Theme A: A3 Unity and Diversity Organisms - A3.1 Diversity Organisms Flashcards
ways of classifying organisms
generally classified based on morphology, but also:
1) feeding habits: carnivore/ herbivore/ makes its own food
2) habitat: land-dwelling/ aquatic
3) movement: sessile/ free moving
4) daily activity: nocturnal/ diurnal
5) risk: harmless/ venemous
6) anatomy: plant/ animal/ vertebrate/ invertebrate
morphology
physical appearance of an organism
taxon (plr. taxon)
each category an organism is placed into
8 levels of taxonomy (largest to smallest)
the largest is domain, followed by:
1) kingdom
2) phylum
3) class
4) order
5) family
6) genus
7) species
discontinuous
when variation can be placed into distinct categories (e.g. type A blood and type B blood)
continuous
when variation has a wide range of possibilities (height of a tree)
binomial nomenclature
first name is capitalised and refers to the genus (Homo)
second name is lowercase and refer to the species (sapiens)
3 main objectives of binomial nomenclature
1) each organism has a unique name that can’t be confused with another organism
2) names can be universally understood
3) the system is stable so people can’t change names of organisms without valid reasons
biological species concept
this definition suggests that in order to be classified the same species individuals must be able to breed together and produce fertile offspring.
speciation
process by which a population is separated into 2 groups that can no longer reproduce together. Overtime, one part evolves in a different way to the other. Gradually the result is two new species with a common ancestor.
diploid
diploid cells have two complete sets of chromosomes, one set from each parent. In humans, this number is 46. Body cells are diploid.
remember: diploid = 2n
gametes
a reproductive/sex cell.
haploid
Haploid cells are those that have only a single set of chromosomes. In humans, this number is 23. Gametes (sperm and egg cells) are haploid.
remember: haploid = n
karyogram
representation of chromosomes found in a cell arranged according to a standard format. the chromosomes are placed according to their size and shape.
karyotype
specific number and appearance of the chromosomes in the indidividual’s cells.
centromere
The part of a chromosome that holds two sister chromatids (copies of the chromosome) together. A chromosomes shape mainly depends on the position of its centromere.
2 characteristics that help identify a chromosome
1) shape (position of centromere)
2) banding pattern
acrocentric shape
centromere at one end, one arm pf the chromosome is much shorter and the other other much larger.
metacentric shape
chromosomes in the shape of an X that have a centromere close to the centre.
telemeres
caps at the tips of chromosomes that contain repeating sequences of DNA (telemetric DNA) and provide protection.
single nucleotide polymorphism (SNP)
a variation involving 1 base pair in a sequence of DNA. around every 100-300 bases n a humans genetic code contains an SNP. most SNPs are neutral and won’t affect one’s phenotype, where around 5% are functional. this DNA variation can lead to genetic disease or increased susceptibility to diseases.
phenotype
a physical expression of a gene, like blood type or colour vision
phylogenetics
the study of evolutionary relationships among organisms. Using whole genome sequencing, scientists compare entire DNA sequences to analyse genetic similarities and differences, which helps construct phylogenetic trees. These trees show common ancestry and the evolutionary divergence of species based on their complete genomes.
personalised medicine
information about a person’s genetic makeup that can be applied to an individual when prescribing treatments