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Garcinia section Xanthochymus (Clusiaceae) is revised for Thailand with four native species, i.e ., G. dulcis , G. nervosa , G. prainiana , and G. xanthochymus . All species are described with updated morphological descriptions, illustrations, and an identification key, together with notes on distributions, distribution maps, habitats and ecology, phenology, conservation assessments, etymology, vernacular names, uses, and specimens examined. Four taxa, G. andamanica , G. andamanica var. pubescens , G. cambodgiensis and G. vilersiana , are synonymized under G. dulcis , and two taxa, G. nervosa var. pubescens and G. spectabilis , are newly synonymized under G. nervosa . Nine names are lectotypified: G. dulcis and its associated synonyms ( G. cambodgiensis and G. vilersiana ), G. nervosa and its associated synonyms ( G. andersonii , G. nervosa var. pubescens , and G. spectabilis ), G. prainiana , and G. xanthochymus . All species have a conservation assessment of Least Concern (LC). The fruits of all species are edible and have a sour or sweet-sour taste.

In this study we dissect the causes of variation in intra‐inflorescence allocation in a sexually polymorphic species, Fragaria virginiana. We separated out the effects of resource competition during flowering from those of inflorescence architecture, as well as identified the effects of sex morph and genotype. We found position‐based variation in petal length, ovule, pollen, and flower number to be influenced more by architecture than by our resource manipulations during flowering. We also found both genotype‐ and sex‐specific intra‐inflorescence patterns. Furthermore, our data indicate that the sex morph‐specific intra‐inflorescence patterns result from architectural modifications of the basic pattern. In fact, sex‐differential intra‐inflorescence patterns suggest that fitness through male and female function may be maximized by different resource distribution patterns within the inflorescence and may have been modified by past selection. Specifically, females invested heavily in ovules at positions where fruit set was most likely (primary and secondary), at the expense of flower number and allocation per flower at more distal positions. Whereas functional males invested minimally in ovules at all flower positions and produced the most abundantly flowered inflorescences, hermaphrodites, on the other hand, showed intermediate patterns, implying a compromise between sex functions. We suggest that consideration of intra‐inflorescence allocation and inflorescence architecture may reveal the mechanism underlying sexual dimorphism in flower allocation and number.

Between March 1993 and May 1995 the floral biology and the phenology of Clusia nemorosa G. Mey. (Clusiaceae) were studied in two dioecious populations in Pernambuco State, and some observations were made in gynodioecious populations, that were encountered only in Bahia State. The species flowers from June to January/February. The flowers are bowl shaped, and last only one day. The floral reward is resin which is produced by staminodia in all types of flowers. The sex ratio was 1:1 for the studied populations. The pollen viability was approximately 98%. Apomixis was not observed. The rate of fruit set, in hermaphrodite individuals, under natural conditions and the sex ratio of the gynodioecious populations studied suggest that the hermaphrodite individuals may behave as males. Clusia nemorosa is melittophilous and was visited by 16 species of bees. The main pollinators were Euplusia mussitans, E. iopyhrra, Eulaema cingulata, E. nigrita, Euglossa cordata and Euglossa sp.