Domestication of the banana
The domestication of the banana is the process that transformed fruits full of seeds into parthenocarpic seedless fruits that develop in the absence of pollination. The founding events took place in the humid tropical belt that extends from India to the Solomon Islands, the natural range of wild species of bananas. The earliest archaeological evidence of domesticated bananas is from Papua New Guinea and has been dated to at least 7,000 years before present.
Cultivated bananas were domesticated from a small subset of wild species of bananas. The best known are Musa acuminata and Musa balbisiana since they are at the origin of the vast majority of cultivars known today. The ancestor of a group of bananas domesticated independently in the Pacific region, the Fei bananas, has not been identified.
Like human beings, wild bananas are diploid, that is their genome is comprised of two sets of gene-bearing chromosomes, only one of which is passed on by each parent during sexual reproduction. The transition from wild seeded bananas to parthenocarpic (the ability to produce a fruit in the absence of pollination) and seedless bananas is two-step process that start with a sexual phase followed by an asexual one.
From wild bananas to edible diploids
The potential to produce parthenocarpic fruits has been traced to genes present in Musa acuminata. Domestication for edibility most likely started with farmers transplanting the offshoots (suckers) of plants that were edible by virtue of having less seeds and more pulp. But since these plants were still fertile, they continued mating with other fertile banana plants. The latter could be plants from the same or different Musa acuminata subspecies or with a Musa balbisiana plant.
Under the nomenclature system developed by Norman Simmonds and Kenneth Shepherd, those sexual events became the foundation of the AA and AB genome groups, the letter A standing in for acuminata and B for balbisiana.
From diploids to triploids
Triploid cultivars were produced when one of the diploid parents normally passed on half of its genome, while the other contributed an unreduced genome (a phenomenon called meiotic restitution). This process produced three main genome groups : AAA, AAB and ABB.
Sterility is believed to be due to a combination of structural and genetic factors. The structural factors are linked to matings between distant relatives (between different subspecies of Musa acuminata or between different species, mainly Musa acuminata and Musa balbisiana), as inheriting mismatched chromosomes made it difficult for the progeny to produce fertile ovules and pollen. But scientists also believe that farmers preferentially propagating the plants that produced fruits with the least seeds might have selected for genes that contribute to sterility. Triploidy made further sexual reproduction extremely unlikely,.
From that point on, further diversity was produced by farmers propagating mutant plants that exhibited desirable traits. Diploid and triploid cultivars that are related to each other through a series of mutations are said to form a subgroup. Two examples are the Plantains of Africa and the East African highland bananas, which have upwards of 100 cultivars each. This diversity is the result of farmers propagating mutants of the triploid ancestors introduced to the continent.
Also on this website
Special issue on the history of banana domestication in Ethnobotany Research & Applications.