56. Herzke D, Kallenborn R, Nygård T (2002) Organochlorines in egg samples from Norwegian
birds of prey: congener-, isomer- and enantiomer specific considerations. Sci Total Environ
291:59–71. https://doi.org/10.1016/S0048-9697(01)01092-0
57. WHO (2019) World malaria report 2019 [en línia]. https://www.who.int/publications-detail/
world-malaria-report-2019 [data de consulta: December 2019]
58. Montgomery CM, Munguambe K, Pool R (2010) Group-based citizenship in the acceptance of
indoor residual spraying (IRS) for malaria control in Mozambique. Soc Sci Med 70:1648–1655.
https://doi.org/10.1016/j.socscimed.2010.01.020
59. Feo ML, Eljarrat E, Manaca MN et al (2012) Pyrethroid use-malaria control and individual
applications by households for other pests and home garden use. Environ Int 38:67–72. https://
doi.org/10.1016/j.envint.2011.08.008
60. Zehringer M, Herrmann A (2001) Analysis of polychlorinated biphenyls, pyrethroid
insecticides and fragrances in human milk using a laminar cup liner in the GC injector.
Eur Food Res Technol 212:247–251. https://doi.org/10.1007/s002170000223
61. Sereda B, Bouwman H, Kylin H (2009) Comparing water, bovine milk, and indoor residual
spraying as possible sources of ddt and pyrethroid residues in breast milk. J Toxicol Environ
Health A 72:842–851. https://doi.org/10.1080/15287390902800447
62. FAO-WHO (2019) Joint FAO/WHO meeting on pesticide residues. https://www.who.int/
foodsafety/areas_work/chemical-risks/jmpr/en/ [data de consulta: December 2019]
63. Corcellas C, Eljarrat E, Barceló D (2014) Enantiomeric-selective determination of pyrethroids:
application to human samples. Anal Bioanal Chem 407:779–786. https://doi.org/10.1007/
s00216-014-7905-6
64. Jin YX, Liu JW, Wang LG et al (2012) Permethrin exposure during puberty has the potential to
enantioselectively induce reproductive toxicity in mice. Environ Int 42:144–151. https://doi.
org/10.1016/j.envint.2011.05.020
65. Zhang SY, Ueyama J, Ito Y et al (2008) Permethrin may induce adult male mouse reproductive
toxicity due to cis isomer not trans isomer. Toxicology 248:136–141. https://doi.org/10.1016/j.
tox.2008.03.018
66. Bossart GD (2011) Marine mammals as sentinel species for oceans and human health.
Vet Pathol 48:676–690. https://doi.org/10.1177/0300985810388525
67. Kajiwara N, Kamikawa S, Amano M et al (2008) Polybrominated diphenyl ethers (PBDEs)
and organochlorines in melon-headed whales, Peponocephala electra, mass stranded along the
Japanese coasts: maternal transfer and temporal trend. Environ Pollut 156:106–114. https://doi.
org/10.1016/j.envpol.2007.12.034
68. Desforges JPW, Ross PS, Loseto LL (2012) Transplacental transfer of polychlorinated
biphenyls and polybrominated diphenyl ethers in arctic beluga whales (Delphinapterus leucas).
Environ Toxicol Chem 31:296–300. https://doi.org/10.1002/etc.750
69. Park B-K, Park G-J, An Y-R et al (2010) Organohalogen contaminants in finless porpoises
(Neophocaena phocaenoides) from Korean coastal waters: contamination status, maternal
transfer and ecotoxicological implications. Mar Pollut Bull 60:768–774. https://doi.org/10.
1016/j.marpolbul.2010.03.023
70. Alonso MB, Feo ML, Corcellas C et al (2015) Toxic heritage: maternal transfer of pyrethroid
insecticides and sunscreen agents in dolphins from Brazil. Environ Pollut 207:391–402. https://
doi.org/10.1016/j.envpol.2015.09.039
71. Hoguet J, Keller JM, Reiner JL et al (2013) Spatial and temporal trends of persistent organic
pollutants and mercury in beluga whales (Delphinapterus leucas) from Alaska. Sci Total
Environ 449:285–294. https://doi.org/10.1016/j.scitotenv.2013.01.072
72. Weijs L, Tibax D, Roach AC et al (2013) Assessing levels of halogenated organic compounds
in mass-stranded long-finned pilot whales (Globicephala melas) from Australia. Sci Total
Environ 461-462:117–125. https://doi.org/10.1016/j.scitotenv.2013.04.090
Bioavailability and Bioaccumulation of Pyrethroid Insecticides in Wildlife and. . .
225
birds of prey: congener-, isomer- and enantiomer specific considerations. Sci Total Environ
291:59–71. https://doi.org/10.1016/S0048-9697(01)01092-0
57. WHO (2019) World malaria report 2019 [en línia]. https://www.who.int/publications-detail/
world-malaria-report-2019 [data de consulta: December 2019]
58. Montgomery CM, Munguambe K, Pool R (2010) Group-based citizenship in the acceptance of
indoor residual spraying (IRS) for malaria control in Mozambique. Soc Sci Med 70:1648–1655.
https://doi.org/10.1016/j.socscimed.2010.01.020
59. Feo ML, Eljarrat E, Manaca MN et al (2012) Pyrethroid use-malaria control and individual
applications by households for other pests and home garden use. Environ Int 38:67–72. https://
doi.org/10.1016/j.envint.2011.08.008
60. Zehringer M, Herrmann A (2001) Analysis of polychlorinated biphenyls, pyrethroid
insecticides and fragrances in human milk using a laminar cup liner in the GC injector.
Eur Food Res Technol 212:247–251. https://doi.org/10.1007/s002170000223
61. Sereda B, Bouwman H, Kylin H (2009) Comparing water, bovine milk, and indoor residual
spraying as possible sources of ddt and pyrethroid residues in breast milk. J Toxicol Environ
Health A 72:842–851. https://doi.org/10.1080/15287390902800447
62. FAO-WHO (2019) Joint FAO/WHO meeting on pesticide residues. https://www.who.int/
foodsafety/areas_work/chemical-risks/jmpr/en/ [data de consulta: December 2019]
63. Corcellas C, Eljarrat E, Barceló D (2014) Enantiomeric-selective determination of pyrethroids:
application to human samples. Anal Bioanal Chem 407:779–786. https://doi.org/10.1007/
s00216-014-7905-6
64. Jin YX, Liu JW, Wang LG et al (2012) Permethrin exposure during puberty has the potential to
enantioselectively induce reproductive toxicity in mice. Environ Int 42:144–151. https://doi.
org/10.1016/j.envint.2011.05.020
65. Zhang SY, Ueyama J, Ito Y et al (2008) Permethrin may induce adult male mouse reproductive
toxicity due to cis isomer not trans isomer. Toxicology 248:136–141. https://doi.org/10.1016/j.
tox.2008.03.018
66. Bossart GD (2011) Marine mammals as sentinel species for oceans and human health.
Vet Pathol 48:676–690. https://doi.org/10.1177/0300985810388525
67. Kajiwara N, Kamikawa S, Amano M et al (2008) Polybrominated diphenyl ethers (PBDEs)
and organochlorines in melon-headed whales, Peponocephala electra, mass stranded along the
Japanese coasts: maternal transfer and temporal trend. Environ Pollut 156:106–114. https://doi.
org/10.1016/j.envpol.2007.12.034
68. Desforges JPW, Ross PS, Loseto LL (2012) Transplacental transfer of polychlorinated
biphenyls and polybrominated diphenyl ethers in arctic beluga whales (Delphinapterus leucas).
Environ Toxicol Chem 31:296–300. https://doi.org/10.1002/etc.750
69. Park B-K, Park G-J, An Y-R et al (2010) Organohalogen contaminants in finless porpoises
(Neophocaena phocaenoides) from Korean coastal waters: contamination status, maternal
transfer and ecotoxicological implications. Mar Pollut Bull 60:768–774. https://doi.org/10.
1016/j.marpolbul.2010.03.023
70. Alonso MB, Feo ML, Corcellas C et al (2015) Toxic heritage: maternal transfer of pyrethroid
insecticides and sunscreen agents in dolphins from Brazil. Environ Pollut 207:391–402. https://
doi.org/10.1016/j.envpol.2015.09.039
71. Hoguet J, Keller JM, Reiner JL et al (2013) Spatial and temporal trends of persistent organic
pollutants and mercury in beluga whales (Delphinapterus leucas) from Alaska. Sci Total
Environ 449:285–294. https://doi.org/10.1016/j.scitotenv.2013.01.072
72. Weijs L, Tibax D, Roach AC et al (2013) Assessing levels of halogenated organic compounds
in mass-stranded long-finned pilot whales (Globicephala melas) from Australia. Sci Total
Environ 461-462:117–125. https://doi.org/10.1016/j.scitotenv.2013.04.090
Bioavailability and Bioaccumulation of Pyrethroid Insecticides in Wildlife and. . .
225
