Effects of Prudhoe bay crude oil on primary production and zooplankton in arctic tundra thaw ponds

The effects of Prudhoe Bay, Alaska, crude oil on the indigenous phytoplankton and zooplankton of tundra thaw ponds were studied under controlled conditions in situ during the summer of 1976. These effects were compared with uncontrolled oil spills on Pond Omega (a year previously) and Pond E (six years previously). In the uncontrolled spills, the phytoplankton species composition of both ponds remained appreciably different compared with control Pond C, although phytoplankton biomass did not differ greatly. Primary production remained low in Pond Omega but had recovered to control levels in Pond E. In controlled subpond experiments, oil caused a decrease of about 90–100% in primary production in five days but recovered to 40–50% of the control level within fifteen days. During that time, phytoplankton biomass decreased initially but recovered within fifteen days. Oil caused a shift in phytoplankton species composition from a predominance of cryptophytes to chrysophytes. Subponds containing two Daphnia middendorffiana and one Brachinecta paludosa per litre of pondwater were also affected by oil, causing zooplankton death within three or four days. After that time, changes in the phytoplankton species composition were similar to control subponds without zooplankton. Oil toxicity to zooplankton or experimental removal resulted in a loss of grazing pressure which caused the elimination of the cryptophyte Rhodomonas sp. This species was still absent from Pond Omega, but was seen in Pond E for the first time, when zooplankton also reappeared after six years. Oil perturbation of tundra thaw ponds causes a loss of zooplankton and a reduction in primary production. Phytoplankton primary production recovers somewhat but algal species composition remains changed because of the loss of zooplankton grazing pressure and the selective effects of oil.     

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.     

A Benthic Terrain Classification Scheme for American Samoa

Coral reef ecosystems, the most varied on earth, continually face destruction from anthropogenic and natural threats. The U.S. Coral Reef Task Force seeks to characterize and map priority coral reef ecosystems in the U.S./Trust Territories by 2009. Building upon NOAA Biogeography shallow-water classifications based on Ikonos imagery, presented here are new methods, based on acoustic data, for classifying benthic terrain below 30 m, around Tutuila, American Samoa. The result is a new classification scheme for American Samoa that extends and improves the NOAA Biogeography scheme, which, although developed for Pacific island nations and territories, is only applicable to a maximum depth of 30 m, due to the limitations of satellite imagery. The scheme may be suitable for developing habitat maps pinpointing high biodiversity around coral reefs throughout the western Pacific.     

Investigations of the East Greenland continental margin between 70° and 72° N by deep seismic sounding and gravity studies

Results are presented from a deep seismic sounding experiment with the research vessel POLARSTERN in the Scoresby Sund area, East Greenland. For this continental margin study 9 seismic recording landstations were placed in Scoresby Sund and at the southeast end of Kong Oscars Fjord, and ocean bottom seismographs (OBS) were deployed at 26 positions in and out of Scoresby Sund offshore East Greenland between 70° and 72° N and on the west flank of the Kolbeinsey Ridge. The landstations were established using helicopters from RV POLARSTERN. Explosives, a 321 airgun and 81 airguns were used as seismic sources in the open sea. Gravity data were recorded in addition to the seismic measurements. A free-air gravity map is presented. The sea operations — shooting and OBS recording — were strongly influenced by varying ice conditions. Crustal structure 2-D models have been calculated from the deep seismic sounding results. Free-air gravity anomalies have been calculated from these models and compared to the observed gravity. In the inner Scoresby Sund — the Caledonian fold belt region — the crustal thickness is about 35 km, and thins seaward to 10 km. Sediments more than 10 km thick on Jameson Land are of mainly Mesozoic age. In the outer shelf region and deep sea a ‘Moho’ cannot clearly be identified by our data. There are only weak indications for the existence of a ‘Moho’ west of the Kolbeinsey Ridge. Inside and offshore Scoresby Sund there is clear evidence for a lower crust refractor characterised byp-velocities of 6.8–7.3 km s^?1 at depths between 6 and 10 km. We believe these velocities are related to magmatic processes of rifting and first drifting controlled by different scale mantle updoming during Paleocene to Eocene and Late Oligocene to Miocene times: the separation of Greenland/Norway and the separation of the Jan Mayen Ridge/Greenland, respectively. A thin igneous upper crust, interpreted to be of oceanic origin, begins about 50 km seaward of the Liverpool Land Escarpment and thickens oceanward. In the escarpment zone the crustal composition is not clear. Probably it is stretched and attenuated continental crust interspersed with basaltic intrusions. The great depth of the basement (about 5000 m) points to a high subsidence rate of about 0.25 mm yr^?1 due to sediment loading and cooling of the crust and upper mantle, mainly since Miocene time. The igneous upper crust thickens eastward under the Kolbeinsey Ridge to about 2.5 km; the thickening is likely caused by higher production of extrusives. The basementp-velocity of 5.8–6.0 km s^?1 is rather high. Such velocities are associated with young basalts and may also be caused by a higher percentage of dykes. Tertiary to recent sediments, about 5000 m thick, form most of the shelf east of Scoresby Sund, Liverpool Land and Kong Oscars Fjord. This points to a high sedimentation rate mainly since the Miocene. The deeper sediments have a rather high meanp-velocity of 4.5 km s^?1, perhaps due to pre-Cambrian to Caledonian deposits of continental origin. The upper sediments offshore Scoresby Sund are thick and have a rather low velocity. They are interpreted as eroded material transported from inside the Sund into the shelf region. Offshore Kong Oscars Fjord the upper sediments, likely Jurassic to Devonian deposits, are thin in the shelf region but thicken to more than 3000 m in the slope area. The crust and upper mantle structure in the ocean-continent transition zone is interpreted to be the result of the superposition of the activities of three rifting phases related to mantle plumes of different dimensions:

1. the ‘Greenland/Norway separation phase’ of high volcanic activity,
2. the ‘Jan Mayen Ridge/Greenland separation phase’ and
3. the ‘Kolbeinsey Ridge phase’ of ‘normal’ volcanic activity related to a more or less normal mantle temperature.

During period 2 and 3 only a few masses of extrusives were produced, but large volumes of intrusives were emplaced. So the margin between Scoresby Sund and Jan Mayen Fracture Zone is interpreted to be a stretched margin with low volcanic activity.     

Two- and three-dimensional inversions of magnetic anomalies in the MARK area (Mid-Atlantic Ridge 23° N)

Magnetic data collected in conjunction with a Sea Beam bathymetric survey of the Mid-Atlantic Ridge south of the Kane Fracture Zone are used to constrain the spreading history of this area over the past 3 Ma. Two-dimensional forward modeling and inversion techniques are carried out, as well as a full three-dimensional inversion of the anomaly field along a 90-km-long section of the rift valley. Our results indicate that this portion of the Mid-Atlantic Ridge, known as the MARK area, consists of two distinct spreading cells separated by a small, zero-offset transform or discordant zone near 23°10′ N, The youngest crust in the median valley is characterized by a series of distinct magnetization highs which coalesce to form two NNE-trending bands of high magnetization, one on the northern ridge segment which coincides with a large constructional volcanic ridge, and one along the southern ridge segment that is associated with a string of small axial volcanos. These two magnetization highs overlap between 23° N and 23°10° N forming a non-transform offset that may be a slow spreading ridge analogue of the small ridge axis discontinuities found on the East Pacific Rise. The crustal magnetizations in this overlap zone are generally low, although an anomalous, ESE-trending magnetization high of unknown origin is also present in this area. The present-day segmentation of spreading in the MARK area was inherited from an earlier ridge-transform-ridge geometry through a series of small (∼ 10 km) eastward ridge jumps. These small ridge jumps were caused by a relocation of the neovolcanic zone within the median valley and have resulted in an overall pattern of asymmetric spreading with faster rates to the west (14 mm yr⁻¹) than to the east (11 mm yr⁻¹). Although the detailed magnetic survey described in this paper extends out to only 3 Ma old crust, a regional compilation of magnetic data from this area by Schoutenet al. (1985) indicates that the relative positions and dimensions of the spreading cells, and the pattern of asymmetric spreading seen in the MARK area during the past 3 Ma, have characterized this part of the Mid-Atlantic Ridge for at least the past 36 Ma.     

Sodium fluoride ion-pairs in seawater

Laboratory investigations were conducted on the formation of NaF° ion-pairs at the ionic strength of seawater using specific ion electrodes. Sodium and fluoride ion electrodes produced results which are consistent with the ion-pairing model for these ionic interactions. The stoichiometric association constant for NaF°, $\text{K}{}^1{}_{\mathrm{<mtext>NaF</mtext>}}$, was determined at 15, 25, and 35°C. It was assumed that $\text{K}{}^1{}_{\mathrm{<mtext>NaF</mtext>}}$ was a function of temperature, pressure, and ionic strength but not of solution composition. The value for $\text{K}{}^1{}_{\mathrm{<mtext>NaF</mtext>}}$ at 25°C and I = 0.7 m is 0.045 ± 0.006. $\text{K}{}^1{}_{\mathrm{<mtext>NaF</mtext>}}$ increased with decreasing temperature. This result was used to recompute values of $\text{K}{}^1{}_{\mathrm{<mtext>MgF</mtext>}}$ and $\text{K}{}^1{}_{\mathrm{<mtext>CaF</mtext>}}$ accounting for the presence of NaF° ion-pairs. The value for $\text{K}{}^1{}_{\mathrm{<mtext>NaF</mtext>}}$ indicates that 1.1% of the fluoride in seawater is ion-paired with sodium at 25°C and 35‰ salinity. This fraction increases to approximately 2% at the lower temperatures found in the deep ocean. The percentage of free fluoride in natural seawater was measured at 15, 25, and 35°C to verify the speciation calculated from equilibrium constants.     

Hepatic CYP1A levels and EROD activity in English sole: biomonitoring of marine contaminants in Vancouver Harbour

To assess chemical contaminant stress in the marine environment, ethoxyresorufin-O-deethylase (EROD) activity and cytochrome P450 1A (CYP1A) expression were measured in 88 English Sole (Pleuronectes vetulus) collected during May and June 1999 from four sites in Vancouver Harbour and at an expected reference site outside the harbour. Hepatic microsomes were prepared from the fish and analyzed for total CYP content, EROD activity, and CYP1A protein levels. Hepatic EROD activity and CYP1A protein levels were elevated in fish from two sites in the inner harbour. A comparison with sediment chemistry data showed that fish with increased EROD activity and CYP1A levels came from sites containing relatively high levels of polycyclic aromatic hydrocarbons and polychlorinated biphenyls. Unexpectedly high levels of EROD activity and CYP1A protein were also found in fish from a reference site near Gibsons, in Howe Sound. The elevated EROD activity and CYP1A expression in fish from this site cannot be explained by the chemical analysis data collected.