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Reptiles are tetrapods and amniotes, animals whose embryos are surrounded by an amniotic membrane. Today they
are represented by four surviving orders:
*Crocodilia (crocodiles, caimans and alligators): 23 species
*Sphenodontia (tuataras from New
Zealand): 2 species
*Squamata (lizards, snakes and
amphisbaenids ('worm-
lizards
')): approximately 7,600 species
*Testudines (turtles): approximately 300
species
Reptiles are found on every continent except for Antarctica, although their main
distribution comprises the tropics and subtropics. Though all cellular metabolism produces some heat, most
modern species of reptiles do not generate enough to maintain a constant body temperature and are thus
referred to as 'cold-blooded' or ectothermic (the Leatherback Sea Turtle is an exception). Instead, they rely
on gathering and losing heat from the environment to regulate their internal temperature, e.g, by moving
between sun and shade, or by preferential circulation - moving warmed blood into the body core, while pushing
cool blood to the periphery. In their natural habitats, most species are adept at this, and can ususally
maintain core body temperatures within a fairly narrow range, comparable to that of mammals and birds, the two
surviving groups of 'warm-blooded' animals. While this lack of adequate internal heating imposes costs
relative to temperature regulation through behavior, it also provides a large benefit by allowing reptiles to
survive on much less food than comparably-sized mammals and birds, who burn much of their food for warmth.
While warm-blooded animals move faster in general, an attacking lizard, snake or crocodile moves very
quickly.
Except for a few members of the Testudines, all reptiles are covered by scales.
Most reptile species are oviparous (egg-laying). Many species of squamates, however, are capable of
giving live birth. This is achieved, either through ovoviviparity (egg retention), or viviparity (babies born
without use of calcified eggs). Many of the viviparous species feed their fetuses through various forms of
placenta analogous to those of mammals (Pianka & Vitt, 2003 pgs: 116-118). They often provide considerable
initial care for their hatchlings.
From the classical standpoint, reptiles included all the
amniotes except birds and mammals
. Thus reptiles were defined as the set of animals that includes crocodiles,
alligators, tuatara, lizards, snakes, amphisbaenians and turtles, grouped together as the class
Reptilia (Latin repere, 'to creep'). This is still the usual definition of the term.
However, in
recent years, many taxonomists have begun to insist that taxa should be monophyletic, that is, groups should
include all descendants of a particular form. The reptiles as defined above would be paraphyletic, since they
exclude both birds and mammals, although these also developed from the original reptile. Colin Tudge
writes:
Mammals are a clade, and therefore the cladists are happy to acknowledge the traditional
taxon Mammalia; and birds, too, are a clade, universally ascribed to the formal taxon Aves. Mammalia and Aves
are, in fact, subclades within the grand clade of the Amniota. But the traditional class reptilia is not a
clade. It is just a section of the clade Amniota: the section that is left after the Mammalia and Aves have
been hived off. It cannot be defined by synamorphies, as is the proper way. It is instead defined by a
combination of the features it has and the features it lacks: reptiles are the amniotes that lack fur or
feathers. At best, the cladists suggest, we could say that the traditional Reptila are ´non-avian,
non-mammalian amniotes´. (Tudge, p.85)
By the same token, the traditional class Amphibia
becomes Amphibia*, because some ancient amphibian or other gave rise to all the amniotes; and the phylum
Crustacea becomes Crustacea*, because it may have given rise to the insects and myriapods (centipedes and
millipedes). If we believe, as some (but not all) zoologists do, that myriapods gave rise to insects, then
they should be called Myriapoda*....by this convention Reptilia without an asterisk is synonymous with
Amniota, and includes birds and mammals, whereas Reptilia
*means non-avian, non-mammalian amniotes. (Tudge, p.85)
Recent college-level references, such as
Benton (2004) [1], offer another compromise by applying traditional ranks to accepted phylogenetic
relationships. In this case, reptiles belong to the class Sauropsida, and mammal-like reptiles to the class
Synapsida, with birds and mammals separated into their own traditional classes.
Hylonomus is the
oldest-known reptile, and was about 8 to 12 inches (20 to 30 cm) long. Westlothiana has been suggested as the
oldest reptile, but is for the moment considered to be more related to
amphibians than amniotes.
Petrolacosaurus and Mesosaurus are other examples. The first true 'reptiles' (Sauropsids) are categorized as
Anapsids, having a solid skull with holes only for nose, eyes, spinal cord, etc. Turtles are believed by some
to be surviving Anapsids, as they also share this skull structure; but this point has become contentious
lately, with some arguing that turtles reverted to this primitive state in order to improve their armor. Both
sides have strong evidence, and the conflict has yet to be resolved.
Shortly after the first
reptiles, two branches split off, one leading to the Anapsids, which did not develop holes in their skulls.
The other group, Diapsida, possessed a pair of holes in their skulls behind the eyes, along with a second pair
located higher on the skull. The Diapsida split yet again into two lineages, the lepidosaurs (which contain
modern snakes, lizards and tuataras, as well as, debatably, the
extinct sea reptiles of the Mesozoic) and the archosaurs (today represented by only crocodilians and birds,
but also containing pterosaurs and dinosaurs).
The earliest, solid-skulled amniotes also gave
rise to a separate line, the Synapsida. Synapsids developed a pair of holes in their skulls behind the eyes
(similar to the diapsids), which were used to both lighten the skull and increase the space for jaw muscles.
The synapsids eventually evolved into mammals, and are often referred to as mammal-like reptiles, though they
are not true members of the class Sauropsida.
Most reptiles have closed circulation via a
three-chamber heart consisting of two atria and one, variably-partitioned ventricle. There is usually one pair
of aortic arches. In spite of this, because of the fluid dynamics of blood flow through the heart, there is
little mixing of oxygenated and deoxygenated blood in the three-chamber heart. Furthermore, the blood flow can
be altered to shunt either deoxygenated blood to the body or oxygenated blood to the lungs, which gives the
animal greater control over its blood flow, allowing more effective thermoregulation and longer diving times
for aquatic species. There are some interesting exceptions among reptiles. For instance, crocodilians have an
incredibly complicated four-chamber heart that is capable of becoming a functionally three-chamber heart
during dives (Mazzotti, 1989 pg 47). Also, it has been discovered that some snake and lizard species (e.g.,
monitor lizards and pythons) have three-chamber hearts that become functional four-chamber hearts during
contraction. This is made possible by a muscular ridge that subdivides the ventricle during ventricular
diastole and completely divides it during ventricular systole. Because of this ridge, some of these squamates
are capable of producing ventricular pressure differentials that are equivalent to those seen in mammalian and
avian hearts (Wang et al, 2003).
Most reptiles reproduce sexually. All male reptiles except
turtles and tortoises have a twin tube like sexual organ called the hemipenes. Turtles and tortoises have a
single penis. All testudines lay eggs, none are live bearing as some lizard and snakes are. All reproductive activity occurs with the cloaca, the
single exit/entrance at the base of the tail where waste and reproduction happens.
Asexual
reproduction has been identified in squamates in six families of lizards and one snake. In some species of
squamates, a population of females are able to produce a unisexual diploid clone of the mother. This asexual
reproduction called parthenogenesis occurs in several species of gecko, and is particularly widespread in the
teiids (especially Aspidocelis) and lacertids (Lacerta). Parthenogentic species are also suspected to occur
among chameleons, agamids, xantusiids, and typhlopids.
Amniotic eggs are covered with leathery or
calcareous shells. An amnion, chorion and allantois are present during embryonic life. There are no larval
stages of development.
Read more: 8 other pages about Reptiles:
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