Derivatives include respiratory system liver pancreas gall bladder and endocrine structures All are endodermal in origin Digestive System includes digestive tract Mouth amp Pharynx Small Intestine ID: 926721
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Slide1
Digestive System and Derivatives
Derivatives include respiratory system, liver, pancreas,
gall bladder and
endocrine
structures
All are endodermal in
origin
Digestive System includes
digestive tract
Mouth & Pharynx — Small Intestine
Esophagus — Large Intestine
Stomach — Cloaca (or derivative)
Also includes associated
digestive glands
: liver, pancreas and gall bladder
Slide2Figure 13.1
Fig 13.1
– Digestive tract components
Slide3Embryonic Origin of Digestive Tube
Embryonic
Origin of Digestive Tube by 2 Basic Methods
Cyclostomes, Actinopterygians, and Amphibians = gastrulation provides a “tube-within-a-tube” arrangement.
Inner
tube is
endodermally
derived and becomes
gut.
All
other vertebrates
have:
The
epiblast
oriented on top of the hypoblast in flat sheets. The hypoblast is
continuous
peripherally with the endoderm of the prospective yolk sac.
Development
of head, lateral body, and tail folds separate the embryo from
extraembryonic
membranes.
The
endoderm folds upon itself to form a tube continuous ventrally with the
yolk sac
forms
the gut
.
Slide4Development of Openings to Gut Tube
Protostomes
= blastopore forms the mouth; the anus is derived secondarily
Includes Annelids, Molluscs, and Arthropods
Deuterostomes
= blastopore becomes the anus; the mouth forms later as an independent
perforation
of the body
wall
Includes
Echinoderms and
Chordates
In vertebrate development the head turns downward over the surface of the yolk, forming an ectodermal pocket (
stomodeum
) which represents the primitive mouth
cavity
Slide5Development of Openings to Gut Tube
Stomodeum
is separated from the pharyngeal region of the gut by a membrane (pharyngeal membrane) that eventually breaks down so that the oral cavity and pharynx become continuous.
Proctodeum is similar invagination at the posterior end of the gut, separated from the gut by the cloacal membrane that eventually disappears, leaving a tube open at both ends
.
The mouth and teeth are
derived from ectoderm.
Slide6Figure 13.2
Fig 13.2
– Embryonic formation of the digestive system
Early
amniote
embryo
Generalized
amniote
embryo
Ventral view of isolated gut
Lateral view of differentiating gut
Slide7Development of Openings to Gut Tube
The
boundary of the mouth ideally is the junction of the stomodeum
(ectodermal) with the pharynx (endodermal). In practice, definite anterior and posterior limits to the mouth are difficult to establish, and differ among vertebrate groups.Landmarks
used in distinction as markers of the mouth (
ectodermally
derived) include:
Nasal Pits (= nasal
placodes
)
Rathke’s
Pouch (=
hypophyseal
pouch)
Evolutionary
trend: toward inclusion of more ectoderm inside the mouth in advanced formsPrimitively, stomodeal structures are forced outside the mouth through differential
growth
Slide8Figure 13.4
Fig 13.4
– boundaries of the mouth cavity
Slide9Mouth Cavity
Lined
by skin, includes teeth and salivary glands as components
Teeth are homologous with the integument of some fishes and placoid scales (denticles) of shark
skin
Location
of teeth
Fish
= found on palate (roof of mouth), margins of jaw, gill
arches
Amphibians/Reptiles
= found on some bones of the palate and margins of
maxillary
,
premaxillary and dentary bones
Mammals = found only on margins of maxillary, premaxillary and
dentary
bones
Slide10Mouth Cavity
Evolutionary trend in mammals = reduction
in numbers of teeth from primitive to advanced mammals
Primitive mammal number is 44 (humans with 32) Whales
have an increased number as a specialization to their very large
mouth
Birds
have no teeth, except for primitive Mesozoic forms
(
associated with reduced weight for flight
)
Turtles
also lack teeth; instead have a hard, keratinized
beak
Number
of generations of teeth is reduced from primitive (continuous replacement) to advanced (1 or 2 sets) vertebrates
Slide11Degree of Tooth Differentiation
Homodontous
Condition = all teeth are similar,
generally conical in shape Most vertebratesHeterodontous
Condition = specialization of
teeth
Typical state for
a few reptiles, Therapsids, and
Mammals
Teeth
include:
Incisors
(front) - used for
croppingCanines - behind the incisors, used for tearing
Molars (cheek teeth) - furthest back in mouth, used for
chewing
Teeth
in
heterodontous
vertebrates are used for capture or cropping of food and
chewing
Chewing
aids in digestion by increasing surface area of food available for
digestion
This
increases digestive efficiency and provides energy necessary to support high rates
of
metabolism
of mammals
Slide12Homodontous
Teeth from salamander
Heterodontous
Teeth from fox
Slide13Salivary Glands
Formed
from invaginations of the mouth lining
Mucous Glands = produce mucous; lubrication of
food
Serous
Glands
=
watery
secretion containing enzymes; initiates digestion of
carbohydrates
(salivary amylase)
Mixed
Glands
= mucous and serous secretionsSnake venom glands are modified serous salivary glands
Slide14Fig 13.37
– Salivary glands in a dog
Slide15Fig 13.35
– Oral glands of reptiles. Venom glands derived from
Duvernoy’s
gland.
Slide16Palate
Forms roof
of mouth
Composed of bone, lined by epithelium and connective tissue Fish, Amphibians and Birds have only a primary palate
present
Crocodilians
and mammals also have a secondary palate, which allows
simultaneous
chewing and breathing in mammals, and breathing while
mouth
is submerged in
crocodiles
Secondary
palate separates nasal passages
from
mouth
Slide17Fig 7.57
– Primary and Secondary palates in vertebrates
Slide18Pharynx
Shared region between
digestive and respiratory systems – Respiratory
system represents a derivative of the digestive tract. Other pharyngeal derivatives
Thyroid
- present in all vertebrates, always derived as
outpocketing
from floor
of
1st
pharyngeal
pouch
Fish
= thyroid tissue becomes dispersed along the ventral aorta in adults
Tetrapods = remains as a single or bilobed gland
Function = produces Thyroid Hormones that increase metabolic rate and regulate early
development
and
growth
C-cells
are also present (only in mammals
); produce
Calcitonin
which decreases blood calcium levels by reducing bone
resorption
Slide19Other Pharyngeal Derivatives
Parathyroids
- not present in fishes; present in all
tetrapodsAmphibians and Reptiles = derived from ventral regions of pouches 2-4
Birds
= from ventral regions of pouches
3-4
Mammals
= from dorsal regions of pouches
3-.
Secrete
parathyroid hormone which increases blood calcium levels by promoting
bone
resorption
Slide20Other Pharyngeal Derivatives
Thymus
- found in all vertebrates except Cyclostomes
Derived from various pouches in the different vertebrate groups
Function
: immunological role, production of T-lymphocytes
cell-mediated
immunity
Ultimobranchial
Bodies
= derivatives of ventral part of 5
th
pharyngeal pouch in all vertebrates
except mammalsSecrete Calcitonin, so they are presumably homologous with C-cells of mammalian
thyroid gland1st
Pharyngeal Pouch forms
spiracle
in
Elasmobranchs
Forms
the tympanic cavity and Eustachian tubes in
Tetrapods
Slide21Comparative
Pharyngeal Pouch
Derivatives in
Vertebrates
Slide22Digestive Tube Proper
General Sequence:
anterior to posterior is Esophagus
Stomach Intestine Cloaca (or anus)
Esophagus
:
Function
= food transport; secretes mucus to aid
passage
Birds
show specialized
Crop
= sac-like structure adapted for food
storage
Slide23Stomach
None present in
Cyclostomes, chimeras, lungfish, and some teleosts
(primitive condition) When present, functions in food storage, physical treatment of food, initiates digestion
Food
storage is the
primary
function (and probably the original evolutionary function
)
Physical treatment evolved somewhat later as food is taken in large
chunks
Digestion
probably is latest function to
evolve
Slide24Stomach
Birds and Crocodiles
Muscular tissue of stomach is concentrated posteriorly as a
gizzard Anterior stomach is glandular (Proventriculus
)
Because
birds lack teeth, many will swallow small pebbles (
grit
) that lodge in the
gizzard
and aid in grinding
food
Functional analog
to teeth in
mammals
Slide25Stomach
Ruminant Mammals
(Cud-chewing Ungulates) Possess
ruminant stomach with 4 chambers When food is eaten it enters rumen and
reticulum
which reduce the food to
pulp
Microorganisms are present that aid in the breakdown of complex carbohydrates in plant
material
The
cud is then regurgitated for more
chewing
After
chewing the cud, the
remasticated
material passes to omasum and abomasum where physical and chemical processing similar to normal mammalian stomach
occursThe rumen, reticulum, and omasum
are derived as modifications
of esophagus
;
abomasum
is the true
stomach
Ruminant-like digestion occurs in one bird, the
Hoatzin
Folivorous
(eats leaves) bird with foregut fermentation similar to ruminant
digestion
Enlarged crop & lower
esophagus house symbiotic
bacteria
Slide26Fig 13.42
– Ruminant digestion in the bovine stomach
Slide27Foregut fermentation in Hoatzin digestive system
Slide28Intestine
Majority
of digestion and absorption occurs here
Sharks and some other fishes have a spiral intestine = cigar-shaped body with spiral valve internallyGreatly
increases surface area for
absorption
Increased
surface area in
Tetrapods
is by elongation and coiling of intestines along with folding of internal
surfaces
Intestine
is
longer
in herbivores than in carnivores because
plant matter is more difficult to digest
Slide29Intestine
Evolutionary
Trend in intestine structure = increased
intestinal surface area (primitive advanced) associated with higher metabolic rates in advanced
vertebrates
Hagfish
lack spiral valve; poorly developed in
lampreys
Spiral
valve is present in sharks and some other
fishes
Elongation
and coiling with internal folding in
Tetrapods
Slide30Fig 13.27
– Stomach and Intestines in non-mammalian vertebrates
Slide31Figure 13.28
Fig 13.28
– Stomach and Intestines in various mammals
Slide32Fig 13.29
– Digestive tracts of various fishes. Note spiral valves in several species and elongation of intestine in perch