Using a combination of morphological, life-history and molecular data, we redescribe Sphaerospora ranae (Morelle, 1929) n. comb. (previously Leptotheca ranae) and emend its taxonomic status. Renal infection was recorded in 2 spp. of frogs (out of 5 amphibian spp. examined), Rana dalmatina (proposed type host) and Rana temporaria, suggesting restricted host specifity of S. ranae. We provide a description of sporogonic stages of S. ranae for the first time and suggest possible modes of its developmental cycle. Phylogenetic analysis inferred from the small-subunit ribosomal DNA revealed a close relationship of S. ranae with piscine Sphaerospora elegans (type species of the genus) and Sphaerospora truttae, forming together with distantly related Leptotheca fugu a ‘Sphaerosporid clade’, the basal branch to all myxosporean species. The close relationship of the 3 Sphaerospora spp. is further supported by the presence of 2 areas with extensive nucleotide insertions in the V4 region of the SSU rDNA (absent in L. fugu), morphology and life-history features. We conclude, that the spore morphology of Sphaerospora s.l., is very simple and probably represents a ‘primitive’, basal morphotype retained in most myxosporean lineages. Based on presented data, we propose emendation of the genus Sphaerospora using morpological, life-history and molecular features.

Time for metamorphosis and metamorph size of moor frogs Rana arvalis and common frogs R. temporaria were measured in 22 ponds for 1–8 years. Environmental data in these ponds were also measured. Metamorphosis of the frogs took place from the beginning of June to the beginning of August. When both species were found in one pond, the common frogs metamorphosed up to 20 days earlier than the moor frogs. Most variation in time for metamorphosis, among ponds and years, is explained by temperature effects, but a causal relationship was not established. Within a pond, metamorphosis was later in cold summers than in warm summers. Size at metamorphosis was affected by tadpole density; at high densities metamorphs were smaller. Size at metamorphosis was not related to time for metamorphosis. There was an effect of pond drying; if ponds were about to dry up, metamorphosis was accelerated by about 2.4 days. Tadpoles from ponds with a late metamorphosis in the field had tadpoles that metamorphosed early in a common garden experiment, suggesting counter gradient selection.

Echinostoma sp. use larval anurans as intermediate hosts. The cercariae enter the tadpoles via the cloacal opening and form metacercarial cysts in the kidneys, pronephroi, and Wolffian ducts. To examine the distribution of Echinostoma metacercariae in Rana sylvatica and Rana clamitans tadpoles, 200 individuals of each species were exposed to free-swimming cercariae. There was a significant left:right bias in the distribution of metacercariae within both R. sylvatica and R. clamitans tadpole hosts, with trematodes preferentially encysting in nephric structures on the right side. In R. sylvatica and R. clamitans, respectively, 56.7% and 96.8% of the metacercariae were on the tadpoles' right side. Asymmetry in the distribution of parasites followed the direction of the asymmetry in tadpole kidney size, but was much greater. Trematodes preferentially encysted in the head kidneys of R. clamitans, which regress at metamorphosis. The right head kidney was the most commonly infected structure in R. clamitans tadpoles, containing 72.7% of all cysts in that species. Despite the preference of trematodes to encyst in the head kidney, there was no correlation between the number of cysts in the right kidney and the number in the right head kidney. This suggests that limited space in the head kidney does not influence metacercarial formation in the kidney proper. The high frequency of unilateral encystment in both anurans, and in the head kidneys of R. clamitans, may be the result of a co-evolved relationship that ultimately benefits both the host and parasite by ensuring host survival.