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146 results for “Wet Tropics”

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zenodo36/100

Data for: "Different dry-wet pulses favor different functional strategies: a test using tropical dry forest tree species" by Vega-Ramos, Flor, Cifuentes Gómez, Lucas, Pineda-García, Fernando, Dawson, Todd, Paz, Horacio

<p>These data represent those published in "Different dry-wet pulses favor different functional strategies: a test using tropical dry forest tree species" by Vega-Ramos, Flor, Cifuentes G&oacute;mez, Lucas, Pineda-Garc&iacute;a, Fernando, Dawson, Todd, Paz, Horacio</p>

opencc-by-sa-4.0Apr 2024View details →
dryad36/100

Local timing of rainfall predicts the timing of moult within a single locality and the progress of moult among localities that vary in the onset of the wet season in a year-round breeding tropical songbird

<p>Rainfall seasonality is likely an important cue for timing key annual cycle events like moult in birds living in seasonally arid environments, but its precise effect is difficult to establish because seasonal rainfall may affect other covarying annual events such as breeding in the same way. In central Nigeria, however, Common Bulbuls <em>Pycnonotus barbatus</em> moult in the wet season but only show weak breeding seasonality. This suggests that moult is more sensitive to rainfall than breeding, but a similar outcome is possible if moult is simply periodic. We tested the relationship between rainfall and moult in Common Bulbuls at a single location over 18 years: on average moult started 5th May (± 41 days: 25th March–15th June), being on average later than the onset of the rains which is usually mid-April. The likelihood of finding a moulting Common bulbul was best predicted by rainfall 9–15 weeks before moult was scored. We then tested the generality of this across populations: the progress of moult should, therefore, correlate with the average timing of the wet season along a spatial environmental gradient where the rains start at different times each year south-to-north of Nigeria. To test this, we modelled moult progress just before the rains across 15 localities 6°–13° N as a function of the onset of the wet season among localities. As predicted, moult progressed further in localities with earlier wet seasons, confirming that the onset of moult is timed to the onset of the wet season in each locality despite weak breeding seasonality in the Common Bulbul. This strategy may evolve to maintain optimal annual cycle routine in seasonal environments where breeding is prone to unpredictable local perturbations like nest predation. It may, however, be less obvious in temperate systems where all annual cycle stages are seasonally constrained, but it may help with explaining the high frequency of breeding–moult overlaps in tropical birds.</p>

opencc-zeroOct 2022View details →
dryad36/100

Hydraulic traits are not robust predictors of tree species stem growth during a drought in a wet tropical forest

<p>Severe droughts have led to lower plant growth and high mortality in many ecosystems worldwide, including tropical forests. Drought vulnerability differs among species but there is limited consensus on the nature and degree of this variation in tropical forest communities. Understanding species-level vulnerability to drought requires examination of hydraulic traits since these reflect the different strategies species employ for surviving drought. Here we examined hydraulic traits and growth reductions during a severe drought for 12 common woody species in a wet tropical forest community in Puerto Rico to ask:</p> <p>Q1. To what extent can hydraulic traits predict growth declines during drought? We expected that species with more hydraulicly vulnerable xylem and narrower safety margins would grow less during drought.</p> <p>Q2. How do species successional association relate to levels of vulnerability to drought and hydraulic strategies? We predicted that early- and mid-successional species would exhibit more acquisitive strategies, making them more susceptible to drought than shade-tolerant species.</p> <p>Q3. What are the different hydraulic strategies employed by species and are there trade-offs between drought avoidance and drought tolerance?</p> <p>We anticipated that species with greater water storage capacity would have leaves that lose turgor at higher xylem water potential and be less resistant to embolism forming in their xylem (P50). We found a large range of variation in hydraulic traits across species; however, they did not closely capture the magnitude of growth declines during drought. Among larger trees (≥10 cm diameter at breast height—DBH), some tree species with high xylem embolism vulnerability and risk of hydraulic failure experienced substantial declines during drought but this pattern was consistent across species. We found a trade-off among species between drought avoidance (capacitance) and drought tolerating (P50) in this tropical forest community. Hydraulic strategies did not align with successional associations. Instead, some of the more drought-vulnerable species were shade-tolerant dominants in the community, suggesting that a drying climate could lead to shifts in long-term forest composition and function in Puerto Rico and the Caribbean.</p>

opencc-zeroNov 2022View details →
dryad36/100

Sunda-Sahul floristic exchange and pathways into the Southwest Pacific: New insights from wet tropical forest trees

<p><strong>Aim</strong> Recent investigations on the floristic exchange between Southeast Asia and Australia have shown a clear dispersal directionality bias (West to East) of wet-adapted plant taxa. However, dispersal routes and directions of wet forest taxa into the South Pacific remain insufficiently known. We here aimed to establish the most likely routes and directions of plant dispersal into the Southwest Pacific islands.</p> <p><strong>Location</strong> Southeast Asia, East Asia, Australia, Southwest Pacific.</p> <p><strong>Taxon</strong> <em>Dysoxylum</em> s.l. (Meliaceae). This includes <em>Dysoxylum</em> s.s., <em>Didymocheton</em>, <em>Epicharis</em>, <em>Goniocheton</em>, <em>Pseudocarapa</em> and <em>Prasoxylon</em>.</p> <p><strong>Method</strong> We sampled 75% of the species diversity in <em>Dysoxylum</em> s.l., covering the entire distribution range, all genera and major lineages. Phylogenetic relationships of 149 accessions were reconstructed using Bayesian Evolutionary Analysis and two internal constraints. The dispersal–extinction–cladogenesis variant, founder-event speciation (DEC+J), was used for reconstructing the biogeographic history, and 100 BSMs were simulated.</p> <p><strong>Results</strong> <em>Dysoxylum</em> s.l. originated and firstly diversified in the western part of its current distribution range (incl. Indochina) during the Miocene to Pliocene, followed by an overall eastern range expansion towards Malesia, Australia and the Southwest Pacific in the Pliocene.</p> <p><strong>Main</strong> <strong>conclusions</strong> The south-eastward expansion of lineages into Wallacea and Australia is in temporal agreement with the convergence of the Asian and Australian tectonic plates since the Miocene. Long-distance dispersal is the main mechanism that led to the current distribution. Two dispersal pathways into the Southwest Pacific are identified, (1) through New Guinea and the Solomon Islands to Fiji, and (2) from New Zealand to Fiji. For both routes, Fiji was an important secondary source area for dispersal into the Southwest Pacific.</p>

opencc-zeroMar 2023View details →
dryad36/100

Laying low: Rugged lowland rainforest preferred by feral cats in the Australian wet tropics

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publicJun 2022View details →
dryad36/100

Tree species controls over nitrogen and phosphorus cycling in a wet tropical forest

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publicSep 2024View details →
dryad36/100

Hydraulic traits are not robust predictors of tree species stem growth during a drought in a wet tropical forest

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publicNov 2022View details →
dryad36/100

Local timing of rainfall predicts the timing of moult within a single locality and the progress of moult among localities that vary in the onset of the wet season in a year-round breeding tropical songbird

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publicOct 2022View details →
dryad36/100

Sunda-Sahul floristic exchange and pathways into the Southwest Pacific: New insights from wet tropical forest trees

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publicMar 2023View details →
zenodo32/100

FIGURE 3 in A protocol for online documentation of spider biodiversity inventories applied to a Mexican tropical wet forest (Araneae, Araneomorphae)

FIGURE 3. Example of a species page documented with standard views Cyrtognatha petila Dimitrov &amp; Hormiga 2009. http:// www.unamfcaracnolab.com/WPGS_TUXV/tuxv.html

opennotspecifiedJan 2020View details →
zenodo32/100

FIGURE 4 in A protocol for online documentation of spider biodiversity inventories applied to a Mexican tropical wet forest (Araneae, Araneomorphae)

FIGURE 4. Species richness estimations. Red triangles with values indicated with (*) correspond to the species estimations for those treatments fitted to a lognormal distribution. White and red triangles over the x axis indicate higher overestimations.

opennotspecifiedJan 2020View details →
zenodo32/100

FIGURE 5. Species richness estimations slopes. Jack 2s in A protocol for online documentation of spider biodiversity inventories applied to a Mexican tropical wet forest (Araneae, Araneomorphae)

FIGURE 5. Species richness estimations slopes. Jack 2s indicates the slope average for these estimations based on incidence (BAT) and abundance (Bat and Estimates). Same averages were calculated for Jack 1s and Chao 1 and 2 estimation slopes. Column indicated with (*) correspond to the slope value for pitfalls under Chao's estimations.

opennotspecifiedJan 2020View details →
zenodo32/100

FIGURE 9 in First record of Synagelides Strand, 1906 (Araneae: Salticidae) from Sri Lanka description of four endemic species from tropical wet forest of the island

FIGURE 9. Synagelides orlandoi sp. nov. A–B, male (A, dorsal view; B, ventral view). C–E left palp (C, prolateral view; D, ventral view; E, retrolateral view). Scale bars: A–B = 0.5 mm, C–E = 0.1 mm.

opennotspecifiedJun 2020View details →
dryad32/100

Data from: Short-term precipitation exclusion alters microbial responses to soil moisture in a wet tropical forest

Many wet tropical forests, which contain a quarter of global terrestrial biomass carbon stocks, will experience changes in precipitation regime over the next century. Soil microbial responses to altered rainfall are likely to be an important feedback on ecosystem carbon cycling, but the ecological mechanisms underpinning these responses are poorly understood. We examined how reduced rainfall affect- ed soil microbial abundance, activity, and community compo- sition using a 6-month precipitation exclusion experiment at La Selva Biological Station, Costa Rica. Thereafter, we ad- dressed the persistent effects of field moisture treatments by exposing soils to a controlled soil moisture gradient in the lab for 4 weeks. In the field, compositional and functional re- sponses to reduced rainfall were dependent on initial condi- tions, consistent with a large degree of spatial heterogeneity in tropical forests. However, the precipitation manipulation sig- nificantly altered microbial functional responses to soil mois- ture. Communities with prior drought exposure exhibited higher respiration rates per unit microbial biomass under all conditions and respired significantly more CO2 than control soils at low soil moisture. These functional patterns suggest that changes in microbial physiology may drive positive feed- backs to rising atmospheric CO2 concentrations if wet tropical forests experience longer or more intense dry seasons in the future.

opencc-zeroDec 2017View details →
dryad32/100

Data from: Ants as ecological indicators of rainforest restoration: community convergence and the development of an Ant Forest Indicator Index in the Australian wet tropics

Ecosystem restoration can help reverse biodiversity loss, but whether faunal communities of forests undergoing restoration converge with those of primary forest over time remains contentious. There is a need to develop faunal indicators of restoration success that more comprehensively reflect changes in biodiversity and ecosystem function. Ants are an ecologically dominant faunal group and are widely advocated as ecological indicators. We examine ant species and functional group responses on a chronosequence of rainforest restoration in northern Australia, and develop a novel method for selecting and using indicator species. Four sampling techniques were used to survey ants at 48 sites, from grassland, through various ages (1–24 years) of restoration plantings, to mature forest. From principal components analysis of seven vegetation metrics, we derived a Forest Development Index (FDI) of vegetation change along the chronosequence. A novel Ant Forest Indicator Index (AFII), based on the occurrences of ten key indicator species associated with either grassland or mature forest, was used to assess ant community change with forest restoration. Grasslands and mature forests supported compositionally distinct ant communities at both species and functional levels. The AFII was strongly correlated with forest development (FDI). At forest restoration sites older than 5–10 years that had a relatively closed canopy, ant communities converged on those of mature rainforest, indicating a promising restoration trajectory for fauna as well as plants. Our findings reinforce the utility of ants as ecological indicators and emphasize the importance of restoration methods that achieve rapid closed-canopy conditions. The novel AFII assessed restoration status from diverse and patchily distributed species, closely tracking ant community succession using comprehensive species-level data. It has wide applicability for assessing forest restoration in a way that is relatively independent of sampling methodology and intensity, and without a need for new comparative data from reference sites.

opencc-zeroDec 2016View details →
zenodo32/100

FIGURES 6–13 in Riekophlebia crocina, a new genus and species of Atalophlebiinae (Ephemeroptera: Leptophlebiidae) from the Wet Tropics bioregion of north-eastern Australia

FIGURES 6–13. Riekophlebia crocina. Nymph: (6) labrum and clypeus; (7) right mandible; (8) maxilla, ventral view; (9) hypopharynx; (10) labium, dorsal view left of midline and ventral view right of midline; (11) segment 3 of labial palp, dorsal view; (12) foreleg; (13) abdominal gill.

opennotspecifiedDec 2009View details →
zenodo32/100

FIGURES 1–5 in Riekophlebia crocina, a new genus and species of Atalophlebiinae (Ephemeroptera: Leptophlebiidae) from the Wet Tropics bioregion of north-eastern Australia

FIGURES 1–5. Riekophlebia crocina. Male imago: (1) wings; (2) hind wing; (3) abdominal terga 3–5; (4) penes and claspers, ventral view. Female imago: (5) ninth abdominal sternum.

opennotspecifiedDec 2009View details →
zenodo32/100

FIGURES 7, 8 in Five new species and new records of Hydroptilidae (Trichoptera) from the Wet Tropics of northeastern Queensland

FIGURES 7, 8. Orthotrichia species, male genitalia in ventral view: 7, O. rentzi sp. nov.; 8, O. andicairnsae sp. nov.

opennotspecifiedDec 2010View details →
zenodo32/100

FIGURES 1–6 in Five new species and new records of Hydroptilidae (Trichoptera) from the Wet Tropics of northeastern Queensland

FIGURES 1–6. Orphninotrichia species, male genitalia in ventral and left lateral views: 1, 2, O. barbarae sp. nov.; 3, 4, O. desleyae sp. nov.; 5, 6, O. alata sp. nov.

opennotspecifiedDec 2010View details →
zenodo32/100

FIGURE 3. A in Two new frog species (Microhylidae: Cophixalus) from the Australian Wet Tropics region, and redescription of Cophixalus ornatus

FIGURE 3. A single representative call of: (A) C. australis sp. nov., Tully Falls, 750 m a.s.l., 18°C; (B) C. hinchinbrookensis sp. nov., Mt Diamantina, Hinchinbrook Island, 770 m a.s.l., 19°C; (C) Cophixalus ornatus, Butchers Ck, 715 m a.s.l., 18.5°C. These calls were selected because they are from similar altitudes and temperatures, and because they fall near the group centroid of variation within each species from analyses in Hoskin et al. (2011). Waveforms display amplitude (y-axis) against time (x-axis, seconds); Spectrograms display call frequency (y-axis) and intensity (degree of shading) against time (x-axis, seconds).

opennotspecifiedDec 2012View details →

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Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record