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Homologous vs. Analogous features
Homologous: equivalent structure, common ancestor; Analogous: equivalent structure, convergent evolution,
Synapomorphy definition + examples
Exclusive shared derived character from most recent common ancestor; Ex: Mammals (hair, mammary glands), Tetrapods (four limbs with digits),
Skeleton classification
Postcranial: Axial (skull, vertebral column, ribs, sternum), Appendicular (girdles, appendages); Cranial: Splanchnocranium, Chondrocranium, Dermatocranium,
Mesenchyme
Undifferentiated stem
Neural crest
Migratory stem cells → teeth, cartilage, smooth muscle, endocrine tissue,
Endoderm
Innermost germ layer → GI tract + organs (pancreas, etc.),
Mesoderm
Middle germ layer → skeletal, muscular, excretory systems,
Ectoderm
Outer germ layer → epidermis, hair, enamel, nervous/endocrine tissue,
What is the somite
Mesodermal blocks → dermatome, myotome, sclerotome,
Dermatome
Forms dermis,
Myotome
Forms skeletal muscles,
Sclerotome
Forms vertebrae + ribs,
Dermatocranium
Outer skull covering, from dermal bone,
Chondrocranium
Brain/support structures,
Splanchnocranium
Gill support → jaws,
Jaw articulation Paleostyly
Arches separate from skull,
Jaw articulation Euautostyly
Jaws attach directly to skull,
Jaw articulation Amphistyly
Double connection (palatoquadrate–braincase + hyomandibula),
Jaw articulation Hyostyly
Lower jaw attached via hyomandibula (sharks),
Jaw articulation Metautostyly
Lower jaw attaches via quadrate,
Jaw articulation Craniostyly
Upper jaw fused to braincase, lower jaw suspended by dermatocranium (mammals),
Cranial kinesis
Skull bone mobility for feeding (snakes, birds),
Modes of cranial kinesis and what they are
Metakinesis (Whole upper jaw), Mesokinesis (Middle of upper jaw), Prokinesis (Front of upper jaw), Streptostyly (Entire lower jaw moves)
Jaw–ear connection
Quadrate and articular bones become incus and malleus of the middle ear.
This illustrates how jaw elements were repurposed for hearing
Temporal fenestrae evolution
Anapsids: none; Synapsids: one low opening; Diapsids: two; Euryapsids: one high opening,
Atlas
Holds head upright,
Axis
Allows head to move side to side
Cervical vertebrae
Support head, increase mobility,
Thoracic vertebrae
With ribs, aid respiration + trunk stability,
Lumbar vertebrae
Rib-free for locomotion and mobility
Sacral vertebrae
Fused, connect pelvis to axial skeleton,
Caudal vertebrae
Tail, locomotion, balance,
Amphicoelous vertebrae
Both ends concave (fish), flexible, weak under compression,
Procoelous vertebrae
Anterior concave, posterior convex (reptiles), stable, flexible,
Opisthocoelous vertebrae
Anterior convex, posterior concave (amphibians/mammals),
Acoelous vertebrae
Flat ends (mammals), resist compression, support weight,
Heterocoelous vertebrae
Saddle
Arcualia
Primitive incomplete vertebral elements (lamprey); precursors to vertebrae,
True ribs
Connected to sternum,
False ribs
Connect to another rib, not sternum,
Floating ribs
No anterior articulation,
Cranial
Toward head,
Caudal
Toward tail,
Rostral
Toward nose,
Anterior
Toward front,
Posterior
Toward back,
Dorsal
Toward back,
Ventral
Toward belly,
Proximal
Closer to origin,
Distal
Away from origin,
Palmar
Toward palm,
Plantar
Toward foot sole,
Pectoral girdle evolution
Originated earlier, supported fins, connected to skull then separated, diverse functions,
Pelvic girdle evolution
Appeared later, anchored to vertebral column, conservative, locomotor support,
Stylopodium evolution
One large proximal element (humerus/femur), conserved,
Zeugopodium evolution
Paired bones (radius/ulna, tibia/fibula), reduction/specialization,
Autopodium evolution
Early polydactyly, standardized pentadactyly, specialized reduction (horses, birds),
Gill theory
paired fins evolved from gill (branchial) arches.
Fin-fold theory
paired fins originated from continuous lateral folds of skin along the body.
Pneumatic bone
Air spaces, lighter (birds, dinosaurs),
Apneumatic bone
Solid, heavy, stronger under compression,
Epidermis
Outer epithelial layer, keratinized,
Basement membrane
Anchors epidermis to dermis,
Dermis
Connective tissue; vessels, glands, follicles,
Hypodermis
Fat storage, insulation, connection to muscle,
Hair
Keratinized, insulation, sensory,
Nails/claws/hooves
Keratinized tips, protection, locomotion,
Beaks/horns
Keratinized coverings, feeding/defense/display,
Glands
Sebaceous, sweat, scent, mammary,
Teeth
From dermal armor, enamel + dentine,
Muscle structure hierarchy
Myofibril → fiber → fascicle → muscle; CT = endomysium, perimysium, epimysium,
Flexion
Decreases angle at joint,
Extension
Increases angle at joint,
Elevation
Up,
Depression
Down,
Abduction
Away laterally,
Adduction
Toward midline,
Pronation
Radius crosses ulna (palm down)
Supination
Radius uncrosses ulna (palm up)
Lateral flexion
Bending sideways,
Internal rotation
Toward body,
External rotation
Away from body,
Epaxial musculature
Dorsal: with vertebrae, ribs, skull base,
Hypaxial musculature
Ventral: locomotion, respiration, prey capture,
What features unite all chordates?
Notochord, dorsal hollow nerve cord, pharyngeal slits, endostyle/thyroid, postanal tail
What additional features define vertebrates?
Cranium, vertebral column, neural crest cells
What chordate like traits are found in echinoderms?
Larvae have bilateral symmetry and are free floating
What chordate like traits are found in hemichordates?
They have pharyngeal slits, some bilateral symmetry, and some are free floating but lack a notochord and dorsal hollow nerve cord
Why is metamorphosis important for understanding chordate origins?
Metamorphosis – Tunicate larvae show chordate traits (notochord, dorsal nerve cord, postanal tail, pharyngeal slits). These traits are lost in adults, suggesting early chordates came from a larval form that retained these features into adulthood (paedomorphosis).
Why is embryology important for understanding vertebrate origins?
Embryology – Embryonic development shows how chordate body plans form. Neurulation creates the dorsal hollow nerve cord; the notochord marks the midline. Somites form in paired blocks (bilateral symmetry). Pharyngeal arches function in filter-feeding in primitive chordates and become jaws/ear structures in vertebrates. Vertebrates also develop a head with specialized sense organs from unique embryonic tissues.
What is dorsoventral inversion in chordates?
Definition: In protostomes the nerve cord is ventral and the heart is dorsal. In chordates this is reversed: a dorsal hollow nerve cord above the notochord and a ventral heart.
Significance: Explains the unique chordate body plan, uniting traits around a dorsal CNS. Shows how a major evolutionary shift in body axes produced efficient, directed locomotion and distinguishes chordates from protostomes while using the same developmental toolkit.
Explain how body symmetry evolved and developed in early chordates and vertebrates.
Radial → Bilateral: Early animals (cnidarians) radial; bilaterians evolved bilateral symmetry for cephalization and movement.
Chordates: Bilateral body plan with notochord midline, paired somites, larval symmetry for swimming.
Vertebrates: Further refinement—cranium, vertebral column, paired appendages; external symmetry maintained for locomotion.
Significance: Bilateral symmetry supports efficient movement, nervous system coordination, and flexibility in paired structures.