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zenodo36/100

Figure 4 in Gall-inducing arthropods in a Neotropical savanna area in the EPA of Rio Pandeiros (Bonito de Minas, MG, Brazil): effects of plant species richness and super-host abundance

Figure 4. Gall morphotypes in host plants in an area of Neotropical savanna in the EPA of Rio Pandeiros (Bonito de Minas, MG, Brazil). (A) Fabaceae = Tachigali alba, (B) Malpighiaceae = Malpighiaceae sp., (C) Malvaceae = Eriotheca gracilipes, (D) Myrtaceae = Eugenia dysenterica, (E) Myrtaceae = Eugenia sp., (F) Myrtaceae = Psidium sp., (G) Ochnaceae = Ouratea hexasperma, (H) Ochnaceae = Ouratea spectabilis.

opencc-by-nc-4.0Jul 2020View details →
zenodo36/100

Figure 3 in Gall-inducing arthropods in a Neotropical savanna area in the EPA of Rio Pandeiros (Bonito de Minas, MG, Brazil): effects of plant species richness and super-host abundance

Figure 3. Gall morphotypes in host plants in an area of Neotropical savanna in the EPA of Rio Pandeiros (Bonito de Minas, MG, Brazil). (A-D) Fabaceae = Copaifera oblongifolia, (E) Fabaceae = Hymenaea stigonocarpa, (F-G) Fabaceae = Machaerium opacum, (H) Fabaceae = Sclerolobium denudatum.

opencc-by-nc-4.0Jul 2020View details →
zenodo36/100

Figure 2 in Gall-inducing arthropods in a Neotropical savanna area in the EPA of Rio Pandeiros (Bonito de Minas, MG, Brazil): effects of plant species richness and super-host abundance

Figure 2. Gall morphotypes in host plants in an area of Neotropical savanna in the EPA of Rio Pandeiros (Bonito de Minas, MG, Brazil). (A) Dilleniaceae = Davilla elliptica, (B) Ebenaceae = Diospyros hispida, (C) Erythroxylaceae = Erythroxylum suberosum, (D-F) Fabaceae = Andira humilis, (G) Fabaceae = Copaifera luetzelburgii, (H) Fabaceae = Copaifera oblongifolia.

opencc-by-nc-4.0Jul 2020View details →
zenodo36/100

Figure 1 in Gall-inducing arthropods in a Neotropical savanna area in the EPA of Rio Pandeiros (Bonito de Minas, MG, Brazil): effects of plant species richness and super-host abundance

Figure 1. Gall morphotypes in host plants in an area of Neotropical savanna in the EPA of Rio Pandeiros (Bonito de Minas, MG, Brazil). (A) Anacardiaceae =Anacardium humile, (B) Bignoniaceae = Handroanthus ochraceus, (C) Calophyllaceae = Kielmeyera speciosa, (D) Caryocaraceae = Caryocar brasiliense, (E) Combretaceae = Terminalia fagifolia, (F-G) Connaraceae = Connarus suberosus, (H) Dilleniaceae = Davilla elliptica.

opencc-by-nc-4.0Jul 2020View details →
zenodo36/100

Figure 1 in First characterization of a taxonomically well-resolved trophic network composed by host plants and gall midges (Diptera: Cecidomyiidae) in the Neotropical region

Figure 1. Bipartite network of host plants and gall midge species at the Restinga of Barra de Maricá (Maricá, RJ, Brazil). Lower bars represent host plant species and upper bars represent gall-midge species; grey bars represent interactions. Bar thickness is proportional to the number of interactions of each species. ble interactions. The observed connectance (C = 0.028) decades), which enhances the sampling of rarer interacwas lower than expected from null model values (Null tions, and consequently increases the specialization of C = 0.032 ± 0.001, p <0.001). Similarly, the observed num- the network. However, this fact reinforces the relevance ber of links per species (L = 0.608) also was lower than of the observed patterns, because even with such a long expected by chance (Null L = 0.710 ± 0.020, p <0.001). sampling, only species-specific plant-galling interactions The observed modularity for plant-galling network was were registered. very high (M = 0.958), but did not differ from null model The structure of the network formed by the gall midgvalues (Null M = 0.959 ± 0.001, p> 0.05). Robustness ob- es and their host plants proved to be highly specialized. served was relatively low (R = 1.343), but was higher than The connectance observed in the present study (2.8%) expected by chance (Null R = 1.334 ± 0.232, p <0.001). was low as compared to other plant-phytophagous networks (review in Araújo et al., 2015). However, comparing with other networks of galling arthropods, the val- DISCUSSION ue observed here was higher than observed by Araújo

opencc-by-nc-4.0Mar 2021View details →
dryad36/100

Data from: Combining experimental evolution and genomics to understand how seed beetles adapt to a marginal host plant

<p>Genes that affect adaptive traits have been identified, but our knowledge of the genetic basis of adaptation in a more general sense (across multiple traits) remains limited. We combined population-genomic analyses of evolve and resequence experiments, genome-wide association mapping of performance traits, and analyses of gene expression to fill this knowledge gap, and shed light on the genomics of adaptation to a marginal host (lentil) by the seed beetle <em>Callosobruchus maculatus</em>. Using population-genomic approaches, we detected modest parallelism in allele frequency change across replicate lines during adaptation to lentil. Mapping populations derived from each lentil-adapted line revealed a polygenic basis for two host-specific performance traits (weight and development time), which had low to modest heritabilities. We found less evidence of parallelism in genotype-phenotype associations across these lines than in allele frequency changes during the experiments. Differential gene expression caused by differences in recent evolutionary history exceeded that caused by immediate rearing host. Together, the three genomic data sets suggest that genes affecting traits other than weight and development time are likely to be the main causes of parallel evolution, and that detoxification genes (especially cytochrome P450s and beta-glucosidase) could be especially important for colonization of lentil by <em>C. maculatus</em>.</p>

opencc-zeroApr 2020View details →
dryad36/100

Struggling to survive: A comparison of Vanessa cardui larval survivorship on putative host plants

<p>The painted lady butterfly (<em>Vanessa cardui</em>) is a generalist herbivore with a global distribution. In North America, over 100 species have been identified as <em>V. cardui</em> larval host plants. This cosmopolitan species is commercially available in all life stages and can be reared on an artificial diet. As a result, <em>V. cardui</em> commonly serves as a model organism for education and outreach. However, gaps in our knowledge remain with regard to <em>V. cardui </em>ecology and larval host plant suitability for supporting complete development of larvae to reproductive adulthood. In a laboratory setting, we tested host plant suitability of five reported host plants commonly found in California sage scrub ecosystems by assessing survival of <em>V. cardui</em> caterpillars in their entirety. We also assessed how commercially sourced larvae survived on an artificial diet: both raising the caterpillars exclusively on an artificial diet, as well as switching diets from artificial to thistle (a commonly reported host plant) and switching from thistle to artificial diet. We found that all commercially-sourced caterpillars exhibited both high larval mortality and low pupation rates when reared on host plants, although larvae reared on <em>Malacothamnus fasciculatus</em> and <em>Sphaeralcea ambigua</em> survived longest. Moreover, <em>M. fasciculatus</em> and <em>S. ambigua </em>were the only host plants tested that supported successful pupation. This contrasted with a 63% higher survival of wild-collected larvae. Our findings suggest that commercially obtained <em>V. cardui </em>may struggle to utilize wild host plants and that future investigations into host plant suitability in wild populations are needed. Additionally, future research using commercial larvae should consider the implications for interpreting host plant suitability as larvae may exhibit adaptations to artificial diet or the loss of adaptation to consuming plant material.</p>

opencc-zeroFeb 2024View details →
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Data and Analyses for Host plant-mediation of viral transmission and its consequences for a native butterfly

<p>This contains R code for all analyses and creation of figures included in the publication entitled "Host plant-mediation of viral transmission and its Q1 consequences for a native butterfly". This article has now been accepted for publication under DOI: 10.1002/ecy.4282. The files containing the data analysis script have been updated to reflect the final analyses included in this paper.&nbsp;</p>

opencc-by-4.0May 2023View details →
dryad36/100

Data for: Local adaptation of a generalist hemiparasitic plant to one of its potential host plants

<p>Coevolution is often found in parasite-host interactions but has not yet been described for hemiparasitic plants and their hosts. Root hemiparasites like <em>Rhinanthus alectorolophus</em> perform photosynthesis but also parasitize other plant species, some of which (e.g. <em>Plantago lanceolata</em>) may defend themselves against parasite attack by blocking the haustoria of the parasites. We grew seedlings of the hemiparasite <em>Rhinanthus alectorolophus</em> and the potential host <em>Plantago lanceolata</em> from seven grassland sites in a factorial design. To detect differences in host defence, we also included hosts from two 'naïve' populations from regions where the parasite does not occur.<em> R. alectorolophus</em> grew consistently larger and had higher fitness with sympatric than with allopatric hosts, suggesting parasite adaptation to local host populations. Moreover, <em>R. alectorolophus</em> remained smallest with allopatric hosts from the same region and reached intermediate sizes with allopatric hosts from other regions or naïve hosts, suggesting host adaptation to parasites at the regional scale. Parasite presence reduced the size of the host plants already after four weeks, but only that of hosts with 'experience' of the parasite, suggesting an early host response. Follow-up experiments confirmed that parasites attach to hosts already after four weeks and hosts respond by changing belowground allocation patterns. However, parasite roots did not preferentially grow towards sympatric hosts. Our results suggest that local adaptation to hosts can occur even in generalist parasites and does not require specialization on individual hosts. We discuss the role of potential mechanisms, including variation in chemical signalling (early) and in host defence (late effects).</p>

opencc-zeroApr 2024View details →
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Figure 6 in Colotis lais (Butler, 1876) and Colotis euippe omphale (Godart, [1819]) use Cadaba aphylla (Thunb.) Wild LC as a host-plant at Tswalu Kalahari, Northern Cape Province, South Africa)

Figure 6 – Location of Tswalu Kalahari in southern Africa.

opencc-by-4.0Dec 2023View details →
zenodo36/100

Evolution of sympatric host-specialized lineages of the fungal plant pathogen Zymoseptoria passerinii in natural ecosystems

<p>This repository contains the data sets from the research paper "Evolution of sympatric host-specialized lineages of the fungal plant pathogen <em>Zymoseptoria passerinii</em> in natural ecosystems"</p>

opencc-by-4.0Aug 2024View details →
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Figures 8–9. Stenelytrana splendens. 8 in New larval host plants and ecological observations on North American Cerambycidae (Coleoptera)

Figures 8–9. Stenelytrana splendens. 8) Female. 9) Male.

opencc-by-4.0Dec 2021View details →
dryad36/100

Parasitic trophic mode of plant host affects the extent of colonization, but does not induce systematic shifts in the composition of foliar endophytic assemblages in temperate meadow ecosystems

<p>1. Foliar endophytic bacteria and fungi are increasingly being recognized as important drivers of plant host phenotype – affecting a wide range of eco-physiological processes. However, we are still lacking fundamental ecosystem-level knowledge about the structure, function, and inter-species interactions in endophytic assemblages associated with plant hosts sharing a common life strategy or ecological specialization.</p> <p>2. In this study, we chose two groups of plants with contrasting physiology as model systems: parasites and their hosts. We assessed whether plant life history strategy, namely differences in nutrient acquisition and accumulation, plays a role in structuring above-ground microbiomes under field conditions.</p> <p>3. We focused on the structure, colonization extent, and potential function of foliar endophytic bacteria and fungi in three root hemiparasitic species (Orobanchaceae), one stem holoparasite (Convolvulaceae), and their potential host plants co-occurring in species-rich temperate grassland ecosystems. For this purpose, we combined next generation amplicon sequencing with quantitative real-time PCR, chemical analyses of leaf tissue, and, in the case of bacteria, functional predictions using information deposited in available databases.</p> <p>4. We found the foliar endophytic assemblages to be diverse, dominated by generalist taxa, but highly similar across all studied species. Despite of the highly contrasting leaf tissue chemistry in the parasitic and non-parasitic plant species, the parasitic trophic mode did not induce systematic shifts in the diversity, composition, or predicted biogeochemical function of the endophytic microbiomes under field conditions. However, compared to their potential hosts, leaves of both hemiparasitic and holoparasitic species harbored significantly lower fungal counts, estimated as <em>ß-actin</em> gene copies ng DNA<sup>-1</sup>, which suggests that parasitic plants may possess mechanisms to regulate the extent of colonization by endophytic fungi.</p>

opencc-zeroFeb 2022View details →
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Pre-processed data for "Does host plant drive variation in microbial gut communities in a recently shifted pest?"

<p>Pre-processed fastqs files generated by Illumina sequencing associated with the publication by Javal et al. entitled &quot;Does host plant drive variation in microbial gut communities in a recently shifted pest?&quot;.</p>

opencc-by-4.0Mar 2022View details →
dryad36/100

Host plant specificity of the monarch butterfly Danaus plexippus: A systematic review and meta-analysis

<p>The preference-performance hypothesis explains host specificity in phytophagous insects, positing that host plants chosen by adults confer the greatest larval fitness. However, adults sometimes oviposit on plants supporting low larval success because the components of host specificity (adult preference, plant palatability, and larval survival) are non-binary and not necessarily correlated. Palatability (willingness to eat) is governed by chemical cues and physical barriers such as trichomes, while survival (ability to complete development) depends upon nutrition and toxicity. Absence of a correlation between the components of host specificity results in low-performance hosts supporting limited larval development. Most studies of specificity focus on oviposition behavior leaving the importance and basis of palatability and survival under-explored. We conducted a comprehensive review of 127 plant species that have been claimed or tested to be hosts for the monarch butterfly Danaus plexippus to classify them as non-hosts, low performance, or high performance. We performed a meta-analysis to test if performance status could be explained by the properties of neurotoxic cardenolides or trichome density. We also conducted a no-choice larval feeding experiment to identify the causes of low performance. We identified 34 high performance, 42 low performance, 33 non-hosts, and 18 species with unsubstantiated claims. Mean cardenolide concentration was greater in high- than low-performance hosts and a significant predictor of host status, suggesting possible evolutionary trade-offs in monarch specialization. Other cardenolide properties and trichome density were not significant predictors of host status. In the experiment, we found, of the 62% of larvae that attempted to eat low-performance hosts, only 3.5% survived to adult compared to 85% of those on the high-performance host, demonstrating that multiple factors affect larval host plant specificity. Our study is the first to classify all known host plants for monarchs and has conservation implications for this threatened species.</p>

opencc-zeroJun 2022View details →
dryad36/100

Defensive mutualists affect outcross pollen transfer and male fitness in their host plant

<p>Ant guards can increase plant fitness by deterring herbivores, but they may also reduce it by interfering with pollination. While ant impacts on herbivory have been well-studied, much less is known about their impacts on pollinators and associated consequences for plant pollination, particularly pollen transfer dynamics and outcrossing/selfing rates. We used field experiments to quantify the effect of ant guards on pollinator community composition, frequency and duration of flower visits, and cascading effects on outcrossing pollen transfer and pollen exports in Turnera velutina (Passifloraceae). Although ant patrolling did not affect pollinator community composition or visitation frequency, it decreased flower visit duration and the time pollinators spent foraging inside flowers. Such behavioural changes resulted in reduced pollen deposition on stigmas, decreased pollen exports (a proxy for male fitness) and significantly doubled outcross pollen transfer. This study contributes to our understanding of how nonpollinator mutualists can shape plant reproductive processes. We discuss the downstream effects that variation in biotic defences, such as rewards for guarding ants, can have on plant pollen transfer patterns and fitness. In conclusion, guarding ants influence pollen transfer patterns in Turnera velutina, increasing outcrossing in a self-compatible species at the cost of male fitness. We show how non-pollinators, such as defensive ant mutualists, can shape plant reproductive traits and discuss the consequences these interactions may have for plant mating systems.</p>

opencc-zeroJun 2022View details →
zenodo36/100

Adaptation of pathogens to their local plant host, Silphium integrifolium, along a precipitation gradient

<p>All figures and code were generated in RStudio 2022.02.3+492 &quot;Prairie Trillium&quot; Release. All packages needed to run the R code are shown in the RMD&rsquo;s.</p> <p>&nbsp;</p> <p>Code to generate figures and statistical analysis:</p> <p>&nbsp;</p> <ul> <li>DVTindex_help.Rmd <ul> <li>Code to generate figure 3</li> </ul> </li> <li>Figure5_PrairieVSCommonGarden <ul> <li>Code to generate figure 5</li> </ul> </li> <li>PATHOFigs_for_Manu_FEB22.Rmd <ul> <li>Code to generate figures 1, 2, 4</li> </ul> </li> <li>SUPP_Figure3_DimPathoEDIT.Rmd <ul> <li>Code to generate supplementary figure 3 (fig S3)</li> </ul> </li> <li>STATSAnalysis_PathoDim2B.Rmd <ul> <li>Code to generate all tables and statistical analysis in the manuscript</li> </ul> </li> </ul> <p>&nbsp;</p> <p>Description of data files:</p> <ul> <li>2019and2020Prairie_data.txt <ul> <li>This file contains data collected from the prairie sites in 2019 and 2020</li> </ul> </li> <li>Dim2b_latlon.csv <ul> <li>The latitudinal and longitudinal coordinates for the common garden sites and prairie sites as well as precipitation data</li> </ul> </li> <li>DVTINDEX_from_DVT.csv <ul> <li>A separate file that contains the data that produced fig 3. This data file is sourced from SEPT2019_2020_COMPILED_2b_DATACOLL.txt</li> </ul> </li> <li>SEPT2019_2020_COMPILED_2b_DATACOLL.txt</li> <li>SEPT2019_2020_COMPILED_2b_DATACOLL_plots.txt</li> <li>SEPT2019_2020_COMPILED_2b_DATACOLL_plots_longversion.txt <ul> <li>These 3 data files are different versions of the same raw data that was collected from the common garden sites in 2019 and 2020. The code calls for all 3 at different points to generate plots and run statistical analyses</li> </ul> </li> <li>Summary [ insert unique name here] <ul> <li>Various data frames generated from r mark downs that contain summary statistics of the data. These are used to produce the figures in PATHOFigs_for_Manu_FEB22.Rmd graphs.</li> </ul> </li> </ul>

opencc-by-4.0Jul 2022View details →
zenodo36/100

Supporting data and code for: Host plant and insecticides shape the evolution of genetic and clonal diversity in a major aphid crop pest

<p>This is the first release of the final data and code for the article accepted for publication in <em>Evolutionary Applications</em> journal. It contains the necessary scripts to produce most of the analyses and figures of the manuscript. All the necessary data can be found in the &#39;data&#39; folder.</p>

openother-openSep 2021View details →
dryad36/100

The role of tetradecane in the identification of host plants by the pest bugs Apolygus lucorum and Adelphocoris suturalis

<p><em><span>Apolygus lucorum </span></em><span>and <em>Adelphocoris suturalis </em>are considered serious pests to many cultures in China. Safe alternatives are needed to manage these mirid pests. </span>The current study identified <span>compounds from  volatiles of the </span>ethanol extracts of <span><em>Phaseolus vulgaris</em> </span><span>pods and the other </span>10 common hosts. GCMS detection showed that t<span>etradecane</span><span>, 2-propyl-1-pentanol, and dodecanal were included in these </span>volatiles and<span>   </span>tetradecane was present in all the volatiles.</p>

opencc-zeroJul 2022View details →
zenodo36/100

Figure 1 in Megalopodidae (Insecta, Coleoptera): new occurrence and host plant records for Brazil

Figure 1. Species of Megalopodinae (Megalopodidae) sampled from forest fragments in southwestern and western Paraná. (A) Mastostethus sobrinus Lacordaire, 1845; (B) Mastostethus pantherinus Lacordaire, 1845; (C) Mastostethus lateritius (Klug, 1834); (D) Mastostethus alternans (Klug, 1834); (E) Mastostethus minutus Monrós, 1947; (F) Megalopus tabidus Klug, 1834; (G) Megalopus waterhousei Baly, 1859; (H) Agathomerus (Euagathomerus) sellatus (Germar, 1823); (I) Agathomerus (Euagathomerus) elegans (Klug, 1834); (J) Agathomerus (Agathomeroides) flavomaculatus (Klug, 1845); (K) Pseudhomalopterus carinatus Pic, 1920.

opencc-by-nc-4.0Oct 2021View details →

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Allen Brain Atlas

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

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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

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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