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485 results for “Cooking”
Figures 22-29 from: Martoni F, Brown SDJ (2018) An annotated checklist of the Cook Islands psyllids with keys to the species and two new records (Hemiptera, Psylloidea). ZooKeys 811: 91-108. https://doi.org/10.3897/zookeys.811.28829
Figures 22-29 Wings, schematic. 22Leptynopterasulfurea (after Crawford 1919) 23Syntomozatahuata (from slide-mounted Rarotonga specimen) 24Triozacf.zimmermani (from photograph of Rarotonga specimen by G. McCormack) 25Heteropsyllacubana (after Tuthill 1959) 26Triozaalifumosa (from slide-mounted Rarotonga specimen) 27Triozazimmermani (after Tuthill 1942) 28Mesohomotomahibisci (after Froggatt 1901) 29Triozavitiensis (after Klyver 1932). Scale bar: 1 mm.
Figures 1-10 from: Martoni F, Brown SDJ (2018) An annotated checklist of the Cook Islands psyllids with keys to the species and two new records (Hemiptera, Psylloidea). ZooKeys 811: 91-108. https://doi.org/10.3897/zookeys.811.28829
Figures 1-10 Syntomozatahuata. 1 lateral habitus of female 2 lateral habitus of male 3 dorsal habitus of female 4 dorsal habitus of male 5 head of female, dorsal view 6 head of male, dorsal view 7 wing of male 8 mesotibia of male 9 terminalia of female, lateral view of left side 10 terminalia of male, lateral view of left side. Abbreviation: par = paramere. Scale bars: 1 mm (1–7); 0.5 mm (8); 0.25 mm (9, 10).
Supplementary material 1 from: González-Moreno P, Lazzaro L, Vilà M, Preda C, Adriaens T, Bacher S, Brundu G, Copp GH, Essl F, García-Berthou E, Katsanevakis S, Moen TL, Lucy FE, Nentwig W, Roy HE, Srėbalienė G, Talgø V, Vanderhoeven S, Andjelković A, Arbačiauskas K, Auger-Rozenberg M-A, Bae M-J, Bariche M, Boets P, Boieiro M, Borges PA, Canning-Clode J, Cardigos F, Chartosia N, Cottier-Cook EJ, Crocetta F, D'hondt B, Foggi B, Follak S, Gallardo B, Gammelmo Ø, Giakoumi S, Giuliani C, Fried G, Jelaska LS, Jeschke JM, Jover M, Juárez-Escario A, Kalogirou S, Kočić A, Kytinou E, Laverty C, Lozano V, Maceda-Veiga A, Marchante E, Marchante H, Martinou AF, Meyer S, Michin D, Montero-Castaño A, Morais MC, Morales-Rodriguez C, Muhthassim N, Nagy ZA, Ogris N, Onen H, Pergl J, Puntila R, Rabitsch W, Ramburn TT, Rego C, Reichenbach F, Romeralo C, Saul W-C, Schrader G, Sheehan R, Simonović P, Skolka M, Soares AO, Sundheim L, Tarkan AS, Tomov R, Tricarico E, Tsiamis K, Uludağ A, van Valkenburg J, Verreycken H, Vettraino AM, Vilar L, Wiig Ø, Witzell J, Zanetta A, Kenis M (2019) Consistency of impact assessment protocols for non-native species. NeoBiota 44: 1-25. https://doi.org/10.3897/neobiota.44.31650
: Data type: statistical data
Supplementary material 2 from: González-Moreno P, Lazzaro L, Vilà M, Preda C, Adriaens T, Bacher S, Brundu G, Copp GH, Essl F, García-Berthou E, Katsanevakis S, Moen TL, Lucy FE, Nentwig W, Roy HE, Srėbalienė G, Talgø V, Vanderhoeven S, Andjelković A, Arbačiauskas K, Auger-Rozenberg M-A, Bae M-J, Bariche M, Boets P, Boieiro M, Borges PA, Canning-Clode J, Cardigos F, Chartosia N, Cottier-Cook EJ, Crocetta F, D'hondt B, Foggi B, Follak S, Gallardo B, Gammelmo Ø, Giakoumi S, Giuliani C, Fried G, Jelaska LS, Jeschke JM, Jover M, Juárez-Escario A, Kalogirou S, Kočić A, Kytinou E, Laverty C, Lozano V, Maceda-Veiga A, Marchante E, Marchante H, Martinou AF, Meyer S, Michin D, Montero-Castaño A, Morais MC, Morales-Rodriguez C, Muhthassim N, Nagy ZA, Ogris N, Onen H, Pergl J, Puntila R, Rabitsch W, Ramburn TT, Rego C, Reichenbach F, Romeralo C, Saul W-C, Schrader G, Sheehan R, Simonović P, Skolka M, Soares AO, Sundheim L, Tarkan AS, Tomov R, Tricarico E, Tsiamis K, Uludağ A, van Valkenburg J, Verreycken H, Vettraino AM, Vilar L, Wiig Ø, Witzell J, Zanetta A, Kenis M (2019) Consistency of impact assessment protocols for non-native species. NeoBiota 44: 1-25. https://doi.org/10.3897/neobiota.44.31650
: Data type: Spreadsheet template
FIGURE 3 in Phytoseiid mites (Acari: Phytoseiidae) of the Cook Islands
FIGURE 3. Knopkirie flascus sp. nov. (female). A. leg I; B. leg II; C. leg III; D. leg IV.
FIGURE 5 in Phytoseiid mites (Acari: Phytoseiidae) of the Cook Islands
FIGURE 5. Kuzinellus rarotonga sp. nov. (female). A. leg I; B. leg II; C. leg III; D. leg IV.
FIGURE 1 in A new species of Proterhinus Sharp, 1878 (Coleoptera: Curculionoidea: Belidae) from Miti'aro, Cook Islands, South Pacific
FIGURE 1. Distribution of known Proterhinus species
Figures 3-6 from: Sublett CA, Cook JL, Janovec JP (2019) Species richness and community composition of sphingid moths (Lepidoptera: Sphingidae) along an elevational gradient in southeastern Peru. Zoologia 36: 1-11. https://doi.org/10.3897/zoologia.36.e32938
Figures 3-6 Regression analysis across the entire gradient for average temperature with (3) estimated species richness, (4) Fisher's alpha, and regression analysis at the three highest elevations for average temperature with (5) estimated species richness, and (6) Fisher's alpha. (3) r2 = 0.5518, p = 0.150; (4) r2 = 0.7264, p = 0.067; (5) r2 = 0.9391, p = 0.159; (6) r2 = 0.7364, p = 0.343.
Figures 8-9 from: Sublett CA, Cook JL, Janovec JP (2019) Species richness and community composition of sphingid moths (Lepidoptera: Sphingidae) along an elevational gradient in southeastern Peru. Zoologia 36: 1-11. https://doi.org/10.3897/zoologia.36.e32938
Figures 8-9 Contribution of sphingid subfamilies to (8) species richness and (9) total abundance. Blue bars = Macroglossinae; orange bars = Sphinginae; grey bars = Smerinthinae. Contributions of each subfamily are similar among sites, and contributions of any particular subfamily to richness and abundance are similar within a site.
Figure 7 from: Sublett CA, Cook JL, Janovec JP (2019) Species richness and community composition of sphingid moths (Lepidoptera: Sphingidae) along an elevational gradient in southeastern Peru. Zoologia 36: 1-11. https://doi.org/10.3897/zoologia.36.e32938
Figure 7 Breakpoint regression analysis for (log)elevation with estimated species richness. Vitobamba (800 m), which was the break point, is included in both graphs. The characteristic mid-elevation unimodal richness pattern can be seen with the increase in species richness with elevation up to Vitobamba (r2 = 0.953, p = 0.139), and the decrease in species richness with elevation above Vitobamba (r2 = 0.999, p = 0.003).
Figure 2 from: Sublett CA, Cook JL, Janovec JP (2019) Species richness and community composition of sphingid moths (Lepidoptera: Sphingidae) along an elevational gradient in southeastern Peru. Zoologia 36: 1-11. https://doi.org/10.3897/zoologia.36.e32938
Figure 2 The relationship between elevation and species richness. There is a clear low-elevation skewed unimodal pattern, which peaks around 800 m.
Fig. 4 in Revision of the genus Attemsostreptus Verhoeff, 1941 with description of a new species from Tanzania and notes on the tribe Trachystreptini Cook, 1896 (Spirostreptida, Diplopoda)
Fig. 4. Attemsostreptus reflexus sp. nov., male holotype (NHMD607065), gonopods. A. Gonopods, anterior view. B. Right gonopod, antero-apical view. C. Telopodite. D. Tip of telopodite. For abbreviations, see Material and methods. Scale bars: A = 1 mm; B–D = 0.5 mm.
Fig. 2 in Revision of the genus Attemsostreptus Verhoeff, 1941 with description of a new species from Tanzania and notes on the tribe Trachystreptini Cook, 1896 (Spirostreptida, Diplopoda)
Fig. 2. Attemsostreptus reflexus sp. nov., male holotype (NHMD607065), head and anteriormost body rings. A. Ventral view. B. Lateral view. Scale bar: 1 mm.
Figure 1. Hygrobates angelieri Cook, 1966 in First description of the male of Hygrobates angelieri Cook, 1966 from Ghana (Acariformes, Hydrachnidia, Hygrobatidae)
Figure 1. Hygrobates angelieri Cook, 1966, ♂, stream Asukuma, Ghana: A – coxal and genital field, partial view; B – I-L-5 and -6; C – palp. Scale bars = 100 µm.
Linked collectors and determiners for: A new species of Lepidium (Brassicaceae) in the Cook Islands.
Natural history specimen data linked to collectors and determiners held within, "A new species of Lepidium (Brassicaceae) in the Cook Islands". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/e4a5a574-cfa4-4824-bf4f-b8b563ac0e7d">https://bionomia.net/dataset/e4a5a574-cfa4-4824-bf4f-b8b563ac0e7d</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/e4a5a574-cfa4-4824-bf4f-b8b563ac0e7d">https://gbif.org/dataset/e4a5a574-cfa4-4824-bf4f-b8b563ac0e7d</a>. Formatted as a Frictionless Data package.
FIGURE 1 in A new species of Lepidium (Brassicaceae) in the Cook Islands
FIGURE 1. Lepidium makateanum, habitat. Photo: Ewen Cameron.
Supplementary material 2 from: Ballesteros-Mejia L, Angulo E, Diagne C, Cooke B, Nuñez MA, Courchamp F (2021) Economic costs of biological invasions in Ecuador: the importance of the Galapagos Islands. In: Zenni RD, McDermott S, García-Berthou E, Essl F (Eds) The economic costs of biological invasions around the world. NeoBiota 67: 375-400. https://doi.org/10.3897/neobiota.67.59116
Tables S2–S5
Supplementary material 1 from: Ballesteros-Mejia L, Angulo E, Diagne C, Cooke B, Nuñez MA, Courchamp F (2021) Economic costs of biological invasions in Ecuador: the importance of the Galapagos Islands. In: Zenni RD, McDermott S, García-Berthou E, Essl F (Eds) The economic costs of biological invasions around the world. NeoBiota 67: 375-400. https://doi.org/10.3897/neobiota.67.59116
Database of Economic costs of biological invasions in Ecuador
Figure 3 from: Crocetta F, Macali A, Furfaro G, Cooke S, Villani G, Valdes A (2013) Alien molluscan species established along the Italian shores: an update, with discussions on some Mediterranean "alien species" categories. ZooKeys 277: 91-108. https://doi.org/10.3897/zookeys.277.4362
Figure 3 - The rate of reporting (as number of species per decade) of alien molluscan species from the Italian territorial seawaters.
Figure 2 from: Crocetta F, Macali A, Furfaro G, Cooke S, Villani G, Valdes A (2013) Alien molluscan species established along the Italian shores: an update, with discussions on some Mediterranean "alien species" categories. ZooKeys 277: 91-108. https://doi.org/10.3897/zookeys.277.4362
Figure 2 - A. Haplotype network of non-native haplotypes of Haminoea japonica Pilsbry, 1895 (haplotype IDs from Hanson et al. 2013). Rectangular haplotype (H20) is most ancestral. Sizes of the haplotype icons are proportional to the total number of individuals sequenced (data from Hanson et al. 2013 and present paper). B. Known European records of Haminoea japonica, including new collection localities. Sizes of the pie charts are proportional to the number of individuals sequenced from the locality. Pie charts and patterns within indicate the proportion of different haplotypes found in each locality.
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