A3.1 diversity of organisms Flashcards
(36 cards)
basis of variation between organisms
-no two individual organisms share the same traits
-patterns of variation are complex and are the basis for naming and categorizing objects
morphological species definition
individuals that belong to the same species have external physical similarities
biological species definition
population whose members can interbreed and produce fertile offspring to be considered same species
what is gene flow
how genes go from on individual/ population to another
categories of taxa (humans)
DOMAIN
KINGDOM (anamalia)
PHYLUM(chordata)
CLASS (mammalia)
ORDER (primate)
FAMILY (hominidae)
GENUS(homo)
SPECIES(sapiens)
discontinuous
continuous
discontinuous= when variation can be placed into distinct categories
continuous=when variation has a wide range of possibilities
original morphological concept
-scientists in 18th centaury had difficulty in identifying plants
Linnaeus idea: to categorize all living organisms, giving them a name using a uniform system
-creating names in latin/greek
-based classification system and names on physical appearance= morphological classification
the binomial systems for naming organisms
-scientific name based on species
-‘‘two-names’’
-nomenclature= system used for naming
first word is GENUS (capital)
second word if species (lower)
-organisms in the same genus will more similar characteristics compared to organisms in another genus
three main rules when using binomial nomenclature
1- each organism has its own name
2- names can be universally understood
3-some stability in system- no one can change without valid reason
biological species concept
(another definition of a species proposed in 1942)
-in order to be classified as the same species, individuals must be able to breed together to produce fertile offspring
what the biological species concept doesn’t show
speciation
process of splitting one species into two or more groups that can no longer reproduce
-very gradual process, rather than a single act, the traits become more different and results in two new species that have a common ancestor
diploid cells
A diploid cell is a cell that contains two complete sets of chromosomes
-most human body cells
-have even chromosome number
2n
haploid cells
A haploid cell has only a single set of chromosomes.
-gamet cells
-n
chromosome number in humans and chimpanzees
humans= 46 (23n x 2)
chimps=48 (24 x 2)
what is a karyogram
representation of the chromosomes found in a cell arranged according to standard format- size/shape
what is a karyotype
specific number and appearance of chromosomes in an organisms cell, represented by a karyogram
what does the shape of a chromosome depend on
THE CENTROMERE= which is a structure that holds the two chromatids together
steps on how karyogam image is obtained
1) cells are stained- prepared on glass slide under light microscope
2)photomicrograph image is obtained during specific parts of cell division
3) image cut, separated
4) image ordered in size and position of centromere
question of human chromosome 2, and its hypothesis
-apes have 48 chromosomes and since we have a common ancestor, what happened with out chromosome number?
2 Hypothesis;
1- complete chromosome disappeared
2- two chromosomes from earlier common ancestor fused together to become a single chromosome
(first hypothesis is unlikely)
characteristics that help identify chromosome
-2 characteristics that help identify chromosome; shape + bonding patterns
‘x’ shape= METACENTRIC
centromere at one end= ACROCENTRIC
evidence for fusion and formation of human chromosome 2
hypothesis= chromosome 2 arose from fusion of chromosomes 12 and 13 in a shared ancestor
EVIDENCE:
-non human acrocentric chromosomes 12, 13 had similar length to human chromosome 2
-centromere positions lined up in chromosome 12
-long arm of chimp chromosome 12 matches short arm of human chromosome 2
-long arm of chimp chromosome 13 matches the long arm of human chromosome 2
-presence of telomeric DNA , that is not supposed to be at center of chromosome, but rather only at tips. Implies fusion
reason for diversity in a species
-humans share the same genes, but not the same version of each gene
-differences are found in DNA sequences of base pairs; small portion of people may have a G rather then T in a base pair
-these variation start out as mutations
this is called SINGLE NUCLEOTIDE POLYMORHISM
what is single nucleotide polymorphism
-variation involving one base
-100-300 bases in human genetic code has a SNP, very small percent are functional, meaning them show in a persons phenotype.