Species distribution models (SDMs) are widely used in ecology and conservation. Presence-only SDMs such as MaxEnt frequently use natural history collections (NHCs) as occurrence data, given their huge numbers and accessibility. NHCs are often spatially biased which may generate inaccuracies in SDMs. Here, we test how the distribution of NHCs and MaxEnt predictions relates to a spatial abundance model, based on a large plot dataset for Amazonian tree species, using inverse distance weighting (IDW). We also propose a new pipeline to deal with inconsistencies in NHCs and to limit the area of occupancy of the species. We found a significant but weak positive relationship between the distribution of NHCs and IDW for 66% of the species. The relationship between SDMs and IDW was also significant but weakly positive for 95% of the species, and sensitivity for both analyses was high. Furthermore, the pipeline removed half of the NHCs records. Presence-only SDM applications should consider this limitation, especially for large biodiversity assessments projects, when they are automatically generated without subsequent checking. Our pipeline provides a conservative estimate of a species’ area of occupancy, within an area slightly larger than its extent of occurrence, compatible to e.g. IUCN red list assessments.

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.

Amazonian forests are extraordinarily diverse, but the estimated species richness is very much debated. Here, we apply an ensemble of parametric estimators and a novel technique that includes conspecific spatial aggregation to an extended database of forest plots with up-to-date taxonomy. We show that the species abundance distribution of Amazonia is best approximated by a logseries with aggregated individuals, where aggregation increases with rarity. By averaging several methods to estimate total richness, we confirm that over 15,000 tree species are expected to occur in Amazonia. We also show that using ten times the number of plots would result in an increase to just ~50% of those 15,000 estimated species. To get a more complete sample of all tree species, rigorous field campaigns may be needed but the number of trees in Amazonia will remain an estimate for years to come.

The Balbina hydropower dam in the Central Amazon basin, established in the Uatumã River in the 1980s, is emblematic for its socio‐environmental disaster. Its environmental impacts go far beyond the reservoir and dam, however, affecting the floodplain forests (igapó) in the downstream area (dam shadow), which have been assessed using a transdisciplinary research approach, synthesized in this review. Floodplain tree species are adapted to a regular and predictable flood pulse, with high‐ and low‐water periods occurring during the year. This was severely affected by the operation of the Balbina dam, which caused the suppression of both the aquatic phase at higher floodplain elevations and the terrestrial phase at lower floodplain elevations (termed the ‘sandwich effect’). During the period of construction and reservoir fill, large‐scale mortality already occurred in the floodplains of the dam shadow as a result of reduced stream flow, in synergy with severe drought conditions induced by El Niño events, causing hydraulic failure and making floodplains vulnerable to wildfires. During the operational period of the dam, permanent flooding conditions at low topographical elevations resulted in massive tree mortality. So far, 12% of the igapó forests have died along a downstream river stretch of more than 125 km. As a result of flood suppression at the highest elevations, an encroachment of secondary tree species from upland (terra firme) forests occurred. More than 35 years after the implementation of the Balbina dam, the downstream impacts caused massive losses of macrohabitats, ecosystem services, and diversity of flood‐adapted tree species, probably cascading down to the entire food web, which must be considered in conservation management. These findings are discussed critically, emphasizing the urgent need for the Brazilian environmental regulatory agencies to incorporate downstream impacts in the environmental assessments of several dam projects planned for the Amazon region.

The construction of hydroelectric dams causes changes in the diversity and floristic composition of floodplain forests due to the irregularity of the hydrological regime in rivers downstream from the dams. In the Amazon Basin, plans for the construction of dams are threatening the igapós, forests flooded by blackwater rivers. In these floodplains, the distribution of tree species is synchronized with periodic flood events of the topographic gradient. Previous studies on the Balbina Dam show an altered flood pulse downstream. This work discusses the potential long-term impacts on the diversity and floristic composition of an igapó downstream of the dam (Uatumã River) and compares it with an area unaffected by the dam (Abacate River). An evaluation of the vegetation strata-adults, saplings, and seedlings-showed that for all strata, diversity was greater in the high igapó (higher topographies) in the Uatumã area. This may be due to the near-total absence of flooding in the high igapó and to the extent of flooding in the low igapó (low topographies). Thus, in the Uatumã area, seeds of species typical of flooded areas cannot reach the high igapó by water and, thus, tend to be replaced by upland forest species (mainly seedlings). In the low igapó, the typical species have difficulty establishing. Therefore, the Uatumã vegetation forms two different communities, which does not occur in the Abacate area. These effects of the dam led to irreversible changes in the diversity and floristic composition across all strata throughout the entire topography in the downstream region.

Vascular epiphytes constitute a life form that is important to maintaining the biological diversity of forest ecosystems, because they provide food resources and specialized microenvironments for fauna in the forest canopy. This study aimed to describe the floristic composition and ecological aspects of vascular epiphytes occurring in the restingas (coastal woodlands) within the Algodoal-Maiandeua Environmentally Protected Area, located in the municipality of Maracanã, in the state of Pará, Brazil. We sampled five 50 × 50 m plots (three in dry restinga forest and two in floodplain restinga forest), the sampled area therefore totaling 1.25 ha. In the plots sampled, vascular epiphytes were identified and described according to their frequency, abundance, importance value (IV), functional group and vertical distribution (trunk, lower crown or upper crown of the host). For both forest types, we identified 477 individuals belonging to five families, nine genera and 11 species. The most species-rich families were Araceae and Orchidaceae. The species with the highest density, frequency and IV were the secondary hemiepiphytes Philodendron acutatum, Anthurium pentaphyllum and Philodendron muricatum, collectively accounting for 92.1% of all sampled individuals. The true epiphytes predominated. Epiphytic species richness and abundance was greater on the host trunk than in the lower or upper crown. The seasonal climate and structure of the forest favored greater abundance of secondary hemiepiphytes and a higher frequency of epiphytes on the trunks of their hosts.

Research focusing on assemblages of vascular epiphytes in the Amazon are scarce. Th is is especially true for Amazonian fl oodplain forests, for which only two previous studies have been published. We compared composition, richness and structure of epiphyte assemblages in white-water and black-water fl oodplains (várzea and igapó) in Central Amazonia in order to close knowledge gaps concerning the distribution and richness of epiphytes. We established sixteen 25x25 m plots in each forest type, and counted and identifi ed all species of vascular epiphytes occurring on trees with a diameter at breast height (DBH) ≥10 cm. We observed a clear distinction in epiphytic species composition (r 2 =0.83, p=0.001) and diversity (t=3.24, P=0.003) between the two environments, with 61.5 % of species being restricted to várzea, 22.9 % restricted to igapó and only 15.6 % common to both ecosystems. Th e fl oodplains were also structurally diff erent for the most abundant species and those with the highest Epiphytic Importance Value (IVe). Th e diversity of trees did not infl uence the epiphyte diversity in either ecosystem. Th e forests were found to diff er in the composition, diversity and structure of their epiphytic assemblages, which must be taken into account when designing conservation action plans for these ecosystems and for their vascular epiphytes.

Vascular epiphytes are a diverse and conspicuous component of biodiversity in tropical and subtropical forests. Yet, the patterns and drivers of epiphyte assemblages are poorly studied in comparison with soil-rooted plants. Current knowledge about diversity patterns of epiphytes mainly stems from local studies or floristic inventories, but this information has not yet been integrated to allow a better understanding of large-scale distribution patterns. EpIG-DB, the first database on epiphyte assemblages at the continental scale, resulted from an exhaustive compilation of published and unpublished inventory data from the Neotropics. The current version of EpIG-DB consists of 463,196 individual epiphytes from 3,005 species, which were collected from a total of 18,148 relevés (host trees and 'understory' plots). EpIG-DB reports the occurrence of 'true' epiphytes, hemiepiphytes and nomadic vines, including information on their cover, abundance, frequency and biomass. Most records (97%) correspond to sampled host trees, 76% of them aggregated in forest plots. The data is stored in a TURBOVEG database using the most up-to-date checklist of vascular epiphytes. A total of 18 additional fields were created for the standardization of associated data commonly used in epiphyte ecology (e.g. by considering different sampling methods). EpIG-DB currently covers six major biomes across the whole latitudinal range of epiphytes in the Neotropics but welcomes data globally. This novel database provides, for the first time, unique biodiversity data on epiphytes for the Neotropics and unified guidelines for future collection of epiphyte data. EpIG-DB will allow exploration of new ways to study the community ecology and biogeography of vascular epiphytes. K E Y W O R D S biodiversity, community ecology, database, forest plot, hemiepiphytes, Neotropics, nomadic vines, taxonomic diversity, vascular epiphytes, vegetation relevé 520 |