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Dr. Allen
Paleozoic era
Cambrian period (~ 541 - 485 million years ago)
Four major continents (after Rodinia broke up):
Gondwanaland/ Gondwana (Southern continent)
Laurentia (North America, Greenland)
Baltica (Scandinavia)
Siberia
Oceans:
Panthalassa
Lapetus
Late Cambrian ~ 514 million years ago
Cambrian Explosion
Appearance of major animal bauplans (body plans) in the fossil record
Metazoans:
Multicellular and eukaryotic
In Kingdom Animalia
Primary germ layers:
Diplobastic vs Triploblastic
Symmetry:
Radial vs Bilateral
Developmental biology
Biomineralized skeletons
Complex food webs and ecology
Predator-Prey arms races
Animal Body Plans
Porifera
Sponges
Cnidaria
Jellyfish
Platyhelminthes
Flatworms
Rotifera
Rotifers
Nematoda
Round worms
Mollusca
Mollusk
Annelida
Segmented worms
Arthropoda
Insects, Crustaceans
Echinodermata
Crinoids, Sea urchins
Chordata
Vertebrates
Burgess shale
~ 509 million years ago (Middle Cambrian) on Laurentia
This drawing depicts a recontruction of the acient reef (Cathedral Escarpment) that hosted the Burgess Shale animals
Superimposed are the quarry site, the town of Field, and the surrounding mountains we see today
The animals lived in the ocean, but today are found on a mountain ridge between Wapta Mountain and Mt. Field
Beginning ~ 175 million years ago, mountain-building forces moved the fossils from their burial grounds on the sea floor eastward on huge faults to their current positions
Burgess shale site
Named after the Burgess Pass in Yoho National Park in the Canadian Rockies, British Columbira, Canada
Black shale formation extends for many miles
Konservat Lagerstatten
Discovered in 1909 by Charles Dolittle Walcott
Excavated ~ 65,000 specimens (now in the Smithsonian)
Significance of the finds wasn’t realized at the time of discovery
Walcott simply placed the unusual new species within the phyla known to exist during that period, a process Stephen Jay Gould dubbed “shoehorning” (lumping) in his book about the Burgess Shale, Wonderful Life (1989)
Some of the fossils represent animals with no known descendants and that are difficult to classify
Opabinia regalis
Anomalocaris canadensis
The Paleo Dive Game features some Cambrian life
Anomalocaris, complete specimen
Disarticulated parts of Anomalocaris were originally assigned to three different animal phyla
Frontal appendages
Thought to be shrimp-like (Arthropoda)
Circular mouth parts
Thought to be a jellyfish (Cnidaria)
Main body
Thought to be a see cucumber (Echinodermata)
In 1978 Simon Conway Morris reexamined some of the specimens
In the 1980’s Harry Whittington and Derek Briggs uncovered intact specimens of Anomalocaris showing all three features connected as parts of an early stem-group arthropod (Radiodonta)
Interesting Burgess Shale Fauna
Haplophrentis carinatus
one-inch fossil
extinct mollusk with an operculum
Marella splended
Ancestrial anthropod
Hallucigenia sparsa
A panarthopod, like a velvet worm
Pikaia gracilens
an early chordate
Metaspriggnia walcotti
an early chordate
Punctuated Equilibrium
Stephen Jay Gould suggested that the great diversity of fossils indicate that life at the time was much more diverse than that surviving today and that many of the unique lineages were evolutionary experiments that became extict
Burgess shale fauna has been used in support of evolution by punctuated equilibrium rather then gradualism (also called phyletic gradualism)
However, much of the radiation in animal life can be traced back to the Precambrian
Radical shift in abundance of hard parts and increase in preservation potential
Chengjiang, China
Another important Lagerstatten of the Cambrian, Yunnan province, China
Maotianshan shales of the Early Cambrian (518 -520 million years ago)
Mostly soft-bodied organisms
Shares ~15% of genera and ~85% of phyla with Burgess Shale
Trilobites as Index Fossils for the Cambrian
Late Cambrain
Monkaspis
Middle Cambrain
Paradoxides
Early Cambrain
Olenellus
Post-Cambrian Life
Cambrian-Ordovician extinction event at ~485 million years ago
Wiped out 10% to 50% of global species such as trilobites and brachiopods, reducing their diversity and abundance
Jawless fish (aganthans) rose in dominance, including armored types called ostracoderms and eel-life conodonts
Conodonts were known for their hard mineralized tooth-like “conodont elements”
Archeognathus primus
Manticolepis subrecta
Ostracoderms
Armored heads
Round or slit-like mouths
No paired fins
Horseshoe Crabs
Lunataspis is a stem xiphosuran
Limulus polypheus (extant)
Eurypterids
“Sea urchins”
Gigantism in Paleozoic arthropods is well documented
Large dragonfly-like flying forms and giant millipedes
High oxygen levels in the atmosphere
Gigantism is also seen in trilobites of the Ordovician and eurypterids of the Devonian
Decline of Eurypterids due to Competition with Vertebrates
Suborder Stylonurina
Benthic scavenger, sweeping feeding
Suborder Eurypterina
Active, nektonic predatory
“Mass-moult-mate” Hypothesis of Eurypterids
Proposed: Mass migrations of Eurypterus in the style of extant horseshoe crab (Limulus)
Moults vs mortalities: Disarticulation patterns support moulted appendaged
Salinity tolerance cannot be tested
Findings didn’t fit with prediction of male dominance in gender ratio (compared to Limulus)
Based on the results, a revised mass-mate-spawn-moult hypothesis was proposed:
Following mating, males left the breeding area to return to deeper waters (where they moulted), whilst females remained behind to fertilize their eggs
Questions remain about whether gender ratio was interpreted correctly