Jan Ludvig Lyche
Jan Ludvig Lyche has a total of 29 co-authors. Here are the top co-authors by number of shared publications:
- Anders Ruus
Department of Biosciences, University of Oslo , Kristine Bonnevies hus, Blindernveien 31, 0316 Oslo
2 shared publications - Clare Andvik
Department of Biosciences, University of Oslo , Kristine Bonnevies hus, Blindernveien 31, 0316 Oslo
2 shared publications - Eve Jourdain
Department of Biosciences University of Oslo Oslo Norway
2 shared publications - Katrine Borgå
Section for Aquatic Biology and Toxicology, Department of Biosciences, University of Oslo, Oslo, Norway
2 shared publications Richard Karoliussen
2 shared publications- Ajay Yadav
Department of Production Animal Clinical Sciences, Norwegian University of Life Sciences, P.O. Box 369 Sentrum, NO-0102, Oslo, Norway; Section for Pharmacology and Pharmaceutical Biosciences, Department of Pharmacy, University of Oslo, P.O. Box 1068, Blindern, NO-0316, Oslo, Norway
1 shared publication
Latest Publications
- Open Access
- 31 July 2026
- Published by Elsevier in Environmental Research
- Vol. 306
Comparing polychlorinated n-alkane occurrence and biomagnification with legacy contaminants in a killer whale food web
- 31 July 2026
- Published by Elsevier in Environmental Research
- Vol. 306
Open AccessComparing polychlorinated n-alkane occurrence and biomagnification with legacy contaminants in a killer whale food web
- 18 June 2026
- Published by Elsevier in Environmental Pollution
- Vol. 406, 128597
Organic phosphorus flame retardants and bisphenols in municipal wastewater, runoff and drinking water in a sub-arctic city
- 18 June 2026
- Published by Elsevier in Environmental Pollution
- Vol. 406, 128597
Organic phosphorus flame retardants and bisphenols in municipal wastewater, runoff and drinking water in a sub-arctic city
- Open Access
- 1 January 2026
- Published by Oxford University Press (OUP) in Conservation Physiology
- Vol. 14 (1)
A sensitive liquid chromatography–tandem mass spectrometry analytical method of steroid hormones in small blubber samples from four whale species
Steroid hormones can give an indication of stress, physiological health and reproductive status in whales; however, analysis is often limited by sample mass. We developed a sensitive analytical method using solid phase extraction–liquid chromatography–electrospray ionization–tandem mass spectrometry (LC–ESI–MS/MS) for the identification and quantification of eight steroid hormones (cortisol, cortisone, testosterone, androstenedione, progesterone, 11-deoxycortisol, 11-deoxycorticosterone and 17-hydroxyprogesterone) in small amounts of whale blubber (≤50 mg). Blubber biopsies were collected from stranded killer whales (Orcinus orca; n = 7), harbour porpoises (Phocoena phocoena; n = 3) and sperm whales (Physeter macrocephalus; n = 4), harvested common minke whales (n = 10; Balaenoptera acutorostrata) and free-living killer whales (n = 2) in Norway and the Barents Sea. Steroid hormones were separated using pentafluorophenyl propyl stationary phase and an optimized gradient programme with a total 20-min run. All samples (n = 26) were analysed at 50-mg sample mass, and a subset (n = 11) at 25 mg or lower. Low limit of detection and limit of quantification values resulted in high detection rates of hormones, and we found similar hormone concentrations between parallel samples and at the lowest tested sample mass (14 mg). Cortisol concentrations in sperm whales (4.3 ± 1.6 ng/g) were four times higher than stranded killer whales (1.1 ± 0.96 ng/g), which in turn were up to four times higher than free-living killer whales (0.23 ± 0.12 ng/g), harbour porpoise (0.64 ± 0.38 ng/g) and harvested minke whales (0.22 ± 0.13), possibly due to fatality type and duration of stress prior to death. We provide the first quantification of blubber steroid hormones in killer whale, minke whale, sperm whale and harbour porpoise, and in less than 50-mg sample mass. By minimizing sample mass without compromising precision or sensitivity, our method allows for steroid hormone analysis even on samples with limited availability, strengthening our ability to monitor and conserve marine mammal populations.
- 1 January 2026
- Published by Oxford University Press (OUP) in Conservation Physiology
- Vol. 14 (1)
Open AccessA sensitive liquid chromatography–tandem mass spectrometry analytical method of steroid hormones in small blubber samples from four whale species
Steroid hormones can give an indication of stress, physiological health and reproductive status in whales; however, analysis is often limited by sample mass. We developed a sensitive analytical method using solid phase extraction–liquid chromatography–electrospray ionization–tandem mass spectrometry (LC–ESI–MS/MS) for the identification and quantification of eight steroid hormones (cortisol, cortisone, testosterone, androstenedione, progesterone, 11-deoxycortisol, 11-deoxycorticosterone and 17-hydroxyprogesterone) in small amounts of whale blubber (≤50 mg). Blubber biopsies were collected from stranded killer whales (Orcinus orca; n = 7), harbour porpoises (Phocoena phocoena; n = 3) and sperm whales (Physeter macrocephalus; n = 4), harvested common minke whales (n = 10; Balaenoptera acutorostrata) and free-living killer whales (n = 2) in Norway and the Barents Sea. Steroid hormones were separated using pentafluorophenyl propyl stationary phase and an optimized gradient programme with a total 20-min run. All samples (n = 26) were analysed at 50-mg sample mass, and a subset (n = 11) at 25 mg or lower. Low limit of detection and limit of quantification values resulted in high detection rates of hormones, and we found similar hormone concentrations between parallel samples and at the lowest tested sample mass (14 mg). Cortisol concentrations in sperm whales (4.3 ± 1.6 ng/g) were four times higher than stranded killer whales (1.1 ± 0.96 ng/g), which in turn were up to four times higher than free-living killer whales (0.23 ± 0.12 ng/g), harbour porpoise (0.64 ± 0.38 ng/g) and harvested minke whales (0.22 ± 0.13), possibly due to fatality type and duration of stress prior to death. We provide the first quantification of blubber steroid hormones in killer whale, minke whale, sperm whale and harbour porpoise, and in less than 50-mg sample mass. By minimizing sample mass without compromising precision or sensitivity, our method allows for steroid hormone analysis even on samples with limited availability, strengthening our ability to monitor and conserve marine mammal populations.
- Open Access
- 1 January 2022
- Published by Elsevier in NeuroToxicology
- Vol. 88, 79-87
Peripherally administered persistent organic pollutants distribute to the brain of developing chicken embryo in concentrations relevant for human exposure
- 1 January 2022
- Published by Elsevier in NeuroToxicology
- Vol. 88, 79-87
Open AccessPeripherally administered persistent organic pollutants distribute to the brain of developing chicken embryo in concentrations relevant for human exposure