25843nas 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/1403001101nas a2200193   4500008004100000020001400041245009400055210006900149260001600218300001200234490000700246520044100253653002400694653002400718653002100742653001900763100002000782856010500802       2010                        eng d  a1341-116000aThe subgenus Tachypterellus of the genus Anthonomus (Coleoptera, Curculionidae) from Laos0 asubgenus Tachypterellus of the genus Anthonomus Coleoptera Curcu  cNovember 30  a203-2110 v163 aThree new species of the subgenus Tachypterellus are described from Laos as the first representatives of the anthonomine subgenus from the Indochina under the names of Anthonomus (Tachypterellus) yoroi sp. nov., A. (T.) spinosus sp. nov., and A. (T.) laoensis sp. nov. All of them occurred sympatrically and were captured on a single fruiting evergreen Prunus tree at the same time. A key to the species of Tachypterellus is also given.10aAnthonomus laoensis10aAnthonomus spinosus10aAnthonomus yoroi10aTachypterellus1 aKojima, Hiroaki  uhttps://weevil.myspecies.info/subgenus-tachypterellus-genus-anthonomus-coleoptera-curculionidae-laos02168nas a2200181   4500008004100000020001400041245011300055210006900168260001100237300001200248490000700260520151100267653002501778100001701803700001601820700001801836856013201854       2011                        eng d  a1021-358900aBiological control of dense-thorned bitter apple, Solanum sisymbriifolium Lam. (Solanaceae), in South Africa0 aBiological control of densethorned bitter apple Solanum sisymbri  cAugust  a427-4330 v193 aSolanum sisymbriifolium Lam. is a weed of disturbed areas in South Africa, particularly in the high-elevation summer rainfall areas of the country. Despite the introduction of the South American leaf-feeding tortoise beetle, Gratiana spadicea (Klug) (Coleoptera: Chrysomelidae: Cassidinae) in 1994, the weed has continued to spread. Although established in a number of regions, beetle populations appear to persist in relatively low numbers, inflicting minimal damage to the weed. Consequently, a number of variables have been investigated in order to explain this lack of efficacy, and in some cases, failure to establish. Gratiana spadicea populations in South Africa are under considerable stress both from abiotic and biotic sources. Population-limiting factors such as disturbance of overwintering sites, climatic incompatibility, and high rates of pupal parasitism translate into low numbers of the agent at the start of each growing season. Small early-season populations which are slow to build-up, coupled with asynchronous development of S. sisymbriifolium, limit the beetles' effective-ness and pre-empt any impact on the weeds' reproductive output. Consequently, G. spadicea alone is unlikely to control S. sisymbriifolium infestations in South Africa. The flower-feeding weevil Anthonomus sisymbrii Hustache (Coleoptera: Curculionidae: Anthonominae), may therefore warrant study as it could have the potential, if released, to curtail fruit production and further spread of S. sisymbriifolium.10aAnthonomus sisymbrii1 aKing, A., M.1 aBrudvig, R.1 aByrne, M., J.  uhttps://weevil.myspecies.info/biological-control-dense-thorned-bitter-apple-solanum-sisymbriifolium-lam-solanaceae-south-africa02351nas a2200181   4500008004500000020001400045245017300059210006900232260001300301300001400314490000800328520159600336653003101932100002101963700002701984700002302011856013502034       2008                        Engldsh    a0022-049300aGenetic profiling to determine potential origins of boll weevils (Coleoptera: Curculionidae) captured in a Texas eradication zone: endemicity, immigration, or sabotage?0 aGenetic profiling to determine potential origins of boll weevils  cDecember  a1729-17360 v1013 aThirty-seven boll weevils, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), were captured in pheromone traps near Lubbock, TX, in the Southern High Plains/Caprock eradication zone during August-October 2006. No boll weevils had been captured in this zone or neighboring zones to the north earlier in the year, and only very low numbers had been captured in neighboring zones to the south and east. Therefore, the captures near Lubbock were unexpected. Five of the weevils captured the last week of August were preserved and genotyped at 10 microsatellite loci for comparison with a database of genotypes for 22 boll weevil populations sampled from eight U.S. states and four locations in Mexico. The Lubbock population itself is an unlikely source, suggesting that the captured weevils probably did not originate from a low-level endemic population. Populations from eastern states, Mexico, and Big Spring, TX, can be confidently excluded as potential source regions. Although the Weslaco and Kingsville, TX, areas cannot be statistically excluded, they are unlikely sources. The most likely sources are nearby areas inNewMexico, TX, or southwest Oklahoma, or from areas of eastern Texas represented by Waxahachie and El Campo populations. Together, genetic and circumstantial evidence suggest either that the trapped boll weevils are the offspring of a lone mated female that immigrated from eastern Texas earlier in thesummeror that weevils originally captured near Waxahachie but now long-dead were planted in the traps by a disgruntled employee of the eradication program.10aAnthonomus grandis grandis1 aKim, Kyung, Seok1 aSappington, Thomas, W.1 aAllen, Charles, T.  uhttps://weevil.myspecies.info/genetic-profiling-determine-potential-origins-boll-weevils-coleoptera-curculionidae-captured-texas-e02594nas a2200205   4500008004100000020001400041245013400055210006900189260001000258300001200268490000800280520181500288653003102103100002102134700002002155700002702175700002402202700002702226856013502253       2009                        eng d  a0022-049300aMolecular diagnostic for boll weevil (Coleoptera: Curculionidae) based on amplification of three species-specific microsatellites0 aMolecular diagnostic for boll weevil Coleoptera Curculionidae ba  cApril  a759-7660 v1023 aThe boll weevil, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), is a serious pest of cultivated cotton, Gossypium hirsutum, L., in the Americas, and reinfestation of zones from which they have been eradicated is of perpetual concerti. Extensive arrays of pheromone traps monitor for reintroductions, but occasionally the traps collect nontarget weevils that can be misidentified by scouts. For example, the congeneric pepper weevil, Anthonomus eugenii Cano, and other superficially similar weevils are attracted to components of the boll weevil lure or trap color. Although morphologically distinguish able by trained personnel, the potential for misidentification is compounded when captured weevils are dismembered or partially consumed by ants or ground beetles that sometimes feed on them in the traps. Because misidentification can have expensive consequences, a molecular diagnostic tool would be of great value to eradication managers. We demonstrate that a cocktail of three primer pairs in a single polymerase chain reaction (PCR) amplify species-specific microsatellites that unambiguously distinguish the boll weevil from three other weevil species tested, including pepper we evil; cranberry weevil, Anthonomus eugenii musculus Say; and pecan weevil, Curculio caryae Horn. However, it does not distinguish the boll weevil from the subspecific "thurberia" weevil. A universal internal transcribed spacer primer pair included in the cocktail cross-amplifies DNA from all species, serving as a positive control. Furthermore, the diagnostic primers amplified the target microsatellites from various boll weevil adult body parts, indicating that the PCR technology using the primer cocktail is sensitive enough to positively identify a boll weevil even when the body is partly degraded.10aAnthonomus grandis grandis1 aKim, Kyung, Seok1 aSzendre, Zsofia1 aRodriguez-Saona, Cesar1 aMulder, Phillip, C.1 aSappington, Thomas, W.  uhttps://weevil.myspecies.info/molecular-diagnostic-boll-weevil-coleoptera-curculionidae-based-amplification-three-species-specific02457nas a2200181   4500008004100000020001400041245009500055210006900150260000900219300001000228490000700238520182100245653002402066100002402090700002502114700002302139856011302162       2007                        eng d  a0191-612200aAlmond, melon, and pigweed pollen retention in the boll weevil (Coleoptera: Curculionidae)0 aAlmond melon and pigweed pollen retention in the boll weevil Col  c2007  a81-930 v313 aThe boll weevil (Anthonornus grandis Boheman) remains a devastating insect pest on cotton (Gossypium hirsutum C. Linnaeus), particularly where it has not been eradicated. Identifying and understanding the survival of overwintered boll weevils, when cotton is not available, is important in designing mitigation programs and controlling this insect pest, especially in areas where boll weevils are active all year. Many non-malvaceous taxa have been listed as possible overwintering adult food sources. The purpose of this research was to determine if pollen from three non-malvaceous taxa could be used as food sources for overwintering boll weevils in the Lower Rio Grande Valley of Texas, where weevils are active year-round and during cotton-free periods. The taxa are almond (Prunus dulcis (Mill.) D.A. Webb), melon (Cucumis melo C. Linnaeus subsp. melo), and pigweed (Amaranthus sp.), Furthermore, it was intended to determine the retention of these pollen types in the boll weevil gut. More weevils (84%) contained almond pollen when they had additional water than those (30%) that did not have additional water. Almond pollen was found in 100% of the examined weevils after 72 hours, and in 80% after 96 hours. Pigweed and melon pollen were never found after 48 hours. Overall, almond pollen was found in more weevils (96%) than pigweed (40%), or melon (12%). In addition, a greater number of almond pollen grains (539) were found than pigweed (41), or melon (21). This shows that these types of pollen were consumed, and could play a part in the survival of overwintering weevils. However, more research is needed to examine the nutritional value of these, and other, pollen grains for overwintering boll weevil survival, and to determine the length of time weevils can survive feeding on these pollen types.10aAnthonornus grandis1 aJones, Gretchen, D.1 aGreenberg, Shoil, M.1 aEischen, Frank, A.  uhttps://weevil.myspecies.info/almond-melon-and-pigweed-pollen-retention-boll-weevil-coleoptera-curculionidae02019nas a2200193   4500008004100000020001400041245013300055210006900188260001400257300001200271490000700283520126100290653002401551100002701575700002901602700003401631700002601665856013401691       2011                        eng d  a0147-172400aParasitoids of Anthonomus sisyphus Clark (Coleoptera: Curculionidae) in Red Nanche Fruits (Malpighia mexicana) in Oaxaca, Mexico0 aParasitoids of Anthonomus sisyphus Clark Coleoptera Curculionida  cSeptember  a351-3610 v363 aMalpighia mexicana, or red nanche, is a plant with edible fruits, used on crafts and medicine, as well as for the establishment of living fences. The objective of this work was to catalog the parasitoids associated with Anthonomus sisyphus Clark (Coleoptera: Curculionidae) in the fruit of M. mexicana in the central valleys of Oaxaca, Mexico. The sampling sites were located in San Lorenzo Cacaotepec and the Ethnobotanical Garden of Santo Domingo. From 2005 to 2007, mature red nanche fruits were collected weekly to determine the emergency of the parasitoids. The fruits were weighed, counted and placed in trays. The greatest infestation was found in San Lorenzo Cacaotepec with 1.16 to 1.44 weevils per fruit while in the Ethnobotanical Garden were 0.74 to 1.18 weevils per fruit. Seven different species of parasitoids belonging to the families Braconidae, Pteromalidae, and Eupelmidae were found associated with A. sisyphus. The most abundant species were Triaspis eugenii, Diospilus sp., and Bracon sp. The Ethnobotanical Garden was the site with the greatest abundance of species of parasitoids and presented the highest level of parasitism. The species with the highest proportion of males were Bracon sp. in 2005 and 2007 and T. eugenii in 2006.10aAnthonomus sisyphus1 aJarquin-Lopez, Roselia1 aMartinez-Martinez, Laura1 aSanchez-Garcia, Jose, Antonio1 aFigueroa, Jose, Isaac  uhttps://weevil.myspecies.info/parasitoids-anthonomus-sisyphus-clark-coleoptera-curculionidae-red-nanche-fruits-malpighia-mexicana01966nas a2200589   4500008004100000245009200041210006900133300001200202490000800214653002200222653001400244653002100258653002400279653002100303653002700324653002200351653002600373653002400399653002900423653002600452653002500478653002400503653001300527653002300540653002900563653003100592653001800623653002700641653002100668653001500689653002200704653002400726653002300750653002900773653003000802653001600832653004800848653002900896653003700925653003000962653002200992653001601014653002601030653002801056653004101084653003701125653002901162653002801191653002101219100001701240856011901257       1940                        eng d00aCurculionides nouveaux de l'Argentine et autres regions sud-americaines (deuxieme note)0 aCurculionides nouveaux de lArgentine et autres regions sudameric  a112-1440 v12910aAcalles tigreanus10aAcariosia10aAcariosia notata10aAeatus carinicollis10aAeatus contiguus10aAeatus oncorrhinoideus10aAeatus puncticeps10aAeatus quadraticollis10aAnthonomus dentipes10aAnthonomus gracilicornis10aAnthonomus obliquatus10aAnthonomus sisymbrii10aAnthonomus tibialis10aAzygides10aAzygides testaceus10aConotrachelus humeridens10aConotrachelus subhumeralis10aDorytosomimus10aDorytosomimus vestitus10aEndalus communis10aErycosimus10aErycosimus bruchi10aEubulus niveipectus10aHenosomus signalus10aMitrephorus albolineatus10aMitrephorus curvilineatus10aNeoazygides10aNeohustachius Neohustachius tuberculipennis10aOxytenopterus maculiceps10aOxytenopterus quadrituberculatus10aOxytenopterus subcaudatus10aPalocopsis vagans10aProdialomia10aProdialomia paranense10aPseudomopsis bolivianus10aSaladorhynckusSaladorhynckus wagneri10aSemnorrhynchus serietuberculatus10aSemnorrhynchus trivialis10aTorcobius canaliculatus10aTyloderma cuprea1 aHustache, A.  uhttps://weevil.myspecies.info/curculionides-nouveaux-de-largentine-et-autres-regions-sud-americaines-deuxieme-note03550nas a2201141   4500008004100000245003600041210003500077300003900112490000600151653001900157653002400176653002200200653003100222653001300253653002400266653002200290653002300312653001500335653002800350653002800378653002500406653002200431653002600453653002500479653002900504653002600533653002700559653002700586653003100613653001700644653002300661653002900684653002000713653002300733653002600756653003200782653002900814653003300843653002500876653003200901653003200933653002700965653003300992653002801025653002801053653001701081653002401098653001501122653002901137653004001166653002001206653001901226653002901245653002601274653002901300653001501329653002401344653002201368653003901390653002701429653003301456653002801489653002201517653002101539653002901560653001501589653002201604653001601626653002801642653002301670653002701693653001701720653002801737653002701765653002701792653003001819653002301849653003101872653001501903653002901918653002701947653002801974653002902002653002602031653001302057653002002070653002402090653002302114653002802137653002702165653002902192653002902221653003102250653002702281653001802308100001702326856006502343       1929                        eng d00aCurculionides de la Guadaloupe.0 aCurculionides de la Guadaloupe  a165-267 (special pagination 1-103)0 v310aAcalles dufaui10aAcalles planipennis10aAcalles squamosus10aAnchonomorpha guadelupense10aAnchonus10aAnchonus scrabrosus10aAnchonus spinosus10aAnchonus tuberosus10aAnthonomus10aAnthonomus biinaculatus10aAnthonomus convexifrons10aAnthonomus differens10aAnthonomus dufaui10aAnthonomus filicornis10aAnthonomus flexuosus10aAnthonomus guadelupensis10aAnthonomus homunculus10aAnthonomus spinipennis10aAnthonomus squamulatus10aAnthonomus thyasocnemoidus10aApion dufaui10aApion guadelupense10aAuletobius guadelupensis10aCamaratus rufus10aCatiline elongatus10aCatiline tuberculatus10aConotrachelus brevicrinitus10aConotrachelus cinnamomus10aConotrachelus codosternoides10aConotrachelus dufaui10aConotrachelus guadelupensis10aConotrachelus hirsutipennis10aConotrachelus obscurus10aConotrachelus obtusedentalus10aDiaprepes distinguendus10aDiaprepes guadelupensis10aDorytomorpha10aDorytomorpha tonsus10aDufaniella10aDufaniella heterorostris10aDufauiella Dufauiella heterorostris10aEuscepes tonsus10aEuscepes ursus10aMicroxypterus maculaalba10aMicroxypterus minutus10aNeochetina guadelupensis10aNeotylodes10aNeotylodes caudatus10aNeotylodes hirtus10aNeotylodes hirtus (Curculionidae).10aNeotylodes ovalipennis10aNeotylodes parallelipipennis10aOxypterus obliquevittis10aOxypterus ornatus10aOzoctenus dufaui10aPandeleteius testaceipes10aParanalcis10aParanalcis dufaui10aParanchonus10aParanchonus latirostris10aParanchonus ovatus10aParanchonus verrucosus10aParaulosomus10aParaulosomus difficilis10aParaulosomus impressus10aParaulosomus maculatus10aParaulosomus puncticollis10aParaulosomus ursus10aPerisacalles guadelupensis10aPhyllotrox10aPhyllotrox callosipennis10aPhyllotrox nigripennis10aPhyllotrox nigroventris10aPolydrosus guadelupensis10aPolydrosus latitarsis10aPrepodes10aPrepodes dufaui10aPrepodes marmoratus10aPrepodes marmoreus10aPromecops sinuatocollis10aPseudanthonomus bellus10aPseudanthonomus pusillus10aPseudanthonomus seriatus10aPseudanthonomus sylvaticus10aRhyparonotus insularis10aUdeus muticus1 aHustache, A.  uhttps://weevil.myspecies.info/curculionides-de-la-guadaloupe00547nas a2200121   4500008004600000245012400046210006900170300001000239490000800249653002800257100000500285856013500290       Submitted                   eng d     00aPopulation structure of the boll weevil in cotton fields and subtropical forests of South America: a bayesian approach.0 aPopulation structure of the boll weevil in cotton fields and sub  a11-200 v13110aAnthonomus, boll weevil1 a  uhttps://weevil.myspecies.info/population-structure-boll-weevil-cotton-fields-and-subtropical-forests-south-america-bayesian-approa02699nas a2200229   4500008004100000020001400041245010900055210006900164260001300233300001200246490000700258520189500265653003102160100002502191700002402216700001902240700002302259700002102282700001902303700002202322856012502344       2007                        eng d  a1672-960900aSurvival of boll weevil (Coleoptera: Curculionidae) adults after feeding on pollens from various sources0 aSurvival of boll weevil Coleoptera Curculionidae adults after fe  cDecember  a503-5100 v143 aThe survival of overwintering boll weevil, Anthonomus grandis grandis (Boheman), adults on non-cotton hosts in the Lower Rio Grande Valley (LRGV) of Texas was examined from 2001 to 2006. The success of the Boll Weevil Eradication Program, which was re-introduced into the LRGV in 2005, depends on controlling overwintering boll weevil populations. Laboratory studies were conducted using boll weevil adults that were captured in pheromone traps from September through March. The number of adults captured per trap declined significantly in the field from fall to the beginning of spring (3.5-7.0-fold). The proportion of trapped males and females did not differ significantly. The mean weight of boll weevil adults captured in September was 13.3 mg, while those of captured adults from November to February were significantly lower and ranged from 6.7 to 7.8 mg. Our results show that boll weevil adults can feed on different plant pollens. The highest longevity occurred when adults were fed almond pollen or mixed pollens (72.6 days and 69.2 days, respectively) and the lowest when they fed on citrus pollen or a non-food source (9.7 days or 7.4 days, respectively). The highest adult survival occurred on almond and mixed pollens [88.0%-97. 6% after 1st feeding period (10 days), 78.0%-90.8% after 3rd feeding period (10 days), 55. 0%-83.6% after 5th feeding period (10 days), and 15.2%-32.4% after 10th feeding period (10 days)). The lowest adult survival occurred on citrus pollen [52.0%-56.0% after 1st feeding period (10 days), 13.3% after 3rd and 5th feeding periods (10 days), and 0 after 6th feeding period (10 days)]. Pollen feeding is not a behavior restricted to adult boll weevils of a specific sex or physiological state. Understanding how boll weevil adults survive in the absence of cotton is important to ensure ultimate success of eradicating this pest in the subtropics.10aAnthonomus grandis grandis1 aGreenberg, Shoil, M.1 aJones, Gretchen, D.1 aEischen, Frank1 aColeman, Randy, J.1 aAdamczyk, J., J.1 aLiu, Tong-Xian1 aSetamou, Mamoudou  uhttps://weevil.myspecies.info/survival-boll-weevil-coleoptera-curculionidae-adults-after-feeding-pollens-various-sources02371nas a2200217   4500008004500000020001400045245011000059210006900169260001300238300001400251490000700265520160000272653002301872653003101895100002201926700002301948700002101971700001601992700001602008856012902024       2008                        Engldsh    a0046-225X00aEffects of photoperiod on boll weevil (Coleoptera: Curculionidae) development, survival, and reproduction0 aEffects of photoperiod on boll weevil Coleoptera Curculionidae d  cDecember  a1396-14020 v373 aEffects of photoperiod on development, survival, feeding and oviposition of boll weevils, Anthonomus grandis grandis Boheman, were assessed under five different photophases (24, 14,12, 10, and 0 h) at a constant 27 [degree]C temperature and 65% RH in the laboratory. Analyses of our results detected positive relationships between photoperiod and puncturing (mean numbers of oviposition and feeding punctures per day), and oviposition (oviposition punctures/oviposition+feeding punctures) activities, and the proportion of squares attacked by boll weevil females. When boll weevil females developed in light: darkness cycles, they produced a significantly higher percentage of eggs developing to adulthood than those developed in 24-h light or dark conditions. In long photoperiod (24:0 and 14:10 h), the number of female progeny),vas significantly higher and their development time was significantly shorter than those developed in short photoperiod (0:24 and 10:14 h). Lifetime oviposition was significantly highest at 12- and 14-h photophase, lowest at 0- and 10-h photophase, and intermediate at 24 h of light. Life table calculations indicated that boll weevil populations developed in a photoperiod of 14:10 and 12:12 (L: D) h will increase an average of two-fold each generation (Ro) compared with boll weevils developed in 24:0- and 10:14-h photoperiods and 15-fold compared with those at 0:24 h. Knowledge of the photoperiod-dependent population growth potential is critical for understanding population dynamics to better develop sampling protocols and timing insecticide applications.10aAnthonomus grandis10aAnthonomus grandis grandis1 aGreenberg, S., M.1 aSappington, T., W.1 aAdamczyk, J., J.1 aLiu, T., X.1 aSetamou, M.  uhttps://weevil.myspecies.info/effects-photoperiod-boll-weevil-coleoptera-curculionidae-development-survival-and-reproduction02782nas a2200241   4500008004100000020001400041245013300055210006900188260001100257300001200268490000700280520193300287653003102220100002202251700001802273700002102291700001602312700002202328700002002350700001602370700001902386856013502405       2009                        eng d  a1672-960900aReproductive potential of field-collected overwintering boll weevils (Coleoptera: Curculionidae) fed on pollen in the laboratory0 aReproductive potential of fieldcollected overwintering boll weev  cAugust  a321-3270 v163 aThe reproductive potential of overwintering boll weevil, Anthonomus grandis grandis (Boheman), females collected from pheromone traps in September, November and January, fed for 1, 3, and 5 weeks on plant pollens, and then provided cotton squares, was determined in the laboratory at 27 [plus or minus] 1[degree]C, 65% RH, and a photoperiod 13 : 11 (L : D) h. Duration of pollen feeding by overwintering boll weevils did not significantly influence egg and feeding punctures, or puncture ratios (egg to total punctures) for any of the three months of parent weevil collections when provided cotton squares on a daily basis. However, punctures and puncture ratios are significantly different when comparing mean data between months of boll weevil collections. When boll weevils were provided with cotton squares daily, the pre-ovipositional periods of female parents captured in September, November and January were 5, 9 and 14 days, respectively. The rate of eggs by females was significantly lower during November and January than September. Female parents collected in September produced a significantly higher percentage of eggs yielding adult progeny than those collected in November and January. Life table parameters indicated that net reproductive rate (Ro) of boll weevil females collected in September was 1.2-fold higher than those collected in November and 10.7-fold higher than those collected in January. Except for testes size, no differences in male reproductive parameters were observed during the cotton-free period compared with males captured during mid-cotton (June). The number of oocytes in the ovarioles and the number of oocytes containing yolk were significantly lower during September, November and January compared with June. The reproductive potential of overwintering boll weevil females collected in different months is an important consideration in determining the success of any control strategy.10aAnthonomus grandis grandis1 aGreenberg, S., M.1 aJones, G., D.1 aAdamczyk, J., J.1 aEischen, F.1 aArmstrong, J., S.1 aColeman, R., J.1 aSetamou, M.1 aLiu, Tong-Xian  uhttps://weevil.myspecies.info/reproductive-potential-field-collected-overwintering-boll-weevils-coleoptera-curculionidae-fed-polle00585nas a2200145   4500008004100000245009600041210006900137300000700206490000700213653003000220653002800250653002400278100002000302856011700322       1953                        eng d00aSexual dimorphism and synonymy in Anthonomus (Anthonomorphus) (Coleoptera-: Cur-culionidae)0 aSexual dimorphism and synonymy in Anthonomus Anthonomorphus Cole  a410 v2910aAnthonomus Anthonomorphus10aAnthonomus peninsularis10aAnthonomus pervilis1 aGilbert, E., E.  uhttps://weevil.myspecies.info/sexual-dimorphism-and-synonymy-anthonomus-anthonomorphus-coleoptera-cur-culionidae02054nas a2200241   4500008004500000020001400045245010100059210006900160300000900229490000700238520122500245653002401470653002501494653002301519653002401542653002601566653002401592653002401616653002601640100001601666700001601682856011401698       1986                        Engldsh    a0010-065X00aRevision of the gularis species group of the genus Anthonomus Germar (Coleoptera: Curculionidae)0 aRevision of the gularis species group of the genus Anthonomus Ge  a1-260 v403 aIt is hypothesized that the 10 species of the gularis species group of the genus Anthonomus Germar constitute a monophyletic group on the basis of morphological characters. Furthermore, some of the species are known to have host plants in the genus Cassica (Fabaceae) and none are known to have host plants in any other genus. Various morphological characters were used as evidence to propose a hypothesis of the phylogenetic relationships of the species to each other. The species are primarily neotropical in distribution although two, A. rufipennis LeConte and A. gularis LeConte, do occur in the eastern United States. A diagnosis and description of the group and of each species in the group, as well as a key to the species and illustrations of important characters, are presented as aids in identifying the species. Six new species are described: A. macarioi from Mexico, A. gallinae from Belize, A. estebani and a. faustinoi from Brazil, A. felipae from Panama, and A. melitoni from Peru. The name A. cossonoides Champion is placed in new synonymy under A. instabilis Faust and the names A. virgo Dietz and A. unicus Blatchley are synonymized with A. rufipennis. [Also include in the group is A. sobrinus Faust].10aAnthonomus estebani10aAnthonomus faustinoi10aAnthonomus felipae10aAnthonomus gallinae10aAnthonomus instabilis10aAnthonomus macarioi10aAnthonomus melitoni10aAnthonomus rufipennis1 aClark, W.E.1 aBurke, H.R.  uhttps://weevil.myspecies.info/revision-gularis-species-group-genus-anthonomus-germar-coleoptera-curculionidae00794nas a2200205   4500008004500000020001400045245011200059210006900171300001200240490000700252653002900259653002400288653002500312653002400337653002700361653002600388653002600414100001600440856013200456       1991                        Engldsh    a0010-065X00aRevision of the Anthonomus alboannulatus and Anthonomus triensis species groups (Coleoptera: Curculionidae)0 aRevision of the Anthonomus alboannulatus and Anthonomus triensis  a206-2260 v4510aAnthonomus alboannulatus10aAnthonomus tricopis10aAnthonomus tricuspis10aAnthonomus triensis10aAnthonomus tripugionis10aAnthonomus trisicifer10aAnthonomus whiteheadi1 aClark, W.E.  uhttps://weevil.myspecies.info/revision-anthonomus-alboannulatus-and-anthonomus-triensis-species-groups-coleoptera-curculionidae02622nas a2200229   4500008004100000020002500041245016200066210006900228260000800297300001200305490000800317520174400325653003102069100002302100700002102123700001402144700002302158700002502181700002402206700002702230856013502257       2011                        eng d  a0013-8746; 1938-290100aTemporal Changes in Genetic Variation of Boll Weevil (Coleoptera: Curculionidae) Populations, and Implications for Population Assignment in Eradication Zones0 aTemporal Changes in Genetic Variation of Boll Weevil Coleoptera   cJul  a816-8250 v1043 aAn existing microsatellite genotype database has been used for several years in population genetic assignment analyses of boll weevils, Anthonomus grandis grandis Boheman (Coleoptera: Curculionidae), captured in eradication zones. It is important to update it in case of changes in genotype frequency at any of the locations over time. Such changes at neutral loci could be caused by drift, immigration, or population bottlenecks. We examined allele frequency distribution for 10 microsatellite loci to determine genetic differentiation among 10 boll weevil populations sampled from Texas and Mexico in 2009. In addition, temporal changes in genetic composition were examined in the eight populations for which samples were available from previous years. Substantial levels of spatial genetic structure were observed, with the 10 populations clustering as four major groups. Pairwise FST estimates in 2009 samples ranged from 0.001 (College Station-Cameron) to 0.492 (College Station-Ojinaga). There was little change in genetic profiles over time at four of the eight locations. Thus, for those four locations, genotype and allele frequency data can be pooled over the two sample dates, which will provide greater statistical power in future population assignment tests. However, genetic profiles changed substantially at Ojinaga, and to a lesser extent at Uvalde, Cameron, and Rosales, so the 2009 genotype data should be substituted in future analyses. Finally, populations from two new locations, Brownsville and Lockhart, TX, were sampled, genotyped, and added to the database. The addition of Lockhart is particularly important given its surprisingly high differentiation from the relatively nearby populations of Cameron and Uvalde.10aAnthonomus grandis grandis1 aChoi, Sung, Kyoung1 aKim, Kyung, Seok1 aLee, Hang1 aAdamczyk, John, J.1 aGreenberg, Shoil, M.1 aWestbrook, John, K.1 aSappington, Thomas, W.  uhttps://weevil.myspecies.info/temporal-changes-genetic-variation-boll-weevil-coleoptera-curculionidae-populations-and-implications01443nas a2200181   4500008004100000020001400041245015700055210006900212260000800281300001200289490000800301520072600309653002601035100002901061700001901090700001701109856013501126       2012                        eng d  a0013-879700aTHE LIFE HISTORY AND IMMATURE STAGES OF THE WEEVIL ANTHONOMUS MONOSTIGMA CHAMPION (COLEOPTERA: CURCULIONIDAE) ON MICONIA CALVESCENS DC (MELASTOMATACEAE)0 aLIFE HISTORY AND IMMATURE STAGES OF THE WEEVIL ANTHONOMUS MONOST  cApr  a173-1850 v1143 aWe describe and illustrate the life history and immature stages of Anthonomus monostigma Champion (Curculionidae: Curculioninae: Anthonomini). This weevil is a fruit borer in Miconia calvescens DC (Melastomataceae), a Neotropical tree that is invasive in Pacific islands. The larva has three instars, and development from egg to adult requires approximately two months. In Costa Rica, A. monostigma larvae were found in three Miconia species, and adults fed only on Miconia species. Host relationships of the A. monostigma group suggest that this group could be related to the A. partiarius and A. albocivitensis groups (sensu Clark 1992, 1993b). The potential of A. monostigma as a biological control agent is discussed.10aAnthonomus monostigma1 aChacon-Madrigal, Eduardo1 aJohnson, Tracy1 aHanson, Paul  uhttps://weevil.myspecies.info/life-history-and-immature-stages-weevil-anthonomus-monostigma-champion-coleoptera-curculionidae-mico02003nas a2200181   4500008004500000020001400045245018300059210006900242260001000311300001200321490000700333520127300340653001501613653002401628100001601652700001801668856013501686       2007                        Turkdsh    a1010-696000aDetermination of Anthonomus species (Coleoptera: Curculionidae) and population changes of the almond pest, Anthonomus amygdali Hustache in Diyarbakir, Elazig and Mardin provinces0 aDetermination of Anthonomus species Coleoptera Curculionidae and  cEylul  a189-2020 v313 aThis study was carried out during years 2002-2004 at the almond orchards of Diyarbakir, Mardin and Elazig provinces located at Southeast and East Anatolian regions. Four species belonging to the genus Anthonomus were determined on almond orchards. Those species were Anthonomus amygdali Hustache, Anthonomus bituberculatus Thomson, Anthonomus brevispennis Pic. and Anthonomus variabIlis (Hoffman). Although 4 species have been found at the almond orchards as a result of the studies, it was determined that the dominant species was A. amygdali. The most population density of A. amygdali in Diyarbakir province was determined in 26th May 2003, during 3 years studies with 154 individuals/100 knock in Ergani district. The most population density of A. amygdali in Elazig province among years of 2002, 2003 and 2004 in almond orchards was determined in 22nd May 2002 with individuals/100 knock in Gezin district. The top population density of pest in Mardin province was founded in Omerli district with 25 individuals/100 knock in 12 May, 2003. In general the population of A. amygdali in Diyarbakir was founded higher than other 2 province. It was determined that flights of the adults in general were occurred between the months from April to June in almond orchards.10aAnthonomus10aAnthonomus amygdali1 aBolu, Halil1 aOezgen, Inanc  uhttps://weevil.myspecies.info/determination-anthonomus-species-coleoptera-curculionidae-and-population-changes-almond-pest-anthono