Axial Skeleton
Notochord
serves as a skeleton but is not made of bone or cartilage
serves as a stiffening/structural feature in chordates
construction
cells with large vacuoles, surrounded by a layer of collagenous tissue and a layer of connective tissue
the two sheaths are functionally the same
acts as a hydrostatic skeleton, medicated by vacuole pressure
longitudinally rigid (resists compression) and latitudinally flexible (allows for bending along length)
Biomechanics
moves via alternation muscle contractions
functions similarly to swimming flippers in movement
side to side movement allows for forward propulsion
along with nerves and muscles, it can create (lateral) undulating power strokes
Manifestations
Urochrodata
lose notochord as adults
present in plankton
Chephalochordata
notochord continues beyond the nerve cord at the front of the body (beyond oral opening)
Craniate (origins)
Conodont
fossils of small teeth from the Cambrian → found worldwide
could be used to map (stratographic fossils)
Belonged to organisms with small eyes→ Fossil found in the 1990s
maybe/possibly craniates
“Agnatha” & “Ostracoderms”
earliest unambiguous fossils of Craniata date from the late Cambrian to the early Ordovician
Ostracoderms
have armored-plated bodies (scale-like) with large head shields
often had ornamentation on bony plating
Tail-like body
had notochord and nerve cord
Head-like structure
nose→ sensing food
eyes→ seeing predators/food
ears→ allows for course corrections during movement (functioned as a balancing structure)
All of this indicated movement for longer distances in open water columns
brain
allowed for sensory processing
developed via the nerve cord getting larger at one end
likely moved to their food
mobile, impatient, active
tendency to be macro-phagus or exhibit predatory behavior
larger than tunicates and cephalochordates (Amphioxus)
have an optimal/efficient tempo for movement
Cyclostomes→ “cylindrical mouths”
remaining agnathans
lamprey → parasitic
has neural arches
blocks of cartilage added on top of notochord
provide extra anchors for musculature
FIRST LEGITIMATE VERTEBRATES
hagfish
have a notochord and dorsal nerve cord
move via ungulatory motion
Notochord → hydrostatic stiffening rod
allows bounce back after bending
resists compression, permits flexion
facilitates aquatic locomotion through side-to-side undulation
Urochordates: notochord only in larval (motile) stages, in tail only
Cephalochordates: notochord persists throughout life & spans the entire body length
Craniates: notochord persists throughout life in primitive forms, but only posterior to the midbrain
In more advanced forms, the notochord is progressively reduced and replaced by a vertebral column
Agnatha (jawless fishes)
Hagfishes (Myxini): notochord persists unrestricted
“Ostracoderms” only trace impressions of vertebral arch elements; presumably, notochord persisted, largely unrestricted
Lampreys (Petromyzontida): notochord persists unrestricted. Arcualia in first few postcranial segments
Placoderms
Bony vertebral arch elements: neural & hemal arches. In between, the notochord was presumably unrestricted (cartilaginous central possible but not fossilized)