01249nas a2200229   4500008004100000245004000041210003700081300001300118490000600131520058900137653002300726653001300749653002400762653003000786653001300816653002400829653002300853653002300876653002300899100002800922856006900950       1938                        eng d00aNew Australian Curculionidae (Col.)0 aNew Australian Curculionidae Col  app. 8-140 v73 aGlaucopela acaciae (Curculionidae): [Sp nov, Australia p. 10]. Imbilius (Curculionidae): [Gen nov, (Hylobiinae), Imbilius araucariae, sp. n., Queensland p. 9 fig.]. Imbilius araucariae (Curculionidae): [Sp nov]. Neomerimnetes flindersiae (Curculionidae): [Sp nov, Queensland p. 8].Omeretes (Curculionidae): [Gen nov, (Cossoninae) p. 12, Omeretespodocarpi, (type), Omeretes onychialis, spp. n., Australia p. 15]. Omeretes onychialis (Curculionidae): [Sp nov]. Pseudapries crux (Curculionidae): [Sp nov, Queensland p. 11]. Stereoderus lucens (Curculionidae): [Sp nov, Queensland p. 12].10aGlaucopela acaciae10aImbilius10aImbilius araucariae10aNeomerimnetes flindersiae10aOmeretes10aOmeretes onychialis10aOmeretes podocarpi10aPseudapries crux .10aStereoderus lucens1 aMarshall, Sir, G. A. K.  uhttps://weevil.myspecies.info/new-australian-curculionidae-col-310273nas a2201117   4500008004100000245003600041210003500077300001600112490000600128520692700134653002107061653002507082653002207107653002607129653002207155653002407177653002407201653001607225653002707241653001707268653002807285653002607313653002807339653003007367653002407397653002807421653001507449653002307464653002207487653002407509653002307533653002207556653002207578653002507600653003007625653002607655653001707681653003007698653003007728653002207758653002507780653001307805653002707818653002207845653001707867653002807884653001607912653002607928653003207954653003207986653004008018653002608058653001808084653002808102653001508130653002808145653001408173653002608187653002308213653001508236653002808251653002608279653002508305653002008330653001508350653002308365653002408388653002008412653002708432653002308459653001908482653002808501653003308529653002208562653002508584653002408609653002908633653002608662653002308688653001608711653002908727653002708756653002708783653002708810653001808837653002708855653001808882653002508900653002708925653002708952653002508979653002909004653003209033100002809065856006209093       1931                        eng d00aCurculionidae. Insects of Samoa0 aCurculionidae Insects of Samoa  app. 249-3460 v43 aAcicnemis biconiferaAcicnemis eludensAcicnemis kraatziAcicnemis signiferaAmorphocerusAphanocorynes humeralisDeretiosus gibberDeretiosus wilderiDiathetes lyrigerDryophthorus armati collisDynatopechus rubronotatusEremonyx rufoplagiatusEremonyx samoanusNesobaris parvungulisNesobaris tutuilaeOttinychus buxtoniOttinychus hopkinsi [Zoology / / ]. Acicnemis variegata [Zoology / / Fairm. (= Acicnemis foveicollis Hell) p. 271 Acicnemis biconifera Fairm. (= Acicnemis kraatzi Hub.) Acicnemis eludens (with var. n Acicnemis signifera p. 274) sp. N Samoa p. 272 [Sp nov]]. Ampagia cribrellicollis [Zoology / / further description p. 306 Ampagia semisuturalis sp. N Samoa p. 307]. Aphanocorynes savaiiensis [Zoology / / p. 333 Aphanocorynes humeralis p. 334 spp. N Samoa fig]. Curculionidae [Zoology / / Curculionidae of Samoa]. Deretiosus scutiger [Zoology / / p. 287 Deretiosus gibber p. 289 Deretiosus wilder p. 290 spp. N Samoa fig].Diathetes buxtoni [Zoology / / p. 316 Diathetes lyriger p. 318 spp. N fig].Dryophthorus muscosus [Zoology / / p. 321 Dryophthorus armati collis p. 322 spp. N Samoa figs].Insecta [Zoology / / Geography Or Faunistic Insular (including New Zealand) Samoa Coleoptera Curculionidae].Microcryptorrhynchus analis [Zoology / / p. 282 Microcryptorrhynchus subscu tellatusp. 283 Microcryptorrhynchus glomus p. 284 spp. N Samoa figs].Pentarthrum hirticolle [Zoology / / Pentarthrum naucum spp. N Samoa p. 324]. Trigonopterus crinipes [Zoology / / p. 298 Trigonopterus caesipes p. 301 Trigonopterus serratipes p. 304Trigonopterus bryani p. 305 spp. nTrigonopterus submetallicus subsp. nTrigonopterus mendax p. 300 Samoa key to Samoan spp. p. 304 figs [Subsp nov]].Acalles samoanus (Curculionidae): [Sp nov, sp. n., Samoa p. 280].Acicnemis biconifera (Curculionidae).Acicnemis eludens (Curculionidae).Acicnemis foveicollis - Hell. (Curculionidae): [Systematics].Acicnemis kraatzi (Curculionidae).Acicnemis signifera (Curculionidae).Acicnemis variegata (Curculionidae).Amblycnemus (Curculionidae): [Gen nov, gen. n., (Anthonominae) p. 265, Amblycnemus stevensoni, sp. n., Samoa p. 266 fig., [Sp nov]].Amblycnemus stevensoni (Curculionidae): [Sp nov].Amorphocerus (Curculionidae).Ampagia cribrellicollis (Curculionidae).Ampagia semisuturalis (Curculionidae): [Sp nov].Aphanocorynes humeralis (Curculionidae).Aphanocorynes savaiiensis (Curculionidae).Calandra punctigera - Pasc. (Curculionidae): [Systematics].Chaetectetorus tutuilae (Curculionidae): [Sp nov, sp. n., Samoa p. 296 fig.].Deretiodes (Curculionidae): [Gen nov, gen. n., (Cryptorrhyn chinae),Deretiodes swezeyi, sp. n., Samoa p. 292 fig., [Sp nov]].Deretiodes swezeyi (Curculionidae): [Sp nov].Deretiosus gibber (Curculionidae).Deretiosus scutiger (Curculionidae).Deretiosus wilderi (Curculionidae).Diathetes buxtoni (Curculionidae).Diathetes lyriger (Curculionidae).Diocalandra frumenti - F. (Curculionidae): [Systematics, (=, Calandra punctigera, Pasc., ) new to Pacific Is. p. 321]. Dryophthorus armati collis (Curculionidae). Dryophthorus muscosus (Curculionidae). Dynatopechus (Curculionidae): [Gen nov, gen. n., (Cossoninae) p. 325, Dynatopechus rubronotatus, (type), sp. n., Samoa p. 326, Dynatopechus aureopilosus, Fairm., from, Amorphocerus, p. 325 fig., [Sp nov]]. Dynatopechus aureopilosus - Fairm. (Curculionidae): [Systematics]. Dynatopechus rubronotatus (Curculionidae). Elytrurus bicolor - Mshl. (Curculionidae): [Systematics, (=, Elytrurus bivittatus, Mshl., ) p. 260]. Eremonyx (Curculionidae): [Gen nov, gen. n., (Baridinae) p. 308, Eremonyx samoanus, (type) p. 300, Eremonyx rufoplagiatus, p. 310, spp. n., [Sp nov]]. Eremonyx rufoplagiatus (Curculionidae). Eremonyx samoanus (Curculionidae). Gitonischius (Curculionidae): [Gen nov, gen. n., (Cossoninae) p. 327, Gitonischius tubicollis, sp. n., Samoa p. 328 fig., [Sp nov]]. Gitonischius tubicollis (Curculionidae): [Sp nov]. Hesychobius (Curculionidae): [Gen nov, gen. n., (Erirrhininae) p. 263, Hesychobius nebulosus, sp. n., Samoa p. 264 fig., [Sp nov]]. Hesychobius nebulosus (Curculionidae): [Sp nov]. Microcryptorrhynchus analis (Curculionidae). Microtribus longiceps (Curculionidae): [Sp nov, sp. n., Samoa p. 330 fig.]. Mystrorrhinus (Curculionidae): [Gen nov, gen. n., (Cossoninae) p. 340, Mystrorrhinus dimorphus, sp. n., Samoa p. 341 figs., [Sp nov]]. Mystrorrhinus dimorphus (Curculionidae): [Sp nov]. Nesendaeus (Curculionidae): [Gen nov, gen. n., (Tychiinae), Nesendaeus seto lineatus, sp. n., Samoa p. 270 fig., [Sp nov]]. Nesendaeus seto lineatus (Curculionidae): [Sp nov]. Nesobaris (Curculionidae): [Gen nov, gen. n., (Baridinae), Nesobaris tutuilae, (type) p. 313, Nesobaris parvungulis, p. 315, spp. n., Samoa figs., [Sp nov]]. Nesobaris parvungulis (Curculionidae). Nesobaris tutuilae (Curculionidae). Nodocnemus (Curculionidae): [Gen nov, gen. n., (Erirrhininae) p. 260, Nodocnemus subfasciatus, sp. n., Samoa p. 261 fig., [Sp nov]]. Nodocnemus subfasciatus (Curculionidae): [Sp nov]. Notiosomus cervicalis (Curculionidae): [Sp nov, sp. n., Samoa p. 335]. Ochronanus pumilus (Curculionidae): [Sp nov, sp. n., Samoa p. 344]. Omobaris lucens (Curculionidae): [Sp nov, sp. n., Samoa p. 310 fig.]. Ottinychus (Curculionidae): [Gen nov, gen. n., (Brachyderinae),Ottinychus buxtoni, (type) p. 253, Ottinychus hopkinsi, p. 256, spp. n., Samoa figs., [Sp nov]]. Ottinychus buxtoni (Curculionidae). Ottinychus hopkinsi (Curculionidae). Oxydema simplex (Curculionidae): [Sp nov, sp. n., Samoa p. 332]. Pentarthrum hirticolle (Curculionidae). Pentarthrum naucum (Curculionidae): [Sp nov]. Phanerostethus (Curculionidae): [Gen nov, gen. n., (Cryptorrhynchinae) p. 285, Phanerostethus dilophus, sp. n., Samoa p. 286 fig., [Sp nov]]. Phanerostethus dilophus (Curculionidae): [Sp nov]. Phloeophogosoma carinirostre (Curculionidae): [Sp nov, sp. n., Samoa p. 331 fig.]. Proeces praeustum (Curculionidae): [Sp nov, sp. n., Samoa p. 339]. Rhabdocnemis obacura - Boisd. (Curculionidae): [Systematics, (=, Sphenophorus promissus, Pasc., ) p. 320]. Rhymhaenus samoanus (Curculionidae): [Sp nov, sp. n., Samoa p. 269]. Rhyncolosoma subsignatum (Curculionidae): [Sp nov, sp. n., Samoa p. 342 fig.]. Rhyncolus fuscicollis (Curculionidae): [Sp nov]. Rhyncolus samoanus - Mshl. (Curculionidae): [Systematics, from, Temnorhamphus, Rhyncolus fuscicollis, sp. n., Samoa p. 346]. Spanochelus (Curculionidae): [Gen nov, gen. n., (Ithyporinae), Spanochelus planirostris, sp. n., Samoa p. 278 fig., [Sp nov]]. Spanochelus planirostris (Curculionidae): [Sp nov]. Sphaerorrhinus mutatis (Curculionidae): [Sp nov, sp. n., Samoa p. 257]. Stenotrupis myristicae (Curculionidae): [Sp nov, sp. n., Samoa p. 320]. Teleodactylus (Curculionidae): [Gen nov, gen. n., (Cryptorrhynchinae) p. 294, Teleodactylus roscidus, sp. n., Samoa p. 295, [Sp nov]]. Teleodactylus roscidus (Curculionidae): [Sp nov]. Trigonopterus crinipes (Curculionidae). Trigonopterus submetallicus (Curculionidae): [Subsp nov].10aAcalles samoanus10aAcicnemis biconifera10aAcicnemis eludens10aAcicnemis foveicollis10aAcicnemis kraatzi10aAcicnemis signifera10aAcicnemis variegata10aAmblycnemus10aAmblycnemus stevensoni10aAmorphocerus10aAmpagia cribrellicollis10aAmpagia semisuturalis10aAphanocorynes humeralis10aAphanocorynes savaiiensis10aCalandra punctigera10aChaetectetorus tutuilae10aDeretiodes10aDeretiodes swezeyi10aDeretiosus gibber10aDeretiosus scutiger10aDeretiosus wilderi10aDiathetes buxtoni10aDiathetes lyriger10aDiocalandra frumenti10aDryophthorus armaticollis10aDryophthorus muscosus10aDynatopechus10aDynatopechus aureopilosus10aDynatopechus rubronotatus10aElytrurus bicolor10aElytrurus bivittatus10aEremonyx10aEremonyx rufoplagiatus10aEremonyx samoanus10aGitonischius10aGitonischius tubicollis10aHesychobius10aHesychobius nebulosus10aMicrocryptorrhynchus analis10aMicrocryptorrhynchus glomus10aMicrocryptorrhynchus subscutellatus10aMicrotribus longiceps10aMystrorrhinus10aMystrorrhinus dimorphus10aNesendaeus10aNesendaeus setolineatus10aNesobaris10aNesobaris parvungulis10aNesobaris tutuilae10aNodocnemus10aNodocnemus subfasciatus10aNotiosomus cervicalis10aOchronanus pumilus].10aOmobaris lucens10aOttinychus10aOttinychus buxtoni10aOttinychus hopkinsi10aOxydema simplex10aPentarthrum hirticolle10aPentarthrum naucum10aPhanerostethus10aPhanerostethus dilophus10aPhloeophogosoma carinirostre10aProeces praeustum10aRhabdocnemis obacura10aRhymhaenus samoanus10aRhyncolosoma subsignatum10aRhyncolus fuscicollis10aRhyncolus samoanus10aSpanochelus10aSpanochelus planirostris10aSphaerorrhinus mutatis10aSphenophorus promissus10aStenotrupis myristicae10aTeleodactylus10aTeleodactylus roscidus10aTemnorhamphus10aTrigonopterus bryani10aTrigonopterus caesipes10aTrigonopterus crinipes10aTrigonopterus mendax10aTrigonopterus serratipes10aTrigonopterus submetallicus1 aMarshall, Sir, G. A. K.  uhttps://weevil.myspecies.info/curculionidae-insects-samoa04163nas a2200853   4500008004100000245004200041210003700083300001200120490001100132653001500143653001000158653004900168653001100217653002800228653007100256653007400327653005700401653006900458653007300527653001200600653006900612653006700681653006200748653007000810653006900880653007200949653006701021653004201088653003601130653004201166653006801208653002801276653001301304653003001317653002301347653002101370653003001391653003701421653002101458653007101479653001301550653001701563653003201580653007101612653006601683653006601749653006201815653005701877653006901934653006902003653007202072653007402144653007102218653002302289653004002312653007102352653002702423653004402450653003902494653003802533653007302571653007502644653006902719653006702788653002502855653007502880653004502955653007203000653006403072653001603136653007403152100002103226856006203247       1932                        eng d00aNotes on the Hylobiinae (Col., Curc.)0 aNotes on the Hylobiinae Col Curc  a341-3550 v(10) 910a) p. 345].10a345].10aAcaerus - Pasc. (Psylloidea): [Systematics].10aAclees10aAclees (Curculionidae).10aAclees, Chitonopterus fasciculatus, Klb., from, Hylobius, p. 345].10aAfrolithinus (Curculionidae): [Gen nov, gen. n., (Hylobiinae) p. 352,10aAfrolithinus bipustulatus (Curculionidae): [Sp nov].10aAfrolithinus bipustulatus, sp. n., Kenya p. 353 fig., [Sp nov]].10aAschpiadorrhynchus, Peyr., ), Chitonopterus floccosus, Fairm., from,10aBiology10aCentor globulicollis - Boh. (Curculionidae): [Systematics, from,10aChamp., ), Pseudanchonus aequatorius, Fst., ( =, Pseudanchonus10aChitonopterus - Fairm. (Curculionidae): [Systematics, (=,10aChitonopterus fasciculatus - Klb. (Curculionidae): [Systematics].10aChitonopterus floccosus - Fairm. (Curculionidae): [Systematics].10aclassification of Hylobiinae (key to groups p. 345) and transfer of10aCleonus dehaani - Fhs. (Curculionidae): [Systematics, Fossil].10aCleonus dehaani, Fhs., p. 346 figs.].10aCurculionidae (Curculionoidea).10aCurculionidae [Zoology / / Characters10aFst., ), Steremnius tuberosus, Boh., a N. American sp. p. 345].10aGeological time periods10aHeilipus10aHeilipus (Curculionidae).10aHeilipus, p. 345].10aHorn, ) p. 345].10aHylobius (Curculionidae).10aHylobius [Zoology / / ] [ / / ].10aJek., ) p. 345].10aMioscapus (Curculionidae): [Gen nov, gen. n., (Paipalesomini) for,10aNew taxa10aNomenclature10aocculta, Champ., ) p. 345].10aOtidocephalus - Chev. (Curculionidae): [Systematics, (=, Cycotida,10aOtidocephalus lineata - Pasc. (Curculionidae): [Systematics].10aOtidocephalus vittatus - Horn (Curculionidae): [Systematics].10aPagiophloeus ruhli - Fst. (Curculionidae): [Systematics].10aPagiophloeus ruhli, Fst., ) from, Hylobius, p. 345].10aPagiophloeus rusticus - Pasc. (Curculionidae): [Systematics, (=,10aPaipalephorus - Jek. (Curculionidae): [Systematics, (=, Acaerus,10aPasc., ), Otidocephalus lineata, Pasc., (=, Otidocephalus vittatus,10aPasc., ), Paipalephorus frontalis, Pasc., (=, Paipalephorus mucoreus,10aPinacopus (Curculionidae): [Gen nov, gen. n., (Hylobiinae) p. 348,10aPinacopus caudatus10aPinacopus caudatus (Curculionidae).10aPinacopus caudatus, (type) p. 349, Pinacopus dentirostris, p. 350,10aPinacopus dentirostris10aPinacopus dentirostris (Curculionidae).10aPinacopus dolosus (Curculionidae).10aPinacopus dolosus [Zoology / / ].10aPinacopus dolosus, p. 352, spp. n., Malay Peninsula fig., [Sp nov]].10aPseudanchonus - Fst. (Curculionidae): [Systematics, (=, Anchonomorpha,10aPseudanchonus aequatorius - Fst. (Curculionidae): [Systematics].10aPseudanchonus occulta - Champ. (Curculionidae): [Systematics].10arelationships and re10aSeleuca - Pasc. (Curculionidae): [Systematics, (=, Ergias, Pasc., ) p.10aseveral genera into allied subfamilies].10aSteremnius - Schh. (Curculionidae): [Systematics, (=, Paraplisthus,10aSteremnius tuberosus - Boh. (Curculionidae): [Systematics].10aSystematics10aTaractes - Kirsch (Curculionidae): [Systematics, (=, Ectinura, Pasc.,1 aMarshall, G.A.K.  uhttps://weevil.myspecies.info/notes-hylobiinae-col-curc-001509nas a2200157   4500008004100000020001400041245011600055210006900171260000900240300001200249490000700261520090800268653002101176100002301197856013101220       2010                        eng d  a1427-433700aResponse of large pine weevil (Hylobius abietis L.) beetles to insecticides with different mechanisms of action0 aResponse of large pine weevil Hylobius abietis L beetles to inse  c2010  a149-1570 v503 aResponses (knock-down and mortality) of large pine weevil (Hylobius abietis L.) beetles to insecticides of different mechanism of action such as neonicotinoids (clotianidin, acetamiprid) acting on nicotinic receptors of acetylcholine (ACh), pyrethroids (deltamethrin, [alpha]-cypermethrin) blocking sodium channels in nerve cell membranes, organophosphates (chlorpiryfos) and carbamates (carbosulfan) both inhibiting acetylcholinesterase (AChE) activity and fenylpirazoles (fipronil) interfering with a-butyric acid (GABA) receptors were studied. Taking into account speed of insect decay the order of examined groups of substances may be established as follows: first place is occupied by insecticides interferring with GABA receptors, second place by insecticides blocking AChE activity, and third place in parallel insecticides blocking sodium channels and those acting on nicotinic receptors of ACh.10aHylobius abietis1 aMalinowski, Henryk  uhttps://weevil.myspecies.info/response-large-pine-weevil-hylobius-abietis-l-beetles-insecticides-different-mechanisms-action-004161nas a2200853   4500008004100000245004200041210003700083300001200120490001100132653001500143653001000158653004900168653001100217653002800228653007100256653007400327653005700401653006900458653007300527653001200600653006900612653006700681653006200748653007000810653006900880653007200949653006701021653004201088653003601130653004201166653006801208653002801276653001301304653003001317653002301347653002101370653003001391653003701421653002101458653007101479653001301550653001701563653003201580653007101612653006601683653006601749653006201815653005701877653006901934653006902003653007202072653007402144653007102218653002302289653004002312653007102352653002702423653004402450653003902494653003802533653007302571653007502644653006902719653006702788653002502855653007502880653004502955653007203000653006403072653001603136653007403152100002103226856006003247       1932                        eng d00aNotes on the Hylobiinae (Col., Curc.)0 aNotes on the Hylobiinae Col Curc  a341-3550 v(10) 910a) p. 345].10a345].10aAcaerus - Pasc. (Psylloidea): [Systematics].10aAclees10aAclees (Curculionidae).10aAclees, Chitonopterus fasciculatus, Klb., from, Hylobius, p. 345].10aAfrolithinus (Curculionidae): [Gen nov, gen. n., (Hylobiinae) p. 352,10aAfrolithinus bipustulatus (Curculionidae): [Sp nov].10aAfrolithinus bipustulatus, sp. n., Kenya p. 353 fig., [Sp nov]].10aAschpiadorrhynchus, Peyr., ), Chitonopterus floccosus, Fairm., from,10aBiology10aCentor globulicollis - Boh. (Curculionidae): [Systematics, from,10aChamp., ), Pseudanchonus aequatorius, Fst., ( =, Pseudanchonus10aChitonopterus - Fairm. (Curculionidae): [Systematics, (=,10aChitonopterus fasciculatus - Klb. (Curculionidae): [Systematics].10aChitonopterus floccosus - Fairm. (Curculionidae): [Systematics].10aclassification of Hylobiinae (key to groups p. 345) and transfer of10aCleonus dehaani - Fhs. (Curculionidae): [Systematics, Fossil].10aCleonus dehaani, Fhs., p. 346 figs.].10aCurculionidae (Curculionoidea).10aCurculionidae [Zoology / / Characters10aFst., ), Steremnius tuberosus, Boh., a N. American sp. p. 345].10aGeological time periods10aHeilipus10aHeilipus (Curculionidae).10aHeilipus, p. 345].10aHorn, ) p. 345].10aHylobius (Curculionidae).10aHylobius [Zoology / / ] [ / / ].10aJek., ) p. 345].10aMioscapus (Curculionidae): [Gen nov, gen. n., (Paipalesomini) for,10aNew taxa10aNomenclature10aocculta, Champ., ) p. 345].10aOtidocephalus - Chev. (Curculionidae): [Systematics, (=, Cycotida,10aOtidocephalus lineata - Pasc. (Curculionidae): [Systematics].10aOtidocephalus vittatus - Horn (Curculionidae): [Systematics].10aPagiophloeus ruhli - Fst. (Curculionidae): [Systematics].10aPagiophloeus ruhli, Fst., ) from, Hylobius, p. 345].10aPagiophloeus rusticus - Pasc. (Curculionidae): [Systematics, (=,10aPaipalephorus - Jek. (Curculionidae): [Systematics, (=, Acaerus,10aPasc., ), Otidocephalus lineata, Pasc., (=, Otidocephalus vittatus,10aPasc., ), Paipalephorus frontalis, Pasc., (=, Paipalephorus mucoreus,10aPinacopus (Curculionidae): [Gen nov, gen. n., (Hylobiinae) p. 348,10aPinacopus caudatus10aPinacopus caudatus (Curculionidae).10aPinacopus caudatus, (type) p. 349, Pinacopus dentirostris, p. 350,10aPinacopus dentirostris10aPinacopus dentirostris (Curculionidae).10aPinacopus dolosus (Curculionidae).10aPinacopus dolosus [Zoology / / ].10aPinacopus dolosus, p. 352, spp. n., Malay Peninsula fig., [Sp nov]].10aPseudanchonus - Fst. (Curculionidae): [Systematics, (=, Anchonomorpha,10aPseudanchonus aequatorius - Fst. (Curculionidae): [Systematics].10aPseudanchonus occulta - Champ. (Curculionidae): [Systematics].10arelationships and re10aSeleuca - Pasc. (Curculionidae): [Systematics, (=, Ergias, Pasc., ) p.10aseveral genera into allied subfamilies].10aSteremnius - Schh. (Curculionidae): [Systematics, (=, Paraplisthus,10aSteremnius tuberosus - Boh. (Curculionidae): [Systematics].10aSystematics10aTaractes - Kirsch (Curculionidae): [Systematics, (=, Ectinura, Pasc.,1 aMarshall, G.A.K.  uhttps://weevil.myspecies.info/notes-hylobiinae-col-curc01507nas a2200157   4500008004100000020001400041245011600055210006900171260000900240300001200249490000700261520090800268653002101176100002301197856012901220       2010                        eng d  a1427-433700aResponse of large pine weevil (Hylobius abietis L.) beetles to insecticides with different mechanisms of action0 aResponse of large pine weevil Hylobius abietis L beetles to inse  c2010  a149-1570 v503 aResponses (knock-down and mortality) of large pine weevil (Hylobius abietis L.) beetles to insecticides of different mechanism of action such as neonicotinoids (clotianidin, acetamiprid) acting on nicotinic receptors of acetylcholine (ACh), pyrethroids (deltamethrin, [alpha]-cypermethrin) blocking sodium channels in nerve cell membranes, organophosphates (chlorpiryfos) and carbamates (carbosulfan) both inhibiting acetylcholinesterase (AChE) activity and fenylpirazoles (fipronil) interfering with a-butyric acid (GABA) receptors were studied. Taking into account speed of insect decay the order of examined groups of substances may be established as follows: first place is occupied by insecticides interferring with GABA receptors, second place by insecticides blocking AChE activity, and third place in parallel insecticides blocking sodium channels and those acting on nicotinic receptors of ACh.10aHylobius abietis1 aMalinowski, Henryk  uhttps://weevil.myspecies.info/response-large-pine-weevil-hylobius-abietis-l-beetles-insecticides-different-mechanisms-action25843nas a2202773   45000080041000002450084000412100069001253000010001944900007002045201748900211653001617700653003117716653002417747653001517771653002617786653002517812653002417837653002317861653002817884653002517912653002617937653002717963653002517990653002618015653002918041653002818070653002318098653001818121653002618139653001218165653002218177653002518199653001518224653002518239653001718264653001518281653002518296653002318321653002918344653001918373653002318392653002118415653002318436653001918459653001718478653001818495653001618513653002318529653002418552653002518576653001418601653002418615653002018639653002518659653002818684653001518712653001518727653001118742653002618753653002718779653001918806653002218825653001618847653001418863653001518877653002718892653002718919653002518946653002818971653002618999653002519025653002719050653003119077653001319108653002519121653001919146653002619165653003019191653001919221653002919240653004819269653002819317653003219345653002719377653003019404653002819434653003419462653002819496653002819524653002019552653001919572653002119591653002419612653002719636653002719663653002819690653002419718653002319742653002219765653002219787653002419809653001919833653002119852653001219873653003419885653002819919653002719947653002719974653002620001653002420027653002520051653002720076653001320103653003020116653002420146653002320170653002520193653002920218653002520247653002820272653002220300653002720322653002920349653003020378653002820408653002720436653002520463653003020488653002720518653002520545653002620570653002720596653002620623653002620649653003320675653002920708653004120737653002620778653002720804653002820831653002420859653002620883653002720909653002720936653002520963653002520988653003021013653002421043653002221067653002721089653002521116653002521141653002621166653002421192653003021216653002521246653002221271653001321293653001221306653001521318653002421333653001821357653002121375653001421396653002521410653001621435653003221451653001621483653002621499653002321525653001721548653001821565653002321583653002621606653001521632653002321647653002621670653002421696653002421720653002721744653002421771653002221795653002721817653001521844653002821859653003221887653002621919653002821945653002721973653002922000653002722029653002822056653002622084653002622110653002522136653002222161653002322183653002722206653001922233653001622252653001622268653003022284653002522314653002422339653001522363653002122378653002722399653002522426653001522451653002522466653001222491653002522503653002122528653002122549653002422570653002522594653002122619653002722640653005822667653003422725653002722759653002322786653003122809653002922840653002622869653001822895653002522913653001522938653001722953653002622970653001222996100001623008856004523024       1950                        eng d00aNuevas sinonimias, revalidaciones y combinaciones (aporte a Col. Curculionidae)0 aNuevas sinonimias revalidaciones y combinaciones aporte a Col Cu  a10-210 v103 aAnchodemus - Lec. (Curculionidae): [Systematics, (=, Lixellus, Lec, Anchodemus hubbardi - Lec. (Curculionidae): [Systematics].Anchonus planipennis - Chevr. (Curculionidae): [Systematics].Antarctobius (Curculionidae). Anthonomus (Curculionidae).Anthonomus chilensis - Schenkl. (Curculionidae): [Systematics].Anthonomus ornatus - Blanch. (Curculionidae): [Systematics, (=, Anthonomus redtenbacheri, Blackw., ) p. 17]. Anthonomus redtenbacheri - Blackw. (Curculionidae): [Systematics]. Baris flavipes (Curculionidae). Baris tenuis - Blanch (Curculionidae): [Systematics]. Berberidicola (Curculionidae): [Gen nov, gen. n., for, Rhyssomatus exaratus, Blanch, (type) (=, Rhyssomatus crenulatus, Blanch., Rhyssomatus ater, Phil., ), Centrinus carinatus, Phil., p. 18].Brachybaris - Faust. (Curculionidae): [Systematics]. Calandra chilensis - Phil. (Curculionidae): [Systematics]. Calandra granaria - L. (Curculionidae): [Systematics]. Calandra laevicosta - Phil. (Curculionidae): [Systematics]. Calandra oryzae - L. (Curculionidae): [Systematics, (=, Calandra  chilensis, Phil., ), Calandra granaria, L., (=, Calandra laevicosta, Phil., ) p. 20]. Calvertius tuberosus - Fairm. & Ger. (Curculionidae): [Systematics, (=, Calvertius araucariae, Sharp, ) from, Heilipus, p. 15]. Centrinus (Curculionidae). Centrinus carinatus - Phil. (Curculionidae): [Systematics]. Ceuthorrhynchus (Curculionidae). Chalcodermus lunatus - Bond. (Curculionidae): [Systematics]. Chalcodermus speculifer - Heller (Curculionidae): [Systematics, (=, Chalcodermus lunatus, Bond., ) p. 18].Chilebaris (Curculionidae): [Gen nov, gen. n., for, Baris tenuis, Blanch, (type), Baris flavipes, Phil. p. 19]. Chileudius (Curculionidae): [Gen nov, gen. n., for, Eudius varians, Blanch, p. 12]. Cholus - Boh. (Curculionidae): [Systematics]. Cholus atropunctellus (Curculionidae). Cholus dealbatus - Boh. (Curculionidae): [Systematics, (=, Cholus ornatus, Chevr., ) p. 17, Cholus atropunctellus, see, Acrotomopus, Cholus trizonatus, see, Dionychus trifasciatus]. Cholus ornatus - Chevr. (Curculionidae): [Systematics]. Cholus trizonatus - Gunth. (Curculionidae): [Systematics]. Cnemecoelus (Curculionidae). Coeliodes (Curculionidae). Conothorax - Jek. (Curculionidae): [Systematics, (=, Conocloeus, Mshl., ), Conothorax luctuosus, Lac., (=, Conothorax variabilis, Kessel, ) p. 12]. Conotrachelus aequalis - Fiedl. (Curculionidae): [Systematics]. Conotrachelus cervinus - Hust. (Curculionidae): [Systematics]. Conotrachelus glaber - Hust. (Curculionidae): [Systematics]. Conotrachelus irroratus - Fiedl. (Curculionidae): [Systematics]. Conotrachelus kirschi - Blackw. (Curculionidae): [Systematics]. Conotrachelus pullus - Fiedl. (Curculionidae): [Systematics]. Conotrachelus striatus - Hust. (Curculionidae): [Systematics]. Conotrachelus subnebulosus - Hust. (Curculionidae): [Systematics, (=, Conotrachelus irroratus, Fiedl., ), Conotrachelus cervinus, Hust., (=, Conotrachelus pullus, Fiedl., ), Conotrachelus glaber, Hust., (=, Conotrachelus aequalis, Fiedl., ), Conotrachelus striatus, Hust., (=, Conotrachelus kirschi, Blackw., ) p. 18]. Cossonus (Curculionidae). Cossonus nigropiceus (Curculionidae). Cryptorhynchus (Curculionidae). Cydianerus chevrolati - Blanch. (Curculionidae): [Systematics]. Cydianerus latruncularius - Perty (Curculionidae): [Systematics, (=, Cydianerus chevrolati, Blanch., ) p. 12]. Cylindrorhinus (Curculionidae). Cylindrorhinus angulatus - Guer. (Curculionidae): [Systematics, (=, Adioristus rubripes, Phil., Adioristus rugatus, Phil., (=, Cylindrorhinus angulatus var. scrobiculatus, Burm., )) p. 12, Cylindrorhinus griseus, Phil., (=, Adioristus apiculatus, Hust., )from, Adioristus, Cylindrorhinus denticulatus, Fairm. & Ger., (=, Cylindrorhinus inquinatus, Lac., ), Cylindrorhinus sulcatus, Fairm., (=, Adioristus fuegianus, Berg, ), Cylindrorhinus lactifer, Burm., (=,Cylindrorhinus quadrilineatus, Bovie, ) p. 13, Cylindrorhinus costatus, Cylindrorhinus sordidus, see, Paulsenius]. Cylindrorhinus angulatus var. scrobiculatus - Burm. (Curculionidae): [Systematics].Cylindrorhinus costatus - Redt. (Curculionidae): [Systematics].Cylindrorhinus denticulatus - Fairm. & Ger. (Curculionidae): [Systematics]. Cylindrorhinus griseus - Phil. (Curculionidae): [Systematics]. Cylindrorhinus inquinatus - Lac. (Curculionidae): [Systematics]. Cylindrorhinus lactifer - Burm. (Curculionidae): [Systematics]. Cylindrorhinus quadrilineatus - Bovie (Curculionidae): [Systematics]. Cylindrorhinus sordidus (Curculionidae). Cylindrorhinus sulcatus - Fairm. (Curculionidae): [Systematics]. Demoda kuscheli - Bond. (Curculionidae): [Systematics, a valid, Demoda sp. vittata, Casey, (=, Demoda lineata, Bond., ) p. 19]. Demoda lineata - Bond. (Curculionidae): [Systematics]. Demoda sp. vittata - Casey (Curculionidae): [Systematics]. Desiantha novica (Curculionidae). Desiantha praemorsa - Lea (Curculionidae): [Systematics]. Dionychus trifasciatus - Hust. (Curculionidae): [Systematics, (=, Cholus trizonatus, Gunth., ) p. 17]. Diplogrammus maculipes - Chevr. (Curculionidae): [Systematics, reduced to form of, Diplogrammus quadrivittatus, Ol., Diplogrammus nitidulus, Fiedl., reduced to form of, Diplogrammus amoenus, Rosensch., p. 18]. Dissopygus metalleacens - Boh. (Curculionidae): [Systematics, (=,Dissopygus oblongus, Casey, ) p. 19]. Dissopygus oblongus - Casey (Curculionidae): [Systematics]. Entimus granulatus - L. (Curculionidae): [Systematics, (=, Entimus speciosus, Er., ) p. 12].Entimus speciosus - Er. (Curculionidae): [Systematics].Erycosomus bruchi - Hust. (Curculionidae): [Systematics].Erycosomus vergarae - Reed (Curculionidae): [Systematics, (=, Erycosomus bruchi, Hust., ) from, Centrinus, p. 18].Eubulus bruchi - Hust. (Curculionidae): [Systematics].Eubulus miniatus - Boh. (Curculionidae): [Systematics, (=, Eubulus bruchi, Hust., ) from, Cryptorhynchus, p. 18]. Eucalus - Lac. (Curculionidae): [Systematics, (=, Gayella, Hust., ) p. 19].Eudius varians - Blanch (Curculionidae): [Systematics].Falklandiellus (Curculionidae): [Gen nov, gen. n., for, Falklandiussuffodens, End., (type), F. inaequalis, Champ., p. 14].Falklandius antarcticus - Stierl. (Curculionidae): [Systematics, (=, Falklandius brachyomma, Enderl., p. 14) from, Otiorhynchus, p. 11,Falklandius suffodens, Falklandius inaequalis, see, Falklandiellus].Falklandius brachyomma - Enderl. (Curculionidae): [Systematics].Falklandius inaequalis (Curculionidae). Falklandius suffodens - End. (Curculionidae): [Systematics]. Graphognathus minor - Buch. (Curculionidae): [Systematics, (=,Naupactus breviscapus, Hust., ) p. 10]. Hammatostylus argala - Er. (Curculionidae): [Systematics, (=,Hammatostylus criniger, Champ., ) p. 17]. Hammatostylus criniger - Champ. (Curculionidae): [Systematics]. Heilipus (Curculionidae). Heilipus bisignatus - Redt. (Curculionidae): [Systematics]. Heilipus concinnus - Phil. (Curculionidae): [Systematics]. Homalostylus aduncus - Er. (Curculionidae): [Systematics, (=,Homalostylus geniculatus, Hust., ) from, Sphenophorus, Homalostylus tornowi, Breth., from, Rhodobaenus, p. 20]. Homalostylus geniculatus - Hust. (Curculionidae): [Systematics]. Homalostylus tornowi - Breth. (Curculionidae): [Systematics]. Hyperodes lineaticollis - Blanch. (Curculionidae): [Systematics]. Hyperodes minutus - Blanch. (Curculionidae): [Systematics]. Hyperodes ornatipennis - Blanch. (Curculionidae): [Systematics, Hyperodes lineaticollis, Blanch., Hyperodes minutus, Blanch., from,Phytonomus, p. 14]. Hypocoeliodes ganglionus - Boh. (Curculionidae): [Systematics, from,Coeliodes, p. 19].Iphipus rudis - Boh. (Curculionidae): [Systematics]. Listroderes (Curculionidae). Listroderes angusticeps - Blanch. (Curculionidae): [Systematics]. Listroderes antarctixa - Ger. (Curculionidae): [Systematics]. Listroderes apicalis - Waterh. (Curculionidae): [Systematics, (=,Listroderes argentinensis, Hust., ), Listroderes rugipennis, Blanch., (=, Listroderes antarctixa, Ger., Listroderes katerensis, Champ., ),Listroderes vulsa, End., (=, Listroderes gibbera, End., ), Listroderes falklandica, End., (=, Listroderes bracteata, End., ), Listroderes cineraria, Blanch., (=, Listroderes liliputana, Ger., ), Listroderes tuberculifera, Blanch., (=, Listroderes binodosa, Ger., ), Listroderes delaiguei, Ger., (=, Desiantha praemorsa, Lea, ), Listroderes obliqua, Klug, Listroderes angusticeps, Blanch., varr. of, Listroderes costirostris, Schonh., Listroderes c. obliqua, (=, Listroderes difficilis, Germ., Listroderes hypocrita, Hust., Desiantha novica, French), Listroderes bimaculata, Boh., (=, Listroderes lugubris, Germ., Listroderes costirostris angusticeps, Blanch., Listroderes slictica, Germ., ) p. 13, Listroderes succincta, Boh., (=, Listroderes vulgaris, Germ., ), Listroderes ovata, Boh., (=, Listroderes chalceata, Blanch., Listroderes nodifera, Boh., Listroderes tristis, Ger., ), Antarctobius, a subgen., Trachodema, a subgen. & transferred from Rhytirhininae p. 14]. Listroderes argentinensis - Hust. (Curculionidae): [Systematics]. Listroderes bimaculata - Boh. (Curculionidae): [Systematics]. Listroderes binodosa - Ger. (Curculionidae): [Systematics]. Listroderes bracteata - End. (Curculionidae): [Systematics]. Listroderes c. obliqua (Curculionidae). Listroderes chalceata - Blanch. (Curculionidae): [Systematics]. Listroderes cineraria - Blanch. (Curculionidae): [Systematics]. Listroderes compressiventris - End. (Curculionidae): [Systematics]. Listroderes costirostris - Schonh. (Curculionidae): [Systematics]. Listroderes costirostris angusticeps - Blanch. (Curculionidae): [Systematics]. Listroderes delaiguei - Ger. (Curculionidae): [Systematics]. Listroderes difficilis - Germ. (Curculionidae): [Systematics]. Listroderes falklandica - End. (Curculionidae): [Systematics]. Listroderes gibbera - End. (Curculionidae): [Systematics]. Listroderes hypocrita - Hust. (Curculionidae): [Systematics]. Listroderes katerensis - Champ. (Curculionidae): [Systematics]. Listroderes liliputana - Ger. (Curculionidae): [Systematics]. Listroderes lugubris - Germ. (Curculionidae): [Systematics]. Listroderes nodifera - Boh. (Curculionidae): [Systematics]. Listroderes nordenskioldi - End. (Curculionidae): [Systematics]. Listroderes obliqua - Klug (Curculionidae): [Systematics]. Listroderes ovata - Boh. (Curculionidae): [Systematics]. Listroderes rugipennis - Blanch. (Curculionidae): [Systematics]. Listroderes schythei - Ger. (Curculionidae): [Systematics]. Listroderes slictica - Germ. (Curculionidae): [Systematics]. Listroderes succincta - Boh. (Curculionidae): [Systematics]. Listroderes tristis - Ger. (Curculionidae): [Systematics].  Listroderes tuberculifera - Blanch. (Curculionidae): [Systematics]. Listroderes vulgaris - Germ. (Curculionidae): [Systematics]. Listroderes vulsa - End. (Curculionidae): [Systematics]. Lixellus - Lec (Curculionidae): [Systematics]. Lixodes - Pasc. (Curculionidae): [Systematics, transferred from Erirhininae to Cholinae p. 15, Lixodes obtusus, see, Acrotomopus]. Madarellus - Casey (Curculionidae): [Systematics, (=, Willinkia, Bond., ) p. 19]. Madarus biplagiatus - Boh. (Curculionidae): [Systematics, (=, Madarus reductus, Casey, ), Madarus latus, Casey, a valid sp. p. 19]. Madarus latus - Casey (Curculionidae): [Systematics]. Madarus reductus - Casey (Curculionidae): [Systematics]. Malvinius (Curculionidae): [Gen nov, gen. n., for, Listroderes compressiventris, End., (type), Listroderes nordenskioldi, End., (=, Malvinius divaricata, End., ) transferred from Cylindrorhininae to Leptopinae p. 11]. Malvinius divaricata - End. (Curculionidae): [Systematics]. Microrhinus - Chevr. (Curculionidae): [Systematics, (=, Brachybaris, Faust., ) transferred from Pterocolinae to Baridinae p. 17].Minurophilus violaceipennis - Fairm. & Ger. (Curculionidae): [Systematics, from, Rhynchites, p. 16].Mionarthrus (Curculionidae): [Gen nov, gen. n., for, Platyomus cinerascens, Blanch., p. 11].Naupactus breviscapus - Hust. (Curculionidae): [Systematics].Omoides variabilis (Curculionidae).Otiorhynchus (Curculionidae).Ovanius niger - Hust. (Curculionidae): [Systematics, raised to sp. (not var. of, Ovanius picipennis, Boh., ) p. 19].Ovanius picipennis - Boh. (Curculionidae): [Systematics].Paulaenius subcostata - Waterh. (Curculionidae): [Systematics, Paulaenius carinicollis, Blanch., (with, Paulaenius var. caudiculata, Fairm., ), Paulaenius percostata, Fairm. & Ger., (=, Cylindrorhinus costatus, Redt., p. 13), Paulaenius cupreosquamosa, Ger., Paulaenius thermarum, Ger., from, Listroderes, Paulaenius sordidus, Burm., (=, Listroderes schythei, Ger., p. 13) from, Cylindrorhinus, p. 12].Paulsenius (Curculionidae).Pentarthrum affine - Woll. (Curculionidae): [Systematics].Pentarthrum castaneum - Blanch. (Curculionidae): [Systematics, (=, Cossonus nigropiceus, Phil., Pentarthrum nitidum, Woll., Pentarthrum affine, Woll., ) p. 21]. Pentarthrum nitidum - Woll. (Curculionidae): [Systematics]. Philippius insignis - Ger. (Curculionidae): [Systematics]. Philippius laesicollis - Fairm. & Ger. (Curculionidae): [Systematics]. Philippius superbus - Reed (Curculionidae): [Systematics, (=, Philippius insignis, Ger., ), Philippius laesicollis, Fairm. & Ger., (=, Anchonus planipennis, Chevr., ) from, Heilipus, p. 13]. Philonis crucifer - Breth. (Curculionidae): [Systematics, from, Cryptorhynchus, p. 18]. Phyllerythrurus laetus - Er. (Curculionidae): [Systematics, (=, Phyllerythrurus luteus, Hust., ) from, Sphenophorus, p. 20]. Phyllerythrurus luteus - Hust. (Curculionidae): [Systematics]. Phytonomus (Curculionidae). Platyaspistes alternans - Bruch 1914 (Curculionidae): [Systematics]. Platyaspistes alternans - Fhs. (Curculionidae): [Systematics]. Platyaspistes argentinensis (Curculionidae): [Nom nov]. Platyaspistes glaucus - Fhs. (Curculionidae): [Systematics, (=, Platyaspistes alternans, Fhs., ), Platyaspistes prasinus, Er., (=, Platyaspistes limbatus, Chevr., ), Platyaspistes marginalis, Fhs., (=, Platyaspistes validus, Chevr., ), Platyaspistes lateralis, Chevr., (=, Platyaspistes prasinus var., Fhs., ), Platyaspistes argentinensis, n. n., for, Platyaspistes alternans, Bruch 1914, Hustache 1938 p. 11]. Platyaspistes lateralis - Chevr. (Curculionidae): [Systematics]. Platyaspistes limbatus - Chevr. (Curculionidae): [Systematics]. Platyaspistes marginalis - Fhs. (Curculionidae): [Systematics]. Platyaspistes prasinus - Er. (Curculionidae): [Systematics]. Platyaspistes prasinus var. - Fhs. (Curculionidae): [Systematics]. Platyaspistes validus - Chevr. (Curculionidae): [Systematics]. Platyomus cinerascens - Blanch. (Curculionidae): [Systematics]. Polydius caelestinus - Perty (Curculionidae): [Systematics, (=, Polydius orbignyi, Chevr., ) p. 12]. Polydius orbignyi - Chevr. (Curculionidae): [Systematics]. Porteriella brevis (Curculionidae). Porteriella singularis - Hust. (Curculionidae): [Systematics].   eudhyperodes - Hust. (Curculionidae): [Systematics]. Relistrodes - Breth. (Curculionidae): [Systematics]. Rhodobaenus (Curculionidae). Rhopalomerus tenuirostris - Blanch. Curculionidae): [Systematics, (=, Anthonomus chilensis, Schenkl., ) p. 15]. Rhyephenes philippii - Fiedl. (Curculionidae): [Systematics]. Rhyephenes sulcatus - Phil. (Curculionidae): [Systematics, (=, Rhyephenes philippii, Fiedl., ) p. 18]. Rhyssomatus ater - Phil. (Curculionidae): [Systematics]. Rhyssomatus crenulatus - Blanch. (Curculionidae): [Systematics]. Rhyssomatus exaratus - Blanch (Curculionidae): [Systematics]. Scirpicola (Curculionidae): [Gen nov, gen. n., for, Sphenophorus chilensis, Blanch., (valid sp. not syn. of, Iphipus rudis, Boh., ) transferred from Amalactinae to Baridinae p. 16]. Sibinia - Germ. (Curculionidae): [Systematics, (=, Teratonychus, Bond., ), Sibinia sellatus, Boh., from, Ceuthorrhynchus, Sibinia albovittatus, Blanch., Sibinia vitticollis, Blanch., Sibinia flavipes, Blanch., from, Tychius, p. 17]. Sibinia albovittatus - Blanch. (Curculionidae): [Systematics]. Sibinia flavipes - Blanch. (Curculionidae): [Systematics]. Sibinia sellatus - Boh. (Curculionidae): [Systematics]. Sibinia vitticollis - Blanch. (Curculionidae): [Systematics]. Solenopus nitidicollis - Chevr. (Curculionidae): [Systematics]. Solenopus sexmaculatus - Ol. (Curculionidae): [Systematics, (=, Solenopus nitidicollis, Chevr., ) p. 17]. Squamamitrus - Voss (Curculionidae): [Systematics]. Stenommatus canus - Phil. (Curculionidae): [Systematics, from, Cossonus, p. 21]. Strongylopterus nitidirostris - Auriv. (Curculionidae): [Systematics]. Strongylopterus ovatus - Boh. (Curculionidae): [Systematics, (=, Strongylopterus nitidirostris, Auriv., ) p. 18]. Tartarisus griseus - Phil. (Curculionidae): [Systematics]. Tartarisus perforatipennis - Blanch. (Curculionidae): [Systematics]. Tartarisus signatipennis - Blanch. (Curculionidae): [Systematics, (=, Heilipus concinnus, Phil., Heilipus bisignatus, Redt., ), Tartarisus perforatipennis, Blanch., Tartarisus griseus, Phil., from, Heilipus, p. 15]. Testalthea versicolor - Bond. (Curculionidae): [Systematics]. Thaliabaridia (Curculionidae): [Gen nov, gen. n., for, Thaliabaris kuscheli, Bond., (type), Testalthea versicolor, Bond., p. 20]. Thaliabaris kuscheli - Bond. (Curculionidae): [Systematics]. Trachodema (Curculionidae). Trichocyphus - Hell. (Curculionidae): [Systematics, (=, Squamamitrus, Voss, ), Trichocyphus formosus, Er., (=, Amitrus nitidicollis, Voss, ) p. 11]. Trichocyphus formosus - Er. (Curculionidae): [Systematics]. Tychius (Curculionidae). Gayella - Hust. (Masaridae): [Systematics].10aAcrotomopus10aAcrotomopus atropunctellus10aAcrotomopus obtusus10aAdioristus10aAdioristus apiculatus10aAdioristus fuegianus10aAdioristus rubripes10aAdioristus rugatus10aAegorhinus eschscholtzi10aAegorhinus fasciatus10aAegorhinus nodipennis10aAegorhinus reticulatus10aAegorhinus strumosus10aAegorhinus subrugosus10aAegorhinus superciliosus10aAegorhinus vermicularis10aAegorhinus vitulus10aAlastoropolus10aAlastoropolus vitulus10aAmitrus10aAmitrus alutaccus10aAmitrus nitidicollis10aAnchodemus10aAnchonus planipennis10aAntarctobius10aAnthonomus10aAnthonomus chilensis10aAnthonomus ornatus10aAnthonomus redtenbacheri10aApion chilense10aApion meorrhynchum10aApion pachymerum10aApion tenebricosum10aBaris flavipes10aBaris tenuis10aBerberidicola10aBrachybaris10aCalandra chilensis10aCalandra laevicosta10aCalvertius tuberosus10aCentrinus10aCentrinus carinatus10aCeuthorrhynchus10aChalcodermus lunatus10aChalcodermus speculifer10aChilebaris10aChileudius10aCholus10aCholus atropunctellus10aCholus dealbatus - Boh10aCholus ornatus10aCholus trizonatus10aCnemecoelus10aCoeliodes10aConothorax10aConotrachelus aequalis10aConotrachelus cervinus10aConotrachelus glaber10aConotrachelus irroratus10aConotrachelus kirschi10aConotrachelus pullus10aConotrachelus striatus10aConotrachelus subnebulosus10aCossonus10aCossonus nigropiceus10aCryptorhynchus10aCydianerus chevrolati10aCydianerus latruncularius10aCylindrorhinus10aCylindrorhinus angulatus10aCylindrorhinus angulatus var. scrobiculatus10aCylindrorhinus costatus10aCylindrorhinus denticulatus10aCylindrorhinus griseus10aCylindrorhinus inquinatus10aCylindrorhinus lactifer10aCylindrorhinus quadrilineatus10aCylindrorhinus sordidus10aCylindrorhinus sulcatus10aDemoda kuscheli10aDemoda lineata10aDesiantha novica10aDesiantha praemorsa10aDionychus trifasciatus10aDiplogrammus maculipes10aDissopygus metalleacens10aDissopygus oblongus10aEntimus granulatus10aEntimus speciosus10aErycosomus bruchi10aErycosomus vergarae10aEubulus bruchi10aEubulus miniatus10aEucalus10aEudius varians Falklandiellus10aFalklandius antarcticus10aFalklandius brachyomma10aFalklandius inaequalis10aFalklandius suffodens10aGraphognathus minor10aHammatostylus argala10aHammatostylus criniger10aHeilipus10aHeilipus (Curculionidae).10aHeilipus bisignatus10aHeilipus concinnus10aHomalostylus aduncus10aHomalostylus geniculatus10aHomalostylus tornowi10aHyperodes lineaticollis10aHyperodes minutus10aHyperodes ornatipennis10aHypocoeliodes ganglionus10aIphipus rudis Listroderes10aListroderes angusticeps10aListroderes antarctixa10aListroderes apicalis10aListroderes argentinensis10aListroderes bimaculata10aListroderes binodosa10aListroderes bracteata10aListroderes c. obliqua10aListroderes chalceata10aListroderes cineraria10aListroderes compressiventris10aListroderes costirostris10aListroderes costirostris angusticeps10aListroderes delaiguei10aListroderes difficilis10aListroderes falklandica10aListroderes gibbera10aListroderes hypocrita10aListroderes katerensis10aListroderes liliputana10aListroderes lugubris10aListroderes nodifera10aListroderes nordenskioldi10aListroderes obliqua10aListroderes ovata10aListroderes rugipennis10aListroderes schythei10aListroderes slictica10aListroderes succincta10aListroderes tristis10aListroderes tuberculifera10aListroderes vulgaris10aListroderes vulsa10aLixellus10aLixodes10aMadarellus10aMadarus biplagiatus10aMadarus latus10aMadarus reductus10aMalvinius10aMalvinius divaricata10aMicrorhinus10aMinurophilus violaceipennis10aMionarthrus10aNaupactus breviscapus10aOmoides variabilis10aOtiorhynchus10aOvanius niger10aOvanius picipennis10aPaulaenius subcostata10aPaulsenius10aPentarthrum affine10aPentarthrum castaneum10aPentarthrum nitidum10aPhilippius insignis10aPhilippius laesicollis10aPhilippius superbus10aPhilonis crucifer10aPhyllerythrurus laetus10aPhytonomus10aPlatyaspistes alternans10aPlatyaspistes argentinensis10aPlatyaspistes glaucus10aPlatyaspistes lateralis10aPlatyaspistes limbatus10aPlatyaspistes marginalis10aPlatyaspistes prasinus10aPlatyaspistes prasinus.10aPlatyaspistes validus10aPlatyomus cinerascens10aPolydius caelestinus10aPolydius orbignyi10aPorteriella brevis10aPorteriella singularis10aPseudhyperodes10aRelistrodes10aRhodobaenus10aRhopalomerus tenuirostris10aRhyephenes philippii10aRhyephenes sulcatus10aRhynchites10aRhyssomatus ater10aRhyssomatus crenulatus10aRhyssomatus exaratus10aScirpicola10aScirpicola chilensis10aSibinia10aSibinia albovittatus10aSibinia flavipes10aSibinia sellatus10aSibinia vitticollis10aSitophilus granarius10aSitophilus oryza10aSolenopus nitidicollis10aSolenopus sexmaculatus Squamamitrus Stenommatus canus10aStrongylopterus nitidirostris10aStrongylopterus ovatus10aTartarisus griseus10aTartarisus perforatipennis10aTartarisus signatipennis10aTestalthea versicolor10aThaliabaridia10aThaliabaris kuscheli10aTrachodema10aTrichocyphus10aTrichocyphus formosus10aTychius1 aKuschel, G.  uhttps://weevil.myspecies.info/node/1403001663nas a2200181   4500008004100000020001400041245007300055210006900128260000900197300001200206490000700218520106900225653002101294100002401315700002101339700002401360856009701384       2009                        eng d  a1388-554500aPhoretic dispersal of entomopathogenic nematodes by Hylobius abietis0 aPhoretic dispersal of entomopathogenic nematodes by Hylobius abi  c2009  a419-4270 v113 aPhoresis is a strategy in which one organism (the phoretic) attaches to another (the host) for the implied purpose of dispersal and is valuable for small flightless invertebrates with limited mobility. Previous work has shown that the relatively immobile larvae of Hylobius abietis (the large pine weevil) are highly susceptible to entomopathogenic nematodes (EPN) and support nematode reproduction whereas adults do not. Here, we demonstrate that the infective juveniles (IJ) of two species of EPN, Heterorhabditis megidis and Steinernema carpocapsae, can use the resistant but highly mobile adults of H. abietis for phoretic dispersal. The ability to use adult H. abietis for phoresis depended on nematode species and habitat (sand vs peat) and there was no evidence of sex-biased dispersal in S. carpocapsae for which the IJ are dioecious. We hypothesise that phoretic dispersal may be a significant mechanism to avoid sibling competition and inbreeding in EPN, which produce tens of thousands of offspring at point sources in a relatively impenetrable habitat.10aHylobius abietis1 aKruitbos, Laura, M.1 aHeritage, Stuart1 aWilson, Michael, J.  uhttps://weevil.myspecies.info/phoretic-dispersal-entomopathogenic-nematodes-hylobius-abietis00769nas a2200265   4500008004100000245004300041210004000084300001600124490000600140653002100146653002300167653001600190653002900206653001500235653001900250653002100269653002500290653002400315653002600339653001100365653002000376653002400396100001300420856007000433       1933                        eng d00aDie Hylobiinen aus Formosa (Col. Curc)0 aDie Hylobiinen aus Formosa Col Curc  app. 182-1890 v710aAclees hirayamai10aAclees taiwanensis10aDysceroides10aDysceroides bipustulatus10aHylobiinae10aHylobius kanoi10aHylobius minowai10aHylobius niitakensis10aHylobius pustulatus10aHylobius rectirostris10aKobuzo10aKobuzo kikuchii10aKobuzo rectirostris1 aKono, H.  uhttps://weevil.myspecies.info/die-hylobiinen-aus-formosa-col-curc01766nas a2200169   4500008004500000245020300045210006900248260001000317300001000327490000600337520102200343653002101365100002101386700002501407700002901432856013501461       2008                        Engldsh  00aInfestation by a Nalepella species induces emissions of alpha - and beta -farnesenes, (-)-linalool and aromatic compounds in Norway spruce clones of different susceptibility to the large pine weevil0 aInfestation by a Nalepella species induces emissions of alpha an  cMarch  a31-410 v23 aThe emissions of spruce grafts (Picea abies), caused by infestation of an acarid species of the genus Nalepella were investigated. Volatiles of three clones, both healthy and infested, with different susceptibility to the large pine weevil Hylobius abietis were collected by solid phase micro extraction (SPME) and analyzed by gas chromatograph coupled to mass-spectrometry (GC-MS). In addition, enantiomers of the main chiral compounds were separated by a two dimensional-gas chromatograph (2DGC). In the characteristic flower-like fragrances emitted by the infested grafts large amounts of E-[beta]-farnesene, E,E-[alpha]-farnesene, (-)-linalool, methyl salicylate and minute amounts of benzyl alcohol, E-anethole, methyl benzoate, neral and geranial were found. All together, these compounds could explain the characteristic scent emitted by the infested seedlings. Large differences in the emissions of E-[beta]- farnesene, E,E-[alpha]-farnesene and methyl salicylate were found between but not within the clones.10aHylobius abietis1 aKannaste, Astrid1 aVongvanich, Namphung1 aBorg-Karlson, Anna-Karin  uhttps://weevil.myspecies.info/infestation-nalepella-species-induces-emissions-alpha-and-beta-farnesenes-linalool-and-aromatic-comp02457nas a2200169   4500008004100000020001400041245016200055210006900217260000800286300001200294490000700306520176300313653002102076100002802097700002702125856013502152       2012                        eng d  a0307-694600aHost activity and wasp experience affect parasitoid wasp foraging behaviour and oviposition on nematode-infected larvae of the forestry pest Hylobius abietis0 aHost activity and wasp experience affect parasitoid wasp foragin  cAug  a269-2820 v373 a1. Entomopathogenic nematodes (EPN) are currently being used as introduced biological control agents against the larvae of the native European forestry pest Hylobius abietis L. which develop under the bark of stumps and roots of newly dead conifer trees. 2. The potential for resource competition between gregarious ectoparasitoid Bracon hylobii Ratz and EPN by recording oviposition and related behaviours of B. hylobii females on EPN-infected H. abietis larvae was investigated. Wasps did not parasitise EPN-infected host larvae that were dead when presented, but naive and experienced wasps parasitised live EPN-infected hosts. Naive wasps parasitised live EPN-infected hosts significantly less frequently than healthy hosts only when the infected larvae were close to death (i.e. died during 24-h trial). Parasitism by experienced wasps was unaffected by host infection. 3. Wasp probing and oviposition were positively associated with the amount of host movement. Preventing H. abietis larvae from chewing on bark significantly reduced parasitism by naive, but not experienced wasps. 4. The number of eggs per clutch was not affected by bark chewing or EPN-infection of H. abietis larvae. 5. Naive and experienced B. hylobii parasitised two abnormal hosts (larvae of coleopteran Rhagium bifasciatum Fabricius and lepidopteran Galleria mellonella L.), both of which moved and chewed on bark during trials. 6. It was concluded that B. hylobii can use vibrational cues generated by host movement and feeding to locate hosts at short range and accepts unsuitable (EPN-infected or abnormal) hosts as long as these create such cues. The implications for competition between B. hylobii and EPN and possible ways of minimising it when applying EPN are discussed.10aHylobius abietis1 aHarvey, Christopher, D.1 aGriffin, Christine, T.  uhttps://weevil.myspecies.info/host-activity-and-wasp-experience-affect-parasitoid-wasp-foraging-behaviour-and-oviposition-nematode02884nas a2200181   4500008004100000020001400041245017900055210006900234260000800303300002200311490000700333520212700340653002102467100002802488700002402516700002702540856013502567       2012                        eng d  a1049-964400aThe impact of entomopathogenic nematodes on a non-target, service-providing longhorn beetle is limited by targeted application when controlling forestry pest Hylobius abietis0 aimpact of entomopathogenic nematodes on a nontarget serviceprovi  cSep  aNIL_0059-NIL_00680 v623 aEntomopathogenic nematodes are being applied to tree stumps on coniferous clearfell sites in Europe for inundative biological control of the large pine weevil (Hylobius abietis; Coleoptera: Curculionidae), a major forestry pest. We investigated the risk that two nematode species, Steinernema carpocapsae and Heterorhabditis downesi (Nematoda: Rhabditidae), present to longhorn beetle Rhagium bifasciatum (Coleoptera: Cerambycidae), a service-providing, non-target saproxylic insect on clearfell sites. In a Petri dish assay, larvae of R. bifasciatum were less susceptible (LC50 24-42) than pupae or adults (LC50 <= 10) to infective juveniles (IJs) of S. carpocapsae and H. downesi. S. carpocapsae and H. downesi reproduced within R. bifasciatum larvae, pupae and adults, with up to 130,000 IJs emerging per insect. When we applied 1.8 million IJs (half the number recommended per tree stump containing pine weevil) to deadwood logs in laboratory and field experiments, both nematode species infected more than 50% of R. bifasciatum within the logs. Field application at a lower, more realistic rate (18,000 IJs per log) resulted in 0-11% infection. The two nematode species caused similar rates of infection within logs and infected R. bifasciatum larvae more than 4 cm deep within the wood. On six clearfell sites sampled one to twelve months after S. carpocapsae had been inundatively applied to tree stumps for suppression of pine weevil, < 10% of deadwood logs contained infected R. bifasciatum and < 4% of 1989 R. bifasciatum individuals in logs were infected. Infection was recorded a year after nematodes had been applied, however, suggesting that nematodes were recycling within logs in the field. Incidence of R. bifasciatum infection decreased significantly with increasing distance between a log and the nearest treated tree stump. Thus, our results indicate that entomopathogenic nematodes can infect and recycle in R. bifasciatum, but that the risk to this and other saproxylic non-target insects is limited by the targeted application of nematodes to tree stumps. (C) 2012 Elsevier Inc. All rights reserved.10aHylobius abietis1 aHarvey, Christopher, D.1 aAlameen, Khalil, M.1 aGriffin, Christine, T.  uhttps://weevil.myspecies.info/impact-entomopathogenic-nematodes-non-target-service-providing-longhorn-beetle-limited-targeted-appl01065nas a2200181   4500008004100000020002500041245004500066210004400111260001300155300001000168490000700178520054500185653002100730100002000751700001900771700002500790856006800815       2009                        eng d  a1815-5103; 1815-511100aOccurrence of Hylobius spp. in Carinthia0 aOccurrence of Hylobius spp in Carinthia  cDezember  a10-140 v483 aThe occurrence of Hylobius spp. was investigated at several localities in the Carinthian districts of Feldkirchen, Klagenfurt-Land and of Valkermarkt in the year 2005. Another aim was to test the lure effect of different tree species as trap material to attract beetles. In total, 5276 adult Hylobius spp. - 5256 H. abietis and 20 H. piceus - were collected. The occurrence of these two species was different during the seasons. in the majority of cases more beetles were collected on spruce bark pieces than on pine and larch log sections.10aHylobius abietis1 aGriesser, Sonja1 aKritsch, Peter1 aWegensteiner, Rudolf  uhttps://weevil.myspecies.info/occurrence-hylobius-spp-carinthia01871nas a2200217   4500008004500000020001400045245007700059210006900136260001000205300001200215490000800227520117200235653001801407653002101425653002401446100002201470700002201492700002301514700001701537856009901554       2008                        Engldsh    a0953-756200aBeauveria caledonica is a naturally occurring pathogen of forest beetles0 aBeauveria caledonica is a naturally occurring pathogen of forest  cMarch  a352-3600 v1123 aIn New Zealand, two introduced scolytid beetles, Hylastes ater and Hylurgus ligniperda (Curculionidae: Scolytinae) are pests in pine plantations. Investigation of the naturally occurring pathogens of these exotic pests revealed that both are attacked by Beauveria caledonica, a species originally isolated and described from soil in Scotland. The isolates in New Zealand were identical in morphology and conserved DNA region (rDNA, elongation factor a) sequence to isolates held in the USDA-ARS insect pathogens culture collection. In bioassay, the B. caledonica isolates were highly pathogenic to adults of H. ligniperda and larvae of Tenebrio molitor. Sporulation. was observed on cadavers, confirming the species can utilise the cadavers. As both species were likely to have been introduced to New Zealand from Europe, a search was made for B. caledonica in the northern UK and Ireland. The fungus was found as a naturally-occurring pathogen of the weevil pest, Hylobius abietis (Curculionidae: Scolytinae), developing in spruce and other beetles in forests in both regions. (C) 2007 The British Mycological Society. Published by Elsevier Ltd. All rights reserved.10aHylastes ater10aHylobius abietis10aHylurgus ligniperda1 aGlare, Travis, R.1 aReay, Stephen, D.1 aNelson, Tracey, L.1 aMoore, Roger  uhttps://weevil.myspecies.info/beauveria-caledonica-naturally-occurring-pathogen-forest-beetles02123nas a2200193   4500008004100000020001400041245016600055210006900221260000800290300001200298490000800310520138200318653002101700100002001721700001401741700001901755700002001774856013501794       2010                        eng d  a0022-201100aThe lethal and sub-lethal consequences of entomopathogenic nematode infestation and exposure for adult pine weevils, Hylobius abietis (Coleoptera: Curculionidae)0 alethal and sublethal consequences of entomopathogenic nematode i  cJul  a195-2020 v1043 aEntomopathogenic nematodes (EPN) frequently kill their host within 1-2 days, and interest in EPN focuses mainly on their lethality. However, insects may take longer to die, or may fail to die despite being infected, but little is known about the effects of EPN infection on insects, other than death. Here we investigate both lethal and sub-lethal effects of infection by two EPN species, Steinernema carpocapsae and Heterorhabditis downesi, on adults of the large pine weevil, Hylobius abietis. Following 12 h nematode-weevil contact in peat, S. carpocapsae killed a significantly higher proportion of weevils (87-93%) than H. downesi (43-57%) at all concentrations tested. Less than 10% of weevils were dead within 2 days, and weevils continued to die for up to 10 days after exposure (LT50 of 3 days or more). In a separate experiment, live weevils dissected 6 days after a 24 h exposure to nematodes on filter paper harbored encapsulated and dead nematodes, showing that weevils could defend themselves against infection. Some live weevils also harbored live nematodes 6 days after they had been removed from the nematode infested medium. Feeding by weevils was not affected by infection with, or exposure to, either species of EPN. We discuss these results in relation to the use of EPN in biological control against H. abietis. (C) 2010 Elsevier Inc. All rights reserved.10aHylobius abietis1 aGirling, R., D.1 aEnnis, D.1 aDillon, A., B.1 aGriffin, C., T.  uhttps://weevil.myspecies.info/lethal-and-sub-lethal-consequences-entomopathogenic-nematode-infestation-and-exposure-adult-pine-wee02478nas a2200181   4500008004100000020001400041245020600055210006900261260001000330300001200340490000700352520172600359653002102085100001602106700002002122700001902142856013502161       2009                        eng d  a0007-485300aCompetition and intraguild predation between the braconid parasitoid Bracon hylobii and the entomopathogenic nematode Heterorhabditis downesi, natural enemies of the large pine weevil, Hylobius abietis0 aCompetition and intraguild predation between the braconid parasi  cApril  a151-1610 v993 aIn biological control programmes introduced natural enemies compete with indigenous enemies for hosts and may also engage in intraguild predation when two species competing for the same prey attack and consume one another. The large pine weevil, Hylobius abietis L. (Coleoptera: Curculionidae), is an important pest of coniferous reforestation in Europe. Among its natural enemies, the parasitoid Bracon hylobii Ratz. (Hymenoptera: Braconidae) and entomopathogenic nematodes have potential as biological control agents. Both parasitoid and nematodes target the weevil larvae and, hence, there is potential for competition or intraguild predation.In this study, we examine the interaction of B. hylobii with the nematode Heterorhabditis downesi Stock, Griffin and Burnell (Nematode: Heterorhabditidae), testing the susceptibility of larvae, pupae and adults of B. hylobii to H. downesi and whether female parasitoids discriminate between nematode-infected and uninfected weevils for oviposition. In choice tests, when weevils were exposed to nematodes 1-7 days previously, no B. hylobii oviposited on nematode-infected weevil larvae. Up to 24 h, healthy weevils were twice as likely as nematode-infected ones to be used for oviposition. Bracon hylobii females did not adjust clutch size; nematode-infected hosts were either rejected or the parasitoid laid a full clutch of eggs on them.When nematodes were applied to the parasitoid feeding on weevil larvae, the nematodes parasitized the parasitoid larvae, there was a reduction in cocoon formation and fewer cocoons eclosed. Eclosion rate was not reduced when nematodes were applied to fully formed cocoons, but nearly all of the emerging adults were killed by nematodes.10aHylobius abietis1 aEverard, A.1 aGriffin, C., T.1 aDillon, A., B.  uhttps://weevil.myspecies.info/competition-and-intraguild-predation-between-braconid-parasitoid-bracon-hylobii-and-entomopathogenic02839nas a2200193   4500008004500000020001400045245012400059210006900183260001200252300001400264490000700278520211900285653002102404100002102425700002102446700002102467700002202488856013502510       2008                        Engldsh    a0098-033100aAntifeedants and feeding stimulants in bark extracts of ten woody non-host species of the pine weevil, Hylobius abietis0 aAntifeedants and feeding stimulants in bark extracts of ten wood  cOctober  a1290-12970 v343 aBark of ten woody species, known to be rejected as a food source by the pine weevil, Hylobius abietis, were sequentially extracted by a Soxhlet apparatus with pentane followed by methanol. Species were alder (Alnus glutinosa), aspen (Populus tremula), beech (Fagus sylvatica), guelder rose (Viburnum opulus), holly (Ilex aquifolium), horse chestnut (Aesculus hippocastanum), lilac (Syringa vulgaris), spindle tree (Evonymus europaeus), walnut (Juglans regia), and yew (Taxus baccata). Bark of each species was collected in southern Scandinavia during the summer. Resulting extracts were tested for antifeedant activity against the pine weevil by a micro-feeding choice assay. At a dose corresponding to that in the bark, methanol extracts from Aesculus, Taxus, Ilex, and Populus were antifeedant active, while pentane extracts of Aesculus, Fagus, Syringa, and Viburnum were stimulatory. Four known antifeedants against H. abietis, the straight-chained carboxylic acids, hexanoic and nonanoic acid (C6 and C9), carvone, and carvacrol were identified by gas chromatography (GC)-mass spectrometry (MS) in several extracts. The major constituents were identified and tested for feeding deterrence. The aromatic compounds benzyl alcohol and 2-phenylethanol are new non-host plant-derived feeding deterrents for the pine weevil. Additionally, two feeding stimulants, [beta]-sitosterol and 5-(hydroxymethyl)-2-furaldehyde, were identified. One active methanol extract of Aesculus bark was sequentially fractionated by liquid chromatography, and major compounds were tentatively identified as branched alcohols and esters of hexanoic acid. Five commercially available hexanoate esters and two commercially available branched alcohols were identified as new active antifeedants. Both stimulatory and inhibiting compounds were found in the same extracts and co-eluted in the same or adjacent fractions. The mix of semiochemicals of opposite activity in each extract or fraction could explain the stimulatory-, inhibitory-, or sometimes neutral activity. Generally, such co-occurrence confounds the isolation of antifeedants.10aHylobius abietis1 aEriksson, Carina1 aMansson, Per, E.1 aSjodin, Kristina1 aSchlyter, Fredrik  uhttps://weevil.myspecies.info/antifeedants-and-feeding-stimulants-bark-extracts-ten-woody-non-host-species-pine-weevil-hylobius-ab02127nas a2200181   4500008004100000020002500041245009400066210006900160260000800229300001200237490000700249520148100256653002101737100002301758700002201781700002701803856011501830       2010                        eng d  a0003-3472; 1095-828200aPine weevils modulate defensive behaviour in response to parasites of differing virulence0 aPine weevils modulate defensive behaviour in response to parasit  cAug  a283-2880 v803 aGrooming and avoidance of contaminated areas are among the behavioural defences employed by animals against parasites. Antiparasite defence behaviour is costly in terms of time, energy and/or food foregone and therefore animals are expected to modulate their defences depending on the risk of attack and/or the severity of the symptoms caused. We tested the hypothesis that an insect host invests more in defence against more virulent (more likely to cause death) than less virulent parasites. We tested avoidance and grooming of adult pine weevils, Hylobius abietis, in response to infective juveniles of two species of entomopathogenic nematodes, the more virulent Steinernema carpocapsae and less virulent Heterorhabditis downesi. Weevils avoided feeding on a substrate contaminated with S. carpocapsae but not H. downesi. Weevils also groomed more when their bodies were contaminated with S. carpocapsae than either H. downesi or water. We also made direct observations of nematodes on weevils. When equal numbers of nematodes were applied to weevils more S. carpocapsae than H. downesi moved actively on the weevil's cuticle. Thus, the differential response of weevils to the two nematode species can be explained by the weevils detecting the more aggressive behaviour of S. carpocapsae than H. downesi, which corresponds to a higher probability of death. [copyright] 2010 The Association for the Study of Animal Behaviour. Published by Elsevier Ltd. All rights reserved.10aHylobius abietis1 aEnnis, Darragh, E.1 aDillon, Aoife, B.1 aGriffin, Christine, T.  uhttps://weevil.myspecies.info/pine-weevils-modulate-defensive-behaviour-response-parasites-differing-virulence02674nas a2200193   4500008004100000020001400041245014700055210006900202260000800271300001200279490000800291520193500299653002102234100002302255700002502278700001602303700002602319856013502345       2011                        eng d  a0013-870300aCordeauxia edulis and Rhododendron tomentosum extracts disturb orientation and feeding behavior of Hylobius abietis and Phyllodecta laticollis0 aCordeauxia edulis and Rhododendron tomentosum extracts disturb o  cFeb  a162-1740 v1383 aThe use of plant-based compounds to control insect pests is an alternative to the use of synthetic pesticides. We evaluated the repellent and antifeedant effects of Cordeauxia edulis Hemsley (Fabaceae) and Rhododendron tomentosum Harmaja (Ericaceae) extracts against Hylobius abietis L. (Coleoptera: Curculionidae) and Phyllodecta laticollis Suffrian (Coleoptera: Chrysomelidae). Repellent properties were evaluated by monitoring responses of adult insects toward the odor from extracts or extraction solvents (controls) in a Y-tube olfactometer, and choice or no-choice feeding tests were conducted by applying extracts or extraction solvents on stems of Scots pine (Pinus sylvestris L. (Pinaceae)) and European aspen (Populus tremula L. (Salicaceae)), host plants of H. abietis and P. laticollis, respectively. Extracts of R. tomentosum repelled adults of both insect species effectively. However, extracts of C. edulis did not repel H. abietis although its ethyl acetate extract showed repellence against the adults of P. laticollis. Feeding by H. abietis was significantly reduced by a methanol extract of C. edulis, and methanol and hexane extracts of R. tomentosum. Feeding by the adults and larvae of P. laticollis was significantly reduced by extracts from both plant species. Concomitant with less feeding, larval growth was retarded by ethyl acetate extracts of both plant species. Gas chromatography-mass spectrometry analyses of the volatile components of the extracts showed that extracts from both plant species were mixtures of various terpene and non-terpene compounds, which showed quantitative and/or qualitative variations between plant species and extraction solvents. This experiment showed that extracts from both plant species effectively manipulated the orientation and/or feeding behavior of the two beetle species. Hence, they may be considered as potential alternatives to synthetic chemical pesticides.10aHylobius abietis1 aEgigu, Meseret, C.1 aIbrahim, Mohamed, A.1 aYahya, Asha1 aHolopainen, Jarmo, K.  uhttps://weevil.myspecies.info/cordeauxia-edulis-and-rhododendron-tomentosum-extracts-disturb-orientation-and-feeding-behavior-hylo01216nas a2200169   4500008004100000020001400041245010600055210006900161260000800230300001200238490000700250520059300257653001100850100003000861700003500891856012000926       2010                        eng d  a0085-562600aMorphological aspects of the genitalia of seven species of Heilus Kuschel (Coleoptera, Curculionidae)0 aMorphological aspects of the genitalia of seven species of Heilu  cApr  a157-1640 v543 aMorphological aspects of the genitalia of seven species of Heilus Kuschel (Coleoptera, Curculionidae). Morphological aspects of the male and female genitalia and their associated sclerites, abdominal tergite and sternite 8, are described, illustrated and discussed for seven species of Hellos Kuschel 1955 of tribe and subtribe Hylobiini-Hylobiina. The seven species arc H. faldermanni (Boheman, 1836); H. fasciculatus (Bohemian, 1843); H.,freyreissi (Boheman, 1836); H. myops (Boheman, 1836); H. pupillatus (Olivier, 1790); H. rufescens (Boheman, 1836) and H. tuberculosus (Perry, 1832).10aHeilus1 aSantos, Geane, Brizzola d1 aRosado-Neto, Germano, Henrique  uhttps://weevil.myspecies.info/morphological-aspects-genitalia-seven-species-heilus-kuschel-coleoptera-curculionidae02342nas a2200193   4500008004500000020001400045245012600059210006900185260001300254300001400267490000800281520161100289653002101900100002201921700002001943700002301963700002701986856013502013       2008                        Engldsh    a0378-112700aEvict of infect? Managing populations of the large pine weevil, Hylobius abietis, using a bottom-up and top-down approach0 aEvict of infect Managing populations of the large pine weevil Hy  cApril 20  a2634-26420 v2553 aHylobius abietis is the most important pest of replanted coniferous sites in Northern Europe, where feeding by adult weevils can result in up to 100% mortality of seedlings. Field trials were conducted with the aim of reducing H. abietis populations developing in Sitka spruce stumps by increasing pressure from natural enemies (top-down pressure), and reducing the quality of stumps for development (bottom-up pressure). Top-down pressure was applied through inundative treatment of stumps with entomopathogenic nematodes (Heterorhabditis downesi or Steinernema carpocapsae). Bottom-up pressure was applied by treating stumps with the wood colonising fungus Trichoderma koningii. Natural levels of parasitism of H. abietis by the parasitoid Bracon hylobii and the effect of applied agents on B. hylobii were also investigated. Heterorhabditis downesi parasitised more immature weevils than S. carpocapsae, and significantly reduced numbers of adults emerging from stumps compared to controls. Entomopathogenic nematodes did not significantly impact on populations of B. hylobii, and over three sites the effects of both agents were additive. Stumps modified by application of the fungus (bottom-up pressure) did not have fewer H. abietis developing in, or emerging from them; however, development of H. abietis was more advanced in these stumps, and the success of natural enemies was differentially affected. T. koningii facilitated B. hylobii while having the opposite effect on entomopathogenic nematodes, suggesting that it affected the outcome of competition between the nematodes and the parasitoid.10aHylobius abietis1 aDillon, Aoife, B.1 aMoore, Colm, P.1 aDownes, Martin, J.1 aGriffin, Christine, T.  uhttps://weevil.myspecies.info/evict-infect-managing-populations-large-pine-weevil-hylobius-abietis-using-bottom-and-top-down-appro03089nas a2200205   4500008004500000020001400045245010200059210006900161260001000230300001200240490000700252520238500259653002102644100001902665700002002684700001802704700001902722700002002741856012202761       2008                        Engldsh    a1051-076100aEstablishment, persistence, and introgression of entomopathogenic nematodes in a forest ecosystem0 aEstablishment persistence and introgression of entomopathogenic   cApril  a735-7470 v183 aEntomopathogenic nematodes (EPN) are currently marketed worldwide for use in inundative biological control, where the applied natural enemy population ( rather than its offspring) is expected to reduce insect numbers. Unlike classical biological control, in inundative control natural enemy establishment is not crucial in order to achieve pest suppression. Field trials in Irish forestry provided the opportunity to test predictions regarding the establishment of two exotic (Steinernema carpocapsae and Heterorhabditis megidis) and two indigenous ( Steinernema feltiae and Heterorhabditis downesi) species. Nematodes were inundatively applied to pine stumps to control populations of pine weevil, Hylobius abietis, on three clearcut sites, and their persistence and spread monitored for up to five years. All species were recovered three years after application but only S. feltiae was recovered in years 4 and 5. Limited horizontal dispersal to 20 cm ( but not 100 cm) was observed, but the majority of nematodes were recovered close to the area of application. Steinernema feltiae was also recovered from nearby stumps to which it had not been applied, indicating possible phoretic dispersal by weevils or other stump-associated fauna. EPN were not recovered from stumps outside the treated area, suggesting that such dispersal is quite localized. Two strains of S. feltiae ( Irish and exotic) were applied. Amplified fragment length polymorphism (AFLP) analysis on 11 populations isolated from soil four years later showed that all had a much closer affinity to the applied Irish strain, suggesting persistence of this genotype and extinction of the exotic one. Some strains were clustered close together, and this is interpreted in the light of possible population genetic scenarios. The findings from the field study confirm predictions based on background knowledge of the species and demonstrate the importance of medium-term studies, as a 3-year study would have overestimated the risk of establishment of exotic species. Short-term persistence and spread of S. carpocapsae, S. feltiae, and H. downesi was also studied in pine forest mesocosms. Similar trends to field results, such as limited horizontal dispersal, even vertical distribution, and more abundant recovery of S. feltiae than of other species, point to the utility of mesocosm studies as a predictive tool.10aHylobius abietis1 aDillon, A., B.1 aRolston, A., N.1 aMeade, C., V.1 aDownes, M., J.1 aGriffin, C., T.  uhttps://weevil.myspecies.info/establishment-persistence-and-introgression-entomopathogenic-nematodes-forest-ecosystem03019nas a2200265   4500008004500000020001400045245015600059210006900215260000800284300001200292490000700304520206700311653001902378653002102397653003202418100002002450700002202470700001902492700002202511700002202533700002202555700002002577700002102597856013502618       2008                        Engldsh    a0737-403800aLong-term evolutionary stability of bacterial endosymbiosis in Curculionoidea: additional evidence of symbiont replacement in the Dryophthoridae family0 aLongterm evolutionary stability of bacterial endosymbiosis in Cu  cMay  a859-8680 v253 aBacterial intracellular symbiosis ( endosymbiosis) is well documented in the insect world where it is believed to play a crucial role in adaptation and evolution. However, although Coleopteran insects are of huge ecological and economical interest, endosymbiont molecular analysis is limited to the Dryophthoridae family. Here, we have analyzed the intracellular symbiotic bacteria in 2 Hylobius species belonging to the Molytinae subfamily ( Curculionoidea superfamily) that exhibit different features from the Dryophthoridae insects in terms of their ecology and geographical spanning. Fluorescence in situ hybridization has shown that both Hylobius species harbor rod- shaped pleiomorphic symbiotic bacteria in the oocyte and in the bacteria- bearing organ ( the bacteriome), with a shape and location similar to those of the Dryophthoridae bacteriome. Phylogenetic analysis of the 16S ribosomal DNA gene sequences, using the heterogeneous model of DNA evolution, has placed the Hylobius spp. endosymbionts ( H- group) at the basal position of the ancestral Rclade of Dryophthoridae endosymbionts named Candidatus Nardonella but relatively distant from the S- clade of Sitophilus spp. endosymbionts. Endosymbionts from the H- group and the R- clade evolved more quickly compared with free- living enteric bacteria and endosymbionts from the S- and D- clades of Dryophthoridae. They are AT biased ( 58.3% A + T), and they exhibit AT- rich insertions at the same position as previously described in the Candidatus Nardonella 16S rDNA sequence. Moreover, the host phylogenetic tree based on the mitochondrial COI gene was shown to be highly congruent with the H- group and the R- clade, the divergence of which was estimated to be around 125 MYA. These new molecular data show that endosymbiosis is old in Curculionids, going back at least to the common ancestor of Molytinae and Dryophthoridae, and is evolutionary stable, except in 2 Dryophthoridae clades, providing additional and independent supplementary evidence for endosymbiont replacement in these taxa.10aDryophthoridae10aHylobius abietis10aHylobius transversovittatus1 aConord, Cyrille1 aDespres, Laurence1 aVallier, Agnes1 aBalmand, Severine1 aMiquel, Christian1 aZundel, Stephanie1 aLemperiere, Guy1 aHeddi, Abdelaziz  uhttps://weevil.myspecies.info/long-term-evolutionary-stability-bacterial-endosymbiosis-curculionoidea-additional-evidence-symbiont01312nas a2200229   4500008004100000020001400041245015500055210006900210260002100279300001200300490000700312520041300319653001300732100003200745700002700777700003000804700003100834700002600865700002800891700002800919856013500947       2007                        eng d  a1519-566X00aGenitalia of three species of Heilipus Germar (Coleoptera: Curculionidae) that damage avocado fruits (Persea americana Mill.) in Mexico and Costa Rica0 aGenitalia of three species of Heilipus Germar Coleoptera Curculi  cNovember-Decembe  a914-9180 v363 aThe male and female genitaliae of three species of the genus Heilipus Germar (H. lauri Boheman, H. pittieri Barber and H. trifasciatus Fabricius) that damage avocado fruits (Persea americana Mill.) in Mexico and Costa Rica are described and illustrated. The aedeagus, spiculum gastrale, styli of 8th sternite are different in each one of the three species studied and can be used for specific identification.10aHeilipus1 aCastaneda-Vildozola, Alvaro1 aValdez-Carrasco, Jorge1 aEquihua-Martinez, Armando1 aGonzalez-Hernandez, Hector1 aRomero-Napoles, Jesus1 aSolis-Aguilar, Juan, F.1 aRamirez-Alarcon, Samuel  uhttps://weevil.myspecies.info/genitalia-three-species-heilipus-germar-coleoptera-curculionidae-damage-avocado-fruits-persea-americ00963nas a2200193   4500008004500000020001400045245012000059210006900179260002100248300001200269490000700281520020700288653001900495100003200514700003300546700002800579700002700607856013500634       2009                        Spandsh    a1519-566X00aPersea schiedeana (Lauraceae), a new host of Heilipus lauri Boheman (Coleoptera: Curculionidae) in Veracruz, Mexico0 aPersea schiedeana Lauraceae a new host of Heilipus lauri Boheman  cNovember-Decembe  a871-8720 v383 aThe presence of the Molytinae Heilipus lauri Boheman is reported for the first time attacking fruits of Persea schiedeana, commonly called "chinene" in Huatusco and Zongolica, state of Veracruz, Mexico.10aHeilipus lauri1 aCastaneda-Vildozola, Alvaro1 aDel Angel-Coronel, Oscar, A.1 aCruz-Castillo, Juan, G.1 aValdez-Carrasco, Jorge  uhttps://weevil.myspecies.info/persea-schiedeana-lauraceae-new-host-heilipus-lauri-boheman-coleoptera-curculionidae-veracruz-mexico00889nas a2200169   4500008004100000020002500041245006000066210005700126260000900183300001200192490000700204520035100211653003200562100001900594700002500613856008100638       2011                        eng d  a1392-1657; 1648-691900aNew records of beetles (Insecta: Coleoptera) in Estonia0 aNew records of beetles Insecta Coleoptera in Estonia  c2011  a235-2370 v213 aThe current article presents faunal data on 3 beetle species from Estonia, two of which, Leiopus linnei Wallin, Nylander et Kvamme, 2009 (Cerambycidae) and Hylobius transversovittatus (Goeze, 1777) (Curculionidae), are reported for the local fauna for the first time. General information on the distribution and bionomy of these species is given.10aHylobius transversovittatus1 aBukejs, Andris1 aBalalaikins, Maksims  uhttps://weevil.myspecies.info/new-records-beetles-insecta-coleoptera-estonia02095nas a2200217   4500008004500000020001400045245011000059210006900169260001000238300001200248490000700260520134700267653002101614100001501635700001901650700001801669700001901687700002501706700002001731856012601751       2008                        Engldsh    a0098-033100aStructure-activity relationships of phenylpropanoids as antifeedants for the pine weevil Hylobius abietis0 aStructureactivity relationships of phenylpropanoids as antifeeda  cMarch  a339-3520 v343 aEthyl cinnamate has been isolated from the bark of Pinus contorta in the search for antifeedants for the pine weevil, Hylobius abietis. Based on this lead compound, a number of structurally related compounds were synthesized and tested. The usability of the Topliss scheme, a flow diagram previously used in numerous structure-activity relationship (SAR) studies, was evaluated in an attempt to find the most potent antifeedants. The scheme was initially followed stepwise; subsequently, all compounds found in the scheme were compared. In total, 51 phenylpropanoids were tested and analyzed for SARs by using arguments from the field of medicinal chemistry (rational drug design). Individual Hansch parameters based on hydrophobicity, steric, and electronic properties were examined. The effects of position and numbers of substituents on the aromatic ring, the effects of conjugation in the molecules, and the effects of the properties of the parent alcohol part of the esters were also evaluated. It proved difficult to find strong SARs derived from single physicochemical descriptors, but our study led to numerous new, potent, phenylpropanoid antifeedants for the pine weevil. Among the most potent were methyl 3-phenylpropanoates monosubstituted with chloro, fluoro, or methyl groups and the 3,4-dichlorinated methyl 3-phenylpropanoate.10aHylobius abietis1 aBohman, B.1 aNordlander, G.1 aNordenhem, H.1 aSunnerheim, K.1 aBorg-Karlson, A., K.1 aUnelius, C., R.  uhttps://weevil.myspecies.info/structure-activity-relationships-phenylpropanoids-antifeedants-pine-weevil-hylobius-abietis01728nas a2200181   4500008004100000020001400041245013000055210006900185260001200254300001200266490000800278520103300286653002101319100002201340700002301362700002601385856013501411       2009                        eng d  a0269-749100aPine weevil feeding on Norway spruce bark has a stronger impact on needle VOC emissions than enhanced ultraviolet-B radiation0 aPine weevil feeding on Norway spruce bark has a stronger impact   cJanuary  a174-1800 v1573 aPlants can respond physiologically to damaging ultraviolet-B radiation by altering leaf chemistry, especially UV absorbing phenolic compounds. However, the effects on terpene emissions have received little attention. We conducted two field trials in plots with supplemented UV-B radiation and assessed the influence of feeding by pine weevils, Hylobius abietis L., on volatile emissions from 3-year old Norway spruce trees (Picea abies L. Karst.). We collected emissions from branch tips distal to the feeding weevils, and from whole branches including the damage sites. Weevil feeding clearly induced the emission of monoterpenes and sesquiterpenes, particularly linalool and (E)-ss-farnesene, from branch tips, and the sums of monoterpenes and sesquiterpenes emitted by whole branches were substantially increased. We discovered little effect of UV-B radiation up to 30% above the ambient level on volatile emissions from branch tips distal to damage sites, but there was a possible effect on bark emissions from damage sites.10aHylobius abietis1 aBlande, James, D.1 aTurunen, Katariina1 aHolopainen, Jarmo, K.  uhttps://weevil.myspecies.info/pine-weevil-feeding-norway-spruce-bark-has-stronger-impact-needle-voc-emissions-enhanced-ultraviolet01808nas a2200157   4500008004500000020001400045245005000059210005000109260001200159300000900171490000700180520134900187653002101536100002201557856007101579       2008                        Engldsh    a0892-755300aCues for shelter use in a phytophagous insect0 aCues for shelter use in a phytophagous insect  cJanuary  a9-230 v213 aMany insects spend a large proportion of their life inactive, often hiding in shelters. The presence of shelters may, therefore, influence where insects feed. This study examines stimuli affecting the use of shelters by adults of the pine weevil, Hylobius abietis (L.) (Coleoptera, Curculionidae). This species is an economically important forest pest in Europe since the adults feed on the stem bark of newly planted conifer seedlings. When there are hiding or burrowing places present in close proximity to a seedling, pine weevils may hide there and repeatedly return to feed on the same seedling. Experiments were conducted in a laboratory arena with above-ground or below-ground shelters and in the presence or absence of wind. Pine weevils were highly attracted to shelters both above and below ground. Weevils in shelters were often observed assuming a characteristic ''resting'' posture. Experiments with opaque and transparent shelters showed that visual stimuli are used for orientation towards shelters and also increase the probability of an individual remaining in a shelter. The presence of wind increased the weevils' propensity to use shelters both above and below ground. The present study indicates that shelters have a major influence on the behavior of the pine weevil and possible implications of the results are discussed.10aHylobius abietis1 aBjorklund, Niklas  uhttps://weevil.myspecies.info/cues-shelter-use-phytophagous-insect01590nas a2200181   4500008004800000020001400048245010100062210006900163260001900232300001200251490000700263520091600270653002201186100002901208700002601237700002301263856012201286       2009                        Portdguese    a0085-562600aStridulation behaving in Heilipus odoratus Vanin & Gaiger (Coleoptera, Curculionidae, Molytinae)0 aStridulation behaving in Heilipus odoratus Vanin Gaiger Coleopte  cJuly-September  a334-3360 v533 aStridulation behaving in Heilipus odoratus Vanin & Gaiger (Coleoptera, Curculionidae, Molytinae). Heilipus odoratus Vanin & Gaiger, 2005 (Coleoptera, Curculionide, Molytinae) is considered the main plague of rosewood fruit. Being recently described, the biological aspects of this species are not very well known. This study aimed at contributing for the knowledge of this species' behavior and providing a method for sexing adults based on stridulation. Individuals were divided into two groups: stridulating and non-stridulating. After dissection, stridulation was associated with the sex of each individual. Most males (92.2 %, N = 115) emitted sound by stridulation due to the presence of stridulatory organs on the posterior internal surface of their elytra and penultimate tergite, while none of the females (N=92) have such organs. This result is the first report of stridulatory activity in H. odoratus.10aHeilipus odoratus1 aNunes, Adilson, Benchaya1 aRonchi-Teles, Beatriz1 aSpironello, Wilson  uhttps://weevil.myspecies.info/stridulation-behaving-heilipus-odoratus-vanin-gaiger-coleoptera-curculionidae-molytinae07256nas a2202581   4500008004100000245004400041210004100085300001200126490001100138653001700149653002600166653002200192653001500214653002800229653001900257653002200276653002600298653002500324653002800349653002300377653002200400653002500422653002400447653002400471653002200495653001200517653002200529653001400551653001600565653002200581653001200603653001300615653001300628653001300641653002600654653001400680653002900694653002400723653001100747653001400758653001500772653001800787653001500805653002800820653002400848653002300872653001300895653001600908653002500924653002600949653001600975653001900991653001601010653001801026653001401044653001801058653002501076653001501101653001601116653002301132653002601155653002201181653001201203653001501215653001501230653001101245653002601256653002701282653002201309653002401331653002401355653002501379653002501404653002701429653002601456653002801482653002701510653001601537653001701553653002701570653001201597653001401609653001201623653002501635653002501660653001301685653001501698653001401713653002401727653002401751653002201775653002601797653002801823653003601851653001801887653001301905653002201918653002001940653002901960653002901989653002302018653001202041653003102053653002602084653001302110653002202123653002202145653001802167653001302185653001302198653001402211653002702225653002502252653001702277653002602294653003002320653002702350653001702377653001502394653002602409653001802435653002502453653001902478653002302497653002902520653001602549653002002565653002502585653002502610653001502635653002902650653002702679653002302706653001402729653001902743653001602762653002102778653001302799653001702812653001302829653002102842653001402863653002602877653002502903653002702928653001302955653002202968653002402990653002203014653002403036653002003060653001203080653002803092653001503120653002403135653001803159653001503177653001403192653001803206653001503224653003203239653001603271653001503287653001703302653002603319653003003345653002803375653002903403653002503432653001603457653002103473653002503494653002603519653002803545653002903573653002203602653002203624653002503646653002403671653003003695653002803725653002603753653004003779653001803819653003103837653002703868653001903895653004403914653003103958653003003989653002304019653002204042653002504064653002604089653002804115653002604143653002104169653002604190653001204216653002404228653001204252653001804264653002804282653002704310653002704337653002704364653001304391653002004404653003104424653003004455653001804485653001204503653001404515653002304529653002604552100002804578856006804606       1952                        eng d00aTaxonomic notes on Curculionidae (Col.)0 aTaxonomic notes on Curculionidae Col  a261-2700 v(12) 510aAcallopistus10aAcallopistus pardalis10aAcanthotrachelini10aAfrodolius10aAfrodolius polylineatus10aAfropolydrosus10aAlcidodes affinis10aAlcidodes aschanticus10aAlcidodes blanchardi10aAlcidodes crythropterus10aAlcidodes dentipes10aAlcidodes elegans10aAlcidodes guessfeldi10aAlcidodes necopinus10aAlcidodes obsoletus10aAlcidodes otiosus10aAmnemus10aAmnemus squamosus10aAmphialus10aAmphyonotus10aAmphyonotus douei10aAmydala10aAmydanus10aAmygdala10aAnchonus10aAncistropterus helmsi10aApotmetus10aApotmetus granuliventris10aApotmetus suturalis10aApries10aArniticus10aBaryopadus10aBrachyderinae10aBryochaeta10aBryochaeta crassicornis10aBryochaeta viridis,10aCadoderus mysticus10aCalandra10aCalidiopsis10aCamptorrhinus lesnei10aCamptorrhinus simplex10aCatolethrus10aChaetectetorus10aCharactopus10aChitonopterus10aColobodes10aCompsus dives10aCorigetus albovarius10aCossoninae10aCratopechus10aCratopechus gedyei10aCryptacrus variegatus10aCryptotelus scops10aCybebus10aCycloderes10aCyphicerus10aCyphus10aDeiradolcus pruinosus10aDeretiosus amblipennis10aDeretiosus aridus10aDeretiosus turbatus10aDeretiosus zopherus10aDiocalandra rugosula10aDorytomodes confusus10aDorytomodes xenorhinus10aDrymophoetus modestus10aEctatopsides cineraceus10aEctatopsides cinerosus10aElattocerus10aEllimenistes10aElytrocallus cyphoides10aEntimus10aEremninae10aEremnus10aEugnathus bracteatus10aEugnathus distinctus10aEupholus10aEurhynchus10aEurrhinus10aEustylus magdalenae10aExapries lophonotus10aHeilipus ludiosus10aHeilipus verruculatus10aHeterocossonus lobeliae10aHoplitotrachelus nigromaculatus10aHoploparochus10aHylobius10aIcmalius abnormis10aIschnotrachelus10aIschnotrachelus burgeoni10aIschnotrachelus curvipes10alcidodes obsoletus10aLeptops10aLeptops quadrituberculatus10aLeptops superciliaris10aLeptosus10aLeptosus tribulus10aLipsanus brunneus10aLobotrachelus10aLycosura10aMachodon10aMacropoda10aMaleuterpes phytolymus10aMaleuterpes spinipes10aMecistocerus10aMecistocerus cuneatus10aMecistocerus denticulatus10aMecistocerus maculipes10aMenemachinae10aMenemachus10aMenemachus nigricauda10aMesitomorphus10aMesphrigodes ornatus10aMetacyphicerus10aMeteremnus obtusus10aMeteremnus subfissuratus10aMicrotribus10aMimopentarthrum10aMnemynurus caloderes10aMnemynurus championi10aMyllocerus10aMyrmacicelus gibbipennis10aNematocerus lineatulus10aNematocerus parvus10aNeocyphus10aNeoepipedosoma10aNerthopinae10aNerthops guttata10aOaphilia10aOdontomaches10aOosomini10aOosomus agrestis10aOrchestes10aOrthorrhinus aethiops10aOrthorrhinus bicolor10aOrthorrhinus carinatus10aOsphilia10aOsphilia gabonica10aOsphilia nigricauda10aOsphilia tibialis10aOxydema subcaudatus10aOxyrrhynchoides10aPactola10aPagiophloeus bidentulus10aParamecops10aParamecops sinuatus10aPhaenomerinae10aPhlyctinus10aPiazomias10aPlatyrhynchus10aPlatytenes10aPorohylobius ligniperdoides10aPseudomimus10aPsidiopsis10aRhadinomerus10aRhadinomerus cuneatus10aRhadinomerus denticulatus10aRhadinoscapus nociturus10aRhadinoscapus variegatus10aRhamphus perpusillus10aRhinoscapha10aRhinoscapha alma10aRhinoscapha arrogans10aRhinoscapha azureipes10aRhinoscapha cobaltinata10aRhinoscapha darnleyensis10aRhinoscapha douei10aRhinoscapha dubia10aRhinoscapha thomsoni10aRhyparonotus celsus10aRhytirrhinus anaglypticus10aRhytirrhinus anaglyptus10aRhytirrhinus namaquus10aRhytirrhinus transversetuberculatus10aScoliopisthen10aScoliopisthen ellenbergeri10aScoliopisthen sordidum10aSiderodactylus10aSiderodactylus (Hadromerus) conirostris10aSiderodactylus conirostris10aSiderodactylus lineolatus10aSmicronyx cuscutae10aSmicronyx roridus10aSomerenius naivashae10aSphadasmus incallidus10aSphenomorpha cingulatus10aSphenomorpha fasciata10aSphrigodes gunni10aSternechus pollinosus10aStyanax10aStyanax bicarinatus10aSynomus10aSyntaphocerus10aSyntaphocerus obsoletus10aSyntaphocerus pusillus10aSyntaphocerus terrenus10aSynthocus triangulifer10aSystates10aTanyrrhynchinae10aTartarisus perforatipennis10aTelephae obliquefasciatus10aTomicoproctus10aTylomus10aUlomascus10aUlomascus claviger10aUlomascus longicornis1 aMarshall, Sir, G. A. K.  uhttps://weevil.myspecies.info/taxonomic-notes-curculionidae-col01630nas a2200553   4500008004500000020001400045245006300059210005700122300001100179653001100190653001300201653002400214653002200238653001900260653002600279653002400305653002400329653002200353653002600375653002900401653001600430653002200446653001400468653001600482653002400498653002400522653002500546653002500571653003000596653001300626653001400639653002200653653001700675653002500692653001200717653001400729653002900743653001700772653002900789653002600818653001800844653002700862653001200889653002800901653002700929653001900956100001700975856008400992       1982                        Engldsh    a0071-126800aThe family Curculionidae of Japan. 1. Subfamily Hylobiinae0 afamily Curculionidae of Japan 1 Subfamily Hylobiinae  a51-12110aAclees10aDyscerus10aDyscerus exsculptus10aDyscerus galloisi10aDyscerus gigas10aDyscerus laeviventris10aDyscerus orientalis10aDyscerus perforatus10aDyscerus roelofsi10aDyscerus shikokuensis10aEuthycus inaequalicollis10aHesychobius10aHesychobius vossi10aHylobiini10aHylobitelus10aHylobitelus futabae10aHylobitelus haroldi10aHylobitelus montanus10aHylobitelus pinastri10aHylobitelus shiroumaensis10aHylobius10aKyliparus10aKyliparus lewisii10aLeptanchonus10aLeptanchonus minatoi10aLepyrus10aLithinini10aMetahylobius rubiginosus10aPagiophloeus10aPagiophloeus tsushimanus10aParamecops granulatus10aPentaparopion10aPentaparopion costatum10aSeleuca10aSeleuca chujoi rugulosa10aSeleuca impressicollis10aSeleuca satana1 aMorimoto, K.  uhttps://weevil.myspecies.info/family-curculionidae-japan-1-subfamily-hylobiinae02625nas a2200349   4500008004500000020001400045245021900059210006900278260000900347300001200356490000800368520142500376653001501801653002501816100001701841700001801858700002101876700002101897700002101918700002301939700001701962700001701979700002101996700001802017700002002035700001702055700001602072700001802088700001802106700001602124856013502140       2007                        Engldsh    a1210-575900aRedescription of a weevil Paramecops sinaitus (Coleoptera: Curculionidae: Molytinae) from the Sinai and an ecological study of its interaction with the Sinai milkweed Asclepias sinaica (Gentianales: Asclepiadaceae)0 aRedescription of a weevil Paramecops sinaitus Coleoptera Curculi  cJuly  a505-5150 v1043 aWe collected specimens of Paramecops sinaitus (Pic, 1930) (Curculionidae: Molytinae) from south Sinai in Egypt, which enabled us to make the first complete description of this species. We also include some taxonomic remarks on the genus. Paramecops solenostemmatis (Peyerimhoff, 1930) is a synonym of Paramecops sinaitus. We propose the new combination Paramecops sogdianus (Nasreddinov, 1978), based on Perihylobius sogdianus Nasreddinov, 1978, which would make Perihylobius and Paramecops synonymous. Like other Paramecops species, P. sinaitus appears to share a close interaction with Asclepiads, in this case the Sinai milkweed Asclepias sinaica (Boiss.) Muschl., 1912 (Asclepiadaceae). We investigated the oviposition behaviour of female weevils to test whether it is linked to larval performance, as predicted by coevolutionary theory. We found that female oviposition preference was positively related to plant size and to the volume of the seed follicles in which the eggs were laid. The survival of eggs was negatively related to plant size, perhaps due to plant differences in the production of defensive cardenolides. Larval survival was not related to plant size but increased with follicle volume, probably as a result of competition for food. Paramecops is relatively sedentary and nocturnal in its behaviour. Night-time observations of behaviour showed that weevils were more active at lower temperatures.10aParamecops10aParamecops sogdianus1 aNewbold, Tim1 aMeregalli, M.1 aColonnelli, Enzo1 aBarclay, Maxwell1 aElbanna, Shereen1 aFandud, Nancy, Abu1 aFlegg, Frank1 aFouad, Rasha1 aGilbert, Francis1 aHall, Vanessa1 aHancock, Claire1 aIsmail, Mona1 aOsamy, Samr1 aSaber, Isra'a1 aSemida, Fayez1 aZalat, Samy  uhttps://weevil.myspecies.info/redescription-weevil-paramecops-sinaitus-coleoptera-curculionidae-molytinae-sinai-and-ecological-s-000882nas a2200169   4500008004800000245010000048210006900148260001900217300001200236490000700248520025500255653001400510653002600524100002300550700002000573856011900593       2003                        Portdguese  00aArniticus brevicollis Pascoe (Coleoptera: Curculionidae), pest of mulberry in Sao Paulo, Brazil0 aArniticus brevicollis Pascoe Coleoptera Curculionidae pest of mu  cJuly-September  a513-5140 v323 aArniticus brevicollis Pascoe (Curculionidae: Molytinae: Hylobiini) is recorded for the first time attacking mulberry plants (Morus alba L.) in the state of Sao Paulo, Brazil. Adult specimens are deposited in the Museum of Zoology, USP, Sao Paulo, SP.10aArniticus10aArniticus brevicollis1 aSanchez-Soto, Saul1 aNakano, Octavio  uhttps://weevil.myspecies.info/arniticus-brevicollis-pascoe-coleoptera-curculionidae-pest-mulberry-sao-paulo-brazil01179nas a2200421   4500008004100000245011900041210006900160300001000229490000700239653001200246653001700258653001600275653001400291653001200305653001700317653001000334653001200344653001400356653001300370653001100383653001300394653001700407653001200424653001300436653001200449653001200461653001100473653001000484653001300494653001400507653001300521653001800534653001900552653001600571653001500587100002000602856013500622       1968                        eng d00aChrzzszcze--Coleoptera. 98c. Ryjkowce-Curculionidae. Podrodziny Tanymecinae, Cleoninae, Tanyrhynchinae, Hylobiinae0 aChrzzszczeColeoptera 98c RyjkowceCurculionidae Podrodziny Tanyme  a1-1060 v1910aAlophus10aChlorophanus10aChromoderus10aCleoninae10aCleonus10aConiocleonus10aDonus10aGronops10aHylobiini10aHylobius10aHypera10aHyperini10aLarinodontes10aLarinus10aLeiosoma10aLepyrus10aLiparus10aLixini10aLixus10aMecaspis10aPlinthini10aPllnthus10aPseudocleonus10aRhabdorhynchus10aTanymecinae10aTanymecini1 aSmreczyuski, S.  uhttps://weevil.myspecies.info/chrzzszcze-coleoptera-98c-ryjkowce-curculionidae-podrodziny-tanymecinae-cleoninae-tanyrhynchinae-hyl01292nas a2200169   4500008004500000020001400045245011600059210006900175260001600244300001200260490000700272520065300279653002200932100002200954700001800976856012800994       2005                        Engldsh    a0085-562600aA new spermophagous species of Heilipus Germar from the Amazonian Region (Coleoptera, Curculionidae, Molytinae)0 anew spermophagous species of Heilipus Germar from the Amazonian   cAbril-Junho  a240-2440 v493 aA new spermophagous species of Heilipus Germar from the Amazonian Region (Coleoptera, Curculionidae, Molyfinae). Heilipus odoratus sp. nov. (type locality: Brazil, Amazonas, Manaus) is described based on adults reared from seeds of Aniba rosaeodora Ducke (Lauraceae), popularly called "pau-rosa". The species is spermophagous and develops from egg to adult inside the seeds. The new taxon is compared with the similar Heilipus draco (Fabricius, 1801). Illustrations of larva, pupa, adult and of important structures for species identification are given, including the male and female genitalia, figured for the first time for a species of Heilipus.10aHeilipus odoratus1 aVanin, Sergio, A.1 aGaiger, Fabio  uhttps://weevil.myspecies.info/new-spermophagous-species-heilipus-germar-amazonian-region-coleoptera-curculionidae-molytinae09666nas a2201969   4500008004500000020001400045245012700059210006900186300001000255490000600265653006400271653004800335653002600383653002700409653000900436653001800445653001800463653007300481653006500554653001500619653006900634653007400703653006700777653007300844653004800917653007400965653003701039653007301076653001701149653001601166653002401182653002401206653003801230653001401268653006301282653007401345653001601419653003001435653004801465653006601513653007401579653003801653653007501691653007101766653007501837653006501912653007501977653007402052653001402126653006802140653002502208653002902233653007102262653007502333653002802408653006902436653003802505653007502543653006102618653007302679653006502752653006502817653005502882653003502937653001002972653001502982653006102997653002403058653007203082653007003154653000803224653000903232653007303241653006703314653007303381653006903454653006703523653007303590653006703663653007003730653001103800653007303811653006503884653006203949653007304011653001904084653006804103653005304171653004604224653004504270653004504315653004504360653006704405653007404472653005004546653002304596653006304619653001304682653001504695653001804710653001704728653001704745653005604762653004704818653007404865653005504939653006904994653007405063653002505137653003205162653003305194653003305227653003105260653003305291653003105324653003105355653003205386653003205418653003105450653003305481653003205514653003705546653007505583653006605658653006905724653006905793653007405862653001705936653006705953653007306020653002406093653005306117653007306170653001506243653001706258653002706275653002406302653002906326653001806355653001106373653007106384653007506455653007206530653006906602653007406671653005606745653001306801653001606814653002306830653005106853653003806904653001306942653007106955653007207026653007107098653007507169653007307244653004207317653007207359653001707431653004607448653002007494653006507514653001007579100001607589856009107605       1987                        Engldsh    a0077-996200aThe subfamily Molytinae (Coleoptera: Curculionidae): general notes and descriptions of new taxa from New Zealand and Chile0 asubfamily Molytinae Coleoptera Curculionidae general notes and d  a11-290 v910a[Designated type species for new genus, Germainius, p. 25].10a[Referred to new genus, Germainius, p. 25].10a14, Cholinae, p. 14].10a14, Euderinae, p. 14].10a14].10a1883, p. 14].10a1892, p. 14].10aAcicnemidinae (Curculionidae): [Downgraded to, Acicnemidini, p. 14].10aAcicnemidini (Curculionidae): [Referred to, Downgraded from,10aaffinities10aAmalactinae (Curculionidae): [Downgraded to, Amalactini, p. 13].10aAmalactini (Curculionidae): [Referred to, Downgraded from, Molytinae,10aAnchoninae (Curculionidae): [Downgraded to, Anchonini, p. 14].10aAnchonini (Curculionidae): [Referred to, Downgraded from, Molytinae,10aAnistome acutifolia (plant), P. 20, fig'd].10aAonychus - Schoenherr (Curculionidae): [Referred to, Erirhininae from10aApiaceae (plant), P. 18, fig'd].10aArthrostenus - Schoenherr (Curculionidae): [Referred to, Erirhininae10aAssociations10aAustralasia10aAustralasian region10aBroun 1883, p. 14].10abursa / / Bursal pouch morphology10aCaenozoic10aCholinae (Curculionidae): [Downgraded to, Cholini, p. 14].10aCholini (Curculionidae): [Referred to, Downgraded from, Molytinae, p.10aCombination10aCryptorhynchinae, p. 14].10aCurculionidae (Curculionoidea): [Parasite].10aCurculionidae [Integument / / Intersegmental membrane pouches10aDesmidophorus - Schoenherr (Curculionidae): [Referred to, Erirhininae10aDiaptrophorus Faust 1882, p. 14].10aDioptrophorus - Faust 1882 (Curculionidae): [Syn nov, Metopotoma Casey10aEmphyastinae (Curculionidae): [Downgraded to, Emphyastini, p. 13].10aEmphyastini (Curculionidae): [Referred to, Downgraded from, Molytinae,10aEuderinae (Curculionidae): [Downgraded to, Euderini, p. 14].10aEuderini (Curculionidae): [Referred to, Downgraded from, Molytinae, p.10aEuodontus - Broun 1883 (Curculionidae): [New synonym, Of Pogonorhinus10aEvolution10afemale / / Vaginal pouch morphology] [Mutualism / / Filamentous10afemales] [Copulatory10afrom Ithyporini, p. 14].10aGalloisiinae (Curculionidae): [Downgraded to, Galloisiini, p. 14].10aGalloisiini (Curculionidae): [Referred to, Downgraded from, Molytinae,10aGeological time periods10aGermainius (Curculionidae): [Gen nov, Of Molytinae, Type species10aGermainius [Chile / / New genus].10aGermainius laesicollis - (Fairmaire & Germaine) (Curculionidae): [Comb10aGuioperini (Curculionidae): [Referred to, Molytinae from10aHaplonychinae (Curculionidae): [Downgraded to, Haplonychini, p. 14].10aHaplonychini (Curculionidae): [Referred to, Downgraded from,10aHeilipus laesicollis - Fairmaire & Germaine (Curculionidae):10aHeilipus laesicollis Fairmaire & Germaine, p. 25].10ahost not given, P. 24, fig'd].10aHosts10aIntegument10aIthyporini (Curculionidae): [Referred to, Molytinae from10aIthyporini, p. 14].10aKarocolens (Curculionidae): [Gen nov, Of Molytinae, Type species K.10aKarocolens pittospori (Curculionidae): [Sp nov, New Zealand, host10aKey10aLand10aLepyrini (Curculionidae): [Referred to, Molytinae from Cleoninae, p.10aLithininae (Curculionidae): [Downgraded to, Lithinini, p. 14].10aLithinini (Curculionidae): [Referred to, Downgraded from, Molytinae,10aLymantes - Schoenherr 1838 (Curculionidae): [Syn nov, Stewpeckia10aLymantinae (Curculionidae): [Downgraded to, Lymantini, p. 14].10aLymantini (Curculionidae): [Referred to, Downgraded from, Molytinae,10aLyperobius coxalis (Curculionidae): [Sp nov, New Zealand, host10aLyperobius nesidiotes (Curculionidae): [Sp nov, New Zealand, host10aMating10aMecysolobinae (Curculionidae): [Downgraded to, Mecysolobini, p. 14].10aMecysolobini (Curculionidae): [Referred to, Downgraded from,10aMetopotoma - Casey 1892 (Curculionidae): [New synonym, Of10aMicraonychus - Lea (Curculionidae): [Referred to, Curculioninae from10amicroorganisms10aMolytinae (Curculionidae): [Included taxa, Taxa listed, p. 13].10aMolytinae [Copulation / / Morphology & behaviour10aMolytinae, p. 13, Petalochilinae, p. 13].10aMolytinae, p. 14, Acicnemidinae, p. 14].10aMolytinae, p. 14, Haplonychinae, p. 14].10aMolytinae, p. 14, Mecysolobinae, p. 14].10aMolytini (Curculionidae): [Key to genera, New Zealand, P. 15].10aNeophycocoetes - O'Brien & Wibmer 1982 (Curculionidae): [New synonym,10aNeophycocoetes O'Brien & Wibmer 1982, p. 13].10aNeotropical region10aNettarhinini (Curculionidae): [Referred to, Molytinae from10aNew taxa10anew taxa].10aNew Zealand].10aNomenclature10aNorth Island10anote] [Phylogeny / / Morphological affinities] [New10anov, Transferred from, Philippius, p. 25].10aOcladius - Schoenherr (Curculionidae): [Referred to, Erirhininae from10aOf Thalasselephas Egorov & Korotyaev 1976, p. 13].10aOmophorinae (Curculionidae): [Downgraded to, Omophorini, p. 14].10aOmophorini (Curculionidae): [Referred to, Downgraded from, Molytinae,10aOsella 1980, p. 14].10ap. 13, Amalactinae, p. 13].10ap. 13, Emphyastinae, p. 13].10ap. 13, Trypetidinae, p. 13].10ap. 14, Anchoninae, p. 14].10ap. 14, Galloisiinae, p. 14].10ap. 14, Lithininae, p. 14].10ap. 14, Lymantinae, p. 14].10ap. 14, Omophorinae, p. 14].10ap. 14, Phrynixinae, p. 14].10ap. 14, Pissodinae, p. 14].10ap. 14, Sternechinae, p. 14].10ap. 14, Styanacinae, p. 14].10aParasites diseases and disorders10aPetalochilinae (Curculionidae): [Downgraded to, Petalochilini, p. 13].10aPetalochilini (Curculionidae): [Referred to, Downgraded from,10aPhilippius laesicollis - (Fairmaire & Germaine) (Curculionidae):10aPhrynixinae (Curculionidae): [Downgraded to, Phrynixini, p. 14].10aPhrynixini (Curculionidae): [Referred to, Downgraded from, Molytinae,10aphylogenetic10aPissodinae (Curculionidae): [Downgraded to, Pissodini, p. 14].10aPissodini (Curculionidae): [Referred to, Downgraded from, Molytinae,10apittospori, p. 15].10aPittosporum crassifolium (plant), P. 16, fig'd].10aPogonorhinus - Broun 1883 (Curculionidae): [Syn nov, Euodontus Broun10aQuaternary10aReproduction10aReproductive behaviour10aReproductive system10aSchoenherr 1838, p. 14].10aSouth America10aStatus10aSternechinae (Curculionidae): [Downgraded to, Sternechini, p. 14].10aSternechini (Curculionidae): [Referred to, Downgraded from, Molytinae,10aStewpeckia - Osella 1980 (Curculionidae): [New synonym, Of Lymantes10aStyanacinae (Curculionidae): [Downgraded to, Styanacini, p. 14].10aStyanacini (Curculionidae): [Referred to, Downgraded from, Molytinae,10aSymbionts attached to female intersegmental pouches10aSynonymy10aSystematics10aTaxonomic position10aTaxonomic significance & presence of symbionts10ataxonomic significance] [Ducts of10aTaxonomy10aTetracyphus - Chevrolat (Curculionidae): [Referred to, Erirhininae10aThalasselephas - Egorov & Korotyaev 1976 (Curculionidae): [Syn nov,10aTrypetidinae (Curculionidae): [Downgraded to, Trypetidini, p. 13].10aTrypetidini (Curculionidae): [Referred to, Downgraded from, Molytinae,10aTymbopiptus (Curculionidae): [Gen nov, Of Molytinae, Type species T.10aTymbopiptus [Holocene / / New Zealand10aTymbopiptus valeas (Curculionidae): [Sp nov, New Zealand, Holocene,10aType species10aultrastructure] [Plant hosts / / New taxa10avaleas, p. 21].10aZealand / / Systematic account & phylogenetic implications].10azones1 aKuschel, G.  uhttp://www.ento.org.nz/nzentomologist/free_issues/NZEnto09_1_1987/Volume%209-11-29.pdf04892nas a2200781   4500008004100000245003500041210003500076300001100111490001000122520268600132653001402818653002202832653002502854653001802879653003802897653002302935653002302958653001702981653001802998653002803016653002803044653002403072653001803096653001503114653002603129653001703155653001203172653002503184653002103209653002003230653002403250653002303274653002303297653002303320653002703343653001403370653001603384653003303400653002303433653002103456653002103477653002203498653003003520653001603550653002303566653002503589653001803614653002903632653002103661653002603682653001603708653002403724653001703748653002503765653002303790653002103813653002303834653002503857653002003882653002903902653002203931653001503953653002403968653002403992653001304016100001404029856006704043       1899                        eng d00aNeue Curculioniden Madagaskars0 aNeue Curculioniden Madagaskars  a26 pp.0 vNo. 23 aAneulobus (Curculionidae): [Gen nov, n. g., Hylobiini, for, Aneulobus decolor, Aneulobus horridipes, n. spp., Madagascar, p. 10, [Sp nov]]. Apion biforme [Zoology / / Madagascar p. 15]. Apoderus (Haplopoderus) aculeatus [Zoology / / Madagascar p. 14 n. spp]. Apoderus femoralis [Zoology / / var. n Apoderus semiruber p. 15]. Calandrides vrais [Zoology / / of Lacord genera tabulated pp. 24-26]. Calandrotopus (Curculionidae): [Gen nov, n. g., Calandrides vrais, for, Calandra punctiger, n. sp., Myanmar, p. 26, [Sp nov]]. Camptorhinus rubicundus [Zoology / / Madagascar p. 17 n. spp]. Cybebus nigritarsis (Apionidae). Cybebus rufus [Zoology / / Cybebus nigritarsis Madagascar p. 14 n. spp]. Dermatodes (Curculionidae).  Desmidophorus hovanus [Zoology / / Madagascar p. 16]. Eremnophilus (Curculionidae): [Gen nov, n. g., for species of, Eremnus, with toothed femora, p. 5]. Eremnus cristicollis (Curculionidae). Eremnus honestus [Zoology / / p. 5  Eremnus humilis p. 6 Eremnus longicornis (Curculionidae). Eremnus rufitarsis (Curculionidae). Eremnus rusticanus (Curculionidae). Eremnus verecundus p. 7 Madagascar n. spp]. Faustiella trifasciata [Zoology / / Madagascar p. 21 n. sp]. Lagenotenes (Curculionidae): [Gen nov, n. g., Brachyderini, p. 2, for, Lagenotenes quinquepunctatus, n. sp., Madagascar, p. 3, [Sp nov]]. Larinus madagassus [Zoology / / Madagascar p. 8 n. sp]. Lithinus hovanus [Zoology / / p. 11 Lithinus nodifer p. 13 Madagascar n. spp]. Lithinus sonticus Mechistocerus lemniscatus [Zoology / / Madagascar p. 16 n. sp]. Neocalandra (Curculionidae): [Gen nov, n. g., Calandrini, for, Neocalandra obsoleta, p. 22, Neocalandra arguta, p. 23, n. spp., Madagascar, [Sp nov]]. Orthomycterus (Curculionidae): [Gen nov, n. g., Strangaliodini, p. 7, for, Orthomycterus coerulipes, n. sp., Madagascar, p. 8, [Sp nov]]. Osphilia vittata (Curculionidae). Otiorrhynchus delatus [Zoology / / Madagascar p. 4 n. spp]. Panoptidius (Curculionidae): [Gen nov, n. g., Zygopini, for, Panoptidius rufipes, n. sp., Madagascar, p. 17, [Sp nov]]. Philophloeus (Carabidae): [Gen nov, n. g., Hylobiini, for, Philophloeus nodifer, n. sp., Madagascar, p. 9, [Sp nov]]. Phoenomerus striga [Zoology / / Madagascar p. 22 n. sp]. Proictes humilis [Zoology / / p. 1 Proictes lateralis p. 2 Madagascar n. spp]. Proictes tessellatus (Curculionidae). Stigmatrachelus [Zoology / / (as Dermatodes but emended on added slip) Stigmatrachelus collaris Madagascar p. 4 n. sp]. Strabus suturalis [Zoology / / Madagascar n. sp]. Timiotatus (Curculionidae): [Gen nov, n. g., Calandrides vrais, for, Timiotatus birmanus, n. sp., Myanmar, [Sp nov]]. Zantes brevirostris [Zoology / / Madagascar p. 15 n. spp].  10aAneulobus10aAneulobus decolor10aAneulobus horridipes10aApion biforme10aApoderus (Haplopoderus) aculeatus10aApoderus femoralis10aApoderus semiruber10aBrachyderini10aCalandrotopus10aCalandrotopus punctiger10aCamptorhinus rubicundus10aCybebus nigritarsis10aCybebus rufus10aDermatodes10aDesmidophorus hovanus10aEremnophilus10aEremnus10aEremnus cristicollis10aEremnus honestus10aEremnus humilis10aEremnus longicornis10aEremnus rufitarsis10aEremnus rusticanus10aEremnus verecundus10aFaustiella trifasciata10aHylobiini10aLagenotenes10aLagenotenes quinquepunctatus10aLarinus madagassus10aLithinus hovanus10aLithinus nodifer10aLithinus sonticus10aMechistocerus lemniscatus10aNeocalandra10aNeocalandra arguta10aNeocalandra obsoleta10aOrthomycterus10aOrthomycterus coerulipes10aOsphilia vittata10aOtiorrhynchus delatus10aPanoptidius10aPanoptidius rufipes10aPhilophloeus10aPhilophloeus nodifer10aPhoenomerus striga10aProictes humilis10aProictes lateralis10aProictes tessellatus10aStigmatrachelus10aStigmatrachelus collaris10aStrabus suturalis10aTimiotatus10aTimiotatus birmanus10aZantes brevirostris10aZygopini1 aFaust, J.  uhttps://weevil.myspecies.info/neue-curculioniden-madagaskars-005169nas a2201753   4500008004100000245007700041210006900118300001000187490000700197653001300204653002200217653002300239653002200262653002400284653002200308653002500330653002400355653002500379653002400404653002400428653002600452653003200478653002100510653001800531653002000549653002600569653002400595653001700619653002800636653001500664653002300679653002400702653001900726653002100745653001200766653002300778653002600801653002800827653002600855653003000881653002500911653002500936653002700961653001800988653002601006653002501032653001401057653002001071653002601091653002801117653003201145653002701177653002701204653001501231653002401246653003201270653003101302653002701333653001701360653002801377653003101405653002701436653002701463653002701490653002901517653002601546653002301572653002101595653002501616653002101641653001401662653002801676653002301704653002201727653002201749653002101771653002101792653002401813653002401837653002601861653001901887653002001906653001901926653002401945653002201969653002001991653002002011653002102031653002102052653002202073653002102095653002002116653001802136653001902154653002202173653002302195653001302218653001502231653001602246653002302262653002302285653001802308653002802326653002502354653002702379653002302406653002302429653002202452653002002474653002102494653002602515653002202541653001302563653002302576653002302599653002502622653001602647653002502663653001502688653002602703653002102729653002602750653003302776653002402809653001602833653002302849653001402872653002402886653002402910653002302934653001702957653002302974653001602997653002303013653002303036653002303059653001603082653002303098653001603121653002403137653002403161653002203185653002403207653001503231653002303246653002703269100001403296856010503310       1899                        eng d00aViaggio di Lamberto Loria nella Papuasia orientale. XXIII. Curculionidae0 aViaggio di Lamberto Loria nella Papuasia orientale XXIII Curculi  a1-1300 vxl10aAchopera10aAcicnemis exclusa10aAcicnemis laqueata10aAcicnemis modesta10aAcicnemis proeculta10aAclees granulosus10aAcythopeus binotatus10aAgametis oeruginosa10aAlcidodes blanchardi10aAmalthus sulcifrons10aAmorphoidea bicolor10aAmorphoidea discedens10aAnchithyrus quadripunctatus10aApion albopictum10aApion gestivi10aApion infaustum10aArachnopus biguttatus10aArachnopus sectator10aAulacocnemus10aAulacocnemus solitarius10aBarinogyna10aBarinogyna ebenina10aChoerodemas setiger10aChoerorhamphus10aCionus usambicus10aCleonis10aCleonis (Konigius)10aConapion sculpturatum10aCoptorhynchus discretus10aCoptorhynchus distans10aCoptorhynchus fraterculus10aCoptorhynchus hospes10aCoptorhynchus pellax10aCoptorhynchus posticus10aCoryssoglymma10aCoryssoglymma enodata10aCoryssoglymma odiosa10aCossonini10aCryptorhynchini10aDeretiosus verrucifer10aDiathetes signaticollis10aDioedimorpha depressicollis10aDryophthorus tricuspis10aDyspeithes suspiciosus10aEctatocyba10aEctatocyba tuberosa10aEctemnomerus nigroplagiatus10aEctemnomerus pertusicollis10aEctemnomerus viridanus10aElassophilus10aElassophilus albopictus10aElytrocheilus crassicornis10aElytrocheilus expansus10aElytrocheilus nigripes10aElytrocheilus proximus10aElytrocheilus ruficollis10aElytrocheilus rufipes10aEupholus bennettii10aEupholus bicolor10aEupholus cinnamomeus10aEupholus coesius10aGuiomatus10aGuiomatus quadrinodosus10aIdiopsis excellens10aIdiopsis maculosa10aIdotasia cribrata10aIdotasia cuneata10aIdotasia densata10aIdotasia difficilis10aIdotasia ephippiata10aIdotasia gibbirostris10aIdotasia illex10aIdotasia illita10aIdotasia melas10aIdotasia morokensis10aIdotasia neglecta10aIdotasia obnixa10aIdotasia polita10aIdotasia pusilla10aIdotasia seclusa10aIdotasia sejuncta10aIdotasia sellata10aIdotasia solida10aIdotasia vana10aImathia brevis10aIsotocerus fallax10aIsotocerus setiger10aMadarini10aMeroleptus10aMicrospathe10aNechyrus concussus10aNechyrus humeralis10aNeoporopterus10aNeoporopterus varicosus10aNiphades interruptus10aOchronanus subreflexus10aOchronanus vicinus10aOdosyllis opposita10aOrthorhinus illex10aOttistira loeta10aOttistira nitida10aOttistira sulcicollis10aOttistira viridis10aOxymelus10aOxymelus concretus10aPantorhytes opacus10aPantorhytes proximus10aPantoxystus10aPholidonotus pilosus10aPoropterus10aPoropterus excitiosus10aPseudoporopterus10aPseudoporopterus leai10aPseudoporopterus sulcicollis10aPtochus violaceipes10aPtyctonotus10aPtyctonotus gibbus10aPyroderes10aRhinoscapha albaria10aRhinoscapha gestroi10aRhinoscapha loriai10aSclerodontus10aSclerodontus comma10aStelechodes10aStelechodes loriai10aStereoderus fronto10aStereoderus hospes10aStereonotus10aStereonotus doriai10aTapinosomus10aTelaugia corpulenta10aTelephae muticollis10aTyrtaeosus ingens10aTyrtaeosus plebeius10aXenospilus10aXenospilus bicolor10aXenospilus fuscicornis1 aFaust, J.  uhttps://weevil.myspecies.info/viaggio-di-lamberto-loria-nella-papuasia-orientale-xxiii-curculionidae09085nas a2202989   4500008004100000245007600041210006900117300001200186490001000198653002200208653002300230653002000253653002000273653002000293653002400313653002300337653001700360653002100377653002100398653002100419653002300440653001900463653002400482653002100506653002300527653001900550653002000569653002000589653002100609653002100630653001800651653002000669653002300689653002300712653002300735653002300758653003700781653004200818653002100860653002100881653002300902653002400925653002700949653002200976653001900998653002301017653002101040653001801061653001601079653002301095653001801118653001801136653002601154653001901180653001201199653001601211653002801227653002701255653002601282653002601308653003601334653002401370653002301394653002601417653003601443653003501479653002401514653003301538653002501571653002501596653001601621653001601637653001701653653002101670653002501691653002601716653002201742653002501764653003001789653001001819653001901829653002601848653002801874653002801902653002401930653002601954653002601980653002202006653002302028653001302051653002502064653001902089653002502108653002202133653002202155653002602177653002302203653002102226653002602247653002402273653002502297653002002322653001902342653003002361653002602391653002502417653002202442653002502464653002702489653002502516653002602541653002302567653002302590653002502613653002302638653003002661653002302691653002402714653002502738653001302763653002902776653001602805653001502821653002202836653002502858653002102883653001402904653002702918653002302945653002402968653003602992653004003028653003303068653003303101653003103134653003903165653003303204653001903237653002303256653001903279653002003298653001503318653002303333653003103356653002103387653002403408653002203432653002603454653001603480653002703496653001403523653001103537653002003548653001703568653002403585653003103609653002603640653002503666653002403691653002603715653002803741653002603769653002803795653002703823653002803850653002603878653002703904653002503931653003003956653002803986653002804014653002604042653002604068653002804094653002604122653002604148653002504174653002404199653002704223653002704250653002604277653003304303653001704336653002704353653001504380653002604395653002404421653001604445653002404461653002004485653001404505653001404519653002104533653002604554653002104580653002604601653002804627653001904655653002704674653003004701653002804731653002504759653002604784653002604810653002404836653002404860653002504884653002804909653001704937653005204954653002505006653002505031653002705056653002705083653002605110653002505136653002605161653002305187653003305210653001905243653004405262653001705306653002905323653002805352653003105380653001505411653003005426653002505456653002205481653002605503653002605529653001805555653003005573653002805603653002605631653002905657653001305686653002505699653002505724653002005749653001705769653002805786653002005814653002705834653001405861653002505875653002205900653002605922653003005948100001405978856010305992       1895                        eng d00aViaggio di Leonardo Fea in Birmania e regioni vicine. LX. Curculionidae0 aViaggio di Leonardo Fea in Birmania e regioni vicine LX Curculio  a153-3700 vxxxiv10aAcicnemis festiva10aAcicnemis mansueta10aAclees birmanus10aAgametis segnis10aAlcides aemulus10aAlcides bimaculatus10aAlcides corniculus10aAlcides feae10aAlcides frenatus10aAlcides funestus10aAlcides haruspax10aAlcides improvidus10aAlcides lichen10aAlcides ludificator10aAlcides mysticus10aAlcides nepalensis10aAlcides obesus10aAlcides pavidus10aAlcides porosus10aAlcides satelles10aAlcides scenicus10aAlcides tutus10aAlcides venosus10aAnaemerus cerberus10aAnius carinicollis10aAplotes bisulcatus10aAplotes lateritius10aApoderus (Centrocorynus) aemulus10aApoderus (Cycnotrachelus) coeruleatus10aApoderus blandus10aApoderus cyclops10aApoderus flaviceps10aApoderus latipennis10aApoderus semiannulatus10aApoderus tentator10aApries histrio10aArhines lanugineus10aArhines sirbenus10aArhines tutus10aAsemus feae10aAsemus lacordairei10aAsemus lentus10aAsemus mixtus10aAsemus pertusiventris10aAsemus plumeus10aAstycus10aAthesapeuta10aAthesapeuta albosparsus10aAthesapeuta aurantiaca10aAthesapeuta bengalica10aAthesapeuta chinensis10aAthesapeuta lineolata fasciatus10aAthesapeuta pinguis10aAthesapeuta secura10aAthesapeuta vinculata10aAttelabus (Lamprolabus) gestroi10aAttelabus (Paramecolabus) feae10aAttelabus humerosus10aAuletes (Auletobius) gestroi10aBaridius albosparsus10aBaridius subsignatus10aBaris amica10aBaris anxia10aBaris doriae10aBaris himalayana10aBaris impressipennis10aBaris quinquemaculata10aBaris speculifera10aCamptorhinus affinis10aCamptorhinus scrobicollis10aCelia10aCelia asperula10aCercidocerus birmanus10aCercidocerus carinensis10aCercidocerus hypocritus10aCercidocerus pictus10aCercidocerus pygmaeus10aCercophorus chloritis10aColobodes hystrix10aConarthrus nasutus10aCopturus10aCorigetus bidentulus10aCorigetus feae10aCorigetus filicornis10aCorigetus gestroi10aCorigetus molitor10aCorigetus subsulcatus10aCorigetus testatus10aCossonus argutus10aCossonus bimaculaltus10aCossonus carinensis10aCossonus foveicollis10aCryptorhynchini10aCryptorhynchus10aCryptorhynchus poricollis10aCyphicerus amphibolus10aCyphicerus confluens10aCyphicerus egenus10aCyphicerus indagator10aCyphicerus interruptus10aCyphicerus lincellus10aCyphicerus marginatus10aCyphicerus mutator10aCyphicerus nubilus10aCyphicerus patricius10aCyphicerus venalis10aCyrtotrachelus birmanicus10aCyrtotrachelus dux10aCyrtotrachelus feae10aDactylotus nitidulus10aDemimoea10aDesmidophorus brachmanum10aDiocalandra10aDyspnoetus10aDyspnoetus dignus10aDyspnoetus lincellus10aDyspnoetus morio10aEpilasius10aEpilasius obtusipennis10aEpilasius querulus10aEpisomus pudibundus10aEpisomus pudibundus auriculatus10aEpisomus pudibundus nigropustulatus10aEpisomus pudibundus profanus10aEpisomus pudibundus repandus10aEpisomus pudibundus sennae10aEpisomus pudibundus var. punctiger10aEpisomus pudibundus versutus10aErgania baulii10aErgania bhamoensis10aErgania doriae10aErgania proximo10aEucopturus10aEugnathus tenuipes10aEuops (Synaptops) fulgidus10aEutornus affinis10aEutornus antennalis10aEutornus crenatus10aEutornus longirostris10aGonipterini10aHeterophasis congruens10aHylobiini10aIxalma10aLamellocopturus10aLepidastycus10aLepidastycus doriae10aLepidastycus submarginalis10aLitorhynchus aberrans10aLitorhynchus anchora10aLitorhynchus noevus10aLitorhynchus robustus10aLitorhynchus separandus10aLitorhynchus turbatus10aLobotrachelus asperulus10aLobotrachelus ingratus10aLobotrachelus leucaspis10aLobotrachelus morosus10aMechistocerus angustus10aMechistocerus bardus10aMechistocerus caliginosus10aMechistocerus concretus10aMechistocerus corticeus10aMechistocerus decisus10aMechistocerus effusus10aMechistocerus fluctiger10aMechistocerus intutus10aMechistocerus mimicus10aMechistocerus mollis10aMechistocerus mucus10aMechistocerus offensus10aMechistocerus petulans10aMechistocerus similis10aMechistocerus subcylindricus10aMenectetorus10aMenectetorus luctuosus10aMimophilus10aMimophilus personatus10aMimophilus tragicus10aMyocalandra10aMyocalandra discors10aNeocleonus feae10aOdoiporus10aOntobaris10aOntobaris jocosa10aOrthosinus salutarius10aOsphilia egregia10aPachyonyx sulcicollis10aPaipalesomus bisulcatus10aParallelodemas10aParallelodemas docilis10aParallelodemas imperfecta10aParallelodemas perfecta10aParallelodemas tarda10aParallelodemas vicina10aPeriphemus pygidialis10aPeriphemus tricolor10aPeriphemus vittiger10aPhamomerus figuratus10aPhyllolytus longicornis10aPhytoscaphus10aPhytoscaphus carinirostrisPhytoscaphus imitator10aPhytoscaphus nubilus10aPhytoscaphus parilis10aPhytoscaphus perversus10aPhytoscaphus porcellus10aPhytoscaphus trepidus10aPhytoscaphus xiphias10aPolytus Porohylobhius10aPorohylobhius feae10aPorohylobhius ligniperdoides10aProdioctes dux10aProdioctes rubricosusProdioctes tristis10aRhabdocnemis10aRhadinomerus conciliatus10aRhadinomerus contemptus10aRhadinomerus granulicollis10aRhadinopus10aRhadinopus centriniformis10aRhadinopus consputus10aRhadinopus parcus10aRhynchites bhamoensis10aRhynchites carinensis10aSphenocorydes10aSphenocorynus impluviatus10aSympiezomias ellipticus10aSympiezomias inflatus10aSympiezomias sulcicollis10aTasactes10aTasactes carinulatus10aTasactes interruptus10aTelephae cupida10aTemnoschoita10aTemnoschoita pygidialis10aTetratopos feae10aTetratopos longicollis10aTryphetus10aTryphetus incarnatus10aTryphetus solidus10aXanthochelus eruditus10aXanthochelus miscellaneus1 aFaust, J.  uhttps://weevil.myspecies.info/viaggio-di-leonardo-fea-birmania-e-regioni-vicine-lx-curculionidae-001399nas a2200421   4500008004100000245008300041210006900124300001200193653001700205653003000222653002000252653002800272653002100300653001700321653001900338653001900357653002100376653002400397653002200421653002500443653003200468653001800500653002500518653003000543653002700573653001800600653002900618653002400647653002600671653002300697653002700720653002500747653002800772653002900800653002600829100001400855856010800869       1892                        eng d00aContributions a la Faune Indo-Chinoise. 10e Memoire. Curculionidae, Brenthidae0 aContributions a la Faune IndoChinoise 10e Memoire Curculionidae   a505-52210aAcallophilus10aAcallophilus scrobicollis10aAclees juvencus10aAmblyrhinus psittacinus10aApion inscriptum10aApion jekeli10aApion versutum10aArhines hirtus10aBaris singularis10aBercthia fairmairei10aCorigetus dejeani10aCorigetus fleutiauxi10aCorigetus nebulosus figulus10aCylas rufipes10aCyphicerus farinosus10aGasterocercus cristulatus10aHeteroptochus globulus10aMacrocordylus10aMacrocordylus wollastoni10aMecysmoderes stigma10aMyllocerus fleutiauxi10aMypomeces fabricii10aNanophyes longirostris10aOmotemnus fleutiauxi10aPhytoscaphus annamensis10aSphenophorus argillaceus10aSternochetus olivieri1 aFaust, J.  uhttps://weevil.myspecies.info/contributions-la-faune-indo-chinoise-10e-memoire-curculionidae-brenthidae00821nas a2200337   4500008004100000245003900041210003800080300001000118490000700128520002800135653001200163653001200175653001200187653001300199653001300212653001300225653001100238653001400249653001200263653001200275653001200287653001300299653001500312653001500327653001300342653001300355653001400368653001700382100001600399856006800415       1963                        eng d00aOrmanyosbogarak 3. Curculionidae 30 aOrmanyosbogarak 3 Curculionidae 3  a1-1040 v643 aKey to species, Hungary10aAcalles10aAlophus10aAnoplus10aCossonus10aEremotes10aHylobius10aHypera10aHyperinae10aLepyrus10aLiosoma10aLiparus10aMagdalis10aMyorrhinus10aPhytonomus10aPissodes10aPlinthus10aRhyncolus10aSphenophorus1 aEndrodi, S.  uhttps://weevil.myspecies.info/ormanyosbogarak-3-curculionidae-300385nas a2200121   4500008004100000245004600041210004300087300002300130490000700153100001800160700001900178856006600197       1920                        eng d00aA new avocado weevil from the Canal Zone.0 anew avocado weevil from the Canal Zone  a111-115 + 3 plates0 v201 aDietz, H., F.1 aBarber, H., S.  uhttps://weevil.myspecies.info/new-avocado-weevil-canal-zone-004880nas a2200133   4500008004500000020001400045245018100059210006900240300001000309490000700319520425000326100003504576856013504611       2008                        Engldsh    a0367-504100aThe types of Palaearctic species of the families Apionidae, Rhynchitidae, Attelabidae and Curculionidae in the collection of Etienne Louis Geoffroy (Coleoptera, Curculionoidea)0 atypes of Palaearctic species of the families Apionidae Rhynchiti  a17-440 v643 aThe Study of 131 more or less complete Curculionoid specimens of the collection Etienne Louis Geoffroy, conserved in the Museum d'Histoire Naturelle de Paris (Entomologie) has permitted the identification of several nominal species that were nomina dubia and the establishment of several new synonymies and combinations, and, in some cases, the reversion of precedence following Art. 23.9 of the Code, declaring nomina protecta and nomina oblita. New synonymies are (the first term is the valid name): Lixus filiformis (Fabricius, 1781) = Curculio longus Gmelin, 1790; Lasiorhynchites cavifrons (Gyllenhal, 1833) nom. protectum Rhinomacer viridis Geoffroy, 1785, nom. oblitum, Byctiscus betulae (Linnaeus, 1758) Rhinomacer auratus Geoffroy, 1785; Neocoenorrhinus pauxillus (Germar, 1824) nom. protectum Rhinomacer caeruleus Geoffroy, 1785, nom. oblitum; Deporaus betulae (Linnaeus, 1758) Curculio nigrostriatus Goeze, 1777 - Curculio niger Geoffroy, 1785 = Curculio fuliginosus Gmelin, 1790; Coniocleonus hollbergii (Fahraeus, 1842) = Curculio sulcatus Goeze, 1777 = Cuurculio sulcatus Geoffroy, 1785 = Curculio sulcatus Gmelin, 1790; Larinus iaceae (Fabricius, 1775) - Curculio carduelis Goeze, 1777; postica (Gyllenhal, 18 13), nom. protectum - Curculio fasciolatus Geoffroy., 1785, nom. oblitum; Charagmus griseus (Fabricius, 1775) = Curculio cupreosquamosus Goeze, 1777 = Curculio intersectus Geoffroy, 1785 = Curculio squamosus Gmelin, 1790; Sitona hispidulus (Fabricius, 1777) Curculio griseus Goeze, 1777 - Curculio modestus Geoffroy, 1785 = Curculio geoffroaei Gmelin, 1790 Aulacobaris cuprirostris (Fabricius, 1787) = Curculio viridisericeus Goeze, 1777; Cleopomiarus plantrum (Germar, 1824), nom. protectum = Curculio nigrostriatus Goeze, 1777 - Curculio floriger Geoffroy, 1785, nom. oblitum - Curculio subglobosus Gmelin, 1790, nom. oblitum; Anisorhynchus scabrousus (Geoffroy, 1785) = Curculio barbatus Rossi, 1794; Hylobius abietis (Linnaeus, 1758) - Curculio tigris Gmelin, 1790; Sitophilus granarius (Linnaeus, 1758) = Curculio contractus Geoffroy, 1785; Phyllobius pomaceus Gyllenhal, 1834 = Curculio auratus Geoffroy, 1785; Hylobius transversovittatus (Goeze, 1777) Curculio fascialis Gmelin, 1790. New combinations are: Leucophyes occidentalis (Dieckmann, 1982) (from Leucosomus) and Anisorhynchus scabrosus (Geoffroy, 1785) (from Curculio). The following names have been reinstated (stat. res.) as valid: Trachyphloeus spinosus (Goeze, 1777) for the species known as Trachyphloeus olivieri Bedel, 1883, Lixus pulverulentus (Scopoli, 1763) for the species known as Lixus angustatus (Fabricius, 1775). Hypera melancholica (Fabricius, 1793) is confirmed as the valid name for the species hitherto named Hypera fuscocinerea (Marsham, 1802) or Hypera murina (Fabricius, 1793). The following narrics are considered nomina dubia, since there is no identifiable type material: Curculio pulex Goeze, 1777, Rhinomacer minutus Geoffroy, 1785, Curculio pulex Gmelin, 1790 (non Goeze, 1777), rhinomacer striatus Geoffroy, 1785, Rhinomacer fulgidus Geoffroy, 1785, Curculio transversofasciatus Goeze, 1777, Curculio fasciatus Geoffroy, 1785 (non Scopoli, 1763, nec Strorm, 1768, nec Degeer, 1775, nec Muller, 1776), Curculio fuscatus Gmelin, 1790, Curculio sulcatus Goeze, 1777: 410 (non Fabricius, 1775, nec Goeze, 1777: 381), Curculio incisus Geoffroy, 1785, Curculio exaratus Gmelin, 1790, Curculio quadratus Goeze, 1777, Curculio quadrilis Geoffroy, 1785, Curculio griseosericeus Goeze, 1777, Curculio communis Geoffroy, 1785, Curculio thoracespinosus Goeze, 1777, Curculio armatus Geoffroy, 1785, Curculio denticulatus Gmelin, 1790 (non Schrank, 1781, nec Geoffroy, 1785), Curculio muricatus Goeze, 1777 (non Drury, 1773), Curculio murinus Geoffroy, 1785 (non Mueller, 1764), Curculio fuscipes Geoffroy, 1785, Curculio tesselatus Geoffroy, 1785 (non Fabricius, 1781), Curculio sericeus Goeze, 1777, Curculio villosus Geoffroy, 1785 (non Fabricius, 1781), Curculio sericeus Gmelin, 1790 (non Goeze, 1777, nec Schaller, 1783, nec Piller & Mitterpacher, 1783), Curculio virgo Goeze, 1777, Curculio virgo Geoffroy, 1785 (non Goeze, 1777), Curculio virgo Gmelin, 1790 (non Goeze, 1777, nec Geoffroy, 1785), Curculio punctulatus Geoffroy, 11 aAlonso-Zarazaga, Miguel, Angel  uhttps://weevil.myspecies.info/types-palaearctic-species-families-apionidae-rhynchitidae-attelabidae-and-curculionidae-collection-e00486nas a2200133   4500008004100000245007800041210006900119300001000188490000700198100001900205700001500224700001600239856009700255       2005                        eng d00aAclees cribratus, nuovo per l’Italia nocivo al fico allevato in vivaio.0 aAclees cribratus nuovo per l Italia nocivo al fico allevato in v  a69-710 v611 aCiampolini, M.1 aPerrin, H.1 aRegalin, R.  uhttps://weevil.myspecies.info/aclees-cribratus-nuovo-l-italia-nocivo-al-fico-allevato-vivaio01459nas a2200181   4500008004500000020001400045245011700059210006900176300001000245490000700255520080800262653001101070100001901081700001601100700001601116700001601132856012901148       2007                        Italdan    a0366-240300aFirst observations on the bioethology of Aclees sp. (Curculionidae, Molytinae) damaging Ficus carica L. in Italy0 aFirst observations on the bioethology of Aclees sp Curculionidae  a51-600 v393 aResults of bioethological observations on Aclees sp., that belongs to a group of species with not well known taxonomy, distributed in East Asia are reported. The observations were carried out from 2005 to 2006 in the Pistoia province (Tuscany). The species recently reported in Italy (as Aclees cribratus Gyllenhal) is, with respect to nutrition and reprodution, strictly related to Ficus carica L. and its cultivar; climatic factors have a significant influence on the life cycle. The xilophagous larvae cause serious damage to hypogeal wood that is completely destroyed resulting in high mortality of feeding larvae. Adults feed on epigeal plant parts. The plants suffering from infestations by Aclees sp. are found in either nurseries or permanent settings in both unmanaged areas or family orchards.10aAclees1 aCiampolini, M.1 aRegalin, R.1 aFarnesi, I.1 aLorenzi, C.  uhttps://weevil.myspecies.info/first-observations-bioethology-aclees-sp-curculionidae-molytinae-damaging-ficus-carica-l-italy02928nas a2200241   4500008004100000245015700041210006900198300001200267490000700279520206700286653001902353653002102372653003202393100001502425700001602440700001602456700001602472700001502488700001502503700001902518700001402537856013502551       2008                        eng d00aLong-term evolutionary stability of bacterial endosymbiosis in Curculionoidea: additional evidence of symbiont replacement in the Dryophthoridae family.0 aLongterm evolutionary stability of bacterial endosymbiosis in Cu  a859-8680 v253 aBacterial intracellular symbiosis ( endosymbiosis) is well documented in the insect world where it is believed to play a crucial role in adaptation and evolution. However, although Coleopteran insects are of huge ecological and economical interest, endosymbiont molecular analysis is limited to the Dryophthoridae family. Here, we have analyzed the intracellular symbiotic bacteria in 2 Hylobius species belonging to the Molytinae subfamily ( Curculionoidea superfamily) that exhibit different features from the Dryophthoridae insects in terms of their ecology and geographical spanning. Fluorescence in situ hybridization has shown that both Hylobius species harbor rod- shaped pleiomorphic symbiotic bacteria in the oocyte and in the bacteria- bearing organ ( the bacteriome), with a shape and location similar to those of the Dryophthoridae bacteriome. Phylogenetic analysis of the 16S ribosomal DNA gene sequences, using the heterogeneous model of DNA evolution, has placed the Hylobius spp. endosymbionts ( H- group) at the basal position of the ancestral Rclade of Dryophthoridae endosymbionts named Candidatus Nardonella but relatively distant from the S- clade of Sitophilus spp. endosymbionts. Endosymbionts from the H- group and the R- clade evolved more quickly compared with free- living enteric bacteria and endosymbionts from the S- and D- clades of Dryophthoridae. They are AT biased ( 58.3% A + T), and they exhibit AT- rich insertions at the same position as previously described in the Candidatus Nardonella 16S rDNA sequence. Moreover, the host phylogenetic tree based on the mitochondrial COI gene was shown to be highly congruent with the H- group and the R- clade, the divergence of which was estimated to be around 125 MYA. These new molecular data show that endosymbiosis is old in Curculionids, going back at least to the common ancestor of Molytinae and Dryophthoridae, and is evolutionary stable, except in 2 Dryophthoridae clades, providing additional and independent supplementary evidence for endosymbiont replacement in these taxa.10aDryophthoridae10aHylobius abietis10aHylobius transversovittatus1 aConord, C.1 aDespres, L.1 aVallier, A.1 aBalmand, S.1 aMiquel, C.1 aZundel, S.1 aLemperiere, G.1 aHeddi, A.  uhttps://weevil.myspecies.info/long-term-evolutionary-stability-bacterial-endosymbiosis-curculionoidea-additional-evidence-symbiont00403nas a2200157   4500008004100000245002500041210002500066300001000091490000700101653001800108653001800126653001300144653001400157100001900171856005500190       1919                        eng d00aAvocado seed weevils0 aAvocado seed weevils  a53-600 v2110aConotrachelus10aCurculionidae10aHeilipus10aMolytinae1 aBarber, H., S.  uhttps://weevil.myspecies.info/avocado-seed-weevils00401nas a2200121   4500008004100000245005600041210005400097300001200151490000700163653001300170100001900183856007700202       1912                        eng d00aNote on the avocado weevil (Heilipus lauri Boheman)0 aNote on the avocado weevil Heilipus lauri Boheman  a181-1830 v1410aHeilipus1 aBarber, H., S.  uhttps://weevil.myspecies.info/note-avocado-weevil-heilipus-lauri-boheman