Dataset.

Appendix 1. Supplementary material: Medicated livestock carcasses and landfill sites: Sources of highly toxic veterinary pharmaceuticals and caffeine for avian scavengers

Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/354970
Digital.CSIC. Repositorio Institucional del CSIC
  • Herrero-Villar, Marta
  • Taggart, Mark A.
  • Mateo, Rafael
-Table A1. Compounds analysed by chemical group, including precursor ion, two main fragmented ions, collision energy (CE) and polarity. -Table A2. Quality control of the analytical method including recovery of the different pharmaceuticals (n = 7 days) at different levels performed in pig liver (31, 63 and 125 ng/g) everyday samples of domestic animal carcasses were processed and analysed, including limit of detection (LOD) and quantification (LOQ) of the analytical technique, and R2 of matrix-matched calibration curves of each compound made in pig liver. -Table A3. Quality control of the analytical method including recovery of the different pharmaceuticals (n = 3 days) at different levels performed in chicken liver (31, 63 and 125 ng/g) everyday samples of avian scavenger tissues were processed and analysed, including limit of detection (LOD) and quantification (LOQ) of the analytical technique, and R2 of matrix-matched calibration curves of each compound made in chicken liver. -Table A4. Quality control of the analytical method including recovery of the different pharmaceuticals and caffeine (n = 1 days) at different levels performed in partridge plasma (18, 39 and 75 ng/mL) everyday samples of avian scavenger plasma samples were processed and analysed, including limit of detection (LOD) and quantification (LOQ) of the analytical technique, and R2 of matrix-matched calibration curves of each compound made in partridge plasma. -Table A5. Veterinary pharmaceutical concentrations detected in domestic animal carcasses by species and tissues supplied at supplementary feeding stations for vultures in Aragon, including average (± SD) and maximum levels (ng/g). -Table A6. Veterinary pharmaceutical and caffeine concentrations detected in positive samples in plasma from avian scavengers captured in Aragon and nearby regions, including average (± SD), minimum and maximum levels (ng/mL). -Fig. A1. Map showing the points where avian scavengers were captured, supplementary feeding stations are shown in black and landfills in orange., Peer reviewed
 
DOI: http://hdl.handle.net/10261/354970
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/354970

HANDLE: http://hdl.handle.net/10261/354970
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/354970
 
Ver en: http://hdl.handle.net/10261/354970
Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/354970

Digital.CSIC. Repositorio Institucional del CSIC
oai:digital.csic.es:10261/354970
Dataset. 2023

APPENDIX 1. SUPPLEMENTARY MATERIAL: MEDICATED LIVESTOCK CARCASSES AND LANDFILL SITES: SOURCES OF HIGHLY TOXIC VETERINARY PHARMACEUTICALS AND CAFFEINE FOR AVIAN SCAVENGERS

Digital.CSIC. Repositorio Institucional del CSIC
  • Herrero-Villar, Marta
  • Taggart, Mark A.
  • Mateo, Rafael
-Table A1. Compounds analysed by chemical group, including precursor ion, two main fragmented ions, collision energy (CE) and polarity. -Table A2. Quality control of the analytical method including recovery of the different pharmaceuticals (n = 7 days) at different levels performed in pig liver (31, 63 and 125 ng/g) everyday samples of domestic animal carcasses were processed and analysed, including limit of detection (LOD) and quantification (LOQ) of the analytical technique, and R2 of matrix-matched calibration curves of each compound made in pig liver. -Table A3. Quality control of the analytical method including recovery of the different pharmaceuticals (n = 3 days) at different levels performed in chicken liver (31, 63 and 125 ng/g) everyday samples of avian scavenger tissues were processed and analysed, including limit of detection (LOD) and quantification (LOQ) of the analytical technique, and R2 of matrix-matched calibration curves of each compound made in chicken liver. -Table A4. Quality control of the analytical method including recovery of the different pharmaceuticals and caffeine (n = 1 days) at different levels performed in partridge plasma (18, 39 and 75 ng/mL) everyday samples of avian scavenger plasma samples were processed and analysed, including limit of detection (LOD) and quantification (LOQ) of the analytical technique, and R2 of matrix-matched calibration curves of each compound made in partridge plasma. -Table A5. Veterinary pharmaceutical concentrations detected in domestic animal carcasses by species and tissues supplied at supplementary feeding stations for vultures in Aragon, including average (± SD) and maximum levels (ng/g). -Table A6. Veterinary pharmaceutical and caffeine concentrations detected in positive samples in plasma from avian scavengers captured in Aragon and nearby regions, including average (± SD), minimum and maximum levels (ng/mL). -Fig. A1. Map showing the points where avian scavengers were captured, supplementary feeding stations are shown in black and landfills in orange., Peer reviewed




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