Download an ADOBE version of
the lecture outline
Chapter 10 - TETRAPOD ORIGINS
Sarcopterygians --lobe-finned fishes (in a paraphyletic sense,
monophyletically includes the tetrapods)
|
Division Rhipidistia (Devonian to Permian)
- Characteristics
- skull roof bones homologous with skull of tetrapods
- proximal paired fin bones homologous with limbs of tetrapods
- labyrinthodont teeth typically present
- Taxa [fig 8-15]
- includes two orders of lobe-finned fish close to the ancestry of the tetrapods
--- the
Orders Osteolepidoidea (including Eusthenopteron) and
Elpistostegida (=Panderichthyida)
--- and the
tetrapods.
|

Eusthenopteron image © BIODIDAC |
- Division TETRAPODA
- tetrapods are weird lobe-finned fish that are adapted to life on land
- Taxa [fig 8-13]
- AMPHIBIA (Gr. amphi = both or double; bios = life)
- living amphibians are "tied to water"
- for reproduction, anamniote eggs
- for
respiration--skin must remain moist
- AMNIOTA (mammals, reptiles, and birds)
THE TRANSITION TO LAND
- Advantages to invasion of land
- new food resources
- avoidance of aquatic predators and competitors
- Oxygen abundant
- Disadvantages (Obstacles)
- water becomes limiting factor in distribution (desiccation, respiration, reproduction)
- gravity - necessitates new morphological designs. Water provides buoyancy and allows for
good support even though it is more difficult to move through than air.
- water has high heat capacity. Most aquatic animals, especially marine species do not
have problems with the drastic temperature changes that occur on land.
Adaptations for Life on Land
Support and Locomotion [fig 8-1]
- modified axial skeleton with zygapotheses
- strengthened shoulder and pelvic girdles
- loss of skull bones, freeing the shoulder from the skull allowing a flexible neck;
shoulder girdle supported by serratus musculature
- attachment of ilium to sacral rib
- evolution of paired limbs
- proximal limb elements are homologous with bones of rhipidistian fin
- elongate, laterally directed humerus and femur
- podials, metapodials, and phalanges
Respiration
- Air versus water
- air has higher O2 content - 20 X more per volume; faster diffusion (500,000
X)
- less energy for ventilation; up to 25% of total metabolism for fish, 1-2% for air
breathers
- air is not hyper- or hypotonic (no salt gain or loss)
- air does not remove as much heat
- air causes problems with desiccation; structures located deep within body; long
passageways moisturize air
- structural adaptations
- absence of internal gills
- reduction and loss of operculum
- better developed lungs than were present in sarcopterygians
- three chambered heart with discrete systemic and pulmonary circulation
- three chambered heart with separation of blood in the ventricle [fig
9-23]
- loss of scales to allow for cutaneous respiration
Water Balance
- Excretion
- urea is the principal nitrogenous waste; Latimeria and the living lungfish can
synthesize urea in their livers; lungfish use urea; retention for water conservation
during estivation
- Dehydration
- still a problem for most amphibians
Sense Organs
- Middle ear
- derived from spiracle
- hyomandibular (freed from jaw support) modified to columella [stapes]; initially
the stapes is large and heavy and when it became solely involved in aerial sound
transmission is questioned
- evolution of otic notch--supports a tympanum
- Vision
- change in shape of lens, associated with different refractive indices of air and water
Reproduction
- usually external fertilization, eggs laid in water (spermatophore in salamanders)
EVOLUTION of TETRAPOD CHARACTERS in an AQUATIC HABITAT
Where?
All lobe-finned fish are initially marine in distribution and later invaded fresh water
habitats.
Why?
Romer proposed climatic conditions. Devonian red beds indicate severe drought. Fish
left the ponds that dried up in search of water.
Thompson proposed ecological conditions. Appearance of wetlands at margins of lakes or
estuaries. Abundant food for fish that could live in very shallow water. Limbs are
adaptation for locomotion in shallow water. E.g., pectoral fins of frogfishes (teleosts)
are modified into structures that function like tetrapod limbs [fig 8-18]. Gradually
amphibians took advantage of terrestrial resources.
Pough indicates early amphibians were adapted for aquatic environments. He suggests
terrestriality is associated with dispersal of juveniles who would feed on terrestrial
invertebrates and have fewer problems with gravity because of small size.
CLASS AMPHIBIA
a paraphlyletic group of non-amniotic tetrapods (recent amphibians are
monophyletic--see below)
Characteristics
- well-developed paired limbs [with digits]--may be secondarily lost
- vertebrae with zygapotheses
- skull freed from shoulder girdle,
- pelvic girdle attached to a single sacral vertebra
- hyomandibular modified to stapes
- operculum absent
- internal gill apparatus absent as adults
Upper Devonian Tetrapods
- Acanthostega, Elginerpeton, Ichthyostega, Tulerpeton, Metaxygnathus
- These five taxa are the earliest known tetrapods and retain many fish-like characters
indicative of an aquatic lifestyle
- median caudal fin rays present on tail
- skull with canals for lateral line system
- preopecular bone present (Acanthostega may have retained internal gills)
- Other primitive characters
polydactyly (more than 5 digits in manus or pes; Acanthostega has 8) [fig
8-16]
- labyrinthodont teeth - synapomorphy shared with osteolepiform
- Ichthyostega from the Devonian of Greenland is one of the best known early
tetrapods.
TEMNOSPONDYLI (Pennsylvanian-Cretaceous)
- it is widely accepted that the three orders of living amphibians (Lissamphibia) are
derived from the temnospondyls [Figs. 8-20d, e, f, g]
- Evidence summarized in Carrol [2002, Journal of Paleontology,
75:1202-1213] suggests that caecilians are most closely related to
lepospondyl microsaurs and that salamanders and frogs are derived from
different families of dissorophoid temnospondyls. However, pedicellate
teeth are present in the earliest caecilian, as well as frogs and
salamanders, but are absent in microsaurs.
- THE ANCESTRY OF THE AMNIOTES
- [numbers refer to numbered nodes in figure 10-2, pp. 266-267]
- REPTILOMORPHA
- skull and vertebral characters differentiate from the Batrachomorpha (temnospondyls and
lyssamphibia)
- ANTHRACOSAUROIDEA
- 11. BATRACHOSAURIA
- SEYMOURIAMORPHA [fig 10-16b]
- 12. COTYLOSAURIA
-
characters
-
sacrum with more than one vertebra
- loss of lateral line system
- robust claws on
forelimbs for digging
- modern atlas-axis complex
- DIADECTOMORPHA [fig 10-16a]
- 13. AMNIOTA
- transverse pterygoid flange for pterygoideus jaw muscle,
etc.
TEMPORAL OPENINGS AND AMNIOTE CLASSIFICATION [fig. 10-21]
- Anapsids
dermal skull roof completely covered with bone; turtles are typically included as
anapsids; this is primitive for the amniotes.
- Synapsids
single opening low on the cheek, bordered by the jugal, squamosal, and postorbital;
condition found in mammals
- Diapsids
two pairs of temporal openings; one pair ventral to the postorbital and squamosal
(as in the synapsids); the second pair dorsal to the postorbital and squamosal and lateral
to the parietal
- Euryapsids
derived from the diapsid condition by loss of the lower temporal opening; evolved
independently in plersiosaurs (lower temporal bar lost) and ichthyosaurs (opening closed
by enlargement of bones of the cheek region
AMNIOTE TAXONOMY
- numbers refer to numbered nodes in figure 10-2, pp. 266-267
- Paleozoic amniotes are illustrated in fig 10-18
- Synapsida (includes Mammalia) [fig 10-18b]
- Sauropsida
- Mesosauridae
- Reptilia
- stem parareptile (Anapsida)
- Milleretidae, etc.
- Testudines (may be diapsids)
- Eureptilia
AMNIOTA
- Characteristics
- Amniote (cleidoic) egg [fig 10-19]
- Amniotes are fully terrestrial and lay eggs on land . Amniotes not "tied to
water" for purposes of reproduction.
- exclusively internal fertilization, No larval stages. No metamorphosis
- four extraembryonic membranes
- amnion--inner part of a double membrane that surrounds the embryo; located directly
outside of the embryo; encloses the developing embryo (fluid-filled sac)
- chorion--outer membrane which is part of the double membrane; located outside of the
amnion; serves as a surface for gas exchange through the shell
- allantois--a chamber which stores nitrogenous wastes [uric acid] produced by the embryo
during development
- yolk sac--contains the embryo's food and energy reserves in the form of lipids
- Albumin--protein source and holds water
- More effective jaw musculature [fig 10-22]
- greatest strength when nearly closed, for crushing prey.
- pterygoid with a transverse flange for attachment of large pterygoidius muscle
- Skeletal structure improved--greater strength and agility
- improved locomotion due to rotation of limbs to support body
- two sacral vertebrae
- otic notch absent
CLASS REPTILIA
Characteristics
- a variety of skull characters [fig 10-2]
- skin tough, leathery, and covered with keratinous scales.
- very few to, usually, no glands in integument; glandless skin is resistant to desication
- "dry" skin of reptiles serves no respiratory function except during embryo
development.
- well-developed lungs
- Heart usually 3-chambered; 4-chambered in crocodiles
- Ectothermic heterotherms
- Paired metanephric kidneys; uric acid is the main nitrogenous waste
- Very well-developed nervous system, especially within the cranium and with regard to
optic nerves and sense organs; very well-developed visual sensory system
- 7000 species total, world wide. 300 species in the U.S.
Return to: