Lactation The transfer of contaminants from mother to pup through
lactation is most likely the largest mass transfer of contaminants, greater than that of in-utero transfers. When the mother begins lactation, blubber lipids are converted into milk lipids to feed her offspring. During this process, toxicants that were stored in
blubber lipids are moved into the milk and subsequently are transferred to the nursing pup. The transfer of toxicants through lactation is driven by the log Kow of the toxicants. Chemical compounds with a high affinity for lipids (a higher log Kow) will more readily be transferred through lactation due to the high lipid content of milk. The transfer of toxicants from blubber to milk is not fully understood, and selective transfer of contaminants has been observed. Mass balance of toxicants is difficult during lactation due to milk lipids originating from blubber lipids as well as being synthesized locally in mammary tissue. The change in toxicant
solubility between blubber and circulatory fluid as well as the breakdown and resynthesis of blubber lipids and circulatory lipids also contributes to the difficulties of mass balance of toxicants between blubber, circulatory, and milk lipids. However, even with difficulties of mass balancing, it has generally been observed in grey seals and harbor porpoises that residues in pup blubber lipids are generally similar or slightly higher than in maternal milk lipids, and are approximately half of the residues in maternal blubber lipids.
Placental Transfer The transfer of POPs from mother to fetus via the
placenta is less than that of lactation but can still cause adverse effects. Fatty acids from the mother's plasma are transported either through diffusion or active transport through the placenta to be used in important processes such as brain development. Sources of fatty acids are mainly derived from blubber in seals, porpoises, and whales. Lipophilic chemicals such as PCBs previously stored within the mother's fatty tissue can be transferred to the fetus via the circulatory fluid. Some lipophilic chemicals can be metabolized by the fetus using mostly
CYP enzymes, but others are quickly incorporated into developing fetal adipose tissue. The storage and release of these chemicals within the fetus can lead to
endocrine disruption,
immunosuppression, thyroid disruption, and
neurotoxicity in seals and orcas. == Implications ==