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\n PI:<\/b> Susumu Honjo and Steve Manganini\n of:<\/b> Woods Hole Oceanographic Institution\n dataset:<\/b> Sediment trap data, biogenic particle fluxes\n dates:<\/b> April 4, 1989 to April 17, 1990\n location:<\/b> N: 48 S: 34 W: -21 E: -21\n project\/cruise:<\/b> North Atlantic Bloom Experiment cruises\n\nNOTES: specific for each trap\n\nTrap #1 at 34N - 21W\nPERIODS 1 THRU 13 TRAP DEPTH = 1071M\nPERIODS 14 THRU 27 TRAP DEPTH = 1248M\nPERIODS 3 THRU 14, RESTRICTED COLLECTION DUE TO PARTIAL CLOGGING OF THE\n SEDIMENT-TRAP APERTURE CAUSED BY A FISH-HEAD.\nPERIOD 14 - NO DATA, MOORING REDEPLOYMENT\nPERIOD 27 - NO DATA, TOTAL CLOGGING OF THE SEDIMENT-TRAP APERTURE DUE TO\n A FISH-HEAD OBSTRUCTION.\n\nTrap #2 at 34N - 21W\nPERIODS 1 THRU 13 TRAP DEPTH = 2067M\nPERIODS 14 THRU 27 TRAP DEPTH = 1894M\nPERIOD 14 - NO DATA, MOORING REDEPLOYMENT\n\nTrap #3 at 34N - 21W\nPERIODS 1 THRU 13 TRAP DEPTH = 4564M\nPERIODS 14 THRU 27 TRAP DEPTH = 4391M\nPERIOD 14 - NO DATA, MOORING REDEPLOYMENT\nPERIODS 9 AND 11 SAMPLES DESTROYED IN TRANSIT\n\nTrap #1 at 48N - 21W\nPERIODS 1 THRU 13 TRAP DEPTH = 1018M\nPERIODS 14 THRU 27 TRAP DEPTH = 1202M\nPERIOD 14 - NO DATA, MOORING REDEPLOYMENT\n\nTrap #2 at 48N - 21W\nPERIODS 1 THRU 13 TRAP DEPTH = 2018M\nPERIODS 14 THRU 27 TRAP DEPTH = 2200M\nPERIOD 14 - NO DATA, MOORING REDEPLOYMENT\nPERIODS 18 THRU 27 NO DATA, SEDIMENT TRAP APERTURE CLOGGED\n\nTrap #3 at 48N - 21W\nPERIODS 1 THRU 13 TRAP DEPTH = 3718M\nPERIODS 14 THRU 27 TRAP DEPTH = 3749M\nPERIOD 14 - NO DATA, MOORING REDEPLOYMENT\n\nReference: Honjo, S and Steven Manganini, 1992. Biogenic Particle Fluxes\nat the 34N 21W and 48N 21W Stations, 1989-1990: Methods and Analytical\nData Compilation. Woods Hole Oceanographic Institution Technical Report\nWHOI-92-15.\n<\/pre>
<\/p>\nSediment Trap Particle Flux data during the North Atlantic Bloom Experiment
\nDr. Susumu Honjo and Dr. Steven J. Manganini\n<\/h2>Woods Hole Oceanographic Institution<\/i><\/p>\n
The following methods documentation was extracted from: <\/p>\n
<\/p>
<\/p>
<\/p>
Two deep ocean mooring arrays were deployed at about 34N (depth
\n to seafloor: 5,261 m and 5,083 m, for phase 1 and 2) and 48N (depth
\n to seafloor: 4,418 m and 4,451 m). Table 1 gives more detailed information
\n on mooring locations, trap depths and names of ships that were used
\n for deployment and recovery. Three PARFLUX Mark 7G-13 time-series
\n sediment traps with 13 rotary collectors on each were deployed on
\n both moorings for a total of 6 traps. At each of the stations, traps
\n were moored at approximately the same depth relative to the surface
\n and the sea- floor (for the deepest trap); 1 km and 2 km from the
\n surface and 0.7 km above bottom. <\/p>\n
\n TABLE 1\n\nSediment Trap deployments, North Atlantic Bloom Exp., Dr. S. Honjo\n\nMooring Stations and Trap Depths \n \nPhase 1: Periods 1 to 13, April 3, 1989 to Sept. 26, 1989 \nPhase 2: Periods 14 to 27, Oct. 16, 1989 to April 16, 1990 \nHiatus : Sept. 26 1989 to Oct 16, 1989\n \n \n 34N 21W Station 48N 21W Station \n Phase 1 Phase 2 Phase 1 Phase 2 \nLatitude 33\u00b049.3'N 33\u00b048.4'N 47\u00b042.9'N 47\u00b043.6'N \nLongitude 21\u00b000.5'W 21\u00b002.2'W 20\u00b052.5'W 20\u00b051.5'W \nBottom Depth ** 5,261 m 5,083 m 4,418 m 4,451 m \n \nTrap Depth 1,070 m 1,248 m 1,018 m 1,202 m \n \" \" 2,067 m 1,894 m 2,018 m 2,200 m \n \" \" 4,564 m 4,391 m 3,718 m 3,749 m \n \nDeployed by R\/V Atlantis II R\/V Endeavor R\/V Atlantis II R\/V Endeavor \nRecovered by R\/V Endeavor RRV Darwin R\/V Endeavor RRV Darwin \n \n** Depths are all corrected values \n\n<\/pre>Arrays were deployed in March and April 1989, recovered and redeployed
\n in September 1989, and totally recovered in April 1990 (Table 1). During
\n the 376-day deployment (including 20 days of hiatus in the middle),
\n each sediment trap was opened and closed 26 times, providing continuous
\n time-series sampling at 14-day intervals, except for two periods. Table
\n 2 lists open\/close schedules for which all the traps were uniformly
\n programmed during the experiment. An independent monitoring mechanism
\n installed with each trap (Honjo and Doherty, 1988) confirmed that the
\n entire program was executed correctly and on schedule. <\/p>\n<\/p>
\n\n TABLE 2 \n \n\nSynchronized Open\/Close Schedule for All Traps \nat the 34N and 48N, 21W Stations\n\nPeriod Mid Date Open\/Close Date Days Open Elapsed Days\n JD* CD* JD* CD* \n \n1 96 04\/06\/89 93 04\/03\/89 5 5\n2 105 04\/15\/89 98 04\/08\/89 14 19\n3 119 04\/29\/89 112 04\/22\/89 14 33\n4 133 05\/13\/89 126 05\/06\/89 14 47\n5 148 05\/29\/89 140 05\/20\/89 17 64\n6 164 06\/13\/89 157 06\/06\/89 14 78\n7 178 06\/27\/89 171 06\/20\/89 14 92\n8 192 07\/11\/89 185 07\/04\/89 14 106\n9 206 07\/25\/89 199 07\/18\/89 14 120\n10 220 08\/08\/89 213 08\/01\/89 14 134\n11 234 08\/22\/89 226 08\/15\/89 14 148\n12 248 09\/05\/89 241 08\/29\/89 14 162\n13 262 09\/19\/89 255 09\/12\/89 14 176\n14 279 10\/06\/89 269 09\/26\/89 20 196 (hiatus)\n15 296 10\/23\/89 289 10\/16\/89 14 210\n16 310 11\/06\/89 303 10\/30\/89 14 224\n17 324 11\/20\/89 317 11\/13\/89 14 238\n18 338 12\/04\/89 331 11\/27\/89 14 252\n19 352 12\/18\/89 345 12\/11\/89 14 266\n20 1 01\/01\/90 359 21\/25\/89 14 280\n21 15 01\/15\/90 8 01\/08\/90 14 294\n22 29 01\/29\/90 22 01\/22\/90 14 308\n23 43 02\/12\/90 36 02\/05\/90 14 322\n24 57 02\/26\/90 50 02\/19\/90 14 336\n25 71 03\/12\/90 64 03\/05\/90 14 350\n26 85 03\/26\/90 78 03\/19\/90 14 364\n27 99 04\/09\/90 92 04\/02\/90 14 378\n\n*CD = Calendar Date; JD = Julien Date\n\n<\/pre><\/li>
Each sediment trap had an aperture of 0.5 m2, covered by baffles
\n with 25mm diameter cells with the aspect ratio of 2.5. The included
\n cone angle was 42 degrees and the structural frame was built of welded
\n titanium The opening and closing of all 6 traps was synchronized with
\n an error of less than one minute. The sample containers, 13 for each
\n trap, were filled with in situ deep sea water were collected by a
\n 30 liter Niskin bottle prior to the deployment. Analytical grade formalin
\n (S. Wakeham; personal communication, 1988) was added to make a 3%
\n solution buffered with 0.1% sodium borate. Each of the 13 sample containers
\n was completely filled with this sea water solution with preservative
\n before the deployment of a trap. Individual sample containers were
\n mechanically sealed from the ambient water before and after each collecting
\n period (Honjo and Doherty, 1988). <\/p>\n<\/li>
The mooring design was based on the PARFLUX Sediment Trap Mooring
\n Dynamics Package that has been used by us since 1979 (Honjo et al.,
\n 1992). A detailed design, parts listing and tension calculation of
\n the NABE mooring array is available in Manganini and Krishfield, 1992,
\n Cruise Report. The arrays were designed to maintain an average of
\n 180 kg of vertical tension throughout the tautline, with a total buoyancy
\n of 1,114 kg that was balanced with a 1,590 kg (in-water weight) cast-iron
\n anchor. Sediment traps were attached to a mooring in-line with three
\n 1-m polyethylene-jacketed bridles. The automatic collection mechanism
\n (Honjo and Doherty, 1988) of the 6 sediment traps worked flawlessly
\n throughout the duration of the experiment and provided us with a total
\n of 156 samples each of which represents an individual key to the time-space
\n matrix for the NABE experiment.\n <\/p><\/li><\/ol>
<\/p>
We measured the pH in supernatant in sample containers immediately
\n after recovery of traps (Manganini and Krishfield, 1992, Cruise Report).
\n Sample containers were then refrigerated on board at approximately
\n 2 to 4 degree C. Particle samples in (original) 250 ml, polyethylene
\n centrifuging sample containers were transported to Woods Hole under
\n refrigeration at approximately 1 to 2 degree C. We identified no swimmers
\n from all samples collected by our experiment. The impact of swimmers,
\n if any, was relatively small; it appears that they were all included
\n with the >1 mm fractions. <\/p>\n<\/li>
In the shore laboratory, first the liquid in a sample container
\n was decanted and then filtered through a 0.45 um pore size Nucleopore
\n filter leaving approximately 1\/3 of the original volume. About 50
\n ml of filtered liquid was then analyzed for total N, NO2, NO3, NH4,
\n P, PO4 and SiO2 using an automatic nutrient analyzer (e.g. Grasshoff
\n et al. 1983). We regarded all excess quantities above the ambient
\n concentration as being dissolved from the trapped particles while
\n stored in situ before the recovery and added to the particle fluxes
\n after being stochastically converted to solids. The remaining liquid
\n in the sampling containers was used as rinse water in the processing
\n of the particulate portion in each specific sample. When additional
\n rinse water was required during the course of analysis, for example,
\n for sample splitting we used filtered and buffered deep Sargasso Sea
\n water containing 3% formalin. <\/p>\n<\/li>
Particle samples were water-sieved through a 1-mm Nitex mesh. This
\n was necessary to maintain precision during splitting of the major
\n portion of the sediment that was 1
\n mm fraction were large aggregates and fragmented gelatinous zooplankton.
\n A sample caught in the 1 mm mesh was then re-suspended in the original
\n seawater, stirred gently and poured onto a grid-printed, 47-mm Nucleopore
\n filter with 2-um pore size, while applying gentle vacuum suction.
\n While a sample on a filter was wet, the filter with the >1 mm fraction
\n was cut into 4 equal pieces along the printed grid by a Teflon-coated
\n blade; each aliquot was then immediately put back into the filtered
\n original water for storage. When a >1 mm sample was too small to split,
\n it was dried and homogenized by pulverization. <\/p>\n
Sediment that passed through the 1 mm mesh was further water- sieved
\n through a 62-um Nitex sieve. Each fraction was split into 1\/4 aliquots
\n and then into 1\/40 aliquots by a rotating wet- sediment splitter with
\n 4 and 10 splitting heads (Honjo, 1980). The average error during the
\n splitting of NABE samples into 4 or 10 aliquots was 3.7% for the \n mm fraction. Wet splitting of the trap-collected sample is justified
\n for multi-disciplinary research including biocoenosis studies. Once
\n particle samples are dried, each becomes inseparable and unidentifiable.
\n Consequently, biocoenosis research such as picking up foraminifera
\n tests or identifying diatom frustules becomes impossible. <\/p>\n<\/li>
Dry mass was determined by weighing two 1\/4 aliquots of >1 mm (whose
\n flux was usually insignificant) and three 1\/10 aliquots of \n on pre-weighed 47 mm, 0.45 um Nucleopore filters. Before weighing,
\n the samples were rinsed 3 times with distilled water, dried in an
\n oven at 60 deg. C for 24 hours and cooled in a desiccator for 4 hours.
\n Total flux was calculated from dry weight of the above aliquots divided
\n by aperture area of the trap and the time it was opened. <\/p>\n<\/li>
The dried sample was pulverized and homogenized, then the two size
\n fractions were recombined proportionally and analyzed with respect
\n to concentrations of: <\/p>\n
\n\n a) Carbonate: as CaCO3\n b) Biogenic Opal\n c) Organic carbon, nitrogen and hydrogen in the decalcified\n fraction\n d) Phosphorus\n\n<\/pre>a) Carbonate content was determined by a method based on a vacuum-gasometric
\n technique developed by Ostermann, et al. (1989). A preweighed sample
\n is introduced into a sealed reaction vessel containing concentrated
\n phosphoric acid. The pressure due to the evolution of CO2 gas is proportional
\n to the carbonate content when calibrated with appropriate standards
\n and was recorded by a transducer. The results were calculated and reported
\n as carbonate percent in the total sample. <\/p>\nb) Biogenic opal was estimated from particulate, reactive Si, selectively
\n leaching decalcified samples in a sodium carbonate solution (Eggimann,
\n et al., 1980) and converting the Si content to SiO2 fluxes. A preweighed
\n sample of approximately 10 mg along with 10 ml of 1 M Na2CO3 was sealed
\n in a Teflon container. The samples were placed in a shaker bath at
\n 90 deg. C for 3 hours and then filtered through a 47-mm-diameter,
\n 0.45 um pore size Nucleopore filter using an all-plastic filtering
\n apparatus. The filtrate at room temperature was neutralized with 0.2
\n N HCl using methyl orange as an indicator. After appropriate dilution,
\n content of Si was determined spectrophotometrically (Strickland and
\n Parsons, 1972). The Si content was then converted to SiO2 and reported
\n as particulate opal flux. <\/p>\nc) Organic carbon, nitrogen and hydrogen were analyzed using a Perkin-Elmer
\n Elemental Analyzer Model 240C. Preweighed samples on precombusted
\n glass fiber filters were decalcified using 1N phosphoric acid. <\/p>\nd) Reactive (biogenic) phosphorus content was determined by the
\n Solorzano and Sharp method that was based on the dissolution of phosphorus
\n by an acid after ashing, using MgSO4 as an oxidant. A preweighed sample
\n was placed into a glass centrifuge tube along with 2 ml of 0.017 M
\n MgSO4 and was dried at 90 degree C. The centrifuge tube containing
\n the sample was ashed at 500 deg. C for 2 hours. After cooling, 5 ml
\n of 0.2 M HCl was added and, with the centrifuge tube capped, was heated
\n at 80 deg. C for 30 min. At room temperature, 5 ml of distilled H2O
\n with one ml of reagent (Strickland and Parsons, 1972) was added and
\n the centrifuge tube was shaken in a vortex shaker, then centrifuged.
\n The concentration of phosphorus was determined spectrophotometrically
\n in the supernatant and the results were reported as particulate phosphorus
\n flux. <\/p>\nUsing the reported method, the lithogenic particles were too small
\n to detect and were usually within the analytical error.\n <\/p><\/li><\/ol>C. Restoration of dissolved components to particulate flux<\/h3>\n
The dissolution of collected particles in a bottle may occur as soon as
\n particles arrive in the bottle while it is open, or later when it is sealed.
\n Assuming that all dissolved portions remained in the recovered bottle, we
\n restored the dissolved components of Si, P and N by analyzing the supernatants
\n in sample bottles. We assumed that the elevated concentration above the
\n sea water initially used to fill the bottles was caused by dissolved components.
\n During the deployment of a trap, the sample bottles were open to the water
\n column only for the duration of collecting periods. While a bottle was open,
\n the bottle water which was placed in the bottle before deployment is exchanged
\n with ambient water. In case the nutrient concentration of the initial bottle
\n water is not equal to that of the ambient water, a correction had to be
\n made; we assumed that one half of the initial water was diluted by the ambient
\n water while the bottle was open. In practice, the effect on calculating
\n particle flux by the difference of nutrients in the initial sea water was
\n within analytical error. <\/p>\n<\/p>
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