In light of recent alarming trends in human population growth, climate change, and other environmental modifications, a “Warning to humanity” manifesto was published in BioScience in 2017. This call reiterated most of the ideas originally expressed by the Union of Concerned Scientists in 1992, including the fear that we are “pushing Earth's ecosystems beyond their capacities to support the web of life.” As subterranean biologists, we take this opportunity to emphasize the global importance and the conservation challenges associated with subterranean ecosystems. They likely represent the most widespread nonmarine environments on Earth, but specialized subterranean organisms remain among the least documented and studied. Largely overlooked in conservation policies, subterranean habitats play a critical role in the function of the web of life and provide important ecosystem services. We highlight the main threats to subterranean ecosystems and propose a set of effective actions to protect this globally important natural heritage.
-The Western Shield of Australia has been above sea level since the Palaeozoic. It is incised by ancient palaeovalieys now containing groundwater calcretes that are found throughout much of arid Australia. The calcretes are deposited, owing to surface evaporation, from a groundwater flow path that increases in salinity from fresh to hypersaline groundwater each terminating at a salt lake (playa). The calcrete aquifers contain a diverse obligate groundwater fauna (stygofauna: predominantly Crustacea) in one of the oldest non-marine landscapes on Earth. Each of the 11 calcrete areas examined so far contains a unique fauna; there are over 210 large discrete calcrete bodies in the Western Australian arid zone. This paper examines a working hypothesis that the stygofauna became isolated in the upper tributaries of the palaeodrainage systems by the progressive upstream movement of salinity from the Eocene onwards. Although each calcrete body does have a unique fauna, as predicted by the hypothesis, the hypothesis has proved too simple because the hydrochemical cycles are repeated along the length of the palaeochannels, each terminating in a saltlake immediately downflow of the calcrete. A new hypothesis has to incorporate these intervals of hypersaline groundwater / calcrete discontinuities acting as barriers to dispersal of the stygofauna. The paper focuses on the geological and landscape setting, and the hydrochemical and groundwater context in which this stygal diversity is found. It is intended to serve as a background resource for further work on this diverse stygofauna. A synopsis is provided of the knowledge of this stygofauna. The presence of such highly diverse and locally endemic stygofauna, often ancient relictual lineages, in a major economic resource within arid Australia poses delicate and chalienging conservation issues. At the same time the scientific challenge is considerable to understand the development and functioning of these systems in order that they can be managed sustainably.
Calcrete aquifers in the arid Yilgarn region of central Western Australia are a biodiversity hotspot for stygofauna. A distinct pattern of interspecific size class variation among subterranean dytiscid beetle species has been observed in 29 of these aquifers where either two or three small, medium and/or large sympatric species are found that are in some cases sister species. We used a 3.5 km(2) grid of bores to sample dytiscids on a fine-scale and employed a comparative phylogeographical and population genetic approach to investigate the origins of a sympatric sister species triplet of diving beetles from a single aquifer. Mitochondrial DNA sequence data from the Cytochrome oxidase c subunit I gene revealed that all three species have high levels of haplotype diversity with ancient (approximately 1 million years ago) intra-specific coalescence of haplotypes, but low levels of nucleotide diversity. Population analyses provide evidence for multiple expansion events within each species. There was spatial heterogeneity in the distribution of genetic variation and abundance both within and among the three taxa. Population analyses revealed significant fine-scale differentiation with isolation by distance for Paroster macrosturtensis and P. mesosturtensis, but not the smallest species P. microsturtensis. Haplotype network analyses provided limited or no evidence for past population fragmentation within the large and small species, but substantial historical divergence was observed in P. mesosturtensis that was not spatially structured. A patchy population structure with contemporaneous and historical isolation by distance in the three species is likely to have been a significant isolating and diversifying force, preventing us from ruling out a potential role for allopatric divergence during speciation of this beetle sister triplet.
The effect of habitat • components (vegetation density at two levels, litter, logs and roads) on the distribution of small mammals was assessed in adjacent areas of native forest and Pinus taeda plantation in north-eastern New South Wales. Rattus fuscipes was associated with structural complexity in native forest but not in pine plantation where it was found on downslope areas. R. rattus was associated with windrows in the pine plantation, R. lutreolus with areas devoid of a shrub layer in the pine plantation, Antechinus stuartii with logs and Melomys cervinipes with habitat components associated with rainforest areas. Road crossing by small mammals was inversely related to road width; roads severely restricted or stopped the movement of small mammals even when the road consisted of a longunused and partly overgrown track.
With 1 plate and 4 figures in the text) Breeding, population dynamics and seasonal changes in physical and physiological parameters were examined in the northern quoll (Dasyurus hallticatus) at Mitchell Plateau, Western Australia, between September 1981 and November 1982. Females gave birth to a single litter of young in July or August. Births were earlier on near-coastal sites than on inland sites. Litter size was greater on inland sites and litter size differed between years. By September all females were either carrying pouch young or were lactating. Lactation ceased by April. Testosterone levels in males peaked in July. There were significantly more male than female pouch young. However, in only one grid was the adult sex ratio different from parity, with an excess of females in September 1981 and 1982. Embryonic mortality was > 53% but loss of pouch young was small. Although males and females moved similar distances between successive recaptures, the extent of movement varied seasonally, being greatest in September. Males were generally larger and heavier than females. Seasonal variations were recorded for most physical and physiological parameters. The most pronounced changes occurred towards the end of the dry season (July to September) for both males and females. Over this period there was a significant decline in weight (males), haematocrit (males), plasma albumin (males) and leucocytes (both males and females) and significant elevations in values of haemoglobin and both free and protein-bound cortisol in both males and females. Few males survived the post-mating period from July to September. They appeared to decline in condition over this period more markedly than females: they lost more weight, their haematocrit and plasma albumin values declined to a greater extent, and they were more heavily infected with lice (Boopia uncinata). Males with lower testosterone and higher free and protein-bound cortisol had increased prospects of surviving the breeding season, which suggests that it is the dominant males that are less likely to survive the breeding season. Individuals in the three major populations at Mitchell Plateau differed greatly in their physiological values. The high-density population in a sandstone area had intermediate levels of free cortisol and higher haematocrit values than both the other populations, and higher levels of haemogl3bin than the population on laterite substratum.
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