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Fig. 11. A. Tranes monopticus Pascoe, 1870 in A review of Paratranes Zimmerman, 1994, Xanthorrhoea-associated weevils of the Tranes group (Coleoptera, Curculionidae, Molytinae), with description of a new species

Fig. 11. A. Tranes monopticus Pascoe, 1870, holotype (NHMUK). B. Tranes xanthorrhoeae Lea, 1898, lectotype (here designated) (SAMA). Scale bars = 5.0 mm.

Fig. 10 in A review of Paratranes Zimmerman, 1994, Xanthorrhoea-associated weevils of the Tranes group (Coleoptera, Curculionidae, Molytinae), with description of a new species

Fig. 10. Female genital structures of Paratranes Zimmerman, 1994. A. P. monopticus (Pascoe, 1870), ovipositor (Homebush, NSW). B. P. zimmermani sp. nov., ditto (Wembley, WA). C. P. monopticus, spermatheca with gland (Homebush, NSW). D. P. zimmermani sp. nov., ditto (Wembley, WA). Scale bars: A–B = 0.5 mm; C–D = 0.2 mm.

Fig. 1 in A review of Paratranes Zimmerman, 1994, Xanthorrhoea-associated weevils of the Tranes group (Coleoptera, Curculionidae, Molytinae), with description of a new species

Fig. 1. Diagnostic external characters of Paratranes Zimmerman, 1994. A. Elytral surface and setae. B. Eyes and prothorax, ventral view. C. Head and base of rostrum, dorsal view. D. Pronotal surface. Scale bars = 1.0 mm.

Fig. 7 in A review of Paratranes Zimmerman, 1994, Xanthorrhoea-associated weevils of the Tranes group (Coleoptera, Curculionidae, Molytinae), with description of a new species

Fig. 7. Terminalia of Paratranes Zimmerman, 1994. A. P. monopticus (Pascoe, 1870), tergite VIII of female. B. P. monopticus, sternite VIII of female. C. P. zimmermani sp. nov., tergite VIII of female. D. P. zimmermani sp. nov., sternite VIII of female. E. P. monopticus, sternite VIII of male. F. P. zimmermani sp. nov., sternite VIII of male. G. P. monopticus, spiculum gastrale. H. P. zimmermani sp. nov., ditto. I. P. monopticus, tegmen. J. P. zimmermani sp. nov., ditto. Scale bars = 0.5 mm.

Fig. 9 in A review of Paratranes Zimmerman, 1994, Xanthorrhoea-associated weevils of the Tranes group (Coleoptera, Curculionidae, Molytinae), with description of a new species

Fig. 9. Endophallus and apex of penis of Paratranes Zimmerman, 1994. A. P. monopticus (Pascoe, 1870), apical sclerite (Griffith Uni., Qld). B. P. monopticus, ditto (Lucindale, SA). C. P. monopticus, ditto (Deepdene, WA). D. P. zimmermani sp. nov., ditto (Kalbarri, WA). E. P. zimmermani sp. nov., apex of penis (Kalbarri, WA). F. P. zimmermani sp. nov., ditto (NSW). Scale bars = 0.2 mm.

Fig. 4. Habitus, lateral view. A–B in A review of Paratranes Zimmerman, 1994, Xanthorrhoea-associated weevils of the Tranes group (Coleoptera, Curculionidae, Molytinae), with description of a new species

Fig. 4. Habitus, lateral view. A–B. Paratranes monopticus (Pascoe, 1870). C–D. P. zimmermani sp. nov. (C. Holotype (ANIC); D. Paratype (ANIC)). A, C. Male. B, D. Female. Scale bars = 5.0 mm.

CO1 Sequences and Material Table of Western Palearctic Weevil Taxa

The ZIP file contains the CO1 sequence dataset and its corresponding material table from the research article: Schütte A, Stüben PE, Astrin JJ (2023) Molecular Weevil Identification Project: A Thoroughly Curated Barcode Release of 1300 Western Palearctic Weevil Species (Coleoptera: Curculionoidea) - Biodiversity Data Journal 11.

Fig. 7 in Phylogeny, diversity and biogeography of flightless amphi-Pacific lymantine weevils (Coleoptera: Curculionidae: Molytinae)

Fig. 7. Maximum likelihood tree of Anchonini and Lymantini relationships reconstructed by RAxML from the three-fragment concatenated matrix. Clades outside of the Anchonini plus Lymantini clade are collapsed. Large and small circles denote strongly and moderately supported clades, respectively. Arrows indicate 26 specimens shown in Figs 1, 2, 8–33. Superimposed globes indicate the current distribution.

Fig. 6 in Phylogeny, diversity and biogeography of flightless amphi-Pacific lymantine weevils (Coleoptera: Curculionidae: Molytinae)

Fig. 6. Maximum likelihood tree of true weevil relationships reconstructed by RAxML from the three-fragment concatenated matrix. Three subclades forming the clade of Anchonini plus Lymantini are collapsed. Large and small circles denote strongly and moderately supported clades, respectively.

Fig. 5 in Phylogeny, diversity and biogeography of flightless amphi-Pacific lymantine weevils (Coleoptera: Curculionidae: Molytinae)

Fig. 5. Morphological diversity of the weevil tribe Lymantini, antennae. Specimen numbers refer to Table 2 and Fig. 7.

Fig. 2 in Phylogeny, diversity and biogeography of flightless amphi-Pacific lymantine weevils (Coleoptera: Curculionidae: Molytinae)

Fig. 2. Morphological diversity of the weevil tribe Lymantini, lateral view. Specimen numbers refer to Table 2 and Fig. 7.

Fig. 4 in Phylogeny, diversity and biogeography of flightless amphi-Pacific lymantine weevils (Coleoptera: Curculionidae: Molytinae)

Fig. 4. Morphological diagnostic features and possible apomorphies of Anchonini (A, B) and Lymantini (C–F). A, C, D: head, left lateral view; B: left antenna; E, F: female genitalia and apical sclerites (E: ventral, F: right dorso-lateral). A: Titilayo geiseri Cristóvão & Lyal, 2018; B: T. barclayi Cristóvão & Lyal, 2018; C: Lymantes scrobicollis Gyllenhal, 1838; D–F: Devernodes chthonia Grebennikov, 2018. A, B: from GREBENNIKOV & ANDERSON (2021a); E, F: from GREBENNIKOV (2018).

Fig. 1 in Phylogeny, diversity and biogeography of flightless amphi-Pacific lymantine weevils (Coleoptera: Curculionidae: Molytinae)

Fig. 1. Morphological diversity of the weevil tribe Lymantini, dorsal view. Specimen numbers refer to Table 2 and Fig. 7.

opencc-by-4.0Apr 2023View details →

Phylogenomics illuminates the phylogeny of flower weevils (Curculioninae) and reveals ten independent origins of brood-site pollination mutualism in true weevils

Phylogenomics illuminates the phylogeny of flower weevils (Curculioninae) and reveals ten independent origins of brood-site pollination mutualism in true weevils (142 /150 characters) Haran J.1*, Li X.2,3,4*, Allio R.5*, Shin S.3,4,6, Benoit L.1, Oberprieler R.G.7, Farrell B.D.8, Brown S.D.J.9, Leschen R.A.B.10, Kergoat G.J.5 & McKenna D.D.3,4 * Equal contribution   Affiliations 1 CBGP, CIRAD, INRAE, IRD, Institut Agro, Univ. Montpellier, Montpellier, France. ORCID: 0000-0001-9458-3785 (JH); 0000-0003-3740-5346 (LB) 2 Department of Entomology, College of Plant Protection, China Agricultural University, Beijing 100193, China. ORCID: 0000-0002-0622-2064 (XL) 3 Department of Biological Sciences, University of Memphis, Memphis, TN 38152 ORCID: 0000-0002-7823-8727 (DDM) 4 Center for Biodiversity Research, University of Memphis, Memphis, TN 38152 5 CBGP, INRAE, IRD, CIRAD, Institut Agro, Univ. Montpellier, Montpellier, France. ORCID: 000-0003-3885-5410 (RA); 0000-0002-8284-6215 (GJK) 6 School of Biological Sciences, Seoul National University, Seoul 08826, Republic of Korea. ORCID: 0000-0002-4258-8661 (SS) 7 CSIRO, Australian National Insect Collection, GPO Box 1700, Canberra, ACT 2601, Australia. ORCID: 0000-0002-1837-580X (RGO) 8 Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, USA. ORCID: 0000-0002-6843-0539 (BDF) 9 Bio-Protection Research Centre, P.O. Box 85084, Lincoln University, Lincoln 7647, New Zealand. Current address: The New Zealand Institute for Plant and Food Research, Mount Albert Research Centre, Private Bag 92169, Auckland 1142, New Zealand. ORCID: 0000-0001-7112-421X (SDJB) 10 Manaaki Whenua - Landcare Research, PB 92170, Auckland, New Zealand. ORCID: 0000-0001-8549-8933 (RABL)   Abstract Weevils are an unusually species-rich group of phytophagous insects, for which there is increasing evidence of frequent involvement in brood-site pollination. This study examines phylogenetic patterns in the emergence of brood-site pollination mutualism among one of the most speciose beetle groups, the flower weevils (subfamily Curculioninae). We analyzed a novel phylogenomic dataset consisting of 214 nuclear loci for 202 weevil species, with a sampling that mainly includes flower weevils as well as representatives of all major lineages of true weevils (Curculionidae). Our phylogenomic analyses establish a uniquely comprehensive phylogenetic framework for Curculioninae and provide new insights into the relationships among lineages of true weevils. Based on this phylogeny, statistical reconstruction of ancestral character states revealed at least ten independent origins of brood-site pollination in higher weevils through transitions from ancestral associations with reproductive structures in the larval stage. Broadly, our results illuminate the unexpected frequency with which true weevils — typically specialized phytophages and hence antagonists of plants — have evolved mutualistic interactions of ecological significance that are key to both weevil and plant evolutionary fitness and thus a component of their deeply intertwined macroevolutionary success.   Figures  Figure 1 (part I). Maximum-likelihood tree resulting from analyses of 214 nuclear protein-coding genes (focus on the CEGH clade and outgroups). Support at node refers to SH-aLRT values ≥ 80% and uBV ≥ 95% (**). Single * refer to SH-aLRT values ≥ 80% only. Clades with black branches and highlighted in blue are classified in Curculioninae sensu Caldara et al. (2014). Taxa displayed on the left: 1 - Hypsomus sp. (Styphlini); 2 - Myllorhinus sp. (Storeini s. lat.); 3 - Encosmia sp. (Storeini s. lat.). Figure 1 (part II). Maximum-likelihood tree resulting from analyses of 214 nuclear protein-coding genes (focus on the CCCMS clade). Node support values refer to SH-aLRT values ≥ 80% and uBV ≥ 95% (**). Single * refer to SH-aLRT values ≥ 80% only. Clades with black branches and highlighted in blue are classified in Curculioninae sensu Caldara et al., (2014). Clades highlighted in darker blue contain genera engaged in brood-site pollination mutualism and the corresponding genera are highlighted in orange (higher taxonomic rank when specific genera are not included in the tree). Other lineages of the CCCMS clade are in bold font. Taxa displayed on the right: 1 - Tychius sp. (Tychiini); 2 - Anthonomus sp. (Athonomini); 3 - Tachyerges sp. (Rhamphini); 4 - Derelomus sp. (Derelomini); 5 - Cionus sp. (Cionini); 6 - Daeneus sp. (Ochyromerini); 7 - Meriphus sp. (Eugnomini); 8 - Archarius sp. (Curculionini); 9 - Dorytomus sp. (Ellescini); 10 - Cleopomiarus sp. (Mecinini). Figure 2. Results of the ASE analysis of larval tissue specialization carried out on the CCCMS clade, with an ER model and using a continuous-time reversible Markov model with 1000 simulations. In addition, red arrows are used to underline the independent origins of brood-site mutualism inferred in another ASE analysis (see Fig. S4). Two clades including brood-site pollinator genera that were not sampled in our study are also highlighted using red rectangles.   Additional files Figure S1. Full ML tree with support values. Figure S2. Support for ML analyses. Figure S3. Results of the ASE analysis of the evolution of the tissue specialization by weevil larvae in the CCCMS clade, with an ER model and using a continuous time-reversible Markov model with 1000 simulations.  Figure S4. Results of the ASE analysis on the evolution of brood-site pollination in the CCCMS clade, with an ER model and using a continuous time-reversible Markov model with 1000 simulations.   Zenodo supplementary files AHE_pipeline.txt shows the detailed step-by-step script used to generate the phylogeny obtained in this study from raw sequencing data. ASE Analyses.zip contains the script and the associated raw results of the ASE analyses. Cole_tcas_probes.fasta contains the Coleopteran probes used. IBA results.zip contains IBA results. IQ-TREE files.zip contains input and output files of the IQ-TREE analysis. Scripts.zip contains the scripts associated with the file AHE_pipeline.txt.

opencc-by-4.0Mar 2023View details →

Рис. 8–13. ΔанΑшафты Южного УраΛа (8–11) и Русской равнины (12–13). 8 – разнотравная степь у поΑножия горы ВербΛюжка, местообитание Cionus rossicus; 9 – ксерофитные Λуга в пойме реки УраΛ вбΛизи горы ВербΛюжка, местообитание Cionus rossicus; 10 – южные степи в районе КзыΛаΑырского карстового поΛя, местообитание Cionus gebleri; 11 – степи низкогорий Южного УраΛа бΛиз с. КиΑрясово, местообитание Smicronyx albopictus; 12 – КаменноброΑские меΛовые горы на юго-запаΑе ПривоΛжской возвышенности, местообитание Mecinus janthiniformis, Smicronyx robustus и S. albopictus; 13 – меΛовой останец КобыΛья ГоΛова в прироΑном парке «Àонской», местообитание Mecinus janthiniformis. Figs 8–13. Landscapes of the Southern Urals (8–11) and the Russian Plain (12–13). 8 – forb steppe at the down of Verblyuzhka Mt., habitat of Cionus rossicus; 9 – xerophytic meadows in the floodplain of the Ural River near Verblyuzhka Mt., habitat of Cionus rossicus; 10 – southern steppes in the Kzyladyr karst area, habitat of Cionus gebleri; 11 – steppes of the low mountains of the Southern Urals near Kidryasovo village, habitat of Smicronyx albopictus; 12 – Kamennobrodsky chalk mountains in the southwest of the Volga Upland, habitat of Mecinus janthiniformis, Smicronyx robustus, and S. albopictus; 13 – Cretaceous outlier Kobyl'ya Golova in the Donskoy Nature Park, habitat of Mecinus janthiniformis. in Interesting records of weevils (Coleoptera: Curculionidae: Curculioninae) in the steppe zone of the European part of Russia and the Urals

Рис. 8–13. ΔанΑшафты Южного УраΛа (8–11) и Русской равнины (12–13). 8 – разнотравная степь у поΑножия горы ВербΛюжка, местообитание Cionus rossicus; 9 – ксерофитные Λуга в пойме реки УраΛ вбΛизи горы ВербΛюжка, местообитание Cionus rossicus; 10 – южные степи в районе КзыΛаΑырского карстового поΛя, местообитание Cionus gebleri; 11 – степи низкогорий Южного УраΛа бΛиз с. КиΑрясово, местообитание Smicronyx albopictus; 12 – КаменноброΑские меΛовые горы на юго-запаΑе ПривоΛжской возвышенности, местообитание Mecinus janthiniformis, Smicronyx robustus и S. albopictus; 13 – меΛовой останец КобыΛья ГоΛова в прироΑном парке «Àонской», местообитание Mecinus janthiniformis. Figs 8–13. Landscapes of the Southern Urals (8–11) and the Russian Plain (12–13). 8 – forb steppe at the down of Verblyuzhka Mt., habitat of Cionus rossicus; 9 – xerophytic meadows in the floodplain of the Ural River near Verblyuzhka Mt., habitat of Cionus rossicus; 10 – southern steppes in the Kzyladyr karst area, habitat of Cionus gebleri; 11 – steppes of the low mountains of the Southern Urals near Kidryasovo village, habitat of Smicronyx albopictus; 12 – Kamennobrodsky chalk mountains in the southwest of the Volga Upland, habitat of Mecinus janthiniformis, Smicronyx robustus, and S. albopictus; 13 – Cretaceous outlier Kobyl'ya Golova in the Donskoy Nature Park, habitat of Mecinus janthiniformis.

opencc-by-4.0Mar 2023View details →

Рис. 1–7. Новые ΑΛя фауны России и маΛоизвестные виΑы жуков-ΑоΛгоносиков. 1–3 – Cionus rossicus: 1 – самец, 2 – эΑеагус, 3 – самка; 4 – Cionus gebleri; 5 – Mecinus janthiniformis; 6 – Smicronyx robustus; 7 – Smicronyx albopictus. Figs 1–7. New to the fauna of Russia and little known species of weevils. 1–3 – Cionus rossicus: 1 – male, 2 – aedeagus, 3 – female; 4 – Cionus gebleri; 5 – Mecinus janthiniformis; 6 – Smicronyx robustus; 7 – Smicronyx albopictus. in Interesting records of weevils (Coleoptera: Curculionidae: Curculioninae) in the steppe zone of the European part of Russia and the Urals

Рис. 1–7. Новые ΑΛя фауны России и маΛоизвестные виΑы жуков-ΑоΛгоносиков. 1–3 – Cionus rossicus: 1 – самец, 2 – эΑеагус, 3 – самка; 4 – Cionus gebleri; 5 – Mecinus janthiniformis; 6 – Smicronyx robustus; 7 – Smicronyx albopictus. Figs 1–7. New to the fauna of Russia and little known species of weevils. 1–3 – Cionus rossicus: 1 – male, 2 – aedeagus, 3 – female; 4 – Cionus gebleri; 5 – Mecinus janthiniformis; 6 – Smicronyx robustus; 7 – Smicronyx albopictus.

opencc-by-4.0Feb 2021View details →

Fig. 1 in A contribution to the fauna of weevil beetles (Coleoptera: Curculionoidea) of the Central Donbass

Fig. 1. Localities of collected weevils in the Central Donbass. 1–13 – Lugansk Region: 1 – Razdol'noe; 2 – Velikotsk; 3 – "Strel'tsovskaya steppe" Natural Reserve; 4 – Chervonaya Dibrova; 5 – Raygorodka; 6 – Trekhizbenka; 7 – "Pridontsovskaya poyma" Natural Reserve (until 2001 "Stanichno-Luganskiy"); 8 – Kondrashevskaya-Novaya railway station; 9 – Kolesnikovka; 10 – Lugansk; 11 – Khrustal'noe; 12 – Ivanovka; 13 – Proval'e and "Proval'skaya steppe" Natural Reserve. 14–87 – Donetsk Region: 14 – Svyatogorsk; 15 – Bogorodichnoe; 16 – Slavyansk, Teplinskiy forest; 17 – Prishib; 18 – Sidorovo; 19 – Cherkasskoe; 20 – Regional Landscape Park "Kramatorskiy"; 21 – Kramatorsk, Belen'koe; 22 – Mayaki; 23 – Drobyshevo; 24 – Shchurovo; 25 – Torskoe; 26 – Yampol; 27 – Il'ichevka; 28 – "Melovaya flora" Natural Reserve; 29 – Dronovka; 30 – Seversk; 31 – Tripol'e; 32 – Artemovsk; 33 – Kurdyumovka; 34 – Debal'tsevo; 35 – Aleksandrovka; 36 – Nikanorovka, Nikanorovskiy forest protected area; 37 – Belokuz'minovka; 38 – Belaya Gora; 39 – Regional Landscape Park "Kleban-Byk"; 40 – Novoocheretovatoe; 41 – Velikaya Novoselka; 42 – Vrem'evka; 43 – Ostroe; 44 – Mar'inka; 45 – Donetsk; 46 – Peski; 47 – Avdeevka; 48 – Yakovlevka; 49 – Mineral'noe; 50 – Yasinovataya; 51 – Vasil'evka; 52 – Mospino; 53 – Makeevka; 54 – Khartsyzsk; 55 – Enakievo; 56 – Ol'khovatka; 57 – Torez; 58 – Petrovskoe; 59 – Regional Landscape Park "Donetskiy kryazh", Saur-Mogila; 60 – Dmitrovka; 61 – Velikoanadol', Velikoanadol'skiy forest; 62 – Novoandreevka; 63 – Zlatoustovka; 64 – Oktyabr'skoe; 65 – Obil'noe; 66 – Starobeshevo; 67 – Novoekaterinovka; 68 – Novopetrovskoe; 69 – Rodniki; 70 – Blagodatnoe; 71 – Amvrosievka; 72 – Karpovo-Nadezhdinka; 73 – Beloyarovka; 74 – Granitnoe; 75 – Zernovoe; 76 – Svobodnoe; 77 – Nazarovka; 78 – "Kamennye mogily" Natural Reserve; 79 – Veseloe; 80 – Volodarskoe, "Azovskaya dacha" Forest Reserve; 81 – Belosarayskaya Spit, National Nature Park "Meotida"; 82 – Mariupol; 83 – Pishсhevik; 84 – "Khomutovskaya steppe" Natural Reserve; 85 – Klinkino; 86 – Novoazovsk; 87 – Sedovo, National Nature Park "Meotida". Рис. 1. МестонахожΔения ΔоΛгоносиков в ЦентраΛьном Àонбассе. 1–13 – Αуганская обΛасть: 1 – РазΔоΛьное; 2 – ВеΛикоцк; 3 – заповеΔник «СтреΛьцовская степь»; 4 – Червоная Àиброва; 5 – РайгороΔка; 6 – Трёхизбенка; 7 – заповеΔник «ПриΔонцовская пойма» (Δо 2001 гоΔа – «Станично-Αуганский»); 8 – жеΛезноΔорожная станция КонΔрашевская- Новая; 9 – КоΛесниковка; 10 – Αуганск; 11 – ХрустаΛьное; 12 – Ивановка; 13 – ПроваΛье и заповеΔник «ПроваΛьская степь». 14–87 – Àонецкая обΛасть: 14 – Святогорск; 15 – БогороΔичное; 16 – СΛавянск, ТепΛинский Λес; 17 – Пришиб; 18 – СиΔорово; 19 – Черкасское; 20 – регионаΛьный ΛанΔшафтный парк «Краматорский»; 21 – Краматорск, БеΛенькое; 22 – Маяки; 23 – Àробышево; 24 – Щурово; 25 – Торское; 26 – ЯмпоΛь; 27 – ИΛьичёвка; 28 – заповеΔник «МеΛовая фΛора»; 29 – Àроновка; 30 – Северск; 31 – ТрипоΛье; 32 – Артёмовск; 33 – КурΔюмовка; 34 – ÀебаΛьцево; 35 – АΛексанΔровка; 36 – Никаноровка, заповеΔное урочище Никаноровкий Λес; 37 – БеΛокузьминовка; 38 – БеΛая Гора; 39 – регионаΛьный ΛанΔшафтный парк «КΛебан-Бык»; 40 – Новоочеретоватое; 41 – ВеΛикая НовосёΛка; 42 – Времьевка; 43 – Острое; 44 – Марьинка; 45 – Àонецк; 46 – Пески; 47 – АвΔеевка; 48 – ЯковΛевка; 49 – МинераΛьное; 50 – Ясиноватая; 51 – ВасиΛьевка; 52 – Моспино; 53 – Макеевка; 54 – Харцызск; 55 – Енакиево; 56 – ОΛьховатка; 57 – Торез; 58 – Петровское; 59 – регионаΛьный ΛанΔшафтный парк «Àонецкий кряж», Саур-МогиΛа; 60 – Àмитровка; 61 – ВеΛикоанаΔоΛь, ВеΛикоанаΔоΛьский Λес; 62 – НовоанΔреевка; 63 – ЗΛатоустовка; 64 – Октябрское; 65 – ОбиΛьное; 66 – Старобешево; 67 – Новоекатериновка; 68 – Новопетровское; 69 – РоΔники; 70 – БΛагоΔатное; 71 – Амвросиевка; 72 – Карпово-НаΔежΔинка; 73 – БеΛояровка; 74 – Гранитное; 75 – Зерновое; 76 – СвобоΔное; 77 – Назаровка; 78 – заповеΔник «Каменные могиΛы»; 79 – ВесёΛое; 80 – ВоΛоΔарское, Λесничество «Азовская Δача»; 81 – БеΛосарайская Коса, национаΛьный прироΔный парк «МеотиΔа»; 82 – МариупоΛь; 83 – Пищевик; 84 – заповеΔник «Хомутовская степь»; 85 – КΛинкино; 86 – Новоазовск; 87 – СеΔово, национаΛьный прироΔный парк «МеотиΔа».

opencc-by-4.0Dec 2016View details →

Figure 4 in First Field Collection of the Rough Sweetpotato Weevil, Blosyrus asellus (Olivier) (Coleoptera: Curculionidae), on Hawaii Island, with Notes on Detection Methods

Figure 4. Average (+ SEM) catch of adult rough sweetpotato weevils/trap/day in green light traps with and without added attractant(s). Treatments having the same letter above the error bar are not significantly different at the α = 0.05 level. Only results of treatments which included green light (Treatments 5–9) are presented here because there was no catch in this trial in traps of any of the treatments where the green light was off (Treatments 1–4).

opencc-by-4.0Dec 2016View details →

Figure 2 in First Field Collection of the Rough Sweetpotato Weevil, Blosyrus asellus (Olivier) (Coleoptera: Curculionidae), on Hawaii Island, with Notes on Detection Methods

Figure 2. Locations on Hawaii island (marked with filled circles) where adult rough sweetpotato weevils have been recovered (map developed using ArcGIS [ESRI 2012]).