Saturday 21 January 2012
AMPHEBIANS
Amphibians (class Amphibia , from Amphi- meaning "on both sides" and -
bios meaning "life") are a class
of vertebrate animals including animals such as toads, frogs, caecilians, and salamanders. They are characterized as non-amniote ectothermic (or cold-blooded) tetrapods. Most Amphibians undergo metamorphosis from a juvenile water-breathing
form to an adult air-breathing
form, but some are paedomorphs that retain the juvenile water-breathing
form throughout life. Mudpuppies, for example, retain juvenile gills in
adulthood. The three modern
orders of amphibians are
Anura (frogs and toads),
Caudata (salamanders and newts ), and Gymnophiona (caecilians, limbless
amphibians that resemble
snakes), and in total they
number approximately 6,500 species.[1] Many amphibians lay their eggs in water.
Amphibians are superficially
similar to reptiles, but reptiles are amniotes, along with
mammals and birds. The study
of amphibians is called
batrachology. Amphibians are ecological indicators,[2] and in recent decades there has been a
dramatic decline in amphibian populations around the globe. Many species are now
threatened or extinct. The earliest amphibians
evolved in the Devonian period from lobe-finned fish that used their strong, bony
fins to venture onto dry land. [3] They were the top predators in the Carboniferous and Permian periods,[4] but they later faced competition
from their descendants, the
reptiles, and many lineages
were wiped out during the Permian–Triassic extinction . One group, the metoposaurs, remained important predators
during the Triassic, but as the world became drier during the Early Jurassic they died out, leaving a handful of relict temnospondyls like Koolasuchus and the modern orders of Lissamphibia. Etymology Amphibian is derived from
the Ancient Greek term ἀμφίβιος amphíbios, which
means both kinds of life,
amphi meaning “both” and bio
meaning life. The term was
initially used for all kinds of
combined natures. Eventually it was used to refer to animals
that live both in the water and on land.[5] Evolutionary history Main article: Labyrinthodontia See also: List of prehistoric amphibians The first major groups of
amphibians developed in the Devonian period from lobe- finned fish similar to the
modern coelacanth and lungfish,[3] which had evolved multi-jointed leg-like
fins that enabled them to
crawl along the sea bottom.
Some fish had developed primitive lungs to help them breath air when the stagnant
pools of the Devonian
swamps were lacking in
oxygen. They could also use
their strong fins to hoist
themselves out of the water and onto dry land if
circumstances required it.
Eventually, their bony fins
would evolve into limbs and
they would become the
ancestors to all tetrapods, including amphibians, reptiles, birds, and mammals. Despite being able to crawl on land,
many of these prehistoric tetrapodomorph fish still spent most of their time in the
water. Amphibians evolved
adaptations which allowed
them to stay out for longer
periods. However, they never
developed the ability to live their entire lives on land,
having a fully aquatic tadpole stage and still needing to
return to water to lay their
shell-less eggs. The first true amphibians
appeared in the Carboniferous Period, by which time they were already moving up the
food chain and occupying the
ecological position currently
claimed by such animals as
crocodiles. Amphibians were
once the top land predators, sometimes reaching several
meters in length, preying on
the large insects on land and
many types of fish in the
water. During the Triassic Period, the better-adapted reptiles began to compete
with amphibians, leading to
the reduction of their size and
importance in the biosphere. Lissamphibia, which includes all modern amphibians and is
the only surviving lineage of
amphibians left, could have
branched off from the extinct
groups Temnospondyli and Lepospondyli anytime between the mid- Permian to the early Triassic, but the relative scarcity of fossil
evidence does not permit an exact date. [4] Taxonomic history Traditionally, amphibians have
included all tetrapod vertebrates that are not amniotes. They are divided into three subclasses, of which two are only known as
extinct subclasses: Subclass Labyrinthodontia † (diverse Paleozoic and early
Mesozoic group) Subclass Lepospondyli † (small Paleozoic group,
sometimes included in the
Labyrinthodontia, which
may actually be more
closely related to amniotes
than Lissamphibia) Subclass Lissamphibia (frogs, toads, salamanders,
newts, etc.) Of these only the last subclass
includes recent species. With the phylogenetic classification Labyrinthodontia
has been discarded as it is a paraphyletic group without unique defining features apart
from shared primitive characteristics. Classification varies according to the
preferred phylogeny of the author, whether they use a stem-based or node-based classification. Traditionally,
amphibians as a class are
defined as all tetrapods with a larval stage, while the group
that includes the common
ancestors of all living
amphibians (frogs,
salamanders and caecilians)
and all their descendants is called Lissamphibia. The
phylogeny of Paleozoic amphibians is by no means
satisfactory understood, and
lissamphibia may possibly
include extinct groups like the temnospondyls (traditionally placed in the subclass
“Labyrinthodontia”), and the
Lepospondyls, and in some
analysis even the amniotes. This means that phylogenetic nomenclature list a large number of basal Devonian and Carboniferous tetrapod groups, undoubtedly were
“amphibians” in biology, that
are formally placed in
Amphibia in Linnaean taxonomy , but not in cladistic taxonomy . All recent amphibians are
included in the subclass
Lissamphibia, superorder
Salientia, which is usually
considered a clade (which means that it is thought that
they evolved from a common
ancestor apart from other
extinct groups), although it
has also been suggested that
salamanders arose separately from a temnospondyl-like
ancestor, and even that
caecilians are the sister group
of the advanced reptiliomorph amphibians, and thus of amniots.[6][7] Authorities also disagree on
whether Salientia is a
Superorder that includes the
order Anura, or whether
Anura is a sub-order of the
order Salientia. Practical considerations seem to favor
using the former arrangement
now. The Lissamphibia,
superorder Salientia, are
traditionally divided into
three orders, but an extinct salamander-like family, the
Albanerpetontidae, is now
considered part of the
Lissamphibia, besides the
superorder Salientia.
Furthermore, Salientia includes all three recent orders plus a
single Triassic proto-frog, Triadobatrachus. Class Amphibia Subclass Lissamphibia Family Albanerpetontidae — Jurassic to
Miocene (extinct) Superorder Salientia Genus Triadobatrachus — Triassic (extinct) —
A stem Anuran Order Anura ( frogs and toads): Jurassic to recent — 5,602
recent species in 48
families Order Caudata or
Urodela
(salamanders, newts ): Jurassic to recent — 571 recent
species in 9 families Order Gymnophiona
or Apoda
(caecilians): Jurassic to recent — 174
recent species in 3
families The actual number of species
partly also depends on the
taxonomic classification
followed, the two most
common classifications being
the classification of the website AmphibiaWeb,
University of California
(Berkeley) and the
classification by herpetologist Darrel Frost and The American
Museum of Natural History,
available as the online
reference database Amphibian Species of the World. [8] The numbers of species cited
above follow Frost. Respiration The lungs in amphibians are
primitive compared to that of
the amniotes, possessing few internal septa, large alveoli and therefore a slow diffusion
rate of oxygen into the blood.
Ventilation is accomplished by buccal pumping. However, most amphibians are able to
exchange gasses with the
water or air via their skin. To
enable sufficient cutaneous
respiration, the surface of
their highly vascularized skin must remain moist in order
for the oxygen to diffuse at a
sufficient rate. Because
oxygen concentration in the
water increases at both low
temperatures and high flow rates, aquatic amphibians in
these situations can rely
primarily on cutaneous
respiration, as in the Titicaca water frog and hellbender salamanders. In air, where oxygen is more concentrated,
some small species can rely
solely on cutaneous gas
exchange, most famously the plethodontid salamanders, which have neither lungs nor
gills. Many aquatic
salamanders and all tadpoles
have gills in their larval stage,
with some (such as the axolotl ) retaining gills as aquatic adults.
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