IB Biology SL A3.1 Diversity of organisms Notes

Diversity begins inside a species. Individuals of the same species are not identical, and that variation is the raw material for natural selection. Continuous variation, such as height or mass, often comes from many genes plus environmental effects, so values form a range rather than neat categories. Darwin noticed that selection can only act when individuals differ.

Notice that a species stays one species even when individuals vary.

Morphology is useful when biologists group organisms by visible structural traits. It works well in fieldwork, fossils, and many plants, where breeding evidence may be unavailable. But morphology can mislead when males and females look different or when there is large variation inside one species. Binomial nomenclature solves a different problem: it gives every species a universal two-part Latin name, with the genus capitalized and the species lowercase, both italicized or underlined.

Keep species grouping by shared traits separate from the formatting rules of binomial names.

The biological species concept tests species by reproduction: members of the same species can interbreed and produce fertile offspring, so gene flow links them. This works well for many sexually reproducing organisms, but it fails or becomes awkward for extinct organisms, asexual organisms, and cases where different forms still exchange genes. Speciation is gradual, so isolated populations may be partly diverged and theoretically able to interbreed, even if they cannot meet. That is why some species boundaries are partly arbitrary.

Chromosomes give another kind of species evidence. Chromosome number is usually constant within a species but varies between species; diploid numbers are even because chromosomes occur in homologous pairs. A karyotype is the full chromosome set, while a karyogram is the arranged display by length, banding pattern, and centromere position. Human chromosome 2 is important because its structure supports fusion from two ancestral ape chromosomes.

Use the visual to move from simple counts to structural evidence.

A genome is all the genetic information in an organism. Members of one species share most of their genome but differ at variants. SNPs, or single nucleotide polymorphisms, are common single-base differences used as biological markers. Across eukaryotes, genomes vary in size and base sequence, and variation between species is much larger than variation within one species. Also, not all DNA codes for proteins, so genome comparison is not just gene counting.

Genome size means the amount of DNA in one chromosome set. A larger genome does not necessarily mean a more complex organism; polyploidy can greatly increase genome size, especially in plants. Whole genome sequencing began at scale with the Human Genome Project and is now used for evolutionary relationships, gene discovery, and pathogen research. Future and growing uses include personalized medicine, diagnosis, disease prevention, and vaccine targets.

Separate the question of DNA amount from the question of what whole genome sequencing can reveal.

For SL, A3.1 is really one evidence map. Variation explains why individuals differ. Morphology and binomial nomenclature help group and name organisms. The biological species concept uses interbreeding and fertile offspring, but boundaries can be difficult during gradual speciation. Chromosomes and karyograms add cellular evidence. Genomes, SNPs, genome size, and whole genome sequencing add molecular evidence. The skill is choosing the right evidence for the question.

Use this for combined SL questions about classification evidence, species concepts, chromosomes, or genomes.