The pentastomid parasite, Raillietiella frenata, is native to Asia where it infects the Asian House gecko, Hemidactylus frenatus. This gecko has been widely introduced and recently R. frenata was found in introduced populations of cane toads (Rhinella marina) in Australia, indicating a host-switch from introduced geckos to toads. Here we report non-native adult R. frenata infecting the lungs of native cane toads in Panama. Eight of 64 toads were infected (median = 2·5, range = 1–80 pentastomids/toad) and pentastomid prevalence was positively associated with the number of buildings at a site, though further sampling is needed to confirm this pattern. We postulate that this pattern is likely due to a host shift of this parasite from an urban-associated introduced gecko. This is the first record of this parasite infecting cane toads in their native range, and the first instance of this parasite occurring in Central America.

Correlations between host phenotype and vulnerability to parasites can clarify the processes that enhance rates of parasitism, and the effects of parasites on their hosts. We studied an invasive parasite (the pentastome Raillietiella frenatus, subclass Pentastomida, order Cephalobaenida) infecting a new host (the invasive cane toad Rhinella marina), in tropical Australia. We dissected toads over a 27-month period to investigate seasonal changes in pentastome population dynamics and establish which aspects of host phenotype are related to infection. Pentastome prevalence and intensity varied seasonally; male toads were 4 times more likely to be infected than were females; and prevalence was highest in hosts of intermediate body size. The strong sex effect may reflect habitat or dietary divergence between the sexes, resulting in males encountering parasites more often. The relationship between pentastome prevalence and host size likely reflects a role for acquired immunity in preventing re-infection. Infection did not influence host body condition (fatbody size), suggesting that R. frenatus does not impose high energy costs in cane toads. Infected toads had heavier spleens (likely an immune response to infection) and larger testes (perhaps since reproductively active hosts have altered microhabitat use and/or immunocompetence) than did uninfected conspecifics. Although experimental studies are required to identify the causal bases of such patterns, our data confirm that infection status within a population can be strongly linked to host phenotypic traits.

Patterns of energy allocation in the cane toad, Bufo marinus, were explored by analysing the seasonal variations in fat bodies and gonads in two populations subjected to different rainfall regimes and water permanency. In both populations, fat deposition occurred shortly after the rainy season due to an increase in feeding activity. In contrast, the timing of reproduction varied between sites according to the availability of suitable water bodies. Nevertheless, females with mature oocytes were predominant during the dry season, even in populations that bred throughout the year in permanent ponds. This suggests that seasonal variations in the nutritional condition of adults may also result in a tendency towards cyclicity in the reproduction of B. marinus in tropical regions. Analyses of allometric relationships of reproductive and storage tissues with body weights indicated that the fractions of weights in reproductive tissues did not vary either with the size of females or between populations. On the contrary, not only did larger toads have proportionally larger fat bodies, but those from wet sites had greater fractions of weight allocated to fat bodies than those from dry sites. This suggests that reproductive output may be fixed in this species and, therefore, excess energy is allocated to fat bodies. Given that the initiation of ovarian cycles depends on the restoration of proper nutritional levels, energy stored in fat bodies during breeding may allow females to resume a new ovarian cycle shortly after spawning and thus maximize the number of reproductive events.

The number, dendritic morphology, and retinal distribution of displaced ganglion cells were studied in two anuran species, Xenopus laevis and Bufo marinus. Horseradish peroxidase or cobaltic lysine complex was applied to the cut end of the optic nerve, and the size, shape, and retinal position of retrogradely filled ganglion cells displaced into the inner nuclear layer were determined in retinal wholemount and sectioned material. Approximately 1% of ganglion cells in Xenopus and 0.1% in Bufo were found to be displaced. In both species, many of the previously described orthotopic ganglion cell types (Straznicky & Straznicky, 1988; Straznicky et al., 1990) were present among displaced ganglion cells. In Xenopus more displaced ganglion cells were found in the retinal periphery than in the retinal center, and they formed 3 or 4 distinct bands around the optic nerve head. In Bufo the incidence of displaced ganglion cells was higher along the visual streak than in the dorsal and ventral peripheral retina. These results indicate that the distribution of displaced ganglion cells approximates the retinal distribution of orthotopic ganglion cells. One of the likely mechanisms to account for this developmental paradox may be that the formation of the inner plexiform layer, adjacent to the ciliary margin, acts as a mechanical barrier by preventing the entry of some of the late developing ganglion cells into the ganglion cell layer.

The main route of information flow through the vertebrate retina is from the photoreceptors towards the ganglion cells whose axons form the optic nerve. Bipolar cells of the frog have been so far reported to contact mostly amacrine cells and the majority of input to ganglion cells comes from the amacrines. In this study, ganglion cells of frogs from two species (Bufo marinus, Xenopus laevis) were filled retrogradely with horseradish peroxidase. After visualization of the tracer, light-microscopic cross sections showed massive labeling of the somata in the ganglion cell layer as well as their dendrites in the inner plexiform layer. In cross sections, bipolar output and ganglion cell input synapses were counted in the electron microscope. Each synapse was assigned to one of the five equal sublayers (SLs) of the inner plexiform layer. In both species, bipolar cells were most often seen to form their characteristic synaptic dyads with two amacrine cells. In some cases, however, the dyads were directed to one amacrine and one ganglion cell dendrite. This type of synapse was unevenly distributed within the inner plexiform layer with the highest occurrence in SL2 both in Bufo and Xenopus. In addition, SL4 contained also a high number of this type of synapse in Xenopus. In both species, we found no or few bipolar to ganglion cell synapses in the marginal sublayers (SLs 1 and 5). In Xenopus, 22% of the bipolar cell output synapses went onto ganglion cells, whereas in Bufo this was only 10%. We conclude that direct bipolar to ganglion cell information transfer exists also in frogs although its occurrence is not as obvious and regular as in mammals. The characteristic distribution of these synapses, however, suggests that specific type of the bipolar and ganglion cells participate in this process. These contacts may play a role in the formation of simple ganglion cell receptive fields.

Using an antibody against serotonin (5-hydroxytryptamine, 5-HT), serotonin-like immunoreactive (serotonin IR) neurons were demonstrated in the retina of adult Bufo marinus. All immunoreactive neurons were identified as amacrine cells (ACs). The dendrites of serotonin-IR ACs branched diffusely and densely throughout all levels of the inner plexiform layer (IPL) of the retina. The great majority of these cell somata were located in the vitread part of the inner nuclear layer (INL) and a few of them (ranging from 9–29 cells) were displaced into the ganglion cell layer (GCL). On the basis of the soma sizes, two populations of serotonin-IR ACs, large (type A) and small (type B), were distinguished. 6-Hydroxydopamine (6-OHDA) injected into the eye abolished immunoreactivity in the recently reported tyrosine hydroxylase (TH)-IR ACs (Zhu & Straznicky, 1990), whereas serotonin-IR ACs remained unaffected.

The number of serotonin-IR cells per retina ranged from 23,750–27,390, with a ratio of 1:1.6 to 1:1.9 between type A and B cells. Both cell types were distributed nonuniformly across the retina. Cell densities were slightly lower in the peripheral (96 cells/mm2) than in the central (164 cells/mm2) retina. Linear regression analysis confirmed the presence of a decreasing density gradient from the retinal center to the retinal margin for both small and large cell types. The analysis of the nearest neighbor distances showed that the retinal distribution of serotonin-IR ACs was orderly.

These results have been taken to indicate that 5-HT-IR cells correspond to a population of serotonincontaining ACs. It is suggested that dopamine and serotonin are contained in two different populations of ACs in the rtina of Bufo marinus.

We analysed the patterns of tick distribution on 2274 adult toads from Venezuela and Brazil, to explore whether these ectoparasites have any impact on the survival of Bufo marinus. A maximum-likelihood analysis showed that aggregation levels of ticks decreased significantly with the mean intensity of infection. This decline could be attributed to a density-dependent reduction of ticks within toads, density-dependent tick-induced toad mortality and/or density-dependent tick-induced changes in toad susceptibility. However, the relationship between the rate of change in tick loads and tick burdens from recaptured toads indicated that neither the loss of ticks within toads nor the toad susceptibility to further infection were dependent upon tick burdens. Therefore, we can indirectly infer that density-dependent tick-induced toad mortality is responsible for the observed decline in aggregation levels with tick age and burdens. On the other hand, a significant negative relationship between tick burdens and the size-specific weight of toads suggested that ticks may also have a significant impact on the patterns of weight deposition of adult toads. This evidence suggests that these ectoparasites may play an important role in regulating the densities of B. marinus in native habitats.

In Hawaii, where there are no native reptiles or amphibians, 27 species of reptiles and amphibians have established (Kraus 2003); however, few have been studied to determine their ecological impacts. For example, little is known about the impacts of the Puerto Rican frog, Eleutherodactylus coqui Thomas, that recently invaded (late 1980s) (Kraus et al. 1999), and has established on all four main Hawaiian Islands (Kraus & Campbell 2002). However, there are likely to be consequences because E. coqui can attain high densities (20 570 frogs ha−1 on average in Puerto Rico) and consume large quantities of invertebrates (114 000 prey items ha−1 per night on average in Puerto Rico) (Stewart & Woolbright 1996).

Infrapopulation dynamics of the nematode Rhabdias cf. hylae within naturally-infected Bufo marinus in north Queensland, Australia, were detailed. Over 80% of 580 toads were infected with Rh. cf. hylae with a mean intensity of 16·1. Distribution of Rh. cf. hylae within the toad population was aggregated, with an increase in the variance-to-mean ratio with increasing toad size. Intensity of infection and length of nematode were both correlated with length of toad in the smaller size classes. Length of nematode was not related to intensity of infection at any time. Mean intensity of infection rose significantly in small toads following initial infection after metamorphosis. Over the same period, average length of nematode did not increase implying constant re-infection of the toads. Larger toads were not reinfected to the same extent, and the number of uninfected toads in the larger size class increased which indicated a natural loss of infections. Changes in parameters of Rh. cf. hylae infection within B. marinus were attributed to seasonal rainfall and its subsequent effect on the behaviour of the toad.