Ұя тозу және организм бөліктерінің түсуі

Shedding of various parts of an organism

Abscission (from Latin ab 'away') is the shedding of various parts of an organism, such as a plant dropping a leaf, fruit, flower, or seed. In zoology, abscission is the intentional shedding of a body part, such as the shedding of a claw, husk, or the autotomy of a tail to evade a predator. In mycology, it is the liberation of a fungal spore. In cell biology, abscission refers to the separation of two daughter cells at the completion of cytokinesis.

A plant will abscise a part either to discard a member that is no longer necessary, such as a leaf during autumn, or a flower following fertilisation, or for the purposes of reproduction. Most deciduous plants drop their leaves by abscission before winter, whereas evergreen plants continuously abscise their leaves. Another form of abscission is fruit drop, when a plant abscises fruit while still immature in order to conserve resources needed to bring the remaining fruit to maturity. If a leaf is damaged, a plant may also abscise it to conserve water or photosynthetic efficiency, depending on the 'costs' to the plant as a whole. The abscission layer is a greenish greyish color. Abscission can also occur in premature leaves as a means of plant defense. Premature leaf abscission has been shown to occur in response to infestation by gall aphids. By abscising leaves that have been made host to aphid galls, plants have been shown to massively diminish the pest population, as 98% of aphids in abscised galls died. The abscission is selective, and the chance of dropping leaves increases as the number of galls increases. A leaf with three or more galls was four times more likely to abscise than a leaf with one, and 20 times as likely to be dropped as a leaf without any galls.

Abscission occurs in a series of three events: 1) resorption, 2) protective layer formation, and 3) detachment. Steps 2 and 3 may occur in either order depending on the species. Nitrogen is found in chlorophyll and is often a limiting nutrient for plants, which need large quantities to form amino acids, nucleic acids, proteins, and certain plant hormones. Once nitrogen and other nutrients have been extracted from chlorophyll, the nutrients will travel to other tissues of the plant. Situated on both sides of the abscission zone are layers of parenchyma cells, which produce and inject suberin and lignin under the abscission zone into the new layer of cork cells. Detachment can occur when layers of parenchyma cells secrete cell wall enzymes to self digest the middle lamella, which holds the cell walls together at the abscission zone.

The reduction of chlorophyll production in leaves due to decreased sunlight in the autumn explains why some leaves turn yellow. However, the yellow color can attract aphids, so some trees turn the leaves red instead by injecting a bright pigment. The loss of chlorophyll may also contribute to the abscission process.

A variety of reactive oxygen species (ROS) are generated by plants during times of stress (biotic and abiotic), including UV light, cool temperatures, excessive light, pathogens, parasites, and high salinity. The presence and continuous production of these ROS causes disruption in the homeostasis of the cellular components, leading to metabolic dysfunction and expression of cell wall degrading enzymes (WDEs).

While researchers originally believed abscisic acid to be the hormone that stimulates abscission (for which the hormone was named), it was later proven that it does not play a primary role. In fact, auxin, a plant hormone, and ethylene have been implicated as prominent regulators of abscission signaling. The two compounds work in a synergistic fashion: As the auxin levels decrease, the flux of auxin to the abscission zone is reduced. Exhaustion of auxin makes the abscission zone sensitive to ethylene. When the plant is then exposed to ethylene, gene expression of cell wall degrading enzymes such as cellulase and polygalacturonase are activated. However, this is not to say that ethylene directly activates WDE gene expression, because the elements responsible for detecting ethylene have not been found in the gene's promoter region. Dwindling auxin levels have also been implicated in autumn leaf color change.