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308 results for “bromeliads”
Figure 3 in Population dynamics, age structure and sex ratio of the bromeliad-dwelling jumping spider, Psecas chapoda (Salticidae)
Figure 3. Climatic data from Itauna farm (5 km from the study site), from May 1998 to April 2000.
Figure 2 in Diet of bromeliad-frog Phyllodytes luteolus (Anura, Hylidae) in Atlantic Forest environments: what have the frogs been eating outside sandy coastal plains?
Figure 2. Non-metric multidimensional scaling (NMDS) plot for prey presence. The represented populations of P. luteolus in lowland forest (triangles), sandy coastal plains (circles) and island (squares) environments in Espírito Santo State, southeastern Brazil.
Figure 1 in Diet of bromeliad-frog Phyllodytes luteolus (Anura, Hylidae) in Atlantic Forest environments: what have the frogs been eating outside sandy coastal plains?
Figure 1. Study sites in Espírito Santo State, southeastern Brazil. Dark gray points represent the sampled Phyllodytes luteolus populations.
Data from: Disentangling the factors that shape bromeliad and ant communities in the canopies of cocoa agroforestry and preserved Atlantic Forest
<p>In tropical forest canopies, host tree characteristics shape epiphyte communities, and both host tree characteristics and epiphytes determine invertebrate communities, e.g., ants. Tree height is among the factors most often mentioned as a strong predictor for both bromeliad and ant communities. However, many factors interact dynamically in shaping the tree-bromeliad-ant association. Here, we investigated the effects of the host tree and canopy structural characteristics on both bromeliads and ants. We sampled bromeliads on 180 trees and ants in 360 bromeliads living on a subset of 60 of those trees in a continuum of native forest fragments and agroforestry systems in the Atlantic Forest, a Brazilian biodiversity hotspot. We found that the host trees' crown area had a positive effect on the abundance of bromeliads. Also, the introduced tree species had higher abundance of bromeliads than native tree species. Moreover, we found that the ant species composition was different between native and introduced trees. In addition, we observed a positive effect of the size of bromeliads and tree crown height on ant species richness on both bromeliad and tree scales, but there was no effect of tree height. Taken together, our findings highlight the importance of trees with large crowns for the maintenance of bromeliads, which are also associated with richer ant communities in both Atlantic Forest and agroforestry systems. These results emphasize the importance of trees with larger crowns for biodiversity conservation in both native forest fragments and agroforestry systems.</p>
Effects of warming on structure of aquatic communities in tropical bromeliad microecosystems
<p><span>Freshwaters are among the most vulnerable ecosystems to climate warming, with projected temperature increases over the coming decades leading to significant losses of aquatic biodiversity. Experimental studies that directly warm entire natural ecosystems in the tropics are needed, </span><span>for understanding the disturbances in aquatic communities.</span><span> Therefore, we conducted an experiment to test the impacts of predicted future warming on density, alpha diversity, and beta diversity of freshwater </span><span>aquatic communities, inhabiting natural microecosystems – Neotropical tank bromeliads. Aquatic communities within the tank bromeliads were experimentally exposed to warming, temperatures ranging from 23.58 to 31.72°C. Linear regression analysis was used to test the impacts of </span><span>warming</span><span>. Next, distance-based redundancy analysis was performed to assess how warming might alter total beta diversity and its components.</span><span> This experiment was conducted across a gradient of habitat size (bromeliad water volume) and availability of detrital basal resources. A combination of the highest detritus biomass and higher experimental temperatures resulted in the greatest density of flagellates. However, the density of flagellates declined in bromeliads with higher water volume and lower detritus biomass. Moreover, the combination of the highest water volume and high temperature reduced density of copepods. </span><span>Finally, warming changed microfauna species composition, mostly through species substitution (βrepl component of total beta-diversity). These findings indicate that warming strongly structures freshwater communities by reducing or increasing densities of different aquatic community groups. It also enhances beta-diversity, and many of these effects are modulated by habitat size or detrital resources. </span></p>
Transcriptome data from silica-preserved leaf tissue reveals gene flow patterns in a Caribbean bromeliad
<p>Transcriptome sequencing is a cost-effective approach that allows researchers to study a broad range of questions. However, to preserve RNA for transcriptome sequencing, tissue is often kept under special conditions, such as immediate ultracold freezing. Here, we demonstrate that RNA can be obtained from six-month-old, field-collected samples stored in silica gel at room temperature. Using these transcriptomes, we explore the evolutionary relationships of the genus Pitcairnia (Bromeliaceae) in the Dominican Republic and infer barriers to gene flow.</p>
Data from: Novel microsatellite markers for epiphytic bromeliad Tillandsia recurvata L., in an urban landscape in South-eastern Brazil
<p><span>The authors present seven novel microsatellite markers for </span><em>Tillandsia recurvata</em> L. The genome assemble sequences of <em>T. recurvata</em> were obtained from NCBI (7.2Gb) (Sayers <em>et al</em>. 2022). The BioProject Accession and accession numbers are PRJNA701548 and SRX10089449, respectively. The microsatellite identification software Krait (0.5.2) (Du <em>et al</em>. 2018) was used to detect suitable microsatellites, both genome-wide and in the noncoding regions of <em>T. recurvata</em>. The single sequence repeats (SSRs) were refined to a minimum number of seven repeats of di-, tri-, or tetra-nucleotide repeat motifs. These sequences were further limited to SSRs of more than 100bp in length and low GC content (<50%). Krait (0.5.2) (Du <em>et al</em>. 2018) was also used to design the primers for the selected SSR sequences, in conjunction with the integrated Primer3 software. The criteria for primer selection included: a primer length of 18-26bp, an optimal melting temperature (Tm) of 54-59°C and GC content of <50%. These designed primers were single-plexed and amplified using the following PCR cycle: initial denaturation (95°C for 3 min), 34 cycles of 95°C for 30s, annealing for 30s (JP01-JP12: 54°C, 4873TD + 35251TD: 56°C, 19286TD: 53°C, 5044TD + 186664TD + 214633TD: 58°C), 72°C for 1 min and a final extension of 72°C for 5 mins. The authors make this information available to other researchers, to continue the investigation of epiphyte genetics.</p>
Data from: Disentangling the factors that shape bromeliad and ant communities in the canopies of cocoa agroforestry and preserved Atlantic Forest
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Height and phytotelm size affect the invertebrate communities of epiphytic bromeliads in the Amazon rainforest
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Data from: Habitat size thresholds for predators: why damselflies only occur in large bromeliads
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Bromeliad populations perform distinct ecological strategies across a tropical elevation gradient
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Data for analyzing the microbiome of bromeliads and fly larvae inhabiting the tropical cloud forest of Mexico
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Effects of warming on structure of aquatic communities in tropical bromeliad microecosystems
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Data from: Novel microsatellite markers for epiphytic bromeliad Tillandsia recurvata L., in an urban landscape in South-eastern Brazil
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Data from: Drivers of bromeliad leaf and floral bract variation across a latitudinal gradient in the Atlantic Forest
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Biogeography of different life forms of the southernmost neotropical tank bromeliad
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RAD-seq data from: Evidence of local adaptation despite strong drift in a Neotropical patchily distributed bromeliad
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Contrasting effects of host tree isolation on population connectedness in two tropical epiphytic bromeliads
<p><b>Premise of the study</b></p> <p>Conversion of primary forests to pastures is a major cause of habitat fragmentation in the tropics. Fragmentation is expected to impede gene flow for many plant species that are restricted to remaining forest fragments. Epiphytes may be especially vulnerable to this effect of forest fragmentation because they depend on host trees. However, trees that remain in pastures may enhance connectivity across the landscape for epiphyte species that can thrive on such trees. To investigate this possibility, we studied the genetic structures of two such species on isolated pasture trees and surrounding forest, in relation to their local abundances in different habitat types and aspects of their reproductive biology including pollen and seed dispersal agents, and looked for evidence of increased or diminished gene flow.</p> <p><b>Methods</b></p> <p>We used microsatellite markers to assess geographic patterns of genetic diversity and differentiation in two epiphytic bromeliads, <i>Catopsis nitida</i> and <i>Werauhia tonduziana,</i> in the Monteverde region of Costa Rica.</p> <p><b>Key results</b></p> <p>About 85%<sup> </sup>of the <i>F</i><sub>ST</sub> value for <i>Catopsis nitida</i> was found among pastures within regions, while for <i>Weruahia tonduziana,</i> about 80% of the <i>F</i><sub>ST </sub>value was contributed by differences between regions, indicating much more gene flow within regions, relative to <i>C. nitida</i>.</p> <p><b>Conclusions</b></p> <p>Although there was substantial genetic differentiation among epiphyte populations, those on isolated pasture trees were not substantially less diverse than those in adjacent forests, suggesting that pasture trees may serve as "stepping stones" that help these species maintain their genetic connectedness and diversity at larger geographic scales.</p>
FIGURE 3 in Checklist of ciliates (Alveolata: Ciliophora) that inhabit in bromeliads from the Neotropical Region
FIGURE 3. Ciliate species from Mexican bromeliads included in the present study: m. Colpoda lucida, n. C. cucullus, o. C. cavicola, p. C. maupasi, q. Emarginatophrya aspera, r. C. inflata, s. Cyclidium glaucoma, t. Paracolpoda lajacola, u. P. steinii, v. Bromeliothrix metopoides macrostome, w. microstomous theront of B. metopoides, x. microstomous trophont of B. metopoides. MA-macronucleus; m, p-x: Cells impregnated with the dry silver nitrate method (Foissner, 2014); n. Cell impregnated with nigrosine; o: Cells with silver carbonate impregnation (Fernández-Galiano 1976). Scale bars: 10µm.
FIGURE 2 in Checklist of ciliates (Alveolata: Ciliophora) that inhabit in bromeliads from the Neotropical Region
FIGURE 2. Ciliate species from Mexican bromeliads included in the present study: a. Fragmocirrus espeletiae, b. Gonostomum bromelicola, c. Leptopharynx bromeliophilus, d. L. brasiliensis, e. L. bromelicola, f. L. costatus, g. Chilodonella uncinata, h. Glaucomides bromelicola, i. Epistylis plicatilis (in vivo), j. Bromeliophrya brasiliensis, k. Drepanomonas revoluta, l. D. sphagni. MA-macronucleus; a, b, g, h, k: cells with protargol procedure (Foissner 2014); c-f, j, l. Cells impregnated with the dry silver nitrate method (Foissner 2014). Scale bars: 10µm.
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Allen Brain Atlas
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