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Spreading Frogtopia: Matt Turpin

September 3, 2020 by admin

Froglife follower and pond-enthusiast, Matt Turpin has been busy building and restoring his neighbours ponds in Nottingham whilst he has been on furlough. Learn more about why he was inspired to do so by his article below!

I was furloughed from my job with an educational charity in June. While I was happy to devote most of the free time I now had to looking after my three year old son, I felt a real need to do something, anything to make the world a better place. It didn’t take long to figure out what that was.

When I moved into a new house a year ago, one of the first things I did – before I’d unfinished unpacking everything – was to get into the back garden and dig a wildlife pond. I’ve been digging ponds since childhood, when my gran I would have varying degrees of success creating frog-friendly habitats for her garden. I would sit by the completed pond for hours once it was finished, taking a sense of peace and serenity from being near water that I still find. Sitting by water, and seeing life beneath the surface – the amphibians, the invertebrates, the tiny, barely-visible tiny creatures – and above the surface – the visiting dragonflies, bees, hoverflies and, if lucky to be out at dusk, bats – was, and has remained one of my favourite ways to relax.

Put water in a garden, and life will proliferate: it’s that simple. I had seen the benefits in my own garden; why not spread that elsewhere? After all, the weather was nice, the gyms were closed and a promising summer lay ahead. It was time to grab some tools, visit some gardens and break some ground. I put out a call over the internet that I would only charge for materials and minor expenses – enough to cover what I lost through furlough, at most – and the offers began to arrive into my inbox.

Some people wanted a pond from scratch, and we’d carefully work out the best place: away from trees and their subterranean roots; plenty of sunlight; near foliage to shade and hide creatures. Often, gardens are full of what seems like rubbish: old rocks, slabs, roof tiles, bricks, remnants from long-completed garden projects. I’d incorporate these into the design, creating caves, banks and other features that would provide the best possible habitat for a range of species. Every pond would have a ‘beach’ – a gently sloping area of shingle that would allow easy entry and exit from the pond -as well as providing a handy area for garden mammals to drink from.

Other clients would want an old  long neglected pond rescuing and transformed into a nature pond. The reeds, sedges and grasses that had run riot in these places would be cut back, replanted and passed onto the new ponds to give them a vegetative kick. I’d spend days thigh- deep in mud, turning an ugly, sterile area into a thriving wildlife sanctuary. It was hugely satisfying, even if my knees were never truly clean during the whole Summer.

After finishing each job, i’d ask the client to keep in touch: partly because I could monitor any issues that arose, partly because I could therefore share any foliage or tips with a growing network of local wildlife pond owners, but mainly because I wanted to find out what happened to the garden once I’d gone.

“Went out this afternoon: never seen so many birds visit, all drinking from the pond. Then this evening three frogs!” said one client, who I’d built a large, rockery lined pond for. “How could we already have newts??” queried another. A swell of pride accompanied these messages: in some tiny way I’d given wildlife a hand, and sported a decent tan too.

Yet the greatest seal of approval came recently, with a pond rescue. After turning a drained and leaf-bound old pond back into a haven for life, I revisited to see how it was a week after the build. 

As I sat by the pond, assessing water levels, seeing if the water buttercups I’d potted and positioned would be better elsewhere, I felt that curious feeling you get when you are being looked at. I glanced to my side, and there, sitting on a rock overhanging the water, was an adult frog, surveying her domain. She seemed oblivious to me, rather she seemed to be joining me in appreciation. We both sat there for a good ten minutes, before I decided I better head off to my next job,  and she decided to go check out a little more of her new home. It felt remarkably satisfying. Next spring, once the ground softens and warms, I’ll be out there again, creating frogtopias across my town.

If you feel inspired to make your own wildlife pond, feel free to download our FREE Just Add Water guide.

Filed Under: Uncategorized Tagged With: lockdown, newts, plants, ponds, wildlife corridor

Croaking Science: Newts that never grow up!

November 21, 2017 by editor

Newts that never grow up – paedomorphosis in salamanders

The majority of pond-breeding salamanders have a biphasic metamorphic life cycle where free-swimming larvae living in ponds and other water bodies metamorphose into terrestrial living adults. The advantage of this life history is that it allows adults to exploit different habitats to larvae, utilise a wider range of ecological niches and escape from potentially hostile environments e.g. a desiccating pond. However, a number of salamander species within Europe and North America have evolved a unique life history where free-swimming larvae to do not metamorphose into terrestrial living adults, but remain within the water and retain larval characteristics. Known as paedomorphosis these individuals develop into sexually reproductive adults but retain larval traits e.g. free-swimming larval form (Figure 1). It appears that the phenomenon of paedomorphosis has evolved several times within salamanders and has been of great interest to biologists for centuries. One theory suggests that paedomorphosis is most likely to evolve when environmental conditions experienced by adults are inhospitable relative to conditions experienced by larvae. For example, if water bodies remain constant throughout the year but temperature regimes and environmental factors on the land are hostile, such as in mountainous regions, arid landscapes or nutrient poor regions, it may be more favourable to remain in the larval form. Within southern Europe, paedomorphic populations often occur in deep, permanent and cool alpine lakes, where the terrestrial habitat has poor nutrient availability (Denoël et al., 2005). In an attempt to resolve many questions relating to the evolution of paedomorphosis in salamanders Bonnett et al. (2014) examined DNA sequences of a sub-family of plethodontid salamanders from North America. The authors concluded that within this group, paedomorphosis is more likely to occur in species dwelling in caves and those occurring in more arid climates. Here there are more resources in water bodies than in terrestrial habitats. An interesting finding of this study is that paedomorphosis has evolved and re-evolved serval times in the same species. The Valdina Farms Salamander (Eurycea troglodytes), from the western Edward Plateau, Texas, existed in a paedomorphic form 22 million years ago, before evolving into a metamorphic form (i.e. larvae metamorphosed into terrestrial adults). Subsequently, several million years later, it re-evolved back into a paedomorphic form (Bonnett et al., 2014). This is likely to be due to changing environmental conditions over this time period. However, there is a cost to being paedomorphic. Bonnett et al. (2014) found that paedomorphic spelerpine plethodontids from eastern North America have significantly smaller geographic range sizes than metamorphosing species and have not dispersed between biogeographic regions.  This has resulted in these species being more at risk from environmental events or human disturbance than species with wider geographic ranges and as a result have a higher rate of extinction.

Figure 1: Cave salamanders such as the Mexican axolotl (Ambystoma mexicanum) exist in paedomorphic forms due to hostile terrestrial habitats. Note the retention of gills which is normally a characteristic of larvae.

In some populations of salamanders, individuals exhibit facultative paedomorphosis, i.e. when both metamorphic and paedomorphic forms coexist and the occurrence of the latter within a given population depends on the advantages of living in the aquatic and terrestrial habitats. Whether an individual is metamorphic or paedomorphic may depend on a range of environmental factors including temperature, pond desiccation rate, terrestrial aridity and resource availability. Facultative paedomorphosis is an adaptive strategy which has been reported from several European newts. For example, great crested newt (Triturus cristatus), palmate newt (Lissotriton helveticus), alpine newt (Ichthyosaura alpestris) and southern banded newt (Omatotriton vittatus) all exhibit paedomorphosis, especially in the south of their range (Oromi et al., 2014). Facultative paedomorphosis has been regularly observed in populations of the smooth newt (L. vulgaris), particularly those in southern and eastern Europe (Figure 2). In this species, the key environmental factors are prey and predator abundance and habitat composition, with paedomorphosis generally occurring in areas with permanent, nutrient-rich water bodies without predators (Bozkurt et al., 2015). When fish are introduced to water bodies, paedomorphosis generally disappears since the aquatic environment becomes a less favourable habitat (Denoël et al., 2005).

Figure 2: Facultative paedomorphosis in the smooth newt (Lissotriton vulgaris) is most common in southern parts of its range. However, it can occur anywhere, such as in this individual from eastern England. Photo © Liz Morrison.

In 2017, Mathiron et al. (2017) tested theories in relation to how climatic factors impact on paedomorphosis in facultative populations of the palmate newt (L. helveticus) living in the Department of Hérault, France. The authors found that temperature and water availability each play a significant role in metamorphosis and explain the persistence of paedomorphosis in certain populations. These results have major implications as they show that droughts through evolutionary history have been a primary factor in promoting the evolution of paedomorphosis in this species. When terrestrial environments experience persistent drought, this has promoted the evolution of paedomorphic populations. This has significance in relation to a warming climate where the occurrence of severe droughts in Mediterranean parts of this species’ range, may result in an increase in paedomorphic populations in the near future. Mathiron et al. (2017) also found a sex-biased effect highlighting the role of sex in the metamorphosis of paedomorphs. Both water level and temperature affected the metamorphosis of males more than females. More metamorphic males occurred than females and, in drying conditions, started metamorphosis earlier than did females, which resulted in a female biased sex-ratio of paedomorphs. The reason why males metamorphose more than do females may be due to differences in levels of hormones in males compared to females. Also, males tend to disperse more than females so being metamorphic and turning into terrestrial adults would allow them to seek new water bodies and promote gene flow between populations.

 

References

Bonnett, R.M., Steffen, M.A., Lambert, S.M., Wiens, J.J. & Chippindale, P.T. (2014) Evolution of paedomorphosis in plethodontid salamanders: ecological correlates and re-evolution of metamorphosis. Evolution 68 (2): 466–482.

Bozkurt, E., Olgun, K. & Wielstra, B. (2015) First record of facultative paedomorphism in the Kosswig’s newt Lissotriton (vulgaris) kosswigi (Freytag, 1955) (Urodela; Salamandridae), endemic to northwestern Turkey. Turkish Journal of Zoology, 39: 976-980.

Denoël, M., Joly, P. & Whiteman, H.H. (2005) Evolutionary ecology of facultative paedomorphosis in newts and salamanders. Biological Reviews, 80: 663–671.

Mathiron, A.G.E., Lena, J., Baouch, S. & Denoël, M. (2017) The ‘male escape hypothesis’: sex-biased metamorphosis in response to climatic drivers in a facultatively paedomorphic amphibian. Proceedings of the Royal Society B: Biological Sciences, 284 (1853):

DOI: 10.1098/rspb.2017.0176.

Oromi, N., Amat, F., Sanuy, D. & Carranza, S. (2014) Life history trait differences between a lake and a stream-dwelling population of the Pyrenean brook newt (Calotriton asper). Amphibia-Reptilia, DOI:10.1163/15685381-00002921.

Filed Under: Uncategorized Tagged With: Croaking Science, Croaks, metamorphosis, newts, paedomorphosis, salamanders

Croaking Science: Courtship & Reproductive Behaviour in Newts and Salamanders

March 27, 2017 by editor

Courtship and reproductive behaviour in newts and salamanders

Courtship behaviour in newts and salamanders is very different to that of frogs and toads (anurans). In anurans, fertilisation is external so the male expels his sperm whilst the female lays her eggs. However, in newts and salamanders, fertilisation is internal. The male deposits a sperm package, the spermatophore, and the female uptakes this into her reproductive tract to fertilize her eggs. Male newts and salamanders have evolved a range of complex behaviours to encourage the female to uptake the spermatophore. This may involve contact between the male and female, but in aquatic newts of the family Salamandridae, there is no contact and the male encourages the female through complex courtship displays.

male showing belly Matt Wilson spring11
Great Crested Newt ©Matt Wilson

Newts in the genera Triturus (e.g. great crested newt) and Lissotriton (e.g. smooth newt), have similar courtship displays. During an initial orientation phase, the male will move in front of a female and attempt to gain her attention. The female may show no interest and swim away. If successful, the male moves into a static display which involves intense tail fanning and wafting pheromones towards the female. Once the female is fully engaged the male will start to retreat backwards facing the female, still tail fanning. He will then turn around, creeping away from the female with his tail quivering and her following. The male will pause, deposit his spermatophore onto the substrate, walk one body length forward and stop, turning 90 degrees. This allows the female to move so that her cloaca is directly over the spermatophore. She now uptakes the spermatophore for successful fertilisation. Unfortunately, spermatophore uptake by the female will not always be successful so the male has to perform the courtship display from the beginning.

Although males will develop secondary sexual characters during the spring (e.g. tail crest, webbing on the feet), the courtship display takes place in underwater in darkness, so visual cues are likely to be irrelevant. Recent research has shown that the courtship pheromones produced by the male are crucial in ensuring mating success. When a male employs tail fanning, he sends sex-specific pheromones towards the female and these directly impact her responses. In the laboratory, female palmate newts (Lissotriton helveticus) exhibit all the sexual responses up until spermatophore uptake, when in the presence of male pheromones, but no male present. This demonstrates the importance of pheromone production and effective transfer to the female during mating. Previous research has demonstrated that male newts which perform their displays more energetically, have higher mating success. In addition, in male smooth newts (L. vulgaris), males with higher body mass and crest height achieve higher mating success, possibly due to enhanced pheromone production and more effective transfer to the female. This research demonstrates the importance of effective transfer of pheromones by the male towards the female for reproduction.

Healthy smooth newt ©Mike Toms
Smooth newt ©Mike Toms

Male pheromones may have additional effects on females. In the aquatic Spanish ribbed newt (Pleurodeles waltlm), which has both contact and non-contact displays, the male has special glands in the cloaca. When these are released they induce the female’s cloaca to expand and uptake the spermatophore. It has previously been thought that the female doesn’t have a choice over whether she receives the spermatophore from a particular male, once he has clasped her and released his pheromones. However, recent research has demonstrated that females of this species may exhibit thanatosis (feigning death) during courtship prior to the crucial moment of pheromone production by the male. This avoids spermatophore uptake by the female and therefore may provide an escape strategy by a female, should she not want to be persuaded by the male to mate. Thanatosis has previously only been known as an escape strategy by amphibians and has not been observed in a sexual context.

Male newts and salamanders exhibit a range of complex sexual displays. Although many of the behaviours exhibited are widely understood, there are still areas where we have less understanding, such as the effects of pheromones, importance of secondary sexual characters and female choice in mate selection.

 

References

Halliday, T. R. (1974) Sexual behaviour of the smooth newt, Triturus vulgaris (Urodela, Salamandridae). Journal of Herpetology, 8 (4): 277-292.

Green, A. J. (1991) Large male crests – an honest indicator of condition, are preferred by smooth newts, Triturus vulgaris (Salamandridae) at the spermatophore transfer stage. Animal Behaviour, 41 (2): 367-369.

Janssenswillen, S. & Bossuyt, F. (2016) Male courtship pheromones induce cloacal gaping in female newts (Salamandridae). Plos One: DOI:10.1371/journal.pone.0144985.

Teyssedre, C. & Halliday, T. (1986) Cumulative effects of male’s displays in the sexual behaviour of the smooth newt, Triturus vulgaris vulgaris (Urodela, Salamandridae). Ethology, 71: 89-102.

Treer, D., Bocxlaer, I.V., Matthijs, S., Four, D. D., Janssenswillen, S., Willaert, B. & Bossuyt, F. (2013) Love is blind: indiscriminate female mating responses to male courtship pheromones in newts (Salamandridae). Plos One, 8 (2): e56538.

Filed Under: Uncategorized Tagged With: Amphibians, courtship, Croaking Science, newts

Are Crassula helmsii Invasions Impacting Our Native Newts?

August 13, 2014 by admin

Croaking science is a new way for student volunteers and scientist to explore what’s occurring in the world of Science. Croaking Science looks at science facts, new research or old debates which are inspired by or affect amphibians and reptiles, and then communicates this in layman’s language to a wider audience. The aim of the feature is to provide a platform for those starting their foray into the world of science communications as well as established scientists. We welcome any submissions from students and scientists. Please note that the views expressed in the articles are not those of the Froglife Trust.

Becky Trippier our Croaking Science reporter, looks at the impact of Crassula helmsii on our native UK newts.

Ashley Basil
Figure 1 – Photo by Ashley Basil

Whilst carrying out some fieldwork I stumbled across a pond where the water’s surface was completely covered in this small thin-leaved plant and thought How am I going to survey this?! I waded through the blanket of plants and attempted to sweep my net through the dense material to take an invertebrate sample, before taking a small piece of the plant home with me to identify later. When searching through my copy of Francis Rose I was horrified to realise it was Crassula helmsii, the deadly and invasive ‘Pond-killing Plant’.

Crassula helmsii, also known as the New Zealand Pigmyweed or Australian Swamp Stonecrop is an aggressively invasive plant,having been present in the UK since 1911 (CAPM: CEH, 2004). The species is one of the biggest threats to ponds in the UK, completely blanketing the surface once established and dominating any available space. It is a pond owner’s nightmare, outcompeting native aquatic plants forming dense mats, shading the underwater environment and depleting the water’s oxygen supply (CAPM: CEH, 2004). The loss of native plants and dissolved-oxygen has been found to have detrimental impacts upon zooplankton and macro-invertebrates, causing knock-on trophic effects such as reducing fish populations (De Vries et al. 2012). The impact the species may be having upon the UK’s amphibians is still fairly unknown with studies suggesting contrasting views.

Figure 2: Shuker et al. 2014
Figure 2: Shuker et al. 2014

A study by Will Watson (1999) looked at the species’ impact upon wetland ecology in the UK finding reductions in the breeding success of the Great-crested newt, Triturus cristatus, which is a highly-protected priority species under the UK BAP and Wildlife and Countryside Act 1981. He also noticed large reductions in float grass and lesser spearwort, emergent plants which are regularly used by the newts for laying their eggs. The populations of palmate or smooth newt present at the pond however, he found to be unaffected, although suggested that the rapid plant growth and silt accumulation may impact upon these species with further Crassula helmsii expansion.

In contrast to this, a more recent study by Langdon et al. (2004) found that the development of Great-crested newts were unaffected by the presence of the invasive species. However, smooth newt eggs were found to hatch at a later development stage when the species was present, which may have detrimental effects on their subsequent development as adults. The most significant findings of the study were that six of the plant species they identified as being important egg-laying plants for newts failed to germinate in the presence of Crassula helmsii.

Although the direct impacts of the plant upon newts are unclear, the indirect effects it is having upon the environmental conditions within ponds and upon native flora do pose several threats to newt species. So what can be done? Well once Crassula helmsii is in a pond, it is very difficult to get it out again. Even the smallest fragments of the plant can grow back, further spreading its presence. Advice for the best chemical treatments are suggested by the Centre for Aquatic Plant Management (CAPM: CEH, 2004) at: http://www.ceh.ac.uk/sci_programmes/documents/australianswampstonecrop.pdf.

However the best way to manage its spread across the UK is by preventing its movement by:

  • Making sure you know what it looks like, especially so you don’t pick it up and bring it home with you!
  • Properly cleaning and drying all equipment, wellies, and clothing which has been in contact with a pond containing Crassula helmsii.
  • Raising awareness of the detrimental impacts the species can have and why people shouldn’t introduce it into their pond.

Ironically it was previously sold as an ornamental “oxygenator” pond plant, however its effects have now been realised and its sale in the UK has now been banned as part of new DEFRA legislation being enforced April this year (Berwick 2009, NNSS 2014).

References:

Berwick, H. (2009). Crassula helmsii at Lound Lakes Management Options. Broads Authority – The broads, a member of the National Park family. Essex and Suffolk Water.

De Vries, W., Rannap, R. and Briggs, L. 2012. Guidelines for eradication of invasive alien aquatic species. Project report: “Securing Leucorrhinia pectoralis and Pelobates fuscus in the northern distribution area in Estonia and Denmark”. LIFE08NAT/EE/000257.

CAPM: CEH, 2004. Information Sheet 11: Australian Swamp Stonecrop, Available from: http://www.ceh.ac.uk/sci_programmes/documents/australianswampstonecrop.pdf [Accessed 29/05/14].

NNSS 2013. Sale of invasive water plants banned to protect wildlife. Available from: http://www.nonnativespecies.org//news/index.cfm?id=107 [Accessed 29/05/14].

Langdon, S.J., Marrs, R.H., Hosie, C.A., McAllister, H.A., Norris, K.M. & Potter, J.A. 2004. Crassula helmsii in U.K. Ponds: Effects on Plant Biodiversity and Implications for Newt Conservation. Weed Technology 18, pp 1349-1352.

Shuker, L., Gurnell, A. & Cockel, C. 2014. Adult New Zealand (Crassula helmsii). Available from: http://beta.urbanriversurvey.org/?attachment_id=91 [Accessed 29/05/14].

Watson, W. 1999. Amphibians & Crassula helmsii. Froglog 31. Available from: http://www.amphibians.org/wp-content/uploads/2012/05/Froglog31.pdf [Accessed 29/05/14].

Filed Under: Uncategorized Tagged With: Australian Swamp Stonecrop, Crassula, Crassula helmsii, Croaking Science, New Zealand Pigmyweed, newts

Last chance: Share your frog thoughts & enter our prize draw

March 5, 2014 by admin

Froglife’s national survey about perceptions of amphibians and reptiles is coming to an end on the 14th of March.  We are asking people what they think about snakes, newts, frogs, lizards and toads as part of a project supported by the Heritage Lottery Fund to investigate how the animals are viewed.  We would love to know your thoughts about wildlife and charity, and you can find the online survey here.

Questions include your favourite animals and thoughts about wildlife conservation, your opinions on amphibians and reptiles, a bit of an ID quiz as well as about the charitable causes closest to your heart.

We’re not looking for right or wrong answers; we’re really interested in honest responses to help us get a better understanding of the challenges we face when talking about our work.  You can find out more about the aims of The Scale of the Problem project here.

Through taking part, you can also enter a prize draw to win over £50 worth of goodies from the Froglife online shop, with a prize for over 18s and under 18s who take part.

Under 18s prize
The prize for under 18s includes a cuddly frog, pond dipping kit and frog back pack from the online shop

The results so far have been really interesting, with Hedgehogs the most popular answer to the favourite animal question. 95% of the respondents so far have seen a frog in the wild in the UK, compared to 64% having seen a snake.  We are also hearing, perhaps unsurprisingly, that many people are affected by  financial concerns when choosing to support charities, and have cut back donations.  All of the information we gather through the survey will be analysed by marketing experts Emerald Frog to help us strengthen our fundraising and campaigning techniques, enabling us to better support amphibians and reptiles into the future.

It would be wonderful if you could take the time to share your thoughts and experiences before the 14th of March, to help shape the future of Froglife’s communications and campaigns. Thank you!

You can find the online survey here

You can read more about the Scale of the Problem project here 

 

Filed Under: Uncategorized Tagged With: competition, consultation, Emerald Frog, favourite animal, feedback, frogs, HLF, lizards, newts, prize draw, quiz, Snakes, survey, toads, win

Croaking Science: Gymnophiona – The Third Amphibian Order

January 8, 2014 by admin

Croaking science is a new way for student volunteers and scientist to explore what’s occurring in the world of Science – science facts, new research or old debates which are inspired by or affect amphibians and reptiles, and then communicate this to a wider audience in their own words. The aim of the feature is to provide a platform for those starting their foray into the world of science communications as well as established scientists. We welcome any submissions from students and scientists. Please note that the views expressed in the articles are not those of the Froglife Trust.

Find out about this hidden order of amphibians from our Croaking Science Volunteer Hannah Graves. 

There are three groups of animals within the amphibians, known as “orders”. We’ve all heard of frogs and toads, the Anura, and salamanders and newts, the Caudata, but what about the third group? These are caecilians, the Gymnophiona, a group which contains just 3% of the amphibian species (1).

Caecilians can be found across most of the tropics except Madagascar and Australia (2). The majority of caecilians are fossorial, meaning they live underground. This type of lifestyle gives caecilians many of their defining characters. They have elongated, limbless bodies, and many are also tailless, allowing them to move through the soil more easily. The skulls are highly ossified, also to aid burrowing. The eyes are covered by skin or bone so they can only sense light or dark, but more refined sight isn’t needed for a life underground (2).

Most adult caecilians feed on soil macro-invertebrates such as earthworms, termites and ants. Some may also be partly detritivorous, meaning they eat dead plant or animal matter (3). The young, however, have a slightly more gruesome diet. After giving birth, the mother remains in a burrow with her young for some time. The young feed on liquid secretions from the mother, similar to young mammals feeding on milk from their mothers.

But caecilians also eat the skin of their mother. The top layer of skin is very fatty and therefore high in energy, and the young have specialised teeth to allow them to peel off the skin. This happens every few days to allow the mother to replenish this fatty layer. In some species the young also eat fatty layers from the mother’s insides before they are born! (4).

There is still much we don’t know about caecilians due to their fossorial nature, particularly surrounding their behaviour and life histories. For example, some scientists believe caecilians may have complex social behaviours due to specimens being found with bite scars from other caecilians and some species having sexual dimorphisms – differences between males and females. There may also be more species we haven’t discovered yet (2).

ARKive image - Common yellow-banded caecilian

 

What can you do to help?

If you’ve just stated out on your journey of discovery into the world of reptiles and amphibians visit our species pages to find out what you may have in your garden or local area.

Use our dragon finder app to report any of your sightings of the species that you find (applicable to species found in the UK).

Support initiatives to inspire the next generation of herpetologists (scientists that specialise in amphibian and reptiles) including our education work.
References

1. AmphibiaWeb: Information on amphibian biology and conservation. [web application]. 2013. Berkeley, California: AmphibiaWeb. Available: http://amphibiaweb.org/. Downloaded on 28 October 2013.
2. Pough, F.H.; Andrews, R.M.; Cadle, J.E.; Crump, M.L.; Savitzky, A.H.; Wells, K.D. (2001) Herpetology 2nd Ed. Prentice Hall Inc., New Jersey.
3. Gaborieau, O.; Measey, G.J. (2004) Termitivore or detritivore? A quantitative investigation into the diet of East African caecilian Boulengerula taitanus. Animal Biology 54:45-56.
4. Wilkinson, M.; Kupfer, A.; Marques-Porto, R.; Jeffkins, H.; Antoniazzi, M.M.; Jared, C. (2008) One hundred million years of skin feeding? Extended parental care in a neotropical caecilian. Biology Letters. 4:358-361.

Filed Under: Uncategorized Tagged With: anura, Caecilians, Croaks, Froglife, frogs, Gymnophiona, newts, salamanders, toads

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