Different time patterns of the presence of red-eared slider influence the ontogeny dynamics of common frog tadpoles.

The coexistence of species in a given community depends on the set of species involved and the timing of their interactions. Many native communities are increasingly forced to face both direct and indirect pressures from new alien predators, which, in extreme cases, can lead to the extinction of prey populations. In this study, we examine the dynamics of the ontogeny of common frog (Rana temporaria) tadpoles under different time patterns of an alien predator-the red-eared slider (Trachemys scripta elegans) presence. We found that the tadpoles had a longer larval period and were smaller in size at metamorphosis and lower in body mass when the predator was present in early development than when the tadpoles developed without a predator. The early presence of a predator conspicuously reduced the growth increments of the tadpoles at early development. After the removal of the predator, growth accelerated above the level measured under the conditions of both the late predator and no predator. However, these growth rates did not exceed the growth rates of equally sized tadpoles in the other treatments and therefore were not sufficient to compensate for the growth slowdown in the first part of development. The presence of a predator in late tadpole development influenced neither the time to metamorphosis nor size/body mass at metamorphosis. In conclusion, the predator had the effect on metamorphosis traits only if it was present in the early development of tadpoles.

Chemical cues of an invasive turtle reduce development time and size at metamorphosis in the common frog.

In aquatic systems, chemical cues are one of the major sources of information through which animals can assess local predation risk. Non-native red-eared sliders (Trachemys scripta elegans) have the potential to disrupt aquatic ecosystems in Central Europe because of their superior competitive abilities and omnivorous diets. In this study, we examined whether continuous predator-borne cues are tied to changes in the developmental rates, growth rates and sizes at metamorphosis of common frog tadpoles (Rana temporaria). Our results show rather rarely documented types of amphibian prey responses to caged predators. The presence of turtles shortened the time at metamorphosis of tadpoles from 110 ± 11.7 days to 93 ± 13.0 days (mean ± S.D.). The first metamorphosed individuals were recorded on the 65th day and on the 80th day from hatching in the predator treatment and in the control group, respectively. The froglets were significantly smaller (12.8 ± 0.99 mm) in the presence of the predator than in the control treatment (15.2 ± 1.27 mm). The growth rate trajectories were similar between the predator treatment and the control. Thus, predator-induced tadpole defences were evident in higher developmental rates and smaller sizes at metamorphosis without significant changes in growth.

Planktonic or non-planktonic food in young-of-the-year European perch Perca fluviatilis in ponds.

Higher biomass especially of some aquatic macrophyte species offered a higher density of phytophilous zoobenthos, but did not increase the proportion of non-planktonic to planktonic prey in young-of-the-year perch Perca fluviatilis. Both abundance and biomass of non-planktonic prey dominated over planktonic prey in the pond with lower biomass of aquatic macrophytes and lower food. Survival of P. fluviatilis was lower (20%) in the pond with lower food than in the other pond (34%), however, specific growth rate (1.3% day(-1) ) and final Fulton's condition factor of P. fluviatilis were similar in both ponds.

Hepatic and branchial glutathione S-transferases of two fish species: substrate specificity and biotransformation of microcystin-LR.

Liver and gills of roach (Rutilus rutilus) and silver carp (Hypophthalmichthys molitrix) were examined for glutathione S-transferases (GSTs) contents and their substrate specificity and capacity to biotransform microcystin-LR (MC-LR). GSTs and other glutathione (GSH) affine proteins were purified using a GSH-agarose matrix and separated by anionic chromatography (AEC). Substrate specificities were determined photometrical for 1-chloro-2,4-dinitrobenzene (CDNB), 1,2-dichloro-4-nitrobenzene (DCNB), 4-nitrobenzyl chloride (pNBC) and ethacrynic acid (ETHA). Biotransformation rate of MC-LR was determined by high performance liquid chromatography (HPLC). Roach exhibited different hepatic and branchial GST activities for used substrates (DNB, pNBC and DCNB) compared to silver carp but not for ethacrynic acid. It suggests that, both fish species have similar amount of pi and/or alpha class, which were the dominant GST classes in liver and gills. Gills of both fish species contained a higher number of GST isoenzymes, but with lower activities and ability of MC-LR biotransformation than livers. GST isoenzymes from roach had higher activity to biotransform MC-LR (conversion rate ranging up to 268 ng MC-LR min(-1) mL(-1) hepatic enzyme) than that isolated from silver carp. Without any prior contact to MC-LR or another GST inducer, roach seems to be better equipped for microcystin biotransformation than silver carp.