Different Forest Types (different + forest_type)

Distribution by Scientific Domains


Selected Abstracts


Early fate of Myristica hypargyraea seeds dispersed by Ducula pacifica in Tonga, Western Polynesia

AUSTRAL ECOLOGY, Issue 4 2005
HAYLEY J. MEEHAN
Abstract Although pigeons from the genus Ducula are considered among the best avian dispersers of large seeds in Asia and the Pacific, little has been documented on their role. The early fate of dispersed and undispersed seeds of the large-seeded tree Myristica hypargyraea A. Gray was studied in order to understand the advantage of seed dispersal by the Pacific Pigeon, Ducula pacifica Gmelin in Tonga. Frequency of visits by frugivores to fruiting trees and dispersal distance of seeds were measured. Pre-dispersal vertebrate seed predation was assessed, then post-dispersal predation was measured over 160 days. Overall, pre-dispersal seed predation by parrots was low but variable among trees sampled. Most seeds (54.7%) in the study area were estimated to be dispersed by D. pacifica; 79.7% of those ingested were expelled directly beneath conspecific fruiting crowns, 20% were dispersed locally and <,0.3% were dispersed more than 300 m into a different forest type. Flying foxes (Pteropus tonganus Quoy and Gaimard) dispersed very few seeds (0.7%) and all were dropped below fruiting crowns. Between 4% and 39% of dispersed and undispersed seeds were still viable, or had established seedlings after 160 days. Most seeds had been removed or killed by rats, and seed survival was highest for locally dispersed seeds (approx. 20 m from source trees and within the M. hypargyraea forest). Although D. pacifica was the only frugivore observed to disperse seeds into this higher zone of survival, overall they did not confer a great advantage to seed survival since significant numbers of seeds/seedlings also persisted under fruiting crowns (27% under crowns compared with 39% locally dispersed). Nevertheless, D. pacifica was the only vector by which seeds were regularly moved within the M. hypargyraea forest and over longer distances, and hence, D. pacifica still plays a significant role in the regeneration of M. hypargyraea. [source]


Assessing the relationship between forest types and canopy tree beta diversity in Amazonia

ECOGRAPHY, Issue 4 2010
Thaise Emilio
Planning of conservation priorities has often taken mapped forest types as surrogates for biological complementarity. In the Brazilian Amazon, these exercises have given equal weight to each forest type as if they were all equally distinct. Here, we examine floristic similarity between forest types to assess the reliability of vegetation maps as a surrogate for canopy tree-community composition. We analyzed floristic differences at the genus level between twelve Amazonian forest types using 1184 one-hectare inventories of large trees with three complementary approaches. First, we compared a map of floristic composition, from a uni-dimensional NMDS ordination of the inventories, with a map of coarser-level forest types commonly recognized as distinct by classification systems across Amazonia. Using Mantel and means-difference tests, we next examined the distance-decay of floristic similarity for all paired samples and for the pairs drawn from within and between twelve more finely divided forest types. Finally, we examined the degree of floristic separation of each pair of the twelve forest types using non-parametric analysis of variance. Maps of floristic composition and coarse-level forest types were highly congruent. At the finer level of classification, similarity was only slightly higher when pairs were drawn from the same versus from different forest types. This was true for all geographic distances. Nonetheless, eighty percent of the 66 paired combinations of forest types were significantly different in the unreduced genus-space and nearly half showed little or no overlap in a two-dimensional ordination. Three types were most distinct from all others: white sand, seasonally dry, and bamboo-dominated forests. Here, we show that forest types exhibit variable degrees of separation. For this reason, treating all fine-level forest types as equally distinct results in poor representation of canopy tree beta diversity. We recommend explicitly considering the degree of floristic separation between all forest types , as presented here for Amazonian flora , as a way to improve the use of this biodiversity surrogate. [source]


Conservation implications of rainforest use patterns: mature forests provide more resources but secondary forests supply more medicine

JOURNAL OF APPLIED ECOLOGY, Issue 6 2009
Michael C. Gavin
Summary 1.,Tropical rainforests are a global conservation priority. Robust arguments supporting rainforest conservation can attract funding and shape land-use management. However, some popular assertions regarding the value of tropical forests remain largely untested. 2.,This study tests the validity of two arguments in support of mature tropical rainforest conservation: first, that these forests should be conserved based on their value as potential sources of medicine. This argument requires mature forests to be better sources of medicine than alternative land-use types, including secondary forests. Second, secondary forest use may help conserve mature forests by providing sufficient resources to buffer against resource extraction in mature forests. 3.,The research was conducted in three communities in the Cordillera Azul, Peru, where 369 individuals from 66 households were surveyed. Participants recorded all flora and fauna collected in mature (>20 years) and secondary forests over 180 days in six use categories (food, medicine, wood, weavings, adornments and ,other'). Ecological knowledge of secondary and mature forest species was assessed for male and female household heads. 4.,Households used 346 folk species (as defined by local classification systems) from 3668 collection events. Individuals had better knowledge of secondary forest species, but more access to mature forests. Participants collected significantly more medicines from secondary than from mature forests. In other major use categories (food, wood, weaving, adornment), secondary forests provided fewer resources than mature forests. Participants collected a different set of species from secondary and mature forests, with only 130 folk species (38%) collected in both secondary and mature forests. 5.,Synthesis and applications. The arguments to protect mature rainforests as sources of new drugs may be overstated, because secondary forests can provide more medicinal plant resources than mature forests, and landscapes that incorporate forests of different ages can maximize availability of medicinal plant species. Conservation efforts must take a landscape level approach given the spread of resource use across different forest types. Because of the heterogeneity of resource availability and use among community members, and the dynamic nature of resource use on forest frontiers, conservation should embrace participatory adaptive management approaches that incorporate a variety of resource users. [source]


Do trails affect relative abundance estimates of rainforest frogs and lizards?

AUSTRAL ECOLOGY, Issue 6 2009
RUDOLF Von MAY
Abstract The selection of a sampling protocol is critical to study amphibian and reptile communities and in many instances researchers have combined the use of visual encounter surveys (VES) conducted on trails and off trails. The effect of human-made trails on relative abundance estimates of amphibians and reptiles has been assessed in a few temperate locations, but data are lacking for tropical sites. Our study was designed to address this issue by comparing abundance estimates of frogs and lizards on and off trails in a lowland rainforest in south-eastern Perú. We used nocturnal VES to sample frogs and lizards along transects established on trails and off trails in two different forest types. We found that the observed relative abundance estimates of frogs and lizards were affected by the location of transects (on trail vs. off trail) and the type of forest (floodplain forest vs. terra firme forest). We also found an interaction between the two main effects, indicating that the effect of transect location with respect to trails varies as a function of habitat. Observed frog abundances were higher on trails than off trails, indicating that studies that include VES on trails will bias relative abundance estimates in contrast to studies that include only VES off trails. We suggest that transects should be established only off trails, especially for monitoring studies because trail use by humans can have a strong influence on observed animal abundance. [source]


Riqueza y Distribución Ecológica de Especies de Pteridofitas en la Zona del Río Yavarí-Mirín, Amazonía Peruana

BIOTROPICA, Issue 5 2007
Glenda G. Cárdenas
ABSTRACT We studied the ecological distribution of pteridophytes (ferns and fern allies) along eight 8-km transects covering 12.7 ha in Peruvian Amazonia. Subunits of 200 m2 of the transects have previously been classified into four different forest types, and here we document and quantify the floristic differences among these forest types. Pteridophytes have been suggested as an indicator group to classify rain forest habitats, but this requires that the ecological preferences of the species are well documented and consistent across geographic regions. Here we analyzed in detail the distribution and diversity patterns of 130 species across the four rain forest types. Relative species abundance and species diversity were similar among some of the forest types and differed among others, but the species composition differed markedly. Our results largely confirmed the earlier interpretation of the edaphic preferences of the pteridophyte species in western Amazonia. This supports the proposition that deterministic processes have an important role in influencing the floristic composition of Amazonian forests. RESUMEN Estudiamos la distribución ecológica de las pteridofitas (helechos y plantas afines) a lo largo de ocho transectos de 8 km cada uno, cubriendo un área total de 12.7 ha en la Amazonía peruana. Subunidades de 200 m2 de los transectos fueron anteriormente clasificadas en cuatro tipos diferentes de bosques, y aquí documentamos y cuantificamos las diferencias florísticas entre estos tipos de bosques. Las pteridofitas han sido recomendadas como un grupo indicador para clasificar los hábitat del bosque húmedo tropical, pero esto requiere que las preferencias ecológicas de las especies sean bien documentadas y consistentes a través de las regiones geográficas. Aquí analizamos en detalle los patrones de distribución y diversidad de 130 especies a través de los cuatro tipos de bosques. La abundancia relativa y la diversidad de especies fueron similares entre algunos de los tipos de bosque y diferentes entre otros, pero la composición florística difirió marcadamente. Nuestros resultados confirmaron en gran parte la previa interpretación de las preferencias edáficas de las especies de pteridofitas en la Amazonía occidental. Esto apoya la propuesta de que procesos deterministas influyen de manera importante en la composición florística de los bosques amazónicos. [source]