Showing posts with label Toads. Show all posts
Showing posts with label Toads. Show all posts

Saturday, 4 October 2014

How an invasive Grass species makes American Toads more vulnerable to Wolf Spiders.


Invasive plants can significantly modify local habitats, particularly if they lack herbivores in the environments they are colonising, by both modifying the structure of the environment and excluding native plants which provide food and homes to native animals. One such plant is the Japanese Stilt Grass (Microstegium vimineum), which has invaded moist forest-floor environments across the eastern United States. Japanese Stilt Grass has been shown to modify soil chemistry and Arthropod diversity and abundance in areas where it invades, and lacks any significant herbivores in the United States, allowing it to spread with little impediment.

Japanese Stilt Grass, Microstegium vimineum. Theresa Yednock/National Park Service/Wikimedia Commons.

One Vertebrate species is also apparently affected by the presence of Japanese Stilt Grass, the American Toad (Anaxyrus americanus), which appears to decline where the Grass becomes established. This could potentially be for a number of reasons. Firstly, like all Amphibians, American Toads have permeable skin through which they exchange fluids and gasses with the environment, which may make them vulnerable to changes in soil chemistry. Secondly they feed almost exclusively on Arthropod prey, notably Mites and Ticks (Acari), Spiders (Araneae), Beetles (Coleoptera), Springtails (Collembola), Flies (Diptera), Bugs (Hemiptera), and Ants, Bees and Wasps (Hymenoptera) and changes in the abundance of these prey items may affect the survival of the Toads. Finally the Toads themselves are vulnerable to predation by larger Arthropods, as they metamorphose (change from tadpoles into adult Toads) very young, achieving most of their growth in the terrestrial environment.

American Toad, Anaxyrus americanus. Brad Glorioso/National Wetlands Research Center/USGS.

In a paper published in the journal Ecology in July 2014, Jayna DeVore of the Warnell School of Forestry and Natural Resources at the University of Georgia and the School of Biological Sciences at the University of Sydney, and John Maerz, also of the Warnell School of Forestry and Natural Resources, describe the results of a series of experiments designed to determine exactly how the presence of Japanese Stilt Grass affects the American Toad.

Firstly DeVore & Maerz created enclosures in four areas of woodland in Georgia State that were enclosed in a way that prevented the entrance or exit of Toads but allowed Arthropods free movement. Within these enclosures the numbers of both Toads and the various Arthropod groups were monitored. No correlation between prey species numbers and Toads was found, but Toad numbers did decline in numbers in pens where Wolf Spiders (Lycopsidae) were present in large numbers.

Wolf Spiders are large predatory Spiders that hunt by waiting in ambush for mobile prey, then running it down. Small Toads, which actively seek out prey, moving about as they forage, are particularly vulnerable to this hunting technique, as they cannot feed it they remain immobile (the Spiders do not themselves forage, and will not find stationary prey) and have no defence against the Spiders.

The Carolina Wolf Spider, Hogna carolinensis. Patrick Edwin Moran/Wikimedia Commons.

DeVore & Maerz then carried out a series of cage experiments where Toads were placed in cages with or without Japanese Stilt Grass, and Wolf Spiders (Hogna carolinensis or Hogna helluo). In cages lacking Spiders the Toads survived well, regardless of the presence of the Stilt Grass, suggesting that it does not affect the soil chemistry in a way that harms the Toads. However in cages with Wolf Spiders the Toads suffered significant mortality, and this rose sharply in cages where both Spiders and Grass were present, suggesting that the Grass modifies the environment in a way that makes it easier for the Spiders to hunt the Toads.

Conceptual diagram of explored mechanisms through which Microstegium vimineum invasion can affect the survival and growth of metamorphic Toads, indicating both direct (solid line) and indirect (dashed line) effects. Black arrows are used to portray connections that were altered following invasion, resulting in significant changes in depicted parameters (e.g., densities, survival rates), whereas those that were unaffected are depicted in gray (i.e., growth rates). Significant changes are also annotated with a sign indicating whether the indicated parameter was positively (+) or negatively (-) affected (as compared with adjacent, uninvaded habitats; see Appendix C for effect sizes). In summary, invasion amplified top-down pressure on toads by increasing structural complexity, which dampened the strength of a pre-existing intraguild (IGP)/cannibalistic trophic linkage among Lycosid Spiders, resulting in higher spider densities and, subsequently, lower Toad survival within invaded habitats. The potential for bottom-up effects occurred via post-invasion changes in detrital food webs, which ultimately decreased the availability of edible invertebrates, but Toad growth was unaffected by these reductions. Although we also documented significant changes in abiotic habitat parameters following invasion, these effects alone did not significantly influence Toad survival (linkage not pictured). DeVore & Maerz (2014).

See also…


Sociality is rare in Spiders, which are by nature solitary and aggressive...


Cryptic species are species which resemble one-another physically, and which cannot generally be separated using traditional taxonomic methodology, but which are nevertheless genetically and reproductively...



Cave Spiders (Nesticidae) are found across the Mediterranean Basin, as well as in the Canary Islands and parts of Asia. They are...

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Monday, 2 June 2014

Frogs and Toads from the Early Eocene of Gujarat State, India.

The Cambay Shale formation from the Vastan Lignite Mine to the northeast of Surat in Gujarat State, India, has produced a diverse and significant Vertebrate fauna, including a diverse assemblage of Bats, the oldest known Ailuravine Rodents in Asia, the oldest known Lagomorphs (Rabbits), the oldest known Tillodont from India, early Adapoid and Omomyid Primates and Artiodactyls (the group that includes Antelopes, Cattle, Deer, Giraffes ect.), as well as Fish, Snakes, Lizards and Birds. A variety of Anuran species (Frogs and Toads) also appear to be present, although these are represented by a large volume of disarticulated bones, and have not therefore been studied in detail to date.

In a paper published in the journal Acta Palaeontologica Polonica on 27 January 2012, a team of scientists led by Annelise Folie of the Department of Paleontology at the Royal Belgian Institute of Natural Sciences, describe these Anuran bones in some detail, and conclude that at least four species from different Anuran families are present.

The majority of the bones are thought to come from a single species within the Fire-bellied Toad family Bombinatoridae. Modern members of this family are aquatic toads with flattened bodies; all extant species being highly toxic, and have colouration that reflects this. Fire-bellied Toads are noted for the ‘Unken reflex’ in which the animal responds to danger by arching its back strongly, exposing its brightly coloured underside as a warning of its toxic nature. Living members of this family are divided into two genera; Bombina, which is found in Europe and East Asia, and Barbourula, which is found in Borneo and the Philippines. The oldest known fossil assigned to this group has previously been a member the genus Bombina from the Miocene of Germany.

Folie et al. assign these bones to the species Eobarbourula delfinoi, where ‘Eobarbourula’ means ‘dawn-Barbourula’ and ‘delfinoi’ honours the Italian paleontologist Massimo Delfino. A total of 58 illia, 120 vertebrae and 12 urostyles are assigned to this species. The vertebrae assigned to Eobarbourula delfinoi have a zygosphene−zygantrum complex on their articulations, in which an anterior process on the vertebra, the zygosphene, inserts into a wedge-shaped cavity on the vertebra in front, the zygantrum. This is found in modern members of the family, as well as in the Salamander Salamandrina, and in Lacertid, Teiid, and Cordylid Lizards, and is associated with the Unken reflex. Similar structures have been seen in some Dinosaur species, and on the cervical (neck) vertebrae of some early Birds, suggesting that these too may have exhibited this behaviour.

Nearly complete ilium of Toad Eobarbourula delfinoi from the Early Eocene of the Vastan Lignite Mine in Gujarat, India. (A) Left ilium in lateral (A1), posterior (A2), medial (A3), and dorsal (A4) views. (B) Left ilium in lateral (B1), posterior (B2), medial (B3), and dorsal (B4) views. (C) Right ilium in medial (C1), posterior (C2), lateral (C3), and dorsal (C4) views. Folie et al. (2012).

Vertebrae of Toad Eobarbourula delfinoi from the Early Eocene of the Vastan Lignite Mine in Gujarat, India. (A) Atlas in anterior (A1), posterior (A2), left lateral (A3), dorsal (A4), and ventral (A5) views. (B). Anterior trunk vertebra in anterior (B1), posterior (B2), left lateral (B3), dorsal (B4), and ventral (B5) views. (C) Trunk vertebra in anterior (C1), posterior (C2), left lateral (C3), dorsal (C4), and ventral (C5) views. (D) Trunk vertebra in anterior (D1), posterior (D2), right lateral (D3), dorsal (D4), and ventral (D5) views. (E) Presacral vertebra in anterior (E1), posterior (E2), right lateral (E3), dorsal (E4), and ventral (E5) views. (F) Sacral vertebra in anterior (F1), posterior (F2), left lateral (F3), dorsal (F4), and ventral (F5) views. (G) Urostyle in anterior (G1), left lateral (G2), dorsal (G3), and ventral (G4) views. Folie et al. (2012).

Close up views of vertebrae of Toad Eobarbourula delfinoi from the Early Eocene of the Vastan Lignite Mine in Gujarat, India. (A) Presacral vertebra in dorsal (A1) and anterior (A2) views. (B) Trunk vertebra in posterior view. Folie et al. (2012).

Secondly a single ilium is thought to come from a member of the Spadefoot Toad family, Pelobatidae. This family only contains a single extant genus, Pelobates, a burrowing Toad known from Europe and West Asia, but has a fossil record going back to the Late Cretaceous (several earlier specimens have been reported, but are now considered dubious). This ilium is assigned to the genus Eopelobates, which has previously been used to describe specimens from the Middle Eocene-Miocene of Germany and the Czech Rebublic, but is not assigned to species level. Eopelobates lacks the adaptations for burrowing seen in the modern Pelobates, and was probably a terrestrial (ground dwelling) Toad, though it has been suggested that it might have lived in trees.

Pelvic girdle of frog Eopelobates. (A) Eopelobates wagneri from the Middle Eocene Messel Shale of Germany. (A1) Complete skeleton in dorsal view; (A2) pelvic girdle in mediodorsal view showing anatomical characters of ilia. (B) Eopelobates sp. from the Early Eocene of the Vastan Lignite Mine in Gujarat, India. Nearly complete right ilium in posterior (B1), lateral (B2), dorsal (B3), and medial (B4) views. Folie et al. (2012).

Thirdly a nearly complete ilia, seven vertebrae and two urostyles are assigned to the True Frog family Ranidae. This family is currently found across much of the globe, with its earliest described fossils coming from the Late Eocene of England and France, and possible specimens reported but never properly described from the Late Cretaceous of Africa and India. It has previously been suggested that this group may have reached Eurasia via the Indian Subcontinent, and the assignment of fossils from Vastan to this group supports this hypothesis.

Nearly complete right ilium of a Frog assigned to the Ranidae from the Early Eocene of the Vastan Lignite Mine in Gujarat, India, in lateral (A), posterior (B), medial (C), and dorsal (D) views. Folie et al. (2012).

Vertebrae of Frog assigned to the Ranidae, from the Early Eocene of the Vastan Lignite Mine in  Gujarat, India. (A) Presacral vertebra in anterior (A1), posterior (A2), left lateral (A3), dorsal (A4), and ventral (A5) views. (B) Last presacral vertebra in anterior (B1), posterior (B2), left lateral (B3), dorsal (B4), and ventral (B5) views. (C) Sacral vertebra in anterior (C1), posterior (C2), left lateral (C3), dorsal (C4), and ventral (C5) views. (D) Fragmentary urostyle in anterior (D1), left lateral (D2), dorsal (D3), and ventral (D4) views. Folie et al. (2012).

Finally an incomplete left ilium and associated pubis, left ischium and half a right ischium are tentatively assigned to the family Rhacophoridae, Shrub Frogs or Old World Tree Frogs. These are currently distributed across tropical parts of Africa, India and Australasia, but have a limited fossil record. Specimens have been reported from the Late Eocene of France, but these have not been described and the presence of such Frogs in the Eocene of Europe is considered doubtful. The only other recorded fossils in this group are from the Pleistocene of Japan, so if the Vastan fossils are Rhacophorids, then they represent the earliest record of this group. These specimens are assigned to a new species, Indorana prasadi, where ‘Indorana’ means ‘Indian Frog’ and ‘prasadi’ honours the Indian palaeontologist Guntupalli Prasad, an expert on Indian Frogs.

Pelvic girdle of Frog Indorana prasadi, from the Early Eocene of the Vastan Lignite Mine in Gujarat, India. (A) Nearly complete left ilium with the two ischia and pubis in lateral (A1), posterior (A2), medial (A3), and dorsal (A4) views. (B) Incomplete left ilium with left ischium in lateral (B1), posterior (B2), medial (B3), and dorsal views (B4). Folie et al. (2012).

See also…


Bush Frogs (Rhacophoridae) are found throughout tropical areas of Africa and Asia. They are tree-dwelling frogs that seldom venture down to the ground, their eggs being laid in a foamy construct...



Flying Frogs of the genus Racophorus are found from Madagascar and Africa across India to Southeast Asia and Japan. They have...




The earliest known Frogs in the fossil record hail from the earliest Triassic of Madagascar, though it is thought the group probably has its origins deeper in the Permian. A number of Frogs have been described from the Early Cretaceous Jehol Biota, a fossil Lagarstätte (rich fossil deposit) from...


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Sunday, 25 May 2014

A new species of Toad from the montane forests of Central Peru.

Toads of the Rhinella margaritifera species group are found in leaf litter on the floors of South American humid rainforests. They are well camouflaged, resembling fallen leaves in colouration, and often possessing a variety of crests and protrusions that help to break up their body outline. Many species are also highly variable, making it hard for a predator (or a herpetologist) to develop a species recognition pattern that might aid in hunting. This makes the taxonomy of the group particularly hard to unravel, and there are thought to be numerous cryptic species within the group.

In a paper published in the journal ZooKeys on 17 January 2014, Jiří Moravec of the Department of Zoology at the National Museum in Prague, Edgar Lehr of the Department of Biology at Illinois Wesleyan University, Juan Carlos Cusi and Jesús Córdova of the Departamento de Herpetología at the Museo de Historia Natural at the Universidad Nacional Mayor de San Marcos and Václav Gvoždík also of the Department of Zoology at the National Museum in Prague, describe a new species of Toad in the Rhinella margaritifera species group, from montane forests of Central Peru.

The new species is named Rhinella yunga, meaning ‘warm valley’ in Quecha; a term widely used for montane rainforests in the eastern Andes of Peru and Bolivia. Rhinella yunga is a 57.5-65.5 mm ‘dead-leaf’ patterned Toad (the females being on average slightly larger than the males), with cephalic (skull) crests and a lateral row of tubercles (warts).

Specimens of Rhinella yunga. (A) Adult male in water, about 5 km west of Oxapampa, and (B) adult female from the area of Rio Huatziroki. Jiří Moravec in Moravec et al. (2014).


Rhinella yunga was found in the Yanachaga-Chemillén National Park in Oxapampa Province, the left bank of the Rio Huancabamba about 5 km west of Oxapampa, the Quebrada Yanachaga Valley, and from the Rio Huatziroki area in the buffer zone of the Pui Pui Protected Forest (a buffer zone around a protected forest is an are where some forms of agriculture etc. are allowed, but there are restrictions in place to protect the environment). This covered elevations of roughly 1800-2230 m above sea-level, and about 60 km northwest to southeast along a buffer zone between transitional montane forest (found roughly 1000-2000 m above sea-level) and montane cloud forest (found roughly 2000-3400 m above sea-level), though it is likely that the Toad is more widely distributed in the montane forests of Central Peru.

Schematic map of central and southern Peru showing known distribution of Rhinella yunga. (1) Quebrada San Alberto (1950 m above sea-level) in the Yanachaga-Chemillén National Park. (2) Quebrada Yanachaga valley at the settlement Prosoya (about 1800 m above sea-level). (3) Rio Huancabamba (about 5 km W of Oxapampa, and about 1885 m above sea-level). (4) Rio Huatziroki (1915–2230 m above sea-level) lying in the buffer zone of the Pui Pui Protected Forest about 60 km straight southeast of Quebrada San Alberto. Edgar Lehr in Moravec et al. (2014).

Habitat of Rhinella yunga, (A) a road margin at Quebrada San Alberto, and (B) closed cloud forest in the area of Rio Huatziroki (about 2200 m above sea level). Jiří Moravec in Moravec et al. (2014).

See also…


Bush Frogs (Rhacophoridae) are found throughout tropical areas of Africa and Asia. They are tree-dwelling frogs that seldom venture down to the ground, their eggs being laid in a foamy construct...



Flying Frogs of the genus Racophorus are found from Madagascar and Africa across India to Southeast Asia and Japan. They have...




The earliest known Frogs in the fossil record hail from the earliest Triassic of Madagascar, though it is thought the group probably has its origins deeper in the Permian. A number of Frogs have been described from the Early Cretaceous Jehol Biota, a fossil Lagarstätte (rich fossil deposit) from...


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Friday, 1 February 2013

A new species of Toad from the coastal restingas of southern Brazil.

True Toads of the Family Bufonidae (a variety of unrelated Frogs from around the world are colloquially known as 'Toads', but the Family Bufonidae are the only group to which this is universally applied) occur naturally on every continent except Antarctica and Australia, and have been introduced to Australia. They occupy a wide variety of environments, including fairly arid, sandy regions where Amphibians are not generally expected. True Toads tend to be warty in appearance and to lack teeth. Most species can excrete toxins through their skins, and in many species male Toads can become female under some circumstances.

In a paper published in the American Museum Novitates on 14 November 2012, a team of scientists led by Pedro Peloso of the Division of Vertebrate Zoology (Herpetology) and Richard Gilder Graduate School at the American Museum of Natural History, describe a new species of Toad from the coastal resingas (shrubby woodland on acidic sandy soils) of Espírito Santo State in southern Brazil.

The new species is placed in the genus Melanophryniscus (South American Redbelly Toads), and given the specific name setiba, meaning 'seashells in abundance' in the local Tupi Guarani language; this being the popular name of the area where the Toads were found living.

Melanophryniscus setiba is a 13-16 mm reddish brown Toad with a warty skin and the majority of its fingers and toes greatly reduced, leaving it with one effective digit on each limb. The males are slightly more robust than the females.

Melanophryniscus setiba, adult male, 16 mm long. Peloso et al. (2012).

The hand (left) and foot (right) of Melanophryniscus setiba. Scale bar is 2 mm. Peloso et al. (2012).

The restinga forest where Melanophryniscus setiba was found. Peloso et al. (2012).


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Friday, 16 November 2012

How Cow pats help the spread of the Invasive Cane Toad in northern Australia.

The Cane Toad, Rhinella marina, is a large, toxic, Amphibian from Central and South America, introduced to 1935 as a biological control of the Cane Beetle, Dermolepida albohirtum, an agricultural pest. Unfortunately the Toad proved to be rather poor at controlling the Beetles, and very good at consuming a variety of Australian invertebrates, as well as poisoning local predators, which evolved in an environment free of poisonous potential prey items and have been slow adapting to the introduction. Since their introduction the Toads have spread across much of northeast Australia, and caused a great deal of problems for local conservation efforts.

A Cane Toad, Rhinella marina. Burrum River & Howard Community Website/Eva Ford.

The spread of the Toads is particularly associated with agricultural land, particularly cattle ranching, which provides year-round irrigation and extended strips of Toad-friendly environment along which to spread. In a paper published in the journal PLoS One on 7 November 2012, Edna González-Bernal, Matthew Greenlees, Gregory Brown and Richard Shine of the School of Biological Sciences at the University of Sydney, discus the results of an investigation into anecdotal evidence that the spread of the Toads is somehow facilitated by the presence of Cow pats (excrement) in the environment.

González-Bernal et al. investigated whether the Toads really did associate with Cow pats, as they were rumored to do, and also whether the Cow pats helped them to retain moisture, to regulate their temperature or to gain access to food. 

They found that Toads in an environment with Cow pats would be found on or near to the pats more than would be expected by random chance, but that the Cow pats, despite being warm and wet, made no difference to the body temperature of Toads upon them, and were, if anything, slightly more likely to absorb moisture from the Toads than the other way around. 

However the Cow pats did appear to contribute to the Toads feeding strategy, with Toads near to pats able to consume Dung Beetles, another introduced species, which apparently make up a considerable proportion of the Toads diet on land used for pasture. This suggests that the presence of cattle farms does indeed facilitate the spread of the Toads.


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Sunday, 4 March 2012

New Spadefoot Toad from southeastern Laos.

Eastern Spadefoot Toads of the genus Leptobrachium are found in India, Southeast Asia, Southern China and the islands of the Sunda Arc. They are related to Horned Toads, Horned Frogs, Spiny Toads, Asian Toads, Mountain Toads, Borneo Frogs and Karin Hill Frogs. Many Eastern Spadefoot Toad species have split coloured irises to their eyes, with the top part of the iris a different colour to the rest of the eye.

I a paper published in the journal Zootaxa on 10 January 2012, a team lead by Bryan Stuart of the North Carolina Museum of Natural Sciences describe a new species of Eastern Spadefoot Toad from southeastern Loas, named as Leptobrachium xanthops, the Yellow-eyed Eastern Spadefoot Toad.

Female Leptobrachium xanthops, the Yellow-eyed Eastern Spadefoot Toad. From Stuart et al. (2012).

Leptobrachium xanthops is a stocky dark grey toad 45-57 mm in (adult) length. It is pale on the underside and has a distinctive pale yellow arc across the top part of its eye. It was not observed to make any vocalizations.

Male Leptobrachium xanthops, the Yellow-eyed Eastern Spadefoot Toad. From Stuart et al. (2012).

The toads were discovered in wet evergreen forest on the Dakchung Plateau, in southeastern Laos, at an altitude of 1450-1500 m. All were found within 15 m of wide, fast flowing rocky streams. Stuart et al. speculate that they are probably also present in other upland areas of southern Laos, and adjacent areas of Vietnam.

Map of Laos and the surrounding countries showing the area where the toads were found (black star). From Stuart et al. (2012).