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archosaurs are the last common ancestor of
crocodilians + birds, and all of its descendant
everything outside that node is a stem archosaur, however “archosaur-like” it looks
archosaurs origins
permian-triassic
they have a fast start after the
end-permian extinction
fast origin -
crown archosaurs appear less than 5 mar after the end-permian extinction
minimum age -
fossils set a floor for the crocodile-line/bird split; no verified molecular date yet
cause unproven
extinction as the trigger of archosaur suc
< 5 Myr from
the end-permian extinction to the first date crown archosaurs
the archosauriform stem
late permian
archosaurian characters
antoribital fenestra; serrated teeth in deep sockets
mandibular fenestra; pronounced 4th trochanter
pubic boot; metatarsal II > IV
advances mesotarsal (hinge) ankle
mapping archosaurian characters on the tree common error
socketed teeth and ant orbital fenestra “define" archosaurs
ankles: ancestral is not
diagnostic
ankles - crocodiles (normal)
rotation between astragals and calcaneum (peg-and-socket)
allows sprawling or an erect “high walk”
ankle - advanced mesotarsal
simple hinge between proximal and distal tarsal
limits the limb to an erect, fore-and-aft (parasagittal) swing
most rornithodirans
ankles - ancestral for the crown
teleocrater, and early bird-line archosaur, still has a crocodile-normal ankle
so it cannot define the crocodile line
triassic peusdosuchians out-diversified
early dinosaurs
triassic pseudosuchians - higher disparity
late triassic crocodile-line archosaurs spanned more body plans than early dinosaurs
triassic pseudosuchians - same pace
rates of character evolution were statically indistinguishable
triassic pseudosuchians - implication
the dinosaurs’ dire reflects which lineages survived the end-triassic extinction, not “superiority”
the end-triassic filter - one survivor
every crocodile-line clade except crocodylomorphs ended at or before the boundary
crocodylomorph radiations - early jurassic
rebound after the end-triassic extinction
mostly small, slender, land-dwelling predators
crocodylomorph radiations - jurassic seas
marine thalattosuchaisn” teleosauroids and metriorhynchoids
crocodylomorph radiations - cretaceous land
neosuchaisn ( the lineage including crocodylians) and the land-dwelling notosuchains
jaw shapes diversify sharply
crocodylomorph radiations - drivers
warm clime raised speciation on land and at sea (not in fresh water_; high sea level raised extinction
neither biotic nor abiotic factor dominated
Alligatoroidea =
alligators, caimans
Crocodyloidea =
true crocodiles
gavials =
gharial
tomistoma =
false gharial
living crocodylians =
25 species in three families
living crocodylians = recent splits
Crocodylus suchus, Mecistops leptorhynchus, Osteolaemus osborni.
living crocodylians - field marks
crocodiles show the 4th lower tooth with the mouth closed; in alligators and caimans it sits hidden in an upper-jaw pit; gavials have long slender snouts
archosaur biology - heart and lungs
divided ventricle - level I’
one-way lung airflow - level I’; alligator has it without air sacs
archosaur biology - metabolism
likely secondary ectotherms - descend from high-metabolism ancestors
evidence - heart and lungs; bone histology; bone chemistry
archosaur biology - bracket check
air sacs, hollow bones, and endothermy in non-avian dinosaurs are level II’ (birds only)
temperature-dependent sex determination distribution
all crocodilians; birds are ZW
no bracket onto dinosaurs
cardiac shunt distribution
crocodylians
no bracket into dinosaurs
jaw sensory organs distribution
crocodyliforms
ectothermy distribution
crocodylians (probably secondary)
crocodilian specializations - not “living” fossils
living crocodilians are derived specialists
temperature-dependent sex determination - males
in the middle (31.7-35.9)
temperature-dependent sex determination - females
ends (<31.7, >35.9)
temperature-dependent sex determination - in all crocodylians
dominant pattern FMF; and MF pattern has never been observed
temperature-dependent sex determination - sensitive window
roughly the middle third of incubation
parental care - embryos call
nile crocodile call inside the egg; calls synchronize hatching and prompt the mother to open the nest
parental care - level I’
care occurs in both brackets, so attentive is likely ancestral; its forms is not inferable
parental care - dinosaurs on nests
oviraptorids and troodontids on clutches; parental care proposed, challenged
conservation seven crododylains
are critical endangered
about half threatened
asia hit hardest
pterosauromorpha
pterosaur-like braincase and inner ear
pterosaur
wing on a highly elongated 4th finger
pterodactyloidea
short tail; long neck and skull
azdarchoidea
toothless jaws
pterosaurs - powered
flight, evolved separately
pterosaurs - range
228-66 Mal gone at the K-Pg
pterosaurs and avialans
evolved flight separately twice within ortinodira line
dinosaur =
the last common ancestor of Triceratops and birds, and all its descendants
birds are dinosaurs, “non-avian dinosaurs” is a paraphyletic grade
dinosauria stable 3 clades
ornithischians (Triceratops, Stegosaurus), sauropodomorphs
(Brachiosaurus), theropods (Tyrannosaurus, birds).
ornithischians
Triceratops, Stegosaurus
sauropodomorphs
(Brachiosaurus
theropods
Tyrannosaurus, birds
Ornithischia =
beaked plant-eaters
Ornithischia shared traits
predentary → extra bone at the lower-jaw tip, sheathed in a beak
backward-pointing pubis → more room for a plant-fermentating gut
leaf-shaped teeth - and likely cheeks
Ornithischian specializations
armor
domes and frills
dental batteries
nesting
Ornithischian specializations - armor
osteoderms in thyreophorans; stegosaur plate f unction debated
Ornithischian specializations - dental batteries
hadrosaurs": interlocked teeth form one grinding surface
Ornithischian specializations - domes and frills
thick skull roofs; frills and a new beak bone
Ornithischian specializations - nesting
maiasaura nests with worn-toothed nestlings: parents likely fed young (inference)
saurop
two legs to four - stance mapped on the
sauropodomorph tree
plateosaurus
two-legged, late triassic
massospondylus
two-legged, early jurassic
mussarus
shifted with age/either
young on four legs, adults on two
ledunahavdi
four-legged, crouched forelimbs
sauropods -
four legs, columnar limbs
two legs to four - more than once
four-legged walking arose separately in the ledmahadi lineage (crouched arms) in sauropods (pillar limbs)
two legs to four - size first
giant size came before the sauropod limb design
how sauropodomorphs went from two legs to four
limb bones
step by step
growth
trackways
how sauropodomorphs went from two legs to four - limb bones
ledumahadi: thick, crouched limbs - a separate route to four legs
how sauropodomorphs went from two legs to four - step by step
sauropod ankle and arm traits added gradually, not all at once
how sauropodomorphs went from two legs to four - growth
mussaurus center of mass moved toward the hip as it grew
how sauropodomorphs went from two legs to four - trackway
two-legged and four-legged sauropodomorph track occurs in late triassic age strata
how sauropodomorphs went from two legs to four - not “stay juvenile”
in mussarus, the shift came from a growing tail, so sauropods probably did not turn quadrupedal by keeping baby proportions
theropods are the
bipedal predators and birds
theropods shared traits
blade-like serrated teeth, large grasping hands, a flexible joint within the lower jaw’ always two-legged
theropods diets - not all
meat-eaters
split into fish-eaters, bone-crushers, and beaked plant- and omnivore-eaters
theropods diets - spinosaurids
long snouts, conical teeth; ate much aquatic food
theropods diets - tyrannosaurus
huge skulls, deep-rooted teeth
bone-crushing bite; tiny two-fingered arms
theropods diets - Ornithomimosaurs
toothless beaks, long legs
omnivores or herbivores
feathers on the theropod tree
evolved in the middle of the tree
maniraptoran traits
larger brain, long arms
half-moon wrist bone lets the hand fold
vaned feathers