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A list of 1719 chemical compounds identified from headspace samples of floral scent is presented. The list has been compiled from some 270 published papers, including analyses of 991 species of flowering plants and a few gymnosperms, a sample including seed plants from 90 families and 38 orders. The compounds belong to seven major compound classes, of which the aliphatics, the benzenoids and phenylpropanoids, and, among the terpenes, the mono- and sesquiterpenes, occur in most orders of seeds plants. C5-branched compounds, irregular terpenes, nitrogen-containing compounds, and a class of miscellaneous cyclic compounds have been recorded in about two-thirds of the orders. Sulfur-containing compounds occur in a third of the orders, whereas diterpenes have been reported from three orders only. The most common single compounds in floral scent are the monoterpenes limonene, (E)-β-ocimene, myrcene, linalool, α-and β-pinene, and the benzenoids benzaldehyde, methyl 2-hydroxybenzoate (methyl salicylate), benzyl alcohol, and 2-phenyl ethanol, which occur in 54–71% of the families investigated so far. The sesquiterpene caryophyllene and the irregular terpene 6-methyl-5-hepten-2-one are also common and occur in more than 50% of the families. Orchidaceae are by far the best investigated family, followed by several families known to have many species with strongly scented flowers, such as Araceae, Arecaceae, Magnoliaceae, and Rosaceae. However, the majority of angiosperm families are still poorly investigated. Relationships between floral scent and pollination, chemistry, evolution, and phylogeny are briefly discussed. It is concluded that floral scent chemistry is of little use for phylogenetic estimates above the genus level, whereas the distribution and combinations of floral .scent compounds at species and subspecific levels is a promising field of investigation for the understanding of adaptations and evolutionary processes in angiosperms. [ABSTRACT FROM AUTHOR]

Although our biological knowledge regarding cactus species is thorough in many areas, only in recent years have ecologists addressed their demographic behavior. Here we attempt a first review of the present knowledge on cactus demography, including an analysis of the published information on species with different growth forms and life-history traits. Our review shows that cactus distribution ranges are determined by environmental heterogeneity and by species-specific physiological requirements. Temperature extremes may pose latitudinal and altitudinal distribution limits. At a more local scale, soil properties dramatically affect cactus distribution. Most cacti show a clumped spatial distribution pattern, which may be the reflection of a patchy resource distribution within their heterogeneous environments. The association of cacti with nurse plants is another factor that may account for this aggregated distribution. Many cacti grow in association with these perennial nurse plants, particularly during early lifecycle phases. The shade provided by nurse plants results in reduced evapotranspiration and buffered temperatures, which enhance cactus germination and establishment. In some cases a certain degree of specificity has been detected between particular cactus species and certain nurse plants. Yet some globose cacti may establish in the absence of nurse plants. In these cases, rocks and other soil irregularities may facilitate germination and establishment. Cacti are slow-growing species. Several abiotic factors, such as water and nutrient availability, may affect their growth rate. Competition and positive associations (i.e., mycorrhizae and nurse--cacti association) may also affect growth rate. Age at first reproduction varies greatly in relation to plant longevity. In general, cactus reproductive capacity increases with plant size. Populations are often composed of an uneven number of individuals distributed in the different size categories. [ABSTRACT FROM AUTHOR]

Examines the plant distribution of Malesherbiaceae, a monogenetic plant group in South America. Characteristics of the habitat; Interrelationship between the rise of the Andes and increased aridity on the western slopes; Occurrence of geological and climatic changes.

Examines the plant distributions in northern Peru. Use of ribes and loasaceae; Phylogenetic relationship between species; Effect of complex tomography on habitat types; Presence of paleoendemics and neoendemics.

Examines the plant distribution of Oxalis tuberosa alliance in South America. Use of cladograms developed from DNA sequence data; Comparison between phylogeny and distribution; Presence of endemic species.