low for both regions in the darwinulids. The slow-down of evolution in ITS1 that has been observed for Darwinula stevensoni (Brady & Robertson) apparently does not occur in other darwinulid species. ITS1 evolves more slowly than COI within non-marine ostracod families, including the darwinulids, but not between superfamilies. The ancient asexuals might have a higher relative substitution rate in ITS1, as would be expected from hypotheses that predict the accumulation of mutations in asexuals. However, the speed-up of ITS could also be ancient, for example through the stochastic loss of most lineages within the superfamily after the Permian–Triassic mass extinction. In this case, the difference in rate would have occurred independently from any effects of asexual reproduction.

How ancient are ancient asexuals?

Ancient asexual animal groups, such as bdelloid rotifers and darwinuloid ostracods, are excellent model organisms to study the effects of long-term asexuality. However, the absolute length of time that these groups have been fully asexual is mostly ignored. In the case of the darwinuloid ostracods, the fossil record shows that sexual reproduction disappeared almost completely after the end of Permian mass extinction (ca. 245 Myr ago), although several putative records of males from the Mesozoic obscure the exact time-frame of obligate asexuality in darwinuloids. Here, we re-examine the Mesozoic darwinuloid records, with regard to the reproductive mode of the assemblages. Three criteria to distinguish males in fossil populations (lack of brood pouch, position of muscle scars and size dimorphism) are used here to test for the presence of males in darwinuloid assemblages. A large, well-preserved assemblage of Darwinula leguminella (Forbes 1885) from the latest Jurassic (ca. 145 Myr ago) of England is found to be markedly variable in size and shape, but nevertheless turns out to be an all female assemblage. The exceptional preservation of the material also allows the re-assignment of this species to the extant darwinuloid genus Alicenula. All other putative dimorphic darwinuloid records from the Mesozoic are re-examined using the same criteria. The hypothesis that these assemblages represent bisexual populations is rejected for all post-Triassic (ca. 208 Myr ago) records.

Comparisons of Physiological Performance in Sexual and Asexual Whiptail Lizards (GenusCnemidophorus): Implications for the Role of Heterozygosity

Many asexual animal species are of hybrid origin, with consequent high levels of heterozygosity. Data from some studies suggest that increased heterozygosity may be functionally correlated with superior performance in a variety of fitness-related traits. Thus, hybrid asexual species could be expected to exhibit some degree of heterosis. This spontaneous heterosis hypothesis is tested in a comparative study of asexual and sexual species of the lizard genus Cnemidophorus. Asexual species of the genus are parthenogenetically reproducing hybrids of the sexual species and as a result have high levels of heterozygosity that have persisted since their origins. Five whole-organism physiological traits (burst speed, endurance, maximal exertion, standard metabolic rate, and evaporative water loss rate) were examined in five asexual species and the sexual species that gave rise to them. Trait values for sexual and asexual species were compared using a nonphylogenetic approach and two phylogenetically controlled approaches capable of dealing with reticulate phylogenies. In contrast to the predictions of the heterosis hypothesis, performance for four of the traits in asexual Cnemidophorus was not statistically different than that in their sexual parental species, and asexuals had significantly worse endurance. On the whole, the overall trend appeared to be toward worse performance in asexuals. An obvious interpretation of these results is that heterozygosity and "vigor" need not be functionally related. However, other factors may be counterbalancing possible beneficial effects of heterozygosity, including detrimental epistatic effects resulting from the karyotypically mixed genome of these hybrids, and the accumulation of deleterious mutations in the asexual lineages via Muller's ratchet.

An integrated approach to life-cycle evolution using selective landscapes

A model which defines fitness in terms of the intrinsic rate of increase of phenotypes is used to analyse which life cycles are appropriate to which ecological circumstances. The following predictions are made for asexual animals and those sexual animals producing on average more than one daughter per brood. If there are no behavioural or physiological interactions between variables, then number of offspring per breeding should be maximized, survival until first/next breeding should be maximized, and time to first/next breeding should be minimized. If interactions occur such that altering one life-cycle variable affects another, then there are trade-offs between variables and the optimum trade-off will maximize fitness. Number of offspring per breeding will generally affect adult survivorship until next breeding. Given certain reasonable assumptions about this trade-off, high juvenile survivorship selects towards semelparity (many offspring per brood), low juvenile survivorship selects towards iteroparity (few offspring per brood). If juvenile survival depends on adult feeding, as in altricial birds, then juvenile survivorship declines as clutch size is increased. Optimal clutch size maximizes the number of surviving offspring per brood. Two trade-offs involve parental care. If parents guard their offspring they should take more risks if brood size is larger. The amount that parents feed their offspring should depend on how effective feeding is in enhancing growth. Growth may also be enhanced by taking risks, in juveniles or adults. The extent of risk-taking should depend on how effective risk-taking is in enhancing growth. If the number of offspring per brood is related to growing conditions for offspring, the prediction is that more offspring per brood should be produced if growing conditions for offspring are better. If the adult can protect the offspring, for example by encapsulating them, the amount of protection provided should depend on how effective the protection is in increasing offspring survivorship.