7.3- Classification Flashcards

(30 cards)

1
Q

What is variation

A

when no two individuals of a population are identical in their traits

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2
Q

What is taxonomy

A

the science of categorising life

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3
Q

What are the two types of variation

A

continuous
discontinuous

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4
Q

Example of continuous variation

A

height

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5
Q

Example of discontinuous variation

A

blood type

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6
Q

What are the two ways of categorising species?

A

morphological
physiological

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7
Q

Morphological species

A

Classified by physical characteristics.

Organisms with shared traits

Sexually and asexually reproducing organisms and fossils

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8
Q

Who first published the morphological species definition

A

Carolus Linnaeus, 1735

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9
Q

Biological species

A

a group of organisms that can breed and produce fertile offspring

cannot apply to fossils, hybrids, bacteria containing DNA from multiple sources

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10
Q

Who proposed the biological species definition

A

Ernst Mayr, 1942

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11
Q

What is binomial nomenclature

A

two-name system of classification

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12
Q

Binomial nomenclature structure

A

First word: genus name (Capitalised)
Second word: species name (lowercase)

has to be underlined in exams.

Homo sapiens (italics)

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13
Q

When are related populations different species in biological species concept

A

when they are reproductively isolated.

doesn’t work when two isolated populations of the same species are slowly evolving to be different. BECAUSE unsure if viable offspring can be produced.

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14
Q

When are related populations different species in the phylogenetic species concept

A

When they differ in a trait or gene

Problems arise when populations exhibit variation, so species would spilt into many species.

Difference in traits is subjective

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15
Q

Name the haploid cells and diploid cells in humans, chimpanzees, and bonobos.

A

number of chromosomes is characteristic of a species

humans, 23 + 46
chimpanzees, 24 + 48
bonobos, 24 + 48

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16
Q

What is a karyogram

A

representation of all chromosomes in a cell arranged according to size, centromere position, banding pattern.

arranged in decreasing order of length

17
Q

Describe XY chromosomes

A

One long, one short

18
Q

What are the two hypotheses to how the chromosome number of humans changed over time from the common ancestor between humans and gorillas.

A
  1. a complete chromosome disappeared
  2. two chromosomes fused to become a single chromosome.
19
Q

3 evidence that supports the hypothesis that human chromosome 2 originated from the fusion of chromosomes 12 and 13 from an ape ancestor

A
  1. chromosome 2 sequence is almost identical to chimpanzee sequences found on two different chromosomes
  2. chromosome 2 has one centromere and one remnant of a centromere
  3. chromosome 2 has telomeres in the centre. Telomeres should only appear at the end of the chromosome.
20
Q

When would the fusion of the chromosomes have happened?

A

Evidence does not say we descended from chimpanzees.
The fusion of the chromosome would have happened after the speciation split of a common ancestor that led to the evolution of chimpanzees in one lineage and the evolution of humans in another.

21
Q

What is a genome

A

the entire genetic information in an organism

22
Q

How is a genome of a species an example of diversity

A

shows variation between members of a species

23
Q

Example of genome showing variation

A

SNPs occur due to mutations.
Source of difference across individuals of a species.

24
Q

The genes of a species are the same, but the alleles??

25
What is the human genome project
international cooperative venture in 1990 - 2003 sequence the entire human genome (3.2 billion bases) currently working to decipher the function of each gene -22,000 genes estimated for humans
26
How has genome sequencing changed over time
increased in speed and decreased in cost
27
What are two benefits of carrying out whole-genome sequencing of organisms
1. Personalised medicine 2. Researching evolutionary relationships
28
Personalised medicine, genome sequencing
information about a person's genetic makeup is used to prescribe medicine. analysing the genome of participants in drug trials increases understanding of a drugs effect. identify patterns and reduce side effects
29
Evolutionary relationships, genome sequencing
information about a species genetic makeup can be used to determine ancestral relationships information used to make phylogenetic trees and map individual pedigrees
30
What is phylogenetics
study of ancestral evolutionary relationships