Para grass, amphibians and reptiles

Understanding mechanisms of weed damage to ecosystems: para grass, amphibians and reptiles

Exotic weeds invade ecosystems and cause reductions in plant and animal biodiversity, alteration of food chains, reduction of species abundances and alteration of assemblage structure of existing flora and faunal communities. These negative effects can severely reduce the ecosystem services provided by a previously valuable area, and important functions of natural ecosystems (such as maintenance of water quality, pollinator services, and maintenance of local biodiversity) can be compromised.

Among the invasive weeds most likely to have negative effects on ecosystems are grasses, because they compete successfully with native species in a wide range of ecosystem types, and can alter critical ecosystem processes, such as fire-proneness and nutrient cycling, of the invaded ecosystem. Introduced pasture grasses comprise a third of the worst environmental weeds in Australia. Para grass ( Brachiaria mutica ) has become established in waterways where it causes economic and ecological problems, such as flow reduction and increases in sedimentation, as well as reduction in the attractiveness of wetlands to water birds, and reduction in fish diversity. Evidence from Australian wetlands invaded by para grass suggests that it turns diverse wetland plant communities into a monoculture, drastically reducing both floral and faunal diversity. These changes are unlikely to be reversed simply by removing vegetation. In this case, vegetation removal on its own may simply degrade habitat further, rather than enhance it.

In this study, we examine the influence of para grass control, on amphibians and reptiles in a northern Australian wetland – the Townsville Town Common Conservation Park. We will also examine uninvaded wetland areas adjacent to the para-grass-affected areas, to quantify the reptile and amphibian assemblages present in uninvaded wetlands. Finally, we will observe the habitat use of an abundant predator (keelback snakes, Tropidonophis marii ) to predict the responses of native fauna to the removal of the weed, and to understand some of the mechanisms responsible for these responses.

Project update:

Surveys of amphibians and reptiles in the woodland adjacent to the paragrass-dominated floodplain reveal a high species richness and abundance in this habitat.  The woodland may be an important site for recruitment of herpetofauna that utilize the Town Common floodplain.

Pitfall and funnel trapping conducted in the woodland during mid-March 2007 was used to gain information regarding seasonal species composition, population demographics, and movement patterns.  The Green Striped Burrowing frog (Cyclorana albogutta) and the Ornate Burrowing frog (Opisthodon ornatus) dominated the amphibian assemblage of 7 species encountered during this period.  The skinks Ctenotus robustus and Carlia pectoralis, and the freshwater keelback snake (Tropidonophis marii) were the dominant reptile species.  In total, nine species of skink, three snakes, two dragons, and one goanna species were encountered during March. 

An early dry season trapping session and additional incidental field observations in mid-April added two species of arboreal gecko, 1 species of legless lizard, and 2 species of frog, indicating a potential shift in the assemblage.  A winter trapping session planned for July will be used to study this further, and it will provide data on habitat use of species relative to burned, grazed, burned and grazed and control plots.

The keelback snake is the most abundant predator found on the Town Common.  During May, snakes were collected over 15 nights for 2-3 hours from dusk along the road bisecting the woodland, and an additional six snake species were identified.  Over winter 2007, we successfully tracked keelback snakes and determined details of their habitat use in woodland and floodplain habitats.  Keelbacks moved almost exclusively in the daytime, and in the early morning and evening were using shelter sites.  On the floodplain, snakes used para grass as shelter sites, whereas snakes released close the border of woodland and para grass used mostly burrows and logs, and occasionally clumps of other grasses as shelter.  Predation on snakes was highest on the floodplain which suggests either that shelter is inadequate in para grass, or that there is another reason why predators may more successfully capture snakes in the para grass.  In spite of this, however, we found no evidence that snakes released for tracking near the edge of para grass moved into woodland habitats.  Snakes were clearly able to use para grass infested floodplain habitats.  We will conduct further tracking during periods of greater activity (warmer months), and will reveal movement patterns when snakes are feeding.


Key References:

Braithwaite, R. W. 1987. Effects of fire regimes on lizards in the wet-dry tropics of Australia. Journal of Tropical Ecology 3 :265-275.

Christensen, P., H. Recher, and J. Hoare. 1981. Responses of open forests (dry sclerophyll forests) to fire regimes. Pages 367-393 in A. M. Gill, R. H. Groves, and I. R. Noble, editors. Fire and the Australian Biota . Australian Academy of Science, Canberra.

Deil, U. 2005. A review on habitats, plant traits and vegetation of ephemeral wetlands - a global perspective. Phytocoenologia 35 (2-3): 533-705.

Douglas, MM; Bunn, SE; Davies, PM. 2005. River and wetland food webs in Australia's wet-dry tropics: general principles and implications for management. Marine and Freshwater Research 56 (3): 329-342.

Finlayson, CM. 2005. Plant ecology of Australia's tropical floodplain wetlands: A review. Annals of Botany 96 (4): 541-555.

Grice, A. C. 1997. Post-fire regrowth and survival of the invasive tropical shrubs Cryptostegia grandiflora and Ziziphus mauritiana . Australian Journal of Ecology 22 :49-55.

Valentine, LE; Roberts, B; Schwarzkopf, L 2007. Mechanisms driving avoidance of non-native plants by lizards. Journal of Applied Ecology, 44 (1): 228-237

Woinarski, J. C. Z. 1990. Effects of fire on the bird communities of tropical woodlands and open forests in northern Australia. Australian Journal of Ecology 15 :1-22.

Woinarski, J.C.Z. & Recher, H.F. (1997) Impact and response: a review of the effects of fire on the Australian avifauna. Pacific Conservation Biology 3 :183-205.

Zavaleta, E.S., Hobbs, R.J. and Mooney, H.A. 2001. Viewing invasive species removal in a whole ecosystem context. Trends in Ecology and Evolution 16 , 454-9.


Administration

Funding: approx $100,000

Contact: Dr. Bronwyn Houlden, BDTNRM Programme Coordinator

Email: Bronwyn.Houlden@bdtnrm.org.au

Project Identification Number: BD8007

Key Management Action: BVH2.3.2

"By 2010, ensure 40% of land managers, including local, state and federal governments are utilizing land management techniques that improve land and biodiversity condition. "

Partners: JCU, CSIRO, EPA/QPWS

Project Manager: Lin Schwarzkopf

Links: website for A/Prof Lin Schwarzkopf, Tropical Biology, JCU