Beruflich Dokumente
Kultur Dokumente
Paulgaard
Biology 30
Notes & Diagrams
Stages of Characteristics
Interphase
Gap 1 Cell growth, protein synthesis, normal cell
functions, about 11 hours
S phase (synthesis) DNA replication, up to 7 hours
Gap 2 Cell growth, protein synthesis, 4 hours
o Cell Division: divided into two parts nuclear division (mitosis or meiosis) and
cytokinesis (10%)
TERMS:
Chromatin Strands of genetic material (DNA) that are unraveled into long thin strands
(accessible DNA) during interphase. Found during the resting phases of the
cell’s life cycle
Chromosome Thick shortened strands of genetic material (DNA) that is inaccessible or
packaged. Noticeable just before cell division (condensed)
Chromatid Replicated, identical chromosomes that are attached at the centromere.
Chromatid pairs are found during cellular division (metaphase of mitosis and
meiosis)
Homologous Chromosomes that contain similar genes or DNA sequences but are not
Chromosomes identical. One of the pair comes from each parent.
Nucleolus Used in the synthesis of ribosomes (protein synthesis)
Spindle fibers Protein strands that attach to the centromere and pull the chromatids to
opposite ends of the cell
Centriole Found in animal cells only. They provide attachment for spindle fibers
Centromere The spot, usually in the middle, on the chromosome where the spindle fibers
attach. This spot holds the two sister chromatids together.
Mitosis: Asexual Reproduction (1 Parent Cell)
Nuclear division characterized by chromosome replication and formation of two identical
daughter nuclei (2n) using one division.
Division normally occurs in most body or somatic cells (exceptions include muscle and
nerve cells and cells in the ovaries and testes)
These cells are used for growth or replacement of dead or damaged cells.
Stages of Mitosis
Prophase Nuclear membrane breaks down, spindle fibers begin to form, chromosomes
condense
Metaphase Spindle fibers formed and attach to centromeres, chromosomes line up across
equatorial plate
Anaphase Chromatids segregate (separate) and move to opposite spindle poles
Telophase Nuclear membrane reforms, chromosomes disappear, cytokinesis occurs
Cytokinesis:
Equal division of the cytoplasm between the two daughter cells.
The parent cell has now split into two new daughter cells, each cell has the same number
of chromosomes as the parent cell (this is called the diploid number of chromosomes)
Stem cells:
Cells that can divide over and over again to form the specialized cells, tissues and organs
that make up our body.
Totipotent stem cells:
o Cells that can have the ability to develop into any cell including extraembryonic
membranes.
Pluripotent stem cell or Embryonic stem cells:
o Cells that can form all cells, tissues and organs in the body except the
extraembryonic membranes.
Committed stem cells/ Adult stem cells:
o Cells that are unique to the organ and can only develop into more specialized
cells of that same organ.
o Example: nerve cells in the brain, or blood cells in the bone marrow
Identical twins:
o Produced from one fertilized egg that divides abnormally, in early development usually before
the blastocyst stage, to produce two separate embryos.
o The twins are identical in every way.
Fraternal twins:
o Produced when two separate eggs are ovulated and fertilized by separate sperm cells. They
will each implant separately producing separate placentas.
o The twins will not be identical.
Stages of Meiosis
Prophase I o Nuclear membrane disappears, chromosomes condense, become
visible, homologous chromosomes pair up (synapsis) forming a tetrad,
crossing over occurs here.
o Homologous chromosomes are chromosomes that have similar
shape, size, and genes
Metaphase I o Homologous chromosomes line up randomly on the equatorial plate,
spindle fibers attach to the centromere
Anaphase I o Homologous chromosome pairs move to opposite poles of the cell in a
process called segregation.
o The chromatids do not separate at the centromere
Telophase I o Cytokinesis occurs forming two cells with half the number of
chromosomes as the parent cell, nuclear membrane forms around the
chromosomes
Prophase II o Spindle fibers form, nuclear membrane disappears
Metaphase II o Chromosomes line up at equatorial plate, spindle fibers attach to
centromeres
Anaphase II o Spindle fibers pull chromatids apart (breaks the centromere) and
chromatids/chromosomes move to opposite poles of the cell
Telophase II o Nuclear membrane reforms around chromosomes, cytokinesis occurs
producing two haploid cells from each cell.
Oogenesis:
o Production of egg cells (ova/ovum) in the ovary.
o Produces 4 cells, 1 larger egg cell (ovum) and 3 smaller cells (called polar bodies) that die
Spermatogenesis:
o Production of sperm cells in the testes.
o Results in the formation of four small sperm cells (from one parent cell).
Crossing Over:
This occurs during prophase I of meiosis.
When the homologous chromosomes pair up the chromatids of the different
chromosomes in one pair will exchange parts (genes).
The significance of this is it adds more variation to the population by producing
individuals with new combinations of characteristics.
New variations will give the population a better chance of surviving by providing
adaptations to the new environment.
Sources of Variation:
Mutations
Random Assortment
If one of these gametes should fertilize a normal gamete the resulting individual will have
an extra chromosome (trisomy), or lack a chromosome (monosomy).
The effects are categorized as ‘syndromes’.
o Examples:
Down syndrome: 3 copies of chromosomes 21 (trisomy 21) with a total
of 47 chromosomes.
Turner syndrome: woman has only one X chromosomes (monosomy X)
and therefore has only 45 chromosomes in her body cells.
Klinefelter’s syndrome: man has an extra X chromosome (XXY) and a
total of 47 chromosomes.
Chromosomal disorders resulting from non-disjunction can be detected during pregnancy
using the fetus’ karyotype.
Karyotype
This is a chart of the pictures of all the chromosomes, arranged in order from longest to
shortest, of an organism.
The human karyotype has 4 rows of 23 pairs of chromosomes (46 chromosomes in all)
o 44 or 22 pairs are called autosomes
o 2 chromosomes or one pair are called sex chromosomes
Strategies of Reproduction:
o Only one measure of its evolutionary success: the proportion of its genes present in
future generations and the reproductive adaptations of organisms are many and varied
1. Sexual reproduction
o Involves different sexes of a species producing gametes that unite to produce and
embryo that grows into a new individual.
o Fertilization can happen externally, as in fish, or internally, as in birds and mammals.
o The embryo can grow internally in a uterus, or externally in an egg.
o There are many variations of these strategies.
2. Asexual reproduction
o Involves one member of a species cloning itself.
o No gametes are required.
o Examples of this include runners in strawberries and poplar trees, and binary fission in
bacteria.
Binary fission
o A form of asexual cell reproduction in which the parent organism splits in half to form
two new (diploid) individuals
Parthenogenesis
o This involves the development of an organism from an unfertilized egg.
o Dandelions, some fish and lizards, as well as many insects perform this.
3. Alternation of Generations (Plants)
o This involves the alternating between diploid and haploid stages within the life cycle of
sexually reproducing plants.
o There are various forms of this process throughout the living world.
o Sporophyte produces, asexually, spores, reproductive cells that can grow into
new individuals without fertilization (gametophytes)
o Gametophyte plant produces gametes which must fuse to produce a cell called a
zygote, which then develops into a new individual
Genetic Material:
o Composed of DNA, RNA, Genes, and Chromosomes
o DNA carries the instructions to put amino acids into sequences that make proteins.
Discovery of DNA:
James Watson and Francis Crick first identified DNA structure in 1953
Structure of DNA
The Watson-Crick model of deoxyribonucleic acid is similar to the shape of a twisted
rope ladder.
o DNA is made up of nucleotides which are made up of:
Five-carbon sugar (deoxyribose).
Phosphate (PO4-)
One of four nitrogen bases
adenine [A] ~ Purine
guanine [G] ~ Purine
thymine [T] ~ Pyrimidine
cytosine [C] ~ Pyrimidine
Genes:
o DNA is subdivided into segments called genes.
o A gene is composed of many nucleotides.
o Each gene codes for a specific protein (one gene-one enzyme hypothesis).
o Allele: the variations of a gene. e.g. eye colour.
Types of Genes:
Introns: meaningless segments that does not code for no specific protein and appear to
have no function.
Exons: parts of the DNA that actually form the gene.
o Structural Genes: these are genes that direct the synthesis of proteins in
individual cells.
The proteins are used to build cell structure or other important
molecules. Ex. hormones, neurotransmitters, hair.
o Regulator Genes: control the production of repressor proteins which switch off
structural genes.
o Oncogenes: are genes that specifically cause cancer.
o Transposons: moveable genes that can ‘jump” along the chromosome.
Chromosomes:
o Chromosomes (DNA molecule) can carry several hundred to several thousand genes,
depending on the size of the chromosome.
o Chromosomes are composed of a long molecule of DNA and proteins that the DNA wraps
around.
o The larger the chromosome the longer the DNA molecule and the more base pairs it has.
Functions of DNA
Self-Replication
Protein-Synthesis: coding for structural proteins and enzymes thereby controlling the
cellular activities of an organism.
Ligase-are enzymes that glue DNA nucleotides together at the nitrogen bases
DNA polymerase- joins the phosphates to the sugars to form the sides of the DNA ladder
Protein Synthesis:
A gene codes for the production of a specific protein by specifying which amino acids to
use, in what order, and how many.
This occurs in two sequences: Transcription and Translation
Types of DNA
o DNA is found in the nucleus, mitochondria and chloroplasts.
o Mitochondrial DNA is inherited only from the mother. It can be compared to determine
ancestry of organisms.
Acquired characteristics:
Characteristics received from the environment and are not passed on to offspring and do
not affect the genes.
Genetics:
The study of the patterns of inheritance as hereditary characteristics or traits passed from
parents to offspring.
Gregor Mendel the “Father of Genetics” studied the mechanisms of inheritance in
garden peas. (1866)
Terms:
Allele: The different forms of a gene. (variation on the trait)
o More than two alleles can exist for any specific gene but only two of them will be
found within any individual.
o Dominant allele = D
o Recessive allele = d
Genotype: the specific allelic combination for a certain gene or set of genes.
Phenotype: "the form that is shown"
o The outward, physical appearance of a particular trait in an individual.
Homozygous: Having two of the same allele, e.g. DD or dd.
o Homozygote: An individual which contains only one allele at the allelic pair
DD is homozygous dominant
dd is homozygous recessive
Pure lines are homozygous for the gene of interest.
o Purebred: an organism having all homozygous gene pairs.
Heterozygous: Having two different alleles e.g. Dd.
o Heterozygote: An individual which contains one of each of the gene pair
Dd is a heterozygote.
o Hybrid: - an organism having at least one heterozygous gene pair.
Monohybrid: - an organism having only one heterozygous gene pair.
Dihybrid: - an organism having two heterozygous genes pairs.
Example: Using Mendel’s peas
Yellow seeds are dominant to green seeds so the alleles for seed color are:
o Y=yellow and y=green.
Genotypes for seed color are:
o h. dom = YY hetero = Yy and h.reces = yy.
o The dominant allele is always written before the recessive allele of the same
characteristic in any genotype.
Phenotypes (what the seeds look like) are:
o YY and Yy are yellow and yy is green
Punnett Squares:
Tables drawn to predict the possible offspring from a cross between two individuals.
Helps predict the outcome of a genetic cross
When doing crosses always use the following problem solving method.
1) State what the alleles mean, assign letters to the dominant and recessive alleles.
2) Identify the parent cross in words and after in genotype symbols.
3) Identify the gametes from each parent and set up the punnett square.
4) Interpret the genotypes and phenotypes from the punnett square and answer the problem.
Single Trait Crosses (Monohybrid Crosses):
A cross between two individuals with respect to a single trait.
Example:
Alleles:
o R= red r= white
P1 (parental generation):
Purebred (homozygous dominant) red X purebred white (homozygous recessive)
o RR X rr (Genotypes)
Gametes (alleles): R r
Example:
Suppose in pea plants tall is dominant to short for the height of the plant. The possible alleles in
the gametes can only be tall (T) or short (t). The cross or punnett square is set up as follows:
Alleles:
o T=tall t=short
P1 (parental generation):
heterozygous tall X heterozygous tall
o Tt X Tt
Example:
Determine whether a red-flowered pea plant is homozygous or heterozygous?
Alleles:
o R = red r = white
P1 (parental generation):
homozygous red flowered X white-flowered homozygous
o RR? X rr
If no offspring showing the recessive phenotype are produced, the unknown parent must be
homozygous.
OR
P1 (parental generation):
heterozygous red flowered X white-flowered homozygous
o Rr? X rr
If any offspring showing the recessive phenotype are produced, the unknown parent must be
heterozygous.
Variations of the Single Trait Cross:
1. Incomplete Dominance:
o This occurs when neither allele for a characteristic is dominant (both alleles are
equal).
o The heterozygous individual expresses neither of the phenotypes of the two alleles
but expresses a new intermediate phenotype.
Example: Flower color of snapdragons is incompletely dominant with red, white and pink in
the hybrid individual.
o Alleles: Red=R, white=W, pink=RW.
P1 (parental generation):
o Red snapdragon X White snapdragon
RR X WW
2. Codominance:
o This occurs when both alleles are dominant (again, both alleles are equal).
o In this case both alleles get expressed in the heterozygous individual producing
mixed phenotype.
Example: Coat color is shorthorn cattle: Red=R, White = W, Roan = RW this is a mixture of
both red and white hairs in the coat giving the animal a reddish grey blotchy coat.
Example: A man that is Type A heterozygous crosses with a woman who is Type B
heterozygous.
P1 (parental generation):
o Type A heterozygous X Type B heterozygous
IAi X IBi
Note: Another form of notation for blood type uses the capital I with a superscript A = A allele, I
with a B = B allele, i = O allele
Two Trait Crosses (Dihybrid Crosses):
This type of cross involves examining the inheritance of two characteristics at the same
time. Example where both parents are heterozygous for both characteristics (called a
dihybrid)
Consequently there will be more gametes with different combinations of alleles that could
be used for fertilization.
Traits are found on separate chromosomes.
o Alleles: plant height: tall= T and short= t, and seed color: yellow= Y and green= y
P1 (parental generation):
o Tall yellow seed plant X tall yellow seed plant (both parents are heterozygous)
TtYy X TtYy
P1 (parental generation):
o White dog X Black dog
WwBb X wwBb
P1 (parental generation):
o rose comb X pea comb (both parents homozygous for rose and pea)
RRpp X rrPP
Ex: A male who is heterozygous for both height and blood type A is crossed with a short woman
who is heterozygous for type B blood. What is the probability of producing a short son with AB
blood? What would be the probability of producing a short daughter with AB blood?
F1 (first offspring generation): Two chromosomes that carry the 4 different alleles
YR yr
YR YYRR YyRr
yr YyRr yyrr
Phenotypes: ¾ yellow round, ¼ green wrinkled
This illustrates that each alleles could not have been on a separate chromosome otherwise we
would see the standard 9:3:3:1 ratio as in example one.
Example 3: Two-trait cross with linked genes and crossing over.
o Alleles: Y=yellow, y=green, R=round seed, r=wrinkled seed
One of the parents’ the homologous chromosomes switch genes during
gamete formation (metaphase I of meiosis) resulting in a different
combination in the gametes.
P1 (parental generation):
o Yellow round X Yellow round (both are still heterozygous)
YyRr X YyRr
F1 (first offspring generation): From one parent: YR and yr, but from the other: Yr and yR
YR yr
Yr YYRr Yyrr
yR YyRR yyRr
Phenotypes: ½ yellow round, ¼ yellow wrinkled, ¼ green round
Example 1:
Genes W X Y Z
W 5 7 8
X 5 2 3
Y 7 2 1
Z 8 3 1
W—5—X—2—Y—1—Z
Example 2:
Genes A B C
A 10 5
B 10 15
C 5 15
Example 3: Drosophila, the following data was obtained from genetic crosses:
13% recombination between bar eye and garnet eye
7% recombination between garnet eye and scalloped wings
6% recombination between scalloped wings and bar eye
Genes Bar Garnet Scalloped
Bar 13 6
Garnet 13 7
Scalloped 6 7
Chromosome Theory: combines Mendel’s Laws with discoveries in cytology over the years.
1. Genes control all traits and are carried on chromosomes
2. Chromosomes undergo segregation (chromosomes separate)during meiosis
3. Chromosomes assort independently (chromosomes line up independently of each
other)during meiosis
4. Each chromosome contains many different genes.
The genes on one chromosome are all linked together
Sex is determined by two chromosomes
Autosomes:
22 pairs of chromosomes (44 in all) that determine most of our characteristics except sex.
Genes that are carried on these chromosomes are called autosomal
o Autosomal dominant (trait named after the dominant condition)
o Autosomal recessive (trait named after the recessive condition)
o Autosomal codominant
o Autosomal incomplete dominant
o These are called the “modes of inheritance”
Sex linked crosses: the alleles are expressed as superscripts only on the X chromosome.
Skips a generation….
Example: a colorblind man marries a normal vision woman with no history of colorblindness.
P1 (parental generation):
o Colorblind man X normal women
XcY X XCXC
Ex: A normal vision man meets and marries a normal vision woman whose material grandfather
was colourblind. When they have a child, what is the possibility that they will have a colourblind
child? What is the possibility of having a son who is colourblind?
Pedigree diagrams are drawn to illustrate the inheritance of a particular trait over several
generations within a family. The following is a key to how the pedigrees are coded:
II
III
Autosomal Dominant Inheritance
Autosomal dominant conditions result from an individual carrying one changed gene. Clues that
geneticists use when looking at pedigrees to determine autosomal dominant inheritance include
the following facts:
II
III
Autosomal Recessive Inheritance
Autosomal recessive inheritance is seen in conditions that are due to having two changed genes..
Characteristics of autosomal recessive traits include:
1. The condition typically appears in one generation (siblings) and nothing in their parents or
offspring ("horizontal inheritance").
2. Males and females are equally affected.
3. Both parents are asymptomatic heterozygotes (carriers) meaning they only have one
changed gene.
4. Two carrier parents have a 1 in 4 (or 25%) chance of having an affected child.
5. Each unaffected full sibling of an affected individual has a 2/3 chance of being a carrier.
6. Offspring of an affected individual will be a carrier and therefore be unaffected unless the
other parent is a carrier or is affected with the same condition.
II
III
X-Linked Dominant Inheritance
There are very few X-linked dominant traits. Characteristics of this mode of inheritance include:
1. Affected males transmit the trait to all of their daughters and none of their sons.
2. Affected females transmit the trait to half of their sons and half of their daughters.
3. There are usually twice as many affected females as affected males but affected females
often express the condition to a milder degree.
II
III
X-linked Recessive Inheritance
X-linked dwarfing conditions are rare. Criteria for this mode of inheritance include:
II
III
I
II
III
II
III
Change in Populations and Communities
Species:
Individuals that can reproduce to produce fertile offspring
Populations:
all the members of a species that occupy a particular area at the same time
E.g. wolves in Jasper
Population Genetics:
genes tend to stay in the same population for generation after generation because
individuals within that area will breed with one another than with other populations of the
same species
Gene Pool is total sum of all the alleles for a characteristic in a population at one time.
o Gene/Allele Frequency: numbers of a specific allele out of the total of that gene
(both alleles) in the population.
Hardy-Weinberg Principle
If a population has a stable gene pool and gene frequencies (not evolving) over
generations if all other factors remain constant
Equilibrium will maintain a population’s gene frequencies if 5 conditions are met:
o Closed population (no immigration or emigration can occur)
o Random mating (no mating preferences)
o No selection pressure (all alleles are equal & have the same reproductive
success)
o No mutations
o Large population
If these factors are not constant the frequency of the allele in the population will change.
Mathematical Expression:
o Allele Frequencies:
p+q=1
p = dominant allele frequency (A)
q = recessive allele frequency (a)
o Genotype Frequencies:
p2 + 2pq + q2 = 1
p2 = Homozygous Dominant Genotype Frequency (AA)
2pq = Heterozygous Genotype Frequency (Aa)
q2 = Homozygous Recessive Genotype Frequency (aa)
All three terms add up to 100% of the population so the equation always equals 1 (100%).
Equilibrium: the values for these three terms stay the same over a period of time.
Ex: Black hair is dominant to blonde hair. If 80 individuals out of a population of 1000
are blonde, then what are the allele (gene) frequencies? How many out of the 1000 are
heterozygous?
Non-Equilibrium: the values change over a period of time (micro-evolutionary change).
Environmental Changes:
Populations have three options when the surrounding environment (habitat) changes:
1. Habitat Tracking: (population’s gene pool does not change) they must move to another
area similar to the habitat they have genes/traits for.
2. Extinction: (population’s gene pool does not change) they not have traits that allow them
to survive in the new habitat and consequently not reproduce as much as possibly other
organisms. (natural selection)
3. Micro-Evolution: (population’s gene pool does change) new genes can enter the
population giving the species a new trait that might allow some members of the species
to survive in that changing environment.
Does not directly cause speciation (a new species formed).
if the population does not demonstrate Hardy-Weinberg equilibrium (i.e. its gene
frequencies are not stable) it is in evolutionary change
o Founder Effect:
The population phenotypes reflect the initial ‘founding’ population.
o Population Bottleneck:
o Random events may bring death to large portion of the population thereby
creating a small population.
Mutation: creating new alleles that would alter the frequencies the gene pool.
o One gene changes into another and therefore alters gene frequencies in the
population.
o chromosome mutation - results from non-disjunction, chromosome
breakage or translocation
o gene mutation - changes in the nucleotides (nitrogen base sequence) of a
DNA molecule
Gene Flow: gene pools of most populations of the same species exchange genes.
Gaining/Losing Alleles
Migration: new members entering or leaving the population.
Selective Mating: preference for a specific phenotype (may have a selective advantage)
then those alleles will occur more frequently in the next generation.
non-random mating, inbreeding
Natural Selection: any agent (viruses, predation, parasites, limits on light availability etc)
that will kill an individual based on its phenotype.
Populations Interacting within the Same Community:
Populations:
Members of the same species in a defined area at a defined time
E.g. wolves in Jasper
Community:
Many populations living in the same area and how they interact with each other.
E.g. wolves, deer, spruce, and bees in Jasper
Ecosystems:
Non-living (abiotic) factors interacting with living (biotic) factors.
o Biotic: the living factors in the environment, other organisms
o Abiotic: the nonliving factors in the environment, wind, temperature, humidity,
precipitation
E.g. wolves, deer, spruce, bees, and river in Jasper
Habitat:
The environment in which an organism survives.
Limited by climate, water, soil conditions, and vegetation.
Geographic Range:
o The total area, extent of locations of habitat, where an organism may live
naturally.
Ecological Niche:
o An organism’s profession, role, trophic level or feeding level
o It is the total environment and way of life of all the members of a particular
species in the ecosystem
o Involves factors like feeding habits, number of offspring per birth, interspecies
(different species) relationships, effect on soil, etc.
o E.g. producer/consumer/decomposer, predator, prey, parasite.
Population Interactions:
Cooperative: relations that occur when two or more species live closely together (coexist)
over a long period of time.
o Species that do coexist for a period of time in proximity to each other have one or
more different factors as part of their niches.
o The relationship may improve the chances of survival for one or both species, or
harm one of the species
Detritivory: occurs when one organism consume the dead organic remains of another
organism (detritus)
o not a symbiotic relationship
Symbiotic relations (symbiosis) are cooperative
Relationship Definition Interaction Symbol
Commensalism Two organisms of different The commensalist benefits (+,0)
species that live together and The host is not harmed
share food, shelter, support.
Mutualism Two organisms of different Mutualist benefits (+,+)
species that coexist and benefit Other mutualist benefits
from each other
Parasitism When one species (parasite) Parasite benefits
lives on or in another (host) Host harmed (+,-)
using the host as a food source Or sometimes not harmed
or other purposes (+,0)
Competitive: relations that occur when two or more species live closely together (coexist)
over a short period of time.
Gause’s competitive exclusion principle: states that two species can not occupy the
same niche at the same time without one eliminating the other
o Interspecific competition: different species compete for a limited resource
(food).
Reduce or limit the size of a population
Select those members that have the best traits for survival in each
species (natural selection).
o Intraspecific competition: members of the same population compete for a
limited resource (food, shelter, and mates).
Reduce population size
Select those members of the population that have the best traits for
survival (natural selection)
Predation: predator is an organism that hunts and kills another organism called the prey
o Predator will cause the prey population to decline, but it is not in its best interest
to kill off all the prey.
Small populations of prey will cause predator populations to migrate or
get weak and become more susceptible to disease
o Prey have also evolved various defense mechanisms to predation:
Mimicry: involves developing a similar color pattern, shape, or behavior
that has provided another organism with some survival advantage.
Protective Coloration: includes the ability of a prey to blend into its
environment by camouflaging itself
Warning Coloration: tell other organisms not to touch them
because they are dangerous.
Trickery: using loud noises, changing body size, expelling body parts,
pretending to be injured, to distract or frighten the predator.
Freeze Response: prey immediately stops so as not to draw attention.
This is effective if the prey has good camouflage
Fight Response: works well against a predator that is not well equipped
to fight itself (cheetah), but is often a last resort often resulting is damage
to the prey.
Flight Response: prey running from the predator
Group Behaviors:
Chemical Defenses:
Ex:
N2012=582 deer N=
Natality=121 deer/year
Mortality=84 deer/year
Immigration=56 deer/year
Emigration=98 deer/year
N2013=?
Ex:
N2011=891 rabbits N(2012 to 2014)=
N2012=1244 rabbits
N2013=1984 rabbits
N2014=2563 rabbits
N(2011 to 2013)=
2. Population Density: refers to the number of organisms per unit area (or per unit volume):
Rate of Change in Density: A negative value for rate of density change means the population is
declining while a positive value means the population is increasing
R= D
t
3. Growth Rate
Rate = N
t
N=
t=
%GR= = N X 100
N t
NF = NI x (1+cgr)t
K strategists:
Population stabilizes near the carrying capacity of their environment (K)
o Live in stable and predictable habitats.
o Slow breeding populations that are able to stabilize at a carrying capacity.
o Characteristics:
o Reach a mature age (live longer)
o Larger body sizes
o Longer parental care of offspring
o Longer gestation periods
o Smaller litter sizes
o Later ages of reproduction
o Examples include elephant, whales, and humans
r-strategists:
Great reproductive potential (high rate of reproduction = r) that causes them to overshoot the
carrying capacity
o Live in an unpredictable rapidly changing habitat.
o Fast growing population with a rapid breeding rate (experience periods of exponential
growth)
o The populations tend follow a crash/death phase after they overshoot the carrying
capacity.
o Characteristics:
o Low maturity age
o Shot life span
o Small body sizes
o Require little or no parental care
o Produce many offspring during each breeding
o Short gestation periods
o Reproduce early and often.
o Examples include fish, flies, mice, and turtles.
Chaos Theory:
Long-term predictions may be impossible since randomness is a basic characteristic of
many complex systems.
o Population growth is difficult to predict.
However, these very complex phenomena usually share a number of features:
1. Outcomes of processes in a complex system are extremely sensitive to small
differences in the conditions that were present when the process began
o The number of factors, both biotic and abiotic, that could influence the
population the overall growth rate are often very large.
2. Once a process is underway, the relationships among the interacting parts of the
phenomena can change as a result of the interactions themselves
o The number of interactions between individuals in a population and
between different populations in a community is also difficult to identify.
3. Two systems that appear similar at the start may end up being very different, but
how the two will differ is unpredictable
Succession:
The sequence of identifiable ecological stages or communities occurring over time in
progress of bare rock to climax community
Primary Succession:
Initial colonization of a barren habitat that never supported life by pioneer species.
Soil is produced during this stage.
e.g. Lichen and mosses growing on rocks.
After a long time of this existence, enough soil, water and organic material are added to the soil to
make it more accessible to other plants (seral communities/stages) which then begin to grow
(by windblown seeds, or other methods).
Secondary succession:
The gradual changes that reclaim land or water that once supported life.
Involves the rebuilding of a certain area that may have at one time supported a well-
developed and stable community.
Implies that good soil already exists in the damaged area.