Density-dependent growth and metamorphosis in the larval bronze frog<Emphasis Type="Italic">Rana temporalis</Emphasis> is influenced by genetic relatedness of the cohort

Effects of density and kinship on growth and metamorphosis in tadpoles ofRana temporalis were studied in a 2×4 factorial experiment. Fifteen egg masses were collected from streams in the Western Ghat region of south India. The tadpoles were raised as siblings or in groups of non-siblings at increasing density levels, viz. 15, 30, 60 and 120/5 l water. With an increase in density level from 15 to 120 tadpoles/5 l water, duration of the larval stage increased and fewer individuals metamorphosed irrespective of whether they belonged to sibling or non-sibling groups by day 100 when the experiments were terminated. The size of individuals at metamorphosis declined significantly with increase in the density of rearing. However, at higher densities (60 and 120 tadpoles/5 l water) sibling group tadpoles performed better compared to mixed groups and took significantly less time to metamorphose. Also, more individuals of sibling groups metamorphosed compared to non-sibling groups at a given density. Mixed rearing retarded growth rates, prolonged larval duration resulting in a wider spectrum of size classes, and lowered the number of individuals recruited to terrestrial life. The study shows that interference competition occurred more strongly in cohorts of mixed relatedness than in sibling groups.     

Brain plasticity over the metamorphic boundary: carry-over effect of larval environment on froglet brain development

Brain development shows high plasticity in response to environmental heterogeneity. However, it is unknown how environmental variation during development may affect brain architecture across life history switch points in species with complex life cycles. Previously, we showed that predation and competition affect brain development in common frog (Rana temporaria) tadpoles. Here, we studied whether larval environment had carry-over effects in brains of metamorphs. Tadpoles grown at high density had large optic tecta at metamorphosis, whereas tadpoles grown under predation risk had small diencephala. We found that larval density had a carry-over effect on froglet optic tectum size, whereas the effect of larval predation risk had vanished by metamorphosis. We discuss the possibility that the observed changes may be adaptive, reflecting the needs of an organism in given environmental and developmental contexts.     

Primary and secondary phenology. Does it pay a frog to spawn early?

This study examines the consequences of variation in the laying and hatching date for the time of metamorphosis in the common frog Rana temporaria . Field data are presented showing that eggs laid early tend to take longer to develop. Thus, the time advantage for early eggs is reduced at the time of hatching. There was an among-year variation in this phenomenon; it was not manifest in a phenologically late year. Also, field data revealed that mortality due to pond freezing is a real risk for early laid eggs. Finally, two experiments in tanks analyse the effects of hatching date variation for the time of metamorphosis. (1) When hatching was experimentally delayed by 7 or 11 days, this resulted in later metamorphosis, however, by only 2 and 5 days, respectively. (2a) When tadpoles from the same pond that naturally hatched at different times were compared, it was found that a hatching time difference of 6 days resulted in later metamorphosis by 2 days only. (2b) A comparison of tadpoles from two different ponds that hatched 11 days apart also resulted in only 2 days' difference in metamorphosis. In this case, the later but faster developing tadpoles metamorphosed at a smaller size. I suggest that eggs from these two ponds differed genetically in the growth and development strategy. Despite the obvious risks, and the moderate gain in terms of early metamorphosis, frogs breed dangerously early in spring. Possible reasons for this are discussed. These include external selective forces that promote early metamorphosis (also at a high cost), within-pond competition among tadpoles with an advantage for early and large tadpoles and finally factors relating to mate choice at the breeding site.     

Effects of temperature-induced variation in anuran larval growth rate on head width and leg length at metamorphosis

We tested whether temperature-induced variation in the growth rate of Rana cascadae tadpoles caused any variation in head width or leg length at metamorphosis, independent of the effects of temperature on body size. Body-size-adjusted head width appears to be insensitive to even large variations in tadpole growth rate. This result mirrors previous observations on the effects of variation in food level and temperature on metric shape in frogs and other ectothermic vertebrates. Leg length, on the other hand, showed a small but statistically significant response to the temperature treatment. Fast-growing tadpoles attained slightly longer legs than slowly growing tadpoles at a common metamorphic body size. This example is the first to show that variation in growth rate per se can influence metric shape (i.e., the rate at which individuals reach a common body size determines their shape at that size). Nevertheless, the induced effects were small, and our results taken together with those of previous studies suggest that environmentally induced variation in growth rate is not a major source of variation in metric shape of skeletal characters in ectothermic vertebrates.     

Multiple paternity in the common frog (Rana temporaria): genetic evidence from tadpole kin groups

Very few studies have investigated the occurrence of multiple paternity and sperm competition in amphibians. We studied genetic relatedness within kin groups of tadpoles of an aquatically breeding anuran Rana temporaria using allozymes. We collected samples from 52 naturally fertilized spawn clumps produced by single females at three breeding sites in two populations. We estimated relatedness (r) within kin groups, and compared the observed genotype distributions of the tadpoles (on average 23 individuals in each group) with the expected distributions based on single mating. Average relatedness over five polymorphic loci was 0.44 and 0.43 in the two populations, the latter being significantly smaller than that expected by single mating (0.5). The number of patrilines, calculated from relatedness estimates, was 1.3 in one population and 1.4 in the other. Genotype distributions deviated significantly from the expected in half of the kin groups and at all breeding sites. The results show that egg clutches of R. temporaria commonly contain multiply sired offspring. We suggest that communal breeding may affect paternity patterns in R. temporaria as well as in anurans in general.     

POPULATION STRUCTURE AND COMPETITION AMONG KIN IN THE CHORUS FROG (PSEUDACRIS TRISERIATA)

In natural populations on Isle Royale, tadpoles of the chorus frog live in small pools on the shore of Lake Superior. Hatchling densities are high and sufficient to cause competitive impact on survivorship, growth, and development. The temporal and spatial pattern of egg laying indicates that tadpoles in many of the pools belong to single sibships. I calculated average coefficients of relationship among tadpoles under the assumption that eggs laid together are the products of the same breeding pair; the coefficients indicate that relationship among competing larvae averages approximately 0.35, and varies widely among larval subpopulations, from less than 0.1 to about 0.5. Two growth experiments were carried out in pens to test whether growth trajectories and larval characteristics at metamorphosis are influenced by relationship among competing tadpoles. In both experiments, initial density was crossed with average relationship; relationship was controlled by varying the number of sibships per pen from one to four. The same sibships were used in both experiments, but one experiment had lower initial densities and less water volume per pen than the other. In both experiments, density reduced growth, developmental rate, size at metamorphosis, survivorship to the onset of metamorphosis, and the proportion of survivors which actually attained metamorphosis by the end of the experiment. Kin effects occurred only in the experiment carried out in small pens at high initial densities: in this experiment, pure sib populations grew faster, and a higher proportion attained metamorphosis. However, there were no kin effects on larval period or body size at metamorphosis. The chorus frog appears to have a population structure conducive to kin-group selection. Furthermore, high variance in the average coefficient of relationship among pools should favor kin recognition and kin-specific interference behavior. The growth experiments suggest that the tadpoles respond to the genetic relationship of competitors, with significant effects on the distribution of fitness at metamorphosis among members of the group.     

Predation- and competition-mediated brain plasticity in Rana temporaria tadpoles

An increasing number of studies have demonstrated phenotypic plasticity in brain size and architecture in response to environmental variation. However, our knowledge on how brain architecture is affected by commonplace ecological interactions is rudimentary. For example, while intraspecific competition and risk of predation are known to induce adaptive plastic modifications in morphology and behaviour in a wide variety of organisms, their effects on brain development have not been studied. We studied experimentally the influence of density and predation risk on brain development in common frog (Rana temporaria) tadpoles. Tadpoles grown at low density and under predation risk developed smaller brains than tadpoles at the other treatment combinations. Further, at high densities, tadpoles developed larger optic tecta and smaller medulla oblongata than those grown at low densities. These results demonstrate that ecological interactions - like intraspecific competition and predation risk - can have strong effects on brain development in lower vertebrates.     

Plasticity in age and size at metamorphosis in Rana temporaria - comparison of high and low latitude populations

Effects of different combinations of stressors (viz. temperature, food level) on growth, developmental and survival rates of Rana temporaria tadpoles from two geographically widely (∼ 1500 km) separated populations were studied in a common garden experiment. In both populations, low temperature and low food level lead to towered growth rates and delayed metamorphosis, whereas high temperature and high food level had the opposite effect. Tadpoles from north metamorphosed earlier and exhibited higher growth rates than tadpoles from south, suggesting local adaptation to shorter growth period and cooler ambient temperature in north. Size at metamorphosis did not differ between the two populations, but when the differences in metamorphic age were accounted for, then the tadpoles from north were larger than those from south. These results suggest considerable adaptive genetic differentiation in growth rates, size and timing of metamorphosis between northern and southern R. temporaria populations. In both populations, high food levels tended to reduce tadpole survival rates and there was a negative correlation between growth and survival rates across different treatments in both populations. In general, tadpoles from north experienced high mortality rates in high food level - low temperature treatments, whereas southern tadpoles experienced high mortality in high food level-high temperature treatments. This suggest that there may be genetic differences among different populations as how they would be influenced by high nutrient loads, such as brought along for example by fertilization of forest or agricultural soils.     

Is bigger really better? Relative and absolute body size influence individual growth rate under competition

Models suggest that the mechanism of competition can influence the growth advantage associated with being large (in absolute body size or relative to other individuals in the population). Large size is advantageous under interference, but disadvantageous under exploitative competition. We addressed this prediction in a laboratory experiment on Rana temporaria tadpoles competing for limited food. There were 166 target individuals spanning a 10‐fold range in body mass reared for 3 days with three other individuals that were either the same size, half as large, or twice as large as the target. Relative growth rate (proportion per day) declined with size, and absolute growth rate (mass per day) reached a peak at intermediate size and declined thereafter. Tadpoles grew slowly if they were large relative to their competitors, although relative body size was less important than absolute size. As a result, size variation declined in groups that were initially composed of individuals of variable size. Thus, bigger was not better under exploitative competition. Our results help connect individual‐level behavior with individual growth and the size distribution of the population.     

Local Competition Between Foraging Relatives: Growth and Survival of Bruchid Beetle Larvae

Kin selection theory states that when resources are limited and all else is equal, individuals will direct competition away from kin. However, when competition between relatives is completely local, as is the case in granivorous insects whose larval stages spend their lives within a single seed, this can reduce or even negate the kin-selected benefits. Instead, an increase in competition may have the same detrimental effects on individuals that forage with kin as those that forage with non-kin. In a factorial experiment we assessed the effects of relatedness and competition over food on the survival and on fitness-related traits of the bruchid beetle Callosobruchus maculatus. Relatedness of competitors did not affect the survival of larvae. Larval survival substantially decreased with increasing larval density, and we found evidence that beetles maturing at a larger size were more adversely affected by competition, resulting in lower survival rates. Furthermore, females showed a reduction in their growth rate with increasing larval density, emerging smaller after the same development time. Males increased their growth rate, emerging earlier but at a similar size when food was more limited. Our results add to the growing number of studies that fail to show a relationship between relatedness and a reduction in competition between relatives in closed systems, and emphasize the importance of the scale at which competition between relatives occurs.     

Responses to competition effects of two anuran tadpoles according to life-history traits

Experimental manipulations of the densities of two larval anurans, Pelodytes punctatus and Bufo bufo , showed that these species compete asymmetrically in semi-natural conditions. Growth, mass at metamorphosis, date of metamorphosis, and survival were used as measures of response to interspecific competition. A mechanistic approach was used to collect information on the behaviour of the two species in different conditions. The competitive superiority of Pelodytes at individual level was correlated with a larger body, faster growth rate, increased per capita competitive impact on conspecifics, and greater reduction in the availability of trophic and spatial resources. In the presence of Pelodytes, Bufo showed slower growth, smaller size at metamorphosis and reduced survival. In the interspecific treatments Bufo individuals modified their behaviour by increasing activity and use of the water column while Pelodytes did not change their foraging activity or space use in the aquaria. However, the presence of Bufo resulted in a reduced larval period and smaller size at metamorphosis. We hypothesise that the presence of Bufo act as a signal of environmental degradation and shorten the larval period of Pelodytes, a typical temporal pond breeder . The smaller Bufo tadpoles are potentially stronger competitors at population level because they use relatively large amounts of energy (greater densities and higher metabolic rates). Consequently, they use larger proportions of the shared resources than their larger competitor. A possible evolutionary response for larger tadpoles is the development of interference mechanisms or "escaping" from ephemeral ponds where mortality by drying represent a high risk.     

The non-consumptive effects of predators and personality on prey growth and mortality

Individual organisms vary in personality, and the ecological consequences of that variation can affect the strength of predator–prey interactions. Prey with bolder tendencies can mitigate the strength of species interactions by altering growth and initiating ontogenetic niche shifts (ONS). While the link between personality and growth has been established, recent research has highlighted the important interplay between ONS and predator cues in community ecology. The objective of this study was to evaluate the effects of prey personality and predator cues on prey growth and ONS. We predicted growth–mortality trade-offs among personalities with higher survival, larger size, and accelerated ONS for bold individuals in comparison with shy individuals. To evaluate this objective, we conducted behavioral assays and a mesocosm experiment to test how southern leopard frog (Rana sphenocephala) tadpole personality and predatory fish (bluegill, Lepomis macrochirus) cues affects tadpole growth and metamorphosis. On average, bold tadpoles had higher mortality across all treatments in comparison with shy tadpoles. The effects of fish cues were dependent on tadpole personality with shy tadpoles metamorphosing significantly later than bold tadpoles. Bold tadpoles were larger than shy tadpoles at metamorphosis; however, that pattern reversed with fish cues as shy individuals metamorphosed larger than bold individuals. Our results suggest personality may be useful for predicting growth and life history for some prey species with predators. Specifically, the threat of predation can interact with personality to incur a benefit (earlier ONS) while also incurring a cost (size at metamorphosis). Hence by incorporating predator cues with personality, ecologists will be able to elucidate growth–mortality trade-offs mediated by personality.     

Relatedness and competitive asymmetry – implications for growth and population dynamics

The members of natural populations often differ in size and relatedness to each other, which may affect the division of limited resources and have consequences on reproductive success and population dynamics. We modeled seasonal growth and dynamics in populations composed of different types of relatives (full-sibs, half-sibs and non-related individuals) under the continuum of competitive scenarios between complete symmetry and asymmetry. Growth was assumed logistic in proportion to individual biomass and the size-differences were weighted by the relatedness of individuals. The symmetric component of competition was experienced by all individuals in proportion to their biomass, whereas the asymmetric component was individual-specific, and influenced only by the individuals larger than the focal individual. Relatedness decreased and competitive asymmetry increased the variability of individual biomasses. Mortality of the smallest individuals and the size threshold of reproduction decreased population density. Population dynamics were stable when there was no size threshold for reproduction but the presence of the threshold led to cyclic dynamics under low competitive asymmetry. The effects of the threshold were greater among related than unrelated individuals. The results suggest that individual differences and the asymmetry of competition can greatly affect population dynamics. Full symmetry of competition may be evolutionarily unstable in populations of related individuals as it may increase the probability of extinction due to demographic stochasticity.     

Interactions between freshwater snails and tadpoles: competition and facilitation

Summary Freshwater snails and anuran tadpoles have been suggested to have their highest population densities in ponds of intermediate size where abiotic disturbance (e.g. desiccation) is low and large predators absent. Both snails and tadpoles feed on periphytic algae and, thus, there should be a large potential for competitive interactions to occur between these two distantly related taxa. In a field experiment we examined the relative strength of competition between two closely related snail species, Lymnaea stagnalis and L. peregra, and between L. stagnalis and tadpoles of the common frog, Rana temporaria. Snail growth and egg production and tadpole size at and time to metamorphosis were determined. Effects on the common food source, periphyton, were monitored with the aid of artificial substrates. Periphyton dry weight was dramatically reduced in the presence of snails and/or tadpoles. There were no competitive effects on growth or egg production of the two snail species when they were coexisting. Mortality of L. peregra was high (95%) after reproduction, but independent of treatment. Growth of L. stagnalis was reduced only at the highest tadpole densities, whereas egg production was reduced both by intraspecific competition and by competition with tadpoles. Differences in egg production were retained after tadpole metamorphosis. Tadpole larval period increased, weight of metamorphosing frogs decreased and growth rate was reduced as a function of increasing tadpole density. However, contrary to expectation, snails had a positive effect on tadpole larval period, weight and growth rate. Further, in experimental containers without snails there was a dense growth of the filamentous green alga Cladophora sp. We suggest that the facilitative effects of snails on tadpoles are due to an indirect mutualistic mechanism, involving competition between food sources of different quality (microalgae and Cladophora sp.) and tadpoles being competitively dominant over snails for the preferred food source (microalgae). In the presence of tadpoles snails will be forced to feed on low-quality Cladophora, increasing nutrient turnover rates, which results in enhanced productivity of microalgae, increasing tadpole food resources. Thus, tadpoles have a negative effect on snails through resource depression, while snails facilitate tadpole growth through an indirect enhancement of food availability.     

Antagonistic indirect interactions between large and small conspecific prey via a heterospecific predator

Intrapopulation size variation strongly influences ecological interactions because individuals belonging to different size groups have distinct functions. Most demonstrations of the impacts of size variation in trophic systems have focused on size variation in predator species, and the consequences of size variation in prey species are less well understood. We investigated how prey size structure shapes intra‐ and interspecific interactions in experiments with a gape‐limited predator (larvae of the salamander Hynobius retardatus) and its heterospecific prey (frog tadpoles, Rana pirica). We found that large and small tadpole size groups each increased mortality in the other group by intensifying salamander predation; this type of indirect interactions is called apparent competition. The antagonistic impacts on the prey size groups were caused by different size‐specific mechanisms. By consuming small tadpoles, the salamanders grew large enough to consume large tadpoles. The activity of large tadpoles, by increasing the activity of the small tadpoles, may increase the number of encounters with the predator and thus small tadpole mortality. These results suggest that the magnitude of a predator's ecological role, such as whether a top–down trophic cascade is initiated, depends on size variation in its heterospecific prey.     

Influence of density and predators on metamorphic size in Rhinella schneideri tadpoles raised in mesocosm conditions

Amphibians exhibit extreme plasticity in the timing of metamorphosis, and several species respond to water availability, accelerating metamorphosis when their ponds dry. We analyzed the plasticity of the developmental response to water volume in Rhinella schneideri tadpoles. We raised tadpoles in mesocosm. Covariation between body size at metamorphosis and timing of development was positive. Nevertheless, the first approximately 53% of the metamorphoses finishing the cycle required between 34 and 56 days, and the covariation between body size at metamorphosis and timing of development was negative. For these tadpoles, the larval density and the presence of predators did not significantly affect their mass to metamorphosis. Nevertheless, predators affected time to metamorphosis. For the remainder of the tadpoles that reached metamorphosis at > 56 days, the relationship between body size at metamorphosis and timing of development was positive. For these tadpoles, larval density was important for mass at metamorphosis and presence of predators was also important for time to metamorphosis. Two dominant features were observed: (i) approximately 53% of metamorphs had morphological features similar to individuals developing in desiccating ponds, and (ii) the other individuals had morphological characteristics comparable to metamorphs developing in an unchanging environment.     

The formation of new characteristics in life cycle of the marsh frog (Rana ridibunda) in thermal pond conditions

Using mark and recapture approach, the long-term population dynamics in the marsh frog (Rana ridibunda) was studied. Group-marking of metamorphs was conducted in a small thermal pond serving as a sedimentation basin for discharged waters from Nizhny Tagil metallurgic works. Depending on the time of metamorphosis, three groups of individuals could be singled out, namely: early ones (group I), middle ones (group II), and late ones that overwinter as tadpoles and complete metamorphosis in May of the next year (group III). Upon metamorphosis completion, individuals of group I were found to be significantly larger than those of group II, and individuals of both these groups to be significantly smaller than those of group III. After first wintering, immature individuals from group I were significantly larger than either individuals from group II or metamorphs from group III, though a growth rate of the latter was significantly higher than in groups I and II. These discrepancies were observed both between immature and adult individuals. Over the period from metamorphosis completion to the first wintering ending, survivorship in group I was significantly higher and did not differ between groups II and III. In adult frogs, maximum survivorship was registered in group III and minimum one in group II; the detected differences recurred in each age class till the fourth wintering. However, in age classes that overwintered 4 and 5 times, maximum survivorship was observed in group II, which can be treated as a compensation for rather low survivorship of this group at younger ages. All the events of tadpoles of this species overwintering (except in other thermal water bodies) that are described in literature, correspond to rare deviations from normal ontogenesis. Therefore, the revealed formation of a numerous group of overwintering tadpoles in successive generations should be considered as a new adaptation which sense is a decrease of competition between tadpole groups when using the highly productive resources of the thermal pond practically year-round. The advantage in body size and growth rate of not only tadpoles but also of metamorphs, immature and adult individuals of group III indicates that after metamorphosis the strategy of this group still remains successful. The reason for that is unusually large body size of metamorphs which provides higher postmetamorphic survivorship and greater female fecundity.     

Non-equivalence of growth arrest induced by predation risk or food limitation: context-dependent compensatory growth in anuran tadpoles

1. To gain insight into the evolution of compensatory growth, we studied the growth patterns of anuran (Rana temporaria) larvae following either a period of exogenous growth depression (food restriction) or a period of endogenous depression (exposure to predators). We also investigated the potential deferred costs that larval compensatory growth could impose on post-metamorphic individuals. 2. Food-deprived larvae exhibited full compensatory growth in response to reduced growth rates caused by food limitation, and the growth trajectories of low- and high-rations tadpoles converged before the onset of metamorphosis. 3. According to our predictions, individuals exposed to larval predators did not show growth compensation following predator removal despite undergoing a significant reduction in growth rate associated with low activity levels. 4. Jumping ability of individuals exposed to predators during only 20 days from the commencement of the larval phase was equivalent to that of non-exposed animals, and greater than the jumping capacity of those maintained with predators until the time of metamorphosis. This pattern was consistent with the pattern observed for variation in relative leg length. 5. These results support the suggestion that submaximum and compensatory growth could have evolved to minimize the overall growth/mortality costs in environments with high spatiotemporal variation in predation intensity.     

Effects of induced variation in anuran larval development on postmetamorphic energy reserves and locomotion

Anuran larvae exhibit high levels of phenotypic plasticity in growth and developmental rates in response to variation in temperature and food availability. We tested the hypothesis that alteration of developmental pathways during the aquatic larval stage should affect the postmetamorphic performance of the Iberian painted frog (Discoglossus galganoi). We exposed tadpoles to different temperatures and food types (animal- vs. plant-based diets) to induce variation in the length of the larval period and body size at metamorphosis. In this species, larval period varied with temperature but was unaffected by diet composition. In contrast, size at metamorphosis was shaped by the interaction between food quality and temperature; tadpoles fed on an animal-based diet became bulkier metamorphs than those fed on plant-based food at high (22°C) but not at low (12°C) temperature. Body condition of newly metamorphosed frogs was unrelated to the temperature or food type experienced during the premetamorphic stage. Frogs maintained at high temperature during the larval period showed reduced jumping ability, especially when fed on the plant-based diet. However, when considering size-independent jumping ability, cold-reared individuals exhibited the lowest performance, and herbivores reared at 17°C the highest. Cold-reared (12°C) frogs accumulated larger amounts of energy reserves than individuals raised at 17°C or 22°C. This was still the case after correction for differences in body mass, thus indicating some size-independent effect of developmental temperature. Despite the higher lipid content of the carnivorous diet, the differences in energy reserves between herbivores and carnivores were relatively weak and associated with differences in body size. These results suggest that the consequences of environmental variation in the larval habitat can extend to the terrestrial phase and influence juvenile growth and survival.     

Spatial variation in abiotic and biotic factors in a floodplain determine anuran body size and growth rate at metamorphosis

Body size at metamorphosis is a critical trait in the life history of amphibians. Despite the wide-spread use of amphibians as experimental model organisms, there is a limited understanding of how multiple abiotic and biotic factors affect the variation in metamorphic traits under natural conditions. The aim of our study was to quantify the effects of abiotic and biotic factors on spatial variation in the body size of tadpoles and size at metamorphosis of the European common toad (Bufo b. spinosus). Our study population was distributed over the riverbed (active tract) and the fringing riparian forest of a natural floodplain. The riverbed had warm ponds with variable hydroperiod and few predators, whereas the forest had ponds with the opposite characteristics. Spatial variation in body size at metamorphosis was governed by the interactive effects of abiotic and biotic factors. The particular form of the interaction between water temperature and intraspecific tadpole density suggests that abiotic factors laid the foundation for biotic factors: intraspecific density decreased growth only at high temperature. Predation and intraspecific density jointly reduced metamorphic size. Interspecific density had a negligible affect on body size at metamorphosis, suggesting weak inter-anuran interactions in the larval stage. Population density at metamorphosis was about one to two orders of magnitudes higher in the riverbed ponds than in the forest ponds, mainly because of lower tadpole mortality. Based on our results, we conclude that ponds in the riverbed appear to play a pivotal role for the population because tadpole growth and survival is best in this habitat.