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83 results for “Cooks 1”

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zenodo28/100

Figure 1 from: Watts C, Thornburrow D, Stringer I, Cave V (2017) Population expansion by Cook Strait giant wētā, Deinacrida rugosa (Orthoptera: Anostostomatidae), following translocation to Matiu/Somes Island, New Zealand, and subsequent changes in abundance. Journal of Orthoptera Research 26: 171-180. https://doi.org/10.3897/jor.26.21712

Figure 1 - Arrangement of tracking tunnel transects (shown in white) along the footpaths on Matiu-Somes Island. Each circle indicates the location of a tracking tunnel. The dark hatched area indicates where Deinacrida rugosa were released in 1996. The light hatched area shows where 186 adult D. rugosa were taken for translocation in 2007 and 2008. Note that no wētā were removed from the North transect.

opencc-by-4.0Dec 2017View details →
zenodo28/100

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).

opencc-by-4.0Jan 2019View details →
zenodo28/100

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

opencc-zeroApr 2019View details →
zenodo28/100

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

opencc-zeroApr 2019View details →
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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

opennotspecifiedSep 2019View details →
zenodo28/100

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.

opencc-by-4.0Sep 2019View details →
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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.

opencc-by-4.0Sep 2019View details →
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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).

opencc-by-4.0Sep 2019View details →
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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.

opencc-by-4.0Sep 2019View details →
zenodo28/100

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.

opencc-by-4.0Mar 2022View details →
zenodo28/100

FIGURE 1 in A new species of Lepidium (Brassicaceae) in the Cook Islands

FIGURE 1. Lepidium makateanum, habitat. Photo: Ewen Cameron.

opennotspecifiedOct 2014View details →
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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

opencc-zeroAug 2021View details →
zenodo28/100

Figure 1 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 1 - A. Haminoea japonica Pilsbry, 1895 from Lago Fusaro, 17/02/2012, approx. 15 mm. Photo: Guido Villani. B. Anteaeolidiella foulisi (Angas, 1864) from Lago di Sabaudia, April 2009, 13 mm. Photo: Paolo Mariottini.

opencc-by-4.0Mar 2013View details →
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Figure 8 from: Morales-Núñez AG, Larsen K, Cooke WJ (2016) Oahutanais makalii, a new genus and species of colletteid tanaidacean (Crustacea, Peracarida) from shelf-waters off Hawaii, with a taxonomic key. Zoosystematics and Evolution 92(1): 1-12. https://doi.org/10.3897/zse.92.5581

Figure 8 - Oahutanais makalii gen. et sp. n., paratype female (SEM images): A ventral view of habitus; B enlargement of mid-anterior part of habitus, lateral view; C enlargement of union of cephalothorax and pereonite-1.

opencc-by-4.0Jan 2016View details →
zenodo28/100

Figure 6 from: Morales-Núñez AG, Larsen K, Cooke WJ (2016) Oahutanais makalii, a new genus and species of colletteid tanaidacean (Crustacea, Peracarida) from shelf-waters off Hawaii, with a taxonomic key. Zoosystematics and Evolution 92(1): 1-12. https://doi.org/10.3897/zse.92.5581

Figure 6 - Oahutanais makalii gen. et sp. n., paratype female (SEM images): A enlargement of anterior end showing part of the carapace, antennules, and carpus to dactylus of left cheliped, dorsal view; B enlargement of the cephalothorax and pereonites-1; C enlargement of anterior part showing how the carapace covers the antennules, antennas, mouthparts, and left cheliped, ventral view.

opencc-by-4.0Jan 2016View details →
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Figure 5 from: Morales-Núñez AG, Larsen K, Cooke WJ (2016) Oahutanais makalii, a new genus and species of colletteid tanaidacean (Crustacea, Peracarida) from shelf-waters off Hawaii, with a taxonomic key. Zoosystematics and Evolution 92(1): 1-12. https://doi.org/10.3897/zse.92.5581

Figure 5 - Oahutanais makalii gen. et sp. n., holotype female: A pereopod-1; B pereopod-2; C pereopod-3; D pereopod-4; E pereopod-5: F pereopod-6; G uropod; H pectinate seta. Scale bars: 0.1 mm.

opencc-by-4.0Jan 2016View details →
zenodo28/100

Figure 1 from: Morales-Núñez AG, Larsen K, Cooke WJ (2016) Oahutanais makalii, a new genus and species of colletteid tanaidacean (Crustacea, Peracarida) from shelf-waters off Hawaii, with a taxonomic key. Zoosystematics and Evolution 92(1): 1-12. https://doi.org/10.3897/zse.92.5581

Figure 1 - Map of study area, indicating the sampling stations where Oahutanais makalii gen. et sp. n., were found.

opencc-by-4.0Jan 2016View details →
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Figure 4 from: Morales-Núñez AG, Larsen K, Cooke WJ (2016) Oahutanais makalii, a new genus and species of colletteid tanaidacean (Crustacea, Peracarida) from shelf-waters off Hawaii, with a taxonomic key. Zoosystematics and Evolution 92(1): 1-12. https://doi.org/10.3897/zse.92.5581

Figure 4 - Oahutanais makalii gen. et sp. n., holotype female: A left cheliped, lateral view; B left chela, inner view. Scale bar: 0.1 mm.

opencc-by-4.0Jan 2016View details →
zenodo28/100

Figure 3 from: Morales-Núñez AG, Larsen K, Cooke WJ (2016) Oahutanais makalii, a new genus and species of colletteid tanaidacean (Crustacea, Peracarida) from shelf-waters off Hawaii, with a taxonomic key. Zoosystematics and Evolution 92(1): 1-12. https://doi.org/10.3897/zse.92.5581

Figure 3 - Oahutanais makalii gen. et sp. n., holotype female: A antennule, lateral view; B antenna, lateral view; C labrum; D left mandible; E right mandible; F labium; G maxillule; H maxilliped. Scale bars: 0.1 mm.

opencc-by-4.0Jan 2016View details →
zenodo28/100

Figure 7 from: Morales-Núñez AG, Larsen K, Cooke WJ (2016) Oahutanais makalii, a new genus and species of colletteid tanaidacean (Crustacea, Peracarida) from shelf-waters off Hawaii, with a taxonomic key. Zoosystematics and Evolution 92(1): 1-12. https://doi.org/10.3897/zse.92.5581

Figure 7 - Oahutanais makalii gen. et sp. n., paratype female (SEM images): A enlargement of mouthparts; B enlargement of posterior end showing pleonites 1 to 5, pleotelson, and uropods.

opencc-by-4.0Jan 2016View details →

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