- Acknowledgement of Country
- Saving Koalas – Science for Wildlife Project Updates (see links below)
- Join Bushcare
- Giant Dragonfly sighted by Council’s Natural Area Operations Team
- Giant Dragonfly – an ancient peat-swamp survivor in the Blue Mountains
- Should we plant or not?
- Regenerating a native ground layer from Trad at Bellata Park Bushcare
- Congratulations Lis Bastian – Environmental Citizen of the Year Award
- Native Plant Propagation Workshop
- How did your environment fare last year? Australia’s Environmental 2020
- Connecting Kids to Nature program update
- Congratulations to our new Environmental Manager
- Seniors Week Recognition Awards
- Clean Up Australia Day in The Gully
- What’s On
- Save the date – Bushcare Picnic 30 October
Article by Dr Ian Baird
Petalura gigantea (Family Petaluridae), commonly known as the Giant Dragonfly or Southeastern Petaltail is a very large dragonfly which may have a wingspan up to 12.5 cm. It is recorded from peat swamps, bogs and seepages along the coast and ranges of NSW from near the Victorian border to around the Qld border. It is listed as Endangered in NSW under the NSW Biodiversity Conservation Act 2016, with habitat loss and degradation identified as the main threats. In addition to the large size and widely separated dark eyes, the species (and genus) is characterised by a long pterostigma (darkened cell) towards the end of the leading edge of the wings, and large, petal-shaped, anal appendages in adult males (Figure 1). Adult females lack the conspicuous anal appendages and are somewhat bulkier than males (Figure 2). These features distinguish it from other very large dragonflies such as Austrophlebia costalis. Various Bushcare and Swampcare sites in the Blue Mountains include peat swamp habitat of Giant Dragonflies.
The Petaluridae (“petaltails”) can be traced back to the late Jurassic and currently includes 11 known species around the world, including the endemic Australian genus Petalura with five species. The family is unique amongst dragonflies, in that larvae of nine of those species (including all Petalura species) excavate (sometimes complex) burrows which extend below the water table in peaty soils and which they occupy and maintain for their entire larval stage. The deepest burrow recorded for a petalurid worldwide was a P. gigantea burrow I investigated, which was 75 cm deep. These dragonflies have very long larval stages; extrapolation from recent studies suggests a larval stage of at least six years in P. gigantea, and possibly 10 or more in some situations. Larvae reach a length of 4.5-5 cm. Larvae feed on a range of small invertebrate prey within their burrows, including worms and nematodes, and are likely to act as ambush predators of larger prey from within their burrow entrances, feeding on above ground invertebrates, such as spiders, crickets, cockroaches, and perhaps small frogs, such as Crinia signifera. Larvae with submerged burrow openings in shallow pools can also prey upon other dragonfly or damselfly larvae within those pools. It is possible (but unknown) that they also leave their burrow openings temporarily to forage under suitable conditions, such as at night and during rain. I have recorded above ground chambers above their burrow openings, within litter layers and Sphagnum hummocks, which they may use for foraging purposes. Larvae leave their burrows and climb the nearest shrub or sedgeland vegetation to undergo emergence (ecdysis) to the adult stage, usually leaving their larval skin (exuvia) attached to their shrub or sedge emergence supports. The presence of exuviae confirms a site as a successful breeding site. Emergence may commence in early October in some years in some sites and extend into January, but normally appears to commence during November, at least in the Blue Mountains.
Adults live for a maximum of one summer flying season, which extends into February at least, with occasional late flying individuals having been observed on one occasion as late as mid-March in the Blue Mountains. Adults are predatory upon other flying insects during flight and consume a range of prey, including other dragonflies and damselflies, butterflies, moths, grasshoppers, cicadas, wasps, and various types of flies, including crane flies. Adults typically return to a perch to consume prey. Adults spend much time perched in sedgeland and shrub vegetation, interspersed with generally short flights associated with foraging, mating, and in the case of males, territorial interactions. Adult females typically leave their larval swamp habitat following emergence and only return to a swamp habitat for breeding purposes. There is no courtship behaviour and mating generally occurs in swamp habitat with the pair perched in sedge or shrub vegetation. Egg-laying (ovipositing) involves insertion of the ovipositor into the wet, organic-rich soil substrate, into fissures in the substrate, or amongst or under live or decomposing plant material overlying the substrate. Females typically walk along the soil surface or perch within covering vegetation or on litter while ovipositing. They do not appear to oviposit into substrate covered by more than 1-2 mm of water. Most adults encountered in swamp breeding habitats are males, who are typically territorial in swamp habitat. Predation of adults by birds, skinks and spiders has been observed and dead individuals have been found in spider webs.
Petalura gigantea is considered to be an obligately groundwater-dependent species. Although the burrowing larval habit confers ecological benefits, including increased environmental stability, and some protection from the effects of fire, flood, drought and above ground predators, the species groundwater dependence and restriction to peat swamp habitats places it at increased risk in the event of any reduction in groundwater levels (e.g., due to groundwater abstraction, tunnel or pipeline boring, and longwall coal mining), more intense fire regimes, and the potential compounding effects of rapid climate change. Loss and degradation of habitat as a result of urban and transport infrastructure development, agriculture, forestry, and longwall coal mining continue to threaten the species through loss and degradation of habitat.
Figure 1. Male Petalura gigantea perched on razor sedge, Lepidosperma limicola, in a Blue Mountains Swamp. Note the conspicuous petal-shaped appendages at the end of the abdomen. Photo: Ian Baird
Figure 2. Female Petalura gigantea perched on Acacia ptychoclada in a Blue Mountains Swamp. Photo: Ian Baird
Bring the family to Wentworth Falls Lake on September 17 to discover more about our local waterways and the
creatures that live there. Our creeks, rivers and lakes are part of what makes the Blue Mountains so special. They are home to unique animals such as giant dragonflies, turtles, water-skinks and much more. Come along and learn about who lives in and around the water, and what we can do to look after them. Meet a crayfish, listen to stories, explore a swamp, create some art, make a difference!
Threatened Species Day is a national day held each year on 7 September to commemorate the death of the last remaining Tasmanian tiger at Hobart Zoo in 1936. On this date every year we reflect on what has happened in the past and how we can protect our threatened species in the future. It is also a day to celebrate our success stories and ongoing threatened species recovery work.
With all this in mind Garguree Swampcare Group hosted a threatened species event on Sunday September 4.
30 fantastic volunteers joined in on the day which started with a restoration planting along the riparian corridor which connects the Blue Mountains Water Skink populations of the “McCrae’s Paddock” swamp and the “middle” swamp in The Gully Aboriginal Place, Katoomba.
At 11am Sandy Holmes greeted us with a most amazing brunch, including giant dragonfly cookies and water skink eclairs (they were definitely threatened species …)
This was followed by Welcome to Country and a smoking ceremony by David King. He also spoke about Garguree Swampcare’s work and the ongoing support from the Environmental Trust and “Protecting our Places” grants.
Council’s Environmental Scientist Michael Hensen spoke about a new 10 year Environmental Trust – Saving our Species grant of $750,000 “Swamped by Threats” which will help protect the Blue Mountains Water Skink and the Giant Dragonfly at a number of priority sites across the Blue Mountains and the Newnes Plateau.
We finished the morning’s formal proceedings with Ian Baird presenting an exciting insight into the biology and identification of two iconic threatened species found in Blue Mountains Swamps: the Giant Dragonfly and the Blue Mountains Water Skink.
After that it was back to more connecting to our place through our stomachs!
A recent journal paper by local ecologist Dr Ian Baird (firstname.lastname@example.org), on larval burrow morphology and groundwater dependence in the endangered Giant Dragonfly, Petalura gigantea, may be of interest to bushcarers.
The following abstract is from the paper:
“Most species of petalurid dragonflies have a fossorial larval stage, which is unique in the Odonata. Larvae typically excavate burrows in soft peaty soils in mires, seepages or along stream margins, which are occupied by a single larva throughout the long larval stage. This paper reports on a study of burrow morphology in Petalura gigantea, with the objectives of describing their burrows, documenting any variability in burrow morphology across the hydrogeomorphic range of habitats used by the species, identifying factors contributing to any such variability, resolving questions in relation to the single previous illustration of a burrow system and identifying the level of groundwater dependence of larvae. The species was found to be an obligate, groundwater dependent, mire-dwelling species with well-maintained and sometimes complex burrows. Burrow complexity and morphological variation are inferred to be a response by larvae to the hydrogeomorphic characteristics of the habitat and substrate attributes. All burrows were occupied by a single larva, consistent with previous observations of other fossorial petalurids, but in contrast to the previous description of a P. gigantea burrow complex occupied by multiple larvae. The functional role of identified burrow features is discussed. Although the fossorial larval habit confers ecological benefits, the species’ groundwater dependence and restriction to mire habitats places it at increased risk in the event of any reduction in groundwater availability, more intense fire regimes, and the potential compounding effects of rapid climate change.”
Baird, I.R.C. (2014). Larval burrow morphology and groundwater dependence in a mire-dwelling dragonfly, Petalura gigantea (Odonata: Petaluridae). International Journal of Odonatology, 17, 101-121. doi:10.1080/13887890.2014.932312