CHANGES IN LEAD BIOGEOCHEMISTRY IN RESPONSE TO DECREASING ATMOSPHERICINPUTS

Citation
Ce. Johnson et al., CHANGES IN LEAD BIOGEOCHEMISTRY IN RESPONSE TO DECREASING ATMOSPHERICINPUTS, Ecological applications, 5(3), 1995, pp. 813-822
Citations number
51
Categorie Soggetti
Ecology
Journal title
ISSN journal
10510761
Volume
5
Issue
3
Year of publication
1995
Pages
813 - 822
Database
ISI
SICI code
1051-0761(1995)5:3<813:CILBIR>2.0.ZU;2-T
Abstract
In the 1970s, the U.S. Congress passed legislation restricting the sal e of gasoline with alkyl-lead additives. In the intervening years, the amount of lead (Pb) consumed in gasoline has declined sharply, result ing in lower rates of atmospheric Pb deposition. At the Hubbard Brook Experimental Forest (HBEF) in New Hampshire, the input of Pb in precip itation has declined by 97% between 1976 and 1989. The purpose of this paper is to evaluate the long-term response of forest and associated aquatic ecosystems to these declining inputs of Pb. Lead continues to accumulate in the forest ecosystem of the HBEF, in spite of lower inpu ts, due to extremely low losses in drainage water. However, between 19 77 and 1987 the Pb content in the forest floor declined by 29%. Lead n ow appears to be accumulating in the mineral soil. The stratigraphy of Pb in sediment from a nearby lake shows continued Pb deposition, thou gh at a declining rate. Much of our understanding of the long-term pat terns of lead accumulation in ecosystems has been shaped by paleoecolo gical studies, in which inputs of lead are assumed to be irreversibly retained. Using a regression model and historical information concerni ng Pb consumption in gasoline, we estimated Pb inputs to the HBEF ecos ystem during the period 1926-1989. Based on this analysis and our fiel d observations, it is clear that Pb mobility at the HBEF is greater th an previously reported: approximate to 30% of the total atmospheric Pb input between 1926 and 1987 was not retained in organic soils or pond sediments. The potential for Pb pollution in drainage water may there fore be greater than suspected in regions with continued high rates of atmospheric Pb deposition.