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Fig. 3 in Seasonal and longitudinal variation in fish assemblage structure along an unregulated stretch of the Middle Uruguay River
Fig. 3. Variation (mean ±standard deviation) in species richness and biomass (CPUEb/100m2) of migratory fishes along the river channel (A and C) and among seasons (B and D), in the Middle Uruguay River. Sites: S1 = upstream; S6 = downstream. Different letters indicate statistical difference (p <0.05).
Fig. 6 in Seasonal and longitudinal variation in fish assemblage structure along an unregulated stretch of the Middle Uruguay River
Fig. 6. Canonical Correspondence Analysis (CCA) applied to investigate the association between fish assemblage structure and environmental variables (spatial, geomorphology and landscape) along the Middle Uruguay River (A), and the influence of species on the ordination (B). Seasons: Au= Autumn; Sp = Spring; Su= Summer and Wi= Winter. Migratory species are marked in bold.
Supplementary material for: Lala, J., Tilahun, S., and Block, P. (2020). Predicting rainy season onset in the Ethiopian Highlands for agricultural planning. Journal of Hydrometeorology.
<p>Supplementary material for: Lala, J., Tilahun, S., and Block, P. (2020). Predicting rainy season onset in the Ethiopian Highlands for agricultural planning. Journal of Hydrometeorology. This includes onsets and cessations for northwestern Ethiopia, climate signals, and MATLAB scripts for calculating hindcasts</p>
Figure 30 in Dasymutilla Ashmead (Hymenoptera, Mutillidae) in Panama: new species, sex associations and seasonal flight activity
Figure 30. Total Dasymutilla specimens captured by month in six years (2001 to 2006) with ten Malaise traps in BCI.
Figures 23–28. Dasymutilla, right forewing. 23 in Dasymutilla Ashmead (Hymenoptera, Mutillidae) in Panama: new species, sex associations and seasonal flight activity
Figures 23–28. Dasymutilla, right forewing. 23) D. araneoides. 24) D. colorado, sp. nov. 25) D. paradoxa. 26) D. phya. 27) D. pulchra. 28) D. spilota.
Figures 17–22 in Dasymutilla Ashmead (Hymenoptera, Mutillidae) in Panama: new species, sex associations and seasonal flight activity
Figures 17–22. Dasymutilla colorado, sp. nov. 17–19) Female photographs. 20–21) Male photographs. 22) Male genitalia illustrations. a) Dorsal view. b) Ventral view. c) Penis valve lateral view. d) Lateral view.
Figure 1 in Dasymutilla Ashmead (Hymenoptera, Mutillidae) in Panama: new species, sex associations and seasonal flight activity
Figure 1. Location of Malaise traps (red spots) on Barro Colorado Island [Modified from Foster and Brokaw 1990].
DATA of 'Quantification of seasonal and diurnal dynamics of subglacial channels using seismic observations on an Alpine Glacier.' from Nanni et al. 2020,
<p>This dataset belongs to the study of <strong>Nanni et al., 2020</strong> "Quantification of seasonal and diurnal dynamics of subglacial channels using seismic observations on an Alpine Glacier." accepted for publication in The Cryosphere on March 9th 2020.</p> <p>You can find additional information on the "<strong>README_data_NANNI_2020_glacier</strong>"</p>
Supplementary material 10 from: Augustinus BA, Lommen STE, Fogliatto S, Vidotto F, Smith T, Horvath D, Bonini M, Gentili RF, Citterio S, Müller-Schärer H, Schaffner U (2020) In-season leaf damage by a biocontrol agent explains reproductive output of an invasive plant species. NeoBiota 55: 117-146. https://doi.org/10.3897/neobiota.55.46874
Number of seeds
Supplementary material 9 from: Augustinus BA, Lommen STE, Fogliatto S, Vidotto F, Smith T, Horvath D, Bonini M, Gentili RF, Citterio S, Müller-Schärer H, Schaffner U (2020) In-season leaf damage by a biocontrol agent explains reproductive output of an invasive plant species. NeoBiota 55: 117-146. https://doi.org/10.3897/neobiota.55.46874
Successful seed formation
Supplementary material 3 from: Augustinus BA, Lommen STE, Fogliatto S, Vidotto F, Smith T, Horvath D, Bonini M, Gentili RF, Citterio S, Müller-Schärer H, Schaffner U (2020) In-season leaf damage by a biocontrol agent explains reproductive output of an invasive plant species. NeoBiota 55: 117-146. https://doi.org/10.3897/neobiota.55.46874
p-values for O. communa
Supplementary material 7 from: Augustinus BA, Lommen STE, Fogliatto S, Vidotto F, Smith T, Horvath D, Bonini M, Gentili RF, Citterio S, Müller-Schärer H, Schaffner U (2020) In-season leaf damage by a biocontrol agent explains reproductive output of an invasive plant species. NeoBiota 55: 117-146. https://doi.org/10.3897/neobiota.55.46874
Raceme length
Supplementary material 8 from: Augustinus BA, Lommen STE, Fogliatto S, Vidotto F, Smith T, Horvath D, Bonini M, Gentili RF, Citterio S, Müller-Schärer H, Schaffner U (2020) In-season leaf damage by a biocontrol agent explains reproductive output of an invasive plant species. NeoBiota 55: 117-146. https://doi.org/10.3897/neobiota.55.46874
Damage ~ abundance
Supplementary material 5 from: Augustinus BA, Lommen STE, Fogliatto S, Vidotto F, Smith T, Horvath D, Bonini M, Gentili RF, Citterio S, Müller-Schärer H, Schaffner U (2020) In-season leaf damage by a biocontrol agent explains reproductive output of an invasive plant species. NeoBiota 55: 117-146. https://doi.org/10.3897/neobiota.55.46874
Figure S2
Supplementary material 2 from: Augustinus BA, Lommen STE, Fogliatto S, Vidotto F, Smith T, Horvath D, Bonini M, Gentili RF, Citterio S, Müller-Schärer H, Schaffner U (2020) In-season leaf damage by a biocontrol agent explains reproductive output of an invasive plant species. NeoBiota 55: 117-146. https://doi.org/10.3897/neobiota.55.46874
Census dates
Supplementary material 1 from: Augustinus BA, Lommen STE, Fogliatto S, Vidotto F, Smith T, Horvath D, Bonini M, Gentili RF, Citterio S, Müller-Schärer H, Schaffner U (2020) In-season leaf damage by a biocontrol agent explains reproductive output of an invasive plant species. NeoBiota 55: 117-146. https://doi.org/10.3897/neobiota.55.46874
Study sites
Supplementary material 6 from: Augustinus BA, Lommen STE, Fogliatto S, Vidotto F, Smith T, Horvath D, Bonini M, Gentili RF, Citterio S, Müller-Schärer H, Schaffner U (2020) In-season leaf damage by a biocontrol agent explains reproductive output of an invasive plant species. NeoBiota 55: 117-146. https://doi.org/10.3897/neobiota.55.46874
Successful raceme formation
Figure 1-4 from: Younis EM, Al-Asgah NA, Abdel-Warith A-WA, Gabr MH, Shamlol FS (2020) Analysis of reproductive biology and spawning season of the pink ear emperor Lethrinus lentjan, from marine ecosystem. Zoologia 37: 1-10. https://doi.org/10.3897/zoologia.37.e48475
Figure 1-4 Photomicrographs of ovarian tissue explain the sex change of L. lentjan: (1)male reproductive cells in mature female ovaries; (2) the central cavity (remaining egg channel) inside the testicle; (3) torsion of the ovary wall to the inside to form the seminal canal; (4) brown masses (the porous layer of the remaining ovaries).
Patterns of annual and seasonal immune investment in a temporal reproductive opportunist
<p> Historically, investigations of how organismal investments in immunity fluctuate in response to environmental and physiological changes have focused on seasonally breeding organisms that confine reproduction to seasons with relatively unchallenging environmental conditions and abundant resources. The red crossbill, <i>Loxia curvirostra,</i> is<i> </i>a songbird that can breed opportunistically if conifer seeds are abundant, on both short, cold, and long, warm days, providing an ideal system to investigate environmental and reproductive effects on immunity. In this study, we measured inter- and intra-annual variation in complement, natural antibodies, PIT54, and leukocytes in crossbills across four summers (2010-2013) and multiple seasons within one year (summer 2011-spring 2012). Overall, we observed substantial changes in crossbill immune investment among summers, with interannual variation driven largely by food resources, while variation across multiple seasons within a single cone year was less pronounced and lacked a dominant predictor of immune investment. However, we found weak evidence that physiological processes (e.g., reproductive condition, moult) or abiotic factors (e.g., temperature, precipitation) affect immune investment. Collectively, this study suggests that a reproductively flexible organism may be able to invest in both reproduction and survival-related processes, potentially by exploiting rich patches with abundant resources. More broadly, these results emphasize the need for more longitudinal studies of trade-offs associated with immune investment.</p>
Supplementary material 5 from: Bieberich J, Feldhaar H, Lauerer M (2020) Micro-habitat and season dependent impact of the invasive Impatiens glandulifera on native vegetation. NeoBiota 57: 109-131. https://doi.org/10.3897/neobiota.57.51331
Table S2. Abbreviations of species names as shown in Figure 5
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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.