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variation
differences between organisms
causes of variation
a mix of environmental and genetic factors
genetic variation
genes determine which proteins an organism is capable of producing, influencing their characteristics
occurs when mutation happens and alleles are combined in different ways during sex
environmental variation
determines whether the organism has the resources needed to produce a particular protein, may affect gene expression
factors affecting environmental variation may be:
temperature
nutrient availability
variation between species
can be used to classify organisms into different groups
variation within species
different individuals have different combinations of alleles, despite similar genetic makeup
sequences can be different due to mutations like SNPs
genome size varies
no 2 individuals are identical, even identical twins (environmental factors)
discontinuous variation
characteristics fall into distinct categories
e.g human blood type
continuous variation
characteristics can be measured incrementally
e.g height, weight
species classification using morphology
putting organisms into groups is called classification
science of classification is taxonomy
problems with classifying by morphology
similarities in observable characteristics doesn’t mean the 2 organisms share a common ancestor
analogous structures
doesn’t consider DNA
morphological species concept
A species is a group of organisms that share observable characteristics
Linnaeus
Linnaeus re-invented classification by giving organisms 2 part latin names instead of long ones
he believed classification based on morphology led to mistakes
binomial nomenclature system
two part Latin names
recognised universally
first part = Genus
second part = species
species in the same genus will have similar characteristics
facilitates understanding and communication between scientists
biological species concept
a group of organisms that can interbreed to produce fertile offspring
limitations of the biological species concept
asexual reproduction
organisms like bacteria can’t be classified
fertile hybrids
rarely, animals of different species breed and make fertile offspring
e.g wholpin
extinction
some species are extinct, so it’s impossible to breed them with members of an existing species to determine fertility of offspring
horizontal gene transfer
the passing of genetic info from one cell to another within the same generation
many organisms contain genetic info from a species that are very distantly related
similarities and differences between morphological and biological species concept
similarities
both state there can be variation within species
both seek to define a species
differences
biological reflects evolutionary relationships, whereas morphological does not
morphological concept is applicable to both asexually and sexually reproducing organisms, biological is only applicable to sexually reproducing ones
other characteristics that can sometimes be used to determine species
morphology
DNA
biochemistry
evolution
process of species change
speciation
when one species gives rise to 2 or more species
can occur when a population becomes isolated from other populations of the same species due to living in a different area
isolation means that members of the separate populations cannot breed together and gene flow cannot take place between them
if environmental conditions affecting each population are different, natural selection could act differently on each population
once speciation has happened, the 2 species can no longer breed to produce fertile offspring; they are reproductively isolated and are said to be separate species
distinguishing between populations and species
in most cases, the ability of 2 populations to interbreed successfully declines gradually, rather than a sudden cut off point
difficult to pinpoint when the 2 populations become different species
decision when to assign separate species status to 2 populations is subjective
diploid cell
a cell containing 2 complete sets of chromosomes
haploid cell
a cell containing one complete set of chromosomes, meaning half the number of chromosomes in normal body cells, in most cases these are gametes
chromosome number and cross breeding
for a zygote to be viable, both gametes have to contain the same number of chromosomes
in the case of closely related species e.g horse and donkey:
the fusion of a horse and donkey gamete produces an uneven number of chromosomes
these chromosomes cannot pair up during meiosis, preventing the formation of gametes
mule is infertile
chromosome number
number of chromosome varies between species, dependent on changes during species’ evolution
each individual in the same species has the same number of chromosomes
humans: 46
chimpanzees: 48
types of chromosomes
metrocentric: centromere is in the middle, arms of equal length
acrocentric: centromere is near the end, arms unequal
chromosomes stained with dye have a banded appearance
karyogram
an image that shows all the chromosomes in a cell
arranged by size, shape and banding pattern, placed with their homologous pair
homologous pair: a pair of chromosomes, one maternal one paternal, with the same shape and size
karyotype
the appearance of a complete set of an individuals chromosomes, including their number, shape, size and banding
chromosome evidence and human evolution
humans share a recent common ancestor with chimps, this raises the question of how humans lost the 2 chromosomes
possible answers:
a pair of chromosomes disappeared from genome
a pair of chromosomes fused with another pair to form a single pair
hypothesis about loss of chromosome pair
chromosomes in pairs 12 and 13 in a common ancestor fused to form the chromosomes in human pair 2
telomere
region of repeating DNA base sequences located at ends of chromosomes
evidence supporting hypothesis
chimp chromosomes 12 and 13 when placed end to end match length of human chromosome 2
locations of centromeres match on chimp chromosome 12 and human chromosome 2
the banding of long arms of acrocentric chimp 12 and 13 matches banding of metrocentric human 2
human chromosome 2 contains telomeric DNA in middle of chromosome
evidence against hypothesis
lengths are not a perfect match, there is a slight overlap
location of centromere of chimp chromosome 13 doesnt match human chromosome 2
testable hypothesis
needs to be access to evidence to support it
hypothesis needs to be a statement that can be accepted or rejected
shouldn’t contain vague statements such as “may” or “could”
shouldn’t make predictions
genomes
all of the genetic information in an organism
alleles
alternative forms of a particular gene with different base sequences
single nucleotide polymorphisms
differences between DNA sequences involving a single base change
area of difference between individuals
comparing eukaryotic genomes
can vary in size, determined by mass of DNA present in a nucleus
plants may have a gene that codes for enzymes involved in photosynthesis, humans don’t need these
vary in base sequencing
diversity between species is much larger than diversity within species
genome size and organism complexity
genome size measured in mega-bases (Mb)
no clear relationship between genome size and organism complexity
some similar species may have very different genome sizes
factors contributing to unexpected numbers (e.g wheat has a larger genome size than humans)
polyploidy in plants causing much larger genomes
a larger genome doesn’t necessarily mean an organism has more genes
DNA sequencing
determining the entire base sequence of the genes within an organisms genome
organisms within the same species share most of their genome
sequencing methods continually advancing to become faster and cheaper, due to advances in tech
genome sequencing and evolutionary relationships
phylogenetics is the classification of species based on evolutionary origins & relationships
advances in sequencing allow scientists to understand true phylogeny of taxa
the more similar the sequences, the more closely related the species are
genome sequencing and personalised medicine
by combining info about the genome with other clinical information, patterns can be identified that can help determine an individuals risk of developing disease
genomes can also be used to work out how patients will respond to specific treatments
dichotomous key
used to identify unfamiliar species
contains a series of paired statements
e.g the organism has 1 pair of wings, the organism has 2 pairs of wings
statements must be yes or no
DNA barcodes
a DNA sequence that can be used to quickly identify a species
usually just a few hundred base pairs in length
eDNA sampling
the process of extracting DNA from a habitat
eDNA sample is taken from habitat of interest containing unknown species
eDNA sample is amplified and sequenced
eDNA sample is compared with data base of known sequences
species is identified