CH 7&8 Flashcards

1
Q

A set of similar ecological niches occupied by a group of (usually) related species, often constituting a higher taxon

A

Adaptive zone

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2
Q

Magnitude of the effect of an allele on a character, measured as half the phenotypic difference between homozygous for that allele compared with homozygous for a different allele

A

Additive

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3
Q

One of several forms of the same gene, presumably differing by mutation of the DNA sequence. Usually recognized by phenotypic effects

A

Allele

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4
Q

Polyploid in which the several chromosome sets are derived from more than one species

A

Allopolyploid

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5
Q

Cell or organism, possessing too many or too few homologous chromosomes, relative to the normal set

A

Aneuploid

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6
Q

Polyploid in which the several chromosomes sets are derived from the same species

A

Autopolyploid

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7
Q

Long-prevailing rate at which taxa become extinct, in contrast to the highly elevated rate that characterize mass extinction

A

Background extinction

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8
Q

Mutation of an allele back to the allele from which it arose by an earlier mutation

A

Back mutation

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9
Q

Population density that can be sustained by limiting resources

A

Carrying capacity

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10
Q

adjacent to the coding sequence

located elsewhere in genome

A

Cis, trans

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11
Q

Nucleotide triplet that encodes an amino acid or acts as a stop signal translation

A

Codon

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12
Q

Extinction of a population due to competition with another species

A

Competitive exclusion

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13
Q

Untranscribed regions of the genome to which products of other genes bind, and which enhances or repress transcription of specific genes

A

Control regions (enhancer and repressors)

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14
Q

Magnitude of variation in morphological or other phenotypic characters among species in a clade or taxon

A

Disparity

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15
Q

Process that have a stronger effect on per capita rates of speciation or extinction when the diversity of species is greater

A

Diversity-dependent factors

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16
Q

Extent to which it produces when hetero the same phenotype,

A

Dominance

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17
Q

Cell or organism, possessing the normal, balanced, number of chromosomes

A

Euploid

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18
Q

Part of a gene that is translated into a polypeptide

A

Exon

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19
Q

Nonlinear increase of a property over time, described by an exponential equation

A

Exponential growth

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20
Q

Carried by entire population (mutation)

A

Fixed

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21
Q

Insertion or deletion of base pairs in a translated DNA sequence that alters the reading frame, resulting in multiple downstream changes in the gene product

A

Frameshift mutation

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22
Q

Functional unit of heredity

A

Gene

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23
Q

Two or more loci with similar nucleotide sequences that have been derived from a common ancestral sequence

A

Gene family

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24
Q

Translation through polypeptides or proteins

A

Genetic code

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25
Readily detected generic variant that is used to trace variation and inheritance of a closely linked region that may include a gene of interest
Genetic marker
26
DNA sequence that differs from homologous sequences at one or more base pair sites
Haplotype
27
Recombination within a gene
Intragenic recombination
28
Part of the gene that is not translated into a polypeptide
Intron
29
A 180° reversal of the orientation of a part of a chromosomes, relative to some standard chromosome
Inversion
30
Chromosome complement of an individual
Karyotype
31
Adaptation that provides the basis for using a new, substantially different habitat or resource
Key adaptation
32
Graph of the apparent change in number of lineages in a clade, often based on a time-calibrated phylogeny
Lineage-through-time plot
33
Site on a chromosomes occupied by a specific gene; more loosely, the gene itself, in all its allelic states
Locus
34
Highly elevated rate of extinction of species, extending over an interval that is relatively short on a geological time scale
Mass extinction
35
Short, highly repeated, untranslated DNA sequence
Microsatellite
36
Error in the replication of a nucleotide sequence, or any other alteration of the genome that is not manifested as reciprocal recombination
Mutation
37
Increment in the genetic variance of a phenotypic character caused by new mutation in each generation
Mutational variance
38
Base pair substitution in DNA that results in an amino acid substitution in the protein product
Nonsynonymous mutations
39
Phenotypic effect of a gene on more than one character
Pleiotropic
40
Mutation that maps to a specific gene locus; change of a singular base pair
Point mutation
41
Of a cell or organism, possessing more than two chromosome complement
Polyploidy
42
Arisen via the retrotransposition of mRNA into cDNA
Processed pseudogene
43
Degree to which the taxonomic composition of a biota is differentiated among major geographic regions
Provinciality
44
Artifact in estimating diversity in the fossil record, whereby taxa that are still alive have apparently longer duration than they would it they had been counted only from fossil data, and so will inflate the count of taxa, compared to the more remote past
Pull of the recent
45
Phenotypically detectable only when homologous
Recessive
46
Recombinational exchange of parts of two nonhomologous chromosome
Reciprocal translocation
47
Repeated origin of mutation of a particular kind within a species
Recurrent mutation
48
Proposition that taxa become extinct at an approximately constant rate because they fail to evolve as fast as other species with which they have antagonistic interaction
Red queen hypothesis
49
Group selection: species with different characteristics increase or decrease in number at different rates because of a difference in their characteristic
Species selection
50
Correlation between a particular character and the rate of diversification among clade
Species sorting
51
Complete replacement of one allele for another within a population or species over evolutionary time
Substitution
52
Multipe codons code for the same thing
Synonymous codon
53
Fixation of a base pair change that does not alter the amino acid in the protein product of a gene
Synonymous mutation
54
One of a group of adjacent duplicates copies of a DNA sequence
Tandem repeat
55
Mutation that changes a nucleotide to another nucleotide in the same class
Transition
56
DNA sequence, copies of which become inserted into various sites in the genome
Transposable element
57
Movement of a copy of a transposable element to a different site in the genome
Transposition
58
Mutation that changes a nucleotide to another nucleotide in the opposite class (purine or pyrimidine)
Transversion
59
Recombination between nonhomologous sites on two homologous chromosomes
Unequal crossing over
60
Allele, genotype, of phenotype that is most prevalent in wild population; with reference to the wild-type allele, other alleles are often termed mutation
Wild type