183 research outputs found
Integrating molecular biogeography and community ecology to understand the evolution of habitat specialization in Amazonian forests
I investigated the origin of western Amazonian white-sand vegetation and the
evolution of plant habitat specialization to different edaphic conditions in
Neotropical lowland forests. In order to address these goals I used complementary
ecological as well as molecular phylogenetic approaches. Amazonian white-sand
forests harbour a flora specialized to nutrient-poor sandy soils, which is distributed as
habitat-islands across the Amazon and Guiana Shield regions. This flora has been
suggested to have many local and regional endemics, therefore making an important
contribution to overall Neotropical plant diversity. The role of habitat specialization
in the origin of this flora and its relationships with other floras within the Amazon-
Guiana regions is not well understood. To shed light onto these questions, this thesis
studies the floristic composition of these forests as well as molecular phylogenetic
patterns of selected plant lineages containing white-sand species. The floristic study
focused on the white-sand forests of the western Amazon region, which contained
1180 species of vascular plants whereas the non-white-sand Amazon and Guiana
Shield dataset consisted of 26,887 vascular plant species. 77% of these species
occurred outside white-sand habitats, in other habitat types of the Amazon region,
while 23% were white-sand specialists. This demonstrates lower endemism in
western Amazonian white-sand forests than previously estimated. 88% of the total
westen Amazon white-sand specialist occur within the limits of the Guiana Shield
region with the remaining 12% being endemics to the white-sand forests of the
western Amazon. Within the Guiana-Shield region, Caquetá Moist Forests (56%),
Guayanan Highlands (55%), and Negro-Branco Moist Forests (53%) were the
biogeographic regions with the highest proportions of western Amazonian whitesand
specialists. Cluster analysis of province level floristic checklists across the
Amazon and Guiana regions showed that western Amazonian white-sand forests are
nested within floras of the western Guiana-Shield region compared to other floras in
the Amazon. Molecular phylogenetic analyses were carried out for the widespread
and species-rich families Sapotaceae and Chrysobalanaceae, which display an
uneven number of white-sand specialists. Sapotaceae had only three white-sand
specialists but Chrysobalanaceae had a larger number of white-sand specialists (14
species). Phylogenetic analysis showed that white-sand specialist species in both
studied families were scattered across the phylogenies. Both families show a marked
absence of edaphic niche conservatism, suggesting that evolutionary switching
amongst habitat types has been frequent. Ancestral state reconstruction of habitat
specialization under a maximum likelihood approach suggests that preference for
poor soils may be ancestral in these clades, especially in Chrysobalanaceae, but that
the evolution of species entirely restricted to white-sand soils is in general much
more recent and has multiple origins. For the white-sand flora of the western
Amazon in particular, there is little evidence that it comprises ancient lineages as
previously hypothesized. The historical construction of the Amazonian white sand
flora is more likely to be the result of a gradual accumulation of species with
different degrees of edaphic specialization, both by on-going speciation driven via
habitat switching from non-white-sand specialists and via regional dispersal events
after these habitats became available in regions such as the western Amazon.
Edaphic transitions between different habitat types were not evolutionary
constrained, which may have favoured edaphic niche evolution and the accumulation
of plant species diversity in Neotropical lowland forests
Diversity, composition, and structure of a highly endangered habitat: the seasonally dry forests of Tarapoto, Peru
Entre marzo y abril de 2006, la flora de los bosques estacionalmente secos en Tarapoto, San Martín fue estudiada en diez localidades. En cada una de estas localidades se estableció una parcela de 0,1 ha; cada tallo mayor de 2,5 cm de diámetro fue medido, contado e identificado a especie. Se encontraron 146 especies en 2814 individuos. En toda la zona de estudio, Myrtaceae fue la familia más diversa con 14 especies, seguida por Leguminosae con 12 especies. Igualmente, Annonaceae y Myrtaceae fueron las familias más abundantes en numero de tallos en toda la zona de estudio (461, y 412 tallos totales), mientras que Sapotaceae, con sólo 160 tallos totales, tuvo el valor más alto en área basal, debido a la Quinilla, Manilkara bidentata (A. DC.) A. Chev., el árbol más importante en la estructura de los bosques estacionalmente secos de Tarapoto. Dos especies estuvieron presentes en todos los sitios de estudio: Coccoloba sp. 1, (Polygonaceae) y Oxandra espintana (Spruce ex Benth.) Baill. (Annonaceae), mientras que 53 especies ocurrieron en un solo sitio. Los bosques estacionalmente secos de Tarapoto presentan una diversidad intermedia comparada con otros bosques secos del Neotrópico y similar diversidad a los bosques secos del Pacífico Peruano. La comunidad de árboles en estos bosques pertenece a especies de amplia distribución comparada con las especies de arbustos que tienen distribución restringida a los hábitats de bosques secos. En términos generales las áreas localizadas cerca de la carretera Tarapoto-Juanjui tienen el grado más alto de amenaza y perturbación debido a la extracción maderera y destrucción de hábitat para la creación de campos de cultivos agrícolas. Los bosques más representativos y mejor conservados de esta región se encuentran al Oeste y Sur de Picota, en el Área de Conservación Municipal El Quinillal, y en la cuenca del Río Bombonajillo y Ponasillo. Estos resultados resaltan la urgencia de conservar estos bosques ante la creciente amenaza de deforestación y pérdida de hábitat prevalente en la región.Between March and April 2006, I studied ten localities with seasonally dry forests located along the Tarapoto- Juanjui road, San Martin. At each site ten 50×2 m transects totalling 1000 m² (0,1 ha) were laid out along a 180 m baseline where all standing trees with diameter at breast height (DBH) greater than 2,5 cm were measured, counted and identified to species. I found a total of 146 species and 2814 individuals with DBH ≥ 2,5 cm. Within the study area, Myrtaceae was the most species rich family with 14 species followed closely by Leguminosae with 12 species. Annonaceae and Myrtaceae had the highest number of individuals (461 and 412, respectively), whereas Sapotaceae, with only 160 stems, had the highest basal area. The latter was mainly due to Manilkara bidentata (A. DC.) A. Chev. (“Quinilla”), the most important tree species in the seasonally dry forests of Tarapoto. Two species were present at all sites: Coccoloba sp. 1 (Polygonaceae) and Oxandra espintana (Spruce ex Benth.) (Annonaceae), whereas 53 species occurred only at one site. The seasonally dry forests of Tarapoto have an intermediate diversity compared to the other dry forests in the Neotropics and similar diversity compared to the Peruvian dry forests of the Pacific coast. Most of the tree community in these forests belong to geographically widespread species compared to shrubs that are mostly restricted to dry forests habitats. The areas located near the Tarapoto-Juanjui road (“carretera marginal”) have the most disturbed forests. The best representations of Tarapoto’s seasonally dry forests are located west and south of the locality of Picota, in the Area de Conservación Municipal “El Quinillal”, and in the Bombonajillo and Ponasillo basins. These results highlight the pressing needs for conservation efforts in the area, before these unique forests are forever lost due to the continuing expansion of agricultural fields and logging activities prevalent in the region
CLASIFICACIÓN DE BOSQUES SOBRE ARENA BLANCA DE LA ZONA RESERVADA ALLPAHUAYO-MISHANA
La Zona Reservada Allpahuayo-Mishana (ZRAM) alberga las áreas más extensas de bosques sobre arena blanca, localmente conocidos como varillales, protegidas actualmente en el Perú. Con el propósito de obtener información que ayude en el manejo y la conservación de este tipo de vegetación, nosotros estudiamos la composición florística, estructura y características ambientales de 44 parcelas, 20 x 20 m, ubicadas en los suelos de arena blanca de la ZRAM, Loreto, Perú (3°53’S, 73°25’O, 110-180 m.s.n.m.). Para la selección de los lugares de muestreo en el área utilizamos una imagen de satélite Landsat TM 5. Seleccionamos los lugares de muestreo, tratando de abarcar la mayor variación posible que podíamos observar en los colores de la imagen de satélite, con el fin de muestrear varillales potencialmente diferentes en el campo. Las parcelas estuvieron ubicadas a lo largo de transectos que atravesaron parches heterogéneos de varillal. En cada parcela registramos, en cinco clases diamétricas, a todos los individuos que tenían al menos un metro de altura e hicimos una estimación de la cobertura herbácea. También medimos la altura del dosel y grosor de la capa orgánica. Realizamos análisis de agrupamiento (cluster analysis), entre las parcelas, usando como variables el número de tallos por parcela, la altura del dosel y la calidad del drenaje expresada por el grosor de la capa orgánica (capa orgánica delgada = buen drenaje, y viceversa). Utilizamos además la abundancia y frecuencia de las especies en los grupos para definir especies indicadoras (indicator species analysis). En el contexto de nuestro estudio, y utilizando la terminología regional para estos bosques, reconocemos la existencia de cinco tipos de varillales en la ZRAM: varillal alto seco, varillal alto húmedo, varillal bajo seco, varillal bajo húmedo y chamizal
Tipos de forrajeo y gremios alimenticios de aves en bosques sobre arena blanca de la Reserva Nacional Allpahuayo Mishana, Loreto, Perú
Desde octubre del 2014 a marzo del 2015 y con el objetivo de conocer los tipos de forrajeo y gremios alimenticios de la avifauna en dos bosques sobre arena blanca de la Reserva Nacional Allpahuayo Mishana (RNAM), se evaluaron dos parcelas de una hectárea (varillal alto húmedo –VAH- y varillal alto seco –VAS-), utilizando el método de Punto de Conteo (PC). Se observó un total de 10 tipos de forrajeo: salir, alcanzar, picar, colgar, cernir, recoger, arrojar, espiar, alcanzar con salto y buscar en rama; en 76 especies de aves encontradas entre los varillales, el más dominante fue salir, seguido de alcanzar y el menos dominante fue espiar. Se registró seis gremios alimenticios: insectívoro, frugívoro, frugívoro/insectívoro, frugívoro/granívoro, nectarívoro y carnívoro, el más dominante fue insectívoro seguido de frugívoro y los menos dominantes fueron nectarívoro y carnívoro
Reducing adverse impacts of Amazon hydropower expansion
Proposed hydropower dams at more than 350 sites throughout the Amazon require strategic evaluation of trade-offs between the numerous ecosystem services provided by Earth\u27s largest and most biodiverse river basin. These services are spatially variable, hence collective impacts of newly built dams depend strongly on their configuration. We use multiobjective optimization to identify portfolios of sites that simultaneously minimize impacts on river flow, river connectivity, sediment transport, fish diversity, and greenhouse gas emissions while achieving energy production goals. We find that uncoordinated, dam-by-dam hydropower expansion has resulted in forgone ecosystem service benefits. Minimizing further damage from hydropower development requires considering diverse environmental impacts across the entire basin, as well as cooperation among Amazonian nations. Our findings offer a transferable model for the evaluation of hydropower expansion in transboundary basins
Floristic diversity, composition and dominance across Amazonian forest types respond differently to latitude
Aim: The latitudinal biodiversity gradient is considered a first-order biogeographical pattern for most taxonomic groups. Latitudinal variation in plant diversity is not always consistent, and this could be related to the particular characteristics of different forest types. In this study, we compare latitudinal changes in floristic diversity (alpha diversity), composition (beta diversity) and dominance across different tropical forest types: floodplain, terra firme and submontane forests. Location: Western Amazonia (Ecuador, Peru and Bolivia). Taxon: Woody plants. Methods: We inventoried 1978 species and 31,203 individuals of vascular plants with a diameter at breast height ≥ 2.5 cm in 118 0.1-ha plots over an 1800 km latitudinal gradient in three different forest types. The relationships between alpha diversity, latitude and forest type were analysed using generalised linear mixed models. Semi-parametric permutational multivariate analysis of variance was used to investigate the effects of latitude and forest type on beta diversity. Dominant species abundances were correlated with non-metric multidimensional scaling ordination axes to reflect their contributions in shaping changes in beta diversity. Results: Alpha diversity increased towards equatorial latitudes in terra firme and submontane forests but remained relatively constant in floodplains. Beta diversity of all forest types changed with latitude, although less clearly in floodplains. Also, in floodplain forests, there were fewer dominant species contributing to beta diversity and more species homogeneous along the gradient. Main Conclusions: Latitudinal diversity patterns are manifested in alpha and beta diversity since latitude summarizes climatic and edaphic changes. However, we found different responses of each forest type. In floodplain forests, inundation regime is a stronger predictor than latitude, limiting floristic diversity and composition. Changes in dominant species abundance over gradients explained species composition, but floodplain forests harboured more homogeneous dominant species than well drained forests. It is key to study environmental trends and habitat characteristics of each forest type to understand their species diversity and dominance pattern
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Rarity of monodominance in hyperdiverse Amazonian forests.
Tropical forests are known for their high diversity. Yet, forest patches do occur in the tropics where a single tree species is dominant. Such "monodominant" forests are known from all of the main tropical regions. For Amazonia, we sampled the occurrence of monodominance in a massive, basin-wide database of forest-inventory plots from the Amazon Tree Diversity Network (ATDN). Utilizing a simple defining metric of at least half of the trees ≥ 10 cm diameter belonging to one species, we found only a few occurrences of monodominance in Amazonia, and the phenomenon was not significantly linked to previously hypothesized life history traits such wood density, seed mass, ectomycorrhizal associations, or Rhizobium nodulation. In our analysis, coppicing (the formation of sprouts at the base of the tree or on roots) was the only trait significantly linked to monodominance. While at specific locales coppicing or ectomycorrhizal associations may confer a considerable advantage to a tree species and lead to its monodominance, very few species have these traits. Mining of the ATDN dataset suggests that monodominance is quite rare in Amazonia, and may be linked primarily to edaphic factors
Understanding different dominance patterns in western Amazonian forests
Dominance of neotropical tree communities by a few species is widely documented, but dominant trees show a variety of distributional patterns still poorly understood. Here, we used 503 forest inventory plots (93,719 individuals ≥2.5 cm diameter, 2609 species) to explore the relationships between local abundance, regional frequency and spatial aggregation of dominant species in four main habitat types in western Amazonia. Although the abundance-occupancy relationship is positive for the full dataset, we found that among dominant Amazonian tree species, there is a strong negative relationship between local abundance and regional frequency and/or spatial aggregation across habitat types. Our findings suggest an ecological trade-off whereby dominant species can be locally abundant (local dominants) or regionally widespread (widespread dominants), but rarely both (oligarchs). Given the importance of dominant species as drivers of diversity and ecosystem functioning, unravelling different dominance patterns is a research priority to direct conservation efforts in Amazonian forests.Publisher PDFPeer reviewe
Geographic patterns of tree dispersal modes in Amazonia and their ecological correlates
Indaga sobre los patrones geográficos y los correlatos ecológicos en la distribución geográfica de los modos de dispersión arbórea más comunes en la Amazonia (endozoocoria, sinzoocoria, anemoocoria e hidrocoria). Se examina si la abundancia proporcional de estos modos de dispersión podría explicarse por la disponibilidad de agentes dispersores (hipótesis de disponibilidad de dispersores) y/o la disponibilidad de recursos para la poducción de frutos zoocorios (hipótesis de disponibilidad de recursos). Para ello se usaron parcelas de inventario de árboles establecidas entre 1934 y 2019, con un diámetro a la altura del pecho (DAP) ≥ 9,55 cm. Ubicados en las selvas tropicales de tierras bajas de la cuenca del río Amazonas y el Escudo Guayanés. Se asignaron modos de dispersión a un total de 5433 especies y morfoespecies en 1877 parcelas de inventario de árboles en bosques de abeto, inundados estacionalmente y permanentemente inundados. Se investigaron los patrones geográficos en la abundancia proporcional de los modos de dispersión. Se realizó una prueba de distancia media entre pares ponderada por abundancia (MPD) y ajustamos modelos lineales generalizados (GLM) para explicar la distribución geográfica de los modos de dispersión. La anemocoria se asoció significativa y positivamente con la velocidad media anual del viento, y la hidrocoria fue significativamente mayor en los bosques inundados. Los modos de dispersión no mostraron consistentemente asociaciones significativas con la disponibilidad de recursos para la construcción de frutos zoochorous. Una menor disimilitud en los modos de dispersión, resultante de una mayor dominancia de la endozoocoria, se produjo en los bosques de abeto (excluyendo los podzoles) en comparación con los bosques inundados. La hipótesis dispersor-disponibilidad fue bien apoyada para los modos de dispersión abióticos (anemochoria e hidrochoria). La disponibilidad de recursos para la construcción de frutos zoocorios parece una explicación poco probable para la distribución de los modos de dispersión en la Amazonia. La asociación entre los frugívoros y la abundancia proporcional de zoocoría requiere más investigación, ya que el reclutamiento de árboles no sólo depende de los vectores de dispersión, sino también de las condiciones que favorecen o limitan el reclutamiento de plántulas en los distintos tipos de bosque.Revisión por pares
Reducing greenhouse gas emissions of Amazon hydropower with strategic dam planning
Hundreds of dams have been proposed throughout the Amazon basin, one of the world’s largest untapped hydropower frontiers. While hydropower is a potentially clean source of renewable energy, some projects produce high greenhouse gas (GHG) emissions per unit electricity generated (carbon intensity). Here we show how carbon intensities of proposed Amazon upland dams (median = 39 kg CO2eq MWh−1, 100-year horizon) are often comparable with solar and wind energy, whereas some lowland dams (median = 133 kg CO2eq MWh−1) may exceed carbon intensities of fossil-fuel power plants. Based on 158 existing and 351 proposed dams, we present a multi-objective optimization framework showing that low-carbon expansion of Amazon hydropower relies on strategic planning, which is generally linked to placing dams in higher elevations and smaller streams. Ultimately, basin-scale dam planning that considers GHG emissions along with social and ecological externalities will be decisive for sustainable energy development where new hydropower is contemplated. © 2019, The Author(s)
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