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3,688 results for “Milling”
We are what we eat, plus some per mill: Using stable isotopes to estimate diet composition in Gyps vultures over space and time
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Data from: Shelf life and quality of tomato (Lycopersicon esculentum Mill.) fruits as affected by neem leaf extract dipping and beeswax coating
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Data from: Analysis of microsatellite loci in tree of heaven (Ailanthus altissima (Mill.) Swingle) using SSR-GBS
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Data from: Population clustering and clonal structure evidence the relict state of Ulmus minor Mill. in the Balearic Islands
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Data from: ‘Fix me another marguerite!’: species delimitation in a group of intensively hybridising lineages of ox-eye daisies (Leucanthemum Mill., Compositae-Anthemideae)
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Data from: High-density genetic map construction and QTL mapping of leaf and needling traits in Ziziphus jujuba Mill.
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Data from: Comparative leaf anatomy of wild Manihot Mill. species (Euphorbiaceae) from Chapada Diamantina, Bahia, Brazil
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Data from: Adaptation to local climate in a multi-trait space: evidence from silver fir (Abies alba Mill.) populations across a heterogeneous environment
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Data from: Postglacial recolonization history of the European crabapple (Malus sylvestris Mill.), a wild contributor to the domesticated apple
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Data from: Population bottlenecks have shaped the genetic variation of Ailanthus altissima (Mill.) Swingle in an area of early introduction
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Data from: Evidence of divergent selection for drought and cold tolerance at landscape and local scales in Abies alba Mill. in the French Mediterranean Alps
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FIG. 5. — A in Annotated checklist of Afrotropical Trogolaphysa Mills, 1938 (Hexapoda: Collembola: Paronellidae) and description of a new species from Madagascar
FIG. 5. — A, Trogolaphysa grassei (Delamare Debouteville, 1952) n. comb. hind claw form Delamare-Deboutteville (1952); B, T. ghesquierei (Marlier, 1945) n. comb. hind claw from Marlier (1945); C, T. fuelleborni n. comb. hind claw from Börner (1903); D, T. monomaculata, hind claw from Barra (1969); E, L. flava, hind claw from Carpenter (1916); F, T. monomaculata, mucro from Barra (1969); G, T. vivieni, mucro from Barra (1969); H, T. beguei (Delamare Debouteville, 1951) n. comb, hind claw complex, modified from Delamare Deboutteville (1951a); I, T. lamottei (Delamare Debouteville, 1950) n. comb. habitus, modified from Delamare Deboutteville (1950b); J, T. beguei n. comb. habitus, modified from Delamare Deboutteville (1951a).
Supplementary material 1 from: Cunha MR, Génio L, Pradillon F, Clavel Henry M, Beaulieu S, Birch J, Campuzano FJ, Carretón M, De Leo F, Gula J, Laming S, Lindsay D, Matos FL, Metaxas A, Meyer-Kaiser K, Mills S, Queiroga H, Rodrigues CF, Sarrazin J, Watanabe H, Young R, Young CM (2020) Foresight Workshop on Advances in Ocean Biological Observations: a sustained system for deep-ocean meroplankton. Research Ideas and Outcomes 6: e54284. https://doi.org/10.3897/rio.6.e54284
Abstracts of keynote talks
Figure 2 from: Cunha MR, Génio L, Pradillon F, Clavel Henry M, Beaulieu S, Birch J, Campuzano FJ, Carretón M, De Leo F, Gula J, Laming S, Lindsay D, Matos FL, Metaxas A, Meyer-Kaiser K, Mills S, Queiroga H, Rodrigues CF, Sarrazin J, Watanabe H, Young R, Young CM (2020) Foresight Workshop on Advances in Ocean Biological Observations: a sustained system for deep-ocean meroplankton. Research Ideas and Outcomes 6: e54284. https://doi.org/10.3897/rio.6.e54284
Figure 2 Sustained meroplankton observations - a basin-scale approach. Low-cost samplers for deep-ocean observations (colonization modules coupled with larval traps) deployed at moorings or mounted on landers of the EMSO-ERIC distributed observatories and covering different water masses (Project LO3CATED; Génio, Cunha and Young). NACW: North Atlantic Central Water; AIW: Antarctic Intermediate Water; MOW: Mediterranean Outflow Water; NADW: North Atlantic Deep Water; MABW: Modified Antarctic Bottom Water.
Figure 1 from: Cunha MR, Génio L, Pradillon F, Clavel Henry M, Beaulieu S, Birch J, Campuzano FJ, Carretón M, De Leo F, Gula J, Laming S, Lindsay D, Matos FL, Metaxas A, Meyer-Kaiser K, Mills S, Queiroga H, Rodrigues CF, Sarrazin J, Watanabe H, Young R, Young CM (2020) Foresight Workshop on Advances in Ocean Biological Observations: a sustained system for deep-ocean meroplankton. Research Ideas and Outcomes 6: e54284. https://doi.org/10.3897/rio.6.e54284
Figure 1 Workshop participants "under the microscope" at the campus of Universidade de Aveiro: Back row, left to right: Fábio Matos, Jonathan Gula, Henrique Queiroga, Rob Young, Sven Laming, Kirstin Meyer-Kaiser, Jozée Sarrazin, Craig M. Young, Fabio De Leo. Front row, left to right: Jim Birch, Morane Clavel Henry, Marina R. Cunha, Clara Rodrigues, Florence Pradillon, Anna Metaxas.
Figure 2 from: Mille C, Jourdan H, Cazères S, Maw E, Foottit R (2020) New data on the aphid (Hemiptera, Aphididae) fauna of New Caledonia: some new biosecurity threats in a biodiversity hotspot. ZooKeys 943: 53-89. https://doi.org/10.3897/zookeys.943.47785
Figure 2 Aphid interceptions in New Caledonia from 2008 to 2018 on fresh imported fruits and vegetables.
Data from: Conservation of the threatened species Pulsatilla vulgaris Mill. (pasqueflower) is aided by reproductive system and polyploidy
Population loss due to habitat disturbance is a major concern in biodiversity conservation. Here we investigate the genetic causes of the demographic decline observed in English populations of Pulsatilla vulgaris and the consequences for conservation. Using ten nuclear microsatellite markers, we compare genetic variation in wild populations with restored and seed-regenerated populations (674 samples). Emergence of genetic structure and loss of allelic variation in natural populations is not as evident as expected from demographic trends. Restored populations show genetic variation comparable to their source populations and, in general, to the wild ones. Genetic homogeneity is observed in regeneration trials, although some alleles not captured in source populations are detected. We infer that polyploidy, longevity and clonal reproduction have provided P. vulgaris with the standing genetic variation necessary to make the species resilient to the effects of demographic decline, suggesting that the use of multiple sources for reintroduction may be beneficial to mimic natural gene flow and the availability of multiple allele copies typical of polyploid species.
Fig. 1 in Beetle Interactions with Poison Ivy and Poison Oak (Toxicodendron P. Mill. sect. Toxicodendron, Anacardiaceae)
Fig. 1. Chauliognathus pennsylvanicus DeGeer.
Fig. 2 in Nine geranylgeranylated derivatives isolated from the roots of Rhus chinensis Mill.
Fig. 2. Key HMBC correlations of compounds 1–7.
FIGURE 1 in Survey of Trogolaphysa Mills (Collembola, Paronellidae) of the Brazilian Amazon including five new species and the description of the dorsal chaetotaxy of the first instar
FIGURE 1. Symbols used in the chaetotaxy descriptions of Trogolaphysa species.
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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.
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