Ch. 32 Part 1: Animal Body Plans Flashcards

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1
Q

In Complex Multicellular Organisms, bulk flow

A

circumvents the limitations of diffusion

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2
Q

Complex multicellularity depends on

A

cell adhesion, communication, and a genetic program for development

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3
Q

Animals

A
  • Multicellular
  • Heterotrophic eukaryotes with tissues that develop from embryonic layers
  • can be characterized by “body plans”
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4
Q

Views of animal phylogeny

A

continue to be shaped by new molecular and morphological data

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5
Q

3 types of body cavities

A

1) Coelomate
2) Pseudocoelomate
3) Acoelomate

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6
Q

Pseudocoelomate

A

exists between the endoderm and mesoderm

false

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7
Q

Acoelomate

A

no body cavity

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8
Q

Coelomate

(eu)coelomate

A

within mesoderm only

true

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9
Q

Unicellular

A
  • cell is autonomous
  • can do all functions by themselves
  • all prokaryotes, many eukaryotes
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10
Q

Simple Multicellularity

Colonial

A
    • Cell adhesion molecules maintain structural integrity (Cadherins)
  • Little intercellular communication or nutrient transfer
  • Very little differentiation; cells retain most/all functions
  • Nearly all cells in direct contact with external environment
  • Little cost to losing a cell
  • Common in algae
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11
Q

Advantages to colonial vs. unicellular

A

1) Avoid being eaten: size can be a deterrent
2) Maintain position in water column
3) Flagellar currents and filter feeding (suspension)

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12
Q

Disadvantages to colonial vs. unicellular

A

Cells no longer act in a corporative manner

-susceptible to “cancer”

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13
Q

Complex Multicellularity

A
  • Highly developed adhesion mechanisms
  • Specialized structures for intercellular communication
  • Complex patterns of tissue and organ development guided by regulatory gene networks
  • 3- dimensional organization
  • plants, fungi, animals
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14
Q

Complex Multicellularity features

A

1) Adhesion
2) Communication
3) Development
4) Key innovation in multicellularity

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15
Q

Adhesion types

A

a) cadherins: cell = cell
b) integoins: cell = extracellular matrix (ECM) (critical in animals - no walls)
c) ECM
d) pectins
e) gap junctions: animal: physical connection and intracellular communication (tubes)
f) plasmodesmata: plant: physical connection and intracellular communication (tubes)

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16
Q

Communication types

A

a) gap junctions
b) plasmodes
c) integral (plasma membrane) receptors
d) intracellular receptors

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17
Q

Development

A

molecular signals direct differential gene expression leads to cellular => tissue => organ differentiation

a) division of labor because of
b) different environments

18
Q

Key innovation in multicellularity

A

ability to enable cells to differentiate in Space instead of Time

19
Q

Biological Design Principles

A

2nd law of Thermodynamics

diffusion

20
Q

2nd Law of Thermodynamics

A
  • disorder is spontaneous in our Universe
  • i.e. high concentration to low concentration
  • disorder to order is not spontaneous, but can occur if work is done (input of energy)
21
Q

Diffusion

A

particles spontaneously move from areas of high concentration to low concentration

has to go through the diffusion path: O2 => membrane (SA) => Cytosol (V) => mitochondria

22
Q

Size limits on cells

A

SA = 4 * pi * r^2
V = (4/3) * pi * r^3
radius is the only thing varied

SA/V ratio decreases as radius increases

23
Q

Fiele’s Law

A

Js = DA (∆c/∆x) => linear Js vs [C]

Js = diffusion rate of s (flux)
D = diffusion coefficient (empirically determined) solubility (how fast)
A = surface area
∆c = concentration gradient
∆x = path length
24
Q

Field’s Law and diffusion

A

increase in D, A, or ∆c will increase Js

decrease in ∆x will increase Js

25
Q

Multicellularity and size of organisms

A

1) Multicellularity (complex)
2) Size
3) Animal Body Design
4) Body Cavities
5)

26
Q

Multicellularity (complex)

A
  • exterior > interior
  • exterior < interior
    (i. e. O2 > ; < CO2)
  • nutrients/waste
  • temperature, pH, light physical force gradients
  • shape
27
Q

Size

A

If small, then diffusion can work

If larger, then diffusion is insufficient (limiting); therefore, resorts to bulk flow

28
Q

Bulk Flow

A

a means by which molecules move through organisms at rates beyond those possible by diffusion alone across a concentration gradient (moving faster)

29
Q

3 types of Animal Body Designs (trends)

A

1) Symmetry
2) Body Cavities
3) Germ layers

30
Q

3 types of Symmetry

A

1) Asymmetric
2) Radial
3) Bilateral

31
Q

Asymmetric

A

no mirror image when cut

i.e. sponge

32
Q

Radial Symmetry

A
  • mirror image
  • many possible planes
  • i.e. circular
  • probably started here
33
Q

Bilateral Symmetry

A
  • mid-sagittal plane (left and right)
  • mirror image
  • one possible plane
  • i.e. humans
34
Q

(frontal) coronal plane

A

dorsal/ventral

35
Q

Traverse plane

A

anterior/posterior

36
Q

Germ Layers

A
embryonic tissues (1st ones)
diploblastic vs. triploblastic
37
Q

Diplobastic

A

2 germ layers:

1) endoderm
2) ectoderm

38
Q

Triploblastic

A

3 germ layers:

1) endoderm
2) mesoderm
3) ectoderm

39
Q

If triploblastic, then

A

protostome vs deuterostome

40
Q

Protostome

A
  • Blastopore first opening: mouth
  • Spiral cleavage
  • Schizocoely = split mesoderm
41
Q

Deuterostome

A
  • Blastopore first opening: anus
  • Blastopore seconde opening: mouth
  • Radial cleavage
  • Enterocoely = grows out of the mesoderm