Dissolved trace metals and their relationship to major elements in the Manuherikia River, a pristine subalpine catchment in central Otago, New Zealand

1991 ◽  
Vol 42 (4) ◽  
pp. 409 ◽  
Author(s):  
WW Ahlers ◽  
JP Kim ◽  
KA Hunter

The spatial distributions of the dissolved trace metals Cu, Ni, Cd, Zn and Pb and of reactive Hg have been measured in parallel with the major elements Na, K, Mg and Ca and electrical conductivity in three sampling events in the Manuherikia River, New Zealand. The geographical span of the sampling sites ranged from a pristine subalpine upper catchment area through lower altitude sites that are increasingly affected by both natural weathering processes and moderate agricultural and domestic runoff. Major-element concentrations in the upper catchment were at or below the 1% frequency minimum of the spectrum of global river compositions, indicating a highly pristine system. Concen- trations increased steadily downstream to levels similar to world average river water. All trace metals exhibited the same spatial trends as the major ions. Typical upper-catchment concentrations were very low by global standards: Cu (150 ng L-1), Ni (100-150 ng L-1), Cd (8 ng L-I), Zn (150-200 ng L-1), Pb (20-30 ng L-1) and Hg (0.3 ng L-1). Oceanic residence times calculated from the data for Zn (80 000 years) and Cd (230 000 years) for which few reliable estimates have been made, are consistent with observed correlations between the oceanographic distributions of these elements and dissolved silicon or phosphate, respectively.

1996 ◽  
Vol 47 (7) ◽  
pp. 919 ◽  
Author(s):  
JP Kim ◽  
MR Reid ◽  
RG Cunninghame ◽  
KA Hunter

Concentrations of the major ions Na+, K+, Mg2+, Ca2+, HCO32-, SO42- and Cl-, of silicate, and of both total and dissolved trace metals Zn, Cu, Pb and Cd were determined at sites along the Clutha River. The major ions exhibited differing behaviour both spatially and temporally. A large proportion of Cl- and Na+ throughout the catchment could be attributed to atmospheric input of sea salt. Contributions from this source for the rest of the major elements were minimal, except perhaps near the mouth of the river (K+, Mg2+). The water composition was dominated by the weathering of carbonate rather than of silicate minerals. Increases in the concentrations of Mg and Na + K indicate the weathering of Mg, K and Na from rock, minerals and clays within the catchment. The concentrations of major ions and Si were relatively low compared with other rivers in New Zealand and elsewhere. Concentrations of dissolved Zn, Cu, Pb and Cd all increased consistently with distance down river, and between 40% and 100%, for a given metal, was found in the dissolved fraction. High correlation among the dissolved trace metals, with essentially constant Cu : Zn : Pb : Cd ratios of 755 : 716 : 223 : 1 (molar basis), indicates that the same weathering process or source may be occurring throughout the catchment.


1987 ◽  
Vol 38 (6) ◽  
pp. 861 ◽  
Author(s):  
BT Hart ◽  
EM Ottaway ◽  
BN Noller

A materials budget was estimated for the Magela Creek system during the 1982-83 wet season. This tropical system in northern Australia consists largely of a well-defined creek (Magela Creek contributes approximately 50% of the total inflow to the floodplain) flowing into an extensive wetlands area and then into the East Alligator River. Intensive sampling of creek water, rainfall and water flowing from the system provided the data base for the budget calculations. The annual transport of both dissolved and particulate matter by Magela Creek (area 600 km2) is very low, even when compared with other low-relief tropical systems. The annual load transported during 1982-83 was 1260 t (21 kg ha-1) of dissolved salts and 2330 t (39 kg ha-1) of particulate matter. Rainfall appeared to contribute all the sodium, potassium and chloride, and part of the calcium (c. 30%) and magnesium (25%) transported during the 1982-83 wet season by Magela Creek. Most of the manganese (c. 60%) (and probably iron) was contributed from weathering processes occurring in the catchment. Only small amounts of the trace metals copper, lead, zinc and uranium were transported by the creek. During the 1982-83 wet season, more trace metals were contributed in rainfall than transported from the catchment by the creek. However, this is probably atypical and resulted from dust particles that had entered the atmosphere in greater numbers due to the extended dry season. The vast bulk of the nutrients (total P 93%, NO3- N 86%, NH4+ N 98%) added to the catchment by rainfall was removed by the catchment, probably via uptake by the vegetation. Consequently, the creek transported only very small amounts of nutrients to the floodplain. An input-output budget for the Magela floodplain was calculated. The uncertainty in the net amounts deposited or released from the floodplain was estimated using a new quantitative method developed for this purpose. The uncertainties in the net values estimated were high, ranging from around 30% for bicarbonate to 500% for uranium. These data suggest that the Magela floodplain is a net source of the major ions (sodium, potassium, calcium, magnesium, chloride, sulfate and bicarbonate) and also of iron, and a net sink for suspended solids, nutrients (total phosphorus, nitrate and ammonia) and manganese. The floodplain also appears to be a net sink for the trace metals copper, lead, zinc and uranium.


1997 ◽  
Vol 48 (3) ◽  
pp. 257 ◽  
Author(s):  
Jonathan P. Kim ◽  
Keith A. Hunter

Concentrations of major ions (Na+, K+, Ca2+, Mg2+, Cl-, SO 4 2–), total alkalinity (TA), silicate (Si) and trace metals (Zn, Cu, Pb, Cd) have been investigated in the Takaka–Cobb River system at the northernmost extremity of the South Island, New Zealand. The range in concentrations of major ions, Si and TAwas large, with Ca2+ and TAdominating. Some waters in the upper catchment were close to saturation with respect to calcite, reflecting limestone dissolution both in the upper Takaka River and in an associated spring system. Dissolved trace metals exhibited different behaviour, with constant or increasing concentrations upriver, especially in the Cobb Valley. Low concentrations found in the upper Takaka River suggest that limestone weathering makes a minor contribution to concentrations of trace metals. The Cobb River exhibited much higher concentrations, implying that the differing compositions of rock types and soils within the separate catchments exercise important controls on trace metals.


2005 ◽  
Vol 69 (4) ◽  
pp. 839-850 ◽  
Author(s):  
William J. Green ◽  
Brian R. Stage ◽  
Adam Preston ◽  
Shannon Wagers ◽  
Joseph Shacat ◽  
...  

2014 ◽  
Vol 226 (1) ◽  
Author(s):  
Jorge Moreda-Piñeiro ◽  
Isabel Turnes-Carou ◽  
Elia Alonso-Rodríguez ◽  
Carmen Moscoso-Pérez ◽  
Gustavo Blanco-Heras ◽  
...  

2013 ◽  
Vol 45 (3) ◽  
pp. 379-390 ◽  
Author(s):  
Anna Maria Szczucińska

The major part of the Polish Plain (central Europe) was shaped during the last glaciation and so far has been considered to be poor in groundwater outflows. The present study aimed to map the groundwater outflows and to analyse their water properties in the Lubuska Upland, western Polish Plain. The mapping of the groundwater outflows was supplemented by hydrochemical analyses (major ions and trace metals) of selected outflows. Altogether, approximately 600 groundwater outflows were recorded, of which 45% were springs. The outflow water discharges ranged from 0.001 to 45 L s−1. Most of them were located at the bottom of the slopes of river valleys. The water was neutral (pH 6.9 to 8.11), with electrical conductivity from 261 to 652 μS cm−1 and average temperature ~10 °C. The most common water type was dominated by bicarbonate, sulphates and calcium ions. The waters often exceeded the quality limits for total Fe and Mn2+. This study revealed that groundwater outflows are a common feature of the areas shaped by former glaciations and are most likely supplied by shallow aquifers.


2020 ◽  
Author(s):  
Jenni L. Hopkins ◽  
Janine E. Bidmead ◽  
David J. Lowe ◽  
Richard J. Wysoczanski ◽  
Bradley J. Pillans ◽  
...  

Abstract. Although analyses of tephra-derived glass shards have been undertaken in New Zealand for nearly four decades (pioneered by Paul Froggatt), our study is the first to systematically develop a formal, comprehensive, open access, reference dataset of glass-shard compositions for New Zealand tephras. These data will provide an important reference tool for future studies to identify and correlate tephra deposits and for associated petrological and magma-related studies within New Zealand and beyond. Here we present the foundation dataset for TephraNZ, an open access reference dataset for selected tephra deposits in New Zealand. Prominent, rhyolitic, tephra deposits from the Quaternary were identified, with sample collection targeting original type sites or reference locations where the tephra's identification is unequivocally known based on independent dating or mineralogical techniques. Glass shards were extracted from the tephra deposits and major and trace element geochemical compositions were determined. We discuss in detail the data reduction process used to obtain the results and propose that future studies follow a similar protocol in order to gain comparable data. The dataset contains analyses of twenty-three proximal and twenty-seven distal tephra samples characterising 45 eruptive episodes ranging from Kaharoa (636 ± 12 cal. yrs BP) to the Hikuroa Pumice member (2.0 ± 0.6 Ma) from six or more caldera sources, most from the central Taupō Volcanic Zone. We report 1385 major element analyses obtained by electron microprobe (EMPA), and 590 trace element analyses obtained by laser ablation (LA)-ICP-MS, on individual glass shards. Using PCA, Euclidean similarity coefficients, and geochemical investigation, we show that chemical compositions of glass shards from individual eruptions are commonly distinguished by major elements, especially CaO, TiO2, K2O, FeOt (Na2O+ K2O and SiO2/K2O), but not always. For those tephras with similar glass major-element signatures, some can be distinguished using trace elements (e.g. HFSEs: Zr, Hf, Nb; LILE: Ba, Rb; REE: Eu, Tm, Dy, Y, Tb, Gd, Er, Ho, Yb, Sm), and trace element ratios (e.g. LILE / HFSE: Ba / Th, Ba / Zr, Rb / Zr; HFSE / HREE: Zr / Y, Zr / Yb, Hf / Y; LREE / HREE: La / Yb, Ce / Yb). Geochemistry alone cannot be used to distinguish between glass shards from the following tephra groups: Taupō (Unit Y in the post-Ōruanui eruption sequence of Taupō volcano) and Waimihia (Unit S); Poronui (Unit C) and Karapiti (Unit B); Rotorua and Rerewhakaaitu; and Kawakawa/Ōruanui, Okaia, and Unit L (of the Mangaone subgroup eruption sequence). Other characteristics can be used to separate and distinguish all of these otherwise-similar eruptives except Poronui and Karapiti. Bimodality caused by K2O variability is newly identified in Poihipi and Tahuna tephras. Using glass shard compositions, tephra sourced from Taupō Volcanic Centre (TVC) and Mangakino Volcanic Centre (MgVC) can be separated using bivariate plots of SiO2/K2O vs. Na2O+K2O. Glass shards from tephras derived from Kapenga Volcanic Centre, Rotorua Volcanic Centre, and Whakamaru Volcanic Centre have similar major- and trace-element chemical compositions to those from the MgVC, but can overlap with glass analyses from tephras from Taupō and Okataina volcanic centres. Specific trace elements and trace element ratios have lower variability than the heterogeneous major element and bimodal signatures, making them easier to geochemically fingerprint.


2020 ◽  
Vol 34 (2) ◽  
pp. 183-194
Author(s):  
Alexandre Chaves ◽  
Luiz Knauer

The hematitic phyllite is a rock that occurs in the São João da Chapada and Sopa-Brumadinho formations of the southern Espinhaço range. Its origin is widely discussed in papers on Espinhaço, but there is no consensus on its protolith due to certain characteristics of the lithotype, such as its chemical composition and textural features. The pattern of rare earth elements strongly enriched [(La/Yb)N 6.80-17.68], with light rare earth elements [(La/Sm)N 2.54-4.83] richer than heavy ones [(Gd/Yb)N 1.28-3,32], suggests that the protolith was an alkaline volcanic rock formed during the rift that generated the Espinhaço basin. The major elements indicate that the alkaline rock met weathering processes, becoming a regolith. During the Brasiliano metamorphism, it finally became hematitic phyllite. Other characteristics of the lithotype, such as the presence of sericite-bearing rounded parts (possibly formed by alteration and deformation of leucite crystals) and the preservation of igneous layering, suggest a potassic volcanic origin for hematitic phyllite. In diagram that allows identifying altered and metamorphic volcanic rocks, the investigated samples have composition similar to a feldspathoid-rich alkali-basalt, probably a leucite tephrite, a leucitite or even a lamproite, rocks from mantle source.


Soil Research ◽  
1990 ◽  
Vol 28 (3) ◽  
pp. 343 ◽  
Author(s):  
RL Parfitt

Studies of allophanes from New Zealand are reviewed, and a definition of the allophane group of minerals is suggested. Three types of allophane are identified, and their structures are discussed under headings Al-rich soil allophanes, Si-rich soil allophanes and stream deposit allophanes. Examples from New Zealand soils and tephras are discussed in relation to properties, identification and weathering processes.


Sign in / Sign up

Export Citation Format

Share Document