Hormonal Changes after Compatible and Incompatible Pollination in Theobroma cacao L.

In order to characterize the self-incompatibility system in Theobroma cacao, the levels of ethylene, indole-3-acetic acid (IAA), and abscisic acid (ABA) were determined after pollination with compatible and incompatible pollen and in unpollinated flowers. Pollen tube growth rates after incompatible and compatible pollinations were identical, and the majority of the pollen tubes reached the ovules between 12 and 20 hours after pollination. ABA levels rose in incompatibly pollinated flowers, and fell in compatibly pollinated flowers, prior to pollen tube—ovule contact. Ethylene evolution remained stable in compatibly pollinated flowers and rose in incompatibly pollinated flowers. IAA concentrations increased in compatibly pollinated flowers, and remained stable in incompatibly pollinated flowers after pollination and subsequent to pollen tube—ovule contact.

Detecting Cross-incompatibility of Three North American Apricot Cultivars and Establishing the First Incompatibility Group in Apricot

Laboratory and orchard tests have shown that the apricot (Prunus armeniaca L.) cultivars `Hargrand', `Goldrich', and `Lambertin-1' are cross-incompatible. All three cultivars are from North American breeding programs and have `Perfection' as a common ancestor. In orchard tests, compatible pollinations resulted in 19% to 74% fruit set, while incompatible pollinations resulted in <2% fruit set. Microscopic examination showed that, in incompatible pollinations, pollen tube growth was arrested in the style, most frequently in its third quarter, and that the ovary was never reached. It is proposed that self-incompatibility in apricot is of the gametophytic type, controlled by one S-locus with multiple alleles, and that these three cultivars are S1S2.

Citrus pollen tube development in cross-compatible gynoecia, self-incompatible gynoecia, and in vitro

The route of 'Orlando' tangelo (Citrus paradisi Macf. × C. reticulata Blanco) pollen tubes was traced and compared in self-incompatible pollinations and cross-compatible pollinations with 'Dancy' tangerine (C. reticulata Blanco). In both crosses, 'Orlando' pollen germinated in the stigmatic exudate and grew between the papillae on the stigma surface and inter-cellularly between the parenchymatous cells until reaching a stylar canal by 3 days. However, in the incompatible pollination, irregular deposition of callose occurred in the pollen tube walls as early as 1 day after pollination. By day 6, pollen tubes were in the upper portion of the ovary in the compatible pollination, whereas most pollen tubes from the incompatible pollination were still in the upper style. 'Orlando' pollen tube growth rate decreased substantially by day 3 in both the self-incompatible pollination and in vitro but increased rapidly after day 3 in the compatible combination. The generative cell divided between 1 and 3 days after pollination in the compatible cross. Generative cell division was observed by day 3 in only a few pollen tubes in the incompatible cross and in cultured tubes. Compatible pollen tubes grew slowly for the first 3 days after pollination, during which time generative cells divided and then grew rapidly until fertilization. In contrast, incompatible pollen tubes showed morphological features indicative of an incompatibility reaction by 1 day after pollination and grew slowly for a period of 6 days, and then ceased growth.

A quantitative and structural comparison of Citrus pollen tube development in cross-compatible and self-incompatible gynoecia

Pollen tube development in Orlando tangelo (Citrus paradisi Macf. × C. reticulata Blanco.) was compared within and between cross-compatible pollinations of Orlando pollen on Dancy tangerine (C. reticulata Blanco.) stigmas and self-incompatible pollinations on Orlando tangelo stigmas. Orlando and Dancy gynoecia were morphologically similar but differed slightly in stigma, style, and ovary lengths. Orlando pollen tube development was studied 1, 3, 6, 9, and 12 days after both cross- and self-pollination to record the number of pollen tubes at each of five levels: stigma surface, upper style, lower style, ovary, and entrance into ovules. In the incompatible cross (self-pollinated Orlando), the stigma was the primary region of pollen tube arrest. In the compatible cross (Orlando pollen on Dancy), some pollen tubes penetrated ovules between 9 and 12 days after cross pollination; however, other pollen tubes were arrested in the stigma. Pollen tubes that successfully penetrated ovules in the compatible cross differed morphologically from pollen tubes arrested in both the compatible and incompatible situations. Successful compatible pollen tubes were straight with thin-walled tips and regularly spaced callose plugs behind the growing tips. Many pollen tube abnormalities associated with the self-incompatible pollination of Orlando were also present among arrested pollen tubes from the compatible cross.

Incompatibility, stamen movement and pollen economy in a heterostyled tropical forest tree, Cratoxylum formosum (Guttiferae)

Cratoxylum formosum shows all the classical features of a distylic species. The two types are: long-styled plants with short stamens and small pollen grains and short-styled plants with long stamens and large pollen grains. Compatible pollinations are only between the two types; incompatible pollen tubes are inhibited in the style. A significant morphological feature distinguishes Cratoxylum from distylic plants in other families. Instead of having a small number of anthers making well separated narrow discs in the two types, Cratoxylum has many anthers (144) and they are arranged on staminal bundles that produce long cylinders of anthers that partially occupy similar height zones in the two types of flower. A novel method of separation of the two height zones is achieved by the bending of the stamens of the long-styled type when the flower opens, which converts the cylinder to a narrow disc of anthers at the same height as the ‘short’ stigma. The bending coincides with anther dehiscence and is slightly later than the first daily insect visitation. The anthers return to the upright position later in the day, when the pollination is complete. There was a 20-fold difference between the amounts of pollen deposited on the two types of stigmas. The ‘long’ stigmas received 1200 pollen grains per flower, in the ratio of 46 ‘long’ to 54 ‘short’, which is close to the ratio of two types of pollen produced in the population. This random deposition of pollen on ‘long’ stigmas is, however, more than adequate for the 36 seeds produced per flower. ‘Short’ stigmas received only 64 pollen grains per flower, in the ratio of 90 ‘long’ to 10 ‘short’, and several flowers had below the critical level of 36 compatible pollen grains for full seed production. Pollen loads of the pollinating bee, Apis javana , consisted of ‘long’ and ‘short’ pollen on the thorax in the ratio found on the ‘long’ stigma, and on the head of the bee in a ratio close to the 9:1 found on the ‘short ’ stigma. The corbicular loads reflected accurately the pollen of the tree in which the bee was caught. For Cratoxylum the accurate positioning of the anthers of the long-styled plant in relation to the visiting bees head was an important evolutionary step in the effective pollination of the short-styled form, which, at least in this species, is one critical and highly selected feature of the system.

The physiology of incompatibility in plants - I. The effect of temperature

Two different genetic systems of incompatibility between pollen and style are known. One, heterogamety, depends upon the genotype of the individual pollen grain; the other, heterostyly, upon the genotype of its parent. We do not know whether the two types are physiologically related. The specificity of heterogamety indicates an immunity reaction. The effect of temperature on pollen-tube growth in the two systems was measured in order to discover their relationship. Compatible pollinations of both systems showed increased rate of growth with increased temperature until the lethal point was approached at about 35°C. Incompatible pollinations of both systems showed an optimum growth rate between 15 and 20°C. The physiological method of inhibition is therefore probably related although its genetic basis is different. The different rate of growth at different temperatures gives different total growth at in­hibition, and at the most favourable temperature there may be no inhibition at all. There is therefore no specific inhibitory zone in these plants, although elsewhere the top of the style may provide such a zone. Certain genotypes of Oenothera organensis show such powerful incompatibility that no temperature sensitivity can be discovered. This extreme modification is determined by the pollen parent’s genotype, like the main action in heterostyly. In heterostyled plants thrum pollen has to grow dowm the longer pin style; it is adapted to this in two ways. In Primula it is larger, in Linum grandiflorum it has a higher osmotic pressure. In either case, presumably, it has the higher dry weight. In two heterostyled Primula species thrum pollen grows faster dowm the long-pin style than pin pollen does down the short-thrum style. But in the illegitimate matings thrum pollen is more strongly inhibited. There is therefore a differentiation of the mechanism adapted to secure equal regularity of cross-fertilization of the two types.