29 research outputs found

    Lignin biomarkers as tracers of mercury sources in lakes water column

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    This study presents the role of specific terrigenous organic compounds as important vectors of mercury (Hg) transported from watersheds to lakes of the Canadian boreal forest. In order to differentiate the autochthonous from the allochthonous organic matter (OM), lignin derived biomarker signatures [Lambda, S/V, C/V, P/(V ? S), 3,5-Bd/V and (Ad/Al)v] were used. Since lignin is exclusively produced by terrigenous plants, this approach can give a non equivocal picture of the watershed inputs to the lakes. Moreover, it allows a characterization of the source of OM and its state of degradation. The water column of six lakes from the Canadian Shield was sampled monthly between June and September 2005. Lake total dissolved Hg concentrations and Lambda were positively correlated, meaning that Hg and ligneous inputs are linked (dissolved OM r2 = 0.62, p\0.0001; particulate OM r2 = 0.76, p\0.0001). Ratios of P/(V ? S) and 3,5-Bd/V from both dissolved OM and particulate OM of the water column suggest an inverse relationship between the progressive state of pedogenesis and maturation of the OM in soil before entering the lake, and the Hg concentrations in the water column. No relation was found between Hg levels in the lakes and the watershed flora composition—angiosperm versus gymnosperm or woody versus non-woody compounds. This study has significant implications for watershed management of ecosystems since limiting fresh terrestrial OM inputs should reduce Hg inputs to the aquatic systems. This is particularly the case for largescale land-use impacts, such as deforestation, agriculture and urbanization, associated to large quantities of soil OM being transferred to aquatic systems

    How to combat cyanobacterial blooms: strategy toward preventive lake restoration and reactive control measures

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    Linking biogeochemical processes and historic primary producer communities in the SE USA sinkhole lake form the mid-Holocene to present.

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    Many freshwater resources receive materials from human development causing a decrease in ecological services when compared to pre-disturbance periods. As a result, the understanding of eutrophication and limnological change has increased, but less attention has been given to systems under intense human impact that have not eutrophied so that drivers precluding eutrophication can be documented. The primary objective of this research was to reconstruct allochthonous inputs and in-lake processes for Long Pond, Georgia, USA from the mid Holocene to present and link them to primary producer community changes. Long Pond is a mesotrophic lake located in a highly altered watershed from agricultural and municipal land use and housing developments. A 5 m sediment core was collected from Long Pond, and organic matter, nutrients (C, N, P), metals (Al, Fe, Cu), and photosynthetic pigments were measured. Long Pond existed in three limnological states spanning the past ~6000 years. Prior to modern lacustrine conditions, Long Pond was a wetland/peat system that experienced the highest primary producer abundance recorded in the core. The modern lacustrine state began in the late Holocene and was characterized by increased connectivity with the surrounding watershed and low productivity. Human impacts began around 1900 AD and included high levels of phosphorus and metal deposition but moderate levels of primary producer abundance. As a result, in-lake dynamics are believed to be regulating the trophic status of Long Pond. Low concentrations of available phosphorus in the water column combined with high concentrations of sedimentary phosphorus may imply the binding of phosphorus to the sediments by certain materials such as aluminum and iron. Long Pond serves as an example of the complex in-lake processes that can occur from allochthonous inputs and autochthonous responses in lake systems thus complicating management decisions

    Mercury trends in fish from rivers and lakes in the United States, 1969–2005

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    A national dataset on concentrations of mercury in fish, compiled mainly from state and federal monitoring programs, was used to evaluate trends in mercury (Hg) in fish from US rivers and lakes. Trends were analyzed on data aggregated by site and by state, using samples of the same fish species and tissue type, and using fish of similar lengths. Site-based trends were evaluated from 1969 to 2005, but focused on a subset of the data from 1969 to 1987. Data aggregated by state were used to evaluate trends in fish Hg concentrations from 1988 to 2005. In addition, the most recent Hg fish data (1996–2005) were compared to wet Hg deposition data from the Mercury Deposition Network (MDN) over the same period. Downward trends in Hg concentrations in fish from data collected during 1969–1987 exceeded upward trends by a ratio of 6 to 1. Declining Hg accumulation rates in sediment and peat cores reported by many studies during the 1970s and 1980s correspond with the period when the most downward trends in fish Hg concentrations occurred. Downward Hg trends in both sediment cores and fish were also consistent with the implementation of stricter regulatory controls of direct releases of Hg to the atmosphere and surface waters during the same period. The southeastern USA had more upward Hg trends in fish than other regions for both site and state aggregated data. Upward Hg trends in fish from the southeastern USA were associated with increases in wet deposition in the region and may be attributed to a greater influence of global atmospheric Hg emissions in the southeastern USA. No significant trends were found in 62% of the fish species from six states from 1996 to 2005. A lack of Hg trends in fish in the more recent data was consistent with the lack of trends in wet Hg deposition at MDN sites and with relatively constant global emissions during the same time period. Although few significant trends were observed in the more recent Hg concentrations in fish, it is anticipated that Hg concentrations in fish will respond to changes in atmospheric Hg deposition, however, the magnitude and timing of the response is uncertain
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