This isolation means that members of the separate populations cannot breed together and gene flow cannot take place between them
If the environmental conditions affecting each population are different, then natural selection could act differently on each population and eventually lead to speciation
genetic drift
random changes in allele frequencies in a population due to chance
how can genetic drift lead to speciation
Once speciation has taken place, the two species can no longer breed to produce fertile offspring; they are reproductively isolated and are said to be separate species
natural selection
the process by which organisms better adapted to their environment survive, reproduce and pass on their advantageous alleles to their offspring, while those less well adapted fail to do so
Speciation can occur when gene flow does not occur between two populations of the same species
The process of speciation occurs over very long time periods, and the differences between isolated populations accumulate gradually
Distinguishing between populations and species
The process of speciation occurs over very long time periods, and the differences between isolated populations accumulate gradually
In most cases, it is likely that the ability of two populations to interbreed successfully declines gradually rather than a sudden cut-off point occurring, meaning that it is difficult to pinpoint the stage at which two separate populations have become two new species
The decision as to when to assign separate species status to two populations can therefore seem arbitrary (and subjective)
diploid cell
a cell that contains two complete sets of chromosomes
Adult body cells are usually diploid cells
haploid cell
contain one complete set of chromosomes (n), meaning that they have half the number of chromosomes compared to normal body cell
these haploid cells are called gametes and they are involved in sexual reproduction
In animals, they are the female egg cell and the male sperm cell
There are some unusual species which have haploid cells for other parts of their life cycle
During fertilisation the nuclei of haploid gametes fuse together to form the nucleus of a diploid zygote
Both gametes must contain the same number of chromosomes in order for the zygote to be viable.
For a diploid zygote this means that the gametes must be haploid
Every body cell that arises from the zygote will contain the same number of chromosomes
Exceptions to this include red blood cells, which have no nucleus and so contain no chromosomes
Chromosome number is halved in gametes, and restored to diploid after fertilisation
chromosome number
The number of chromosomes possessed by different species varies and is dependent upon changes that have occurred during that species' evolution
Each individual in a species always has the same number of chromosomes
There are a few rare instances where a chromosome mutation has occurred, giving a different chromosome number
Differences in chromosome number is one reason why organisms from different species are unable to breed together successfully
stating the chromosome number give:
The number of chromosomes found in a diploid cell
The number of pairs of chromosomes found in a diploid cell
This will be the same as the haploid chromosome number
The number of chromosomes found in a haploid cell
The diploid number must always be an even number
This is because the diploid number (2n) must always be divisible by two to produce a whole haploid number (n)
humans have 46 chromosomes and chimpanzees have 48
chromosomes
strands of DNA
gene
a section of DNA that codes for one polypeptide
Chromosomes that have undergone DNA replication have the appearance of an 'X' shape, where the 'legs' of the X are made up of two strands of DNA attached at a region known as the centromere
Chromosomes with a centromere located roughly in the middle are known as metacentric chromosomes
Chromosomes with the centromere near the end are acrocentric
Chromosomes that have been stained with a dye have a banded appearance
karyogram
an image that shows all of the chromosomes in a cell, arranged by size, shape, and banding pattern, and placed with their homologous pairs
polypeptide
a polymer consisting of a large chain of amino acids bonded together by peptide bonds
A karyogram shows the karyotype of an individual
karyotype
The appearance of a complete set of an individual's chromosomes, including their number, size, shape, and banding
homologous pairs
a pair of chromosomes(maternal and paternal) that are the same size and shape, and have the same gene loci. they are not necessarily identical as they may have different alleles
A karyogram contains an individual's chromosomes arranged in homologous pairs. It shows a karyotype; the appearance of a complete set of chromosomes arranged by size, shape, and banding pattern
making a karyogram
Cells are stained and viewed under a light microscope
Photographs are taken of the contents of the nucleus during metaphase of cell division
The photographs of the chromosomes are cut up and arranged by size, shape, and banding pattern
This can be done with paper and scissors or on a computer
why do humans have 46 chromosones while chimpanzees have 48
A pair of chromosomes disappeared from the genome
A pair of chromosomes fused with another pair to form a single pair
why is it unlikely that A pair of chromosomes disappeared from the genome in humans
The loss of an entire pair of chromosomes would have had a significant effect on the characteristics of human ancestors, and may have put their survival at risk
Evidence that supports the hypothesis that Chromosomes in pairs 12 and 13 in a common ancestor fused to form the chromosomes in human pair 2
Human chromosome 2 contains a region of non-coding DNA known as satellite DNA that corresponds to the location of the centromere in chimpanzee chromosome 13; this could be a remnant of a centromere
The banding of the long arms of acrocentric chimpanzee chromosomes 12 and 13 corresponds to the banding of metacentric human chromosome 2
Human chromosome 2 contains telomeric DNA in the middle of the chromosome
Evidence that supports the hypothesis that Chromosomes in pairs 12 and 13 in a common ancestor fused to form the chromosomes in human pair 2
Chimpanzee chromosomes 12 and 13, when placed end-to-end, match the length of human chromosome 2
The location of the centromere of chimpanzee chromosome 12 matches that of human chromosome 2
Evidence that does not supports the hypothesis that Chromosomes in pairs 12 and 13 in a common ancestor fused to form the chromosomes in human pair 2
The length of chimpanzee chromosomes 12 and 13 combined is not a perfect match for human chromosome 2; there is a slight overlap
The location of the centromere of chimpanzee chromosome 13 does not match that of human chromosome 2
Chromosome fusion evidence diagram
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For a hypothesis to be testable, it must have the following characteristics
There needs to be access to evidence that supports it or refutes it
The hypothesis needs to be a testable statement
A hypothesis should not contain vague statements that use terms like 'may' or 'could
A hypothesis should not make predictions
A hypothesis should not draw causal conclusions
how can the hypothesis be tested
the fusion of ancestral chromosomes 12 and 13 can be tested by examining chromosome evidence from humans and modern chimps
genome
All of the genetic information in an organism
This refers to the DNA present within every cell of an organism
This includes genes that code for proteins as well as non-coding DNA sequences
Mitochondrial DNA and chloroplast DNA are included in the genome of eukaryotic cells
In a prokaryote cell, plasmid DNA is included in the genome
Advances in technology have allowed scientists to determine the entire base sequence of the genes within an organism's genome
DNA sequencing
Determining the base sequence of DNA
Genome-wide comparisons can now be made between individuals and between species
Comparisons show that there is a high level of genome similarity within, and even between, species
Humans share around 99.9 % of their DNA with other humans
Humans share around 99 % of their DNA with chimpanzees
Organisms in the same species share most of their genome but variations such as single-nucleotide polymorphisms give some diversity.