RESUMO
Abandonment of agricultural lands promotes the global expansion of secondary forests, which are critical for preserving biodiversity and ecosystem functions and services. Such roles largely depend, however, on two essential successional attributes, trajectory and recovery rate, which are expected to depend on landscape-scale forest cover in nonlinear ways. Using a multi-scale approach and a large vegetation dataset (843 plots, 3511 tree species) from 22 secondary forest chronosequences distributed across the Neotropics, we show that successional trajectories of woody plant species richness, stem density and basal area are less predictable in landscapes (4 km radius) with intermediate (40-60%) forest cover than in landscapes with high (greater than 60%) forest cover. This supports theory suggesting that high spatial and environmental heterogeneity in intermediately deforested landscapes can increase the variation of key ecological factors for forest recovery (e.g. seed dispersal and seedling recruitment), increasing the uncertainty of successional trajectories. Regarding the recovery rate, only species richness is positively related to forest cover in relatively small (1 km radius) landscapes. These findings highlight the importance of using a spatially explicit landscape approach in restoration initiatives and suggest that these initiatives can be more effective in more forested landscapes, especially if implemented across spatial extents of 1-4 km radius.
Assuntos
Ecossistema , Florestas , Biodiversidade , Árvores , PlantasRESUMO
Tropical forests are globally important for biodiversity conservation and climate change mitigation but are being converted to other land uses. Conversion of seasonally dry tropical forests (SDTF) is particularly high while their protection is low. Secondary succession allows forests to recover their structure, diversity and composition after conversion and subsequent abandonment and is influenced by demographic rates of the constituent species. However, how these rates vary between seasons for different plant sizes at different successional stages in SDTF is not known. The effect of seasonal drought may be more severe early in succession, when temperature and radiation are high, while competition and density-dependent processes may be more important at later stages, when vegetation is tall and dense. Besides, the effects of seasonality and successional stage may vary with plant size. Large plants can better compete with small plants for limiting resources and may also have a greater capacity to withstand stress. We asked how size-dependent density, species density, recruitment and mortality varied between seasons and successional stages in a SDTF. We monitored a chronosequence in Yucatan, Mexico, over six years in three 0.1 ha plots in each of three successional stages: early (3-5 years-old), intermediate (18-20 years-old) and advanced (>50 years-old). Recruitment, mortality and species gain and loss rates were calculated from wet and dry season censuses separately for large (diameter > 5 cm) and small (1-5 cm in diameter) plants. We used linear mixed-effects models to assess the effects of successional stage, seasonality and their changes through time on demographic rates and on plant and species density. Seasonality affected demographic rates and density of large plants, which exhibited high wet-season recruitment and species gain rates at the early stage and high wet-season mortality at the intermediate stage, resulting in an increase in plant and species density early in succession followed by a subsequent stabilization. Small plant density decreased steadily after only 5 years of land abandonment, whereas species density increased with successional stage. A decline in species dominance may be responsible for these contrasting patterns. Seasonality, successional stage and their changes through time had a stronger influence on large plants, likely because of large among-plot variation of small plants. Notwithstanding the short duration of our study, our results suggest that climate-change driven decreases in rainy season precipitation may have an influence on successional dynamics in our study forest as strong as, or even stronger than, prolonged or severe droughts during the dry season.
RESUMO
Floral phenology and breeding system of Tillandsia streptophylla (Bromeliaceae) were studied in a low inundated forest in Yucatan, Mexico. During the flowering season, from March to August, terminal scapose 1-branched, paniculate inflorescences are produced with one flower per branch opening per day, over a period of 11-29 days. Flowers are tubular, light violet, with the stigma placed below the anthers, both protruding above the corolla. Flowers are protandrous, with anthers releasing pollen from 0500 hours and stigma becoming receptive around 0900 hours. Controlled experimental crosses suggest that Tillandsia streptophylla is self incompatible and therefore, pollinator-dependent.
Assuntos
Polinização/fisiologia , Tillandsia/fisiologia , Cruzamento , Flores/fisiologia , México , Estações do AnoRESUMO
The crude ethanolic extract of leaves, stem-bark and roots of J. flammea were tested for their cytotoxic effect against two mammalian cell lines (HeLa and RAW 264.7) and four bacterial species (Staphylococcus aureus, Bacillus subtilis, Escherichia coli and Pseudomonas aeruginosa). When tested at the concentration of 100 microg/mL, the root extract showed the highest cytotoxic activity against mammalian cells followed by the stem-bark extract while the leaves extract did not show significant activity. No antibacterial activity was detected for all extracts when tested up to 500 microg/disc in the disc diffusion assay. The cytotoxic root extract was subjected to fractionation using solvents of ascending polarity: petroleum ether, chloroform, ethylacetate, butanol and water. The water fraction which showed cytotoxic activity was further subjected to routine bioassay-guided fraction to lead to the isolation of sakurasosaponin as the active principle. The recorded IC50 value for sakurasosaponin was 11.3 +/- 1.52 and 3.8 +/- 0.25 microM (n=3) against HeLa and RAW 264.7 respectively. The identification of sakurasosaponin was based on analysis of spectroscopic data.
Assuntos
Antibacterianos/química , Antibacterianos/toxicidade , Antineoplásicos Fitogênicos/química , Antineoplásicos Fitogênicos/toxicidade , Plantas Medicinais/química , Saponinas/química , Saponinas/toxicidade , Animais , Bactérias/efeitos dos fármacos , Sequência de Carboidratos , Linhagem Celular Tumoral , Ensaios de Seleção de Medicamentos Antitumorais , Células HeLa , Humanos , Metanol , México , Camundongos , Testes de Sensibilidade Microbiana , Dados de Sequência Molecular , Extratos Vegetais/química , Extratos Vegetais/toxicidade , Raízes de Plantas/química , SolventesRESUMO
Floral phenology and breeding system of Tillandsia streptophylla (Bromeliaceae) were studied in a low inundated forest in Yucatan, Mexico. During the flowering season, from March to August, terminal scapose 1-branched, paniculate inflorescences are produced with one flower per branch opening per day, over a period of 11-29 days. Flowers are tubular, light violet, with the stigma placed below the anthers, both protruding above the corolla. Flowers are protandrous, with anthers releasing pollen from 0500 hours and stigma becoming receptive around 0900 hours. Controlled experimental crosses suggest that Tillandsia streptophylla is self incompatible and therefore, pollinator-dependent. Rev. Biol. Trop. 57 (3): 761-770. Epub 2009 September 30.
Estudiamos la fenología floral y el sistema de cruzamiento de la bromelia Tillandsia streptophylla (Bromeliaceae) en una selva baja inundable en Yucatán, México. Durante la estación de floración (marzo a agosto), las plantas producen una inflorescencia terminal, escaposa, paniculada, 1-dividida, con una flor abriendo por rama por día para un período de floración de 11-29 días por inflorescencia. Las flores son tubulares, de corola violeta claro, con el estigma y anteras exertos, pero las anteras más largas que el estigma en antesis. Las flores son protandras, con las anteras liberando el polen desde las 0500 horas y la receptividad del estigma comenzando a las 0900 horas. Los cruces experimentales controlados sugieren que Tillansdia streptophylla es auto incompatible y por ende, dependiente de los polinizadores.
Assuntos
Polinização/fisiologia , Tillandsia/fisiologia , Cruzamento , Flores/fisiologia , México , Estações do AnoRESUMO
Hechtia schottii is a terrestrial, rosetofilous, dioecious, polycarpic succulent herb, that grows mainly in shrubby associations, and less frequently, in secondary low caducifolious forests, both on calcareous soils or limestone outcrops in Yucatan and Campeche States, Mexico. We studied phenology, floral and pollination biology, and breeding system at Calcehtok, Yucatan, during two flowering seasons. Plants bloom mainly during the dry season (November-April) and disperse seeds during the rainy season (May-October). Both floral morphs have diurnal anthesis; pollen is removed ca. 1 h after anthesis starts and both floral morphs are visited by several insect species, especially bees, but results suggest that the introduced honey bee, Apis mellifera, is the pollinator. Controlled crossings show that the species is functionally dioecious and requires to be serviced by pollinators based on fruit setting only in unassisted cross pollination crosses.
Hechtia schottii es una hierba terrestre, suculenta, rosetófila, dioica y policárpica, que crece en asociaciones arbustivas y selva baja caducifolia secundaria, ambos en suelos calcáreos o limosos. Estudiamos la fenología, la biología floral, reproductiva y de la polinización en una población en Calcehtok, Yucatán, México, durante dos estaciones de floración. Las plantas florecen principalmente en la época de secas (noviembre-abril) y la dispersión de semillas es durante la estación de lluvias (mayo-octubre). Ambas formas (morphs) florales tienen antesis diurna; el polen es removido ca. 1 h después del comienzo de la antesis y ambas formas florales son visitadas por varias especies de insectos, especialmente abejas, pero los resultados sugieren que la abeja introducida, Apis mellifera, es el polinizador. Cruces controlados muestran que la especie es funcionalmente dioica y que requiere de un polinizador, ya que solo produce frutos por polinización no asistida entre formas.