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Triassic faunas
Almost no Ornithiscians
Relatively small
Oldest well-preserved remains are early Triassic
Dominated by archaic mammal and reptile groups and labyrinthodont amphibians
Late Triassic to Early Jurassic distribution
Cosmopolitan —> faunas are very similar throughout the world
Middle Jurassic onwards distribution
Endemic faunas developed as the continents divided
Late Triassic dinosaur faunas
Theropods include basal members such as Herrerasaurus and Coelophysis
Prosauropods first appear and are abundant
Ornithischians are rare and poorly known
End Triassic extinctions
~200 mya
Rhynchosaurs, most labyrinthodonts, large mammal relatives like dicynodonts, and large crocodylian relatives (aetosaurs, rauisuchids, phytosaurs) go extinct
Large marine extinction
Immense volcanic activity
Increased atmospheric CO2
Greenhouse conditions
Early Jurassic dinosaur faunas
Low diversity
No rapid radiation after End Triassic extinctions
Prosauropods common —> sauropods rare
Basal theropods
Ornithischians growing more common
Middle Jurassic dinosaur faunas
Poorly known part of the fossil record
Sauropods are common but not diverse
Ornithischians begin to diversify
Ankylosaurs, stegosaurs, and basal members
Theropods are diverse
When did Ornithischians begin to diversify?
Middle Jurassic
Late Jurassic dinosaur faunas
Sauropods dominate
Large theropods such as Allosaurus are present with small coelurosaurs including the earliest bird, Archaeopteryx
Ornithischians are diverse but not common
Ornithopods, ceratopsians, ankylosaurs, stegosaurs
Some endemism as Pangaea begins to split up
Early Cretaceous dinosaur faunas
Gondwana and Laurasia begin to develop endemic faunas
Basal ceratopsians such as Psittacosaurus common in Laurasian faunas
Iguanodonts are common in Gondwanan and Laurasian faunas
Sauropods common, mainly titanosaurs
Coelurosaurs, including birds, are diverse
When did the first flowering plants (angiosperms) appear?
Early Cretaceous
Early floras
Dominated by conifers, cycads, and ginkgoes
Cretaceous Terrestrial Revolution
The diversification of angiosperms and the related insect pollinators and herbivores in the Cretaceous
Late Cretaceous dinosaur faunas
Best known part of Mesozoic
Laurasia
Faunas of North America, Europe, and Asia are similar
Ceratopsians, ankylosaurs and hadrosaurs are common
Tyrannosaurids are the dominant large theropod
Titanosaur sauropods are present in many areas but not in the best known faunas of northern North America
Gondwana
Faunas of South America, Africa, Madagascar, India, Australia, and Antarctica are similar
Rich known faunas in South America and Madagascar
Titanosaur sauropods are common
Ornithischians are rare
No ceratopsians or pachycephalosaurs
Abelisaurid ceratosaurs are the dominant large theropod
Vicariance
Geographic distribution of groups within a taxon due to the breakup of regions by non-biological forces —> taxa have not moved, the Earth has changed
Dispersal
Geographic distribution due to movement of organisms between regions
How features that are not preserved are inferred using phylogeny and optimization
If we know the conditions in living animals they can be optimized (mapped) on a cladogram to infer the condition in extinct relatives for which we have no data —> if all living relatives have the same condition we would infer that the extinct forms have that condition
Character optimization
Infer genomic information about extinct taxa using genomes of living animals
Ancestral gene sequences inferred using the sequences of the living representatives and outgroups
Proteins can be manufactured from the inferred ancestral genome sequence and subjected to experiments
Can be done for the archosaur common ancestor of birds and crocodylians, but not for dinosaurs
Large size of many non-avian dinosaurs may have required them to evolve new features that are not found in living archosaurs
Osteological correlates
Features on bones indicative of particular soft tissues
Archosaur features (derived features of birds and crocodylians)
Extensive air sacs in the skull
Unidirectional air flow during respiration
Parental care of young
Vocalization
Four chambered heart with completely separated circulation in the heart
Egg shells are hard, not leathery
Males had a penis
Scales and possibly feathers were composed of Beta keratin
Features of birds that may have evolved within non-avian dinosaurs
Endothermic (warm-blooded)
High metabolic rate
Incubated eggs within their nests
High growth rate and age of sexual maturity
Had nasal turbinates (or similar soft tissue to cool the brain)
Completely divided blood flow
Had a crop/gizzard
Been active fliers
Breathed by moving their sternum
Extensive air sacs throughout body
Had a cerebellum and cerebrum
Ears sensitive to sound
Genetic sex determination
Evidence for endothermy in non-avian dinosaurs
Surface area does not increase as fast as volume when animals get larger
Large animals have a problem getting rid of body heat (which is done mostly through the skin) once they have warmed up
Bone tissues indicate that dinosaurs were active, possibly warm-blooded animals (Robert Bakker)
Extensive vascular canals
Predator-prey ratios
There are fewer carnivores in warm-blooded communities
Dinosaurs were built like active animals
Erect posture of hindlimb bones
Dinosaurs out-competed the mammals during the Mesozoic, which cold-blooded animals could not do
Birds are warm-blooded, and since they descended from dinosaurs then dinosaurs may have been warm-blooded
Feathers in non-avian dinosaurs suggest that they insulated internally produced heat
Dinosaur localities known near the poles, only endotherms can survive those regions today
Lipid oxidation byproducts in fossils suggest the ancestral condition in dinosaurs was endothermy
Evidence against endothermy in non-avian dinosaurs
Vascular canals are found in reptile bones occassionally
Not directly linked to endothermy
Biases of the fossil record make predator-prey ratios difficult to measure
It is difficult to tell how active an animal is from the shape of its bones
Mammals evolved endothermy during the Mesozoic, yet dinosaurs “out-competed” them
Growth lines in dinosaur bone indicate they had a lower metabolism during the winter, like ectotherms
No evidence of nasal turbinates in dinosaurs (like in birds)
Lines of Arrested Growth (LAGs)
Mammal and bird bones do not have growth lines
For most, growth doesn't slow in the winter
Growth rates in living animals are correlated with metabolic rate
High metabolic rates of endotherms produce faster growth
Maximum growth rates should only consider growth during the rest of the year, and not be an average for an entire year
Exclude slower seasonal growth
A 2014 calculation using whole growth rings shows dinosaurs have a mesothermic growth rate, lower than mammals and birds but higher than crocodylians
Endothermy
Warm-blooded
Relatively constant high body temperature
Higher metabolic rates
Enzymes are most effective with a narrow range of temperatures in which they are active
Ex. birds and mammals
Ectothermy
Cold-blooded
Gain heat from outside the body
Maintain a relatively constant body temperature through behavior
Ex. sunning themselves, evaporative cooling
Ex. reptiles, crocodylians
Poikilotherms
Ectothermic animals that can vary their body temperature
Homeothermy
Variation in body temperature in endotherms
Evidence suggests that large sauropods were homeothermic due to thermal inertia in the huge bodies
Stable isotopes suggest homeothermy in many dinosaurs
End Cretaceous (K-P) extinctions
Large marine extinction
Ammonites and belemnites
Species on sea floor were impacted less
All dinosaur species except birds extinct
Plants suffered extinctions in some areas
A “fern spike” (a layer dense with fern spores) occurred at the very end of the Cretaceous, lasting about 1,000 years
Freshwater animals like turtles, fish, amphibians and crocodilians suffered less than fully terrestrial animals
Impact Theory
Leading hypothesis for the cause of the extinction of non-avian dinosaurs
Iridium is a rare earth element that is 10,000 times more common in extraterrestrial dust and meteorites than in the Earth’s crust
At an end-Cretaceous rock section at Gubbio, Italy, Walter Alvarez found a sharp increase in Iridium
In 1980 he and his father proposed the theory that the extinction was caused by the impact of an extraterrestrial object
Soon after the discovery of Iridium, the same layers produced granules of quartz that were “shocked”
Shocked quartz results from extremely strong stresses, and is rare on Earth except in volcanic eruptions and meteor craters
Shocked quartz and iridium were soon found in a number of localities around the world preserving the K-P boundary
Tektites are found at known meteor impact sites and at times of suspected large impacts
Occur at the K-P boundary in deep sea cores
Chicxulub crater in the Yucatan
Alternative hypothesis for the extinction of non-avian dinosaurs
Climates change during the Cretaceous
Became warmer until about 90 mya then gradually cooling until the very end 66 mya, rising again just before the end of the Cretaceous
Sea level dropped very low at the end of the Cretaceous
This caused the continental seaway across North America to disappear, so that much of the continental shelf was above water
Probably caused some marine invertebrate extinction
Greenhouse conditions resulting from volcanic eruptions
How extinctions are studied in the fossil record
Extinction is recognized by the disappearance in the fossil record of a species or group of species present in older rocks
Examining taxa a particular taxonomic level
Species-level diversity is largely artifactual because species have limited geographic ranges, and species diversity often reflects only the abundance of available rocks in an area or at a particular time, or the number of geographically separated sites
Pseudoextinctions, in which one taxon evolves into another (like dinosaurs and birds), must be recognized and ignored
Fossil record has many biases and gaps
Evidence for dinosaur diets
Indirect
Tooth structure and correlations with diet in living animals
Gastroliths
Stable isotopes
May reflect the diet of animals, since the food is metabolized and its byproducts incorporated into bone and teeth
Direct
Fossilized stomach contents
Coprolites
Rarely associated with skeletons, so difficult to identify the maker
Tooth marks on bone indicate prey
Fossilized predator-prey interactions
How trackways are used to estimate speed
Most trackways preserve stride length
The length of the limbs can be inferred from the size of the footprint and the identity of the trackmaker
In general, stride increases with speed
Relationship differs between species
Dimensionless speed (DS)
DS = speed/√(leg length x gravity)
Estimating leg length and assuming gravity has always been 9.8 m/sec2, we can calculate speed from DS
Evidence for color in feathers and eggshells
Study pigment cells (melanosomes)
Different melanosomes of bird feathers have different shapes
Pigment chemicals or their decay products can sometimes be found preserved in fossils
Only the colors due to melanosomes have been reconstructed
Does not account for other types of pigment cells
Biomolecules known in non-avian dinosaurs
Once fossils petrify, they trap molecules with the bone matrix, as do cross-linkages
Studies in 2018 and 2019 found that crosslinking processes such as glycoxidation and lipoxidation could preserve as flexible 3D polymers
Proteins such as keratin and collagen but not DNA are known from non-avian dinosaur fossils
How DNA and amino acid sequences are used to infer phylogeny
Same gene or protein in different organisms is aligned
Aligning them shows which sites on the gene are the same in all species and which are variable
Alignment is complicated because there are gaps and insertions in some sequences
How to sex dinosaurs
Must be differences in the skeletons of the two sexes (sexual dimorphism)
When female birds lay eggs, calcium is taken from the bone to be deposited in the egg
Often first deposited as medullary bone
Only present in some females