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Figure 2 from: Xie M-L, Wei T-Z, Fu Y-P, Li D, Qi L-L, Xing P-J, Cheng G-H, Ji R-Q, Li Y (2020) Three new species of Cortinarius subgenus Telamonia (Cortinariaceae, Agaricales) from China. MycoKeys 69: 91-109. https://doi.org/10.3897/mycokeys.69.49437
Figure 2 Basidiocarps of three newly-described species. a, bCortinarius laccariphyllus (a, b HMJAU44449, holotype); c, dCortinarius neotorvus (c HMJAU44441, holotype; d HMJAU44439); e, fCortinarius subfuscoperonatus (e HMJAU44444, holotype; f HMJAU44445). Scale bars: 2 cm (a, b, d–f). Photographs by Meng-Le Xie.
Figure 2 from: Rizzoli A, Battelli R, Conedera M, Jermini M (2020) First record of Erasmoneura vulnerata Fitch, 1851 (Hemiptera, Cicadellidae, Typhlocybinae) in Switzerland. Alpine Entomology 4: 151-156. https://doi.org/10.3897/alpento.4.53967
Figure 2 Foliage lesions and Erasmoneura vulnerata excrement. A Leaf lesions, excrement and specimens of E. vulnerata. B Details of leaf lesions and excrement left by E. vulnerata. Photographs taken in Bellinzona, Switzerland, 46.19212 N, 9.02190 E, 15 July 2019.
Figure 1 from: Xie M-L, Wei T-Z, Fu Y-P, Li D, Qi L-L, Xing P-J, Cheng G-H, Ji R-Q, Li Y (2020) Three new species of Cortinarius subgenus Telamonia (Cortinariaceae, Agaricales) from China. MycoKeys 69: 91-109. https://doi.org/10.3897/mycokeys.69.49437
Figure 1 Maximum Likelihood tree inferred from ITS sequences. The tree is rooted with section Armillati. Bayesian posterior probabilities (≥ 0.95) and ML bootstrap values (≥ 75%) are shown on each branch (BPP / ML). New species in bold.
Figure 1 from: Rizzoli A, Battelli R, Conedera M, Jermini M (2020) First record of Erasmoneura vulnerata Fitch, 1851 (Hemiptera, Cicadellidae, Typhlocybinae) in Switzerland. Alpine Entomology 4: 151-156. https://doi.org/10.3897/alpento.4.53967
Figure 1 Study area and monitoring design. Green area: vineyard area in Canton Ticino; circles: experimental plots; black dots: Erasmoneura vulnerata presence.
Figure 1 from: Xu X-L, Yang C-L, Jeewon R, Wanasinghe DN, Liu Y-G, Xiao Q-G (2020) Morpho-molecular diversity of Linocarpaceae (Chaetosphaeriales): Claviformispora gen. nov. from decaying branches of Phyllostachys heteroclada. MycoKeys 70: 1-17. https://doi.org/10.3897/mycokeys.70.54231
Figure 1 Phylogram of RAxML analysis based on a combined ITS, LSU, SSU and TEF-1α sequence dataset within order Chaetosphaeriales. Bootstrap support values for maximum likelihood (ML, left) greater than 70% and Bayesian posterior probabilities (PP, right) equal to or greater than 0.95 are indicated at the nodes. The tree is rooted to Gelasinospora tetrasperma (CBS 178.33) and Sordaria fimicola (CBS 508.50). All sequences from ex-type strains are in bold. The newly-generated sequence is in red.
Figure 2 from: Xu X-L, Yang C-L, Jeewon R, Wanasinghe DN, Liu Y-G, Xiao Q-G (2020) Morpho-molecular diversity of Linocarpaceae (Chaetosphaeriales): Claviformispora gen. nov. from decaying branches of Phyllostachys heteroclada. MycoKeys 70: 1-17. https://doi.org/10.3897/mycokeys.70.54231
Figure 2 Claviformispora phyllostachydis (SICAU 16-0007, holotype) a, bStromata on host substrate c section through ascoma with ascomata d ostiole with periphyses e peridium f paraphyses g–j asci k–o ascospores p germinated ascospore q, r colony on PDA after 7 days. Scale bars: 2 mm (a), 500 μm (b), 100 μm (c), 20 μm (d, e), 10 μm (f–p).
Supplementary material 1 from: Xu X-L, Yang C-L, Jeewon R, Wanasinghe DN, Liu Y-G, Xiao Q-G (2020) Morpho-molecular diversity of Linocarpaceae (Chaetosphaeriales): Claviformispora gen. nov. from decaying branches of Phyllostachys heteroclada. MycoKeys 70: 1-17. https://doi.org/10.3897/mycokeys.70.54231
Figure S1
Supplementary material 2 from: Xu X-L, Yang C-L, Jeewon R, Wanasinghe DN, Liu Y-G, Xiao Q-G (2020) Morpho-molecular diversity of Linocarpaceae (Chaetosphaeriales): Claviformispora gen. nov. from decaying branches of Phyllostachys heteroclada. MycoKeys 70: 1-17. https://doi.org/10.3897/mycokeys.70.54231
Figure S2
Evidence that male sea lamprey increase pheromone release after perceiving a competitor: raw data, R-code, R analyses
<p class="CxSpFirst">Sexual signals evolve via selective pressures arising from male-male competition and female choice, including those originating from unintended receivers that detect the signal. For example, males can acquire information from other males signaling to females and alter their own signal. Relative to visual and acoustic signals, less is known about how such communication networks influence chemical signaling among animals. In sea lamprey (<i>Petromyzon marinus</i>), chemical communication system is essential for reproduction, offering a useful system to study a pheromone communication network that includes signalers and both intended and unintended receivers. Male sea lamprey aggregate on spawning grounds where individuals build nests and signal to females using sex pheromones. We examined how exposure to a major component of the male pheromone, 3keto-petromyzonol sulfate (3kPZS), influenced male pheromone signaling, and whether females had a preference for males that altered their signal. Exposure to 3kPZS, at a concentration of 5x10<sup>-10 </sup>M, simulated the presence of other male(s) and led to increased 3kPZS release rates within 10 min, followed by a return to baseline levels within 30 min. Exposure also led to increases in hepatic synthesis and circulatory transport of pheromone components. In behavioral assays, females preferred the odor of males that had been exposed to 3kPZS; therefore, males likely benefit from upregulating 3kPZS release after detecting competition for mates. Here, we define how a specific pheromone component influences chemical signaling during intrasexual competition, and show a rare example of how changes in chemical signaling strategies resulting from male competition may influence mate choice.</p>
Phase portrait and potential energy function of the dynamical system corresponding to modified ZK equation for ion-acoustic waves in a magnetized electron-ion plasma with generalized (r, q) distributed electrons
<p>These figures (a) and (b) represent phase portrait and potential energy function of the dynamical system corresponding to the mZK equation for ion-acoustic waves in a magnetized electron-ion plasma with generalized (r, q) distributed electrons for q = 5 and r = 0.1. These figures contain three fixed points P<sub>0,</sub> P<sub>1 </sub>and P<sub>2</sub> with one separatrix. The figure (a) contains one family of supernonlinear periodic orbits, two families of periodic orbits and one pair of homoclinic orbits at P<sub>0. </sub>The figure (b) contains the potential energy function with two local minima and one maxima which is necessary condition for supernonlinear wave. </p>
Figure 2 from: Samarakoon BC, Phookamsak R, Wanasinghe DN, Chomnunti P, Hyde KD, Mckenzie EHC, Promputtha I, Xu J-C, Li Y-J (2020) Taxonomy and phylogenetic appraisal of Spegazzinia musae sp. nov. and S. deightonii (Didymosphaeriaceae, Pleosporales) on Musaceae from Thailand. MycoKeys 70: 19-37. https://doi.org/10.3897/mycokeys.70.52043
Figure 2 Spegazzinia deightonii (MFLU 19-2908) a–c fungal colonies on host surface d conidiophore mother cell of α conidia e–g α conidia i a developmental stage of β conidia h, k conidia l colonies on PDA after 28 days showing sporulation j, m–p β conidia. Scale bars: 500μm (a), 200μm (b), 50 μm (c), 20μm (e–h), 10μm (d, k, m–p), 5 μm (i, j).
Figure 1 from: Samarakoon BC, Phookamsak R, Wanasinghe DN, Chomnunti P, Hyde KD, Mckenzie EHC, Promputtha I, Xu J-C, Li Y-J (2020) Taxonomy and phylogenetic appraisal of Spegazzinia musae sp. nov. and S. deightonii (Didymosphaeriaceae, Pleosporales) on Musaceae from Thailand. MycoKeys 70: 19-37. https://doi.org/10.3897/mycokeys.70.52043
Figure 1 Maximum likelihood tree revealed by RAxML from an analysis of SSU, LSU and ITS and TEF1-α sequence data of selected genera of family Didymosphaeriaceae, showing the phylogenetic position of Spegazzinia musae (MFLUCC 20-0001) and S. deightonii (MFLUCC 20-0002). ML bootstrap supports (≥60 %) and Bayesian posterior probabilities (≥ 0.95 BYPP) are given above in the branches, respectively. The tree was rooted with Pleospora herbarum and Stemphylium botryosum (Pleosporaceae). Strains generated in this study are indicated in red-bold. Ex-type species are indicated in bold. The scale bar represents the expected number of nucleotide substitutions per site. A best scoring RAxML tree is shown with a final ML optimization likelihood value of -13516.66. The matrix had 795 distinct alignment patterns, with 33.60% of undetermined characters or gaps. Estimated base frequencies were: A = 0.239862, C = 0.245185, G = 0.277025, T = 0.237927; substitution rates AC = 1.626982, AG = 2.468452, AT = 1.211822, CG = 1.092437, CT = 6.295657, GT = 1.000000; proportion of invariable sites I = 0.484119; gamma distribution shape parameter α = 0.445929.
Figure 3 from: Samarakoon BC, Phookamsak R, Wanasinghe DN, Chomnunti P, Hyde KD, Mckenzie EHC, Promputtha I, Xu J-C, Li Y-J (2020) Taxonomy and phylogenetic appraisal of Spegazzinia musae sp. nov. and S. deightonii (Didymosphaeriaceae, Pleosporales) on Musaceae from Thailand. MycoKeys 70: 19-37. https://doi.org/10.3897/mycokeys.70.52043
Figure 3 Spegazzinia musae (MFLU 19-2907, holotype) a–c fungal colonies on host surface d mature conidia e conidiophore of α conidia with the mother cell f, g α conidia h–q β conidia r colony on PDA after 28 days. Scale bars: 200 μm (a–c), 20 μm (d–g, j), 10 μm (h, i, k–q).
Figure 3 from: Houghton DC, Lardner R (2020) Ash-free dry mass values for northcentral USA caddisflies (Insecta, Trichoptera). ZooKeys 951: 37-46. https://doi.org/10.3897/zookeys.951.49790
Figure 3 Comparison of mean specimen abundance (% of total specimens) and AFDM biomass (% of total biomass) for the caddisfly FFGs of a Michigan first order stream, based on 13 blacklight samples from each of 5 sites collected weekly from June to August 2012 (Houghton and Wasson 2013). AFDM biomass determined by multiplying determined AFDM values reported herein for each species by the number of specimens of that species in each sample.
Figure 2 from: Houghton DC, Lardner R (2020) Ash-free dry mass values for northcentral USA caddisflies (Insecta, Trichoptera). ZooKeys 951: 37-46. https://doi.org/10.3897/zookeys.951.49790
Figure 2 The Log10 high, low, and mean biomass values for each of the 20 different caddisfly families measured. Number of species measured within each family above each bar.
Figure 1 from: Houghton DC, Lardner R (2020) Ash-free dry mass values for northcentral USA caddisflies (Insecta, Trichoptera). ZooKeys 951: 37-46. https://doi.org/10.3897/zookeys.951.49790
Figure 1 The northcentral US, showing localities from where our AFDM-determined specimens were collected.
Supplementary material 3 from: Mederly P, Černecký J, Špulerová J, Izakovičová Z, Ďuricová V, Považan R, Švajda J, Močko M, Jančovič M, Gusejnov S, Hreško J, Petrovič F, Štefunková D, Šatalová B, Vrbičanová G, Kaisová D, Turanovičová M, Kováč T, Laco I (2020) National ecosystem services assessment in Slovakia – meeting old liabilities and introducing new methods. One Ecosystem 5: e53677. https://doi.org/10.3897/oneeco.5.e53677
Individual ES graphical outputs
Supplementary material 1 from: Mederly P, Černecký J, Špulerová J, Izakovičová Z, Ďuricová V, Považan R, Švajda J, Močko M, Jančovič M, Gusejnov S, Hreško J, Petrovič F, Štefunková D, Šatalová B, Vrbičanová G, Kaisová D, Turanovičová M, Kováč T, Laco I (2020) National ecosystem services assessment in Slovakia – meeting old liabilities and introducing new methods. One Ecosystem 5: e53677. https://doi.org/10.3897/oneeco.5.e53677
Specification of data used and legend of all used spatial layers
Supplementary material 2 from: Mederly P, Černecký J, Špulerová J, Izakovičová Z, Ďuricová V, Považan R, Švajda J, Močko M, Jančovič M, Gusejnov S, Hreško J, Petrovič F, Štefunková D, Šatalová B, Vrbičanová G, Kaisová D, Turanovičová M, Kováč T, Laco I (2020) National ecosystem services assessment in Slovakia – meeting old liabilities and introducing new methods. One Ecosystem 5: e53677. https://doi.org/10.3897/oneeco.5.e53677
Computational algorithms for 18 ES
Supplementary material 1 from: Müller A, Prosi R, Taylor S, Richter H, Herrmann M, Weibel U (2020) Unique nesting biology of Osmia ( Melanosmia) uncinata, a Palaearctic osmiine bee specialized on thick-barked conifers (Hymenoptera, Megachilidae). Alpine Entomology 4: 157-171. https://doi.org/10.3897/alpento.4.53489
List of distributional data of Osmia uncinata
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.
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.
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.
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.
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.