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Figure 7 from: SUN B-D, Chen AJ, Houbraken J, Frisvad JC, Wu W, Wei H, Zhou Y, Jiang X, Samson R (2020) New section and species in Talaromyces. MycoKeys 68: 75-113. https://doi.org/10.3897/mycokeys.68.52092
Figure 7 Talaromyces aspriconidius CBS 141835Ta colonies from left to right (top row) CYA, MEA, YES and OA; (bottom row) CYA reverse, MEA reverse, DG 18 and CREAb–g conidiophores and conidia. Scale bars: 10 μm (b–g).
Figure 4 from: SUN B-D, Chen AJ, Houbraken J, Frisvad JC, Wu W, Wei H, Zhou Y, Jiang X, Samson R (2020) New section and species in Talaromyces. MycoKeys 68: 75-113. https://doi.org/10.3897/mycokeys.68.52092
Figure 4 Phylogeny of BenA for species classified in Talaromyces section Subinflati. Branches with values more than 1 pp and 95% bs are thickened, supports lower than those values are indicated with a dash (-). Talaromyces trachyspermus (CBS 373.48T) was chosen as outgroup. T: ex-type.
Figure 2 from: SUN B-D, Chen AJ, Houbraken J, Frisvad JC, Wu W, Wei H, Zhou Y, Jiang X, Samson R (2020) New section and species in Talaromyces. MycoKeys 68: 75-113. https://doi.org/10.3897/mycokeys.68.52092
Figure 2 Phylogeny of BenA for species classified in Talaromyces section Talaromyces. Branches with values more than 1 pp and 95% bs are thickened, supports lower than those values are indicated with a dash (-). Talaromyces dendriticus (CBS 633.80T) was chosen as outgroup. T: ex-type.
Figure 1 from: SUN B-D, Chen AJ, Houbraken J, Frisvad JC, Wu W, Wei H, Zhou Y, Jiang X, Samson R (2020) New section and species in Talaromyces. MycoKeys 68: 75-113. https://doi.org/10.3897/mycokeys.68.52092
Figure 1 Concatenated phylogeny of the ITS, BenA, CaM and RPB2 gene regions of species from Talaromyces. Branches with values more than 1 pp and 95% bs are thickened, supports lower than those values are indicated with a dash (-). Trichocoma paradoxa (CBS 788.83T) was chosen as outgroup. T: ex-type.
Supplementary material 5 from: SUN B-D, Chen AJ, Houbraken J, Frisvad JC, Wu W, Wei H, Zhou Y, Jiang X, Samson R (2020) New section and species in Talaromyces. MycoKeys 68: 75-113. https://doi.org/10.3897/mycokeys.68.52092
Phylogeny of CaM for species classified in Talaromyces section Trachyspermi
Figure 10 from: SUN B-D, Chen AJ, Houbraken J, Frisvad JC, Wu W, Wei H, Zhou Y, Jiang X, Samson R (2020) New section and species in Talaromyces. MycoKeys 68: 75-113. https://doi.org/10.3897/mycokeys.68.52092
Figure 10 Talaromyces resedanus CBS 181.71Ta colonies from left to right (top row) CYA, MEA, YES and OA; (bottom row) CYA reverse, MEA reverse, DG 18 and CREAb–g conidiophores and conidia. Scale bars: 10 μm (b–g).
Figure 11 from: SUN B-D, Chen AJ, Houbraken J, Frisvad JC, Wu W, Wei H, Zhou Y, Jiang X, Samson R (2020) New section and species in Talaromyces. MycoKeys 68: 75-113. https://doi.org/10.3897/mycokeys.68.52092
Figure 11 Talaromyces rufus CBS 141834Ta colonies from left to right (top row) CYA, MEA, YES and OA; (bottom row) CYA reverse, MEA reverse, DG 18 and CREAb synnemata on MEA after 1 wk incubation c, d conidiophores and conidia e ascomata f, g ascospores. Scale bars: 200 μm (b), 10 μm (c, d, f), 50 μm (e), 2 μm (g).
Supplementary material 6 from: SUN B-D, Chen AJ, Houbraken J, Frisvad JC, Wu W, Wei H, Zhou Y, Jiang X, Samson R (2020) New section and species in Talaromyces. MycoKeys 68: 75-113. https://doi.org/10.3897/mycokeys.68.52092
Phylogeny of RPB2 for species classified in Talaromyces section Trachyspermi
Figure 8 from: SUN B-D, Chen AJ, Houbraken J, Frisvad JC, Wu W, Wei H, Zhou Y, Jiang X, Samson R (2020) New section and species in Talaromyces. MycoKeys 68: 75-113. https://doi.org/10.3897/mycokeys.68.52092
Figure 8 Talaromyces brevis CBS 141833Ta colonies from left to right (top row) CYA, MEA, YES and OA; (bottom row) CYA reverse, MEA reverse, DG 18 and CREAb–d conidiophores and conidia e ascomata on OA after two weeks f–g ascospores. Scale bars: 10 μm (b–d, f), 1000 μm (e), 2 μm (g).
Supplementary material 7 from: SUN B-D, Chen AJ, Houbraken J, Frisvad JC, Wu W, Wei H, Zhou Y, Jiang X, Samson R (2020) New section and species in Talaromyces. MycoKeys 68: 75-113. https://doi.org/10.3897/mycokeys.68.52092
Phylogeny of ITS for species classified in Talaromyces section Subinflati
Figure 3 from: SUN B-D, Chen AJ, Houbraken J, Frisvad JC, Wu W, Wei H, Zhou Y, Jiang X, Samson R (2020) New section and species in Talaromyces. MycoKeys 68: 75-113. https://doi.org/10.3897/mycokeys.68.52092
Figure 3 Phylogeny of BenA for species classified in Talaromyces section Trachyspermi. Branches with values more than 1 pp and 95% bs are thickened, supports lower than those values are indicated with a dash (-). Talaromyces purpurogenus (CBS 286.36T) was chosen as outgroup. T: ex-type.
Data from: Toward a precision behavioral medicine approach to addressing high-risk sun exposure: a qualitative analysis
Objectives: Precision behavioral medicine techniques integrating wearable ultraviolet radiation (UVR) sensors may help individuals avoid sun exposure that places them at-risk for skin cancer. As a preliminary step in our patient-centered process of developing a just-in-time adaptive intervention, this study evaluated reactions and preferences to UVR sensors among melanoma survivors. Materials and Methods: Early stage adult melanoma survivors were recruited for a focus group (n=11) or 10-day observational study, which included daily wearing a UVR sensor and sun exposure surveys (n=39). Both the focus group moderator guide and observational study exit interviews included questions on UVR sensing as a potential intervention strategy. These responses were transcribed and coded using an inductive strategy. Results: Most observational study participants (84.6%) said they would find information provided by UVR sensors to be useful to help them learn about how specific conditions (e.g., clouds, location) impact sun exposure and provide in-the-moment alerts. Focus group participants expressed enthusiasm for UVR information and identified preferred qualities of a UVR sensor, such as small size and integration with other devices. Participants in both studies indicated concern that UVR feedback may be difficult to interpret and some expressed that a UVR sensor may not be convenient or desirable to wear in daily life. Discussion: Melanoma survivors believe that personalized UVR exposure information could improve their sun protection and want this information delivered in a method that is meaningful and actionable. Conclusion: UVR sensing is a promising component of a precision behavioral medicine strategy to reduce skin cancer risk.
Figure 4 in Feeding ecology of the common sun skink, Eutropis multifasciata (Reptilia: Squamata: Scincidae), in the plains of central Vietnam
Figure 4. Dispersion diagrams from Pearson's correlations between (A) snout-vent length and mouth width (r = 0.775, P <0.001), (B) mouth width and body mass (r = 0.775, P <0.001) and (C) snout-vent length and body mass (r = 0.902, P <0.001), of male (open circles and broken lines) and female (filled circles and solid lines) Eutropis multifasciata in the plains of central Vietnam.
Figure 1 in Feeding ecology of the common sun skink, Eutropis multifasciata (Reptilia: Squamata: Scincidae), in the plains of central Vietnam
Figure 1. Map of Thua Thien-Hue Province in central Vietnam showing the three localities – (1) Quang Dien; (2) Huong Tra; (3) Xuan Phu – where the stomach contents of Eutropis multifasciata skinks were collected for this study.
Figure 3 in Feeding ecology of the common sun skink, Eutropis multifasciata (Reptilia: Squamata: Scincidae), in the plains of central Vietnam
Figure 3. Percent volumes of major food items (mean ± standard error, SE) in the diet of Eutropis multifasciata from the plains of central Vietnam. Ort = Orthoptera; Lar = insect larvae; Ara = Araneae; Ach = Achatinidae; Plant = plant materials. Different letters above the two lizard groups for the same food item indicate a significant difference (P <0.05) in proportional volumes. The remaining prey categories in Table 2 were excluded from this analysis due to low frequencies of occurrence (i.e. %F <5%).
Figure 4 from: Sun J, Zhang D-G, Huang X-H, Tojibaev K, Yang J-Y, Wang H-C, Deng T (2020) Primula sunhangii (Primulaceae): a new species from Hubei, Central China. PhytoKeys 156: 103-112. https://doi.org/10.3897/phytokeys.156.49137
Figure 4 Bayesian tree of selected species in Primula, focused on Sect. Aleuritia. Based on a combined sequences from nuclear ITS and rbcL, matK of cpDNA genes. Numbers above the branches represent the Bayesian posterior probabilities, and below showing the maximum likelihood values. (* multifurcation in Maximum-likelihood tree).
Figure 2 from: Sun J, Zhang D-G, Huang X-H, Tojibaev K, Yang J-Y, Wang H-C, Deng T (2020) Primula sunhangii (Primulaceae): a new species from Hubei, Central China. PhytoKeys 156: 103-112. https://doi.org/10.3897/phytokeys.156.49137
Figure 2 Images of live Primula sunhangii T. Deng, D. G. Zhang & Jiao Sun, sp. nov. A habitat B inflorescence C leaves D flower, front and back side E toot. Scale bars: 1 cm in (C, D, E). Photographer: Qun Liu.
Supplementary material 1 from: Sun J, Zhang D-G, Huang X-H, Tojibaev K, Yang J-Y, Wang H-C, Deng T (2020) Primula sunhangii (Primulaceae): a new species from Hubei, Central China. PhytoKeys 156: 103-112. https://doi.org/10.3897/phytokeys.156.49137
Taxa, specimen collection information, GenBank accession numbers of all studied samples
Figure 5 from: Yang L-H, Wen F, Kong H-H, Sun Z-X, Su L-Y, Kang M (2020) Two new combinations in Oreocharis (Gesneriaceae) based on morphological, molecular and cytological evidence. In: Shui Y-M, Chen W-H, Ren M-X, Wen F, Hong X, Qiu Z-J, Wei Y-G, Kang M (Eds) Taxonomy of Gesneriaceae in China and Vietnam. PhytoKeys 157: 43-58. https://doi.org/10.3897/phytokeys.157.32609
Figure 5 Geographical distribution of Oreocharis guileana (green dot), O. baolianis (red triangle) and O. pilosopetiolata (blue square).
Figure 3 from: Yang L-H, Wen F, Kong H-H, Sun Z-X, Su L-Y, Kang M (2020) Two new combinations in Oreocharis (Gesneriaceae) based on morphological, molecular and cytological evidence. In: Shui Y-M, Chen W-H, Ren M-X, Wen F, Hong X, Qiu Z-J, Wei Y-G, Kang M (Eds) Taxonomy of Gesneriaceae in China and Vietnam. PhytoKeys 157: 43-58. https://doi.org/10.3897/phytokeys.157.32609
Figure 3 Bayesian (> 50%) tree resulting of the combined nuclear (ITS) and plastid (trnL-F) data matrices. Posterior probability (PP) from the BI analysis are indicated above branches and Bootstrap value (BS) from the ML analysis are indicated below. The asterisk indicates a BS < 50. The dash indicates the topological discordance between ML and Bayesian tree. The two species, O. baolianis and O. guileana, are highlighted in bold.
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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.
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.