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Objectives To determine the prevalence of penicillin susceptibility among MSSA causing bloodstream infections (BSIs) in 16 Spanish hospitals and to characterize the penicillin-susceptible MSSA (MSSA-PENS) isolates. Methods A total of 1011 Staphylococcus aureus isolates were collected from blood cultures in 16 Spanish hospitals during 2018–19 (6–12 months) and their susceptibility to 18 antimicrobials was determined. The MSSA-PENS isolates were selected and examined by PCR to determine the presence of the blaZ gene, other resistance genes and the genes lukF/lukS-PV, eta, etb and tst. The immune evasion cluster (IEC) type was also analysed. All the MSSA-PENS isolates were submitted to S. aureus protein A (spa) typing and the clonal complexes (CCs) were assigned according to their spa type. Results The prevalence of MSSA was 74.6% (754/1011) and 14.9% (151/1011) were MSSA-PENS-blaZnegative. MSSA-PENS-blaZnegative isolates (n = 151) were ascribed to 88 spa types and 11 CCs. The most frequent CCs were CC5 (35/151) and CC398 (25/151), with t002-CC5 and t571-CC398 being the most common lineages. Pan-susceptibility was identified in 117 of the 151 MSSA-PENS-blaZnegative isolates (77.5%). In the remaining isolates, erythromycin and clindamycin resistance was the most frequent resistance found, although tobramycin, ciprofloxacin, fusidic acid, mupirocin and/or tetracycline resistance was also detected. Thirty-eight MSSA-PENS-blaZnegative isolates were IEC negative and four isolates were Panton–Valentine leucocidin (‘PVL’) positive. Conclusions A high penicillin susceptibility rate was detected among MSSA, opening therapeutic opportunities for BSIs. The emergence of new successful MSSA-PENS clones could be responsible for these data. The detection among MSSA-PENS-blaZnegative isolates of the clonal lineage CC398 or the absence of an IEC raises questions about their possible animal origin, requiring further analysis.

BackgroundLivestock-associated (LA)-CC398-MRSA is closely related to pigs, being unfrequently detected in human invasive infections. CC398-MSSA is emerging in human invasive infections in some countries, but genetic and epidemiological characteristics are still scarcely reported.ObjectivesTo determine the prevalence of Staphylococcus aureus (SA) CC398, both MRSA and MSSA, among blood cultures SA isolates recovered in Spanish hospitals located in regions with different pig-farming densities (PD) and characterize the recovered isolates.MethodsOne thousand twenty-two SA isolates (761 MSSA, 261 MRSA) recovered from blood cultures during 6–12 months in 17 Spanish hospitals (2018–2019) were studied. CC398 lineage identification, detection of spa-types, and antibiotic resistance, virulence and human immune evasion cluster (IEC) genes were analyzed by PCR/sequencing.ResultsForty-four CC398-MSSA isolates (4.3% of SA; 5.8% of MSSA) and 10 CC398-MRSA isolates (1% of SA; 3.8% of MRSA) were detected. Eleven spa-types were found among the CC398-MSSA isolates with t571 and t1451 the most frequent spa-types detected (75%). Most of CC398-MSSA isolates were Immune-Evasion-Cluster (IEC)-positive (88.6%), tetracycline-susceptible (95.5%) and erythromycin/clindamycin–inducible-resistant/erm(T)-positive (75%). No statistical significance was detected when the CC398-MSSA/MSSA rate was correlated to PD (pigs/km2) (p = 0.108). On the contrary, CC398-MRSA isolates were all IEC-negative, predominately spa-t011 (70%), and the CC398-MRSA/MRSA rate was significantly associated to PD (p < 0.005).ConclusionCC398-MSSA is an emerging clade in invasive infections in Spanish hospitals. CC398-MRSA (mostly t011) and CC398-MSSA (mostly t571 and t1451) show important differences, possibly suggesting divergent steps in host-adaptation evolutionary processes. While CC398-MRSA is livestock-associated (lacking IEC-system), CC398-MSSA seems to be mostly livestock-independent, carrying human-adaptation markers.

2 pages.-- Nomenclatural notes., Article was realized with a research grant by the Ministerio de Educación y Ciencia of Spain (Research project: Fauna Ibérica VII; Research sub-project: Fauna íbero-balear de Aphidinae (Hemiptera: Aphididae): tribu Aphidini y primera parte de la tribu Macrosiphini, code number: REN2001-1956-C17-03/GLO.

Reasons for performing study: Staphylococcus intermedius group (SIG) bacteria can colonise the nares of some animals but are also emerging pathogens in humans and animals. Objectives: To analyse SIG nasal carriage in healthy donkeys destined for food consumption in Tunisia and to characterise recovered isolates. Methods: Nasal swabs from 100 healthy donkeys were tested for SIG recovery, and isolates were identified by biochemical and molecular methods. Antimicrobial susceptibility of isolates was tested and detection of antimicrobial resistance and virulence genes was performed. Isolates were typed at the clonal level by multilocus sequence typing and SmaI pulsed-field gel electrophoresis. Results: Staphylococcus delphini and Staphylococcus pseudintermedius (included in SIG) were obtained in 19% and 2% of the tested samples, respectively, and one isolate per sample was characterised. All isolates were meticillin susceptible and mecA negative. Most S.delphini and S.pseudintermedius isolates showed susceptibility to all antimicrobials tested, with the exception of 2 isolates resistant to tetracycline (tet(M) gene) or fusidic acid. The following toxin genes were identified (percentage of isolates): lukS-I (100%), lukF-I (9.5%), siet (100%), se-int (90%), seccanine (19%) and expA (9.5%). Thirteen different pulsed-field gel electrophoresis profiles were identified among the 21 SIG isolates. Additionally, the following 9 different sequence types (STs) were detected by multilocus sequence typing, 6 of them new: ST219 (6 isolates), ST12 (5 isolates), ST220 (3 isolates), ST13, ST50, ST193, ST196, ST218 and ST221 (one isolate each). Conclusions: Staphylococcus delphini and S.pseudintermedius are common nasal colonisers of donkeys, generally susceptible to the antimicrobials tested; nevertheless, these SIG isolates contain virulence genes, including the recently described exfoliative gene (expA) and several enterotoxin genes, with potential implications for public health. This is the first description of S. delphini in Tunisia. The Summary is available in Chinese - see Supporting information. © 2014 EVJ Ltd.

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Melolontha emarginata Gyllenhal, 1817 is designated as the type species of Elaphocerida Reitter, 1902. The type specimens of the species of genus Elaphocera Gené, 1836, from the entomological collections of Museo Nacional de Ciencias Naturales (Madrid, Spain), are studied. Lectotypes are designated for species Elaphocera (Elaphocerida) ampla Báguena, 1955, Elaphocerida segurensis Escalera, 1923, Elaphocerida pygmaea Escalera, 1923 and Elaphocera (Elaphocerida) torressalai Báguena, 1955. The type material of the following species is also revised: Elaphocera pardoi Escalera, 1931, Elaphocera (Elaphocerida) ibicensis Escalera, 1926, Elaphocerida abdelkrimi Escalera, 1934 and Elaphocera baguenae Mancini, 1926.En este trabajo se designa Melolontha emarginata Gyllenhal, 1817 como la especie tipo de Elaphocerida Reitter, 1902. Se revisan las series típicas de las especies del género Elaphocera Gené, 1836 conservadas en las colecciones de Entomología del Museo Nacional de Ciencias Naturales (Madrid, España). Se designan los lectotipos de Elaphocera (Elaphocerida) ampla Báguena, 1955, Elaphocerida segurensis Escalera, 1923, Elaphocerida pygmaea Escalera, 1923 y Elaphocera (Elaphocerida) torressalai Báguena, 1955. Además, se proporcionan nuevos datos sobre el material típico de las especies Elaphocera pardoi Escalera, 1931, Elaphocera (Elaphocerida) ibicensis Escalera, 1926, Elaphocerida abdelkrimi Escalera, 1934 y Elaphocera baguenae Mancini, 1926, conservado en estas colecciones.

A review of extinct and living amphibians known from fossils (Allocaudata, Anura and Caudata) has revealed several cases that require nomenclatural changes in order to stabilize the taxonomy of the group. Nomenclatural changes include homonym replacements, corrections of spelling variants and authorships, name availabilities, and in particular, the proposal of new combinations. These changes will allow the incorporation of some palaeontological taxa to the current evolutionary models of relationship of modern forms based on molecular phylogenies. Rana cadurcorum for Rana plicata Filhol, 1877, Rana auscitana for Rana pygmaea Lartet, 1851, and Rana sendoa for Rana robusta Brunner, 1956. Anchylorana Taylor, 1942 is considered a new synonym of Lithobates Fitzinger, 1843. New combinations proposed are: Anaxyrus defensor for Bufo defensor Meylan, 2005; Anaxyrus hibbardi for Bufo hibbardi Taylor, 1937; Anaxyrus pliocompactilis for Bufo pliocompactilis Wilson, 1968; Anaxyrus repentinus for Bufo repentinus Tihen, 1962; Anaxyrus rexroadensis for Bufo rexroadensis Tihen, 1962; Anaxyrus spongifrons for Bufo spongifrons Tihen, 1962; Anaxyrus suspectus for Bufo suspectus Tihen, 1962; Anaxyrus tiheni for Bufo tiheni Auffenberg, 1957; Anaxyrus valentinensis for Bufo valentinensis Estes et Tihen, 1964; Ichthyosaura wintershofi for Triturus wintershofi Lunau, 1950; Incilius praevius for Bufo praevius Tihen, 1951; Lithobates bucella for Rana bucella Holman, 1965; Lithobates dubitus for Anchylorana dubita Taylor, 1942; Lithobates fayeae for Rana fayeae Taylor, 1942; Lithobates miocenicus for Rana miocenica Holman, 1965; Lithobates moorei for Anchylorana moorei Taylor, 1942; Lithobates parvissimus for Rana parvissima Taylor, 1942; Lithobates rexroadensis for Rana rexroadensis Taylor, 1942; Lithobates robustocondylus for Anchylorana robustocondyla Taylor, 1942; Ommatotriton roehrsi for Triturus roehrsi Herre, 1955; Pelophylax barani for Rana barani Rückert-Ülkumen, 1980; Pelophylax meriani for Rana meriani Meyer, 1853; Pelophylax pueyoi for Rana pueyoi Navás, 1922a; Pelophylax quellenbergi for Rana quellenbergi Navás, 1922; Philoria borealis for Kyarranus borealis Tyler, 1991; Pseudepidalea belogorica for Bufo belogoricus Ratnikov, 1993; Pseudepidalea plana for Bufo planus Ratnikov, 1993; Pseudepidalea prisca for Bufo priscus Spinar, Klembara et Meszáros, 1993, and Pseudepidalea stranensis for Bufo stranensis Nemec, 1972. The names Geyeriellinae Brame, 1958, Palaeurodelidae Brame, 1958, Prosalamandridae Stefano, 1903, Lipelucidae Huene, 1956, Rana temporaria fossilis Stefanov, 1951, Salteniidae Kuhn, 1962, Vieraellidae Reig, 1961, and Voigtiellinae Brame, 1958 are nomenclaturally deemed unavailable. The family name based on Scapherpeton Cope, 1876 is Scapherpetidae and not Scapherpetonidae nor Scapherpetontidae.Una revisión de anfibios extintos y actuales en estado fósil (Allocaudata, Anura y Caudata) ha permitido detectar diversos casos que precisan cambios nomenclaturales a fin de estabilizar la taxonomía del grupo. Los cambios nomenclaturales incluyen homonimias, correcciones de variantes gramaticales y autorías, disponibilidad de nombres, y en especial la propuesta de nuevas combinaciones, necesarias para ajustar algunos taxones paleontológicos a los modelos de relaciones evolutivas entre formas vivientes, fundamentados en filogenias moleculares. Las nuevas combinaciones que se proponen son: Anaxyrus defensor para Bufo defensor Meylan, 2005; Anaxyrus hibbardi para Bufo hibbardi Taylor, 1937; Anaxyrus pliocompactilis para Bufo pliocompactilis Wilson, 1968; Anaxyrus repentinus para Bufo repentinus Tihen, 1962; Anaxyrus rexroadensis para Bufo rexroadensis Tihen, 1962; Anaxyrus spongifrons para Bufo spongifrons Tihen, 1962; Anaxyrus suspectus para Bufo suspectus Tihen, 1962; Anaxyrus tiheni para Bufo tiheni Auffenberg, 1957; Anaxyrus valentinensis para Bufo valentinensis Estes et Tihen, 1964; Ichthyosaura wintershofi para Triturus wintershofi Lunau, 1950; Incilius praevius para Bufo praevius Tihen, 1951; Lithobates bucella para Rana bucella Holman, 1965; Lithobates dubitus para Anchylorana dubita Taylor, 1942; Lithobates fayeae para Rana fayeae Taylor, 1942; Lithobates miocenicus para Rana miocenica Holman, 1965; Lithobates moorei para Anchylorana moorei Taylor, 1942; Lithobates parvissimus para Rana parvissima Taylor, 1942; Lithobates rexroadensis para Rana rexroadensis Taylor, 1942; Lithobates robustocondylus para Anchylorana robustocondyla Taylor, 1942; Ommatotriton roehrsi para Triturus roehrsi Herre, 1955; Pelophylax barani para Rana barani Rückert-Ülkumen, 1980; Pelophylax meriani para Rana meriani Meyer, 1853; Pelophylax pueyoi para Rana pueyoi Navás, 1922a; Pelophylax quellenbergi para Rana quellenbergi Navás, 1922; Philoria borealis para Kyarranus borealis Tyler, 1991; Pseudepidalea belogorica para Bufo belogoricus Ratnikov, 1993; Pseudepidalea plana para Bufo planus Ratnikov, 1993; Pseudepidalea prisca para Bufo priscus Spinar, Klembara et Meszáros, 1993, y Pseudepidalea stranensis para Bufo stranensis Nemec, 1972. Los nombres Geyeriellinae Brame, 1958, Palaeurodelidae Brame, 1958, Prosalamandridae Stefano, 1903, Lipelucidae Huene, 1956, Rana temporaria fossilis Stefanov, 1951, Salteniidae Kuhn, 1962, Vieraellidae Reig, 1961, y Voigtiellinae Brame, 1958 se consideran nomenclaturalmente no disponibles. El nombre de familia basado en Scapherpeton Cope, 1876 es Scapherpetidae y no Scapherpetonidae ni Scapherpetontidae.

International audience; Nasal swabs of 423 healthy humans who showed different levels of contact with animals (frequent, 168; sporadic, 94; no contact, 161) were obtained in Tunisia (2008-2009), and 99 of them presented other associated risk factors. Methicillin-resistant (MRSA) was detected in one of these 423 samples (0.24%), retrieved from a veterinarian. The MRSA isolate was -positive, typed as ST80-t203-SCCIVc-III, and contained , , and genes encoding tetracycline, streptomycin, and kanamycin resistance, respectively. This MRSA isolate also contained the virulence gene encoding Panton-Valentine leukocidin. Fifty-four (12.8%) additional nasal samples contained methicillin-susceptible (MSSA) and one isolate/sample was characterized. A high diversity of types ( = 43; 4 new) and pulsed-field gel electrophoresis (PFGE) types ( = 37) was detected among the 55 recovered strains. The percentages of antimicrobial resistance/detected resistance genes were as follows: tetracycline [22%/--], erythromycin [5%/], ciprofloxacin [14.5%], trimethoprim-sulfamethoxazole [2%/], streptomycin [11%/], kanamycin [7%/], amikacin [5%], and chloramphenicol [2%]. Four and two isolates carried the and and/or genes, respectively, and always in individuals with contact with animals. Eleven isolates carried the gene and were recovered from individuals with different levels of contact with animals.

We present an up to date synonymic list of the Iberian and Balearic fauna of Meloidae (Coleoptera). This current list includes all synonymies for 65 taxa at the species level. We have checked most of the original references for all taxa and names cited in the catalogue. This revision leads to various corrections and changes in the spelling of some names and in publication dates and pagination of original references with respect to previous catalogues. The work is illustrated with photographs of 13 type specimens. Some nomenclatural and taxonomic problems require additional work, and their solution might produce further changes in the current list. Most relevant among these problems are the revision of M. maculosopunctata nomenclature, the confirmation of the specific identification of the single Iberian record for M. tricincta, the revision of the taxonomic status of Meloe ibericus, herein maintained at the species level while waiting for the needed revision of the M. brevicollis species group, the evaluation of the taxonomic status of Sitaris melanura and the taxonomic problem of the subgenus Meloe in the Balearic Islands. En este trabajo presentamos un listado sinonímico actualizado de la fauna de Meloidae (Coleoptera) de la Península Ibérica e Islas Baleares. En el listado actual se recogen las sinonimias correspondientes a 65 táxones de nivel especie. Se han revisado las publicaciones donde se incluyen las descripciones originales de la mayoría de los táxones y nombres de las especies ibero baleares de Meloidae. Esta revisión ha llevado a diversas correcciones y actualizaciones tanto en la grafía de algunos nombres, como en las las referencias originales, incluyendo cambios de fechas o de paginación con respecto a catálogos anteriores. El trabajo se ilustra con fotografías de 13 ejemplares tipo. Existen una serie de problemas nomenclaturales y taxonómicos aún por resolver, que podrían producir cambios en el listado actual. Entre estos problemas destacan el caso de la nomenclatura de M. maculosopunctata que requiere revisión, la adscripción específica correcta de la cita ibérica de M. tricincta, la revisión del estatus taxonómico de Meloe ibericus, que se mantiene a nivel específico en espera de la revisión del grupo de especies afines a M. brevicollis, la revisión del estatus de Sitaris melanura y el problema taxonómico del subgénero Meloe en las Islas Baleares.

This study was financially supported by the Project SAF2009-08570 from the Ministerio de Ciencia e Innovación of Spain and FEDER. C.L. has a fellowship FPI from the Ministerio de Ciencia e Innovación of Spain. Sí

The study of 131 more or less complete Curculionoid specimens of the collection Étienne Louis Geoffroy, conserved in the Muséum 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 = Rhinomacer niger Geoffroy, 1785 = Curculio fuliginosus Gmelin, 1790; Coniocleonus hollbergii (F√•hraeus, 1842) = Curculio sulcatus Goeze, 1777 = Curculio sulcatus Geoffroy, 1785 = Curculio sulcatus Gmelin, 1790; Larinus iaceae (Fabricius, 1775) = Curculio carduelis Goeze, 1777; Hypera postica (Gyllenhal, 1813), 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 plantarum (Germar, 1824), nom. protectum = Curculio nigrostriatus Goeze, 1777 = Curculio floriger Geoffroy, 1785, nom. oblitum = Curculio subglobosus Gmelin, 1790, nom. oblitum; Anisorhynchus scabrosus (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 names 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 striatusi> Geoffroy, 1785, Rhinomacer fulgidusi> Geoffroy, 1785, Curculio transversofasciatus Goeze, 1777, Curculio fasciatus Geoffroy, 1785 (non Scopoli, 1763, nec Str√∂m, 1768, nec Degeer, 1775, nec Mu.ller, 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 Müller, 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, 1785.El estudio de 131 ejemplares de Curculiónidos, más o menos completos, de la colección Étienne Louis Geoffroy conservados en el Muséum d’Histoire Naturelle de París (Entomología) ha permitido identificar varias especies nominales que eran consideradas nomina dubia y establecer varias nuevas sinonimias y combinaciones, e incluso, en algunos casos, recuperar la prioridad de acuerdo con el Art. 23.9 del Código, declarando nomina protecta y nomina oblita. Las nuevas sinonimias son (se indica en primer lugar el nombre válido): 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 = Rhinomacer niger Geoffroy, 1785 = Curculio fuliginosus Gmelin, 1790; Coniocleonus hollbergii (Fåhraeus, 1842) = Curculio sulcatus Goeze, 1777 = Curculio sulcatus Geoffroy, 1785 = Curculio sulcatus Gmelin, 1790; Larinus iaceae (Fabricius, 1775) = Curculio carduelis Goeze, 1777; Hypera postica (Gyllenhal, 1813), 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 plantarum (Germar, 1824), nom. protectum = Curculio nigrostriatus Goeze, 1777 = Curculio floriger Geoffroy, 1785, nom. oblitum = Curculio subglobosus Gmelin, 1790, nom. oblitum; Anisorhynchus scabrosus (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. Las nuevas combinaciones son: Leucophyes occidentalis (Dieckmann, 1982) (desde Leucosomus) y Anisorhynchus scabrosus (Geoffroy, 1785) (desde Curculio). Se han restablecido como válidos los siguientes nombres (stat. res.): Trachyphloeus spinosus (Goeze, 1777) para la especie conocida como Trachyphloeus olivieri Bedel, 1883, y Lixus pulverulentus (Scopoli, 1763) para Lixus angustatus (Fabricius, 1775). Se confirma como nombre válido Hypera melancholica (Fabricius, 1793) para la especie denominada hasta ahora Hypera fuscocinerea (Marsham, 1802) o Hypera murina (Fabricius, 1793). Al no poder indentificar el material tipo se consideran nomina dubia los siguientes nombres: 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 Ström, 1768, nec Degeer, 1775, nec Müller, 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 Müller, 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, 1785.