FLFrançois Lacan

François Lacan

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François Lacan has a total of 552 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Open Access

    Iron isotope insights into equatorial Pacific biogeochemistry

    by Capucine Camin, Marie Labatut, Catherine Pradoux, James W. Murray, François Lacan

    The EUCFe cruise (RV Kilo Moana, 2006) was designed to characterize sources of Fe to the western equatorial Pacific and its transport by the Equatorial Undercurrent (EUC), a narrow and fast eastward current flowing along the equator, to the eastern equatorial Pacific High Nutrient Low Chlorophyll (HNLC) region. This study presents seawater dissolved (DFe) and particulate (PFe) iron concentrations and isotopic compositions (δ56DFe and δ56PFe) from 15 stations in the equatorial band (2° N–2° S) between Papua New Guinea and 140° W, over more than 8500 km along the equator and in the upper 1000 m of the water column. δ56DFe and δ56PFe ranged from −0.22 ‰ to +0.79 ± 0.07 ‰ and from −0.52 ‰ to +0.43 ± 0.07 ‰, respectively (relative to IRMM-14, 95 % confidence interval). Source signatures, biogeochemical processes and transport all contribute to these observations. Two distinct areas, one under continental influence (the western equatorial Pacific) and an open ocean region (the central equatorial Pacific), emerged from the data. In the area under continental influence, high PFe concentrations along with δ56DFe values systematically heavier than that of δ56PFe indicated an equilibrium fractionation and the co-occurrence of chemical fluxes from both phases toward the other. This exchange occurs through non-reductive processes, as previously proposed from three of the eight stations of this area (Labatut et al., 2014) and extends up to 1200 km from the coast. In the open ocean area, preservation of a DFe isotopic signature of ∼ +0.36 ‰ within the EUC, from Papua New Guinea to the central equatorial Pacific (7800 km), confirmed the origin of the DFe carried within this current toward the HNLC region. At the same depth, bordering the EUC at 2° N and 2° S at 140° W, light isotopic signatures suggested that iron was originating from the eastern Pacific oxygen minimum zones. These light signatures were also observed in deeper central waters, between 200 and 500 m. Our data did not allow conclusions about fractionation during uptake by phytoplankton, but indicated that any fractionation, if present, must be small, no larger than a few tenths of a per mil.

  • Open Access

    Reply on RC2

    by Capucine Camin, François Lacan, Marie Labatut, Catherine Pradoux, James W. Murray

    The EUCFe cruise (RV Kilo Moana, 2006) was designed to characterize sources of Fe to the western equatorial Pacific and its transport by the Equatorial Undercurrent (EUC), a narrow and fast eastward current flowing along the equator, to the eastern equatorial Pacific High Nutrient Low Chlorophyll (HNLC) region. This study presents seawater dissolved (DFe) and particulate (PFe) iron concentrations and isotopic compositions (δ56DFe and δ56PFe) from 15 stations in the equatorial band (2° N–2° S) between Papua New Guinea and 140° W, over more than 8,500 km along the equator and in the upper 1,000 m of the water column. δ56DFe and δ56PFe ranged from -0.22 to +0.79 ± 0.07 ‰ and from -0.52 to +0.43 ± 0.07 ‰, respectively (relative to IRMM-14, 95 % confidence interval). Source signatures, biogeochemical processes and transport all contribute to these observations. Two distinct areas, one under continental influence (the western equatorial Pacific) and an open ocean region (the central equatorial Pacific), emerged from the data. In the area under continental influence, high PFe concentrations along with δ56DFe values systematically heavier than that of δ56PFe indicated a permanent and reversible dissolved-particulate exchange. This exchange occurs through non-reductive processes, as previously proposed from three of the eight stations of this area (Labatut et al., 2014). In the open ocean area, preservation of a DFe isotopic signature of ~+0.36 ‰ within the EUC, from Papua New Guinea to the central equatorial Pacific (7,800 km), confirmed the origin of the DFe carried within this current toward the HNCL region. At the same depth, bordering the EUC at 2° N and 2° S at 140° W, light isotopic signatures suggested that was iron originating from the eastern Pacific oxygen minimum zones. These light signatures were also observed in deeper central waters, between 200 and 500 m. Our data did not allow conclusions about fractionation during uptake by phytoplankton, but indicated that this fractionation must be if any, is small, no larger than a few tenths of a per mil.

  • Open Access

    Reply on RC1

    by Capucine Camin, François Lacan, Marie Labatut, Catherine Pradoux, James W. Murray

    The EUCFe cruise (RV Kilo Moana, 2006) was designed to characterize sources of Fe to the western equatorial Pacific and its transport by the Equatorial Undercurrent (EUC), a narrow and fast eastward current flowing along the equator, to the eastern equatorial Pacific High Nutrient Low Chlorophyll (HNLC) region. This study presents seawater dissolved (DFe) and particulate (PFe) iron concentrations and isotopic compositions (δ56DFe and δ56PFe) from 15 stations in the equatorial band (2° N–2° S) between Papua New Guinea and 140° W, over more than 8,500 km along the equator and in the upper 1,000 m of the water column. δ56DFe and δ56PFe ranged from -0.22 to +0.79 ± 0.07 ‰ and from -0.52 to +0.43 ± 0.07 ‰, respectively (relative to IRMM-14, 95 % confidence interval). Source signatures, biogeochemical processes and transport all contribute to these observations. Two distinct areas, one under continental influence (the western equatorial Pacific) and an open ocean region (the central equatorial Pacific), emerged from the data. In the area under continental influence, high PFe concentrations along with δ56DFe values systematically heavier than that of δ56PFe indicated a permanent and reversible dissolved-particulate exchange. This exchange occurs through non-reductive processes, as previously proposed from three of the eight stations of this area (Labatut et al., 2014). In the open ocean area, preservation of a DFe isotopic signature of ~+0.36 ‰ within the EUC, from Papua New Guinea to the central equatorial Pacific (7,800 km), confirmed the origin of the DFe carried within this current toward the HNCL region. At the same depth, bordering the EUC at 2° N and 2° S at 140° W, light isotopic signatures suggested that was iron originating from the eastern Pacific oxygen minimum zones. These light signatures were also observed in deeper central waters, between 200 and 500 m. Our data did not allow conclusions about fractionation during uptake by phytoplankton, but indicated that this fractionation must be if any, is small, no larger than a few tenths of a per mil.

  • Open Access

    Reply on RC3

    by Capucine Camin, François Lacan, Marie Labatut, Catherine Pradoux, James W. Murray

    The EUCFe cruise (RV Kilo Moana, 2006) was designed to characterize sources of Fe to the western equatorial Pacific and its transport by the Equatorial Undercurrent (EUC), a narrow and fast eastward current flowing along the equator, to the eastern equatorial Pacific High Nutrient Low Chlorophyll (HNLC) region. This study presents seawater dissolved (DFe) and particulate (PFe) iron concentrations and isotopic compositions (δ56DFe and δ56PFe) from 15 stations in the equatorial band (2° N–2° S) between Papua New Guinea and 140° W, over more than 8,500 km along the equator and in the upper 1,000 m of the water column. δ56DFe and δ56PFe ranged from -0.22 to +0.79 ± 0.07 ‰ and from -0.52 to +0.43 ± 0.07 ‰, respectively (relative to IRMM-14, 95 % confidence interval). Source signatures, biogeochemical processes and transport all contribute to these observations. Two distinct areas, one under continental influence (the western equatorial Pacific) and an open ocean region (the central equatorial Pacific), emerged from the data. In the area under continental influence, high PFe concentrations along with δ56DFe values systematically heavier than that of δ56PFe indicated a permanent and reversible dissolved-particulate exchange. This exchange occurs through non-reductive processes, as previously proposed from three of the eight stations of this area (Labatut et al., 2014). In the open ocean area, preservation of a DFe isotopic signature of ~+0.36 ‰ within the EUC, from Papua New Guinea to the central equatorial Pacific (7,800 km), confirmed the origin of the DFe carried within this current toward the HNCL region. At the same depth, bordering the EUC at 2° N and 2° S at 140° W, light isotopic signatures suggested that was iron originating from the eastern Pacific oxygen minimum zones. These light signatures were also observed in deeper central waters, between 200 and 500 m. Our data did not allow conclusions about fractionation during uptake by phytoplankton, but indicated that this fractionation must be if any, is small, no larger than a few tenths of a per mil.

  • Open Access

    Comment on egusphere-2025-4525

    by Capucine Camin, François Lacan, Marie Labatut, Catherine Pradoux, James W. Murray

    The EUCFe cruise (RV Kilo Moana, 2006) was designed to characterize sources of Fe to the western equatorial Pacific and its transport by the Equatorial Undercurrent (EUC), a narrow and fast eastward current flowing along the equator, to the eastern equatorial Pacific High Nutrient Low Chlorophyll (HNLC) region. This study presents seawater dissolved (DFe) and particulate (PFe) iron concentrations and isotopic compositions (δ56DFe and δ56PFe) from 15 stations in the equatorial band (2° N–2° S) between Papua New Guinea and 140° W, over more than 8,500 km along the equator and in the upper 1,000 m of the water column. δ56DFe and δ56PFe ranged from -0.22 to +0.79 ± 0.07 ‰ and from -0.52 to +0.43 ± 0.07 ‰, respectively (relative to IRMM-14, 95 % confidence interval). Source signatures, biogeochemical processes and transport all contribute to these observations. Two distinct areas, one under continental influence (the western equatorial Pacific) and an open ocean region (the central equatorial Pacific), emerged from the data. In the area under continental influence, high PFe concentrations along with δ56DFe values systematically heavier than that of δ56PFe indicated a permanent and reversible dissolved-particulate exchange. This exchange occurs through non-reductive processes, as previously proposed from three of the eight stations of this area (Labatut et al., 2014). In the open ocean area, preservation of a DFe isotopic signature of ~+0.36 ‰ within the EUC, from Papua New Guinea to the central equatorial Pacific (7,800 km), confirmed the origin of the DFe carried within this current toward the HNCL region. At the same depth, bordering the EUC at 2° N and 2° S at 140° W, light isotopic signatures suggested that was iron originating from the eastern Pacific oxygen minimum zones. These light signatures were also observed in deeper central waters, between 200 and 500 m. Our data did not allow conclusions about fractionation during uptake by phytoplankton, but indicated that this fractionation must be if any, is small, no larger than a few tenths of a per mil.

  • Open Access

    Comment on egusphere-2025-4525

    by Capucine Camin, François Lacan, Marie Labatut, Catherine Pradoux, James W. Murray

    The EUCFe cruise (RV Kilo Moana, 2006) was designed to characterize sources of Fe to the western equatorial Pacific and its transport by the Equatorial Undercurrent (EUC), a narrow and fast eastward current flowing along the equator, to the eastern equatorial Pacific High Nutrient Low Chlorophyll (HNLC) region. This study presents seawater dissolved (DFe) and particulate (PFe) iron concentrations and isotopic compositions (δ56DFe and δ56PFe) from 15 stations in the equatorial band (2° N–2° S) between Papua New Guinea and 140° W, over more than 8,500 km along the equator and in the upper 1,000 m of the water column. δ56DFe and δ56PFe ranged from -0.22 to +0.79 ± 0.07 ‰ and from -0.52 to +0.43 ± 0.07 ‰, respectively (relative to IRMM-14, 95 % confidence interval). Source signatures, biogeochemical processes and transport all contribute to these observations. Two distinct areas, one under continental influence (the western equatorial Pacific) and an open ocean region (the central equatorial Pacific), emerged from the data. In the area under continental influence, high PFe concentrations along with δ56DFe values systematically heavier than that of δ56PFe indicated a permanent and reversible dissolved-particulate exchange. This exchange occurs through non-reductive processes, as previously proposed from three of the eight stations of this area (Labatut et al., 2014). In the open ocean area, preservation of a DFe isotopic signature of ~+0.36 ‰ within the EUC, from Papua New Guinea to the central equatorial Pacific (7,800 km), confirmed the origin of the DFe carried within this current toward the HNCL region. At the same depth, bordering the EUC at 2° N and 2° S at 140° W, light isotopic signatures suggested that was iron originating from the eastern Pacific oxygen minimum zones. These light signatures were also observed in deeper central waters, between 200 and 500 m. Our data did not allow conclusions about fractionation during uptake by phytoplankton, but indicated that this fractionation must be if any, is small, no larger than a few tenths of a per mil.

  • Open Access

    Comment on egusphere-2025-4525

    by Capucine Camin, François Lacan, Marie Labatut, Catherine Pradoux, James W. Murray

    The EUCFe cruise (RV Kilo Moana, 2006) was designed to characterize sources of Fe to the western equatorial Pacific and its transport by the Equatorial Undercurrent (EUC), a narrow and fast eastward current flowing along the equator, to the eastern equatorial Pacific High Nutrient Low Chlorophyll (HNLC) region. This study presents seawater dissolved (DFe) and particulate (PFe) iron concentrations and isotopic compositions (δ56DFe and δ56PFe) from 15 stations in the equatorial band (2° N–2° S) between Papua New Guinea and 140° W, over more than 8,500 km along the equator and in the upper 1,000 m of the water column. δ56DFe and δ56PFe ranged from -0.22 to +0.79 ± 0.07 ‰ and from -0.52 to +0.43 ± 0.07 ‰, respectively (relative to IRMM-14, 95 % confidence interval). Source signatures, biogeochemical processes and transport all contribute to these observations. Two distinct areas, one under continental influence (the western equatorial Pacific) and an open ocean region (the central equatorial Pacific), emerged from the data. In the area under continental influence, high PFe concentrations along with δ56DFe values systematically heavier than that of δ56PFe indicated a permanent and reversible dissolved-particulate exchange. This exchange occurs through non-reductive processes, as previously proposed from three of the eight stations of this area (Labatut et al., 2014). In the open ocean area, preservation of a DFe isotopic signature of ~+0.36 ‰ within the EUC, from Papua New Guinea to the central equatorial Pacific (7,800 km), confirmed the origin of the DFe carried within this current toward the HNCL region. At the same depth, bordering the EUC at 2° N and 2° S at 140° W, light isotopic signatures suggested that was iron originating from the eastern Pacific oxygen minimum zones. These light signatures were also observed in deeper central waters, between 200 and 500 m. Our data did not allow conclusions about fractionation during uptake by phytoplankton, but indicated that this fractionation must be if any, is small, no larger than a few tenths of a per mil.

  • Open Access

    Iron isotope insights into equatorial Pacific biogeochemistry

    by Capucine Camin, François Lacan, Marie Labatut, Catherine Pradoux, James W. Murray

    The EUCFe cruise (RV Kilo Moana, 2006) was designed to characterize sources of Fe to the western equatorial Pacific and its transport by the Equatorial Undercurrent (EUC), a narrow and fast eastward current flowing along the equator, to the eastern equatorial Pacific High Nutrient Low Chlorophyll (HNLC) region. This study presents seawater dissolved (DFe) and particulate (PFe) iron concentrations and isotopic compositions (δ56DFe and δ56PFe) from 15 stations in the equatorial band (2° N–2° S) between Papua New Guinea and 140° W, over more than 8,500 km along the equator and in the upper 1,000 m of the water column. δ56DFe and δ56PFe ranged from -0.22 to +0.79 ± 0.07 ‰ and from -0.52 to +0.43 ± 0.07 ‰, respectively (relative to IRMM-14, 95 % confidence interval). Source signatures, biogeochemical processes and transport all contribute to these observations. Two distinct areas, one under continental influence (the western equatorial Pacific) and an open ocean region (the central equatorial Pacific), emerged from the data. In the area under continental influence, high PFe concentrations along with δ56DFe values systematically heavier than that of δ56PFe indicated a permanent and reversible dissolved-particulate exchange. This exchange occurs through non-reductive processes, as previously proposed from three of the eight stations of this area (Labatut et al., 2014). In the open ocean area, preservation of a DFe isotopic signature of ~+0.36 ‰ within the EUC, from Papua New Guinea to the central equatorial Pacific (7,800 km), confirmed the origin of the DFe carried within this current toward the HNCL region. At the same depth, bordering the EUC at 2° N and 2° S at 140° W, light isotopic signatures suggested that was iron originating from the eastern Pacific oxygen minimum zones. These light signatures were also observed in deeper central waters, between 200 and 500 m. Our data did not allow conclusions about fractionation during uptake by phytoplankton, but indicated that this fractionation must be if any, is small, no larger than a few tenths of a per mil.

  • Open Access

    Iron isotopes suggest significant aerosol dissolution over the Pacific Ocean

    by Capucine Camin, François Lacan, Catherine Pradoux, Marie Labatut, Anne Johansen, James W. Murray

    This study presents aerosol iron isotopic compositions (δ56Fe) in the western and central equatorial and tropical Pacific Ocean. Aerosols supply iron (Fe), a critical element for marine primary production, to the open ocean. Particulate aerosols, > 1 µm, were sampled during the EUCFe (Equatorial Undercurrent Fe) cruise (RV Kilo Moana, PI: James W. Murray, 2006). One aerosol sample was isotopically lighter than the crust (δ56Fe = −0.16 ± 0.07 ‰, 95 % confidence interval), possibly originating from combustion processes. The nine other aerosol samples were isotopically heavier than the crust, with a rather homogeneous signature of +0.31 ± 0.21 ‰ (2 SD, n= 9). Given (i) this homogeneity compared to the diversity of their modeled geographic origin and (ii) the values of the Fe/Ti ratios used as a lithogenic tracer, we suggest that these heavy δ56Fe signatures reflect isotopic fractionation of crustal aerosols caused by atmospheric processes. Using a fractionation factor of Δsolution-particle= −1.8 ‰, a partial dissolution of ≈ 13 % of the initial aerosol iron content, followed by the removal of this dissolved fraction, would explain the observed slightly heavy Fe isotope signatures. Such fractionation has been observed previously in laboratory experiments but never before in a natural environment. The removal of the dissolved fraction of the aerosols has not been previously documented either. This work illustrates the strong constraints provided by the use of iron isotopes for atmospheric process studies.


  • Open Access

    Comment on egusphere-2024-3777

    by Capucine Camin, François Lacan, Catherine Pradoux, Marie Labatut, Anne Johansen, James W. Murray

    This study presents aerosol iron isotopic compositions (δ56Fe) in Western and Central Equatorial and Tropical Pacific Ocean. Aerosols supply iron (Fe), a critical element for marine primary production, to the open ocean. Particulate aerosols, > 1 µm, were sampled during EUCFe cruise (RV Kilo Moana, PI: J. W. Murray, 2006). One aerosol sample was isotopically lighter than the crust (δ56Fe=-0.16 ± 0.07 ‰, 95 % confidence interval), possibly originating from combustion processes. The nine other aerosol samples were isotopically heavier than the crust, with a rather homogeneous signature of 0.31 ± 0.21 ‰ (2SD, n=9). Given i) this homogeneity compared to the diversity of their modeled geographic origin and ii) the values of the Fe/Ti ratios used as a lithogenic tracer, we suggest that these heavy δ56Fe signatures reflect isotopic fractionation of crustal aerosols caused by atmospheric processes. Using a fractionation factor of Δsolution - particle=-1.1 ‰, a partial dissolution of ≈20 % of the initial aerosol iron content, followed by the removal of this dissolved fraction, would explain the observed slightly heavy Fe isotope signatures. Such fractionation has been observed previously in laboratory experiments, but never before in a natural environment. The removal of the dissolved fraction of the aerosols has not been previously documented either. This work illustrates the strong constrains provided by the use of iron isotopes for atmospheric process studies.