Reptiles, amphibians and fire


The Sticky Tongue Project in Canada says about this video:

The Importance of Fire

Wildfires can be devastating to property and lives. But the fact is many of our native habitats are fire-dependent and will eventually burn sooner or later.

“The great outdoors is the foundation of all life on Earth, including yours.”

Episode 14 of a year-long 24 episode education-outreach video series starring Whit Gibbons (Herpetologist and Author), produced in cooperation with The Amphibian and Reptile Conservancy.

This series features “fascinating facts and helpful conservation tips” for everyone “from homeowners to professional land and wildlife managers.”

Save South African frogs


Pickersgill's reed frog

From SAPA news agency in South Africa:

South Africa: Endangered Frogs Get Luxury Suite At Pretoria Zoo

17 May 2013

Johannesburg — The Pretoria zoo is going to start a breeding programme with 10 critically endangered Pickersgill’s Reed Frogs to help save them from extinction, Beeld reported on Friday.

A special “frog room” had been equipped for the six-month project, the zoo’s reptile expert Mike Adams told the newspaper.

According to Beeld, the small, yellow-green frogs, are smaller than a man’s thumb and are endemic to South Africa, but are found in only 18 small habitats.

“Because they are so small, conservation has been difficult,” the newspaper quoted Adams as saying.

The Johannesburg Zoo had caught 40 of the frogs, of which 10 had been moved to Pretoria.

“No one knows at this point how to breed the frogs, so with these 10 we hope to write a breeding manual so that the programme can be replicated elsewhere,” Adams said.

Pretoria zoo spokeswoman Angeline Schwan told Beeld amphibians were among the most endangered species on earth.

“There are about 7000 species, of which 3900 are threatened and 170 are apparently already extinct,” she said.

World’s rarest mammals, amphibians on new map


From Wildlife Extra:

World’s rarest and most extraordinary species mapped for the first time

Sunda pangolin

Sunda pangolin occurs in Southeast Asia and is threatened by illegal poaching for its meat and for its scales – Used in traditional medicine. Courtesy of Carnivore and Pangolin Conservation Programme

EDGE species added to the map

May 2013. The black-and-white ruffed lemur, Mexican salamander and Sunda pangolin all feature on the first map of the world’s most unique and threatened mammals and amphibians, created by the Zoological Society of London(ZSL).

Scientists pinpointed areas of the world where Evolutionarily Distinct and Globally Endangered (EDGE) mammals and amphibians occur. Regions containing the highest concentrations of these species are highlighted as global conservation priorities.

Different regions for different groups
The map reveals that high priority conservation areas for mammals and amphibians are different, reflecting the varied evolutionary histories and threats facing the two groups. For mammals, management efforts are best focused in Southeast Asia, southern Africa and Madagascar. For amphibians, central and southern America are highlighted as priorities.

Very few protected areas
Professor Jonathan Baillie, ZSL’s Director of Conservation says: “The results of the mapping exercise are alarming. Currently only five percent of the areas we’ve identified as priorities for EDGE mammals and 15 percent of the EDGE amphibian areas are protected.

“These areas highlighted should all be global conservation priorities because they contain species that are not only highly threatened but also unique in the way they look, live and behave. These new maps will inform the development of larger-scale work to help secure the future of some of the most remarkable species on Earth,” Professor Baillie added.

The Mexican salamander, or axolotl, is critically endangered due to urbanization, polluted waters, and the introduction of non-native fish which eat the axolotl’s young. Scroll down to see the map of EDGE amphibians

The Mexican salamander, or axolotl, is critically endangered due to urbanization, polluted waters, and the introduction of non-native fish which eat the axolotl’s young. Scroll down to see the map of EDGE amphibians.

Black-and-white ruffed lemur & Sunda pangolin
Madagascar’s black-and-white ruffed lemur is the largest lemur in the world and is threatened by hunting and the loss of its forest habitat to logging, mining and cutting and burning for agriculture. The Sunda pangolin, also known as the scaly anteater, occurs in Southeast Asia and is threatened by illegal poaching for its meat which is a culinary delicacy, as well as its scales which are thought to have high medicinal value. Other mammal species occurring in priority areas include the black rhino and western lowland gorilla.

Amphibians
Amphibians are facing a terrifying rate of extinction making them the most threatened vertebrates in the world. The Mexican salamander, or axolotl, is critically endangered due to urbanization, polluted waters, and the introduction of non-native fish which eat the axolotl’s young. With the aid of the global map of EDGE amphibians, it will now be possible to concentrate efforts in countries such as, Mexico, Costa Rica and Guatemala where the most distinct and threatened species are found.

Dr. Kamran Safi, lead author of the paper from the Max Planck Institute for Ornithology says: “This is the first global map to take into account species’ uniqueness as well as threat. Now that we’ve identified EDGE priority areas for mammals and amphibians we can more effectively continue to ensure their protection.”

It is critical that conservationists prioritise the allocation of limited resources for the best conservation outcomes. ZSL’s EDGE of Existence programme has already launched targeted conservation projects for more than 40 EDGE species around the world.

The research paper is published in PLOS ONE.

Mammalian and amphibian EDGE zones

How animals learned to eat plants


Right lateral aspect of the skull of a juvenile specimen of Orobates pabsti. Credit: Dr Amy Henrici, Carnegie Museum, Pittsburgh; Photo permission: Dr Thomas Martens, Stiftung Schloss Friedenstein Gotha, Germany

From the University of Lincoln in England:

Land animals kept fish-like jaws for millions of years

09 May 2013 University of Lincoln

Research has confirmed how early land vertebrates, which evolved from fish, developed weight-bearing limbs and other adaptations long before their feeding systems adjusted to a vegetation-based diet.

Now, for the first time, fossil jaw measurements have demonstrated this gap in evolutionary development.

Scientists from the University of Lincoln (UK), the University of Massachusetts, Amherst, and the University of Oxford (UK), examined the lower jaws of 89 fossils of early tetrapods (four-footed animals) and their fish-like predecessors.

The fossils ranged in age from about 300 to 400 million years old and the team were interested in how the mechanical properties of the jaws of these animals differed through time.

They used 10 biomechanical metrics to describe jaw differences. One of these, called mechanical advantage, measured how much force an animal can transfer to its bite.

Dr Marcello Ruta, from the School of Life Sciences, University of Lincoln, said: “Our study is the first of its kind to address changes in biomechanical properties of the lower jaw across the transition from fish to land vertebrates using a diverse range of extinct species. This work paves the way to in-depth analyses of the rates of evolutionary transformation in other anatomical structures during this major episode in vertebrate history. It also lays the foundations for integrative research that explores themes as diverse as the origin of the first terrestrial food webs, the impact of acquisition of new structures on the diversification of major animal groups, and patterns and processes of functional change.”

So it turns out that just moving into a new environment is not always enough to trigger functional adaptations.

The team discovered that the mechanical properties of tetrapod jaws did not show significant changes in patterns of terrestrial feeding until some 40 to 80 million years after the four-legged creatures initially came out of the water. Until then, tetrapod jaws were still very fish-like, even though their owners had weight-bearing limbs and the ability to walk on land.

In the paper, which has been published in an early online edition of the journal Integrative and Comparative Biology, the authors say the results may be explained by an earlier hypothesis: a shift from gilled to lung breathing in later four-footed animals was necessary before they could adapt their jaw structure to eating plants.

This finding suggests tetrapods may have shown a limited variety of feeding strategies in the early phases of their evolution on land.

Lead author Dr Phil Anderson, from the University of Massachusetts, said: “The basic result was that it took a while for these animals to adapt their jaws for a land-based diet. They stayed essentially fish-like for a long time.”

Dr Matt Friedman, lecturer in palaeobiology at the University of Oxford, said: “The thing that is really interesting is that the diversity of jaw function didn’t really take off until around the origin of amniotes – creatures that lay hard-shelled eggs on land rather than being tied to water for reproduction like fishes and amphibians. It is in amniotes and their closest relatives that we see the first evidence for dedicated herbivory – until that point tetrapods had basically been carnivores. So this means it took at least 50 million years of evolution after the origin of features like limbs, fingers and toes before tetrapods achieved dietary diversity that began to resemble what we see today.”

The statistical methods developed in this work could be used in future studies of more subtle biomechanical patterns in fossil animals that may not be initially clear.

Helping amphibians, reptiles in your own backyard


This video from Canada says about itself:

Backyard Wildlife Tips

Here are few quick tips to help you conserve amphibian and reptile populations in your own backyard.

“The great outdoors is the foundation of all life on Earth, including yours.”

Episode 13 of a year-long 24 episode education-outreach video series starring Whit Gibbons (Herpetologist and Author), produced in cooperation with The Amphibian and Reptile Conservancy.

This series features “fascinating facts and helpful conservation tips” for everyone “from homeowners to professional land and wildlife managers.”

Linnet, mistle thrush and World War II


1 May 2013.

After yesterday, still in the Drents-Friese Wold.

Male brackcap, 1 May 2013

In the garden, a male blackcap.

First to the Doldersumse veld.

Linnet male, 1 May 2013

On the edge of heathland and forest, a male linnet.

Mistle thrush, 1 May 2013

A bit further, a mistle thrush, high up a tree.

On the Wapserveld, a brimstone butterfly.

Young edible frogs, just over a centimeter in size.

Common redstart, 1 May 2013

A common redstart male in a tree. See on the migration of this species here.

A speckled wood butterfly.

Not far away, in Berkenheuvel nature reserve, is the Onderduikershol.

Here, in 1943, local anti-nazis built a secret hiding place in a sandy hill. Here, people persecuted by the nazi occupiers, and British and US American pilots whose planes had been downed, hid.

In November 1944, the German SS and Wehrmacht discovered the hiding place. They arrested eleven people and sent them to concentration camps. Like with Anne Frank‘s family, only one person of those eleven prisoners survived those camps.

In front of the Onderduikershol, fresh flowers put there by schoolchildren.

Near a lake at Oude Willem, a white stork.

Tufted ducks and mallards swimming.

Coelacanth DNA and tetrapod evolution


This video says about itself:

DNA From Fish May Explain How Feet Evolved From Fins

18 April 2013

Decoding the coelacanth fish genome has put scientists closer to reconstructing how animal ancestors crawled out of the sea 400 million years ago.

By Philip Guelpa:

Genome sequencing of “living fossil” fish sheds light on the evolution of land animals

30 April 2013

In a newly published article in the scientific journal Nature (496, 311–316), scientists report a significant step in the understanding of the evolutionary process that led certain ancient fish to develop limbs and emerge onto dry land, becoming the ancestors of all amphibians, reptiles, birds, and mammals. This transition is one of the most important in the development of life on earth.

The new research is based on the decoding of the genome of a so-called “living fossil” fish, the “coelacanth” (pronounced SEE-luh-canth). This group of fishes, known from fossils dating as far back as 400 million years ago, was long thought to have gone extinct 70 million years ago, in the Late Cretaceous Era. However, the discovery of a living specimen in the West Indian Ocean off of South Africa in 1938 demonstrated that a reclusive population still survived. More recently, a second species of living coelacanth, both belonging to the genus Latimeria, was discovered in Indonesia.

Coelacanths have been colloquially known as living fossils because of their close resemblance, at least outwardly, to fossil specimens dating back tens and even hundreds of millions of years. But perhaps the most interesting aspect of these fish is their apparent close evolutionary relationship to the first land vertebrates.

It has long been thought, based on paleontological and anatomical evidence, that all tetrapods (four-limbed, vertebrate animals—amphibians, reptiles, birds, and mammals) evolved, somewhere in the neighborhood of 400 million years ago, from fish closely resembling the now mostly extinct group of lobe-finned fish belonging to the class Sarcopterygia.

Lobe-finned fish have a well-developed bony skeleton inside their fins, in contrast to the common ray-finned (teleost) fish. Living representatives of this lineage include lungfish, which are actually able to breathe air with lungs that are homologous (have the same genetic origin) as those of tetrapods, and the coelacanth.

Basic anatomical similarities between the skeletal structures in the fins of lobe-finned fish and the limbs of tetrapods strongly suggested an evolutionary link. However, the details of the mechanism for the transformation of fins into limbs had yet to be understood. The newly reported research begins to fill in that gap.

The technique of DNA sequencing, which in recent years has permitted the decoding of the human genome and those of a growing number of other species, has now been used to document the coelacanth’s DNA sequence. Among the resulting discoveries is a genetic mechanism that controls the growth of both the lobe-shaped fins in the coelacanth and of limbs in tetrapods.

Scientists have long wondered whether lungfish or coelacanths were more closely related to tetrapods. In other words, which group is closer to the common ancestor of the earliest vertebrate animals to walk on land? Genetic sequencing holds the potential to answer such questions. Unfortunately, lungfish have an incredibly large genome, which cannot be effectively sequenced by existing methods. It should be noted that the size of a species’ genome has no necessary correlation with the complexity of the organism, due to duplications of DNA sequences and other “baggage” accumulated during the course of evolution, which is not a particularly neat process.

Despite this, the scientific team whose research was published in Nature was able to decode segments of the lungfish genome and compare it to their newly completed full coelacanth sequence as well as to those from a sample of tetrapods. This permitted the conclusion that lungfish are more closely related to tetrapods than are coelacanths. Nevertheless, since the two groups of lobe-finned fish are closely related to each other, knowledge of the coelacanth genome is revealing much regarding the evolution of the first land-dwelling vertebrates.

The first and highly necessary step for the investigators was to determine whether the living coelacanth had evolved only very slowly from its ancestors millions of years ago, as suggested by its ancient outward appearance. This was critically important because the relevance of further analysis would depend on whether the genetic patterns observed in the modern coelacanth could be expected to resemble those of the common ancestor of lobe-finned fish and tetrapods.

The results of this analysis indicate that coelacanths have evolved very slowly as opposed to a number of other species to which they were compared. Many factors influence the rate of evolution in any given lineage of organisms. Evolution is a dialectical interaction between a species and all the elements of its environment. A stable environment means that there is little selective pressure that would prompt adaptive changes. The relatively static environment in which the surviving coelacanths live, and a lack of predators, are likely to have been factors in their slow evolution.

With that understanding, the researchers focused on studying genes that control the expression of structural genes (i.e., genes that build body parts). Such control genes regulate such factors as the degree, rate, and timing of expression of the structural genes.

Among the categories of regulatory genes identified as being newly evolved in tetrapods (that did not exist in the ancestral lobe-finned fish) were ones associated with sensing of chemicals, through taste and smell, driven by the need to more fully perceive the complex terrestrial environment.

Other categories of new control genes include those related to radial pattern formation (body form), hind limb development, kidney development, and the immune system. Again, all of these would have been important in evolutionary adaptation to the new constraints and opportunities of terrestrial existence.

In all, the team identified over 44,000 control genes that evolved after the appearance of tetrapods.

The researchers paid particular attention to the genetic control of the development of hands and feet by comparing genes of teleost (ray-finned) fishes, coelacanths, and tetrapods. They found a specific gene sequence that is common to the latter two, but not found in the former. This sequence was identified as affecting limb development. Experimental insertion of the coelacanth genes into mouse embryos demonstrated that they could provide much of the regulation needed to produce tetrapod limbs, thus demonstrating that this gene complex existed in lobe-finned fishes and was repurposed in the evolution of land animals.

Also identified was a gene in coelacanths that appears later to have become important in the development of the mammalian placenta. Coelacanths give birth to live young which develop inside the mother’s body, but don’t receive direct nourishment from the mother during gestation, as is the case with placental mammals.

The research reported by this team demonstrates the great power and potential of genetic sequencing in helping to elucidate the patterns and mechanisms of biological evolution, complimenting evidence from the fossil record. In a broader sense, this work shows that biological evolution is a process that can be objectively studied and understood as part of the development of the material world.

Toads mating season, video


This video shows a female Eurasian toad with six males during the mating season.

The video was recorded on 14 April 2013 by Dick Schinkel from the Netherlands.

International conservation award winners announced


This video says about herself:

In 2012 a team of young conservationists from Kenya were awarded a CLP Future Conservationist Award to carry out scientific research on blue and black marlins and raise awareness of their plight. Team leader, Nelly Kadagi, recently attended the CLP’s international training course and tells about her experience in the Canadian Rockies.

From BirdLife:

2013 Conservation Leadership Programme awards winners announced!

Wed, Apr 10, 2013

The Conservation Leadership Programme (CLP) has announced this year’s 28 award-winning projects in 22 different countries, worth a total of $470,000.

“For many awardees, this is the first time that they have received funding to manage their own conservation projects so it’s a great boost in their careers. This year, for the first time, we’ll be supporting people in Afghanistan, Bhutan, Cape Verde, Moldova and Samoa to carry out their work,” said Kiragu Mwangi, BirdLife’s CLP Programme Manager.

This year’s projects are extremely diverse from Food Resource Evaluation in Chinese Snow Leopards to Saving the Endangered Giant West African Squeaker Frog in Ghana. One of the bird projects focuses on the little-known Tooth-billed Pigeon from Samoa, also known as the ‘little dodo’ due to its resemblance to its famous namesake.

However, one thing is the same for all projects. The chance to get access to conservation expertise and receive training.

All award-winning team members will become part of the CLP alumni network that supports approximately 3,500 conservation leaders. The network offers an opportunity for alumni to share and learn from each other as they deliver conservation outcomes in often challenging and isolated environments.

“Through this programme, we are building the capabilities of future conservation leaders and providing them with knowledge, skills and experience to address the most pressing conservation issues of our time”, said Kiragu.

Alumni members also receive access to additional grants, mentoring from CLP staff and training. A representative from each award-winning team will take part in CLP’s two-week Conservation Leadership & Management Training Workshop in June 2013 at a remote ecological research station in the foothills of the Canadian Rockies.

Eight of the 2013 project teams working on diverse threatened species of birds, plants and sharks will be mentored by BirdLife partners in Argentina, Bolivia, Cambodia, Kazakhstan, Moldova, Nepal, Paraguay and Zimbabwe.

The CLP has supported 530 projects since the programme’s inception in 1985.

The CLP is a partnership of BirdLife International, Conservation International, the Wildlife Conservation Society and Fauna & Flora International.

Full list

Future Conservationist Awards (up to $15,000)

Wildlife Survey in a Proposed Protected Area in Afghanistan
Saving the Endangered Marsupial Frogs in Yungas Forests of Argentina
Involving Anglers As Key Stakeholders in a Shark Conservation Programme, Argentina
Conserving Endangered Frog Species in Somuncura Plateau, Argentina.
Ecological and Distribution Assessment of Hicatee in Southern Belize
Hornbills: Connecting Environment, Economy and Culture in Bhutan
Conserving Quirusillas Reserve: a Key Area for the Alder Amazon, Bolivia
Conservation of the Critically Endangered Bolivian Frog Psychrophrynella illimani
Conservational Ecology of Giant Ibis in Western Siem Pang Iba, Cambodia
Integrative Conservation of the Terras Salgadas, Cape Verde
Migration Corridor and Habitat Survey in Xia’Erxili, China
Food Resource Evaluation for Snow Leopards, China
Participatory Conservation of the Critically Endangered Ecuadorian Brown-Headed Spider Monkey, Ecuador
Saving the Endangered Giant West African Squeaker Frog, Ghana
Monitoring Key Sites for White-Headed Duck in Kazakhstan
Initiating Conservation of New Hog Deer Population, Myanmar
Enhancing Community-Based Vulture Conservation in Western Lowland of Nepal
Ecology and Conservation of Ganges River Dolphin in Karnali Nepal
Reforestation with Native Species in the Dry Lands of Panama
Population Status Assessment and Conservation Measures of Butia marmorii Palm, Paraguay
Monitoring Important Bird Areas in Moldova to Improve Conservation Management
European Ground Squirrel Population from Eastern Romania
The Samoan “Dodo”: Saving the Manumea
Community-Based Conservation of Sea Turtles on Kolombangara, Solomon Islands

Follow-up Awards ($25,000)

Conservation of the Critically Endangered Togo Slippery Frog in Ghana
On-going Protection of Red Siskins in South Rupununi, Guyana
Scaling-up Mitigation of Human-Crane Conflict in Driefontein Grasslands, Zimbabwe

Leadership Awards ($50,000)

Improving the Community-Based Conservation of Lake Kuyucuk Ramsar Site, Turkey