On the use of compliant fairings on conventional moorings

Abstract

Compliant fairing made of plastic ribbons or flexible rubber filaments can be attached to the cables of taut‐line moorings to reduce the drag force of the currents. The efficiency of such fairing depends upon its orientation in the flow and the Reynolds number of the cable. Results of using filament fairing manufactured by ENDECO Inc. on a 337‐m long mooring in the mouth of Hudson Strait are discussed. The fairing was found to be detrimental in this application because of twisting of the wire rope, producing a “bottle‐brush” configuration, and because the normal drag coefficient Cd ? 2.5 ± 0.45 was found to exceed that of a bare cable by 65 per cent on average. The Reynolds number range for this drag coefficient was 2.6 × 10³ to 4.2 × 10³ and was determined by force measurements in a flume. It is concluded that the problems of correctly orienting the fairing in the flow, and the true drag coefficient for Reynolds numbers less than about 5 × 10⁴ must be carefully addressed in the design of conventional taut‐line moorings. Drag coefficients found in this study imply that compliant fairings would not be warranted for Reynolds numbers below about 5 × 10⁴ unless strumming was expected for bare cables.     

Early Cretaceous uplift and erosion of the northern Appalachian Basin, New York, based on apatite fission track analysis

The thermal history of outcropping Devonian sediments of the northern Appalachian Basin, New York, has been investigated using fission track analysis of detrital apatites from 57 sandstone samples. Based on lengths and apparent age measurements using fission tracks in apatite it is concluded that Lower Devonian sediments presently at the surface in the Catskill region were cooled rapidly from temperatures higher than about 110°C during Early Cretaceous times (120–140 Ma ago). In the western part of New York (Wellsville-Buffalo) data from late Devonian sediments are consistent with cooling at the same time as that identified for the Catskill region but from lower temperatures, in the range of approximately 80–110°C, the maximum temperature these sediments experienced since deposition. For a pre-uplift paleogeothermal gradient of 25–35°C/km, the confined track length data indicates uplift and erosion of 2–3 km for western New York and greater than 3–4 km for the Catskill region, a differential uplift pattern which is consistent with the historical stratigraphic data from the region. This conclusion is at variance with earlier interpretations put forth by others.Rapid broad scale uplift and erosion of the scale identified imply that large volumes of sediment could have been supplied from the northern Appalachian Basin during the Early Cretaceous. This timing for the dominant post-Devonian cooling phase in the basin is not accounted for by recent models of the tectonic evolution of the Appalachian Orogen but is compatible with the change from carbonate to siliciclastic deposition in the Atlantic coastal plain. It is suggested that this style of broad regional uplift without significant deformation is characteristic of a tectonic regime associated with, and subsequent to, continental rifting.Apatite fission track analysis is shown to be a basic tool in providing fundamental limits for thermal history assessment in regional tectonic problems.     

Measured elastic moduli of single-crystal MgO up to 1800 K

Using the rectangular parallelepiped resonance method we measured the temperature dependence of the adiabatic elastic moduli of single-crystal MgO over the temperature range 300–1800 K. The high temperature limit of our measurements extends by 500 K the upper limit over which elasticity data on MgO are now available. Although our measured temperature dependence of C _ij ^s are generally in good agreement with previous measurements over a more narrow range in temperature, we found that C ₄₄ ^s decreases more rapidly with temperature, for T > 1000 K, than previous studies suggest. We also found that each of the slopes (?C ₁₁ ^s /?T)_p, (?K_s/?T)_p, and (C ₄₄ ^s /?T)_p become less negative with increasing temperature for T > 1400 K. From our measurements on elasticity we are able to confirm that the Grüneisen parameter at zero pressure is nearly constant with temperature up to 1800 K, with only a slight decrease above 1000 K. Utilizing our new data we present calculations showing the temperature dependence of thermodynamic parameters important in studies of earth's interior.     

Effects of F,B2O3 and P2O5 on the solubility of water in haplogranite melts compared to natural silicate melts

The effects of F, B₂O₃ and P₂O₅ on the H₂O solubility in a haplogranite liquid (36 wt. % SiO₂, 39 wt. % NaAlSi₃O₈, 25 wt. % KAlSi₃O₈) have been determined at 0.5, 1, 2, and 3 kb and 800, 850, and 900°C. The H₂O solubility increases with increasing F and B content of the melt. The H₂O solubility increase in more important at high pressure (2 and 3 kb) than at low pressure (0.5 kb). At 2 kb and 800°C, the H₂O solubility increases from 5.94 to 8.22 wt. % H₂O with increasing F content in the melt from 0 to 4.55 wt. %, corresponding to a linear H₂O solubility increase of 0.53 mol H₂O/mol F. With addition of 4.35 wt. % B₂O₃, the H₂O solubility increases up to 6.86 wt. % H₂O at 2 kb and 800°C, corresponding to a linear increase of 1.05 mol H₂O/mol B₂O₃. The results allow to define the individual effects of fluorine and boron on H₂O solubility in haplogranitic melts with compositions close to that of H₂O-saturated thermal minima (at 0.5–3 kb). Although P has a dramatic effect on the phase relations in the haplogranite system, its effect on the H₂O solubility was found to be negligible in natural melt compositions. The concominant increase in H₂O solubility and F can not be interpreted on the basis of the available spectroscopic data (existence of hydrated aluminofluoride complexes or not). In contrast, hydrated borates or more probably boroxol complexes have been demonstrated in B-bearing hydrous melts.     

Determination of part-per-trillion levels of atmospheric dimethyl sulfide by isotope dilution gas chromatography/mass spectrometry

Stable isotopic dilution was applied to the determination of dimethyl sulfide (DMS) in ambient air at the low part-per-trillion by volume (pptrv) levels. Perdeuterated DMS was used as an internal standard in the gas chromatography/mass spectrometry determination. The isotopically labelled internal standard provided insensitivity to possible losses of DMS in sampling and analysis. The lower limit of detection (LLD) was 1 pptrv with a sample acquisition time of 2 min.     

Variograms with zonal anisotropies and noninvertible kriging systems

Zonal anisotropies are usually simply defined as those that are not geometric (i.e., that cannot be removed by an affine transformation). Such anisotropies have often been associated with zonations and models have been proposed to reflect that association. It is shown by example that such models can lead to noninvertible coefficient matrices in kriging systems, because the models are only (conditionally) semidefinite instead of positive definite. The relationship to the construction used in turning bands algorithm and also to spatial-temporal models is discussed.     

Age and paleoclimatic significance of the Stansbury shoreline of Lake Bonneville, Northeastern Great Basin

The Stansbury shoreline, one of the conspicuous late Pleistocene shorelines of Lake Bonneville, consists of tufa-cemented gravel and barrier beaches within a vertical zone of about 45 m, the lower limit of which is 70 m above the modern average level of Great Salt Lake. Stratigraphic evidence at a number of localities, including new evidence from Crater Island on the west side of the Great Salt Lake Desert, shows that the Stansbury shoreline formed during the transgressive phase of late Pleistocene Lake bonneville (sometime between about 22,000 and 20,000 yr B.P.). Tufa-cemented gravel and barrier beaches were deposited in the Stansbury shorezone during one or more fluctuations in water level with a maximum total amplitude of 45 m. We refer to the fluctuations as the Stansbury oscillation. The Stansbury oscillation cannot have been caused by basin-hypsometric factors, such as stabilization of lake level at an external overflow threshold or by expansion into an interior subbasin, or by changes in drainage basin size. Therefore, changes in climate must have caused the lake level to reverse its general rise, to drop about 45 m in altitude (reducing its surface area by about 18%, 5000 km²), and later to resume its rise. If the sizes of Great Basin lakes are controlled by the mean position of storm tracks and the jetstream, which as recently postulated may be controlled by the size of the continental ice sheets, the Stansbury oscillation may have been caused by a shift in the jetstream during a major interstade of the Laurentide ice sheet.     

Estimating Geohydrologic Properties from Borehole-Geophysical Logs

Borehole-geophysical logs can be used to estimate geohydrologic properties based on in situ measurement of rock and water properties. Estimates of properties of both formation and water, such as coefficient of diffusion, formation factor, cementation exponent, hydraulic conductivity, irreducible water content and specific yield can be assessed from borehole-geophysical data and selected algorithms and graphs.
Water properties, such as resistivity, sodium chloride concentration, viscosity and density, can also be estimated using data from borehole-geophysical logs. Water resistivity using the spontaneous-potential method can be estimated if an empirical correction for fresh water is applied.
Estimates of formation properties, such as porosity and permeability, can also be made using borehole-geophysical data.     

The Batu Hijau porphyry copper-gold deposit, Sumbawa Island, Indonesia

The Batu Hijau porphyry Cu---Au deposit lies in southwest Sumbawa Island, Indonesia. It is a world-class porphyry Cu deposit in an island are setting, and is typical of this deposit type in most features, including igneous association, morphology, hydrothermal alteration and mineralisation style.The region was not previously recognised as a porphyry Cu province; disseminated Cu sulphides were first recognised in float samples in southwest Sumbawa in 1987. Associated stream sediment sampling identified a broad area of anomalous Au and Cu in an area of greater than 5 km² around Batu Hijau, including 169 ppb Au in BLEG samples and 580 ppm Cu in stream silts 1 km from the deposit. Mineralisation in bedrock at surface contains > 0.1 wt % Cu and > 0.1 ppm Au over an area of 0.6 km × 1.2 km, including a zone 300 m × 900 m containing > 0.3 wt % Cu. Areas with elevated Mo (> 30 ppm) form a distinctive annulus around this Cu-rich zone.Batu Hijau mineralisation is hosted in a tonalite intrusive complex, and diorite and metavolcanic wallrocks. There are no post-mineralisation igneous intrusions or breccia pipes within the deposit. The main tonalite intrusion forms a stock in the centre of the deposit, where it generally displays intensely pervasive potassic (biotite with magnetite-quartz) alteration and hosts most of the higher grade mineralisation. Younger tonalite dykes intruding the centre of this stock are generally less altered and mineralised than the older tonalite.The core zone of potassic alteration grades outward into extensive propylitic alteration (chlorite-epidote), with both variably overprinted by widespread fracture controlled intermediate argillic alteration (sericite-chlorite), and minor phyllic (sericite-pyrite) and sodic (albite) alteration. Argillic (sericite-kaolinite) and advanced argillic (kaolinite-alunite-pyrophyllite) assemblages occur near surface.Copper and Au grades within the orebody show a positive correlation with quartz stockwork intensity, although disseminated Cu sulphides are also common. Chalcopyrite and bornite are the principle hypogenal minerals, with minor chalcocite. Oxidation extends to a depth of 5 m to 85 m below surface across the deposit, and is underlain by weak supergene mineralisation. Drill testing of the deposit down to 650 m below surface reveals a single cylindrical to conical orebody of 334 million tonnes grading 0.8 wt % Cu and 0.69 gm per tonne Au; the depth extent of mineralisation is unknown.     

The geochemistry of Ca,Sr, Ba and Ra sulfates in some deep brines from the Palo Duro Basin,Texas

The geochemistry of Ca, Sr, Ba and Ra sulfates in some deep brines from the Palo Duro Basin of north Texas, was studied to define geochemical controls on radionuclides such as ⁹⁰Sr and ²²⁶Ra. Published solubility data for gypsum, anhydrite, celestite, barite and RaSO₄ were first reevaluated, in most cases using the ion interaction approach of Pitzer, to determine solubility products of the sulfates as a function of temperature and pressure. Ionic strengths of the brines were from 2.9 to 4.8 m, their temperatures and pressures up to 40°C and 130 bars. Saturation indices of the sulfates were computed with the ion-interaction approach in one brine from the arkosic granite wash fades and four from the carbonate Wolfcamp Formation. All five brines are saturated with respect to gypsum, anhydrite and celestite, and three of the five with respect to barite. All are undersaturated by from 5 to 6 orders of magnitude with respect to pure RaSO₄. ²²⁶Ra concentrations in the brines, which ranged from 10^?11.3 to 10^?12.7 m, are not controlled by RaSO₄ solubility or adsorption, but possibly by the solubility of trace Ra solid solutions in sulfates including celestite and barite.