Wild bees (Apoidea: Anthophila) of South-West France: more than 10 years of inventories in mosaic landscapes of ZA-PYGAR
Última versión Publicado por Institut national de recherche pour l’agriculture, l’alimentation et l’environnement (INRAE) en Dec 5, 2024
We provide here data for the 24,329 wild bee specimens (Apoidae: Anthophila) held in the collection of DYNAFOR Lab (UMR 1201 INRAE, INP-ENSAT, EI PURPAN), located at INP-ENSAT (Toulouse, France). These data have been published as a datapaper in Biodiversity Data Journal (Ollivier et al, 2024).
Registros
Los datos en este registros biológicos recurso han sido publicados como Archivo Darwin Core(DwC-A), el cual es un formato estándar para compartir datos de biodiversidad como un conjunto de una o más tablas de datos. La tabla de datos del core contiene 24,329 registros. también existen 1 tablas de datos de extensiones. Un registro en una extensión provee información adicional sobre un registro en el core. El número de registros en cada tabla de datos de la extensión se ilustra a continuación.
- Occurrence (core)
- MeasurementOrFact
Este IPT archiva los datos, sirviendo así como repositorio de datos. Los datos y metadatos están disponibles para descargar en la sección de descargas. La tabla de versiones muestra otras versiones del recurso que se han hecho accesibles al público y permite el seguimiento de los cambios hechos al recurso en el tiempo.
Descargas
Descargue la última versión de los datos como un Archivo Darwin Core (DwC-A) o los metadatos como EML o RTF:
| Datos como un archivo DwC-A | descargar 24,329 registros en Inglés (763 KB) - Frecuencia de actualización: no planeado |
|---|---|
| Metadatos como un archivo EML | descargar en Inglés (87 KB) |
| Metadatos como un archivo RTF | descargar en Inglés (33 KB) |
Versiones
La siguiente tabla muestra sólo las versiones publicadas del recurso que son de acceso público.
¿Cómo referenciar?
Los usuarios deben citar este trabajo de la siguiente manera:
Ollivier M, Rivers-Moore J, Pichon M, Andrieu E, Carrié R, Rudelle R, Sarthou J, Ouin A (2024): Wild bees (Apoidea: Anthophila) of South-West France: more than 10 years of inventories in mosaic landscapes of ZA-PYGAR. v1.4. Institut national de recherche pour l’agriculture, l’alimentation et l’environnement (INRAE). Dataset/Occurrence. http://dynids.toulouse.inra.fr:8180/ipt/resource?r=baseabeilles&v=1.4
Derechos
Los usuarios deben respetar los siguientes derechos de uso:
El publicador y propietario de los derechos de este trabajo es Institut national de recherche pour l’agriculture, l’alimentation et l’environnement (INRAE). This work is licensed under a Creative Commons Attribution (CC-BY) 4.0 License.
Registro GBIF
Este recurso ha sido registrado en GBIF con el siguiente UUID: 0aff18f0-6774-4294-b424-ce79bdbdc6a7. Institut national de recherche pour l’agriculture, l’alimentation et l’environnement (INRAE) publica este recurso, y está registrado en GBIF como un publicador de datos avalado por GBIF France.
Palabras Clave
Occurrence; Observation
Contactos
¿Quién creó el recurso?:
¿Quién puede resolver dudas acerca del recurso?:
¿Quién documentó los metadatos?:
¿Quién más está asociado con el recurso?:
Cobertura Geográfica
The Apoidea specimens come from south-west France, in the LTSER Vallées et Coteaux de Gascogne embedded in the ZA Pygar (Ouin et al. 2021).
| Coordenadas límite | Latitud Mínima Longitud Mínima [43.14, 0.49], Latitud Máxima Longitud Máxima [43.59, 1.12] |
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Cobertura Taxonómica
The dataset contains at least 270 species of the families Andrenidae (2,958 specimens), Apidae (2,805 specimens), Colletidae (167 specimens), Halictidae (18,007 specimens), Megachilidae (377 specimens) and Melittidae (15 specimens). Thirty-three genera have been identified, the most represented being Lasioglossum , Andrena and Halictus. Of the 275 taxon (comprising 270 species and 5 species complexes), 29 taxon are represented by more than 100 specimens, and 134 taxon are represented by 1 to 5 individuals, 56 being singletons.
| Familia | Andrenidae, Apidae, Colletidae, Halictidae, Megachilidae, Melittidae |
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| Género | Seladonia Robertson, 1918, Hylaeus Fabricius, 1793, Lasioglossum Curtis, 1833, Sphecodes Latreille, 1804, Eucera Scopoli, 1770, Andrena Fabricius, 1775, Nomada Scopoli, 1770, Osmia Panzer, 1806 |
| Especie | Seladonia tumulorum (Linnaeus, 1758), Lasioglossum pauxillum (Schenck, 1853), Lasioglossum politum (Schenck, 1853), Andrena variabilis Smith, 1853, Bombus lapidarius (Linnaeus, 1758), Halictus scabiosae (Rossi, 1790), Lasioglossum puncticolle (Morawitz, 1872), Lasioglossum villosulum (Kirby, 1802), Bombus pratorum (Linnaeus, 1761), Lasioglossum malachurum (Kirby, 1802), Melitta nigricans Alfken, 1905, Bombus terrestris (Linnaeus, 1758), Lasioglossum glabriusculum (Morawitz, 1872), Eucera nigrifacies Lepeletier, 1841, Halictus compressus (Walckenaer, 1802), Bombus Latreille, 1802, Halictus Latreille, 1804, Andrena labialis (Kirby, 1802), Lithurgus cornutus (Fabricius, 1787), Andrena flavipes Panzer, 1799, Andrena impunctata Perez, 1895, Seladonia seladonia (Fabricius, 1794), Lasioglossum interruptum (Panzer, 1798), Halictus simplex Bluthgen, 1923, Halictus maculatus Smith, 1848, Andrena wilkella (Kirby, 1802), Andrena ventricosa Dours, 1873, Lasioglossum corvinum (Morawitz, 1877), Bombus sylvarum (Linnaeus, 1761), Nomada kohli Schmiedeknecht, 1882, Nomada distinguenda Morawitz, 1873, Heriades truncorum (Linnaeus, 1758), Lasioglossum leucozonium (Schrank, 1781), Seladonia subaurata (Rossi, 1792), Xylocopa violacea (Linnaeus, 1758), Hylaeus clypearis (Schenck, 1853), Sphecodes longulus Hagens, 1882, Sphecodes puncticeps Thomson, 1870, Seladonia smaragdula (Vachal, 1895), Hylaeus variegatus (Fabricius, 1798), Hylaeus brevicornis Nylander, 1852, Hylaeus euryscapus Forster, 1871, Bombus pascuorum (Scopoli, 1763), Lasioglossum albipes (Fabricius, 1781), Bombus hortorum (Linnaeus, 1761), Lasioglossum zonulum (Smith, 1848), Nomada stigma Fabricius, 1804, Andrena decipiens Schenck, 1861, Eucera nigrescens Perez, 1880, Halictus quadricinctus (Fabricius, 1777), Dasypoda hirtipes (Fabricius, 1793), Eucera taurica Morawitz, 1871, Lasioglossum discus (Smith, 1853), Eucera longicornis (Linnaeus, 1758), Lasioglossum lativentre (Schenck, 1853), Eucera clypeata Erichson in Waltl, 1835, Lithurgus chrysurus Fonscolombe, 1834, Hylaeus difformis (Eversmann, 1852), Osmia gallarum Spinola, 1807, Lasioglossum marginatum (Brulle, 1832), Lasioglossum nigripes (Lepeletier, 1841), Heriades crenulata Nylander, 1856, Ceratina cyanea (Kirby, 1802), Lasioglossum punctatissimum (Schenck, 1853), Andrena ranunculi Schmiedeknecht, 1884, Coelioxys afer Lepeletier, 1841, Lasioglossum morio (Fabricius, 1793), Halictus langobardicus Bluthgen, 1944, Osmia rufohirta Latreille, 1811, Andrena ovata Schenck, 1853, Stelis punctulatissima (Kirby, 1802), Hylaeus hyalinatus Smith, 1842, Lasioglossum laticeps (Schenck, 1869), Osmia caerulescens (Linnaeus, 1758), Andrena aeneiventris Morawitz, 1872, Megachile burdigalensis Benoist, 1940, Anthidium oblongatum (Illiger, 1806), Ceratina cucurbitina (Rossi, 1792), Hoplitis tridentata (Dufour & Perris, 1840), Andrena chrysosceles (Kirby, 1802), Hoplitis leucomelana (Kirby, 1802), Nomada fucata Panzer, 1798, Rophites algirus Perez, 1895, Anthidium manicatum (Linnaeus, 1758), Melitta leporina (Panzer, 1799), Tetralonia alticincta (Lepeletier, 1841), Andrena agilissima (Scopoli, 1770), Hylaeus gibbus Saunders, 1850, Andrena bicolor Fabricius, 1775, Andrena florea Fabricius, 1793, Anthophora pubescens (Fabricius, 1781), Hylaeus tyrolensis Forster, 1871, Seladonia submediterranea Pauly, 2015, Seladonia vestita (Lepeletier, 1841), Megachile rotundata (Fabricius, 1787), Megachile willughbiella (Kirby, 1802), Megachile maritima (Kirby, 1802), Ceratina chalybea Chevrier, 1872, Megachile apicalis Spinola, 1808, Xylocopa valga Gerstacker, 1872, Osmia spinulosa (Kirby, 1802), Sphecodes rufiventris (Panzer, 1797), Xylocopa iris (Christ, 1791), Hylaeus gredleri Forster, 1871, Nomada basalis Herrich-Schaffer, 1839, Hylaeus punctulatissimus Smith, 1843, Amegilla albigena (Lepeletier, 1841), Lasioglossum semilucens (Alfken, 1914), Trachusa interrupta (Fabricius, 1781), Sphecodes ferruginatus Hagens, 1882, Sphecodes monilicornis (Kirby, 1802), Pseudoanthidium scapulare (Latreille, 1809), Bombus ruderarius (Muller, 1776), Anthidiellum strigatum (Panzer, 1802), Bombus humilis Illiger, 1806, Hylaeus confusus Nylander, 1852, Hylaeus nigritus (Fabricius, 1798), Ceratina dallatorreana Friese, 1896, Andrena alfkenella Perkins, 1914, Andrena minutula (Kirby, 1802), Sphecodes ephippius (Linnaeus, 1767), Lasioglossum calceatum (Scopoli, 1763), Bombus confusus Schenck, 1861, Bombus lucorum (Linnaeus, 1761), Nomada flavoguttata (Kirby, 1802), Andrena propinqua Schenck, 1853, Hylaeus communis Nylander, 1852, Lasioglossum fulvicorne (Kirby, 1802), Andrena afzeliella (Kirby, 1802), Megachile ericetorum Lepeletier, 1841, Bombus vestalis (Geoffroy in Fourcroy, 1785), Colletes daviesanus Smith, 1846, Megachile centuncularis (Linnaeus, 1758), Hylaeus annularis (Kirby, 1802), Nomada flavopicta (Kirby, 1802), Colletes similis Schenck, 1853, Hylaeus sinuatus (Schenck, 1853), Halictus rubicundus (Christ, 1791), Megachile albisecta (Klug in Germar, 1817), Lasioglossum pygmaeum (Schenck, 1853), Nomada furva Panzer, 1798, Melitta tricincta Kirby, 1802, Osmia melanogaster Spinola, 1807, Bombus hypnorum (Linnaeus, 1758), Panurgus dentipes Latreille, 1811, Osmia aurulenta (Panzer, 1799), Halictus patellatus Morawitz, 1873, Sphecodes crassus Thomson, 1870, Sphecodes marginatus Hagens, 1882, Lasioglossum subhirtum (Lepeletier, 1841), Sphecodes gibbus (Linnaeus, 1758), Stelis annulata (Lepeletier, 1841), Megachile melanopyga Costa, 1863, Andrena minutuloides Perkins, 1914, Lasioglossum majus (Nylander, 1852), Lasioglossum minutissimum (Kirby, 1802), Tetralonia malvae (Rossi, 1790), Andrena nana (Kirby, 1802), Andrena hedikae Jaeger, 1934, Andrena trimmerana (Kirby, 1802), Andrena angustior (Kirby, 1802), Anthophora plumipes (Pallas, 1772), Andrena dorsata (Kirby, 1802), Andrena nitida (Muller, 1776), Andrena haemorrhoa (Fabricius, 1781), Osmia bicornis (Linnaeus, 1758), Andrena lagopus Latreille, 1809, Halictus tetrazonius (Klug in Germar, 1817), Andrena distinguenda Schenck, 1871, Andrena pusilla Perez, 1903, Andrena livens Perez, 1895, Andrena gravida Imhoff, 1832, Andrena nigroaenea (Kirby, 1802), Lasioglossum pallens (Brulle, 1832), Andrena fulvata Stoeckhert, 1930, Andrena cineraria (Linnaeus, 1758), Colletes cunicularius (Linnaeus, 1761), Lasioglossum laevigatum (Kirby, 1802), Lasioglossum pauperatum (Brulle, 1832), Andrena combinata (Christ, 1791), Andrena helvola (Linnaeus, 1758), Andrena ferox Smith, 1847, Andrena pallitarsis Perez, 1903, Lasioglossum xanthopus (Kirby, 1802), Lasioglossum crassepunctatum (Bluthgen, 1923), Andrena nigroolivacea Dours, 1873, Lasioglossum nitidulum (Fabricius, 1804), Andrena bucephala Stephens, 1846, Osmia bicolor (Schrank, 1781), Anthophora plagiata (Illiger, 1806), Osmia cornuta (Latreille, 1805), Bombus sylvestris (Lepeletier, 1833), Andrena scotica Perkins, 1916, Lasioglossum truncaticolle (Morawitz, 1877), Andrena strohmella Stoeckhert, 1928, Andrena nitidula Perez, 1903, Andrena rufula Schmiedeknecht, 1883, Andrena fulvago (Christ, 1791), Andrena bicolorata (Rossi, 1790), Andrena pilipes Fabricius, 1781, Andrena bimaculata (Kirby, 1802), Andrena humilis Imhoff, 1832, Lasioglossum griseolum (Morawitz, 1872), Hoplitis adunca (Panzer, 1798), Lasioglossum tricinctum (Schenck, 1874), Andrena griseobalteata Dours, 1872, Melecta albifrons (Forster, 1771), Andrena russula Lepeletier de Saint-Fargeau, 1841, Andrena flavilabris Schenck, 1874, Chelostoma florisomne (Linnaeus, 1758), Andrena leucolippa Perez, 1895, Lasioglossum costulatum (Kriechbaumer, 1873), Eucera interrupta Bar, 1850, Sphecodes ruficrus (Erichson in Waltl, 1835), Chelostoma emarginatum (Nylander, 1856), Lasioglossum mesosclerum (Perez, 1903), Eucera numida Lepeletier, 1841, Seladonia confusa (Smith, 1853), Andrena impressa Warncke, 1967, Melecta italica Radoszkowski, 1876, Andrena rhenana Stoeckhert, 1930, Hylaeus cornutus Curtis, 1831, Halictus fulvipes (Klug in Germar, 1817), Andrena chrysopyga Schenck, 1853, Osmia brevicornis (Fabricius, 1798), Bombus muscorum (Linnaeus, 1758), Lasioglossum angusticeps (Perkins, 1895), Andrena simontornyella Noskiewicz, 1939, Andrena lathyri Alfken, 1899, Lasioglossum medinai (Vachal, 1895), Osmia niveata (Fabricius, 1804), Andrena viridescens Viereck, 1916, Andrena labiata Fabricius, 1781, Andrena vetula Lepeletier, 1841, Nomada striata Fabricius, 1793, Nomada goodeniana (Kirby, 1802), Bombus pomorum (Panzer, 1802), Andrena subopaca Nylander, 1848, Nomada fabriciana (Linnaeus, 1767), Nomada sexfasciata Panzer, 1799, Nomada bifasciata Olivier, 1811, Nomada melathoracica Imhoff, 1834, Sphecodes pseudofasciatus Bluthgen, 1925, Nomada zonata Panzer, 1797, Nomada lathburiana (Kirby, 1802), Andrena fulva (Muller, 1766), Andrena mitis Schmiedeknecht, 1883, Nomada flava Panzer, 1797, Lasioglossum bluethgeni Ebmer, 1971, Andrena thoracica (Fabricius, 1775), Rhodanthidium septemdentatum (Latreille, 1809), Stelis breviuscula (Nylander, 1848), Sphecodes majalis Perez, 1903, Osmia leaiana (Kirby, 1802), Nomada ruficornis (Linnaeus, 1758), Anthophora retusa (Linnaeus, 1758), Nomada tridentirostris Dours, 1873, Panurgus calcaratus (Scopoli, 1763), Nomada leucophthalma (Kirby, 1802), Andrena colletiformis Morawitz, 1873, Nomada panzeri Lepeletier, 1841, Nomada succincta Panzer, 1798, Megachile ligniseca (Kirby, 1802), Andrena hattorfiana (Fabricius, 1775), Hylaeus rubicola Saunders, 1850, Nomada villosa Thomson, 1870, Sphecodes rubicundus Hagens, 1875, Andrena synadelpha Perkins, 1914, Nomada hirtipes Perez, 1884, Nomada bluethgeni Stockhert, 1944 |
| Subespecie | Megachile argentata argentata (Fabricius, 1793), Bombus terrestris terrestris (Linnaeus, 1758), Bombus terrestris lusitanicus Kruger, 1956, Bombus pascuorum maculatus Vogt, 1909, Anthophora retusa retusa (Linnaeus, 1758), Lasioglossum discus discus (Smith, 1853), Andrena angustior impressa Warncke, 1967 |
Cobertura Temporal
| Fecha Inicial / Fecha Final | 2010-05-26 / 2022-04-12 |
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Datos del Proyecto
The reported massive decline of arthropods, and particularly of pollinators such as wild bees, in terms of abundance and richness, is a threat for crop production and wild plant biodiversity conservation. This decline is mainly explained by a combination of drivers at local- and landscape-scale related to intensive farming practices. Assessing the evolution of wild bee communities in agricultural ecosystems and their response to such practices is needed to address conservation purposes. We provide here data for the 24,329 wild bee specimens held in the collection of DYNAFOR Lab (UMR 1201 INRAE, INP-ENSAT, EI PURPAN), located at INP-ENSAT (Toulouse, France). All bee specimens were collected from the long term socio-ecological research site, ZA-PYGAR, located in South-West France, for more than 10 years (2010 to 2022) in the frame of different research programs conducted by the DYNAFOR Lab. At least 270 species, representative of the six wild bee families, were identified from this area. The identified specimens are considered reliable as identifications were performed or have been verified by community-recognized experts. In addition, ongoing DNA barcoding performed on certain specimens helped clarify questionable morphological characters and provided cross-validation of species identification.
| Título | Wild bees (Apoidea) of South-West France: more than 10 years of inventories in mosaic landscapes of ZA-PYGAR |
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| Identificador | baseabeilles |
| Fuentes de Financiación | Bilisse (French Ministry of Ecology and Sustainable Development - GIP Ecofor), Farmland (ANR-11-EBID-0004), ForestBees (Défi chercheur Inrae 2021), BioBio (EU FP7 project KBBE- 227161), Sebioref (PSDR 4 Occitanie) |
| Descripción del Área de Estudio | The LTSER ZA PYGAR site took place in South Western of France in the foothills of the Pyrénées mountains. It is characterised by mixed crops and extensive livestock farming systems. These agronomic features and topographic constraints have designed highly heterogeneous landscapes where wooded elements (hedgerows, scattered trees, small forests) are embedded in a mosaic of annual crops and permanent or temporary meadows (Ouin et al. 2022). According to the scientific question investigated, sample sites were chosen along gradients of landscape heterogeneity (composition and configuration) and production system (conventional to organic farming). |
| Descripción del Diseño | See sampling methods. |
Personas asociadas al proyecto:
Métodos de Muestreo
Wild bees were sampled in various habitat types (cultivated and semi-natural, Figure 1) including field margins of crops and inner crops (12,701 individuals), small forests and their edges (7,856 individuals), hedgerows (119 individuals) and permanent grasslands (294 individuals). The precision of the GPS coordinates given in the dataset has been reduced to preserve the locality of vulnerable species. Depending on the project, two sampling methods were implemented : 1) insect net catching along transects for 3,888 individuals belonging to 183 species (described in Rivers-Moore et al. 2020), or 2) one to two sets of three to six coloured pan traps per sampling site (blue, yellow and white UV colour paint) (e.g. Rivers-Moore et al. 2023) for 20,441 individuals belonging to 203 species.
| Área de Estudio | The Apoidea specimens come from south-west France, in the LTSER Vallées et Coteaux de Gascogne embedded in the ZA Pygar. 22,505 specimens were collected in the French department Haute-Garonne and 1,824 in the department Gers. Data range: 2010-7-02 - 2022-4-12. Sampling is inconsistent over time, depending on the projects being carried each year and the protocols chosen. The number of sampling events varies from 10 to 452 between 2010 and 2022, with an average of 127 samplings per year over this period. |
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| Control de Calidad | Before 2015, depending on the project and on the people involved, the most obvious and common species were identified by Samantha Bailley, Romain Carrié, Clara Singh and Léa Frontero, all the others were sent to experts (see below), except for BioBio project for which all specimens were sent to David Genoud. After 2015, all sampled specimens were sorted out to order and family ranks and pinned, before being sent to national experts of Apoidea apiformes group : Rémi Rudelle, David Genoud, Eric Dufrêne, Alain Pauly and Pierre Rasmont. For four species complexes ( Bombus gr. Terrestris , Halictus gr. Simplex , Seladonia gr. Smaragdula and Hylaeus gr. brevicornis ), the taxonomy is not stabilized for the female individuals, and the current identification tools (dichotomous keys) do not allow for a clear separation of the species within these complexes. Taxonomists agree to use the name of the complex for specimen identification when it could be one of the following species: Bombus terrestris , Bombus lucorum , Bombus magnus , and Bombus cryptarum (4 species of the Bombus gr. terrestris ), Halictus simplex , Halictus eurygnathus , Halictus langobardicus , Halictus crenicornis , Halictus tridivisus , Halictus adjikenticus , Halictus carinthiacus , Halictus gruenwaldti , and Halictus pyrenaeus (9 species of the Halictus gr. simplex ), Seladonia smaragdula , Seladonia gemmella and Seladonia submediterranea (3 species of the Seladonia gr. Smaragdula , Pauly et al. 2015), or one of the 22 species from Hylaeus gr. Brevicornis (Dathe et al. 2022). In the present dataset, the specimens belonging to these groups have been identified either to the species level (when morphological characters allowed) or to its complex species group (for female individuals). Ongoing barcoding initiatives may help to clarify the reliable morphological characteristics for identifying species within these complexes. Recently, a fraction of the specimens contained in the collection (534 specimens) and covering 60% of wild bee diversity sampled in ZA-PYGAR has been used to generate DNA barcoding reference sequences, allowing a cross-validation of the specimen identification. For each specimen chosen, one front leg was sampled and used for further molecular processes involving DNA extraction, marker amplification and sequencing (articles in prep., Hebert et al 2003, Folmer et al 1994, Clarke et al 2014). Because of the existence of groups of species particularly recalcitrant to sequencing of the standard CO1 marker, two complementary markers were targeted: CO1 and 16S (Sheffield et al 2017, Villalta et al 2021). A total of 110 and 347 specimens were sampled to provide CO1 marker barcodes and 16S marker barcodes, respectively, while 76 specimens were used to generate reference barcodes for both markers. DNA barcoding results are currently being analysed and discussed with experts. In case of incongruence between morphological and molecular identifications, the specimens are subjected to re-observation of morphological characters. This process is under progress. |
Descripción de la metodología paso a paso:
- See Sampling description and Quality control
Datos de la Colección
| Nombre de la Colección | DYNAFOR Lab (UMR 1201 INRAE, INP-ENSAT, EI PURPAN), located at INP-ENSAT, Av. de l'Agrobiopole, 31326 Auzeville-Tolosane, FRANCE |
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| Métodos de preservación de los ejemplares | Montado con alfileres, Secado |
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Referencias Bibliográficas
- Clarke L, Soubrier J, Weyrich L, Cooper A (2014) Environmental metabarcodes for insects: in silico PCR reveals potential for taxonomic bias. Molecular Ecology Resources 14 (6): 1160‑1170. https://doi.org/10.1111/1755-0998.12265
- Dathe H (2022) Contributions to a revision of the Hylaeus brevicornis group (Hymenoptera, Anthophila, Colletidae). Contributions to Entomology 72 (1): 37‑66. https://doi.org/10.3897/contrib.entomol.72.e87230
- Folmer O, Black M, Hoeh W, Lutz R, Vrijenhoek R (1994) DNA primers for amplification of mitochondrial cytochrome c oxidase subunit I from diverse metazoan invertebrates. Molecular Marine Biology and Biotechnology 3 (5): 294‑299.
- Hebert PN, Cywinska A, Ball S, deWaard J (2003) Biological identifications through DNA barcodes. Proceedings of the Royal Society of London. Series B: Biological Sciences 270 (1512): 313‑321. https://doi.org/10.1098/rspb.2002.2218
- Ollivier M, Rivers-Moore J, Pichon M, Andrieu E, Carrié R, Rudelle R, Sarthou J-P, Ouin A (2024) Wild bees (Apoidea, Anthophila) of south-west France: more than 10 years of inventories in mosaic landscapes of "Vallées et Coteaux de Gascogne" (ZA-PYGAR). Biodiversity Data Journal 12: e135157. https://doi.org/10.3897/BDJ.12.e135157
- Ouin A, Andrieu E, Vialatte A, Balent G, Barbaro L, Blanco J, Ceschia E, Clement F, Fauvel M, Gallai N, Hewison AJM, Jean-François D, Kephaliacos C, Macary F, Probst A, Probst J, Ryschawy J, Sheeren D, Sourdril A, Tallec T, Verheyden H, Sirami C (2021) Chapter Two - Building a shared vision of the future for multifunctional agricultural landscapes. Lessons from a long term socio-ecological research site in south-western France. Advances in Ecological Research. 65. https://www.sciencedirect.com/science/article/pii/S0065250421000155
- Pauly A, Devalez J, Sonet G, Nagy ZT, Boevé J (2015) DNA barcoding and male genital morphology reveal five new cryptic species in the West Palearctic bee Seladonia smaragdula (Vachal, 1895) (Hymenoptera: Apoidea: Halictidae). Zootaxa 4034 (2): 257‑290. https://doi.org/10.11646/zootaxa.4034.2.2
- Rivers-Moore J, Andrieu E, Vialatte A, Ouin A (2020) Wooded Semi-Natural Habitats Complement Permanent Grasslands in Supporting Wild Bee Diversity in Agricultural Landscapes. Insects 11 (11). https://doi.org/10.3390/insects11110812
- Rivers-Moore J, Ouin A, Vialatte A, Carrié R, Ladet S, Andrieu E (2023) Contrasting effects of wooded and herbaceous semi-natural habitats on supporting wild bee diversity. Agriculture, Ecosystems & Environment 356 https://doi.org/10.3390/insects11110812
- Sheffield C, Heron J, Gibbs J, Onuferko T, Oram R, Best L, deSilva N, Dumesh S, Pindar A, Rowe G (2017) Contribution of DNA barcoding to the study of the bees (Hymenoptera: Apoidea) of Canada: progress to date. The Canadian Entomologist 149 (6): 736‑754. https://doi.org/10.4039/tce.2017.49
- Villalta I, Ledet R, Baude M, Genoud D, Bouget C, Cornillon M, Moreau S, Courtial B, Lopez-Vaamonde C (2021) A DNA barcode-based survey of wild urban bees in the Loire Valley, France. Scientific Reports 11 (1). https://doi.org/10.1038/s41598-021-83631-0
Metadatos Adicionales
| Identificadores Alternativos | 0aff18f0-6774-4294-b424-ce79bdbdc6a7 |
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| http://dynids.toulouse.inra.fr:8180/ipt/resource?r=baseabeilles |