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Tokolyi, J.

Publications and source records attributed to Tokolyi, J..

2 recordsLinked to original sources

Seasonal variation of genotypes and reproductive plasticity in a facultative clonal freshwater invertebrate animal (Hydra oligactis) living in a temperate lake

Facultative sexual organisms combine sexual and asexual reproduction within a single life cycle, often switching between reproductive modes depending on environmental conditions. These organisms frequently inhabit variable seasonal environments, where favourable periods alternate with unfavourable periods, generating temporally varying selection pressures that strongly influence life history decisions and hence population dynamics. Due to the rapidly accelerating changes in our global environment today, understanding the dynamics of and genetic changes in facultative sexual populations inhabiting seasonal environments is critical to assess and prepare for additional challenges that will affect such ecosystems. In this study we aimed at obtaining insights of the seasonal population dynamics of the facultative sexual freshwater cnidarian Hydra oligactis through a combination of Restriction-site Associated Sequencing (RAD-Seq) genotyping and the collection of phenotypic data on the reproductive strategy of field-collected hydra strains. We found no significant genetic change during the two years in the study population. Clone lines were detected between seasons and even years, suggesting that clonal lineages can persist for a long time in a natural population. We also found that distinct genotypes differ in sexual reproduction frequency, but these differences did not affect whether genotypes reappeared across samplings. Our study describes changes in population genetic structure across the seasons in a hydra population for the first time, providing key insights into the biology of the species, while also contributing to understanding the population biology of facultative sexual species inhabiting freshwater ecosystems.

ecology↗

Reproductive mode, stem cells and regeneration in a freshwater cnidarian with post-reproductive senescence

In many basal metazoans both somatic and reproductive functions are performed by cellular derivatives of a single multipotent stem cell population. Reproduction can drain these stem cell pools, imposing a physiological cost with subsequent negative effects on somatic maintenance functions. In the freshwater cnidarian Hydra oligactis both asexual (budding) and sexual reproductive modes (production of resting eggs) are present, and both of these are dependent on a common pool of interstitial stem cells. Resting eggs tolerate abiotic conditions which neither the parental animals, nor asexual offspring can survive (e.g. freezing). Therefore, when facing unfavorable conditions and increased mortality risk, hydra polyps are expected to show higher differentiation of interstitial stem cells into germ cells (i.e. sexual reproduction), compared to other cell types needed for selfmaintenance or asexual reproduction. Here, by comparing sexually and asexually reproducing individuals to non-reproductives, we studied the physiological costs of reproduction (size of interstitial stem cell pools, their somatic derivatives and regeneration rate, which is dependent on these cell types) in H. oligactis polyps from a free-living Hungarian population prior to the onset of winter. Sexual individuals (but not asexuals) were characterized by significantly smaller interstitial stem cell pools, fewer somatic derivatives (nematoblasts involved in food capture) and lower regeneration ability compared to non-reproductives. We also found a negative correlation between germ cell counts and stem cell numbers in males (but not in females). These results show that the physiological costs of reproduction are higher for sexual individuals. They also suggest that increased differentiation of stem cells into gametes might limit investment into somatic functions in hydra polyps. Exhaustion of cellular resources (stem cells) could be a major mechanism behind the extreme post-reproductive senescence observed in this species.

evolutionary biology↗