EVALUATION OF DIFFERENT TAXONOMIC LEVELS AS SURROGATES OF ANT DIVERSITY IN GREEN AREAS IN AN URBANIZED ENVIRONMENT E. B. A. KOCH1, T. S. MELO2,3,4, A. R. S. ANDRADE2,3, M. LEPONCE5 & J. H. C. DELABIE2,4 1Programa de Pós-graduação em Ecologia e Evolução, Universidade Estadual de Feira de Santana (UEFS), CEP: 44.036-900 - Feira de Santana, Bahia, Brazil, e-mail: elmoborges@gmail.com; 2Programa de Pós-graduação em Ecologia, Universidade Federal da Bahia (UFBA), Salvador, Bahia, Brazil; 3Centro de Ecologia e Conservação Animal, Universidade Católica do Salvador (UCSal), Salvador, Bahia, Brazil; 4Laboratório de Mirmecologia, Convênio Universidade Estadual de Santa Cruz (UESC)/Comissão Executiva do Plano da Lavoura Cacaueira (CEPLAC), Ilhéus, Bahia, Brazil; 5Biodiversity Monitoring & Assessment, Royal Belgian Institute of Natural Sciences (RBINS), Bruxelas, Belgium. In cities located in environments of high biological importance, urbanization leads to changes in biotic diversity, while monitoring these changes can be difficult. Studies have pointed to the use of metrics that replace species as an alternative. Surrogate models are easily determined measures of biodiversity that correlate strongly with species richness and with what you want to investigate, being useful for detecting or monitoring environmental changes. The use of higher taxonomic levels has been applied to groups of megadiverse organisms, such as arthropods, since difficulties in identifying species are predictable. The aim of this study was to evaluate the practicality of using taxonomic diversity of ants as a surrogate of green area coverage in an urban environment. Four levels of "surrogate resolutions" (subfamily, genus, indicator taxa, and intermediate resolution) were assessed to the taxonomic diversity of ants across three levels of urban green areas (Small = 0 to 35%
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RBINS Staff Publications 2023
Photo-initiators are widely used to cure ink on packaging materials used in food applications such as plastic films or cartonboards. In migration studies, food simulants are very often used to simulate food, like Tenax®, which is the simulant for dry foodstuffs. In this paper a fast and reliable confirmation method for the determination of the following photoinitiators in Tenax® is described: benzophenone (BP), 4,4´-bis(diethylamino)benzophenone (DEAB), 2-chloro-9H-thioxanthen-9-one (CTX), 1-chloro-4-propoxy-9H-thioxanthen-9-one (CPTX), 2,4-diethyl-9H-thioxanthen-9-one(DETX), 2,2-dimethoxy-2-phenyl acetophenone (DMPA), 4-(dimethylamino)benzophenone (DMBP), 2-ethylanthraquinone(EA), ethyl-4-dimethylaminobenzoate (EDMAB), 1-hydroxylcyclohexyl phenyl ketone (HCPK), 2-hydroxy-4´- (2-hydroxyethoxy)-2-methylpropiophenone (HMMP), 2-isopropyl-9H-thioxanthen-9-one (ITX), 4-methylbenzophenone(MBP), Michler’s ketone (MK), and 4-phenylbenzophenone (PBZ). After the migration study was completed, the simulant Tenax® was extracted using acetonitrile, followed by analysis on ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). Quantification was carried out using benzophenone-d10 (BP-d10) as internal standard. The presented method is validated in terms of matrix effect, specificity, linearity, recovery, precision and sensitivity, showing the method can detect all photo-initiators at very low concentrations (LOD < 0.125 μg g–1 for all substances). Finally, the procedure was applied to real samples, proving the capabilities of the presented method.
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