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146 results for “Wet Tropics”
Canopy opening increased leaf shredding arthropods and nutrient mineralization but not mass loss in a wet tropical forest
Canopy opening increased leaf shredding arthropods and nutrient mineralization but not mass loss in a wet tropical forest Support for this work was provided by grants BSR-8811902, DEB-9411973, DEB-9705814 , DEB-0080538, DEB-0218039 , DEB-0620910 , DEB-1239764, DEB-1546686, and DEB-1831952 from the National Science Foundation to the University of Puerto Rico as part of the Luquillo Long-Term Ecological Research Program. Additional support provided by the University of Puerto Rico and the International Institute of Tropical Forestry, USDA Forest Service.
Fig. 3. – Geosiris australiensis B. Gray & Y.W. Low. A in First record of Geosiris (Iridaceae: Geosiridoideae) from Australasia: a new record and a new species from the Wet Tropics of Queensland, Australia
Fig. 3. – Geosiris australiensis B. Gray & Y.W. Low. A. Habit; B. Close-up of a flower bud with bracts; C. Close-up of extrorse stamens showing anthers with a longitudinal slit and forming a tight ring around the style; D. Top view of stigma showing truncate apex with short fimbriate margin.
Fig. 2. – Geosiris australiensis B. Gray & Y.W. Low. A in First record of Geosiris (Iridaceae: Geosiridoideae) from Australasia: a new record and a new species from the Wet Tropics of Queensland, Australia
Fig. 2. – Geosiris australiensis B. Gray & Y.W. Low. A. Habit showing underground rhizome; B. Close-up of stigma with a truncate apex; C. Side view of a flowering head with an unopened flower bud; D. Cross section of an open flower showing stamens in a tight ring around the style just above the corolla throat.
Fig. 1. – Stigmatic heads. A. Geosiris albiflora Goldblatt & J.C in First record of Geosiris (Iridaceae: Geosiridoideae) from Australasia: a new record and a new species from the Wet Tropics of Queensland, Australia
Fig. 1. – Stigmatic heads. A. Geosiris albiflora Goldblatt & J.C. Manning; B. G. aphylla Baill. C. G. australiensis B. Gray & Y.W. Low.
Linked collectors and determiners for: A remarkable new plant bug genus and species (Hemiptera, Heteroptera, Miridae, Deraocorinae) from the Australian wet tropics.
Natural history specimen data linked to collectors and determiners held within, "A remarkable new plant bug genus and species (Hemiptera, Heteroptera, Miridae, Deraocorinae) from the Australian wet tropics". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/6037268b-0c87-43b5-94b9-a6319301b792">https://bionomia.net/dataset/6037268b-0c87-43b5-94b9-a6319301b792</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/6037268b-0c87-43b5-94b9-a6319301b792">https://gbif.org/dataset/6037268b-0c87-43b5-94b9-a6319301b792</a>. Formatted as a Frictionless Data package.
Figures 12–17 in A New Subspecies of Philiris diana Waterhouse & Lyell, 1914 (Lepidoptera: Lycaenidae) from the Wet Tropics of Northern Australia
Figures 12–17. Adults of Philiris diana fortuna ssp. nov.: (12, 13) holotype male, showing dorsal and ventral views (ANIC); (14) paratype male, dorsal view showing variation (BHC); (15, 16) paratype female, showing dorsal and ventral views (ANIC); (17) paratype female, dorsal view showing variation (BHC). Scale bar = 10 mm.
Figures 18–29 in A New Subspecies of Philiris diana Waterhouse & Lyell, 1914 (Lepidoptera: Lycaenidae) from the Wet Tropics of Northern Australia
Figures 18–29. Male genitalia of the Philiris diana species-group in Australia and Papua New Guinea: (18–20) P. diana fortuna ssp. nov. showing posterior, left lateral and right lateral views; (21–23) P. diana diana showing posterior, left lateral and right lateral views; (24–26) P. papuanus kerri showing posterior, left lateral and right lateral views; (27–29) P. papuanus papuanus showing posterior, left lateral and right lateral views. Scale bar = 1 mm.
Figures 4–11 in A New Subspecies of Philiris diana Waterhouse & Lyell, 1914 (Lepidoptera: Lycaenidae) from the Wet Tropics of Northern Australia
Figures 4–11. Adults of Philiris diana diana: (4, 5, 7) lectotype male in AMS, showing dorsal and ventral views and label data; (8, 9, 11) paralectotype female in AMS, showing dorsal and ventral views and label data; (6) male, dorsal view, reared from larva from near Kuranda (BHC); (10) female, dorsal view, reared from larva from near Cairns (EPC). Scale bar = 10 mm.
Figure 3 in A New Subspecies of Philiris diana Waterhouse & Lyell, 1914 (Lepidoptera: Lycaenidae) from the Wet Tropics of Northern Australia
Figure 3. Neighbor Joining phylogenetic tree of Philiris diana based on mitochondrial cytochrome c oxidase subunit I (658 bp "barcode" region). Outgroups are not shown. Scale bar represents number of substitutions/site.
Figures 30–37 in A New Subspecies of Philiris diana Waterhouse & Lyell, 1914 (Lepidoptera: Lycaenidae) from the Wet Tropics of Northern Australia
Figures 30–37. Life history and habitus of Philiris diana fortuna ssp. nov.: (30, 31) larva instar III, showing examples of variation in colour pattern, with lightly-marked and heavily-marked forms; (32, 33) larva instar VI, showing examples of variation in colour pattern, with yellow-brown striped and red-brown striped forms; (34, 35) pupa, showing examples of variation in colour pattern, with lightly marked and heavily marked forms; (36) adult female, newly-emerged at rest on foliage of Litsea leefeana; (37) adult pair in copula, with male on left and female on right.
Figures 1–2 in A New Subspecies of Philiris diana Waterhouse & Lyell, 1914 (Lepidoptera: Lycaenidae) from the Wet Tropics of Northern Australia
Figures 1–2. Right fore- and hindwings of Philiris diana diana, showing measurements of quantitative characters for traits 1–5 (see Materials and Methods): (1) female; (2) male. Letters denote the following characters: A = area of forewing; B = area of forewing white central patch; C = curved area of forewing enclosed between termen and line between end of veins R5 and 1A+2A; D = width of black terminal band of forewing at vein M3; E = length of forewing from base to end of vein M3; F = width of black terminal band of hindwing at vein M3; G = length of hindwing from base to end of vein M3.
FIGURE 5 in Timing Is Everything: Acoustic Niche Partitioning in Two Tropical Wet Forest Bird Communities
FIGURE 5 | Comparison of observed and expected number of pairs of species with overlapping vocalization frequencies in each location (significance "**"α = 0.01). The null distributions were generated using 500 randomizations of species distribution across locations (keeping species richness per location unchanged).
FIGURE 4 in Timing Is Everything: Acoustic Niche Partitioning in Two Tropical Wet Forest Bird Communities
FIGURE 4 | Comparison of observed and expected number of heterospecific pairs of vocalizations with overlapping vocalization times and frequencies in each location (significance "***"α = 0.001, "**"α = 0.01). The null distributions were generated using 500 randomizations of the beginning of vocalizations (keeping number, length and spectral characteristics unchanged).
FIGURE 3 in Timing Is Everything: Acoustic Niche Partitioning in Two Tropical Wet Forest Bird Communities
FIGURE 3 | Comparison of species vocalization characteristics (A,B), the number of vocalizations per 5-min record (C), and number of species recorded per location (D) between Costa Rica (CR) and Hawai'i (HI) (P-value indicates the significance of Wilcoxon's rank sum test).
FIGURE 2 in Timing Is Everything: Acoustic Niche Partitioning in Two Tropical Wet Forest Bird Communities
FIGURE 2 | List of detected species with their vocalization ranges (left figures) and their locations of occurrence (right figures) in Costa Rica and Hawai'i. On the left figures, gray background represents potential overlapping in a given frequency, the darker the background, the higher the number of species using this frequency.
FIGURE 1 in Timing Is Everything: Acoustic Niche Partitioning in Two Tropical Wet Forest Bird Communities
FIGURE 1 | Species accumulation curves (mean of 500 iterations) for each of six recording locations in Costa Rica and Hawai'i.
Data: Avian cultural services peak in tropical wet forests
Open the record for dataset details and reuse information.
Data for: "Above and below ground trait coordination in tree seedlings depend on the most limiting resource: A test comparing a wet and a dry tropical forest in Mexico" by L. Sanaphre-Villanueva, F. Pineda-Garcia, W. Dattilo, L. F. Pinzon-Perez, A. Ricaño Rocha, H. Paz.
<p>These data represent those published in “Above and below ground trait coordination in tree seedlings depend on the most limiting resource: A test comparing a wet and a dry tropical forest in Mexico” by L. Sanaphre-Villanueva, F. Pineda-Garcia, W. Dattilo, L. F. Pinzon-Perez, A. Ricaño Rocha, H. Paz. PeerJ. 2022.</p>
Laying low: Rugged lowland rainforest preferred by feral cats in the Australian wet tropics
<p>Invasive mesopredators are responsible for the decline of many species of native mammals worldwide. Feral cats have been causally linked to multiple extinctions of Australian mammals since European colonisation. While feral cats are found throughout Australia, most research has been undertaken in arid habitats, thus there is a limited understanding of feral cat distribution, abundance, and ecology in Australian tropical rainforests. We carried out camera-trapping surveys at 108 locations across seven study sites, spanning 200 km in the Australian Wet Tropics. Single-species occupancy analysis was implemented to investigate how environmental factors influence feral cat distribution. Feral cats were detected at a rate of 5.09 photographs/100 days, 11 times higher than previously recorded in the Australian Wet Tropics. The main environmental factors influencing feral cat occupancy were a positive association with terrain ruggedness, a negative association with elevation, and a higher affinity for rainforest than eucalypt forest. These findings were consistent with other studies on feral cat ecology but differed from similar surveys in Australia. Increasingly harsh and consistently wet weather conditions at higher elevations, and improved shelter in topographically complex habitats may drive cat preference for lowland rainforest. Feral cats were positively associated with roads, supporting the theory that roads facilitate access and colonisation of feral cats within more remote parts of the rainforest. Higher elevation rainforests with no roads could act as refugia for native prey species within the critical weight range. Regular monitoring of existing roads should be implemented to monitor feral cats, and new linear infrastructure should be limited to prevent encroachment into these areas. This is pertinent as climate change modelling suggests that habitats at higher elevations will become similar to lower elevations, potentially making the environment more suitable for feral cat populations.</p>
Fig. 4 in First record of Geosiris (Iridaceae: Geosiridoideae) from Australasia: a new record and a new species from the Wet Tropics of Queensland, Australia
Fig. 4. – Distribution of the three Geosiris Baill. species.
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Allen Brain Atlas
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
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OpenNeuro
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