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554 results for “Wilson”
Supplementary material 3 from: Nelufule T, Robertson MP, Wilson JRU, Faulkner KT (2022) Native-alien populations—an apparent oxymoron that requires specific conservation attention. NeoBiota 74: 57-74. https://doi.org/10.3897/neobiota.74.81671
File S3
Supplementary material 2 from: Nelufule T, Robertson MP, Wilson JRU, Faulkner KT (2022) Native-alien populations—an apparent oxymoron that requires specific conservation attention. NeoBiota 74: 57-74. https://doi.org/10.3897/neobiota.74.81671
File S2
Supplementary material 1 from: Nelufule T, Robertson MP, Wilson JRU, Faulkner KT (2022) Native-alien populations—an apparent oxymoron that requires specific conservation attention. NeoBiota 74: 57-74. https://doi.org/10.3897/neobiota.74.81671
File S1
Supplementary material 1 from: Wilson CR, Cooke-McEwen C, Gilligan TM, Tembrock LR (2022) Detection of Centistes sp. (Hymenoptera, Braconidae) from intercepted Diabrotica undecimpunctata (Coleoptera, Chrysomelidae) using CO1 DNA barcodes and larval morphology. Journal of Hymenoptera Research 91: 69-81. https://doi.org/10.3897/jhr.91.84139
DNA alignments and figures
Supplementary material 1 from: Jacobs LEO, Richardson DM, Lepschi BJ, Wilson JRU (2017) Quantifying errors and omissions in alien species lists: The introduction status of Melaleuca species in South Africa as a case study. NeoBiota 32: 89-105. https://doi.org/10.3897/neobiota.32.9842
Appendix and Supplementary Figures : Explanation note:
Supplementary material 1 from: Novoa A, Kumschick S, Richardson DM, Rouget M, Wilson JRU (2016) Native range size and growth form in Cactaceae predict invasiveness and impact. In: Daehler CC, van Kleunen M, Pyšek P, Richardson DM (Eds) Proceedings of 13th International EMAPi conference, Waikoloa, Hawaii. NeoBiota 30: 75–90. https://doi.org/10.3897/neobiota.30.7253
Selected species and traits : Explanation note: NA = No information available.
Supplementary material 2 from: Novoa A, Kumschick S, Richardson DM, Rouget M, Wilson JRU (2016) Native range size and growth form in Cactaceae predict invasiveness and impact. In: Daehler CC, van Kleunen M, Pyšek P, Richardson DM (Eds) Proceedings of 13th International EMAPi conference, Waikoloa, Hawaii. NeoBiota 30: 75–90. https://doi.org/10.3897/neobiota.30.7253
List of the sources of information used for the impact scoring according to GISS :
Supplementary material 1 from: Williamson TE, Brusatte SL, Wilson GP (2014) The origin and early evolution of metatherian mammals: the Cretaceous record. ZooKeys 465: 1-76. https://doi.org/10.3897/zookeys.465.8178
List of taxa and characters used in phylogenetic analysis.:
Supplementary material 2 from: Williamson TE, Brusatte SL, Wilson GP (2014) The origin and early evolution of metatherian mammals: the Cretaceous record. ZooKeys 465: 1-76. https://doi.org/10.3897/zookeys.465.8178
Taxon-Character Matrix with characters ordered (TNT file).:
Figure 9 from: Back J, Lee W (2017) Two new species of the genus Emertonia Wilson, 1932 from Korean waters (Copepoda, Harpacticoida, Paramesochridae). ZooKeys 718: 35-64. https://doi.org/10.3897/zookeys.718.19959
Figure 9 - Emertonia simplex sp. n., (♀). A last two segments of urosomite and caudal rami B P5 C P6 and genital field. Scale bars are in µm.
Figure 5 from: Back J, Lee W (2017) Two new species of the genus Emertonia Wilson, 1932 from Korean waters (Copepoda, Harpacticoida, Paramesochridae). ZooKeys 718: 35-64. https://doi.org/10.3897/zookeys.718.19959
Figure 5 - Emertonia koreana sp. n., SEM photographs. A caudal rami, ventral (♀) B P5 (♀) C P6 (♀) D sixth and seventh somites, ventral (♂) E P1 (♂) F P2 and P3 (♂) G P5 (♂) H P6 (♂).
Figure 6 from: Back J, Lee W (2017) Two new species of the genus Emertonia Wilson, 1932 from Korean waters (Copepoda, Harpacticoida, Paramesochridae). ZooKeys 718: 35-64. https://doi.org/10.3897/zookeys.718.19959
Figure 6 - Emertonia simplex sp. n., (♀) A habitus, dorsal B habitus, lateral C antennule (C1 fifth, sixth, and seventh segments C2 last segment). Scale bars are in µm.
Figure 10 from: Back J, Lee W (2017) Two new species of the genus Emertonia Wilson, 1932 from Korean waters (Copepoda, Harpacticoida, Paramesochridae). ZooKeys 718: 35-64. https://doi.org/10.3897/zookeys.718.19959
Figure 10 - Emertonia simplex sp. n., (♂). A habitus, dorsal B antennule (B1 last two segments B2 fifth segment) C P5 D P6. Scale bars are in µm.
Figure 1 from: Back J, Lee W (2017) Two new species of the genus Emertonia Wilson, 1932 from Korean waters (Copepoda, Harpacticoida, Paramesochridae). ZooKeys 718: 35-64. https://doi.org/10.3897/zookeys.718.19959
Figure 1 - Emertonia koreana sp. n., holotype (♀). A habitus, dorsal B habitus lateral C urosome, ventral D caudal rami, dorsal E caudal seta IV and V. Scale bars are in µm.
Figure 4 from: Back J, Lee W (2017) Two new species of the genus Emertonia Wilson, 1932 from Korean waters (Copepoda, Harpacticoida, Paramesochridae). ZooKeys 718: 35-64. https://doi.org/10.3897/zookeys.718.19959
Figure 4 - Emertonia koreana sp. n., (♂). A habitus, dorsal B antennule (B1 fifth segment B2 last segment) C P5 D P6. Scale bars are in µm.
Figure 7 from: Back J, Lee W (2017) Two new species of the genus Emertonia Wilson, 1932 from Korean waters (Copepoda, Harpacticoida, Paramesochridae). ZooKeys 718: 35-64. https://doi.org/10.3897/zookeys.718.19959
Figure 7 - Emertonia simplex sp. n., (♀). A antenna (A1 end of second segment in antenna endopod) B mandible (B1 palp) C maxillule D maxilla (D1 first endite D2 second endite D3 first segment of endopod D4 second segment of endopod) E maxilliped. Scale bar is in µm.
Figure 11 from: Back J, Lee W (2017) Two new species of the genus Emertonia Wilson, 1932 from Korean waters (Copepoda, Harpacticoida, Paramesochridae). ZooKeys 718: 35-64. https://doi.org/10.3897/zookeys.718.19959
Figure 11 - Emertonia simplex sp. n. (♀), SEM photographs. A habitus, lateral B first and second segment, lateral C P1 D P3 C P3 E P5 F caudal rami, lateral.
Figure 2 from: Back J, Lee W (2017) Two new species of the genus Emertonia Wilson, 1932 from Korean waters (Copepoda, Harpacticoida, Paramesochridae). ZooKeys 718: 35-64. https://doi.org/10.3897/zookeys.718.19959
Figure 2 - Emertonia koreana sp. n., holotype (♀). A antennule (A1 fourth segment A2 fifth, sixth, and seventh segments A3 last segment) B antenna C mandible (C1 plap) D maxillule E maxilla F maxilliped. Scale bar is in µm
WOLO: Wilson Only Looks Once – 3D scanned insects
<h1>WOLO: Wilson Only Looks Once – Estimating ant body mass from reference-free images using deep convolutional neural networks</h1> <h2>Abstract</h2> <p>Size estimation is a hard computer vision problem with widespread applications in quality control in manufacturing and processing plants, livestock management, and studies on animal behaviour. Typically, image-based size estimation is facilitated by either well-controlled imaging conditions, the provision of global cues, or both. Reference-free size estimation is challenging, because objects of vastly different sizes can appear identical if they are of similar shape. Here, we attempt to implement automated and reference-free body size estimation to facilitate large-scale experimental work in a key model species in sociobiology: the leaf-cutter ants. Leaf-cutter ants are a suitable testbed for reference-free size-estimation, because their workers differ vastly in both size and shape; in principle, it is therefore possible to infer body mass, a proxy for size, from relative body proportions alone. Inspired by earlier work by E.O. Wilson, who trained himself to discern ant worker size from visual cues alone, we used various deep learning techniques to achieve the same feat automatically, quickly, and at scale from a single reference image: <strong>Wilson Only Looks Once</strong> (<strong>WOLO</strong>). Utilizing over 3 million hand-annotated and computer-generated images, a set of deep neural networks---including regressors, classifiers, and detectors---were trained to estimate the body mass of ants from image cut-outs. The WOLO networks approximately matched human performance, measured for a small group of both experts and non-experts, but were about 1000 times faster. Further refinement may enable accurate, high-throughput, and non-intrusive body mass estimation at scale, and so eventually contribute to a more nuanced and comprehensive understanding of the complex division of labour that characterises polymorphic insect societies.</p> <h2>3D Models</h2> <p>This repository contains the 20 3D scanned, retopologised, colour-corrected, and rigged models used to generate all data used in the original study. Refer to the manuscript for model generation and dataset generation details.</p> <p>As the full-frame datasets are too large to host online permanently, please get in touch with the lead author (Fabian Plum) if you require access. </p>
Figure 7 from: Paton AJ, Mwanyambo M, Govaerts RHA, Smitha K, Suddee S, Phillipson PB, Wilson TC, Forster PI, Culham A (2019) Nomenclatural changes in Coleus and Plectranthus (Lamiaceae): a tale of more than two genera. PhytoKeys 129: 1-158. https://doi.org/10.3897/phytokeys.129.34988
Figure 7 Species of Equilabium 2. AEquilabium laxiflorum (Photo: Bart Wursten) BE. petiolare (Photo: Neil Crouch) CE. subincisum (Photo: K. Smitha) DE. stenophyllum (Photo: Bart Wursten).
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