World's only known eyeless wasp discovered mummified in Nullarbor cave
Jess Marsh had spent 45 minutes crawling and twisting through the claustrophobic limestone tunnels of the Nullarbor Plain when she first saw it.
Perched on the wall of a cave chamber was the almost perfect mummified remains of small, reddish wasp about 2 centimetres long with translucent wings.
Its stand-out feature? It had no eyes.
"This wasp is the only wasp in the world that is known to have adapted like that to a cave life," said Dr Marsh, an entomologist and arachnologist — an insect and spider expert — at the University of Adelaide.
"The first specimen was actually climbing up the wall of the cave ... like they'd been freeze-dried."
The preserved insect, yet to be taxonomically described, was one of the crowning discoveries from a research expedition in April with cavers from the Australian Speleological Federation (ASF).
Eleven caves on the Western Australia side of the 200,000 square kilometre Nullarbor region were examined in a biological survey, funded by the Australian Research Council and the Hermon Slade Foundation.
The caves were selected based on previous sightings of underground critters by cave-exploring citizen scientists.
ASF president Andrew Stempel said the trip, which found specimens at five of the sites, had been an "incredible" collaboration connecting caver knowledge with expert scientists.
"It took many years and many cavers and a lot of hard yards," he said.
The wasp was found in a cave that contains passages that run for about 10 kilometres, which had previously been mapped out by scientists.
It wasn't the only remains the researchers found either.
The cave was full of thousands of mummified bodies of spiders, cockroaches, centipedes and other insects, preserved thanks to the salty cave conditions.
Dr Marsh said when she first locked eyes on the site she was captured by its otherworldly beauty.
"It's not like anything I've ever seen before," she said.
"[It had] the most amazing cave decorations I've ever seen, so stalactites, stalagmites and huge long salt straws [thin pillars of salt that sway in the cave breeze].
No living critters remain because of some sort of invertebrate world-ending cataclysm that occurred an unknown number of years ago.
What excited Dr Marsh was the potential relationship between the blind arachnids and the wasp, which she thought was from the spider-hunting family called Pompilidae.
"It's a really interesting story if they've both evolved to a cave-adapted lifestyle where they've lost their eyes independently but are linked through parasitism," she said.
Matt Shaw, a collection manager at the Australian Museum and not part of the recent expedition, said finding a wasp and spiders with regressed features was fantastic for science.
"Because as [Charles] Darwin pointed out ... regressed animals including cave animals were an important source of evidence for understanding evolution," he said.
The exact age of the invertebrates in the mummy mausoleum was yet to be analysed, but Dr Marsh said they were so well preserved "they could have died yesterday".
Elsewhere on the trip, the expedition found some creatures that were still kicking, including two species of eyeless spiders.
Both could fill up the palm of your hand but are incredibly different.
One, which hangs underneath a web weaved between rocks is believed to be from the genus Tartarus, named after the prison for titans in Greek mythology.
The second is large, hairy and probably part of the Troglodiplura genus but distantly related to tarantulas, funnel webs and trapdoor spiders.
"We don't know yet if it's a new species or if it's one of the already described ones," Dr Marsh said.
There are five spiders in Troglodiplura, including four that were described only a few years ago from tiny fragments found in museum collections.
Both Tartarus and Troglodiplura spiders have only been found on the Nullarbor.
And there is a belief among arachnologists that some Nullarbor spider species may only be found in single caves rather than multiple sites.
Dr Marsh said the latest trip, along with other research, challenged the idea the region was not particularly special for biodiversity.
"The number and the diversity of species that may be surviving and living in the caves on the Nullarbor is actually much higher than we we initially thought," she said.
With the growing knowledge of underground species comes a greater awareness of potential threats.
In caves accessible to mammals, Dr Marsh said invasive foxes proposed a big threat to blind spiders. A site with living arachnids from the most recent trip had fox scat that contained spider fangs.
"The risk of extinction for a lot of those [underground] species through development, impact by humans, changes to water movement across the landscape ... is really very high," she said.
While the South Australia side of the Nullarbor is in the process of being made a World Heritage site, the WA side is not. All of the recent cave surveys were done within an area ear-marked for the largest proposed green energy project in Australia.
The 70 gigawatt Western Green Energy Hub would see about 3,000 turbines and six million solar panels installed across 20,000sqkm of land.
The project has come under scrutiny from cavers concerned about potential impacts to the unique cave systems.
Project chief executive Raymond Macdonald said less than 5 per cent of the total surface area would be impacted, and that the company was currently mapping a directory of caves, sink holes and karst feature locations.
"This new accuracy will ensure that significant features are totally avoided when selecting infrastructure locations," he said.
The project's management is currently in discussion with state and federal regulators about what environmental studies will be needed as the project proposal is reviewed.
An Indigenous land-use agreement is also being negotiated with the area's Traditional Owners, the Mirning.
A WA Mirning People Aboriginal Corporation spokesperson said the whole ecosystem in the Nullarbor was significant.
"Our priority is always to protect the environment as a whole, while placing particular emphasis on rare and endangered species," they said.
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles

ABC News
2 hours ago
- ABC News
Wildlife experts say ugly endangered animals are being ignored in conservation efforts
West Australian wildlife experts say countless threatened animal species are not getting the attention and conservation efforts they deserve because they are considered ugly. WA's South West region is synonymous with endemic, adorable marsupials, such as the vulnerable western ringtail possum or the near-threatened quenda. In fact, the region is home to more than 144 threatened animal species, but lesser-known, uglier species are being left behind in research efforts because of their appearance. The phenomenon is known as "conservation bias", referring to the disproportionate focus on species deemed cute by the public. University of WA research fellow Jeremy Wilson said favouritism was limiting knowledge and leaving some species in danger of extinction. "There's sort of a bias towards studying these groups that, to be honest, we already know a lot about, which are all the cute fluffy things," he said. Dr Wilson's area of expertise is arachnology, the study of spiders. In WA alone, there are more than 200 different species of identified trapdoor spiders, and the South West is a trapdoor hotspot. "In any given area, there may be 10 different species of trapdoors and their relatives, but a lot of them we don't have the necessary information to know how to manage them," Dr Wilson said. "They're around Bunbury, all through the South West forests and all the way up to Perth, and the shortfall of information is everywhere." Independent ecologist Bob Bullen studies bats — a species equally undervalued in terms of public opinion. "The issue with bats is that people just don't see them, they operate at night, and people don't know they're there," Dr Bullen said. Dr Bullen said bats were largely insectivores, which helped to manage pest populations. "If you have a barbecue in your backyard in summer, the sun goes down, and the mosquitoes come and swarm for 20–30 minutes and tend to disappear again, and the reason they tend to disappear is because the bats come out." Dr Wilson said the biggest bottleneck for conservation of ugly animals was taxonomy, or the process of officially naming and classifying a species. "We can't conserve things if we don't know where they are and how to identify them, and that's the main issue," Dr Wilson said. Edith Cowan University wildlife ecologist Leanda Mason said finding and classifying countless unknown species was unviable. "You can definitely conserve things without having a name to them, it's something I find really frustrating," Dr Mason said. Dr Mason said the South West region was brimming with endemic species that needed protection. "[The South West] has extremely high rates of endemism, which means that there are species that are only found here and are very special to this place and don't occur anywhere else in the world," they said. Dr Mason said conservation efforts should be broadly applied to the region's key habitats, such as local cave systems. "There are extra high rates of endemism in those areas because they're so special and so ancient and haven't changed in a long time," they said. "Caves kind of remain the same because they go underground [where] the humidity and temperature doesn't change as much, so a lot of species retreat into cave systems and use them as bases for surviving."

ABC News
4 hours ago
- ABC News
Brain Rot: Is internet addiction real?
Plenty of people will say they are addicted to the internet. But how well-recognised, scientifically, is an addiction ... to your screen? In episode four of Brain Rot, we dig into how behavioural addictions work. And we hear from self-described internet addicts about the treatment programs helping them manage their relationship with technology. Brain Rot is a new five part series from the ABC's Science Friction about how tech is changing our brains, hosted by Ange Lavoipierre. Guests: Jillian and Kate Internet and Technology Addiction Anonymous members Hilarie Cash Psychologist and Co-Founder, reSTART Anna Lembke Professor of Psychiatry and Addiction Medicine, Stanford University School of Medicine Anastasia Hronis Clinical Psychologist; Author, The Dopamine Brain Dar Meshi Associate Professor, Michigan State University Credits: Presenter: Ange Lavoipierre Presenter: Ange Lavoipierre Producer: Fiona Pepper Producer: Fiona Pepper Senior Producer: James Bullen Senior Producer: James Bullen Sound Engineer: Tim Symonds This story was made on the lands of the Gadigal and Menang Noongar peoples. More Information: Changes and correlates of screen time in adults and children during the COVID-19 pandemic: A systematic review and meta analysis. Internet-addicted South Korean children sent to digital detox boot camp.

News.com.au
6 hours ago
- News.com.au
Biocurious: CSL's R&D chief says drug development is like falling in love
CSL's hereditary angioedema prophylactic Andembry is one of only a handful of FDA-approved, Australian-developed drugs Andembry reflects CSL's R&D approach of sticking with 'adjacent' competencies CSL spends around $2.3 billion a year on R&D, but it's still outgunned by rivals and needs to play smart CSL (ASX:CSL) global head of research and development Bill Mezzanotte likens drug development to falling in love. 'If you don't put your whole heart into it, it won't work,' the Pennsylvania-based Mezzanotte told Stockhead. 'But when you do, you are at risk of having your heart broken and that sometimes happens.' The blood plasma giant certainly has had its share of heartbreak along the way, including a failed heart attack mega trial. But as a 'hopeless romantic', Mezzanotte remains confident about the life-saving potential of the company's circa US$1.5 billion ($2.3 billion) a year R&D program. Justifying this optimism, CSL last week won US Food and Drug Administration (FDA) assent for Andembry (garadacimab), a new treatment for the severe swelling condition hereditary angioedema (HAE). In commercial terms, it's the most significant win in years for the $116 billion market cap behemoth. Rare local drug success for rare disease Developed over close to two decades, Andembry is one of only a handful of Australian-developed drugs to be approved by the FDA. It's also the first non-plasma derived monoclonal antibody to be discovered and developed entirely by CSL. Monoclonal antibodies are lab-engineered proteins that bind to a specific target such as a cancer cell or a virus. Because they're not produced from painstakingly collected blood, these remedies have much more attractive margins. Fittingly, CSL's new facility at Broadmeadows in northern Melbourne will make Andembry. Regulators in Europe, the UK, Japan, Switzerland, the United Arab Emirates and locally already had approved Andembry. But to re-phrase Paul Keating, if you are not approved in the US – the world's biggest reimbursed drug market – you are only camping out. Same but very different Andembry is intended as a powerful prophylactic for HAE, which affects about one in every 50,000 people. The disease can cause fatal swelling throat swelling. Andembry stemmed from an antibody 'library' of potential targets which CSL in licensed from the Nasdaq-listed Dyax Corp (later acquired by Shire Pharmaceuticals). CSL discovered garadacimab on the 'bookshelves', along with some other molecules. From that base, CSL did all the research and clinical development, including a 64-patient global trial dubbed Vanguard. 'We took the lead very early,' Mezzanotte says. 'We bought it all the way from research to product development.' CSL's HAE armamentum consists of the injected Haegarda and the infused Berinert (for use during attacks). Haegarda requires twice-weekly injections, while Andembry is administered monthly via a 'patient friendly' auto injector. Mezzanotte says Andembry is 'completely different' to Haegarda. Haegarda is a plasma-derived version of the C1 esterase inhibitor, which HAE patients lack. With a more 'upstream' action, Andembry targets an associate pathway called factor XIIa. 'Both are effective but effective in different ways,' Mezzanotte says, adding that Andembry is 'darned effective' with low side effects. The Vanguard trial showed Andembry reduced the median number of HAE attacks by more than 99% compared to placebo. Blockbuster potential But won't Andembry simply cannibalise Haegarda (and Berinert) revenue? Haegarda chalked up US$491 million of sales in the 2023-24 year, with Berinert contributing US$242 million. Mezzanotte says patients may prefer C1 inhibitors 'because they may do a little more than necessary'. Haegarda works well for pregnant women and it possibly is better for more severe attacks. 'Scientifically they live well together,' he says. But management hopes Andembry will steal plenty of share from Takeda's Takhzyro, the market-leading HAE drug turning over US$3 billion but also requiring twice-weekly injections. Bell Potter analyst Thomas Wakim dubs Andembry 'CSL's most commercially attractive near-term new product.' His peer at Wilsons, Dr Shane Storey estimates Andembry will achieve peak annual sales of US$600 million within five years. In the pipeline Andembry exemplifies CSL's R&D approach of not straying too far from what it's good at, whilst not being afraid to disrupt its own products. 'I'm a big believer in adjacency – utilising our plasma platform – or sticking to an area we know like HAE and disrupting ourselves,' Mezzanotte says. 'When we get too far away from our base of operations it gets a little tricky for us.' CSL's annual R&D manifesto outlines a dense agenda of advanced and nascent programs across its Behring (core plasma and specialty) and Seqirus (flu vaccine) arms. An adjuvanted trivalent cell-based flu vaccine – which includes three flu strains to be more effective – is the most advanced. The program is in phase III and may not need more data to win approval. CSL is also trialling CSL300 (clazakizumab) for patients on dialysis for end-stage kidney disease (to reduce inflammation and heart attacks). CSL inlicensed clazakizumab from another company that had tried the drug for kidney transplants without success. Vifor? I'll tell you Investors periodically have criticised CSL for its $18 billion, seemingly left-field acquisition of the Swiss kidney health and iron deficiency group, Vifor. One of CSL's stated reasons for the purchase was to expand its R&D pipeline. 'Vifor gave us an insight into kidney disease, which allowed us to use a drug we had ,' Mezzanotte says. 'It helps us to be efficient with a great chance of success.' CSL's global head of research and development Bill Mezzanotte. Pic: supplied Checking out of Heartbreak Hotel In February last year CSL experienced heartbreak – literally and figuratively – with the failure of its drug program, CSL-112, to prevent secondary heart attacks via cholesterol-reducing mechanisms. The company's 18,000 patient phase III trial failed the primary endpoint. The therapy showed the desired activity, but just not enough. Mezzanotte says the candidate had passed futility analysis, which – as the name suggests – appraises whether continuing a program makes sense. Mezzanotte says CSL took the conscious risk of eschewing a smaller intermediary trial. 'It was a particularly tough choice, a smaller trial would only have led to the bigger trial,' he says. 'We decided the most cost efficient was to go straight to the big trial but it was a risky approach and we failed.' He says the lesson of such setbacks is to 'fail well'. CSL-112 has gone back to the labs for researchers to have another look-see – but it won't be subject to another big-ticket trial. AI speeds up the 'unsexy' drudge work Mezzanotte says while AI is still immature, it could expedite early-stage drug discovery by enabling programs to skip early-stage animal modelling and to go directly to human studies. 'In theory it should improve speed and the probability of success, but we are in the infancy of using that,' he says. 'Automation has improved our productivity, but I'm hoping AI can bridge the gap with all the big laboratory work we can't afford to do. 'We haven't seen the tangible benefit yet, but we see the promise of it.' He says while AI advocates focus on the 'sexy' research side, the technology is helpful for prosaic tasks such as preparing regulatory and safety reports. 'We create a lot of documents in R&D,' Mezzanotte says. 'We used to send it by trailer, now we email it.' Getting bang for 2.3 billion bucks CSL targets an R&D spend of 10-11% revenue, equating to the $2.3 billion at present. While this sounds capacious, rivals are spending up to US$5 billion annually. Given that, the company needs to glean maximum efficiencies from its global complement of 2000 R&D staff, about one-third of which are in Australia. 'We pick and choose carefully,' Mezzanotte says. 'We can't build huge research palaces and we try keep lean and use partners whenever we can to extend our reach.' Having held senior roles at Boehringer Ingelheim and Astrazeneca, Mezzanotte says commerciality should not be a 'four letter word' in R&D. 'We look for areas of unmet need and rational targets to work on,' he says. 'There is plenty of commercial input early on, but the first few years of Andembry all about the science.' Mezzanotte says through 'great successes and some disappointments', investors have long supported CSL's R&D endeavours. 'I hope shows them the power of R&D and what we can do at CSL.'