Environmental effects on a host-pathogen system: frogs and Batrachochytrium dendrobatidis in wet and dry habitats
Puschendorf, Robert (2009) Environmental effects on a host-pathogen system: frogs and Batrachochytrium dendrobatidis in wet and dry habitats. PhD thesis, James Cook University.
|PDF (Thesis front) - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader|
|PDF (Thesis whole) - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader|
The global increase in emerging infectious diseases poses a substantial threat to wildlife, especially for small, fragmented and populations exposed to novel pathogens. The emergence of the chytrid fungus Batrachochytrium dendrobatidis is one of the clearest cases of this to date. Batrachochytrium dendrobatidis colonises keratinised cells of the amphibian epidermis and causes the disease chytridiomycosis when pathogen populations on hosts reach a threshold density. Host mortality usually occurs shortly after clinical disease symptoms become evident. Chytridiomycosis is fatal to a wide range of amphibian species, while other, less vulnerable species can serve as asymptomatic carriers. This has allowed chytridiomycosis to cause widespread local and global declines as well as extinctions in a wide range of amphibians. Many of the affected species occur in relatively pristine, protected areas; declines of these species have been termed “enigmatic” declines. Previous research has demonstrated that the physical environment plays a major role in determining whether infected hosts recover, coexist with sublethal infections or develop chytridiomycosis and die. The optimal environment for B. dendrobatidis is cool and moist, as is typical of tropical high elevation rainforests, where amphibian diversity is usually high. In tropical Central America and Australia, lowland populations of species that are widely distributed along elevational gradients often persist, while upland populations decline or suffer local extinction. It appears that the warmer, sometimes drier or more seasonal environments of lowlands are less favourable for the pathogen, permitting otherwise susceptible species to coexist with B. dendrobatidis. These areas are therefore climatic refuges from disease-driven amphibian declines and extinctions. The aim of this thesis was to gain an increased understanding of the operation of climatic refuges. I addressed this aim using three objectives: a) to determine how the climate within refuges affects the biology of B. dendrobatidis, b) to compare the epidemiology of the interaction between B. dendrobatidis and its amphibian hosts between refugial and non-refugial sites, and c) to elucidate the underlying mechanisms that enable amphibians in climatic refuges to coexist with this potentially lethal pathogen.
To attain the first objective, I used species distribution models for B. dendrobatidis to predict areas that are unsuitable for the pathogen and should therefore have low probabilities of suffering from disease-driven amphibian declines. I initially examined data from Costa Rica, collected during my Masters’ research. In Costa Rica, areas of low probability of pathogen occurrence are mostly dry forests, which coincidentally support a large population of Craugastor ranoides, a critically endangered species that has disappeared from most of its range (in rainforest) in conjunction with outbreaks of chytridiomycosis. As predicted data on prevalence between dry and wet areas suggest, B. dendrobatidis is much more common in wet areas. This supports the proposed hypothesis that areas with environments that are hostile to B. dendrobatidis can serve as refuges for frogs that have broader environmental niches. I collected preliminary survey data that indicated that dense populations of the frog Litoria nannotis, which had declined across its distribution range above 400 m elevation in rainforest of the Australian Wet Tropics, occurred in dry forest areas adjacent to the western boundary of the rainforest. Species distribution models for B. dendrobatidis constructed using data on its known Australian distribution, predicted that these areas were not suitable for the pathogen. However, surveys of the prevalence of B. dendrobatidis in frogs in these dry forest areas, which were the first to be conducted showed that B. dendrobatidis is present at very high prevalences, higher than in adjacent wet forest areas. This contrasts strongly with low elevation refuges in the Australian Wet Tropics and with the dry-forest refuges in Costa Rica, where prevalences are lower than at high elevation sites. These results suggest that the mechanisms by which high elevation dry forests adjacent to the Australian Wet Tropics serve as climatic refuges differ from those in other areas. Rather than excluding B. dendrobatidis or limiting its prevalence, the high-elevation dry forests promote coexistence between frogs and the pathogen.
To better understand how the host-pathogen interaction differs between areas where frogs were extirpated and now occur in low abundance (wet sites) and adjacent refugial areas where dense frog populations persist (dry sites), I carried out a comparative epidemiological study. Despite the wet and dry study sites being less than 1 km apart, the pathogen-susceptible L. nannotis were up to five times more abundant in the dry site than in the wet site. The intensities of infections in animals positive for B. dendrobatidis did not differ significantly between the sites, however chytridiomycosis-induced mortality was only detected in wet environments. Surveys carried out over a 15-month period showed that prevalence at the dry forest site remained consistently high, significantly higher than at the wet forest site. Also, dry forest frog populations remained much denser than wet forest populations. Given the very high prevalences of B. dendrobatidis infection occurring at the dry forest site, this strongly indicates that infected frogs at this location can tolerate infections for extended periods. The suggestion that the environment at the dry forest site leads to increased tolerance is supported by my discovery of a population of Litoria lorica a short distance downstream. This species was considered a rainforest endemic; it disappeared from all known localities in the early 1990s, had not been seen in 18 years, and was generally thought to be extinct. This newly-discovered population is dense and tolerates high prevalences of B. dendrobatidis infection, similar to those of dry forest L. nannotis. This discovery also demonstrates that it is essential to look for poorly-known species outside the “limits” of their distributions; in this case, it is clear that L. lorica is not, as had been thought a rainforest endemic, but is endemic to high elevation torrents and waterfalls, rather than the surrounding terrestrial habitat.
To further understand the mechanisms leading to the differences in epidemiological patterns between wet and dry habitats, I examined frog behaviour such as microhabitat use. In contrast to the wet forest, where L. nannotis use moist rock crevices as diurnal retreat sites, most tracked L. nannotis in the dry forest spent the day submerged under the water, in fast flowing sections of the stream. This could reduce rates of re-infection rates of individuals by flushing zoospores away from the frog as they are released, and thus reduce the rate of growth of pathogen populations on the hosts. The open canopy at dry forest sites leads to substantial heating of the large boulders that form the substrate usually occupied by frogs during nocturnal activity. When dry forest frogs emerge from their diurnal aquatic retreat sites at dusk, the rocks that they perch on, having been heated in the sun, are dry and substantially warmer than the air temperature. This has the potential to control pathogen loads on their ventral surfaces, the body region most susceptible to infection. The nocturnal perches of wet forest frogs receive little direct sunlight, and are typically moist and cool when frogs emerge, which are conditions conducive to the build up of pathogen populations on the ventral surface.
At present, captive breeding is presumed to be the only viable conservation strategy to prevent chytridiomycosis from causing the extinction of many susceptible amphibian species. Climatic refuges that exclude the pathogen or enhance the ability of frogs to coexist with it, may allow natural amphibian populations to persist and eventually to evolve increased resistance and potentially recolonise non-refugial areas from which they have been extirpated. Any threat, such as chytridiomycosis, which is most severe in the core habitat of many species, can make populations living on the margins of species geographic or ecological ranges, vital to species’ persistence.
|Item Type:||Thesis (PhD)|
|Keywords:||amphibian declines, extinctions, frogs, Litoria nannotis, Litoria lorica, pathogens, chytridiomycosis, environmental refuges, climatic refuges, Batrachochytrium dendrobatidis, epidemiology, host-pathogen interaction, tolerance, wet forests, dry forests, Wet Tropics, Australia|
|FoR Codes:||05 ENVIRONMENTAL SCIENCES > 0502 Environmental Science and Management > 050202 Conservation and Biodiversity @ 100%|
|SEO Codes:||96 ENVIRONMENT > 9608 Flora, Fauna and Biodiversity > 960806 Forest and Woodlands Flora, Fauna and Biodiversity @ 50%|
97 EXPANDING KNOWLEDGE > 970105 Expanding Knowledge in the Environmental Sciences @ 50%
|Deposited On:||15 Jun 2011 08:45|
|Last Modified:||15 Jun 2011 08:45|
Last 12 Months: 136
Repository Staff Only: item control page