week 2 Flashcards

(53 cards)

1
Q

what is systematics?

A

making sense of biological diversity

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2
Q

what is taxonomy?

A

one aspect of systematics - the naming of biological groups

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3
Q

who is linnaeus?

A

swedish biologist who devised the binomial system still used today for naming organisms

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4
Q

what are the main hierarchical groups we are interested in from animal taxonomy?

A
phylum
class
order
family
genus
species
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5
Q

what are the three major schools of hierarchical classification?

A

phenetics
cladistics
evolutionart taxonomy

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6
Q

what is phenetics?

A

also known as numerical taxonomy

builds hierarchies on the basis of physical similarities and therefore emphasises adaptation

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7
Q

what is cladistics?

A

is concerned with relatedness or phylogenetics

classifying organimss based on shared evolutionary origin

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8
Q

what is evolutionary history?

A

mixture of both cladistics and phenetics

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9
Q

what is a clade?

A

a lineage within a tree containing the descendants of a common ancestor

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10
Q

what is a phylogenetic or evolutionary tree?

A

branching diagram representing the history of a group of species

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11
Q

what does cladistics reject?

A

groups that contain some but not all the descendants of a common ancestor e.g. birds and reptiles
PARAPHYLETIC groups

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12
Q

what sort of features does cladistics use?

A

shared derived characteristics because of common ancestry

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13
Q

what is homology?

A

similar structures inherited from a recent common ancestor e.g. vertebrate forearm

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14
Q

what is analogy?

A

similar function evolved independently not from a common ancestor

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15
Q

the utility of different character types in systematics =
character is analagous?
character is homologous and primitive?
character is homologous and derived?

A

no use
limited use
great use for systematics

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16
Q

what are the three kinds of similarity in phylogenetics?

A

primitive
convergent
derived

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17
Q

the character state convergent is also known as

A

homoplasy

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18
Q

the character state primitive is also known as

A

plesiomorphy

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19
Q

shared primitive characters are —

A

symplesiomorphies

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20
Q

the character state derived is also known as

A

apomorphy

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21
Q

shared derived characters are also known as

A

synapomorphies

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22
Q

characters unique to a group are known as

A

autopomorphies

23
Q

what is dollos law?

A

loss of features is more likely

24
Q

what is the principle of parsimony?

A

take the simplest explination the tree with the least number of changes

25
what is a monophyletic group?
group contains a common ancestor and all its descendants
26
what is the main thing you need to be aware of when building a tree?
confounding effect of convergent evolution
27
what is the most important source of information for systematics?
dna sequence data
28
5 reasons molecular data is better than morphological data?
``` cheaper easier to obtain non invasice objective comparable across all living things ```
29
why do you have to be specific about selecting the correct gene to work with in evolutionary studies?
appropriate rate to be informative | easy to work with in lab and analysis
30
what would mitochondrial genes reveal?
maternal lineages
31
do mitochondrial genes have a high or low mutation ratee?
high mutation rate so good for within species | no recombination
32
what do y chromosome genes reveal?
paternal lineages | low mutation rate so good for looking far back
33
austosomal genes can also be used for trees but what is a major problem?
complex to interpret as results can be influenced by recombination and lineage sorting processes
34
what is the brief outline of methodology for obtaining moelcular data?
extract dna target and amplify region of interest using specific primers and the polymerase chain reaction sequence the target dna analyse sequence
35
what do sequence differences arise from?
mutations (substitution, insertion or deletion of bases) accumulate over time
36
what are the 3 character state methods of building trees?
maximum parsimony maximum likelihood baysian statistics
37
what are the 2 distance based methods?
neighbour joining | UPGMA (unweighted pair group method with arithmetic averages)
38
likelihood and bayesian methods often perform better than parsimony or distance methods why?
they involve building a mathematical model of the process of substitution and calculating the probability of observing particular sequences at the ends of particular branches
39
what gives us a molecular clock to calculate divergence times?
calibrating sequences
40
what is a stochastic clock?
where it is not linear, mutations may accumulate with time at different rates
41
what is a metronomic clock?
the stochastic clock plotted linearly
42
Rates of change along lineages can be constant but stochastic how so?
because the same amount fo mutations occur on the lineages but they do not occur at regular intervals. one lineage may have 3 mutations close to each other and the other lineage may have 3 mutations evenly spaced
43
molecular phylogenetic may often disagree with morphological phylogenies why? (3)
homoplasy or misinterpretation of morphology incorrect analysis of molecular data overconfidence in molecular results
44
what is a shared primitive character?
a character that is shared by two or more taxa within the group because it has been inherited from the common ancestor of the entire group
45
what is a shared derived character?
a character shared by two or more taxa within the group that has evolved within the group
46
2 reasons why mutations may not survive through many generations
selection | genetic drift
47
what is one of the assumptions of the molecular method to build a tree?
the gene tree reflects the species tree or the deeper phylogeny (this is not always the case)
48
very often when reconstructing evolutionary trees we look at mitochondrial DNA why?
because it is often passed through the mother line and is simple inheritance
49
the rate of evolution vs level of detail
some genes change faster than others and this has a bearing on building our phylogenies rRNAs very slow evolving microsattelites very fast evolving
50
still have to be aware of homoplasy in molecular building of phylogenetic trees, why?
it is even harder to filter out convergent evolution from shared derived when looking at dna sequences
51
problem with multiple substitutions?
If we are looking at an ancestral sequence at the top there, if overtime look at what can happen in those 2 descendent DNA sequences, various things can happen including sequence substitution, but over time you could get multiple substitutions, if you pick a fast evolving gene then this sort of thing happens all the time e.g. an A goes to a C and then to a T. You will miss the changes as when you sequence it you see the T only and not the changes that occurred between them.
52
problem with gene trees vs species tree
* when looking at gene trees one hope is that reflects the branching pattern of species but not always the case * look at this diagram to make that point * time scale * gene in species a and that gene starts to obtain some mutations when you make the tree you have 2 different lineages * what does that mean in reality? * It could just mean a different phenotype not species * Gene will start to diverge and you get differences in the molecular gene tree way before speciation events occur * at what point does genetic difference give you a different species not a polymorphism
53
calibration of molecular clocks
* hypothesis over time mutations arise they get fixed and those differences get larger as time goes by * the more genetically different the further back in time it was that they shared a common ancestor or sequence * some how need to calibrate this - reliable way to calibrate this molecular clock * surely we know what the mutation rate is in DNA? We actually don’t it is a hard thing to calculate and it is going to differ between different organisms need to find another way to calibrate * also the mutation rate is different ot the observed substitution rate * are mutations constant with time * are they constant within lineages? Defo no