211 results on '"Pelletier V"'
Search Results
2. CHANGES IN BODY COMPOSITION THROUGH A LIFESTYLE INTERVENTION PROGRAM LEAD TO REMISSION OF TYPE 2 DIABETES, PREDIABETES, AND EARLY INSULIN RESISTANCE
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Iglesies-Grau, J., primary, Paradis, A., additional, Dionne, V., additional, Bherer, L., additional, Latour, E., additional, Lamoureux, K., additional, Pelletier, V., additional, Bisaillon, M., additional, Aubut, L., additional, Yasconi, C., additional, Besnier, F., additional, Gagnon, C., additional, Berthiaume, A., additional, Simard, F., additional, Nigam, A., additional, L'Allier, P., additional, Juneau, M., additional, and Gayda, M., additional
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- 2023
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3. TYPE 2 DIABETES REMISSION WITH AN INTENSIVE MULTIDISCIPLINARY INTERVENTION: THE DIABEPIC 2 PILOT STUDY
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Dionne, V., primary, Iglesies-Grau, J., additional, Latour, E., additional, Besnier, F., additional, Maxime, D., additional, Gagnon, C., additional, Gayda, M., additional, Juneau, M., additional, Nigam, A., additional, L'Allier, P., additional, Simard, F., additional, Bherer, L., additional, and Pelletier, V., additional
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- 2023
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4. The Influence of Soil Biodiversity on Hydrological Pathways and the Transfer of Materials between Terrestrial and Aquatic Ecosystems
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Bardgett, R. D., Anderson, J. M., Behan-Pelletier, V., Brussaard, L., Coleman, D. C., Ettema, C., Moldenke, A., Schimel, J. P., and Wall, D. H.
- Published
- 2001
5. An Exploratory Study of Acculturation and Reproductive Health Among Haitian and Haitian-American Women in Little Haiti, South Florida
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Cyrus, E., Gollub, E. L., Jean-Gilles, M., Neptune, S., Pelletier, V., and Dévieux, J.
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- 2016
6. Reducing cranberry heat stress and midday depression with evaporative cooling
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Pelletier, V., Pepin, S., Gallichand, J., and Caron, J.
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- 2016
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7. The need for widely available genomic testing in rare eye diseases: an ERN-EYE position statement
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Black G. C., Sergouniotis P., Sodi A., Leroy B. P., Van Cauwenbergh C., Liskova P., Gronskov K., Klett A., Kohl S., Taurina G., Sukys M., Haer-Wigman L., Nowomiejska K., Marques J. P., Leroux D., Cremers F. P. M., De Baere E., Dollfus H., Ashworth J., Audo I., Bacci G., Balciuniene V. J., Bargiacchi S., Bertelsen M., Black G., Boon C., Bremond-Gignac D., Buzzonetti L., Calvas P., Thomsen A. C., Chirita-Emandi A., Chokoshvili D., Cremers F., Daly A., Downes S., Fasolo A., Fasser C., Fischer D., Fortunato P., Gelzinis A., Hall G., Hamann S., Heon E., Iarossi G., Iberg C., Jouanjan G., Kaariainen H., Kahn K., Keegan D., Laengsfeld M., Leon A., Leroux B., Lorenz B., Maggi R., Mauring L., Melico P., Meunier I., Mohand-Said S., Monterosso C., Morandi P., Parmeggiani F., Passerini I., Pelletier V., Peluso F., Perdomo Y., Rapizzi E., Roos L., Roosing S., Rozet J. -M., Simonelli F., Sowden J., Stingl K., Suppiej A., Testa F., Tracewska A., Traficante G., Valeina S., Wheeler-Schilling T., Yu-Wai-Man P., Zeitz C., Zemaitiene R., Leroux, Dorothée [0000-0002-1412-6611], Apollo - University of Cambridge Repository, Ophthalmology, ANS - Complex Trait Genetics, Black, G. C., Sergouniotis, P., Sodi, A., Leroy, B. P., Van Cauwenbergh, C., Liskova, P., Gronskov, K., Klett, A., Kohl, S., Taurina, G., Sukys, M., Haer-Wigman, L., Nowomiejska, K., Marques, J. P., Leroux, D., Cremers, F. P. M., De Baere, E., Dollfus, H., Ashworth, J., Audo, I., Bacci, G., Balciuniene, V. J., Bargiacchi, S., Bertelsen, M., Black, G., Boon, C., Bremond-Gignac, D., Buzzonetti, L., Calvas, P., Thomsen, A. C., Chirita-Emandi, A., Chokoshvili, D., Cremers, F., Daly, A., Downes, S., Fasolo, A., Fasser, C., Fischer, D., Fortunato, P., Gelzinis, A., Hall, G., Hamann, S., Heon, E., Iarossi, G., Iberg, C., Jouanjan, G., Kaariainen, H., Kahn, K., Keegan, D., Laengsfeld, M., Leon, A., Leroux, B., Lorenz, B., Maggi, R., Mauring, L., Melico, P., Meunier, I., Mohand-Said, S., Monterosso, C., Morandi, P., Parmeggiani, F., Passerini, I., Pelletier, V., Peluso, F., Perdomo, Y., Rapizzi, E., Roos, L., Roosing, S., Rozet, J. -M., Simonelli, F., Sowden, J., Stingl, K., Suppiej, A., Testa, F., Tracewska, A., Traficante, G., Valeina, S., Wheeler-Schilling, T., Yu-Wai-Man, P., Zeitz, C., and Zemaitiene, R.
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0301 basic medicine ,Eye Diseases ,lcsh:Medicine ,CHILDREN ,Position statement ,Sensory disorders Donders Center for Medical Neuroscience [Radboudumc 12] ,MOLECULAR-GENETICS ,0302 clinical medicine ,HISTORY ,Health care ,Medicine and Health Sciences ,Genetics(clinical) ,Pharmacology (medical) ,Child ,Genetics (clinical) ,medicine.diagnostic_test ,General Medicine ,Genomics ,Europe ,TRIALS ,ERN-EYE ,Rare eye diseases ,medicine.symptom ,Genetic and genomic testing ,Human ,medicine.medical_specialty ,Visual impairment ,LEBER CONGENITAL AMAUROSIS ,Socio-culturale ,DIAGNOSIS ,03 medical and health sciences ,Rare Diseases ,medicine ,Humans ,Genetic Testing ,Intensive care medicine ,Genetic testing ,business.industry ,CLINICAL-FEATURES ,lcsh:R ,Rare eye disease ,Eye Disease ,Human genetics ,Clinical trial ,030104 developmental biology ,Genomic ,030221 ophthalmology & optometry ,Personalized medicine ,business ,Rare disease - Abstract
Background Rare Eye Diseases (RED) are the leading cause of visual impairment and blindness for children and young adults in Europe. This heterogeneous group of conditions includes over 900 disorders ranging from relatively prevalent disorders such as retinitis pigmentosa to very rare entities such as developmental eye anomalies. A significant number of patients with RED have an underlying genetic etiology. One of the aims of the European Reference Network for Rare Eye Diseases (ERN–EYE) is to facilitate improvement in diagnosis of RED in European member states. Main body Technological advances have allowed genetic and genomic testing for RED. The outcome of genetic testing allows better understanding of the condition and allows reproductive and therapeutic options. The increase of the number of clinical trials for RED has provided urgency for genetic testing in RED. A survey of countries participating in ERN-EYE demonstrated that the majority are able to access some forms of genomic testing. However, there is significant variability, particularly regarding testing as part of clinical service. Some countries have a well-delineated rare disease pathway and have a national plan for rare diseases combined or not with a national plan for genomics in medicine. In other countries, there is a well-established organization of genetic centres that offer reimbursed genomic testing of RED and other rare diseases. Clinicians often rely upon research-funded laboratories or private companies. Notably, some member states rely on cross-border testing by way of an academic research project. Consequently, many clinicians are either unable to access testing or are confronted with long turnaround times. Overall, while the cost of sequencing has dropped, the cumulative cost of a genomic testing service for populations remains considerable. Importantly, the majority of countries reported healthcare budgets that limit testing. Short conclusion Despite technological advances, critical gaps in genomic testing remain in Europe, especially in smaller countries where no formal genomic testing pathways exist. Even within larger countries, the existing arrangements are insufficient to meet the demand and to ensure access. ERN-EYE promotes access to genetic testing in RED and emphasizes the clinical need and relevance of genetic testing in RED.
- Published
- 2021
8. The short-term impact and sustainability of multiple lifestyle interventions on metabolic health and remission of prediabetes and type 2 diabetes: a two-year experience
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Iglesies-Grau, J, primary, Dionne, V, additional, Latour, É, additional, Pelletier, V, additional, Bisaillon, M, additional, Tessier, G, additional, Aubut, L, additional, Hamrioui, N, additional, Gagnon, C, additional, Simard, F, additional, Nigam, A, additional, L Allier, PL, additional, Bherer, L, additional, Bouabdallaoui, N, additional, and Juneau, M, additional
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- 2022
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9. P62 - Plaie fongique : étude médico-économique d’un médicament versus un pansement
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Dumet, A.F., Leroux, A., Pelletier, V., Vérin, E., and Dieu, B.
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- 2017
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10. Vehicle Tracks on High Arctic Tundra: Their Effects on the Soil, Vegetation, and Soil Arthropods
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Kevan, P. G., Forbes, B. C., Kevan, S. M., and Behan-Pelletier, V.
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- 1995
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11. IMPACT OF MULTIPLE LIFESTYLE INTERVENTION ON BODY WEIGHT, INSULIN SENSITIVITY AND REMISSION OF TYPE 2 DIABETES: A SINGLE-CENTER EXPERIENCE
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Iglesies-Grau, J, primary, Dionne, V, additional, Latour, E, additional, Pelletier, V, additional, Bisaillon, M, additional, Aubut, L, additional, Hamrioui, N, additional, Bherer, L, additional, Bouabdallaoui, N, additional, Nigam, A, additional, and Juneau, M, additional
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- 2021
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12. Mesoaxial polydactyly is a major feature in Bardet–Biedl syndrome patients with LZTFL1 (BBS17) mutations
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Schaefer, E., Lauer, J., Durand, M., Pelletier, V., Obringer, C., Claussmann, A., Braun, J.-J., Redin, C., Mathis, C., Muller, J., Schmidt-Mutter, C., Flori, E., Marion, V., Stoetzel, C., and Dollfus, H.
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- 2014
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13. CHANGES IN BODY COMPOSITION THROUGH A LIFESTYLE INTERVENTION PROGRAM LEAD TO REMISSION OF TYPE 2 DIABETES, PREDIABETES, AND EARLY INSULIN RESISTANCE
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Iglesies-Grau, J., Paradis, A., Dionne, V., Bherer, L., Latour, E., Lamoureux, K., Pelletier, V., Bisaillon, M., Aubut, L., Yasconi, C., Besnier, F., Gagnon, C., Berthiaume, A., Simard, F., Nigam, A., L'Allier, P., Juneau, M., and Gayda, M.
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- 2023
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14. TYPE 2 DIABETES REMISSION WITH AN INTENSIVE MULTIDISCIPLINARY INTERVENTION: THE DIABEPIC 2 PILOT STUDY
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Dionne, V., Iglesies-Grau, J., Latour, E., Besnier, F., Maxime, D., Gagnon, C., Gayda, M., Juneau, M., Nigam, A., L'Allier, P., Simard, F., Bherer, L., and Pelletier, V.
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- 2023
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15. Microarthropods
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Behan-Pelletier, V, primary and Winter, J, additional
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- 2007
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16. Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech
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Bonnet, C, Andrieux, J, Béri-Dexheimer, M, Leheup, B, Boute, O, Manouvrier, S, Delobel, B, Copin, H, Receveur, A, Mathieu, M, Thiriez, G, Le Caignec, C, David, A, de Blois, M C, Malan, V, Philippe, A, Cormier-Daire, V, Colleaux, L, Flori, E, Dollfus, H, Pelletier, V, Thauvin-Robinet, C, Masurel-Paulet, A, Faivre, L, Tardieu, M, Bahi-Buisson, N, Callier, P, Mugneret, F, Edery, P, Jonveaux, P, and Sanlaville, D
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- 2010
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17. Confirmation of TFAP2A Gene Involvement in Branchio-Oculo-Facial Syndrome (BOFS) and Report of Temporal Bone Anomalies
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Stoetzel, C., Riehm, S., Greene, Bennouna V., Pelletier, V., Vigneron, J., Leheup, B., Marion, V., Hellé, S., Danse, J. M., Thibault, C., Moulinier, L., Veillon, F., and Dollfus, H.
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- 2009
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18. Video games and their associations with physical health: a scoping review
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Huard Pelletier, V., Lessard, A., Piché, F., Tétreau, C., Descarreaux, M., Huard Pelletier, V., Lessard, A., Piché, F., Tétreau, C., and Descarreaux, M.
- Abstract
Objective The objective of this scoping review is to investigate the possible links between the practice of video games and physical health. It seeks to answer the following question: What are the physical health consequences of playing video games in healthy video game player? and How is it currently investigated?.Methods A scoping review was conducted to identify observational and experimental studies pertaining to our research question. Retrieved papers were screened using a two-phase method first involving a selection based on titles and abstracts. Then, potentially relevant studies were read and triaged. The final set of included studies was analysed, and data were subsequently extracted. Observational studies and experimental studies were assessed using the appropriate Cochrane Risk of Bias Tool and data were synthetised according to specific physical health and related health behaviours.Results Twelve peer-reviewed articles were retained for further analyses. Results of this scoping review suggest preliminary evidence that time spent gaming is associated with some health outcomes indicators. Our results indicate preliminary evidence that increased gaming time is associated with higher body mass index and lower self-reported general health status. There is insufficient evidence to conclude on a possible association between gaming time and physical activity or sedentary behaviours, sleep or fatigue, musculoskeletal pain or dietary behaviours.Conclusion The results of this sopping review suggest an association between increased video game playing time and a deterioration in some physical health indicators but available evidence is scarce, precluding from any strong conclusion.
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- 2020
19. Biodiversity of oribatid mites (Acari: Oribatida) in tree canopies and litter.
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Behan-Pelletier, V., primary and Walter, D. E., additional
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- 2000
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20. Protein losing enteropathy-hepatic fibrosis syndrome in Saguenay-Lac St-Jean, Quebec is a congenital disorder of glycosylation type Ib
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Vuillaumier-Barrot, S, Le Bizec, C, de Lonlay, P, Barnier, A, Mitchell, G, Pelletier, V, Prevost, C, Saudubray, J M, Durand, G, and Seta, N
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- 2002
21. Levosimendan added to dobutamine in acute decompensated heart failure refractory to dobutamine
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Juguet, W., primary, Faivre, L., additional, Deguillard, C., additional, Fard, D., additional, Pelletier, V., additional, Oliver, L., additional, Damy, T., additional, Mongardon, N., additional, Mekontso-Dessap, A., additional, Dubois Randé, J.L., additional, Gallet, R., additional, Huguet, R., additional, and Lim, P., additional
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- 2020
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22. Anthropometric and cardiometabolic evolution during DIABEPIC 2 pilot study: type 2 diabetes remission program designed for cardiovascular prevention
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Dionne, V, Iglesies-Grau, J, Latour, E, Besnier, F, Gagnon, C, Gayda, M, Pelletier, V, Debray, A, Juneau, M, Nigam, A, L'allier, P, Simard, F, and Bherer, L
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- 2024
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23. Refining the phenotype associated with biallelic DNAJC21 mutations
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D'Amours, G., primary, Lopes, F., additional, Gauthier, J., additional, Saillour, V., additional, Nassif, C., additional, Wynn, R., additional, Alos, N., additional, Leblanc, T., additional, Capri, Y., additional, Nizard, S., additional, Lemyre, E., additional, Michaud, J.L., additional, Pelletier, V.-A., additional, Pastore, Y.D., additional, and Soucy, J.-F., additional
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- 2018
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24. Protein losing enteropathy-hepatic fibrosis syndrome in Saguenay-Lac St-Jean, Quebec is a congenital disorder of glycosylation type lb. (Letter to JMG)
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Vuillaumier-Barrot, S., Bizec, C. Le, Lonlay, P. de, Barnier, A., Mitchell, G., Pelletier, V., Prevost, C., Saudubray, J.M., Durand, G., and Seta, N.
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Behavioral assessment of children -- Research ,Digestive organs -- Abnormalities -- Genetic aspects -- Research ,Genetic disorders -- Research -- Genetic aspects ,Immunization -- Abnormalities -- Research ,Glycosylation -- Abnormalities -- Genetic aspects -- Research ,Diarrhea -- Genetic aspects -- Research ,Infants -- Abnormalities -- Research ,Medical genetics -- Research ,Liver -- Abnormalities -- Research ,Health - Abstract
Congenital disorders of glycosylation (CDG) are newly described inborn errors of metabolism involving glycan moiety synthesis. CDG lb is caused by a deficiency of cellular phosphomannose isomerase (EC 5.4.2.28) (1-1) [...]
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- 2002
25. Global soil biodiversity atlas
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Orgiazzi, A. (ed.), Bardgett, R.D. (ed.), Barrios, E. (ed.), Behan-Pelletier, V. (ed.), Briones, M.J.I. (ed.), Chotte, Jean-Luc (ed.), De Deyn, G.B. (ed.), Eggleton, P. (ed.), Fierer, N. (ed.), Fraser, T. (ed.), Hedlund, K. (ed.), Jeffery, S. (ed.), Johnson, N.C. (ed.), Jones, A. (ed.), Kandeler, E. (ed.), Kaneko, N. (ed.), Lavelle, P. (ed.), Lemanceau, P. (ed.), Ladislav Miko, L. (ed.), Montanarella, L. (ed.), Moreira, F.M.S. (ed.), Ramirez, K.S. (ed.), Scheu, S. (ed.), Singh, B.K. (ed.), Six, J. (ed.), van der Putten, W.H. (ed.), and Wall, D.H. (ed.)
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Life Science ,Soil Biology ,EPS ,Laboratory of Nematology ,PE&RC ,Laboratorium voor Nematologie ,Bodembiologie - Abstract
What is soil biodiversity ? How does it vary in space and time ? What does it provide to society ? What are the main threats to soil biodiversity ? What can we do to preserve it ? The first ever Global Soil Biodiversity Atlas uses informative texts, stunning photographs and striking maps to answer and explain these and other questions. Going through its nine chapters, every reader will learn what soils are and about the amazing creatures living in them. You will discover the factors influencing the distribution of soil organisms, how soil biodiversity supports food production, the pressures affecting soil life and the possible interventions to preserve it. The Global Soil Biodiversity Atlas is an essential reference to understand and appreciate the incredible world living under our feet. Soil is an extremely complex system resulting from the essential interactions between inert and living components. Soils host a myriad of soil organisms ranging in size from a few micrometres to several centimetres, from the microscopic bacteria and archaea to the "giant" earthworms and moles. All these organisms are distributed over space and time, and each ecosystem and season has its unique soil community. Soil organisms interact to provide essential ecosystem services to human beings and the environment, ranging from supporting plant growth to the regulation of climate. Soils are increasingly under pressure and so are the organisms living in them. Intensive agriculture, loss of above ground biodiversity, soil erosion and land degradation are among the most relevant threats to soil life. We can protect soil creatures by taking specific actions. No-tillage, diversification of crops, increasing reforestation and greater use of natural amendments are examples of interventions that may promote life in soils. People need to know about the fascinating world below ground and understand its value. The Global Soil Biodiversity Atlas presents the often neglected protagonists in the environment that surrounds us all.
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- 2016
26. Plaie fongique : étude médico-économique d’un médicament versus un pansement
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Dumet, A.F., primary, Leroux, A., additional, Pelletier, V., additional, Vérin, E., additional, and Dieu, B., additional
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- 2017
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27. Global soil biodiversity atlas
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Orgiazzi, A., Bardgett, R.D., Barrios, E., Behan-Pelletier, V., Briones, M.J.I., Chotte, J.L., de Deyn, G.B., Eggleton, P., Fierer, N., Fraser, T., Hedlund, K., Jeffery, S., Johnson, N.C., Jones, A., Kandeler, E., Kaneko, N., Lavelle, P., Lemanceau, P., Miko, L., Montanarella, L., Moreira, F.M.S., Ramirez, K.S., Scheu, S., Singh, B.K., Six, J., van der Putten, W.H., Wall, D.H., Orgiazzi, A., Bardgett, R.D., Barrios, E., Behan-Pelletier, V., Briones, M.J.I., Chotte, J.L., de Deyn, G.B., Eggleton, P., Fierer, N., Fraser, T., Hedlund, K., Jeffery, S., Johnson, N.C., Jones, A., Kandeler, E., Kaneko, N., Lavelle, P., Lemanceau, P., Miko, L., Montanarella, L., Moreira, F.M.S., Ramirez, K.S., Scheu, S., Singh, B.K., Six, J., van der Putten, W.H., and Wall, D.H.
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- 2016
28. Terrestrial and freshwater invertebrates
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Hodkinson, I.D., Babenko, A., Behan-Pelletier, V., and de Smet, Willem H.
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Biology - Published
- 2013
29. Synthesis of section 2 - From genes to ecosystem services
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Van der Putten, W.H., Ritz, K., Wall, D.H., Bardgett, R.D., Behan-Pelletier, V., Herrick, J.E., Jones, T.H., Six, J., Strong, D.R., and Terrestrische Ecologie (TE)
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- 2012
30. Soil Ecology and Ecosystem Services
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Wall, D.H., Bardgett, R.D., Behan-Pelletier, V., Herrick, J.E., Jones, T.H., Ritz, K., Six, J., Strong, D.R., Van der Putten, W.H., and Terrestrische Ecologie (TE)
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biologische bodemactiviteit ,agroecosystems ,bodemflora ,ecosysteemdiensten ,soil biodiversity ,bodemecologie ,plant genetics ,PE&RC ,bodembiodiversiteit ,soil flora ,soil biology ,agro-ecosystemen ,soil ecology ,biological activity in soil ,plantengenetica ,Laboratory of Nematology ,ecosystem services ,Laboratorium voor Nematologie ,bodembiologie - Abstract
This book synthesizes contributions from leading soil scientists and ecologists, describing cutting-edge research that provides a basis for the maintenance of soil health and sustainability. It covers these advances from a unique perspective of examining the ecosystem services produced by soil biota across different scales - from biotic interactions at microscales to communities functioning at regional and global scales. The book leads the user towards an understanding of how the sustainability of soils, biodiversity, and ecosystem services can be maintained and how humans, other animals, and ecosystems are dependent on living soils and ecosystem services.
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- 2012
31. Introduction to section 1 - The living soil and ecosystem services
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Ritz, K., Van der Putten, W.H., Wall, D.H., Bardgett, R.D., Behan-Pelletier, V., Herrick, J.E., Jones, T.H., Six, J., Strong, D.R., van der Putten, W.H., and Terrestrische Ecologie (TE)
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- 2012
32. 1.2 Soil Biodiversity and Functions
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Wurst, S., De Deyn, G.B., Orwin, K., Wall, D.H., Bardgett, R.D., Behan-Pelletier, V., Herrick, J.E., Jones, T.H., Ritz, K., Six, J., Strong, D.R., van der Putten, W.H., Multitrophic Interactions (MTI), and Terrestrial Ecology (TE)
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- 2012
33. 3.6 Biogeography and phylogenetic community structure of soil invertebrate ecosystem engineers
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Brussaard, L., Aanen, D.K., Briones, M.J.I., Decaëns, T., De Deyn, G.B., Fayle, T.M., James, S.W., Nobre, T., Wall, D.H., Bardgett, R.D., Behan-Pelletier, V., Herrick, J.E., Jones, T.H., Ritz, K., Six, J., Strong, D.R., van der Putten, W.H., and Terrestrial Ecology (TE)
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- 2012
34. Introduction to section 2 - From genes to ecosystem services
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Van der Putten, W.H., Ritz, K., Wall, D.H., Bardgett, R.D., Behan-Pelletier, V., Herrick, J.E., Jones, T.H., Six, J., Strong, D.R., and Terrestrische Ecologie (TE)
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- 2012
35. Synthesis of section 1 - The living soil and ecosystem services
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Ritz, K., Van der Putten, W.H., Wall, D.H., Bardgett, R.D., Behan-Pelletier, V., Herrick, J.E., Jones, T.H., Six, J., Strong, D.R., van der Putten, W.H., and Terrestrische Ecologie (TE)
- Published
- 2012
36. Oribatella texana Behan-Pelletier 2011, sp. nov
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Behan-Pelletier, V. M.
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Oribatella ,Oribatellidae ,Arthropoda ,Arachnida ,Animalia ,Oribatella texana ,Biodiversity ,Sarcoptiformes ,Taxonomy - Abstract
Oribatella texana sp. nov. (Figs. 23E, 24, 25) Material examined. Holotype: adult female. USA: Texas, Kendall Co., Guadeloupe State Park, 29’ 52.443N 98’ 29.139W, 3.iii.2007 (VBP) from palmetto and oak litter; deposited in the CNC, type number 23958. Paratypes: same data as holotype, 2 males; Texas, Bandera Co., Lost Maples State Natural Area, 29’ 48.984N 99’ 34.599W, 28.ii.2007 (VBP) 1 female from wash of oak twigs; Uvalde Co., Garner State Park, 29°34.090N 99°44.876, 2.iii.2007 (VBP) 1 female, 1 male from mesic deep oak and cedar litter in depression; deposited in the CNC and RNC. Diagnosis. Total length of adult 298–326 µm. Integument of notogaster, ventral and anal plates and coxisternal region micropunctate. Lamella (including cusp) about 108 µm long, cusp about 77 µm long, about 36 µm wide at level of insertion of seta le. Lamellar cusps fused posteromedially along length of about 24 µm, leaving prodorsum only visible through small oval opening, about 10 µm wide; translamella without tooth, about 10 µm at greatest width, 24 µm deep. Medial dens on lamellar cusp about 31 µm long, without teeth; lateral dens about 41 µm long with 3–4 teeth on lateral margin. Bothridial setae with barbed, narrowly fusiform head, rounded distally. Epimeral setae 3c about 19 µm long, thickly barbed, and 4c about 32 µm long, much thicker and more heavily barbed that other epimeral setae. Genital setae 1+5 or 2+4, 1 or 2 pairs of genital setae on anterior margin of genital plates. Ten pairs of long, curved, smooth to weakly barbed notogastral setae present; about 41 µm long, positioned so that lm posteromedial of Aa, and lp anterior of A1. Tarsi heterotridactylous. Description. Adult. Dimensions: Mean total length: female (n = 2) 323 µm (320, 326); male (n = 4) 304 µm (range 298–322). Mean notogastral width: female (n =2) 223 µm (220, 226); male (n =3) 209 µm (range 206–216). Integument: Prodorsum, lateral of lamellae, notogaster, anal plate, pedotectum I with widely spaced micropuncta. Coxisternum, lamella, pedotectum I, tutorium and anterior of pteromorph with fine to very fine striae (Fig. 25). Mentum and genital plate microtuberculate. Prodorsum: Rostrum with medial crest dorsally; rostral margin undulating, with pair of minute dens laterally (Fig. 25). Lamella (including cusp) about 108 µm long, cusp about 77 µm long, about 36 µm wide at level of insertion of seta le. Lamellar cusps converging then diverging or parallel anteromedially; fused posteromedially, leaving prodorsum only visible through small oval opening, about 10 µm wide; translamella without tooth, about 10 µm at greatest width, about 24 µm deep (Figs. 23E arrow, 24). Medial dens on cusp about 31 µm long, without teeth; lateral dens about 41 µm long with 3–4 teeth (Fig. 24), varying among specimens and on either side of same specimen. Setae ro about 53 µm long, strongly barbed along length, acuminate, curved anteromedially. Setae le about 58 µm long, thick, heavily barbed, tapered. Setae in about 103 µm long, thick (less so than le), heavily barbed, tapered; mutual distance of pair about 31 µm. Bothridial setae 72–77 µm long, with barbed, narrowly fusiform head, rounded to tapered distally, stalk short, smooth; head directed slightly anterodorsally (Figs. 23E, 24). Exobothridial setae about 19 µm long, thin, barbed tapered. Lateral aspect of podosoma: Genal tooth broad, subrectangular, with dens ventrodistally, with longitudinal ridge ventrally. Tutorium about 108 µm long, of which cusp about 50 µm long, rectangular, distal margin with 3–5 dens. Custodium about 29 µm long (Fig. 25). Porose area Al about 10 µm in diameter. Notogaster: Length subequal to width. Anterior margin undulating, convex lateral of bothridium, with 5–7 transverse ridges (Fig. 24). Pteromorph with short ridges at anterior margin forming reticulate pattern; with small dens on anteroventral margin. Octotaxic system in form of 4 relatively small porose areas, about 8 µm in diameter. Ten pairs of long, curved, smooth to weakly barbed notogastral setae present; about 41 µm long, lm posteromedial of Aa, and lp anterior of A1 (Fig. 24). Distance setae h 1 –h 1 subequal to distance p 1 –p 1 , 14–16 µm. Subtriangular lenticulus present (not illustrated). Ventral region: Epimeral setae 1a, 1b, 1c, 2a, 3a, 3b about 8–10 µm long, weakly barbed; 4a, 4b about 13 µm long, weakly barbed; 3c about 19 µm long, thickly barbed; 4c about 32 µm long, much thicker and more heavily barbed than other epimeral setae (Fig. 25). Genital, aggenital, anal and adanal setae weakly barbed, about 8–10 µm long. Genital setae positioned in curved row, 1 or 2 pairs on anterior margin of plates. Postanal porose area oval, 12 x 6 µm. Gnathosoma: Mentum with transverse carina anteriorly. Axillary saccule about 5 x 2 µm. Legs: Setation (I to IV): trochanters, 1-1-2-1; femora, 5-5-3-2; genua, 3(1)-3(1)-1(1)-2; tibiae 4(2)-4(1)-3(1)- 3(1); tarsi, 20(2)-15(2)-15-12. Seta l” of genu I about 32 µm, l” of genu II about 29 µm. Tarsi heterotridactylous. Etymology. The specific epithet ‘texana’ refers to the provenance of this species, Texas, USA. Remarks. This species is similar to O. pusilla, but differs from the latter in depth of the translamella about 24 µm (15 µm deep in pusilla), and epimeral seta 4c being thick and barbed (subequal in shape, but more distinctly barbed in pusilla). Distribution and Ecology. This species is known only from thick deciduous and coniferous litter from various parts of Texas., Published as part of Behan-Pelletier, V. M., 2011, Oribatella (Acari, Oribatida, Oribatellidae) of eastern North America, pp. 1-56 in Zootaxa 2973 (1) on pages 47-50, DOI: 10.11646/zootaxa.2973.1.1, http://zenodo.org/record/5295835
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37. Oribatella flagellata Behan-Pelletier 2011, sp. nov
- Author
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Behan-Pelletier, V. M.
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Oribatella ,Oribatellidae ,Arthropoda ,Arachnida ,Animalia ,Biodiversity ,Sarcoptiformes ,Oribatella flagellata ,Taxonomy - Abstract
Oribatella flagellata sp. nov. (Figs. 5, 6A–C) Material examined. Holotype: male USA: Virginia, Grayson Co., Hwy 603 at Fox Creek, 6km W Troutdale, 5.viii.1986 (EEL) from Trametes versicolor (L.) polypore fungi and lichen on hardwood, deposited in the CNC, type number 23954. Paratypes: 1 female with same data as holotype; Virginia, Nelson Co., Washington National Forest, Blue Ridge Parkway, Wintergreen Trail, 1.x.1992 (VBP) 1 male from litter under dead shagbark hickory in oak/hemlock forest; Canada, Québec, Gatineau Park, 22.x.1965 (W.G. Matthewman) 1 from Fomes fomentarius; 9.v.–31.x.1968 (D.P. Pielou) 24 from Polyporus betulinus. Paratypes deposited in the CNC. Diagnosis. Total length of adult 410–440 µm. Integument of prodorsum, notogaster, anal plates, genital plates, venter and mentum microtuberculate. Rostrum with medial indentation and 2 strong lateral teeth; without strong medial crest. Lamella (including cusp) about 133 µm long; cusp about 90 µm long, about 38 µm wide at level of insertion of seta le. Translamella without tooth, interlamellar region distinctly V-shaped posteriorly. Ten pairs of smooth, flagellate notogastral setae present; about 50 µm long (tips of some setae broken on specimens), lm posterior of Aa, and lp anteromedial of A1; mutual distance p 1 –p 1 about 20 µm, narrower than distance h 1 –h 1 (about 35 µm). Tarsi heterotridactylous. Description. Adult. Dimensions: Total length: paratype female 440 µm; holotype male 410 µm. Notogastral width: paratype female 310 µm; holotype male 275 µm. Integument: Prodorsum, notogaster, anal plates, genital plates, venter and mentum microtuberculate, microtubercles and striae on coxisternum. Tutorium with small reticulate pattern dorsally. Lamellae with widely spaced, faint longitudinal striae. Prodorsum: Rostrum with medial indentation and 2 strong lateral teeth; without strong medial crest (Fig. 6A). Lamella (including cusp) about 133 µm long, cusp about 90 µm long, about 38 µm wide at level of insertion of seta le. Lamellar cusps contiguous anteromedially; separated posteromedially, leaving prodorsum visible through oval opening, about 13 µm wide x 33 µm long. Translamella without tooth, about 13 µm at greatest width, interlamellar region distinctly V-shaped posteriorly (Fig. 5). Medial dens on lamellar cusp about 40 µm long, without teeth; lateral dens about 50 µm long with 0–1 tooth on lateral margin (Fig. 5). Setae ro about 88 µm long, strongly barbed along length, acuminate, curved anteromedially. Setae le about 85 µm long, thick, heavily barbed, tapered. Setae in about 130 µm long, thick (less so than le), barbed, tapered, parallel; mutual distance of pair about 40 µm. Bothridial setae about 75 µm long, with barbed, club-shaped head, tapered distally, stalk short, smooth; head directed slightly anteromedially (Fig. 5). Exobothridial setae about 16 µm long, thin, smooth. Lateral aspect of podosoma: Genal tooth broad, subrectangular, with dens ventrodistally, with longitudinal ridge ventrally (Fig. 6A). Tutorium broad, rectangular about 133 µm long, of which cusp about 68 µm long, rectangular, distal margin with 5–6 dens (Fig. 6B). Custodium about 31 µm long, extending to middle of pedotectum II (Fig. 6C). Porose area Al about 7 µm in diameter. Notogaster: Length subequal to width. Anterior margin undulating, convex lateral of bothridium, with 2–3 transverse ridges. Pteromorph without striae; with or without small dens on anteroventral margin. Octotaxic system in form of porose areas, 10–12 µm in diameter. Ten pairs of smooth, flagellate notogastral setae present; about 50 µm long (tips of some setae broken on specimens), with c seta longest; lm posterior of Aa, and lp anteromedial of A1; distance p 1 –p 1 about 20 µm, narrower than distance h 1 –h 1 (about 35 µm) (Fig. 5). Diffuse subtriangular lenticulus present (not illustrated). Ventral region: Epimeral setae mostly about 11–21 µm long, weakly barbed acuminate, 3c about 32 µm long, distinctly barbed, 4c about 32 µm long, thick and heavily barbed, much thicker than other epimeral setae (Fig. 6C). Genital, anal and adanal setae weakly barbed, about 13 µm long; genital setae 3 + 3, 3 setae on anterior margin of plate. Aggenital setae about 5 µm. Lyrifissure iad anterolateral of and almost parallel to anal plate. Postanal porose area about 30 x 5 µm. Gnathosoma: Mentum without transverse carina anteriorly, without tectum. Axillary saccule about 4 x 2 µm. Legs: Setation (I to IV): trochanters, 1-1-2-1; femora, 5-5-3-2; genua, 3(1)-3(1)-1(1)-2; tibiae 4(2)-4(1)-3(1)- 3(1); tarsi, 20(2)-15(2)-15-12. Setae l” on genu I about 38 µm; l” on genu II about 43 µm. Tarsi heterotridactylous. Etymology. The specific epithet refers to the flagellate form of the notogastral setae. Distribution and Ecology. This species is known only from different species of polypore fungi. The 1965 record from Gatineau Park, Québec was included in the study of the fauna of Fomes fomentarius (Pielou & Matthewman 1966), incorrectly identified as Oribatella quadricornuta., Published as part of Behan-Pelletier, V. M., 2011, Oribatella (Acari, Oribatida, Oribatellidae) of eastern North America, pp. 1-56 in Zootaxa 2973 (1) on page 13, DOI: 10.11646/zootaxa.2973.1.1, http://zenodo.org/record/5295835, {"references":["Pielou, P. D. & Matthewman, W. G. (1966) The fauna of Fomes fomentarius (Linnaeus ex Fries) Kickx. growing on dead birch in Gatineau Park, Quebec. The Canadian Entomologist, 98, 1308 - 1312."]}
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38. Oribatella Banks 1895
- Author
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Behan-Pelletier, V. M.
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Oribatella ,Oribatellidae ,Arthropoda ,Arachnida ,Animalia ,Biodiversity ,Sarcoptiformes ,Taxonomy - Abstract
Oribatella Banks, 1895 Type species: Oribatella quadridentata Banks, 1895, p. 8. Diagnosis. Adult. Species comprising this genus are unique among Oribatellidae (Grandjean 1953b, Bernini 1978) in having the following combination of character states. Notogaster with immovable pteromorphs. Octotaxic system as 4 pairs of porose areas or saccules; usually without sexual dimorphism, when present that of male modified. Notogaster with 10 to 14 pairs of short to very long setae. Lamellae long, broad, with large cusps, medially converging or contiguous; cusps usually with large medial and lateral dens; translamella (Fig. 4B arrow) variable in width and depth, with or without medial tooth. Bothridial wall distally expanded. Genal tooth with longitudinal ridge ventrally, either broad, subtriangular to subrectangular in shape, with dens ventrodistally (Fig. 1B arrow), or broad, subrectangular, rounded distally, without dens ventrodistally (Fig. 2E arrow). Tutorium broad, lamelliform, cusp rectangular or subrectangular, with dens distally, lying parallel to dorsal contour of prodorsum in lateral aspect, extending well anterior to insertion of rostral seta. Custodium usually present, with short to long, free distal point. Axillary saccule present at base of palp. Chelicera chelate-dentate, elongated in one species. Mentum with or without tectum, with or without recurved ridge distally (Fig. 2D). Palp setal formula 0–2–1–3–9(1) or 0–2–1–3– 8(1); eupathidium acm subequal in length to solenidion, forming double horn with solenidion along length or distally; in one species solenidion almost 2.5x length of acm (Fig. 20E). Humerosejugal porose organ Ah expressed as porose area (Fig. 9C) or saccule; porose area Al present or absent, when present expressed as porose area or saccule. Legs monodactylous, heterobidactylous or heterotridactylous. Femur III with seta l’ present or absent; seta v' of genua I and II present or absent. Setae l” of genua and tibiae I and II thicker, more heavily barbed and longer than setae l’ on these segments. Setae l' on genu and tibia IV thicker, more heavily barbed and longer than other setae on these segments. One or two anterodorsal spines may be present on tibia I close to, or between, solenidia φ 1 and φ 2 (Fig. 2F arrow). Immatures. Apopheredermous, with scalps of preceding instar maintained away from dorsal integument by modified setae da and dorsally directed h 1. Body colorless, cuticle without plicae. All or most gastronotic setae long; setation usually unideficient; larva with 11 or 12 pairs, protonymph with 15 pairs (adult loses at least c 1 ), deutonymph and tritonymph with 13 to 15 pairs. Setae dm and dp subequal in length to da in all immatures, or much shorter than da in deutonymph and tritonymph, or dm and dp absent from deutonymph and tritonymph. Hysterosomal sclerites absent. Pair of humeral organs present laterally in sejugal region. Without apodemato-acetabular tracheal system or porose homologues. Paraprocts atrichous in larva, protonymph and deutonymph. Genital setal formula (larva to adult): 0–1–3–5–6. Aggenital setal formula 0–0–1–1–1, or aggenital seta absent. Opisthonotal gland present in all instars. Cupule development normal. Bothridium and bothridial seta fully formed in all instars. Setation of protonymphal leg IV normal (0–0–0–0–7). Larva to deutonymph with circular line of dehiscence, such that dorsal scalp separates from ventral piece at ecdysis., Published as part of Behan-Pelletier, V. M., 2011, Oribatella (Acari, Oribatida, Oribatellidae) of eastern North America, pp. 1-56 in Zootaxa 2973 (1) on pages 3-4, DOI: 10.11646/zootaxa.2973.1.1, http://zenodo.org/record/5295835, {"references":["Banks, N. (1895) On the Oribatoidea of the United States. Transactions of the American Entomological Society, 22, 1 - 16.","Grandjean, F. (1953 b) Essai de classification des oribates (acariens). Bulletin de la Societe. Zoologique de France, 78, 421 - 446.","Bernini, F. (1978) Notulae Oribatologicae XX. Il genere Oribatella in Italia (Acarida, Oribatida). Redia, 61, 503 - 538."]}
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39. Oribatella nortoni Behan-Pelletier 2011, sp. nov
- Author
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Behan-Pelletier, V. M.
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Oribatella ,Oribatellidae ,Arthropoda ,Arachnida ,Animalia ,Biodiversity ,Sarcoptiformes ,Taxonomy ,Oribatella nortoni - Abstract
Oribatella nortoni sp. nov. (Figs. 15–18, 19A, B) Material examined. Holotype: adult female. USA: Alabama: Lee Co., nr. Auburn in coastal plain, 7.xi.1975 (unknown), RAN 75–150; deposited in the CNC, type number 23957. Paratypes: 20 (15 females, 5 males) with same data as holotype; deposited in the CNC, RNC and the FM. Other material examined. New York, Newcomb, Lake Harris Campground, i. vii.1971 (EEL) 1 from moss on tree trunk; Arkansas, Polk Co., N. slope Rich Mountain, below 272–82 intersection, 25.iii.1992 (HWR) 4 from oldgrowth; Canada, New Brunswick, Kent Co., Kouchibouguac National Park, 21.vii.1978 (IMS) 3 from moss and litter at base of red oak (living); same data except 3 from bark and litter at base of red oak (dead); same data except, 15.vi.1978 (R. Cope) 1 from moose dung in mixed woods; same data except, 9.viii.1977 (EEL) 2 from mixed deciduous litter. Diagnosis. Length of adult 295–320 µm. Rostrum flattened medially with minute lateral teeth. Translamella without tooth, about 9 µm at greatest width, 13 µm at greatest depth. Medial dens on lamellar cusp about 7–10 µm long, without marginal teeth, less than third length lateral dens; latter about 31 µm long, without marginal teeth. Bothridial setae about 100 µm long, with barbed, long bacilliform head, tapered distally, stalk short, smooth; head directed slightly anterodorsally. Ten pairs of short, smooth notogastral setae present, 24 to 41 µm long, with c seta longest, setae lm medial to Aa, lp anteromedial to A1; distance h 1 –h 1 about 27 µm, wider than distance p 1 –p 1 about 21 µm. Epimeral seta 3c barbed, about 32 µm, and 4c smallest, thinnest epimeral seta, about 8 µm long. Genital setae in single curved line, or 2+4. Mentum with thickened, reverted transverse ridge anteriorly, with tectum. Femur III with 2 setae, l’ absent. Tarsi monodactylous. Description. Adult. Dimensions: Mean total length female (n = 10) 317 µm (range 310–320), mean total length male (n = 9) 301 µm (range 295–310). Mean notogastral width female (n = 3) 208 (range 205–210); mean notogastral width male (n = 4) 208 µm (range 200–225). Integument: Prodorsum, notogaster, venter and mentum faintly micropunctate. Coxisternum, lamellae and pedotectum I with fine striae, lamella laterally with strong striae (Fig. 15). Prodorsum: Rostrum flattened medially with minute lateral teeth (Fig. 16). Lamella (including cusp) about 118 µm long, cusp about 70 µm long, about 41 µm wide at level of insertion of seta le. Lamellar cusps contiguous, or not, anteromedially, separated posteromedially, leaving prodorsum visible through long oval opening, 9 µm wide x 16 µm long; translamella without tooth, about 9 µm at greatest width, 13 µm at greatest depth (Fig. 15). Medial dens on lamellar cusp about 7–10 µm long, without marginal teeth, less than third length lateral dens; latter about 31 µm long, without marginal teeth (Figs. 15, 19A). Setae ro about 80 µm long, strongly barbed along length, acuminate, curved anteromedially. Setae le about 93 µm long, thick, heavily barbed, tapered. Setae in about 133 µm long, thick (less so than le), heavily barbed, tapered; mutual distance of insertions of pair about 47 µm. Bothridial setae about 100 µm long, with barbed, long bacilliform head, tapered distally, stalk short, smooth; head directed slightly anterodorsally (Fig. 15). Exobothridial setae about 20 µm long, thin, acuminate. Lateral aspect of podosoma: Genal tooth broad, subrectangular, with dens ventrodistally, with longitudinal ridge ventrally (Fig. 19B). Tutorium about 120 µm long of, which cusp about 72 µm long, rectangular; distal margin variable, with distinct dorsal and ventral dens (Fig. 19B), or with 6–10 dens along anterodorsal and distal margin. Custodium about 29–40 µm long, tapered (Fig. 16). Porose area Al about 11 µm in diameter. Notogaster: Length subequal to width. Anterior margin undulating, convex lateral of bothridium, with 5–7 transverse ridges. Pteromorph with striae along margin; with small dens on anteroventral margin. Octotaxic system in form of small porose areas, about 7 µm in diameter. Ten pairs of short, smooth notogastral setae present; 24 to 41 µm long, with c seta longest, setae positioned medially and laterally, lm medial to Aa, lp anteromedial of A1; distance h 1 –h 1 about 27 µm, wider than distance p 1 –p 1 , about 21 µm (Fig. 15). Subtriangular lenticulus present. Ventral region: Seta 3c largest epimeral seta, barbed, about 32 µm, 4c smallest, thinnest, about 8 µm long; other epimeral setae mostly 14–18 µm long, smooth. Genital, aggenital, anal and adanal setae weakly barbed, about 11 µm long. Genital setae in single curved line or 2+4. Lyrifissure iad anterior of anterolateral corner of anal plates. Postanal porose area oval 18 x 6 µm. Gnathosoma: Mentum with thickened, reverted transverse ridge anteriorly, with tectum. Axillary saccule about 5 x 2 µm. Legs: Setation (I to IV): trochanters, 1-1-2-1; femora, 5-5-2-2; f, 3(1)-3(1)-1(1)-2; tibiae 4(2)-4(1)-3(1)-3(1); tarsi, 20(2)-15(2)-15-12. Seta l’ absent from femur III. Setae l” on genua I and II 22-24 µm. Tarsi monodactylous. Description. Immatures. Dimensions: Length: larva (n = 1) (specimen distorted, not measured); protonymph (n = 1) 235 µm; tritonymph (n = 1) 290 µm. Larva. Prodorsum: Setae ro le, in and ex strongly barbed, tapered, in thickest seta, about 32, 49, 73 and 37 µm long, respectively. Mutual distance of setae ro about 9 µm, of setae le about 13 µm and of setae in about 20 µm. Setae ex directed laterally, other prodorsal setae directed anteriorly or anterolaterally (Fig. 17). Bothridial seta setiform, heavily barbed, about 80 µm long, almost blunt distally (Fig. 17). Gastronotic region: Rounded; outline slightly uneven, caused by swelling around setal tubercles (Fig. 17). Humeral organ as for tritonymph (Fig. 17 arrow). Gastronotal setae, other than h 2 , long, broad, heavily barbed, tapered, seta h 2 thin, weakly barbed, acuminate; seta h 1 absent; all setae, other than h 2 , directed posteriorly, h 2 directed laterally; setae c 1 , da and dm overlapping in larva and on larval scalps carried by protonymph. Setal lengths (in µm) approximate (due to difficulty in measurement): c 1 (78), c 2 (81), c 3 (54), da (52), dm (49), dp (36), la (48), lm (44), lp (35), h 3 (32), h 2 (21); distance da–da and dm–dm subequal 14–15 m, distance dp–dp about 23 µm. Ventral region: Epimeral setation 3-1-2; setae all smooth, about 5 µm, except 1c scaliform. Tritonymph. Integument: weakly sclerotized; weakly microtuberculate. Prodorsum: Setae ro le, in and ex broad, strongly barbed, tapered, about 36, 84, 90 and 60 µm long, respectively. Mutual distance of setal pair ro about 12 µm, of pair le about 17 µm and of pair in about 38 µm. Setae ex directed laterally, other prodorsal setae directed anteriorly or anterolaterally (Fig. 18A). Bothridial seta setiform, heavily barbed, about 120 µm long (Fig. 18A). Gastronotic region: Margin carinate except anteriorly; outline slightly uneven, caused by weak swelling around setal tubercles (Fig. 18A). Two oval porose regions closely medial to each seta lp; about 13 µm at widest dimension (not illustrated). Opisthonotal gland opening ventromedial to seta lp (Fig. 18B). Humeral organ present as small saccule 3 x 3 µm, ventral to seta c 3 (Fig. 18A, arrow). Setae c 2 broken from specimen examined. Other gastronotal setae long, broadened, heavily barbed, tapered; c 1, da , directed posteriorly. Setal lengths (in µm) approximate (due to some terminal breakage and difficulty in measurement): c 1 (45), c 2 (broken), c 3 (108), da (75), dm (90), dp (50), la (105), lm (110), lp (108), h 1 (97), h 2 (81), h 3 (103), p 1 (52), p 2 (47), p 3 (24). Distance da–da about 22 µm, dm–dm about 42 µm and dp–dp about 82 µm; c 1 and dp broadest setae, subequal in shape and length; da narrowest seta, subequal in shape to bo; setae p 1 and p 2 subequal in size and shape, broader than p 3 . Ventral surface of scalps with pair of sheathlike callosities, accommodating seta da of previous instar; sheaths browner, more sclerotized than rest of scalp. Ventral region: Epimeral plates contiguous medially. Epimeral setation 3-1-3-3; all smooth, about 5 µm, except 3c barbed, about 8 µm. Five pairs of genital setae, about 6 µm, aligned in longitudinal row. Aggenital seta smooth, about 8 µm. Three pairs of adanal setae about 8 µm, ad 1 barbed, ad 2 and ad 3 smooth (Fig. 18B); two pairs of anal setae smooth, about 5µm; cupule iad present. Axillary saccule present, about 4 x 2 µm. Legs: Setae l” of femur, genu and tibia I, II and l’ of genu III very broad, barbed, spinous, almost blunt distally. Protonymph. Similar to tritonymph in form and proportions. Epimeral setation 3-1-2-1. Paraprocts atrichous in protonymph. Scalps of protonymph with molded integument to accommodate setae da of larval scalp. Legs: Ontogeny of leg setae and solenidia for known immatures and adult given in Table 3. Etymology. This species is named in honour of my friend, colleague and preeminent expert on oribatid mites, Dr. Roy A. Norton. Remarks. Adults of Oribatella nortoni sp. nov. are very similar to those of O. sexdentata, described from Italy on the basis of a single specimen (Berlese 1916), see also Mahunka and Mahunka-Papp (1995). This species was redescribed by Bernini (1977) and Chistyakov (1984a), and is keyed to species in Bernini (1978) and in Weigmann (2006). The redescription of this species by Bernini (1977) and Chistyakov (1984a) is used for comparison herein, and character states for O. sexdentata are in parentheses below. In O. nortoni sp. nov. seta bo is tapered distally (blunt distally); notogastral seta lm is medial of Aa (posterior to posteromedial of Aa: Bernini 1977, his Fig. XII b; Chistyakov 1984a, his Fig. 13; see also, Weigmann 2006, his Fig. 193 a and Shtanchaeva & Subías 2009, their Fig. 7). Epimeral seta 4c is the smallest, thinnest epimeral seta in O. nortoni (a character state also found in O. eutricha Berlese, 1908 known from Italy); unfortunately, this character is broken on the type of O. sexdentata (Bernini 1977) and is not illustrated in Chistyakov (1984a). The immatures of O. sexdentata were described by Chistyakov (1984a). These differ markedly from immatures of O. nortoni in the shape of gastronotal setae. Furthermore, seta c 1 of all nymphs of O. sexdentata are smooth and shorter than other gastronotal setae, whereas in known nymphs of O. nortoni seta c 1 are equally well barbed and broad as other gastronotal setae. Bernini (1977) questioned the record of O. sexdentata from Virginia, USA (Sengbusch 1957). It is possible that this record related instead to O. nortoni. However, Sengbusch’s specimens are not available, so both species are included in the key to species (see below). Development of leg setae is similar to that given for Oribatella canadensis (Behan-Pelletier & Eamer 2010) except on leg II, v’ is tritonymphal on the genu and pair (v) are tritonymphal on the tibia (adult in O. canadensis); on leg III, l’ is absent from the femur; and on legs III and IV, (l) is tritonymphal on the tibia (adult in O. canadensis). Distribution and Ecology. This species is known only from a few localities in eastern North America from New Brunswick, Canada to Alabama, USA (Table 1)., Published as part of Behan-Pelletier, V. M., 2011, Oribatella (Acari, Oribatida, Oribatellidae) of eastern North America, pp. 1-56 in Zootaxa 2973 (1) on pages 30-36, DOI: 10.11646/zootaxa.2973.1.1, http://zenodo.org/record/5295835, {"references":["Berlese, A. (1916) Centuria terza di Acari nuovi. Redia, 12, 283 - 338.","Mahunka, S. & Mahunka-Papp, L. (1995) The Oribatid species described by Berlese (Acari). Hungarian Natural History Museum, Budapest, 325 pp.","Bernini, F. (1977) Notulae Oribatologicae XVII. Nuovi dati sul genere Oribatella in Italia (Acarida, Oribatei). Redia, 60, 457 - 505.","Chistyakov, M. P. (1984 a) The postembryonic development of Oribatella sexdentata Berlese, 1916 (Oribatei). Gor'kovskiy Gosudarstvennyy Pedagogicheskiy Institut imeni A. M. Gor'kogo. Gor'kiy. Deponirovano v VINITI. 68, 1 - 28. [In Russian]","Bernini, F. (1978) Notulae Oribatologicae XX. Il genere Oribatella in Italia (Acarida, Oribatida). Redia, 61, 503 - 538.","Weigmann, G. (2006) Hornmilben (Oribatida). Die Tierwelt Deutschlands, 76. Teil. Goecke & Evers, Keltern, 520 pp.","Shtanchaeva, U. Ya. & Subias, L. S. (2009) A review of oribatid mites of the family Oribatellidae (Acariformes, Oribatida) from the Caucasus. Entomological Review, 89 (2), 218 - 238. (English version)","Berlese, A. (1908) Elenco di generi e specie nuovi di Acari. Redia, 5, 1 - 15.","Sengbusch, H. G. (1957) Checklist of Oribatoid mites in the vicinity of Mountain Lake Biological Station - Virginia. Virginia Journal Science, 8 (2), 128 - 134.","Behan-Pelletier, V. M. & Eamer, B. (2010) The first sexually dimorphic species of Oribatella (Acari, Oribatida, Oribatellidae) and a review of sexual dimorphism in the Brachypylina. Zootaxa, 2332, 1 - 20."]}
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40. Oribatella metzi Behan-Pelletier 2011, sp. nov
- Author
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Behan-Pelletier, V. M.
- Subjects
Oribatella ,Oribatella metzi ,Oribatellidae ,Arthropoda ,Arachnida ,Animalia ,Biodiversity ,Sarcoptiformes ,Taxonomy - Abstract
Oribatella metzi sp. nov. (Figs. 10–13) Material examined. Holotype: female USA: North Carolina, Durham Co., Duke Forest, 4.v.1979 (L. Metz), deposited in the CNC, type number 23956. Paratypes: 7 (5 males, 2 females) with same data as holotype; North Carolina, Buncombe Co., Bent Creek Experimental forest (A.P. Jacot) (RNC) (2 males) (“montum” of Jacot, see Remarks); West Virginia, Mercer Co., 1.5 mi N on Brushcock Falls Trail, 13.vi.1971 (W. Sheer) 1 female from deep litter near cliff (RNC); Missouri, Boone Co., Hinkson Creek, Columbia, S.U. Mo. Campus, 25.iv.1985 FMHD #85–127 (J. Kethley, R.A. Norton) 1 female from mixed deciduous litter on dry ridgetop (FM); Alabama, DeKalb Co., De Soto State Park, Lost Falls Trail 26.ix.1992 (VBP) 1 female from moist maple litter by Lost Falls; same data except, 27.ix.1992, Rhodendron Trail, 1 male from moss at base of hemlock. Diagnosis. Total length of adult 275–290 µm. Rostral margin rounded, undulating in ventral aspect with 2 small lateral dens. Microtubercles aligned on striae on posterior of notogaster, on coxisternum, on genital plates and on ventral plate laterally and posteriorly of anal plates. Translamella without tooth. Lamella (including cusp) 105–109 µm long, cusp 72–77 µm long, about 38 µm wide at level of insertion of seta le. Medial dens on cusp about 31 µm long, without teeth; lateral dens about 37 µm long with at most 1 tooth on lateral margin. Bothridial seta 90–111 µm long, with barbed, fusiform head, tapered distally. Notogastral porose areas small, about 5 µm in diameter. Ten pairs of short, smooth notogastral setae present, 16–27 µm long, with c seta longest, setae positioned laterally; lm posterior of Aa, and directed laterally, lp anterior of A1. Mutual distance p 1 –p 1 about 19 µm, subequal to distance h 1 –h 1 . Aggenital setae absent. Tarsi monodactylous. Description. Adult. Dimensions: Mean total length: female (n = 3) 288 µm (range 285–290); male (n = 5) 279 µm (range 275–280). Mean notogastral width: female (n =3) 198 µm (range 195–200); male (n =5) 188 µm (range 180–190). Integument: Prodorsum, notogaster, anal plates, genital plates, venter and mentum microtuberculate, microtubercles aligned on striae on posterior of notogaster, coxisternum, genital plates and on ventral plate laterally and posterior of anal plates (Fig. 10). With striae on tutorium, pteromorph and pedotectum I. Lamellae smooth medially, with longitudinal striae laterally (Fig. 10). Prodorsum: Rostrum rounded triangle in dorsal aspect; margin rounded, undulating in ventral aspect with 2 small lateral dens. (Fig. 11). Lamella (including cusp) 105–109 µm long, cusp 72–77 µm long, about 38 µm wide at level of insertion of seta le. Lamellar cusps contiguous anteromedially; separated posteromedially, leaving prodorsum visible through oval opening, about 14 µm wide x 21 µm long; translamella without tooth, about 11 µm at greatest width, 6 µm depth (Fig. 10). Medial dens on lamellar cusp about 31 µm long, without teeth; lateral dens about 37 µm long with at most 1 tooth on lateral margin. Long striae extending longitudinally along outer margin of lamella and cusp; lamella without striae medially (Fig. 10). Setae ro about 73 µm long, strongly barbed along length, acuminate, curved anteromedially (Fig. 11). Setae le about 57–66 µm long, thick, heavily barbed, tapered. Setae in 113–124 µm long, thick (less so than le), heavily barbed, tapered; mutual distance of pair 52–54 µm. Bothridial setae about 90–111 µm long, with barbed, fusiform head, tapered distally, stalk short, smooth; head directed slightly anterodorsally (Fig. 10). Exobothridial setae about 11 µm long, thin, smooth. Lateral aspect of podosoma: Genal tooth broad, subrectangular, with dens ventrodistally, with longitudinal ridge ventrally. Tutorium broad, rectangular about 97 µm long of which cusp about 54 µm long, rectangular, distal margin with 5–6 dens. Custodium about 26 µm long, extending to middle of pedotectum II (Fig. 11). Porose area Al about 10 µm in diameter. Notogaster: Length subequal to width. Anterior margin undulating, convex lateral of bothridium, with 5–9 transverse ridges. Pteromorph with striae; with or without small dens on anteroventral margin (Fig. 11). Octotaxic system in form of relatively small porose areas, about 5 µm in diameter. Ten pairs of short, smooth notogastral setae present, 16–27 µm long, with c seta longest, setae positioned laterally, so that lm posterior of Aa, and directed laterally, and lp anterior of A1 (Fig. 10); distance p 1 –p 1 about 19 µm, subequal to distance h 1 –h 1 about 19 µm. Diffuse subtriangular lenticulus present (not illustrated). Ventral region: Epimeral setae mostly about 6–8 µm long, smooth, 4c about 32 µm long, thick and heavily barbed. Genital, anal and adanal setae smooth, about 6–8 µm long; genital setae 3 + 3, 3 setae on anterior margin of plate. Aggenital setae absent. Lyrifissure iad anterolateral and almost parallel to anal plate. Postanal porose area oval 11 x 5 µm. Gnathosoma: Mentum with transverse carina anteriorly, with short tectum (Fig. 11). Axillary saccule about 4 x 2 µm. Legs: Setation (I to IV): trochanters, 1-1-2-1; femora, 5-5-2/3-2; genua, 3(1)-3(1)-1(1)-2; tibiae 4(2)-4(1)-3(1)- 3(1); tarsi, 20(2)-15(2)-15-12. Setae l” on genua I and II 21 µm; l” on tibiae I and II 14 µm. Tarsi monodactylous. Description. Immatures. Dimensions: Mean length: larva (n = 1) 200 µm; deutonymph (n = 1) 209 µm; tritonymph (n = 7) 282 µm (range 275–290). Larva. Integument weakly microtuberculate. Prodorsum: Setae ro le, in and ex long, barbed, tapered, about 50, 70, 80 and 70 µm long, respectively. Mutual distance of pair ro about 9 µm, of pair le about 10 µm and of pair in about 30 µm. Setae ex directed laterally, other prodorsal setae directed anteriorly or anterolaterally (Fig. 12). Bothridial seta fusiform, heavily barbed, about 80 µm long, tapered distally (Fig. 12). Gastronotic region: Margin carinate except anteriorly; outline uneven, caused by weak swelling around setal tubercles. Twelve pairs of setae, long, barbed, tapered, subequal in shape. Setal lengths (in µm) approximate (due to some terminal breakage and difficulty in measurement): c 1 (92), c 2 (90), c 3 (90), da (100), dm (90), dp (70), la (80), lm (80), lp (60), h 1 (?), h 2 (?), h 3 (27). Tritonymph: Integument of gastronotal region weakly microtuberculate medially, with short striae laterally. Integument of prodorsum weakly microtuberculate. Prodorsum: Setae ro le, in and ex barbed, tapered, about 38, 59, 66 and 45 µm long, respectively. Mutual distance of setae ro about 15 µm, of setae le about 16 µm and of setae in about 33 µm. Setae ex directed laterally, other prodorsal setae directed anteriorly or anterolaterally (Fig. 13). Bothridial seta bacilliform, heavily barbed, about 76 µm long, blunt distally (Fig. 13). Gastronotic region: Margin carinate except anteriorly; outline slightly uneven, caused by weak swelling around setal tubercles (Fig. 13). Setae barbed, tapered, with c 1 thinnest seta and da thickest seta; dm and dp absent (Fig. 13). Setae c 1, c 2, da , directed posteriorly; c 1 generally lying beneath scalps of previous instars. Setae c 3 la, lm, lp, h 3, h 2 directed posterolaterally. Setal lengths (in µm) approximate (due to some terminal breakage and difficulty in measurement): c 1 (23), c 2 (36), c 3 (41), da (30), la (42), lm (40), lp (37), h 1 (30), h 2 (32), h 3 (34), p 1 (26), p 2 (22), p 3 (22). Ventral surface of scalps with pair of setiform, sheathlike callosities, accommodating seta da of preceding instar; sheaths browner, more sclerotized than rest of scalp. Ventral region: Epimeral plates contiguous medially. Epimeral setation 3-1-3-3; all smooth, about 6 µm. Five pairs of genital setae, about 6 µm, aligned in longitudinal row. Aggenital seta absent. Three pairs of adanal setae barbed, about 9–13 µm; two pairs of anal setae barbed, about 9µm; cupule iad present. Axillary saccule present, about 4 x 2 µm. Other nymphal instars: Similar to tritonymph in form and proportions, except as follows. Setae of d series of deutonymph as for tritonymph, i.e., setae dm and dp absent. Setae of d series of protonymph (observation from protonymphal scalp; no specimen available) represented by da, similar in shape to that of tritonymph, about 24 µm long and dp, similar in shape to l series, about 38 µm long; setae dm absent; distance setal bases da and dp about 74 µm, three times length da. Legs: Ontogeny of leg setae and solenidia for known nymphs and adult given in Table 2. Etymology. This species in named in honour of the late Dr. Louis J. Metz, who contributed extensively to oribatid mite research and soil faunal studies in North America. Remarks. This species made it necessary to modify the diagnosis of Oribatella (see above) for characters relating to the ontogeny of gastronotic setae. In other species the protonymph, deutonymph and tritonymph have 15 pairs of gastronotal setae (adult loses at least c 1 ). Oribatella metzi is unique among Oribatella, and among all known brachypyline Oribatida, in that deutonymphal and tritonymphal gastronotal setal loss differs from that of the protonymph, the protonymph having 14 pairs of gastronotal setae (seta dm lost) and the deutonymph and tritonymph with 13 pairs of gastronotal setae (setae dm and dp lost). The development of leg setae is similar to that given for Oribatella canadensis (Behan-Pelletier & Eamer 2010), which is the only species of Oribatella for which this is known. The only clear exception is that seta l’ is deutonymphal on tibia III and tritonymphal on tibia IV (both form in adult in O. canadensis). In 1 tritonymph, femur III on 1 side bears seta l’. Jacot frequently labeled slides with names that were used in internal USDA reports, but which were never published, such as ‘montum’ noted in the Material Examined Section. Distribution and Ecology. This species is known only from litter in mideastern states of the USA (Table 1)., Published as part of Behan-Pelletier, V. M., 2011, Oribatella (Acari, Oribatida, Oribatellidae) of eastern North America, pp. 1-56 in Zootaxa 2973 (1) on pages 21-27, DOI: 10.11646/zootaxa.2973.1.1, http://zenodo.org/record/5295835, {"references":["Behan-Pelletier, V. M. & Eamer, B. (2010) The first sexually dimorphic species of Oribatella (Acari, Oribatida, Oribatellidae) and a review of sexual dimorphism in the Brachypylina. Zootaxa, 2332, 1 - 20."]}
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41. Oribatella brevicornuta Jacot 1934
- Author
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Behan-Pelletier, V. M.
- Subjects
Oribatella ,Oribatellidae ,Arthropoda ,Oribatella brevicornuta ,Arachnida ,Animalia ,Biodiversity ,Sarcoptiformes ,Taxonomy - Abstract
Oribatella brevicornuta Jacot, 1934 Oribatella brevicornuta Jacot, 1934, p. 707. (Figs. 2A–F, 3A–D) Type material examined. Specimens (3 females, 1 male) on 4 slides labelled paratype: USA, New York: Ithaca, Buttermilk Creek, 21.v., 26B81d, Remtd v. 1947, A.P. Jacot Coll. (MCZ). Specimens on 3 slides labelled Cotypes: New York: Danby to West Danby, 19.v.1917 (A.P. Jacot), slides labelled 171 Oo 1a (dissected female), 171 Oo 1b (1 female), 171 Oo 1c (1male, 1 female) (MCZ). Other material examined. USA, Missouri: Roaring Rocks State Park, Trail to lookout tower, 13.v.1999 (VBP) 1 from soil under rotting oak; Arkansas: Montgomery Co., Crystal/Collier area, 3.iv.1992 (HWR); Newton Co., Richland Creek Wilderness, 35°46’308N 092°56’016”W, 21.ix.2001 (HWR) 2; Scott Co., Dry Creek Wilderness Area, NE boundary at 2100’, 6.iii.1999 (HWR) 2 from old growth; Georgia: Okefenokee, (RNC) 1; Glynn Co., Jekyll Island, 31°07.22’N 081°24.58W, 28.ii.2005 (VBP) 3 from Serenoa litter on seashore; Camden Co., Crooked River State Park, coastal shell midden forest, 30°50.79’N 081°32.80W, 26.ii.2005 (VBP) 2 from Quercus myrthifolia Willd. litter; same data, except 2 from litter of old Quercus laurifolia Michx.; Mississippi, Oktibbeha Co., HWY 25, 11 mi S from Starkville, 21.ix.1988 (G.T. Baker) 1; Texas, Aransas Co., Aransas National Wildlife Refuge, 28°16’24”N 096°47’56”W, 3.iii.1995 (VBP) 1 from moist yaupon, live oak, persimmon litter on sand by bay; Bandera Co., Lost Maples State Natural Area, East Trail, 29°48.984’N 099°34.999W, 27.ii.2007 (VBP) 1 from bigtooth maple and oak litter; Canada: Québec: Mont Orford Park, 2.viii.1985 (VBP) 1 from beech litter, some Lycopodium; Mont Joli, 25.x.1954 (J.E.H. Martin) 1; Cedarville, 45°01’30.35”N 72°13’58.97”W, Descente 20, 23.viii.1985 (VBP) 2 from litter under Hericium on fallen dead beech; Nova Scotia, Cape Breton Highlands National Park, Mackenzie Mountain, 25.viii.1983 (M. Sharkey) 1 from litter and moss. Diagnosis. Total length of adult 470–572 µm. Notogastral width 300–382 µm. Integument of prodorsum, notogaster, venter and mentum micropunctate. Integument of coxisternum with distinct striae (Fig. 2D). Rostrum flattened, undulating, with (Fig. 2F, arrow) or without minute lateral teeth. Lamella (with cusp) 177–188 µm long, cusp 121–133 µm long, 61–65 µm wide at level of insertion of seta le. Lamellar cusps diverging or parallel anteromedially; separated posteromedially, leaving prodorsum visible through oval opening 35–54 µm long x 17–23 µm wide. Medial dens of lamellar cusps 38–50 µm, subequal or slightly shorter than lateral dens (48–65 µm long); medial dens smooth; lateral dens with 0–4 small teeth on lateral edge (varying among specimens and on either side of same specimen). Long striae extending longitudinally along outer margin of lamella. Translamella without tooth, about 17–19 µm at greatest width, about 13–16 µm deep (Fig. 2C). Setae ro 108–128 µm long, strongly barbed along length, acuminate, strongly directly medially. Setae le about 105–115 µm long, thick, heavily barbed, tapered. Setae in 197–228 µm long, thick (less so than le), heavily barbed, tapered; mutual distance of pair about 57–74 µm. Bothridial setae 133–149 µm long, subequal in shape to seta le; with barbed, bacilliform head, rounded distally, stalk short, smooth; head directed slightly anteromedially (Fig. 2A). Exobothridial setae about 43–65 µm long, thin, smooth, acuminate. Genal tooth broad, subrectangular, rounded distally, without dens ventrodistally, with longitudinal ridge ventrally (Fig. 2D black arrow, 2E arrow). Tutorium 168–201 µm long, of which cusp about 106–127 µm long, rectangular, convex ventrally, distal margin with 5 to 7 dens (Fig. 2E). Custodium about 48–62 µm long, with 2 adjacent knobs along length (Fig. 3C) (1 cotype specimen with knob distally). Porose area Al about 10 µm in diameter. Anterior margin of notogaster undulating, convex lateral of bothridium, with about 10 transverse ridges (Fig. 2A–C). Pteromorph with short ridges at anterior margin; with dens anteroventrally. Porose areas present, Aa about 22 µm in diameter. Ten pairs of long, barbed notogastral setae present; c series 99–127 µm, l and h series 90–100 µm, p series about 77 µm long; c, l and h directed laterally, positioned so that lm medial of Aa, and lp anteromedial of A1. Distance h 1 –h 1 about 58–67 µm, almost twice distance p 1 –p 1 (38–41 µm). Lenticulus subtriangular. Epimeral setae about 22–65 µm long, barbed, 3b, 3c about 48 µm long, 4c about 65 µm long and more barbed than other epimeral setae, reaching tip of custodium (Fig. 3C). Genital setae in longitudinal row, 1+5, one seta on anterior of genital plate; genital and aggenital setae about 29 µm long; anal and adanal setae barbed, about 23–38 µm long. Postanal porose area oval, about 50 µm wide. Mentum with small reticulate pattern, with anterior tectum covering base of gena, with transverse carina anteriorly (Fig. 2D). Axillary saccule about 8 x 3 µm. Leg setation (I to IV): trochanters, 1-1-2-1; femora, 5-5-3-2; genua, 3(1)-3(1)-1(1)-2; tibiae 4(2)-4(1)-3(1)-3(1); tarsi, 20(2)-15(2)-15-12. Seta l" on genua and tibiae I and II about 43–55 µm. Tarsi heterotridactylous. Remarks. Jacot (1934 a, p. 710) described the subspecies O. brevicornuta extensa, from Florida, Illinois, Indiana, Iowa, Ohio and Virginia. He distinguished the subspecies on the basis of lamellar cusps being longer and more slender than those of O. brevicornuta sensu stricto. Subsequently this subspecies was elevated to species status (Johnston 1965), without any rationale given. I examined one type specimen of O. brevicornuta extensa, specifically: cotype female (with 5 eggs) labelled Cotype: “26Ew147, Arcola Ill, July 4, 06. B147. K. & P. in 80% alc. M. July 7, ’06. H. e. Ewing” (MCZ). All character states fall within the range of variation in O. brevicornuta sensu stricto noted in the diagnosis given above. More specifically the length and width of lamellar cusps and the length and width at midlength of cusp dens fall within the range of variation for the type material of brevicornuta sensu stricto. Thus, the elevation of the subspecies to species by Johnston (1965) should be rejected, but I consider it premature to reject subspecific status, i.e., retention of O. brevicornuta extensa, until the species is studied with molecular methods. Jacot usually denoted his type material as “cotypes”. The word “ paratype ” on labels for the 4 specimens from USA, New York: Ithaca, Buttermilk Creek, 21.v.,.26B81d, Remtd v. 1947, A.P. Jacot Coll., noted in the Material Examined Section is not in Jacot’s handwriting. Distribution and Ecology. Oribatella brevicornuta is widely distributed in deciduous forests throughout eastern North America, from Nova Scotia, Canada to Texas, USA (Table 1). In addition to the Material examined above, it has been recorded from Connecticut and North Carolina (refs. in Marshall et al. 1987)., Published as part of Behan-Pelletier, V. M., 2011, Oribatella (Acari, Oribatida, Oribatellidae) of eastern North America, pp. 1-56 in Zootaxa 2973 (1) on pages 7-10, DOI: 10.11646/zootaxa.2973.1.1, http://zenodo.org/record/5295835, {"references":["Jacot, A. P. (1934) A new four-horned mossmite (Oribatoidea-Acarina). American Midland Naturalist, 15, 706 - 712.","Johnston, D. E. (1965) A catalog of the determined species of Acari (excl. Ixodides) in the collections of the Institute of Acarology. Institute of Acarology, Ohio Agricultural experimental Station, Department of Zoology and Entomology, Series, 29, iv + 67 pp.","Marshall, V. G. Reeves, R. M. & Norton, R. A. (1987) Catalogue of the Oribatida of continental United States and Canada. Memoirs of the entomological Society of Canada 139. 418 pp."]}
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42. Oribatella (Acari, Oribatida, Oribatellidae) of eastern North America
- Author
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Behan-Pelletier, V. M.
- Subjects
Oribatellidae ,Arthropoda ,Arachnida ,Animalia ,Biodiversity ,Sarcoptiformes ,Taxonomy - Abstract
Behan-Pelletier, V. M. (2011): Oribatella (Acari, Oribatida, Oribatellidae) of eastern North America. Zootaxa 2973 (1): 1-56, DOI: 10.11646/zootaxa.2973.1.1, URL: https://biotaxa.org/Zootaxa/article/view/zootaxa.2973.1.1
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- 2011
43. Oribatella jacoti Behan-Pelletier 2011, sp. nov
- Author
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Behan-Pelletier, V. M.
- Subjects
Oribatella ,Oribatellidae ,Arthropoda ,Arachnida ,Animalia ,Biodiversity ,Sarcoptiformes ,Oribatella jacoti ,Taxonomy - Abstract
Oribatella jacoti sp. nov. (Figs. 7, 8) Material examined. Holotype: female, USA, Missouri, Boone Co., Hinkson Creek S Univ. Mo. Campus, 25.iv.1985 FMHD #85–128 (J. Kethley, R.A. Norton) from red and chestnut oak, sugar maple litter on ridge top (FM). Paratypes (all in FM if not indicated otherwise): Missouri, Boone Co., Hinkson Creek S Univ. Mo. Campus, 24.iv.1985 FMHD #85–115 (J. Kethley, R.A. Norton) 1 female from moss on base of tree; 25.iv.1985 FMHD #85– 122 (J. Kethley, R.A. Norton) 1 female from red chestnut oak litter in limestone pit; 25.iv.1985 FMHD #85–126 (J. Kethley, R.A. Norton) 1 female from wood of rotten log at base of slope; 25.iv.1985 FMHD #85–127 (J. Kethley, R.A. Norton) 1 female from mixed deciduous litter on dry ridge top; 25.iv.1985 FMHD #85–130 (J. Kethley, R.A. Norton) 2 males from floodplain litter in mixed mesophytic forest; 29.iv.1985 FMHD #85–160 (J. Kethley, R.A. Norton) 1 male from red and chestnut oak, sugar maple litter at log; 30.iv.1985 FMHD #85–166 (J. Kethley, R.A. Norton) 1 male from red cedar litter on ridge top; Lake of the Ozarks State Park, Woodland Trail, elv. 900’, 38°05’N 92°37’W, 14.v.1999 (VBP) 1 female from soil in dried up stream (CNC). Other material examined: Wisconsin: Nicolet National Forest, Scott Lake Nature Trail, 45°46’N 89°W; 25.x.1998 (VBP and M. Behan) 2 from hemlock litter in 200+ year old stand, some birch; Illinois, Pope Co., Shawnee National Forest, Bell Smith Springs, 37°30’10”N 88°3’30”W, 23.ix.1992 (VBP) 2 from lichens, moss, cedar litter on sandstone ridge above canyon; Arkansas, Scott Co., Dry Creek Wilderness Area, NE boundary at 2100’, 6.iii.1999 (HWR) 4 from old growth; Polk Co., Bard Springs, 6.vi.1992 (HWR) 2; Newton Co., Richland Creek Wilderness, 35°46’308”N 92°56’016”W, viii, 2002 (HWR) 1; Canada, Ontario, Leeds-Grenville Co., nr. Otter Lake, 44°34.85’N 76°20’W, 23.vii.2003 (J. Chen, VBP, J. Johnson) 1 from rotting paper birch litter; Nova Scotia, Cape Breton Highlands National Park, Mica Mt. Trail, 7.ix.1983 (VBP) 1 from lichen, Ledum, shrub Abies and Vaccinium litter in hollow; North Mountain Bog, 26.viii.1983 (M. Sharkey) 2. Diagnosis. Total length of adult 576–634 µm. Integument of prodorsum, notogaster, genital and ventral plate micropunctate, mentum microtuberculate; short striae present on lenticulus and long striae on lateral of lamellae and in coxisternal region. Lamella (including cusp) about 226 µm long, cusp about 163 µm long, about 71 µm wide at level of seta le. Medial dens about 72 µm long, without teeth, lateral dens about 72 µm with 0–6 teeth on lateral margin. Bothridial setae 115–156 µm long, with barbed, fusiform head, rounded to tapered distally. Tutorium extending well anterior of rostrum, about 228 µm long of which cusp about 144 µm long, rectangular, distal margin with about 10 dens. Custodium about 62 µm long, tapered. Notogastral setae 72–86 µm long, lm posterior or posteromedial to Aa, lp anterior to A1. Setal pair h 1 closely adjacent, directed posteriorly, blunt distally; distance h 1 – h 1 about 24 µm, equidistant to distance p 1 –p 1 . Epimeral seta 3c 75 µm, thickest and longest seta, subequal in shape to other epimeral setae. Mentum with transverse carina anteriorly; with tectum. Seta l” of genu I about 53 µm, l” of genu II about 62 µm. Tarsi heterotridactylous. Description. Adult. Dimensions: Mean total length: female (n = 4) 631 µm (range 624–634); male (n = 4) 588 µm (range 576–595). Mean notogastral width: female (n =2) 471 µm (461, 480); male (n =3) 439 µm (range 432– 442). Integument: Prodorsum, notogaster, genital and ventral plate micropunctate, mentum microtuberculate; short striae present on lenticulus and long striae on lateral of lamellae (Fig. 7) and in coxisternal region. Prodorsum: Rostral margin rounded to undulating with minute dens laterally (as in Fig. 2F). Lamella (including cusp) about 226 µm long, cusp about 163 µm long, about 71 µm wide at level of seta le. Lamellar cusps contiguous, or not, anteromedially, separated posteromedially, leaving prodorsum visible through oval opening, about 62 µm long by up to 24 µm wide. Medial dens about 72 µm long without teeth; lateral dens about 72 µm with 0–6 teeth (Fig. 7) on lateral margin, varying among specimens and on either side of same specimen. Translamella without tooth, about 19 µm at greatest width, about 19 µm deep (Fig. 7). Setae ro about 120 µm long, strongly barbed along length, acuminate, strongly directly medially. Setae le about 96 µm long, thick, heavily barbed, tapered. Setae in about 211 µm long, thick (less so than le), heavily barbed, tapered; mutual distance of pair about 72 µm. Bothridial setae 115–156 µm long, with barbed, fusiform head, rounded to tapered distally, stalk short, smooth; head directed slightly anteromedially. Exobothridial setae thin, smooth, about 60 µm. Lateral aspect of podosoma: Genal tooth broad, subrectangular, rounded distally, without dens ventrodistally, with longitudinal ridge ventrally (as for Fig. 2E). Tutorium extending well anterior of rostrum; about 228 µm long, of which cusp about 144 µm long, rectangular, distal margin with about 10 dens. Custodium about 62 µm long, tapered (Fig. 8). Porose area Al about 21 µm in diameter. Notogaster: Length subequal to width. Anterior margin undulating, convex lateral of bothridium, with 10–12 transverse ridges (Fig. 7). Pteromorph with ridges at anterior and ventral margins (Fig. 7); with or without small dens on anteroventral margin (Fig. 8). Porose areas large, about 17 µm in diameter, clearly defined. Ten pairs of long, barbed, tapered (other than seta h 1 ), notogastral setae present, 72–86 µm long, with c, la and h setae longest; lm posterior to posteromedial of Aa, and directed laterally, lp anterior of A1. Setae h 1 closely adjacent, directed posteriorly, blunt distally (Fig. 7); distance h 1 –h 1 about 24 µm, subequal to distance p 1 –p 1 . Lenticulus U-shaped, with fine short striae (Fig. 7). Ventral region: Epimeral setae mostly 24–36 µm long, setal length (in µm) approximate, 1b 36, 2a 24, 3a, 24, 4a 24; 3c 75, thickest and longest seta and more barbed than 4c 72, which subequal in shape to other epimeral setae, though more barbed. Genital, aggenital, anal and adanal setae smooth, about 10–14 µm long. Genital setae about 10 µm, positioned 1+5, with 1 seta on anterior margin of plate. Postanal porose area oval, 25 x 12 µm. Gnathosoma: Mentum with transverse carina anteriorly; with tectum (Fig. 8, as for Fig. 2D). Axillary saccule about 8x3 µm. Legs: Setation (I to IV): trochanters, 1-1-2-1; femora, 5-5-3-2; genua, 3(1)-3(1)-1(1)-2; tibiae 4(2)-4(1)-3(1)- 3(1); tarsi, 20(2)-15(2)-15-12. Setae l” of genu I about 53 µm, l” of genu II about 62 µm. Tarsi heterotridactylous. Etymology. This species is named in honour of A. P. Jacot, (1890–1939), the world-renowned acarologist, who was and is seminal to our knowledge of North American Oribatida. A short biographical overview of his life is given in Metz et al. (1977). Remarks. This species is similar in size and shape to O. brevicornuta from which it is easily distinguished by the closely adjacent, posteriorly directed setae h 1 , and the distance h 1 – h 1 being subequal to the distance p 1 –p 1, about 24 µm. Distribution and Ecology. This species is widely distributed throughout eastern North America, from Nova Scotia to Arkansas., Published as part of Behan-Pelletier, V. M., 2011, Oribatella (Acari, Oribatida, Oribatellidae) of eastern North America, pp. 1-56 in Zootaxa 2973 (1) on pages 16-20, DOI: 10.11646/zootaxa.2973.1.1, http://zenodo.org/record/5295835, {"references":["Metz, L. J., Reeves, R. M. & Norton, R. A. (1977) The works of A. P. Jacot. In: Dindal D. L. (ed.) Biology of Oribatid mites. State University of New York, Syracuse: 1 - 31."]}
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- 2011
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44. Revision of the genus Afroleius Mahunka, 1984 (Acari: Oribatida)
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Coetzee, Louise, Van As, J. G., Behan-Pelletier, V. M., Coetzee, Louise, Van As, J. G., and Behan-Pelletier, V. M.
- Abstract
English: The genus Afroleius Mahunka, 1984 originally comprised three species (A. deformis Mahunka, 1984 (type), A. minor Mahunka, 1984 and A. simplex Mahunka, 1984), but with an uncertain relationship, at first placed in the family Haplozetidae (Oripodoidea). In this study the genus is redescribed and its relationship investigated. Specimens from the acarology collection of the National Museum referable to new species are described, two species originally described in other genera are recombined, a key to the species of the genus is proposed and its phylogeny investigated on the basis of molecular data. It is concluded that Afroleius is a member of the superfamily Ceratozetoidea, based on the presence of the axillary saccule, genal tooth, and the shape of pedotectum I. Its relationship in the family Punctoribatidae is based on the presence of the posterior notogastral tectum and desclerotized hinge of the pteromorph. Nine new species are described (A. crassus Coetzee, 2013; A. decurvatus Coetzee, 2013; A. deformatoides Coetzee, 2013; A. natalensis Coetzee, 2014; A. caudatus Coetzee, 2014; A. amieae Coetzee, 2014; A. inae Coetzee, 2014; A. valerieae Coetzee 2014; A. lucidus Coetzee, In Press). Two species are recombined namely A. polygonatus (Mahunka, 1985) from the genus Kilimabates Mahunka, 1984 and A. floridus (Mahunka, 1985) from the genus Magyaria Balogh, 1963. Afroleius undulatus (Balogh, 1959) (previously recombined from Africoribates) from Tanzania is discussed. Juvenile instars of two species (A. floridus and A. polygonatus) are described. The genus now comprises 15 species. The phylogenetic analysis based on molecular data of 28S rDNA of A. floridus, A. deformis, A. minor en A. polygonatus, additional Ceratozetoidea sequences and outgroup sequences retrieved from GenBank, indicates Mycobates and Trichoribates as the sister genera of Afroleius. Ceratozetidae is shown to be paraphyletic. This analysis emphasises the need for a large-scale phylogenetic analys, Afrikaans: Die genus Afroleius Mahunka, 1984 het uit drie spesies bestaan (A. deformis Mahunka, 1984 (tipe), A. minor Mahunka, 1984 en A. simplex Mahunka, 1984), en die verwantskap was onseker. Dit is oorspronklik in die familie Haplozetidae (Oripodoidea) geplaas. In hierdie studie is die genus herbeskryf en die verwantskap bestudeer. Eksemplare van hierdie genus in die akarologie-versameling van die Nasionale Museum wat nuwe spesies uitmaak, is beskryf, twee spesies wat oorspronklik in ander genera beskryf is, is herkombineer, ‘n sleutel tot die spesies in die genus is opgestel en ‘n molekulêre filogenetiese studie is gedoen. Dit is bevind dat Afroleius aan die superfamilie Ceratozetoidea behoort, gegrond op die teenwoordigheid van die oksellêre sakkulus, laterale insnyding aan die gnathosoma, en die vorm van die eerste pedotektum. Die verwantskap aan die familie Punctoribatidae is gegrond op die teenwoordigheid van ‘n posterior notogastrale tektum en die beweegbaarheid van die pteromorf. Nege nuwe spesies is beskryf (A. crassus Coetzee, 2013; A. decurvatus Coetzee, 2013; A. deformatoides Coetzee, 2013; A. natalensis Coetzee, 2014; A. caudatus Coetzee, 2014; A. amieae Coetzee, 2014; A. inae Coetzee, 2014; A. valerieae Coetzee 2014; A. lucidus Coetzee, In Druk). Twee spesies is na Afroleius oorgeplaas naamlik A. polygonatus (Mahunka, 1985) vanaf die genus Kilimabates Mahunka, 1984 en A. floridus (Mahunka, 1985) vanaf die genus Magyaria Balogh, 1963. Afroleius undulatus (Balogh, 1959) (voorheen oorgeskuif vanaf Africoribates) van Tanzanië is bespreek. Onvolwasse stadia van twee spesies (A. floridus en A. polygonatus) is beskryf. Die genus bestaan nou uit 15 spesies. Die filogenetiese ondersoek gegrond op molekulêre data van 28S rDNA van A. floridus, A. deformis, A. minor en A. polygonatus, bykomende Ceratozetoidea data en buitegroep data wat van GenBank afgelaai is, dui daarop dat Mycobates en Trichoribates die sustergenera van Afroleius is. Die analise dui ook aan d, National Museum
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- 2015
45. An Exploratory Study of Acculturation and Reproductive Health Among Haitian and Haitian-American Women in Little Haiti, South Florida
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Cyrus, E., primary, Gollub, E. L., additional, Jean-Gilles, M., additional, Neptune, S., additional, Pelletier, V., additional, and Dévieux, J., additional
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- 2015
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46. L’immunothérapie épicutanée (EPIT®) induit une protection contre l’anaphylaxie à d’autres allergènes
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Mondoulet, L., primary, Dioszeghy, V., additional, Ligouis, M., additional, Dhelft, V., additional, Puteaux, E., additional, Wavrin, S., additional, Pelletier, V., additional, Dupont, C., additional, and Benhamou, P.H., additional
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- 2015
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47. Médialisation cordale : quelles sont les substances exogènes disponibles en France en 2010 ?
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Lagier, A., Polle-Pelletier, V., Giovanni, A., and Marie, J.-P.
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- 2011
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48. Vocal fold medialization: Which are the available fillers in France in 2010?
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Lagier, A., Polle-Pelletier, V., Giovanni, A., and Marie, J.-P.
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- 2011
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49. Ecosystem processes in natural and managed terrestrial soils and the role of soil organisms in the sustainable delivery of ecosystem goods and services
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van der Putten, W.H., Anderson, J.M., Bardgett, R.D., Behan-Pelletier, V., Bignell, D.E., Brown, G.G., Brown, V.K., Brussaard, L., Hunt, H.W., Ineson, P., Jones, T.H., Lavelle, P., Paul, E.A., St. John, M., Wardle, D.A., Wojtowicz, T., and Wall, D.H.
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Life Science ,Soil Biology ,Laboratory of Nematology ,PE&RC ,Laboratorium voor Nematologie ,Bodembiologie - Published
- 2004
50. The Sustainable Delivery of Goods and Services Provided by Soil Biota
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Van der Putten, W.H., Anderson, J.M., Bardgett, R.D., Behan-Pelletier, V., Bignell, D.E., Brown, G.G., Brown, V.K., Brussaard, L., Hunt, H.W., Ineson, P., Jones, T.H., Lavelle, Pa., Paul, E.A., St. John, M., Wardle, D.A., Wojtowicz, T., Wall, D.H., and Multitrofe Interacties (CTE / MTI)
- Published
- 2004
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