Module 4 Flashcards

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1
Q

What is Biodiversity?

A

− variety in an ecosystem
− variety of habitats and variety of species

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2
Q

Benefit of high species diversity?

A

− Stable ecosystem
− each species is less likely to become extinct (due to high genetic diversity)
− & if a species does become extinct it will not affect the food chain as there are other species available

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3
Q

How to measure Species Diversity for an area?

A

− Species Diversity Index
− takes into account the number of different species and how many individuals there are for each species
− the larger the species diversity index, the larger the species diversity

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4
Q

How does deforestation lower species diversity?

A

− (deforestation is the removal of trees for wood & space)
− decreases plant species diversity
− less variety of habitats
− less variety of food sources
− decreases animal species diversity

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5
Q

How does agriculture/farming lower species diversity?

A

− deforestation to make space for farm
− only grow a few plants & keep a few animal species
− selectively breed plants & animals
− use pesticides to kill other species

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6
Q

What is Classification?

A

placing organisms into groups

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7
Q

What is Hierarchical Classification?

A

− large groups divided into smaller groups with no overlap
− domain, kingdom, phylum, class, order, family, genus, species

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8
Q

What is Binomial Naming System?

A

− using Genus name and Species name to name organism
− Genus name first in capital, Species name second in lower case
− e.g. tiger = Felix tigris

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9
Q

What is a Species?

A

​a group of individuals with similar characteristics that can interbreed to produce fertile ​offspring

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10
Q

Why are the offspring from 2 different species mating infertile?

A

− offspring will have a odd number of chromosomes
− therefore, cannot perform meiosis, cannot produce gametes
− example: ​horse + donkey = mule,
​mule is infertile,
​horse has 64 chromosomes/donkey has 62 chromosomes,
​horse gamete has 32 chromosomes/donkey gamete has 31 chromosomes,
​therefore, mule has 63 chromosomes

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11
Q

What is Phylogenetic Classification?

A

based on evolutionary relationships – how closely related different species are and how ​recent a common ancestor they have

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12
Q

3 ways of comparing relationship between different species?

A

DNA Hybridisation: comparing DNA base sequence

​- take DNA from 2 species to be compared
​- radioactively label one of the DNA
​- heat both sets so double strand separates
​- cool so single strands join together
​- look for Hybrid DNA (one strand from species A, one strand from species B)
​- identify Hybrid DNA by 50% radioactivity
​- heat Hybrid DNA to measure similarity

​results =​higher temperature required
​more hydrogen bonds present
​more complementary base pairing
​more similar the base sequence
​more similar the species
​more closely related
​more recent a common ancestor

AA Sequence: comparing AA sequence for the same protein (e.g. haemoglobin in mammals)

​results = ​more similar the AA sequence
​more similar the DNA base sequence
​more similar the species
​more closely related
​more recent a common ancestor

​(comparing DNA sequence better then comparing AA sequence:
​DNA sequence provides information on INTRONS and triplet code is DEGENERATE)

Protein Shape:​ comparing shape of the same protein (e.g. albumin) using immunological technique

​- comparing species A and species B
​- take albumin from species A
​- place in a blood of rabbit
​- rabbit will make antibodies against albumin of species A
​- takes these antibodies and place in blood from species B
​- if the albumin in species B has a similar shape to species A,
​the antibodies will bind to form antigen-antibody complexes,
​this will then form a precipitate

​results = ​more precipitate
​more complexes
​more similar shape
​more similar the species
​more closely related
​more common recent ancestor

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13
Q

What is Variation?

A

difference in characteristics between organisms

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14
Q

Types of Variation?

A

intraspecific = differences between organisms of the same species
​interspecific = differences between organisms of different species

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15
Q

Causes of Intraspecific Variation?

A

Genetic Factors = same genes but different alleles (allele are different type/forms of genes)

​Environmental Factors

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16
Q

Causes of Interspecific Variation?

A

Genetic Factors = different genes and different alleles

​Environmental Factors

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17
Q

Types of Characteristics?

A

Discontinuous and Continuous

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18
Q

Properties of Discontinuous Characteristics?

A

characteristics fall into certain groups with no overlap (e.g. blood group) – determined by ​genetics only (a single gene)

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19
Q

Properties of Continuous Characteristics?

A

characteristics show a range (e.g. height) – determined by genetics (a few genes, polygenes) ​and environment

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20
Q

What is Genetic Diversity?

A

genetic variation, the variety of alleles within a population of a species

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21
Q

Benefit of high genetic diversity?

A

species able to adapt with changes in the environment ​ e.g. if a new disease arises, some individuals will have characteristics to survive, and will reproduce passing on their alleles, so the species does not become extinct

22
Q

What can lower genetic diversity?

A

small population size (e.g. founder effect – where the numbers ​start low, or genetic bottleneck – where the numbers decrease)

23
Q

What is natural selection and adaptation?

A

− variation in population of species
(genetic diversity/genetic variation/variety in gene pool)
− new alleles arise by random mutation
− environment applies a selection pressure on the population
− those with favourable characteristics/favourable alleles/selection advantage/better adapted survive, the others die [natural selection]
− the ones that survive will reproduce, passing on their favourable alleles
− if this happens for many generations, then that characteristic will become most common – the allele will become more frequent [adaptation]

24
Q

What are the 2 types of selection?

A

stabilising and directional

25
Q

What is stabilising selection?

A

− when the environment favours those with the most common characteristic – those on the extreme dies out
− the common characteristic increases in proportion
− the range (standard deviation) will reduce

26
Q

What is directional selection?

A

− when the environment favours those individuals with characteristics on one of the extremes
− over time this will become the most common characteristic
− normal distribution will shift to that extreme

27
Q

What is a Gene?

A

− a section of DNA that codes for a protein
− made out of intron and exon
− intron = non-coding DNA (function e.g. turns gene on or off)
− exon = coding DNA (codes for protein)

28
Q

How does a Gene/Exon code for a Protein?

A

− made out of a sequence of bases
− each 3 bases code for 1 amino acid (called triplet code)
− therefore,
− sequence of bases
− determines sequence of triplet codes
− which determine the sequence of AAs
− = polypeptide chain/primary structure (folds to secondary, then to tertiary/quaternary)

29
Q

Properties of triplet code?

A

− degenerate = each AA has more than one triplet code
− non-overlapping = each base is read only once
− stop codes = occur at end of sequence – do not code for an AA

30
Q

How does a mutation lead to a non-functional enzyme?

A

− change in base sequence
− change in sequence of triplet codes
− change in sequence of AAs
− change in primary structure
− change in hydrogen/ionic/disulfide bonds
− change in tertiary structure (3D shape)
− change in active site shape
− substrate no longer complementary
− can no longer form enzyme-substrate complex

31
Q

How is a protein assembled?

A

− by transcription and translation
− transcription = production of a single stranded complementary copy of a gene (called ​ mRNA)
− translation = use sequence of codons on mRNA to assemble protein (tRNA brings in ​ AAs)
DNA vs RNA?

− deoxyribose sugar vs ribose sugar
− thymine vs uracil
− double stranded vs single stranded
− one type vs two types (mRNA and tRNA)

32
Q

What is mRNA?

A

− messenger RNA
− single stranded complementary copy of a gene
− carries the code for assembling protein (on DNA called triplet code, on mRNA called ​ codon)

33
Q

What is tRNA?

A

− transfer RNA
− single stranded RNA folded over into a ‘clover leaf’ shape (held by hydrogen bonds ​ between the bases)
− has an AA attachment site on the top
− has 3 specific bases on the bottom (anticodon)
− anticodon binds to complementary codons on mRNA

34
Q

What is Transciption?

A

− occurs in nucleolus of nucleus
− producing a single stranded complementary copy of a gene (called mRNA)
− DNA is double stranded, 1 strand called coding strand & 1 strand called template strand, the template strand will be used to build mRNA
− process,
− DNA Helicase breaks the hydrogen bonds between complementary bases in the gene
− the double strand of the gene unwinds
− leaves 2 separate strands (1 coding strand and 1 template strand)
− complementary RNA nucleotides bind to exposed bases on the template strand
− RNA Polymerase joins the sugar-phosphate backbone of the RNA strand
− leaves pre-mRNA (contains introns and exons)
− the copies of the introns are removed by splicing
− leaves mRNA

35
Q

What is Translation?

A

− takes place on ribosomes of Rough Endoplasmic Reticulum
− uses the sequence of codons on the mRNA to assemble the protein (tRNA brings in AAs)
− process,
− mRNA leaves nucleus via nuclear pore
− mRNA attaches to a ribosome
− complementary tRNA carrying specific AAs bind to the codons on mRNA via their anticodon
− the AAs on the tRNA are joined by peptide bonds

36
Q

What does Meiosis produce?

A

​4 genetically different cells, haploid (half the amount of chromosome/DNA)

37
Q

Benefits of Meiosis?

A

produces gametes which will be used in sexual reproduction in animals & plants
​(2 gametes fuse to form a zygote, zygote develops into organisms)

38
Q

Stages of Meiosis?

A

Interphase/Meiosis I/Meiosis II/Cytokinesis

39
Q

Interphase? ​

A

G1: protein synthesis
​S: DNA replication (doubles set of DNA)
​G2: organelle synthesis

40
Q

Meiosis I?

A

​Prophase I: DNA coils to form chromosomes, nucleus breaksdown, spindle fibres form, ​ ​ crossing over occurs
​Metaphase I: homologous pair of chromosomes line up in middle of cell and attach to ​ ​ spindle fibre via centromere
​Anaphase I: spindle fibres pull, homologous pair of chromosomes separate to opposite sides ​ by independent assortment
​Telophase I: chromosomes uncoil, nucleus reforms (left with 2 nuclei)

41
Q

Meiosis II?

A

Prophase II: DNA coils to form chromosomes, nucleus breaksdown, spindle fibres form
​Metaphase II: chromosomes line up in middle of cell and attach to spindle fibre via ​ ​centromere
​ Anaphase II: spindle fibres pull, centromere splits, sister chromatids move to opposite sides ​ by independent assortment
​Telophase II: chromatids uncoil, nucleus reforms (left with 4 genetically different nuclei)

42
Q

Cytokinesis?

A

separating cell into 4 (each receives a nucleus and organelles/cytoplasm)

43
Q

How does Meiosis produce Variation?

A

Crossing Over and Independent Assortment

44
Q

What is crossing over?

A

occurs in Prophase I of Meiosis I
​homologous pairs of chromosomes wrap around each other and swap equivalent sections of ​chromatids – produces new combination of alleles

45
Q

What is independent assortment?

A

​- in Anaphase I of Meiosis I – the homologous pairs of chromosomes separate
​- in Anaphase II of Meiosis II – the chromatids separate
​- independent assortment produces a mix of alleles from paternal and maternal ​ ​ ​ chromosomes in gamete

46
Q

What happens to DNA mass in meiosis?

A

quarters

47
Q

What happens to Chromosome number in meiosis?

A

halves (haploid)

48
Q

What is Mutation?

A

− Change in DNA
− 2 types: Chromosome Mutation and Gene Mutation

49
Q

What causes mutation?

A

random or due to mutagens (e.g. chemicals, radiation)

50
Q

What is a Chromosome Mutation?

A

− In plants, inherit more than one diploid set of chromosomes – called polyploidy
− In animals, homologous pair of chromosome do not separate in meiosis, so either inherit one extra or one less chromosome – called non-disjunction

51
Q

What is a Gene Mutation?

A

− a change in the base sequence of DNA
− 2 types = substitution and insertion/deletion
− substitution = replace one base for another, changes one triplet code
​can be silent (new triplet code codes for same AA), mis-sense (codes for a different ​AA, so protein shape changes slightly), non-sense (codes for a stop codon, so ​polypeptide chain not produced)
− insertion = adding a base, deletion = removing a base
​both insertion/deletion causes frameshift, all the triplet codes after the mutation ​changes, so normal polypeptide chain/protein not produced