Younger Dryas glaciolacustrine rhythmites and cirque glacier variations at Kråkenes, western Norway: depositional processes and climate

Kråkenes faces the open sea on the west coast of Norway. During the Younger Dryas a cirque glacier deposited a large outer and a smaller inner moraine in a cirque at the site and melt-water entered a small lake depositing glaciolacustrine sediments. The glaciolacustrine succession can be divided into three sub-units corresponding to the advance, the still-stand and the retreat phases of the glacier. The sediment succession contains both varves and other types of rhythmites, the latter being mainly deposited as turbidity underflows caused by localized slumping events. Lee-side accumulation of snow by wind and avalanching into the cirque was crucial to form and maintain the cirque glacier once summer temperatures were low enough. At maximum, the glacier likely was in equilibrium with climate. The initial retreat from the maximum position might have been triggered by fall-out of volcanic ash from Iceland, but the continued retreat was due to increased ablation season temperatures. The most rapid change in climate at the Younger Dryas/Preboreal transition occurred after the cirque glacier had melted away completely.     

A level-set corrector to an adaptive multiscale permeability prediction

We consider the inverse problem of permeability estimation for two-phase porous-media flow. The novel approach is based on regularization by zonation, where the geometry and size of the regions are chosen adaptively during the optimization procedure. To achieve this, we have utilized level-set functions to represent the permeability. The available data are sparsely distributed in space; hence, it is reasonable to confine the estimation to coarse-scale structures. The level-set approach is able to alter the boundaries between regions of different permeability without strict restrictions on their shape; however, when the data are sparse, a reasonable initial guess for the permeability is required. For this task, we use adaptive multiscale permeability estimation, which has the potential of identifying main permeability variations. These are described by a piecewise constant function, where the constant values are attained on rectangular zones. In the current work, we develop a level-set corrector strategy, assuming adaptive multiscale permeability estimation as a predictor.     

Measurement of the redox speciation of iron in seawater by catalytic cathodic stripping voltammetry

Catalytic cathodic stripping voltammetry (CSV) preceded by adsorptive collection of complexes of 1-nitroso-2-napthol (NN) can be used to determine iron in seawater. It is shown here that iron(II) is effectively masked in the presence of 2,2-dipyridyl (Dp) so that iron(III) is measured selectively. The concentration of iron(II) is then calculated as the difference between the concentrations of reactive iron (Fe_R) in the absence and presence of 2 μM Dp, Fe_R being defined as that which was complexed by 20 μM NN at pH 6.9 in the presence of 1.8 mM H₂O₂ and 5 ppm sodium dodecyl sulphate. A 30 min reaction time was allowed for Dp to react with iron(II) in seawater prior to the determination of reactive iron(III) using the same conditions as used for Fe_R. Detection limits of 0.08 nM, 0.077 nM and 0.12 nM were obtained for Fe_R, iron(III) and iron(II), respectively, using a 60 s deposition time.The method was utilised to determine the redox speciation of iron in the northern North Sea. Concentrations of Fe_R ranged between 0.8 and 3.5 nM with nutrient-like depth profiles. Iron(II) was found to be present at concentrations up to 1.2 nM, the highest concentrations occurring in the upper 20 m of the water column.     

Responses of marine phytoplankton in iron enrichment experiments in the northern North Sea and northeast Atlantic Ocean

Short-term iron enrichment experiments were carried out with samples collected in areas with different phytoplankton activity in the northern North Sea and northeast Atlantic Ocean in the summer of 1993. The research area was dominated by high numbers of pico-phytoplankton, up to 70,000 ml⁻¹. Maximum chlorophyll a concentrations varied from about 1.0 μg l⁻¹ in a high-reflectance zone (caused by loose coccoliths, remnants from a bloom of Emiliania huxleyi) and about 3.5 μg l⁻¹ in a zone in which the phytoplankton were growing, to about 0.5 μg l⁻¹ in the northeast Atlantic Ocean. From the high-reflectance zone to the northeast Atlantic Ocean, nitrate concentrations increased from 0.5 μM to 6.0 μM. Concentrations of reactive iron in surface water showed an opposite trend and decreased from about 2.6 nM in the high-reflectance zone to <1.0 nM in the northeast Atlantic Ocean. In the research area, no signs of true iron deficiency were found, but iron enrichments in the high-reflectance zone, numerically dominated by Synechococcus sp., resulted in increased nitrate uptake. Ammonium uptake was hardly affected. Strong support for the effect of Fe on cell physiology is given by the increase in the f-ratio. Net growth rates of the phytoplankton (changes in cell numbers over 24 h) were almost unchanged. Phytoplankton collected from the northeast Atlantic Ocean, did not show changes in the nitrogen metabolism upon addition of iron. Net growth rates in these incubations were low or negative, with only slightly higher values with additional iron.     

III. Mitteilung. Die hydrothermale Zersetzung des Peridotits bei der Bildung der Magnesitlagerstätte am Galgenberg bei Zobten

Ohne ZusammenfassungAbgeschlossen im Juni 1947.     

Life histories of large,grazing copepods in a subarctic ocean gyre: Neocalanus plumchrus,Neocalanus cristatus, and Eucalanus bungii in the Northeast Pacific

Life histories for the dominant, larger copepods of the subartic Pacific have been constructed by sampling from weatherships patrolling Ocean Station P (50°N, 145°W) during 1980 and 1981. Neocalanus plumchrus reproduced at depths below 250 m from July through February. Copepodite stages were present in surface layers from October through August with a large peak in numbers and biomass in spring. Fifth copepodites prepared for diapuse in 38 days during spring and descended to depths below 250 m. They commenced immediately to mature, and the females reproduced without renewed feeding. This schedule contrasts with that of the population in the Strait of Georgia, which remains in diapause from July to January and matures exclusively in January and February. There appears to be a difference between the coastal and oceanic habitats in preparing the diapausing individuals for maturation.Maturation of the diapausing stock of N. plumchrus maintained constant adult populations, averaging 714 males m^?2 from June through October and 1,434 females m^?2 from August through January. This constancy, together with the exponential pattern of decline in the diapause stock from September through February, suggests that density of adults may regulate maturation of fifth copepodites. Offspring of individuals delaying maturation and, thus, reproduction would benefit from the resulting moderation of intraspecific competition, probably that among copepodites.Reproduction of Neocalanus cristatus also occurred below 250 m, and, while spawning was continuous through the year, there was a substantial peak in November. That resulted in a peak of abundance for early copepodite stages in mid-winter, and a peak for the fifth copepodite stage in June. Stocking of the population of fifth copepodites in diapause below 250 m occurred from July through October. Some fifth copepodites were present in surface layers through the entire summer, and some younger copepodites persisted through the summer in progressively declining abundance just below the mixed layer. In autumn 1980 resurgence of early copepodite populations was rapid, occurring during the course of a prolonged October storm. The storm may have improved the habitat either by cooling the mixed layer or by resupplying nutrients to the euphotic zone.Eucalanus bungii reproduced in the mixed layer in early May and in early July. The first event was a spawning by females that had previously spawned in 1979 and then had returned to diapause. The second, heavier spawning (more females, more eggs per female) was by newly matured females from stocks that had overwintered as fifth copepodites. Nauplii peaked sharply in abundance on 19 July, one week after the peak in spawning. First and second copepodites peaked on 1 August, and all had advanced to the third copepodite stage by September. The diapause stock was established by September, principally between 250 and 500 m, and consisted of copepodite stages from third to sixth. Duration of the E. bungii life cycle appears to be typically two years. New nauplii develop as far as the third or fourth copepodite stage during their first summer, then enter diapause. The second summer they advance to the fifth copepodite stage and reenter diapause. Fifth copepodites mature in their third summer at two years of age. The males remain at depth and mate without subsequent feeding. Females migrate at night to the mixed layer where spawning occurs. About 20% of females that had already spawned in 1980 reentered diapause. They would reproduce again in their fourth summer at three years of age. All aspects of the life cycle suggest low mortality rates for copepodite stages, particularly at depth in the habitat occupied during diapuse. There can be no premium on rapid reproduction for E. bungii in the subartic Pacific, and there must even be benefit from spreading reproduction between years. This iteroparity may amount to a “bet-hedging” tactic, the young from a given mother having more than one chance to find sustaining conditions. It also produces gene flow between the year classes of the biennial life cycle.     

Ecohydrological responses to surface flow across borders: Two decades of changes in vegetation greenness and water use in the riparian corridor of the Colorado River delta

Hydrological and bioclimatic processes that lead to drought may stress plants and wildlife, restructure plant community type and architecture, increase monotypic stands and bare soils, facilitate the invasion of non-native plant species and accelerate soil erosion. Our study focuses on the impact of a paucity of Colorado River surface flows from the United States (U.S.) to Mexico. We measured change in riparian plant greenness and water use over the past two decades using remotely sensed measurements of vegetation index (VI), evapotranspiration (ET) and a new annualized phenology assessment metric (PAM) for ET. We measure these long-term (2000–2019) metrics and their short-term (2014–2019) response to an environmental pulse flow in 2014, as prescribed under Minute 319 of the 1944 Water Treaty between the two nations. In subsequent years, small-directed flows were provided to restoration areas under Minute 323. We use 250 m MODIS and 30 m Landsat imagery to evaluate three vegetation indices (NDVI, EVI, EVI2). We select EVI2 to parameterize an optical-based ET algorithm and test the relationship between ET from Landsat and MODIS by regression approaches. Our analyses show significant decreases in VIs and ET for both the 20-year and post-pulse 5-year periods. Over the last 20 years, EVI _Landsat declined 34% (30% by EVI_MODIS) and ET_Landsat-EVI declined 38% (27% by ET_MODIS-EVI), overall ca. 1.61 mm/day or 476 mm/year drop in ET; using PAM ET_Landsat-EVI the drop was from 1130 to 654 mm/year. Over the 5 years since the 2014 pulse flow, EVI_Landsat declined 20% (13% by EVI_MODIS) and ET_Landsat-EVI declined 23% (4% by ET_MODIS-EVI) with a 0.77 mm/day or a 209 mm/year 5-year drop in ET; using PAM ET_Landsat-EVI the drop was from 863 to 654 mm/year. Data and change maps show the pulse flow contributed enough water to slow the rate of loss, but only for the very short-term (1–2 years). These findings are critically important as they suggest further deterioration of biodiversity, wildlife habitat and key ecosystem services due to anthropogenic diversions of water in the U.S. and Mexico and from land clearing, fires and plant-related drought which affect hydrological processes.     

Marine geochemistry—2: scavenging redux

Inorganic surfaces sorb dissolved and particulate phases from seawater onto organic films from a variety of sources. Heavy metals such as Au, Pt, Mn and Cd come to the coatings primarily from particulate phases. This observation confirms a previous finding of this laboratory for the uptake of U, Pu and Po. With depth in the open ocean there are greater contributions from the dissolved phases. Microbial and photochemical processes can enrich surfaces in some metals through reduction reactions. Copper and Mn enrichments in the films are attributed to the photo-reductions of Cu(II) to Cu(I) and manganese oxides to Mn(II), respectively, while the uptake of Mo is a consequence of the reduction, mediated by organisms, of molybdate to Mo(V) or Mo(IV). Cadmium, on the other hand, appears to be bioaccumulated in the films.     

Salt marsh cliff stability in the oosterschelde

Salt marsh cliff erosion in the Oosterschelde, due to basal scour and small-scale failure, was monitored during a two-year period using reference stakes. The composite marsh cliffs have a cantilever profile. Their stability is evaluated from beam failure analysis. A model is proposed, in which the cantilever weight is taken as the motive force; the major resistive force is the tensile strength. By substituting height, undermining width and soil mechanical properties of the cliff in the model, one can identify the cliffs that are likely to fail. Salt marsh cliffs, which combine a large tensile strength due to roots at the top of the profile with a large compressive stress at the cliff base due to the sandy texture of the subsoil, display the highest resistance to beam failure. The critical cliff dimensions, observed in the field, correspond with the values calculated from the proposed model of beam failure.