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60 Cards in this Set

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  • Back

Group Selection

Notion largely discredited by the rise of darwinian theory proposing that animals act for the good of their social group or of their species.

kin selection

Principle that animals behave preferentially toward their genetic kin; formulated by william hamilton.

inclusive fitness

Reproductive success of an organism plus the fitness of its close kin.

adaptationism

A premise that all aspects of an organism have been molded by natural selection to a form optimal for enhancing reproductive success.

reductionism

Paradigm that an organism is the sum of many evolved parts and that organisms can best be understood through an adaptationist approach.

null hypothesis

The strarting assumption for scientific inquiry that ones research results occur by random chance. Ones hypothesis must challenge this initial assumption.

hardy-weinberg equilibrium

The theoretical distribution of alleles in a given population in the absence of evolution, expressed as a mathematical equation.

parapatric speciation

Speciation occurring when two populations have continuous distributions and some phenotypes in that distribution are more favorable than others.

gradualism

Darwinian view of slow, incremental evolutionary change

macroevolution

large scale evolutionary change over a long time period or evolution of major phenotypic changes over relatively short time periods.

punctuated equilibrium

model of evolution characterized by rapid bursts of change, followed by long periods of stasis.

reproductive isolating mechanisms (RIMs)

any factor behavioral, ecological, or anatomical that prevents a male and female of two different species from hybridizing

anagenesis

evolution of trait or a species into another over a period of time

cladogenesis

evolution through the branching of a species or a lineage.

allopatric speciation

speciation occuring via geographic isolation.

analogous

having similar traits due to similar use, not due to shared ancestry.

convergent (or parallel) evolution

similiar form or function brought about by natural selection under similiar environments rather than shared ancestry

cladogram

branching diagram showing evolved relatiohips among members of a lineage

species

an innterbreeding group of animals or plants that are reproductivelly isoltaed through anatomy, ecology, behavior, or geographic distribution from all other such groups.

speciation

formation of one or more new species via reproductive isolation

biological species concept

defines species as interbreeding populations reproductively isolated from other such populations

systematics

branch of biology that describes patterns of organismal variation

homology

similarity of traits resulting from shared ancestry

genetic bottleneck

temporary dramatic reduction in size of a population or species

sexual selection

differntial reproductive success within one sex of any species

sexual dimorphism

difference in size, shape, or color, between the sexes

reproductive potential

the possible offspring output by one sex

reproductive variance

measure of variation from the mean of a population in the reproductive potential of one sex compared with the other

gene flow

movement of genes between populations

inbreeding

mating between close relatives

genetic drift

random changes in gene frequency in a population

founder effect

a component of genetic drift theory, stating that new populations that become isolated from the parent population carry only the gentic variation of the founders

directional selection

natural selection that drives evolutionary change by selecting for greater or lesser frequency of a given trait in a population

stabilizing selection

selection that maintains a certain phenotype by selecting against deviations from it.

phenylketonuria (PKU)

autosomal recessive condition that leads to the accumulation of large quantities of the amino acid phenylalanine, causing mental retardation and other phenotypic abnormalities

polygenic traits

phenotypic traits that result from the combined action of more than one gene; most complex traits are polygenic

pleiotropy

the phenomenon of a single gene having multiple phenotypic effects

heritability

the proportion of toatl phenotypic variability observed for a given trait that can be ascribed to genetic factors.

quantitative variation

phenotypic variation that is characterized by the distribution of continuous variation (expressed using numerical measure) within a population (for example, in a bell curve)

qualitative variation

phenotypic variation that can be characterized as belonging to discrete, observable categories.

x-linked disorders

genetic conditions that result from mutations to genes on the X chromosome. They are almost always expressed in males, who have only one copy of the X chromosome; in females, the second X chromosome containing the normally functioning allele protects them from developing x-linked disorders.

insertion mutation

a change in the base sequence of a gene that results from the addition of one or more base pairs in the DNA

deletion mutation

A change in the base sequence of a gene that results from the loss of one or more base pairs in the DNA

trinucleotide repeat diseases

A family of autosomal dominat diseases that is caused by the insertion of multiple copies of a three-base pair sequence (CAG) that codes for the amino acid glutamine. Typically, the more copies inserted into the gene, the more serious the disease.

autosomal dominant disease

A disease that is caused by a dominant allele: only one copy needs to be inherited from either parent for the disease to develop.

point mutation

A change in the base sequence of a gene that results from the change of a single base to a different base

sickle cell disease

An autosomal recessive disease caused by a point mutation in an allele that codes for one of the polypeptide chains of the hemoglobin protein.

autosomal recessive disease

A disease caused by a recessive allele; one copy of the allele must be inherited from each parent for the disease to develop.

linkage

Genes that are found on the same chromosome are said to be linked. The closer together two genes are on a chromosome, the greater the linkage and the less likely they are to be separated during crossing over.

mendels law of independent assortment

Genes found on differ chromosomes are sorted into sex cells independently of one another

mendels law of segregation

The two alleles of a gene found on each of a pair of chromosomes segregate independently of one another into sex cells.

particulate inheritance

The concept of heredity based on the transmission of genes (alleles) according to Mendelian principles.

codominant

In a diploid organism, two different alleles of a gene that are both expressed in a heterozygous individual

dominant

In a diploid organism, an allele that is expressed when present on only one of a pair of homologous chromosomes.

recessive

In a diploid organism, refers to an allele that must be present in two copies (homozygous) in order to be expressed.

ABO blood type system

Refers to genetic system for one of the proteins found on the surface of red blood cells. Consists of one gene with three alleles: A,B, and O.

Phenotype

An observable or measurable feature of an organism Phenotype's can be anatomical,


biochemical, or behavioral.

Genotype

The genetic makeup of an individual. Genotype, can refer to the entire genetic complement or more narrowly to the alleles present at a specific locus on two homologous chromosomes.

Regulatory genes

Guide the expression of structural genes, without, coding for a protein themselves.

Structural genes

Genes that contain the information to make a protein.