Transcript Lecture #14
Lecture #14
Phylum Chordata
Phylum Chordata
• • only 45,000 species
characteristics:
– 1. bilaterally symmetrical – –
2. notochord 3. pharyngeal gill slits
– –
4. dorsal, hollow nerve cord 5. post-anal tail
– – 6. complete digestive system 7. thyroid gland – 8. ventral, contractile heart Numbers 2 – 5 may be in a unique combination and are found at some stage in development
Chordates Craniates Vertebrates Gnathostomes Osteichthyans Lobe-fins Tetrapods Amniotes Brain Notochord Milk Amniotic egg
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Legs
•
Lung derivatives
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Lobed fins Mineralized skeleton
• •
Jaws Vertebral column Head
• • • •
Ancestral deuterostome
• • •
Chordate classification characteristics:
Notochord? No echinoderms Brain? No Urochordate (tunicate) Head/Cranial cavity? No Cephalochordate (lancelet) Vertebral column? No Hagfish Jaws? No Lampreys Bony skeleton? No Rays Sharks, Lobed fins? No? Ray finned fish Lungs? lung derivatives? Coelocanth Legs? No Lungfish Amniotic egg? No Amphibian Milk? No Reptile
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Phylum Chordata
notochord:
– supportive rod that extends most of the animal’s length – extends into the tail – dorsal to the body cavity – flexible to allow for bending but resists compression – composed of large, fluid-filled cells encased in a fairly stiff fibrous tissue – will become the vertebral column in many chordates
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Phylum Chordata
dorsal, hollow nerve cord:
– runs along the length of the body – dorsal to the notochord – expands anteriorly as the brain – develops from ectoderm – BUT: in most vertebrates – nerve cord is solid and is ventral to the vertebral column
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Phylum Chordata
pharyngeal gill slits:
– series of openings in the pharyngeal region of the embryo – develop as a series of pouches separated by grooves – in some embryos – grooves develop into slits – used in primitive chordates for filter feeding – in aquatic vertebrates – transformed these slits/pouches into gills – embryonic in terrestrial chordates
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Phylum Chordata
SubPhyla:
– Urochodata: sea squirts (tunicates) • notochord, pharyngeal gill slits, and tail present in free swimming larvae –
Cephalochordata: amphioxus
• all four chordate traits persist through life –
Hyperotreti: hagfishes
• jawless, no paired appendages –
Vertebrata: vertebrates
• • • • • •
Subphylum Cephalochordata
known as the
lancelets
earliest diverging group of chordates get their name (Lancelet) from their blade-like shape
embryos develop: a notochord, a dorsal, hollow nerve cord, pharyngeal gill slits and a post-anal tail filter-feeders
– cilia draw water into the mouth swim like fishes – chevron shaped muscles on either side of the notochord
Muscle segments Notochord Dorsal, hollow nerve cord Brain Mouth Anus Muscular, post-anal tail Pharyngeal slits or clefts
Subphylum Urochordata
• • • • •
tunicates
embryonic/larval stage has the characteristics of the chordate
Incurrent siphon to mouth
larva swims to a new substrate and
undergoes metamorphosis
– to form the adult tunicate
Excurrent siphon retain the pharyngeal gill slits in the adults
water flows in through an incurrent siphon - filtered by a net of mucus on the pharyngeal gill slits
Atrium Pharynx with numerous slits Tunic Excurrent siphon Anus Intestine Esophagus Stomach
• • •
Early Chordate Evolution
research on lancelets had provided information on the chordate brain the same Hox genes that organize the vertebrate brain into forebrain, midbrain and hindbrain are found in lancelets tunicates have also been sequenced – numerous similarities with vertebrates
BF1 Otx Hox3
Nerve cord of lancelet embryo
BF1 Otx Hox3
Brain of vertebrate embryo (shown straightened) Forebrain Midbrain Hindbrain
Craniates
• • • • • •
chordates with a head
head – consists of a brain, surrounded by a skull, and other sensory organs living craniates all share a series of unique characteristics one characteristic is the development of
neural crest cells
aquatic craniates possess pharyngeal gill slits not clefts or pouches most basic craniate – hagfish
Neural Crest Cells
• • • • collection of cells that form as bilateral bands of cells near the developing neural tube migrate throughout the body major roles in forming the skull also play roles in forming many kinds of nervous cells – certain neurons – sensory structures
The cells give rise to some of the anatomical structures unique to vertebrates, including some of the bones and cartilage of the skull.
Vertebrates
• • • • branching off from the chordates involved innovations in the nervous system and skeleton –
more extensive skull
– development of the
vertebral column
composed of vertebrae • most vertebrates – vertebrae enclose a spinal cord (replaces the notochord) – development of fin rays in aquatic vertebrates adaptations in respiration and circulation –
more efficient gas exchange system – gills are modified
–
more efficient heart
adaptations in thermal regulation –
warm blooded vs. cold blooded
adaptations in reproduction –
amniotic egg
–
placental animals
Vertebrate Taxonomy
• • • • • most basal vertebrate – lamprey – jawless development of jaws marked the evolution of the
gnathostomes
development of lungs marked the evolution of
ray-finned fishes
development of lobed fins marked the evolution of
lobe finned fishes
development of limbs marked the development of
amphibians and reptiles
• • • •
The Jaw
lamprey have no jaws evolution of the jaw marked the development of the gnathostomes gnathostomes have jaws that evolved from skeletal supports of the pharyngeal slits
gnathostome characteristics:
– 1.
hinged jaws with teeth
– 2.
duplication of Hox genes
chordates – four sets of Hox genes vs. one set in early – 3.
enlargened forebrain
– with highly developed sensory structures – 4.
lateral line system
– in aquatic gnathostomes • for the detection of vibration
Gill slits Cranium Skeletal rods Mouth
Vertebrates & Thermoregulation
• • • • thermoregulation in vertebrates has two sources
1. internal metabolism – internal source of heat 2.
external environment – external source of heat
animals can be classified based on the heat that influences their body temperature –
ectotherms
– animals whose body temperatures are determined by external sources of heat – can also be considered to be poikilotherms (variable body temperature) –
endotherms
– animals whose body temperatures are determined by internal sources of heat – usually also considered homeotherms (constant body temperature)
Thermoregulation in Vertebrates
• • • • when energy from food is transformed into ATP and ATP is transferred into work – energy is lost in the form of heat – seen in both ectotherms and endotherms
endotherms produce more heat
– cells are less efficient at using energy vs. ectotherms – endotherm cells are “Leaky” to ions – endotherm must spend energy to keep its ionic “balance” – this causes an increase in the production of heat via ATP hydrolysis ectotherms = e.g. amphibians & reptiles endotherms = e.g. mammals & birds
Thermoregulation in Vertebrates
• • ectotherms regulate their body temperature through
behavioral mechanisms
– known as
behavioral thermoregulation
endotherms regulate their body temperature by altering internal metabolic heat production – can also use behavioral thermoregulation
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Thermoregulation in Vertebrates
ectotherms and endotherms can influence their body temperature using
4 ways of heat exchange:
– 1. Radiation - heat transfer from a warmer medium to a cooler one via the exchange of infrared radiation – 2. Convection – heat transfer to a surrounding medium (e.g. air or water) as it flows over a surface – 3. Conduction – heat transfer directly between two objects – 4. Evaporation – heat transfer away from a surface as water evaporates
Balancing Heat Loss and Gain
• • • • thermoregulation depends on the animal’s ability to
control the exchange of heat
essence of thermoregulation is to maintain rates of heat loss with equal rates of heat gain animals do this by either: – reducing overall heat exchange – favoring heat exchange in a particular direction many mechanisms involve the integumentary system – – 1. Insulation – fat, feathers & fur
2. Circulatory Adaptations
– 3. Evaporative Heat Loss – sweating & panting – 4. Behavioral Responses – hibernation, basking –
5. Adjusting Metabolism
Circulatory Adaptations
• • •
heat exchange between the internal environment and the skin is through blood flow
as body temp rises – blood flow to the skin increases – heat in the blood is lost to the environment through the 4 methods described in the previous slide ectotherms and endotherms can use blood flow to the skin to control their internal temperatures
• • • • • • •
Counter Current Exchange
seen in many birds and mammals
transfer of heat between fluids flowing in opposite directions
same principle as the exchange of respiratory gases seen in fish arteries and veins are adjacent to one another warm blood moves from the body core into the arteries – transfers its heat
to the cooler blood leaving via the veins
heat is exchanged along the entire length of these vessels – maximizes heat exchange also keeps the heat localized to that specific body area
Evaporative Heat Loss
• • • • • • endotherms must also be able to dissipate heat as environmental temperatures rise
1. increase of blood flow to the skin 2. evaporation of moisture
off the skin’s surface through sweating or across the oral mucosa through panting BUT water falling from the body in the form of saliva or excess sweat does not evaporate and does not cool the body thus, when the need for heat loss is greatest – excess sweating is a waste of that water sweating and panting are also active processes and require expending metabolic energy –
so a sweating animal generates heat when it needs to dissipate heat!!
• • • • • •
Metabolic Heat Production
heat production =
thermogenesis
chemical energy is derived from food nutrients from food are used to generate ATP the production and use of ATP generates heat the more ATP produced/used – the more heat generated
metabolic heat is used to establish core body temperature in endotherms
Physiologic Thermostats
• • • • • regulation of body temperature in mammals is brought about by a complex system based on feedback mechanisms sensors for thermoregulation found in the
hypothalamus functions as a thermostat
activates mechanisms that will promote heat loss – dilation of surface blood vessels – production of sweat activates mechanisms that will promote heat gain – shivering heat production
Energy Allocation and Use
• • bioenergetics = overall flow and transformation of energy in an animal – – determines the animal’s nutritional needs ATP production for : cellular work + biosynthesis, growth, storage and reproduction metabolic rate = sum of all the energy used in biochemical reactions over a given time interval – – energy is measured in Joules or in calories/kilocalories 1 kilocalorie = 4,184 joules – calorie use by nutritionists is actually a kilocalorie
Metabolic Rate
• • • • physiologists can determine an animal’s metabolic rate by 1. measuring its consumption of O2 ( or production of CO2) 2. measuring heat loss – e.g. using a calorimeter 3. measuring the rate of food consumption and
waste production
– used over the long term
Metabolism
• • • • within a narrow range of environmental temps – the metabolic rate of an endotherm is at a low level and independent of external temperature =
thermoneutral zone
the thermoneutral zone is bounded by an upper and a lower critical environmental temperature (UCT and LCT) when environmental temperature is within the zone – the animal does not need to expend much energy to regulate its temp – its thermoregulatory responses are passive – e.g. fluffing fur, controlling blood flow to the skin but outside this zone – the animal must expend metabolic energy – thermoregulatory responses are active – e.g. shivering and non-shivering heat production
Metabolism
• • • the metabolic rate of a resting endotherm in the thermoneutral zone is called the basal
metabolic rate or BMR
BMR is measured when the animal is quiet but awake and not using energy for digestion, reproduction or growth
BMR = minimal amount of energy needed to carry out minimal body functions
•
Standard metabolic rate (SMR) is the
metabolic rate of an ectotherm at rest at a specific temperature
Metabolism
• •
BMR correlates to body size – increased size = increased BMR
BUT increased size = decreased BMR per gram of body tissue – BMR of an elephant – 7,000 times greater than that of a mouse – BUT per gram tissue – mouse uses energy 15X faster than the elephant – – – why?
as an animal increases in size – its surface area to volume decreases heat dissipation relies on surface area – theorized that larger animals have decreased BMRs per gram tissue to avoid overheating
Metabolic Adaptations
• • • when environmental temps fall below the lower critical level of the TZ – endotherms
must produce heat
thermogenesis can be through: –
1. shivering heat production
–
2. non-shivering heat production
most non-shivering heat production- occurs in specialized adipose tissue called brown fat – high numbers of mitochondria and blood vessels
Metabolic Adaptations
• • • •
in the mitochondria: ATP production is uncoupled from metabolic fuel consumption – yet heat is produced (heat is produced rather than ATP)
brown fat is prevalent in newborn humans – decreases in adulthood – metabolic activity can be stimulated upon cold exposure – less brown fat activity in obese individuals also present in large amounts in certain animals – cold weather animals – animals that hibernate other adaptations have evolved to help endotherms retain heat –
thick layers of fur, feathers or fat
– ability to decrease blood flow to the skin – counter-current exchange of heat in the appendages of many animals
Metabolic Adaptations
• • • regulated hypothermia can also be used – by many birds and mammals hummingbirds – high metabolic rate – drop their body temps by 10 to 20C when they are inactive – – lowers their metabolic rate and conserves energy called daily torpor regulated hypothermia that lasts for days or weeks =
hibernation
– metabolic rate needed for hibernation may be 1/50 the animal’s BMR th of – many animals can maintain body temp’s close to freezing!
– arousal from hibernation requires the hypothalamus to reset the body’s internal thermostat
Thermoregulation in Ectotherms
–
amphibians
• assume the temperature of the water when submerged • on land – the body temp can differ from the environment • cooling - evaporative loss across the thin skin • warming –radiation from the sun & from from warm surfaces • to prevent overheating – many amphibians are nocturnal or will hide in shady areas
Thermoregulation in Ectotherms
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reptiles: wide variety of behaviors
• seen best in the lizards - radiation – to heat up – bask perpendicular to sun’s rays – to cool down – parallel to rays • some reptiles can pant to regulate temp - heat loss through evaporative cooling across the mouth • some reptiles can increased body temp through increased metabolism – brooding snakes curl around their eggs • many reptiles endure cold temps by “hibernating” in large groups
Thermoregulation in Ectotherms
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fish
• rare in most fish - most assume the temperature of the surrounding water • • two kinds of thermoregulation strategies 1. “hot” fish – tuna, mackeral, sharks – blood is oxygenated at gills – most of this cold blood is moved to the body via arteries under the skin – blood flows into muscles and is warmed by the venous blood flowing out of the muscle – counter- current exchange – so blood that returns to the heart via veins under the skin is cool –
SO: this strategy keeps the heat within the muscle mass
• 2. “cold” fish – most fish species – blood is oxygenated and cooled to seawater temperature at the gills – – –
cold blood is carried into the tissues via a large aorta
veins return warmed blood to the heart
blood is warmed by the metabolism of muscles
– pumped to the gills – re-cooled