In the Atlantic Forest, the lowland tapir is at risk of extinction

Lowland tapir populations in the Atlantic Forest in South America are at risk of almost complete disappearance, scientists have estimated. The main long-term threat to their well-being is population isolation, as hunting and highways keep populations away from each other. Urgent measures need to be taken to connect isolated populations and ensure the long-term conservation of tapirs, warn the authors of a new study published in the open-access journal Neotropical Biology and Conservation.

Lowland tapir populations in the Atlantic Forest in South America are at risk of almost complete disappearance, scientists have estimated. Weighing up to 250 kg, the animal can adapt to most habitats in South America—but its populations continue to decline across its range.

Today, its survival is seriously threatened: it can be found in just 1.78% of its original distributional range in the Atlantic Forest biome, which covers parts of Brazil, Argentina and Paraguay. The main long-term threat to its well-being is population isolation, as hunting and highways keep populations away from each other.

Lowland tapir. Photo by Patricia Medici

Urgent measures need to be taken to connect isolated populations and ensure the long-term conservation of tapirs, warn the authors of a new study on the distribution and conservation status of lowland tapirsin the South American Atlantic Forest, published in the open-access journal Neotropical Biology and Conservation

The research was done by Kevin Flesher, PhD, researcher at the Biodiversity Study Center, Michelin Ecological Reserve, Bahia, and Patrícia Medici, PhD, coordinator of the Lowland Tapir Conservation Initiative, a project developed by the Institute for Ecological Research in Brazil, and chair of the Tapir Specialist Group at the Species Survival Commission in the International Union for Conservation of Nature.

 “Of the 48 tapir populations identified during the study, between 31.3% and 68.8% are demographically unviable (low number of individuals), and between 70.8% and 93.8% of the populations are genetically unviable (low gene flow). Only 3-14 populations are still viable in the long run when both criteria are considered. The evidence suggests that with the appropriate conservation actions, the lowland tapir could be broadly distributed throughout the Atlantic Forest,” says Kevin Flesher. 

Lowland tapir. Photo by Alexander Blanco

“Tapirs have low reproductive potential, including a long reproductive cycle with the birth of just one young after a gestation period of 13-14 months and intervals of up to three years between births. Our populational simulations clearly show how, in the case of small populations, even the loss of a single individual per year can result in rapid extinction of an entire local population,” adds Medici. 

Lowland tapir. Photo by Bill Konstant

Kevin Flesher dedicated 15 years to visiting 93 reserves in the Atlantic Forest, talking to people and analyzing 217 datasets, before he compiled the necessary data to design conservation actions that can ensure the survival of tapirs in the area. 

The states of São Paulo and Paraná in Brazil have the largest number of remaining populations: 14 and 10, respectively. The two largest populations are in Misiones, Argentina, and in the neighboring Iguaçu and Turvo reserves, in Paraná and Rio Grande do Sul, Brazil.

“As far as our knowledge goes, there is no evidence of movement of tapirs between these populations,” points out Medici.

The distance between population fragments, however, is not what is stopping them.

“The central problem is the multiple threats they face while crossing the habitat,” explains Flesher. Highways are one major obstacle that limits the access of tapirs to forests with adequate habitat. “For example, the heavy traffic on highway BR-101 (which cuts the Brazilian Atlantic Forest from North to South) is a death trap to wildlife. Tapirs often die when attempting to cross it,” explains Medici. 

The construction of highways and expansion of traffic in and around natural areas is a serious threat to large tapir populations that might otherwise have the chance to thrive, like those in Misiones, Argentina, and Serra do Mar, Brazil. 

“Roadkill is a significant cause of death in six of the eight reservations in which highways cross tapir populations, and the expansion of the roadway grid in the country threatens to cause population fragmentation in at least four populations,” points out Flesher. This is why finding ways to allow tapirs to cross highways safely is an urgent conservation priority.

Lowland tapir. Photo by Patricia Medici

The results of the study, however, give cause for “cautious optimism” for the future of tapirs in the area: after decades of dedicated conservation efforts, the situation is starting to improve. 

“Despite these continuing challenges for tapir conservation, most populations appear to be stable or increasing and the conservation outlook for the species is better than several decades ago, when the first efforts to protect the species began,” Kevin Flesher concludes.

Research article:

Flesher KM, Medici EP (2022) The distribution and conservation status of Tapirus terrestris in the South American Atlantic Forest. Neotropical Biology and Conservation 17(1): 1-19. https://doi.org/10.3897/neotropical.17.e71867

Scientists discover White-handed gibbons that have been evolving in the south of Malaysia

Genetic assessment of captive gibbons to identify their species and subspecies is an important step before any conservation actions. A group of wildlife researchers recently discovered a previously unknown population of white-handed gibbons (subspecies lar) from Peninsular Malaysia. Their findings are now published in the open-access journal ZooKeys. Betsy and Lola are among the captive white-handed gibbons undergoing a strict rehabilitation process before being released back to the wild.

Many captive gibbons kept in zoos and rescue centres have been seized from illegal pet trade, private collectors, and plantations where their natural habitats are getting destroyed. 

In 2013, the National Wildlife Rescue Centre (NWRC) of the Department of Wildlife and National Parks (PERHILITAN) was established in Peninsular Malaysia to help with the rehabilitation of wildlife species – including gibbons – before they are reintroduced or translocated back to the wild. Under the Primate Rehabilitation Programme initiated by PERHILITAN, captive gibbons have to go through a number of procedures and assessments, where their taxonomy and genetics might be examined, before they can go back to living in the wild.

Members of the research team at National Wildlife Forensic Laboratory of DWNP. Photo by PERHILITAN

Following the Guidelines for Reintroductions and Other Conservation Translocations provided by the IUCN Species Survival Commission, researchers Dr Jeffrine J. Rovie-Ryan from Universiti Malaysia Sarawak and Millawati Gani and colleagues from the National Wildlife Forensic Laboratory of PERHILITAN conducted a genetic assessment on 12 captive white-handed gibbons in NWRC. Determining the subspecies and origin of the animals is an important step that informs further decisions on their translocation and reintroduction.

In a research paper published in the open-access journal ZooKeys, the team describes a previously unknown southern population of the white-handed gibbon subspecies lar living in Peninsular Malaysia. In what started as a straightforward species and subspecies identification process using DNA technology, the researchers discovered unusual mutations in the DNA of the studied gibbons. This is how the researchers found themselves before a distinct population, which they concluded must have been evolving in isolation.

Lola (left) and Betsy (right), two of the White-handed gibbons of the Hylobates lar lar subspecies undergoing rehabilitation process at Pulau Ungka, NWRC. Photo by Hani Nabilia and PERHILITAN

“Given the prolonged isolation, it is likely that the southern population has undergone some local speciation, but this finding should be regarded as preliminary and requires further investigation,” explained Dr Jeffrine. Furthermore, the researchers suggest there might be a northern population inhabiting Southern Thailand.

Still going through rehabilitation, the gibbons from the study have been pre-released into a semi-wild enclosure known as Pulau Ungka (Gibbon Island), where their recovery is closely monitored by primate experts of PERHILITAN.

Research article:

Gani M, Rovie-Ryan JJ, Sitam FT, Mohd Kulaimi, NA, Zheng, CC, Atiqah AN, Abd Rahim, NM, Mohammed AA (2021) Taxonomic and genetic assessment of captive White-Handed Gibbons (Hylobates lar) in Peninsular Malaysia with implications towards conservation translocation and reintroduction programme. ZooKeys 1076: 25–41 (2021), doi: 10.3897/zookeys.1076.73262

First moth species on Alpenrose discovered

Discovery of the first moth species to mine the leaves of the highly poisonous Alpine rose

 Rust-red alpine rose, one of the most popular alpine plants. Photo by Ingrid Huemer

An Austrian-Swiss research team was able to find a previously unknown glacial relic in the Alps, the Alpine rose leaf-miner moth. It is the first known species to have its caterpillars specializing on the rust-red alpine rose, a very poisonous, widely distributed plant that most animals, including moths and butterflies, strictly avoid. The extraordinary record was just published in the peer-reviewed scientific journal Alpine Entomology.

Poisonous host plant

The rust-red alpine rose (Rhododendron ferrugineum) is among the best-known and most attractive plants due to its flowering splendor – at least for humans. It is, in fact, a highly poisonous plant, strictly avoided by grazing animals. For insects, the alpine rose is attractive at most as a nectar plant; insect larvae, on the other hand, develop on it only in exceptional cases. This also applies to Alpine butterflies and moths, which leave Alpine roses largely untouched despite their wide distribution. Therefore, the discovery of a highly specialized species in the Alps came as a complete surprise.

Chance find

Since alpine roses are unattractive to caterpillars and no insect the entire Alpine region was previously known to specialize on them, butterfly and moth experts had considered them rather uninteresting and ignored them in their research. The discovery of the alpine rose leaf-miner wasn’t the result of a targeted search: it was a pure stroke of luck.

During a cloudy spell in July this year, researchers surveying the butterflies in Ardez in the Engadine valley, Switzerland, happened to take a break exactly at an infested alpine rose bush. 

“The accidental sighting of the first caterpillar in an alpine rose leaf was an absolute adrenaline rush, it was immediately clear that this must be an extraordinary species,”

Peter Huemer, researcher and head of the natural sciences department of the Tyrolean State Museums

Peter Huemer, researcher and head of the natural sciences department of the Tyrolean State Museums, and Swiss butterfly and moth expert Jürg Schmid came back in late July and early August to look for caterpillars and pupae and find out more about this curious insect. The extended search yielded evidence of a stable population of a species that was initially a complete enigma. 

Life in the leaf

The alpine rose leaf-miner moth drills through the upper leaf skin and into the leaf interior immediately after the caterpillar hatches. The caterpillar then spends its entire life until pupation between the intact leaf skins, eating the leaf from the inside. Thanks to this behavior, the caterpillar is just as well protected from bad weather as from many predators such as birds, spiders, or some carnivore insects. The feeding trail, called a leaf mine, begins with a long corridor and ends in a large square-like mine section. The feces are deposited inside this mine. When the time comes for pupation, the caterpillar leaves the infested leaf and makes a typical web on the underside or a nearby leaf. With the help of several fine silk threads, it produces an elaborate “hammock”, in which the pupation finally takes place. In the laboratory, after about 10 days, the successful breeding to a moth succeeded, with a striking result.

Enigmatic glacial relic

Final instar larva of the alpine rose leaf-miner moth on Rhododendron ferrugineum in Ardez, Graubünden, Switzerland. Photo by Jürg Schmid

Huemer and Schmid were surprised to find out that the moths belonged to a species that was widespread in northern Europe, northern Asia and North America – the swamp porst leaf-miner butterfly Lyonetia ledi. By looking at its morphological features, such as wing color and pattern, and comparing its DNA barcodes to those of northern European specimens, they were able to confirm its identity.

Habitat of the alpine rose leaf-miner moth in Engadine/Switzerland with Rhododendron ferrugineum. Photo by Jürg Schmid

The Engadine population, however, is located more than 400 km away from the nearest other known populations, which are on the border of Austria and the Czech Republic. Furthermore, the species lives in northern Europe exclusively on swamp porst and Gagel bush – two shrubs that are typical for raised bogs and absent from the Alps. However, the researchers suggest that in earlier cold phases – some 22,000 years ago – the swamp porst and the alpine rose did share a habitat in perialpine lowland habitats north of the Alps. It is very likely that after the last cold period and the melting of the glaciers, some populations of the species shifted their host preference from the swamp porst to the alpine rose. The separation of the distribution areas of the two plants caused by subsequent warm phases inevitably led to the separation of the moth populations. 

Extinction risk

The Alpine Rose Leaf-miner Moth is so far only known from the Lower Engadine. It lives in a steep, north-exposed, spruce-larch-pine forest at about 1,800 m above sea level. The high snow coverage in winter and the largely shady conditions in summer mean that alpine roses don’t get to bloom there. The scientists suspect that the moth species can still be discovered in places with similar conditions in the northern Alps, such as in neighboring Tyrol and Vorarlberg. Since the moth is likely nocturnal and flies late in the year, probably hibernating in the adult stage, the search for the caterpillars and pupae is more promising. However, the special microclimate of the Swiss location does not suggest that this species, which has so far been overlooked despite 250 years of research, is widespread. On the contrary, there are legitimate concerns that it could be one of the first victims of climate change.

Research article:

Huemer P, Schmid J (2021) Relict populations of Lyonetia ledi Wocke, 1859 (Lepidoptera, Lyonetiidae) from the Alps indicate postglacial host-plant shift to the famous Alpenrose (Rhododendron ferrugineum L.). Alpine Entomology 5: 101-106. https://doi.org/10.3897/alpento.5.76930

Pakistan’s amphibians need more research efforts and better protection

In Pakistan, amphibians have long been neglected in wildlife conservation, management decisions and research agendas. To counter this, scientists have now published the first comprehensive study on all known amphibian species in the country in the open-access scholarly journal ZooKeys. The little we currently know about the occurrence of the chytrid fungus, which has already eradicated many amphibian species globally, is a grim example of how urgent it is to acquire further information.

Amphibians are bioindicators of an ecosystem’s health and may also serve as biological control of crop and forest pests. The First Herpetological Congress, organized in 1989, presented alarming findings about the decline in amphibian populations. Currently, amphibians include the highest percentage of threatened species (>40%), as well as the highest number of data deficient species (>1500 species). The little we currently know about the occurrence of the chytrid fungus, which has already eradicated many amphibian species globally, is a grim example of how urgent it is to acquire further information.

Asian Common Toad. Photo by Herpetology Lab, Arid Agriculture University Rawalpindi

Researchers just published the first comprehensive study on all known amphibian species of Pakistan in the open-access journal ZooKeys. In it, they report 21 species from the country, providing their identification key and photographic guide. However, as many of Pakistan’s potential amphibian habitats are difficult to access and study, especially the high-altitude northern and arid western mountains, it is highly likely that a lot of species are yet to be discovered.

Burrowing Frog (in amplexus). Photo by Herpetology Lab, Arid Agriculture University Rawalpindi

In particular, the authors point out that habitats facing destruction, urbanization, pollution, unsustainable utilization and other human-caused threats need to be put on high priority, so that suitable conservation strategies can be devised. This way, amphibian populations would be better controlled with less financial, administrative, and human resources.

So far, amphibians have been excluded from all current legislative and policy decisions in the country. Likewise, they are not protected under any law. Hence, the legislation pertaining to rare and endemic species needs to be updated. Schedule III, which includes protected species, provincial and federal wildlife laws, and CITES appendices are in particular need of revision.

Common Skittering Frog. Photo by Herpetology Lab, Arid Agriculture University Rawalpindi

Currently, wildlife conservation projects in Pakistan mainly focus on carnivores, ungulates and birds. Therefore, the authors of the study propose adopting an inclusive wildlife conservation approach in Pakistan. This approach would advocate the integration of poorly documented taxa, such as amphibians, in wildlife conservation and management projects. It is by highlighting the significance of their existence and the intrinsic values of all wildlife species that local ecosystems can remain healthy in the long run.

“There is also a dire need to change social attitudes towards the appreciation and significance of amphibians in our society. This could be achieved by initiating community awareness, outreach and school classrooms, and through citizen science programs,” add the researchers.

Research article:
Rais M, Ahmed W, Sajjad A, Akram A, Saeed M, Hamid HN, Abid A (2021) Amphibian fauna of Pakistan with notes on future prospects of research and conservation. ZooKeys 1062: 157-175. https://doi.org/10.3897/zookeys.1062.66913

Man’s best friend could be a jaguar’s next meal: A case study from the Mexican Caribbean

Events of jaguars predating on and attacking dogs are poorly documented throughout the Americas. Researchers from Mexico and Germany report in detail jaguar attacks on 20 dogs at a tourist site in the Mexican Caribbean. In addition, they describe an initiative proposed by locals as well as national and international NGOs to prevent human-jaguar conflicts due to pet predation. The study was published in the open-access journal Neotropical Biology and Conservation.

Mahahual is a small fishing village in the Mexican Caribbean that receives a large number of tourists every year. Over the past 15 years, its population has increased rapidly, and, as a result, people have started to settle in areas away from the main center of the village, sometimes encroaching on jaguar habitats. As most of those people keep guard dogs on their properties, jaguars have taken advantage of this situation by wandering near people’s houses at night, and sometimes those dogs end up as a night-time snack for the big cats.

A jaguar is photographed wandering around houses looking for dogs. Photo by Víctor Rosales

Unlike jaguar attacks on livestock, attacks and predation on other domestic species such as dogs have only been documented anecdotally (through interviews or from remains found in faeces). Such attacks can indeed lead to pet predation conflict, which can ultimately have a negative impact on the jaguar populations. Attachment to pets may lead humans to start killing the big cats, which is of particular concern for an endangered species like the jaguar. Furthermore, it is possible that a wide range of pathogens may be transmitted from dogs to jaguars, further threatening the health of jaguar populations in Mahahual.

A dog injured as a result of a jaguar attack in Mahahual, Quintana Roo, Mexico. Photo by Víctor Rosales

This is why a multidisciplinary team made up of veterinarians, conservationists, locals, NGOs (Aak Mahahual A.C. and International Fund for Animal Welfare (IFAW)) and researchers (El Colegio de la Frontera Sur and Universidad Tecnológica de Calakmul), led by Dr Jonathan Pérez Flores, began investigating the occurrence of jaguar predation and attacks on dogs at the Mexican Caribbean tourist site from almost 10 years ago. Their research was just published in the open-access journal Neotropical Biology and Conservation.

According to their report, the behaviour of Mahahual’s jaguars resembles that of Indian leopards, which have already turned dogs into an important component of their diet, preferring them over livestock. Jaguars and leopards usually attack from a blindside, biting the dogs on the neck or head to avoid counterattacks. Similarly to leopards, jaguars attack at night and kill more dogs during the dry season. This is likely due to the fact that it’s easier for jaguars to hunt dogs than their natural prey: armadillo, lowland paca, brocket deer, white-tailed deer. Furthermore, the latter are less available during the dry season.

One of the night houses built by the people of Mahahual, Aak Mahahual A.C. and International Fund for Animal Welfare (IFAW). Photo by Francisco Rubén Castañeda

In 2017, the people of Mahahual partnered with Aak Mahahual A.C. and IFAW to build protective night houses made of wood and wire mesh meant to keep dogs safe at night. So far, they’ve built 38 such houses to prevent jaguar attacks. Sterilisation and vaccination campaigns have also been intensified since late 2020 to prevent the transmission of diseases between the two species.

Thanks to this study, we now have a better understanding of the adaptability and persistence of jaguars in human-dominated landscapes and the impact of dog predation by jaguars. However, the authors call for more research in the area to help paint the full picture.

Research article:
Carral-García M, Buenrostro I, Weissenberger H, Rosales V, Pérez-Flores J (2021) Dog predation by jaguars in a tourist town on the Mexican Caribbean. Neotropical Biology and Conservation 16(4): 461-474. https://doi.org/10.3897/neotropical.16.e68973

Are zoos inadvertently complicit in wildlife trade? The case of a rare Borneo lizard

Should zoos display legally protected species that have been smuggled out of their range countries? A new study suggests that a pause and rethink may be needed, as it reports that accredited zoos have acquired a rare and legally protected reptile, the earless monitor lizard endemic to Borneo, without any evidence that the animals were legally exported.

The earless monitor lizard occurs only on the island of Borneo and has been described as a “miniature Godzilla” and “the Holy Grail of Herpetology.” Discovered by western scientists almost 150 years ago, for most of this period the species was known largely from pickled specimens in natural history collections, and wasn’t recorded from the wild for decades. In the 1970s, the three countries that make up Borneo – Indonesia, Malaysia and Brunei – added it to their protected species lists. This means that the species can neither be legally traded within these countries, nor legally exported out of them.

Earless monitor lizard. Photo by Chien C. Lee, Wild Borneo.

Despite legal protection and lack of export permissions, reptile enthusiasts and unscrupulous traders have long been smuggling small numbers of earless monitor lizards out of Indonesia and Malaysia, eventually bringing them to Europe. This greatly accelerated in 2012, when the species’ rediscovery was announced in a scientific journal. In 2016, all 183 countries that are signatory to the Convention on international trade in endangered species agreed to regulate global trade in earless monitor lizards in order to limit the negative effects of smuggling on wild populations. Agreed export numbers were set at zero.

Enforcing the laws has proven to be challenging, however, and to date only two smuggling attempts have been thwarted. In both cases, German smugglers were apprehended at Indonesian airports while attempting to move respectively eight and seventeen earless monitor lizards out of the country.

The first zoo that proudly announced it had obtained earless monitor lizards was Japan’s iZoo in 2013. This zoo is not accredited, and the ways in which the animals were obtained remain questionable. In Europe, the first zoos to openly display earless monitor lizards were located in Hungary, Austria and the Czech Republic. The animals were obtained from what zoos referred to as “private individuals” or “dedicated hobby breeders”, and, in one instance, from iZoo. Just like in Japan, how these animals ended up in Europe is questionable, but perhaps not illegal – and it is evident that no export permits were ever issued.

In recent years, more and more zoos in Europe, and since the beginning of this year also in the United States, have started displaying earless monitor lizards. Some cases were part of zoo exchanges, others were obtained from private individuals, and a handful were placed in zoos by authorities after they were seized, but it is clear that many were at one point illegally exported out of Indonesia, Malaysia or Brunei, or were illegally imported into non-range countries.

The acquisition of these protected lizards by zoos is neither in line with the intentions of national laws of their countries of origin, nor with international wildlife trade regulations. Moreover, it is diametrically opposed to the commitments the international zoo community has made to address illegal wildlife trade.

“To me, the current situation concerning the purchasing and proudly displaying of earless monitor lizards by accredited zoos can be compared with a road safety organisation posting online videos of its CEO doing wheelies on a motorbike and then adding that it was done on a private road where neither wearing a helmet nor having a driver’s licence is required,” said Vincent Nijman of the Oxford Wildlife Trade Research Group, author of the study that was published in the open-access journal Nature Conservation. “Both may be legal in a technical sense, but the optics are not good.”

“Modern, scientifically managed zoos are increasingly organising themselves with set ethical values and binding standards which go beyond national legislation on conservation and sustainability, but, unfortunately, this still only counts for a small proportion of zoos worldwide,” said Dr Chris R. Shepherd, Executive Director of Monitor Research Conservation Society. “Zoos that continue to obtain animals that have been illegally acquired, directly or indirectly, are often fuelling the illegal wildlife trade, supporting organised crime networks and possibly contributing to the decline in some species.”

Seven years ago, the price for a single earless monitor lizard was in the order of EUR 8,000 to 10,000 , so any zoo or hobbyist wanting to have one or more pairs had to make a serious financial commitment. These high prices put a restriction on the number of people that wanted to acquire them and could afford them. It probably also gave potential buyers a tacit reminder that the trade was illicit. In recent years, however, prices have come down, to less than EUR 1,000. Now that earless monitor lizards are more affordable, and with accredited zoos giving a sense of legitimacy, Nijman is concerned that it might become more and more acceptable to keep these rare animals as pets.

“When I grew up in the 1970s, it was still perfectly acceptable for what we now see as accredited zoos to regularly buy rare and globally threatened birds, mammals and reptiles from commercial animal traders. Few questions were asked about the legitimacy of this animal trade. This has dramatically changed for the better, and now many of the animals we see in zoos today have been bred in captivity, either in the zoo itself, or in partner zoos”, Nijman said. He added that in many ways zoos are a force for good in the global challenge to preserve species and conserve habitats. “It is imperative that these efforts are genuinely adopted by all in the zoo community, and, when there is doubt about the legitimacy of animals in trade, that a cautionary approach is adopted.”

Original source:

Nijman V (2021) Zoos consenting to the illegal wildlife trade – the earless monitor lizard as a case study. Nature Conservation 44: 69-79. https://doi.org/10.3897/natureconservation.44.65124

When conservation work pays off: After 20 years, the Saker Falcon breeds again in Bulgaria

The Saker Falcon (Falco cherrug) is a bird of prey living in plains and forest-steppes in the West and semi-desert montane plateaus and cliffs in the East. The majority of its Central and Eastern European population is migratory and spends winters in the Mediterranean, the Near East and East Africa. With its global population estimated at 6,100-14,900 breeding pairs, the species is considered endangered according to the IUCN Red List.

Saker falcon, Bulgaria

In Bulgaria, the Saker Falcon, considered extinct as a breeding species since the early 2000s, was recovered in 2018 with the discovery of the first active nest from its new history in Bulgaria. The nest is built by two birds that were reintroduced back in 2015 as part of the first ever Saker Falcon reintroduction programme. The results of the 5-year programme are described in detail in the open-access, peer-reviewed Biodiversity Data Journal.

Saker falcon, Bulgaria

Many factors contributed to the decline of the Saker Falcon in Bulgaria and globally, and most of them are human-caused. Populations lost big parts of their habitat due to changes in land use – the transition from grazing to arable crops led to the diminishing of key food sources. Other reasons include the use of poisonous baits and the accumulation of pesticides in the food chain, illegal trade of nest-poached chicks and eggs, power line electrocution, and lack of suitable nesting places.

Even after European legislation for the protection of wildlife was implemented, and regulations were issued on the use of pesticides in Bulgaria, the Saker Falcon population did not stabilise. Its endangered status further prompted joint conservation efforts between NGOs and national authorities.

As a result, a re-introduction programme for the Saker Falcon in Bulgaria was initiated in 2015, aiming to release a number of birds over a certain period of time using adaptation aviaries, or hacks. The Green Balkans Wildlife Rehabilitation and Breeding Centre (WRBC) in Stara Zagora facilitated the captive breeding of a group of Saker Falcons imported from Austria, Hungary, Germany, Slovakia and Poland by constructing ten breeding aviaries and two stock cages for juvenile falcons and equipping them with internal surveillance cameras.

Saker falcon fledges, Bulgaria

Between 2015 and 2020, a total of 80 Saker Falcons – 27 females and 53 males, were released via the hacking method from four aviaries near the town of Stara Zagora. Out of them, 64 had been bred and hatched at the WRBC.

Observation records from 2018 confirmed that at least one pair of the falcons released in 2015 was currently breeding in the wild in Bulgaria. This observation proves that with the help of hacking, Sakers can survive in the wild until maturity, return to the region of their release and breed successfully. In 2020, the female bird in the breeding pair was changed with a Saker Falcon released in 2016, and the new pair bred successfully.

In 2020, the programme was restarted for another 5 years, with the aim to release 100 Saker Falcons and have six pairs breeding in the wild. This will help restore the Saker Falcon population in the southern Balkans and facilitate gene flow amongst fragmented populations from Central Europe to Kazakhstan.

Helping this iconic species successfully establish a self-sustaining population in Bulgaria has profound implications for conservation in the country – not only in terms of public awareness of species conservation, but also as an indicator of wider environmental issues.

Original source:

Lazarova I, Petrov R, Andonova Y, Klisurov I, Dixon A (2021) Re-introduction of the Saker Falcon (Falco cherrug) in Bulgaria – preliminary results from the ongoing establishment phase by 2020. Biodiversity Data Journal 9: e63729. https://doi.org/10.3897/BDJ.9.e63729

Under Extinction Pressure: Rare Australian bee found after 100 years

A widespread field search for a rare Australian native bee (Pharohylaeus lactiferus) that had not been recorded for almost a century found the species has been there all along – but is probably under increasing pressure to survive. Prior to this study, only six individuals had been found, with the last published record of this Australian endemic bee species, from 1923 in Queensland.

Male Pharohylaeus lactiferus bee. Photo by James Dorey.

A widespread field search for a rare Australian native bee (Pharohylaeus lactiferus) that had not been recorded for almost a century found the species has been there all along – but is probably under increasing pressure to survive. Prior to this study, only six individuals had been found, with the last published record of this Australian endemic bee species, from 1923 in Queensland.

“This is concerning because it is the only Australian species in the Pharohylaeus genus and nothing was known of its biology,”

Flinders University researcher and biological sciences PhD candidate James Dorey says in the new scientific paper in the peer-reviewed, open-access Journal of Hymenoptera Research.

The ‘hunt’ began after bee experts Olivia Davies and Dr Tobias Smith raised the possibility of the species’ extinction based on the lack of any recent sightings. The ‘rediscovery’ followed an extensive sampling of 225 general and 20 targeted sampling sites across New South Wales and Queensland.

Along with extra bee and vegetation recordings from the Atlas of Living Australia, which lists 500 bee species in New South Wales and 657 in Queensland, the Flinders researchers sought to assess the latest levels of true diversity, warning that habitat loss and fragmentation of Australia’s rainforests, along with wildfires and climate change, are likely to put extinction pressure on this and other invertebrate species.  

“Three populations of P. lactiferous were found by sampling bees visiting their favoured plant species along much of the Australian east coast, suggesting population isolation,”

Mr Dorey reports.

Highly fragmented habitat and potential host specialisation might explain the rarity of P. lactiferus.

Additionally, the scientists remind of previous findings that Australia has already cleared more than 40% of its forests and woodlands since European colonisation, leaving much of the remainder fragmented and degraded.

“My geographical analyses used to explore habitat destruction in the Wet Tropics and Central Mackay Coast bioregions indicate susceptibility of Queensland rainforests and P. lactiferus populations to bushfires, particularly in the context of a fragmented landscape,”

Mr Dorey says.

The study also warns the species is even more vulnerable as they appear to favour specific floral specimens and were only found near tropical or sub-tropical rainforest – a single vegetation type.

“Collections indicate possible floral and habitat specialisation with specimens only visiting firewheel trees (Stenocarpus sinuatu), and Illawarra flame trees (Brachychiton acerifolius), to the exclusion of other available floral resources.”

Known populations of P. lactiferus remain rare and susceptible to habitat destruction (e.g. caused by changed land use or events such as fires), the paper concludes.

“Future research should aim to increase our understanding of the biology, ecology and population genetics of P. lactiferus.”

Female Pharohylaeus lactiferus bee. Photo by James Dorey.

“If we are to understand and protect these wonderful Australian species, we really need to increase biomonitoring and conservation efforts, along with funding for the museum curation and digitisation of their collections and other initiatives,”  

Mr Dorey says.

Research paper:

Dorey JB (2021) Missing for almost 100 years: the rare and potentially threatened bee, Pharohylaeus lactiferus (Hymenoptera, Colletidae). Journal of Hymenoptera Research 81: 165-180. https://doi.org/10.3897/jhr.81.59365

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Failure to respond to a coral disease epizootic in Florida: causes and consequences

By 2020, losses of corals have been observed throughout Florida and into the greater Caribbean basin in what turned out to be likely the most lethal recorded case of Stony Coral Tissue Loss Disease. A Perspectives paper, published in the open-access peer-reviewed journal Rethinking Ecology, provides an overview of how Florida ended up in a situation, where the best that could be done is rescuing genetic material from coral species at risk of regional extinction.

Guest blog post by William F. Precht

A colony of the large grooved brain coral, Colpophyllia natans, infected by Stony Coral Tissue Loss Disease. The photo shows the progressive, rapid advance of disease, left-to-right, across the colony.
Image by William Precht.

Dredging projects conducted in association with coral reefs typically generate concern by environmental groups, resulting in careful monitoring by government agencies. Even though the aim of those dredge projects is to widen or deepen existing ship channels, while minimizing damage to coral reef resources, there are often the intuitive negative assumptions that dredging kills corals.

The recent Port Miami Dredge Project started as an uncomplicated case story. However, significant problems arose, caused by a concurrent and unprecedented coral disease epidemic that killed large numbers of corals, which was initiated following a regional thermal anomaly and coral bleaching event.

The coral disease, known as Stony Coral Tissue Loss Disease (SCTLD), was first observed in September 2014 near Virginia Key, Florida. In roughly six years, the disease has spread throughout Florida and into the greater Caribbean basin. The high prevalence of SCTLD and the resulting high mortality in coral populations, coupled with the large number of susceptible species affected, suggest that this disease outbreak is one of the most lethal ever recorded on contemporary coral reefs. The disease is still presently active and continues to ravage coral reefs throughout the region.

The initial response to this catastrophic disease by resource managers with purview over the ecosystem in Southeast Florida was slow. There is generally a noticeably short window of opportunity to intervene in disease amelioration or eradication in the marine environment. This slow response enabled the disease to spread unchecked. Why was the response to the loss of our coral reefs to a coral disease epidemic such a massive failure? This includes our failure as scientists, regulators, resource managers, local media, and policy makers alike. With this Perspectives paper, published in Rethinking Ecology, my intention was to encapsulate the numerous reasons for our failures during the first few years of the outbreak, reminiscent of the early failures in the U.S. response to the COVID-19 pandemic.

First, the Port Miami dredging project was ongoing when the coral disease epidemic began. Some managers and local environmental groups blamed dredging, rather than SCTLD for the coral losses, reported in the project’s compliance monitoring program. Second, this blame was amplified in the media, because dredging projects are intuitively assumed to be bad for coral reefs. Third, during this same time, the State of Florida prohibited government employees from acknowledging global warming in their work. This was problematic because ocean warming is a proximal cause of many coral diseases.

As a result, some managers ignored the well-known links between warming and coral disease. A consequence of this policy was that the dredging project provided an easy target to blame for the coral mortality noted in the monitoring program, despite convincing data that suggested otherwise. 

Specifically, the intensive compliance monitoring program, conducted by trained scientific divers, was statistically significant. SCTLD that was killing massive numbers of corals throughout the region was also killing corals at the dredge site. Further, this was happening in the same proportions and among the same suite of species. 

Finally, when the agencies responded to the outbreak, their efforts were too little and much too late to make a meaningful difference. While eradication of the disease was never a possibility, early control measures may have slowed its spread, or allowed for the rescue of significant numbers of large colonies of iconic species. Because of the languid management response to this outbreak, we are now sadly faced with a situation where much of our management efforts are focused on the rescue of genetic material from coral species already at risk of regional extinction.

The delayed response to this SCTLD outbreak in Southeast Florida has many similarities to the COVID-19 pandemic response in the United States and there are lessons learned from both that will improve disease response outcomes in the future, to the benefit of coral reefs and human populations.

Publication:

Precht W (2021) Failure to respond to a coral disease epizootic in Florida: causes and consequences. Rethinking Ecology 6: 1-47. https://doi.org/10.3897/rethinkingecology.6.56285

Eurasian eagle owl diet reveals new records of threatened giant bush-crickets

Bird diets provide a real treasure for research into the distribution and conservation of their prey, conclude scientists after studying the Eurasian Eagle Owl in southeastern Bulgaria. In their paper, published in the open-access, peer-reviewed journal Travaux du Muséum National d’Histoire Naturelle “Grigore Antipa”, they report the frequent presence of the threatened Big-Bellied Glandular Bush-Cricket, and conclude that studies on the Eurasian Eagle Owl could be used to identify biodiversity-rich areas in need of protection.

Male specimen of the Big-Bellied Glandular Bush-Cricket (Bradyporus macrogaster)
Photo by Dragan Chobanov

Bird diets provide a real treasure for research into the distribution and conservation of their prey, such as overlooked and rare bush-cricket species, point out scientists after studying the diet of the Eurasian Eagle Owl (Bubo bubo) in southeastern Bulgaria.

In their paper, published in the open-access, peer-reviewed journal Travaux du Muséum National d’Histoire Naturelle “Grigore Antipa”, Dr Dragan Chobanov (Institute of Biodiversity and Ecosystem Research, Bulgaria) and Dr Boyan Milchev (University of Forestry, Bulgaria) report the frequent presence of the threatened with extinction Big-Bellied Glandular Bush-Cricket (Bradyporus macrogaster) in the diet of Eurasian Eagle Owls, and conclude that the predatory bird could be used to identify biodiversity-rich areas in need of protection.

While the Balkan Peninsula has already been recognised as the area with the highest diversity of orthopterans (grasshoppers, crickets and bush-crickets) in Europe and one of the generally most biologically diverse areas in the whole Palearctic realm, it is also home to a worrying number of threatened species. Additionally, a thorough and updated country assessment of the conservation status of the orthopterans found in Bulgaria is currently lacking. This is why the Bulgarian team undertook a study on the biodiversity of these insects by analysing food remains from pellets of Eurasian Eagle Owls, collected from 53 breeding sites in southeastern Bulgaria.

As a result, the scientists reported three species of bush crickets that have become a significant part of the diet of the studied predatory birds. Curiously enough, all three species are rare or threatened in Bulgaria. The case of the Big-Bellied Glandular Bush-Cricket is of special concern, as it is a species threatened by extinction. Meanwhile, the local decline in mammals and birds that weigh between 0.2 and 1.9 kg, which are in fact the preferred prey for the Eurasian Eagle Owl, has led the highly opportunistic predator to increasingly seek large insects for food. The researchers even suspect that there might be more overlooked species attracting the owls.

Taking into account the hereby reported interconnected inferences of conservation concern, as well as the vulnerability of the Big-Bellied Glandular Bush-Cricket, a species with a crucial role in the food chain, the scientists call for the newly provided data to prompt the designation of a new Natura 2000 site. Additionally, due to the species’ requirements for habitats of low disturbance and high vegetation diversity, and its large size and easy location via singing males, they point out that it makes a suitable indicator for habitat quality and species community health.

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Original source:

Chobanov D, Milchev B (2020) Orthopterans (Insecta: Orthoptera) of conservation value in the Eurasian Eagle Owl Bubo bubo food in Bulgaria. Travaux du Muséum National d’Histoire Naturelle “Grigore Antipa” 63(2): 161-167. https://doi.org/10.3897/travaux.63.e53867