*2018/06/20 10:16:27.99 *IOS HEADER VERSION 1.10 2011/10/26 2011/10/26 *FILE START TIME : UTC 2018/02/20 22:39:44.000 TIME INCREMENT : 0 0 0 0.416667E-01 0 ! (day hr min sec ms) NUMBER OF RECORDS : 2 DATA DESCRIPTION : Bottle:Rosette:Up:Stop + CTD:Up FILE TYPE : ASCII CRC : A7E7C59D NUMBER OF CHANNELS : 23 $TABLE: CHANNELS ! No Name Units Minimum Maximum !--- ----------------------------------- --------------- -------------- -------------- 1 Sample_Number n/a 33 34 2 Bottle_Number n/a 1 2 3 Bottle:Firing_Sequence n/a 1 2 4 Pressure:CTD dbar 5.1 5.1 5 Temperature:CTD deg_C_(ITS90) 8.5188 8.5208 6 Salinity:CTD PSS-78 31.128 31.1308 7 Sigma-t:CTD kg/m^3 24.1856 24.1875 8 Transmissivity:CTD %/m 42.1 42.3 9 Oxygen:Dissolved:CTD:Volume ml/l 6.72 6.73 10 Oxygen:Dissolved:CTD:Mass µmol/kg 292.9 293.3 11 Fluorescence:CTD:Seapoint mg/m^3 0.76 0.772 12 PAR:CTD µE/m^2/sec 40.6 40.8 13 Salinity:Bottle PSS-78 31.1229 31.1229 14 Flag:Salinity:Bottle n/a 15 Nitrate_plus_Nitrite:Bottle µmol/l 8.02 8.02 16 Flag:Nitrate_plus_Nitrite:Bottle n/a 17 Phosphate:Bottle µmol/l 0.746 0.746 18 Flag:Phosphate:Bottle n/a 19 Silicate:Bottle µmol/l 17.32 17.32 20 Flag:Silicate:Bottle n/a 21 Chlorophyll:Extracted:Bottle mg/m^3 0.72 0.72 22 Flag:Chlorophyll:Extracted:Bottle n/a 23 Phaeo-Pigment:Extracted:Bottle mg/m^3 0.62 0.62 $END $TABLE: CHANNEL DETAIL ! No Pad Start Width Format Type Decimal_Places !--- ---- ----- ----- ------ ---- -------------- 1 -99 ' ' 5 I I 0 2 -99 ' ' 3 I I 0 3 -99 ' ' 3 I I 0 4 -99 ' ' 7 F ' ' 1 5 -99 ' ' 9 F ' ' 4 6 -99 ' ' 9 F ' ' 4 7 -99 ' ' 9 F R4 4 8 -99 ' ' 6 F ' ' 1 9 -99 ' ' 7 F ' ' 2 10 -99 ' ' 6 F ' ' 1 11 -99 ' ' 8 F ' ' 3 12 -99 ' ' 7 F ' ' 1 13 -99 ' ' 9 F R4 4 14 0 ' ' 3 NQ C ' ' 15 -99 ' ' 7 F R4 2 16 0 ' ' 3 NQ C ' ' 17 -99 ' ' 8 F R4 3 18 0 ' ' 3 NQ C ' ' 19 -99 ' ' 7 F R4 2 20 0 ' ' 3 NQ C ' ' 21 -99 ' ' 7 F R4 2 22 0 ' ' 3 NQ C ' ' 23 -99 ' ' 7 F R4 2 $END *ADMINISTRATION MISSION : 2018-001 AGENCY : IOS, Ocean Sciences Division, Sidney, B.C. COUNTRY : Canada PROJECT : Line P SCIENTIST : Robert M. PLATFORM : Sir Wilfrid Laurier *LOCATION GEOGRAPHIC AREA : North-East Pacific STATION : P3 EVENT NUMBER : 18 LATITUDE : 48 37.58000 N ! (deg min) LONGITUDE : 126 20.07000 W ! (deg min) WATER DEPTH : 780 *INSTRUMENT TYPE : Sea-Bird CTD MODEL : SBE-911plus SERIAL NUMBER : 1222 *COMMENTS Sample Number 33: SAL:Bottle - mistakenly recorded as sample 35. Sample is most likely the missing sample 33. Analysis methods: ----------------- Salinity samples were collected in 200 ml type ll glass bottles with disposable nylon inserts and screw caps supplied by Ocean Scientific International Limited. They were analyzed in a temperature-controlled lab on a Guildline 8400B Salinometer standardized with IAPSO standard seawater within 13 - 30 days after collection. For details on duplicate analysis see file 2018-001_SAL.pdf. Oxygen samples were analyzed at sea using an automated Winkler titration system (Metrohm Dosimat model 876 and a UV light source and detector with a 365nm filter controlled by LV02_876 software designed and constructed by Scripps Institution of Oceanography) with modifications based on Carpenter (1965) and adhering to WOCE protocols (Culberson 1991). For details on duplicate analysis see file 2018-001_OXY.pdf. Nutrient samples were collected in plastic tubes. One set of samples was collected and immediately quick frozen in aluminum blocks stored in -20 freezer. Another set of samples from 400 dbar and deeper (to be used for silicate analysis) was collected and stored at 4C in the dark. All samples were returned to IOS for analysis using an Astoria analyzer following methods described in IOS Nutrient Methods (1996) Barwell-Clarke and Whitney. For precision and duplicate analysis see file 2018-001_NUT.pdf. Chlorophyll samples were filtered onto 25mm GF/F filters and stored in glass scintillation vials at -80C prior to analysis. Samples were extracted in 90% acetone at -20C for 24 hours and analyzed on a Turner 10AU fluorometer calibrated with commercially pure chlorophyll a standard (Sigma). Fluorescence readings taken before and after acidification were used to calculate chlorophyll and phaeopigment concentrations (Holm-Hansen et al 1965). Chlorophyll samples were analyzed at IOS ~4 weeks after the cruise. When duplicate samples were collected the average of two samples is reported. Variability is assessed as the CV% (std dev / mean*100). Flags and comments apply to chlorophyll values only. No flags or comments are assigned for Phaeopigment values. Precision Statement: Chlorophyll values ranged from 0.01-8.51 µg/l. Average %CV for this cruise was 3.86% with 3 out of 56 duplicate pairs having a CV > 10% and 0 out of 56 duplicate pairs having a CV > 30%. Our average dataset %CV is 3.73% for 2013 - 2017 so the overall quality of this dataset is very good. For details on duplicates see file 2018-001_CHL.pdf. DMS samples were collected in 250 ml ground glass stoppered bottles and stored in a fridge, in the dark and removed one at a time before analysis. A sample was loaded onto the stripper and purged with UHP Nitrogen for 10 minutes at ~100 ml/min. The DMS was extracted from the water and absorbed on to a Tenax TA trap kept at -80C. The trap was subsequently desorbed at 100C (with a Dewar containing boiling water) onto a Chromasorb 330 column which eluted onto a Flame Photometric Detector (FPD). All samples were run as soon as possible after being collected. The minimum detectable level for DMS is 0.10 nmol/l, so “0” values should be interpreted as < 0.1 nmol/l. For more details see file 2018-001_DMS_report.pdf and for duplicate analysis see 2018-001_DMS.pdf. DMSP-D: 20-75 ml of seawater were allowed to flow directly from the Niskin into a magnetic filtration funnel containing a 0.7 µm GF/F filter. The first 3.5 ml were collected in a polypropylene tube containing 50 µl of a 50% sulphuric acid solution. DMPS-T: 3.5 ml of seawater were collected directly from the Niskin into a polypropylene tube containing 50 µl of a 50% sulphuric acid solution. DMSP-D and DMSP-T: Samples were stored in the dark at 4 degrees C for a minimum of 24 hours. They were hydrolized and analyzed later at the Institute of Ocean Sciences. The minimum detectable level is 0.1 nmol/l, so “0” values should be interpreted as < 0.1 nmol/l. For more details see file 2018-001_DMS_report.pdf. References: 1. Holm-Hansen, O., Lorenzen, C.J., Holmes, R.W., and Strickland J.D.H. 1965. Fluorometric Determination of Chlorophyll. J.du Cons. Intl. Pour l’Epl. De la Mer. 30:3-15. 2. Carpenter, J.H. 1965. The Chesapeake Bay Institute Technique for the Winkler Dissolved Oxygen Method. Limmnol. & Oceanogr., 10: 141-143. 3. Culberson, C.H. 1991. Dissolved oxygen. WOCE Hydrographic Programme Operations and Methods (July 1991). 15pp. 4. Barwell-Clarke, J. and Whitney, F. 1996. Institute of Ocean Sciences Nutrient Methods and Analysis. Canadian Technical Report of Hydrography and Ocean Sciences, No. 182, 43 pp. Data Processing Notes: ---------------------- Transmissivity, Fluorescence and PAR data are nominal and unedited except that some records were removed in editing temperature and salinity. NOTE: While the Fluorescence:CTD data are expressed in concentration units, they do not always compare well to extracted chlorophyll samples, particularly for casts far from shore. It is recommended that users check extracted chlorophyll values where available. Oxygen:Dissolved:CTD was calibrated using the method described in Sea-Bird Application Note #64-2, June 2012 revision (Sea-Bird_64-2_Jun2012.pdf), except that a small offset in the fit was allowed. For details on the processing see the report: 2018-001-proc.pdf. $REMARKS Quality flags have the following significance: ---------------------------------------------------------------------------------- 0 = Acceptable measurement with no header comment. 1 = Sample for this measurement was collected but not analyzed. Sample lost. 2 = Acceptable measurement with header comment. 3 = Questionable measurement (probably good). 4 = Poor measurement (probably bad). 5 = Measurement not reported (bad). 6 = Mean of replicate measurements. 7 = Manual chromatographic peak measurement. 8 = Irregular digital chromatographic peak integration. 9 = Sample was planned for this measurement from this bottle but was not collected. ----------------------------------------------------------------------------------- $END !-1-- 2- 3- --4--- ---5---- ---6---- ---7---- --8-- --9--- --10- ---11-- --12-- ---13--- 14 --15-- 16 ---17-- 18 --19-- 20 --21-- 22 --23-- !Samp Bo Bo Pressu Temperat Salinity Sigma-t: Trans Oxygen Oxyge Fluores PAR: Salinity Fl Nitrat Fl Phospha Fl Silica Fl Chloro Fl Phaeo- !le_ tt tt re:CTD ure:CTD :CTD CTD missi :Disso n:Dis cence: CTD :Bottle ag e_plus ag te: ag te: ag phyll: ag Pigmen !Numb ~u ~u vity: lved: solve CTD: ~o _Nitri ~o Bottle ~o Bottle ~o Extrac ~o t:Extr !er mb en CTD CTD: d:CTD Seapoin tt te: tt tt tt ted: tt acted: ! er ce Volume :Mass t le Bottle le le le Bottle le Bottle !---- -- -- ------ -------- -------- -------- ----- ------ ----- ------- ------ -------- -- ------ -- ------- -- ------ -- ------ -- ------ *END OF HEADER 34 2 2 5.1 8.5188 31.1280 24.1856 42.1 6.72 292.9 0.772 40.6 -99.0000 0 -99.00 0 -99.000 0 -99.00 0 -99.00 0 -99.00 33 1 1 5.1 8.5208 31.1308 24.1875 42.3 6.73 293.3 0.760 40.8 31.1229 3 8.02 0 0.746 0 17.32 0 0.72 6 0.62