single species ID Flashcards

1
Q

Why are phenotypic ID’s challenging?

A

because they are susceptible to variation in expertise.

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2
Q

What are the results and impacts of invasive earthworms?

A

tree seedlings, ferns, wildflowers, and water quality decline given changes in physical and chemical properties of soil

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3
Q

what is a universal species test?

A

this is a primer set to amp a spectrum of species

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4
Q

what kind of species test is challenging to exclude other species?

A

species-specific test

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5
Q

what is a mixed species test?

A

you can amplify a set of species

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6
Q

T/F: universal tests will amplify all species equally.

A

false

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7
Q

what are the implications of species tests?

A
  • specificity
  • sensitivity
  • validation
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8
Q

what are the advantages of small DNA segments?

A

more likely to get viable profiles, and since this is most likely degraded it will still work

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9
Q

what is the disadvantages to small DNA segments?

A

too small they might not contain genetic variation

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10
Q

what is the problem with too much variation?

A

primers might not work or stick on properly.

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11
Q

what is often the first and only question for a wildlife forensic or non-human foresnic scientist?

A

species identification

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12
Q

T/F: universal tests are required prior to running tests for individual identification or population assignments.

A

false, species specific tests are required

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13
Q

how can you get DNA from an egg?

A

scrapping the exterior or swabbing the interior of an egg

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14
Q

T/F: in cases such as shark finning DNA can be tracked back to geographic regions where population stocks can be identified.

A

true

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15
Q

what is a biological species?

A

group of individuals that can breed together but not with other groups

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16
Q

biological species are ____ from other groups.

A

reproductively isolated

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17
Q

what is the phylogenetic species concept?

A

group whose members are descended from a common ancestor and who all possess a combination of certain defining or derived traits

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18
Q

T/F: forensic DNA profiles are determined based on similarity or disimilarity of different markers

A

true

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19
Q

What are the exceptions to morphological species identifications?

A

cryptic species and ecotypes.

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20
Q

A species that looks the same but genetically is different is considered what?

A

a cryptic species.

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21
Q

T/F: ecotypes can be defined as a species that has strong selective pressures amongst the same species and they are reproductively isolated.

A

false, they are NOT reproductively isolated.

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22
Q

what is a monophyletic group?

A

an ancestral population and all descendants

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23
Q

what does incomplete lineage mean?

A

the species that may be monophyletic might have very similar DNA as they haven’t been apart for long enough

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24
Q

what is the ideal DNA barcode?

A

something that is:
- present in all organisms
- distinguishes all species
- easily amplified and sequenced

25
Q

what is the ideal DNA barcode for animals?

A

COI, mtDNA

26
Q

what is the ideal DNA barcode for plants?

A

matK + rbcL, cpDNA

27
Q

what is the ideal DNA barcode for fungi?

28
Q

why do plants not require mtDNA identification?

A

it does not have a lot of genetic variation

29
Q

What does the ITS stand for? what is it used for and why?

A

nuclear ribosomal internal transcribed spacer used to identify fungi because it is highly repeated, contains variable regions and is flanked by conserved sequences

30
Q

T/F: you can get a good profile from a yellow/brown leaf.

A

false, it will be the best for green as they have more chloroplasts.

31
Q

what are the specific genes that plant species ID can be gained from?

A

matK and rbcL genes

32
Q

what kind of specific identification does mtDNA work well with? (inter/intra)

A

interspecific variation

33
Q

T/F: mtDNA is paternally inherited.

A

false, maternally

34
Q

what enzyme does mtDNA and cpDNA lack?

A

proofreading enzyme

35
Q

what are the commonly used genes for mtDNA?

A

cyt b, COI, 12s and 16s rRNA

36
Q

T/F: COI works well in bats.

A

false, not well

37
Q

what gene has the best in-house database?

38
Q

T/F: cyt b is invariable making primer design not easy across species.

A

false it is great for primer design

39
Q

what is the 2% rule?

A

there is an approximate 2% sequence divergence in COI genes if it is below 2% then it is a different species

40
Q

what is the barcode of life project?

A

inventory of biodiversity and under representation of diversity of life from general taxonomy

41
Q

Why is the NCDI worse than BOLD?

A

because bold is validated over and over where as the NCDI is just user uploaded and could contain errors

42
Q

What DNA does hybridization occur with?

43
Q

what is heteroplasmy? what is a famous example?

A

having more than one mtDNA profile, the Romanovs had 2

44
Q

what is reticulate evolution?

A

two species with the same mtDNA

45
Q

what is interspecific introgression?

A

also hybridization where things come back together then diverge then come back together

46
Q

what is the problem with intraspecific divergent lineages?

A

its in insects mostly but it can kill gametes leading to species ID issues.

47
Q

what are nuclear pseudogenes? how do you fix it?

A

caused by retroviruses which pull out pieces of the genome and put them other places, fixed by dilution

48
Q

when nuclear pseudogenes are run through gels what does the gel look like?

A

gel will look like inactive versions of the genome resulting in more than one band.

49
Q

T/F: hybrids will have the same maternal mtDNA

50
Q

what does hybridization lead to?

A

speciation along spatial and temporal gradients

51
Q

what is an example of hybrids that is causing issues in Canada/Alaska?

A

grizzly bear and polar bears

52
Q

what does BLAST stand for?

A

basic local assignment search tool

53
Q

what do you generally search for in a blast search?

A

nucleotides

54
Q

in context of the 2% rule what number in BLAST is very important?

A

the ident number which will give you percentage

55
Q

T/F: on BLAST you will always get a full sequence overlap

A

false, not always

56
Q

how are species specific markers best accomplished?

A

via qPCR with TaqMan assay

57
Q

what do universal primers do?

A

look for regions of no/less variation adjacent to variation