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The Northland region of New Zealand includes numerous high-value, macrophyte-dominated dune lakes. Recent water policy reforms offer limited guidance on managing for aquatic macrophytes. In addition, dune lake histories are poorly known as regular monitoring dates to 2005 AD. Here, ca. 4000 years of lake functional behaviour is reconstructed from sedimentary archives in two Northland dune lakes (Humuhumu and Rotokawau). Results demonstrated that macrophyte dominance is sensitive to catchment erosion and hydrological drawdown. Degradation of macrophyte communities occurred in the nineteenth and twentieth centuries, earlier at Lake Humuhumu than Lake Rotokawau (post-1880 AD and post-1930 AD, respectively). In both lakes, increased erosional influx reduced macrophyte productivity, before later increases to wider trophic state (post-1970 AD). Lake-level decline is linked to increased nutrient loading at Lake Rotokawau but less so, Lake Humuhumu which is more strongly groundwater-fed. In Northland dune lakes, water-level reduction and erosional influx from land use have driven macrophyte degradation. 相似文献
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K–Ar dating of illitic minerals is commonly used in studies of diagenetic series applied to oil prospecting. In spite of a great number of specialized papers, some problems remain unresolved. These are mostly due to a misunderstanding of the argon accumulation process during illitization. Criteria for identifying detrital–authigenic mineral mixtures, crystal ripening, fast precipitation or continuous nucleation‐growth processes are discussed using K–Ar data available in the literature. Using different parameters, such as Δage (ageK–Ar ? agestrati), Δcryst (diagenetic ageK–Ar ? agestrati) or Δfrac (ageK–Arfraction ?ageK–Arfinest), it is shown that the K–Ar age significance depends on the illite nucleation–growth processes. A ‘diagenetic age’ is obtained when these processes are rapid (the K2O accumulation period is shorter than 2σ). If lower than this value, the K–Ar ratio depends on the proportions of new and old particles, respectively, which are controlled by the relative rates of nucleation, crystal growth and ripening. 相似文献
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High levels of Cd and Zn in Jamaican soils observed in geochemical surveys are related to the presence of phosphorites of possible Late-Miocene or Pliocene age. The trace element and REE geochemistry of the phosphorites, together with SEM studies, indicate a guano origin for the phosphorites. No specific host minerals for Cd could be identified in the fossiliferous phosphorite which is characterized by uniquely high levels of Cd, Zn, Ag, Be, U and Y. However, in the soil Cd is present in lithiophorite and a complex history of pedological development is preserved in the aluminous–goethite present in the soil. The unique guano signature is preserved in the soil despite the fact that guanos themselves have either not been observed or have been destroyed by continuing karst and soil development. The phosphorite geochemical signature can be traced in the data of a 1988 island-wide soil geochemical survey, identifying areas where the Palaeo-environment that supported bird ‘rookeries’ existed in the Late-Miocene or Pliocene. 相似文献
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Lucas G. Adamson Donald W. Quigley H. Ross Ainsworth George V. Chilingar 《Engineering Geology》1966,1(6):451-459
Most previous studies and applications of electrochemical stabilization of soils through electroosmosis have been made on clayey soils. The object of this investigation was to find out if relatively small amounts of clay (1.5%–3.5%, by weight) present in a sandy soil would be enough for stabilization and strengthening to be possible. The results indicate increases of cohesion of the order of 100–200 lb./sq.ft. X-ray analyses of treated soils indicate that sheet structures of clays are reduced and silicates destroyed upon treatment by electroosmosis. Newly-formed minerals also cement the soil. These neoformations include gibbsite, limonite, calcite, hydrohematite, hydrogoethite (hydrolepidocrocite), hisingerite, allophane, allophanoid, gypsum, hematite, magnetite, nontronite, trona and natron (Na2 CO3, 10H2O). The process seems to be irreversible. 相似文献