Spatial Distribution, Seasonal Variation, and Ecological Risk Assessment of Benzotriazole UV Stabilizers in Waters from Canadian Tributaries and Coastal Systems.

Benzotriazole UV stabilizers (BZT-UVs) are industrial additives of emerging environmental concern, with UV-328 recently listed under the Stockholm Convention on Persistent Organic Pollutants and several congeners listed as Substances of Very High Concern in Europe. However, their distribution and fate in coastal environments remain poorly understood. This study investigated the spatial and seasonal variations of dissolved and suspended particulate matter (SPM)-bound BZT-UVs in surface water from the St.

Atmospheric fate and deposition of polyhalogenated carbazoles in urban environment.

Polyhalogenated carbazoles (PHCZs) are of emerging environmental concern due to their dioxin-like toxicity and widespread distribution in the aquatic environment. However, knowledge of the occurrence, fate, and impacts of PHCZs in the atmospheric environment is limited. The present study investigated air concentrations and atmospheric deposition of 11 PHCZs in Toronto, Canada, during the winter of 2024.

Organic UV absorbents in the deepwater redfish (Sebastes mentella) from the St. Lawrence Estuary and Gulf: Distribution and human health risk assessment.

UV absorbents (UVAs), such as organic UV filters (UVFs) and benzotriazole UV stabilizers (BZT-UVs), are used in a wide range of consumer and industrial products and they are contaminants of emerging concern in the environment. However, their occurrence and fate in the deep-sea environments are inadequately understood. This study investigated the occurrence and distribution of five UVFs and ten BZT-UVs in the muscle (n = 127) of 2019-collected deepwater redfish (Sebastes mentella) from the St.

Spatial distribution and speciation of mercury in a recovering deepwater redfish (Sebastes mentella) population from St. Lawrence Estuary and Gulf, Canada.

Mercury (Hg) pollution poses a significant threat to the environment, particularly in the form of methylmercury (MeHg). However, little is known about the distribution and influencing factors of Hg in deep-sea (>200m) fish, which is crucial for assessing potential health risks to fish and humans. In Canada, the deepwater redfish (Sebastes mentella) has been designated as an endangered species.

Marennine, promising blue pigments from a widespread Haslea diatom species complex.

In diatoms, the main photosynthetic pigments are chlorophylls a and c, fucoxanthin, diadinoxanthin and diatoxanthin. The marine pennate diatom Haslea ostrearia has long been known for producing, in addition to these generic pigments, a water-soluble blue pigment, marennine. This pigment, responsible for the greening of oysters in western France, presents different biological activities: allelopathic, antioxidant, antibacterial, antiviral, and growth-inhibiting.

Complex metabolic interactions between benzo(a)pyrene and tributyltin in presence of dichlorodiphenyltrichloroethane in South American catfish Rhamdia quelen.

In an attempt to explore complex metabolic interactions between toxicants present in polluted freshwater, hepatic metabolism of benzo(a)pyrene (BaP) and tributyltin (TBT) in fish was investigated when these compounds were administrated alone, mixed together and along with dichlorodiphenyltrichloroethane (DDT). Ten Rhamdia quelen per group were treated with a single intra-peritoneal (IP) dose (5-day experiment) or three successive doses (15-day experiment) either containing BaP (0.3; 3 or 30mgkg(-1)) or TBT (0.

Regioselective pivaloylation of N-phthaloylchitosan: a promising soluble intermediate for chitosan chemistry.

A simple and efficient pivaloylation of primary alcohols was realized on N-phthaloylchitosan that was regioselectively and entirely protected. The selectivity of this mild esterification was demonstrated by comparison with (1)H NMR chemical shifts of H-1 and H-3 of complete 3,6-O-dipivaloylated derivatives. The selective hydrazinolysis of N-phthaloyl groups in the presence of pivaloyl ester was achieved in ethanol/water.