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Von Herzen, R. P., Robinson, P. T., et al., 1991 Proceedings of the Ocean Drilling Program, Scientific Results, Vol. 118 7. GEOCHEMISTRY AND MINERALOGY OF SEDIMENTS, ATLANTIS II FRACTURE ZONE, SOUTHWEST INDIAN OCEAN 1 Eileen Van der Flier-Keller 2 ABSTRACT Thirteen sediment samples, including calcareous ooze, sandy clay, volcanic sand, gravel, and volcanic breccia, from Ocean Drilling Program (ODP) Sites 732B, 734B, 734G and Conrad Cruise 27-9, Station 17, were examined. Contents of major and trace elements were determined using XRF or ICP (on samples <0.5 g). Determinations of rare earth elements (REE) were performed using ICP-MS. Mineralogy was determined using XRD. On the basis of the samples studied, the sediments accumulating in the Atlantis II Fracture Zone are characterized by generally high MgO, Cr, and Ni contents compared with other deep-sea sediments. A variety of sources are reflected in the mineralogy and geochemistry of these sediments. Serpentine, brucite, magnetite, and high MgO, Cr, and Ni contents indicate derivation from ultramafic basement. The occurrence of albite, analcime, primary mafic minerals, and smectite/chlorite in some samples, coupled with high SiO 2 , A1 2 O 3 , TiO 2 , Fe 2 O 3 , V, and Y indicate contribution from basaltic basement. A third major sediment source is characterized as biogenic material and is reflected primarily in the presence of carbonate minerals, and high CaO, Sr, Pb, and Zn in certain samples. Kaolinite, illite, quartz, and some chlorite are most likely derived from continental areas or other parts of the ocean by long-distance sediment transport in surface or other ocean currents. Proportions of source materials in the sediments reflect the thickness of the sediment cover, slope of the seafloor, and the nature of and proximity to basement lithologies. REE values are low compared to other deep-sea sediments and indicate no evidence of hydrothermal activity in the Atlantis II Fracture Zone sediments. This is supported by major- and trace-element data. INTRODUCTION Fracture zones are ubiquitous features in all ocean basins; however, little is known regarding their sediment characteris- tics. Representative samples of major sediment types from the Atlantis II Fracture Zone were taken at ODP Sites 732B, 734B, 734G, and during Conrad Cruise 27-9, Station 17, to study the geochemical and mineralogical properties of sedi- ments occurring in this tectonic setting. The purpose of this research is (1) to characterize the Atlantis II Fracture Zone sediments by mineralogy and compositions of major and trace elements, (2) to isolate characteristics that are unique to the fracture-zone environment by comparison with other parts of the Indian Ocean and elsewhere, (3) to determine sources and associations of components in the sediments, and (4) to examine the evidence for hydrothermal influences on the sediments using REE data. The Atlantis II Fracture Zone is one of several major transform faults that offset the slow-spreading (approximately 0.8 cm/yr [Fisher and Sclater, 1983]) Southwest Indian Ridge. The transform has an offset of approximately 210 km, trends approximately north-south, and has substantial relief (on the order of 5800 m). Although the walls of the valley are steep, typically 30° to 40°, more subdued slopes exist locally. The sediment cover on the valley walls generally is thin (less than 10 m), irregular, or nonexistent (Robinson, Von Herzen, et al., 1989). A median ridge bisects the valley and is covered with sediment and rubble of varying thickness. Two isolated sediment ponds were identified on the fracture-zone floor north of the transform (Conrad Cruise 27-9). Rubble compo- sition is dominated by serpentinized peridotites, basalt, dia- 1 Von Herzen, R. P., Robinson, P. T., et al., 1991. Proc. ODP, Sci. Results, 118: College Station, TX U.S.A. (Ocean Drilling Program). 2 Department of Geography, University of Victoria, P.O. Box 1700, Victo- ria, British Columbia V8W 2Y2. base, and subsidiary gabbro, greenstone, amphibolite, and sedimentary rock. SAMPLES Thirteen sediment samples (Table 1) from the Atlantis II Fracture Zone were examined. Samples were taken from Hole 732B (Core 1 at 32°32.81'S, 57°03.289'E), Hole 734B (Core 1 at 32°06.82'S, 57°07.80'E), Hole 734G (Core 3 at 32°06.87'S, 57°08.24'E) and from the Conrad Cruise 27-09, Station 17 (pilot Core 1 at 31°34.l'S, 57°08.4'E). Site 732 is located on top of the median tectonic ridge, on a flat surface near the slope break and ridge crest. The ridge crest is covered by up to 5 m of soft sediment overlying sand and coarse bouldery gravel. Site 734 is on the east wall of the transform fault, on a steep (25° to 35°), straight slope that exhibits no evidence of slump- ing or landsliding (Robinson, Von Herzen, et al., 1989, p.78). Sediment at this site consists of rubble, breccia, and sand overlain by foraminiferal ooze. Sediment sections 80 cm and 6 m long were recovered at Holes 734B and 734G, respectively. Station 17 of Conrad Cruise 27 is located in a sediment basin (4.5 to 5 km water depth and 10 to 20 km wide) on the east flank of the Atlantis II Fracture Zone. All samples analyzed in this study were retrieved from within 150 cm of the sediment surface, most commonly from the top 30 cm of the sediment column (Table 1). Sediment ages, on the basis of calcareous nannofossil biomarkers, are middle Pleistocene (Core 118- 732B-1H), Holocene (Core 118-734B-1H), and early Pleis- tocene (Core 118-734G-1H) (Robinson, Von Herzen, et al., 1989). The samples are representative of the range of sediment types encountered in this fracture zone and include calcareous (foraminiferal) ooze, sandy clay, volcanic sand (fine and coarse), gravel, and volcanic breccia. METHODS All samples were washed with distilled water prior to analysis. Eight samples were split into <62 μm and >62 μm size fractions. The mud was separated after freeze drying, 145
Transcript
Page 1: 7. GEOCHEMISTRY AND MINERALOGY OF … › publications › 118_SR › VOLUME › CHAPTERS › s…GEOCHEMISTRY AND MINERALOGY OF SEDIMENTS, ATLANTIS II FRACTURE ZONE, SOUTHWEST INDIAN

Von Herzen, R. P., Robinson, P. T., et al., 1991Proceedings of the Ocean Drilling Program, Scientific Results, Vol. 118

7. GEOCHEMISTRY AND MINERALOGY OF SEDIMENTS, ATLANTIS II FRACTURE ZONE,SOUTHWEST INDIAN OCEAN1

Eileen Van der Flier-Keller2

ABSTRACT

Thirteen sediment samples, including calcareous ooze, sandy clay, volcanic sand, gravel, and volcanic breccia,from Ocean Drilling Program (ODP) Sites 732B, 734B, 734G and Conrad Cruise 27-9, Station 17, were examined.Contents of major and trace elements were determined using XRF or ICP (on samples <0.5 g). Determinations ofrare earth elements (REE) were performed using ICP-MS. Mineralogy was determined using XRD.

On the basis of the samples studied, the sediments accumulating in the Atlantis II Fracture Zone arecharacterized by generally high MgO, Cr, and Ni contents compared with other deep-sea sediments. A variety ofsources are reflected in the mineralogy and geochemistry of these sediments. Serpentine, brucite, magnetite, andhigh MgO, Cr, and Ni contents indicate derivation from ultramafic basement. The occurrence of albite, analcime,primary mafic minerals, and smectite/chlorite in some samples, coupled with high SiO2, A12O3, TiO2, Fe2O3, V, andY indicate contribution from basaltic basement. A third major sediment source is characterized as biogenic materialand is reflected primarily in the presence of carbonate minerals, and high CaO, Sr, Pb, and Zn in certain samples.Kaolinite, illite, quartz, and some chlorite are most likely derived from continental areas or other parts of the oceanby long-distance sediment transport in surface or other ocean currents. Proportions of source materials in thesediments reflect the thickness of the sediment cover, slope of the seafloor, and the nature of and proximity tobasement lithologies. REE values are low compared to other deep-sea sediments and indicate no evidence ofhydrothermal activity in the Atlantis II Fracture Zone sediments. This is supported by major- and trace-elementdata.

INTRODUCTION

Fracture zones are ubiquitous features in all ocean basins;however, little is known regarding their sediment characteris-tics. Representative samples of major sediment types from theAtlantis II Fracture Zone were taken at ODP Sites 732B,734B, 734G, and during Conrad Cruise 27-9, Station 17, tostudy the geochemical and mineralogical properties of sedi-ments occurring in this tectonic setting. The purpose of thisresearch is (1) to characterize the Atlantis II Fracture Zonesediments by mineralogy and compositions of major and traceelements, (2) to isolate characteristics that are unique to thefracture-zone environment by comparison with other parts ofthe Indian Ocean and elsewhere, (3) to determine sources andassociations of components in the sediments, and (4) toexamine the evidence for hydrothermal influences on thesediments using REE data.

The Atlantis II Fracture Zone is one of several majortransform faults that offset the slow-spreading (approximately0.8 cm/yr [Fisher and Sclater, 1983]) Southwest Indian Ridge.The transform has an offset of approximately 210 km, trendsapproximately north-south, and has substantial relief (on theorder of 5800 m). Although the walls of the valley are steep,typically 30° to 40°, more subdued slopes exist locally. Thesediment cover on the valley walls generally is thin (less than10 m), irregular, or nonexistent (Robinson, Von Herzen, etal., 1989). A median ridge bisects the valley and is coveredwith sediment and rubble of varying thickness. Two isolatedsediment ponds were identified on the fracture-zone floornorth of the transform (Conrad Cruise 27-9). Rubble compo-sition is dominated by serpentinized peridotites, basalt, dia-

1 Von Herzen, R. P., Robinson, P. T., et al., 1991. Proc. ODP, Sci.Results, 118: College Station, TX U.S.A. (Ocean Drilling Program).

2 Department of Geography, University of Victoria, P.O. Box 1700, Victo-ria, British Columbia V8W 2Y2.

base, and subsidiary gabbro, greenstone, amphibolite, andsedimentary rock.

SAMPLESThirteen sediment samples (Table 1) from the Atlantis II

Fracture Zone were examined. Samples were taken from Hole732B (Core 1 at 32°32.81'S, 57°03.289'E), Hole 734B (Core 1 at32°06.82'S, 57°07.80'E), Hole 734G (Core 3 at 32°06.87'S,57°08.24'E) and from the Conrad Cruise 27-09, Station 17(pilot Core 1 at 31°34.l'S, 57°08.4'E). Site 732 is located on topof the median tectonic ridge, on a flat surface near the slopebreak and ridge crest. The ridge crest is covered by up to 5 mof soft sediment overlying sand and coarse bouldery gravel.Site 734 is on the east wall of the transform fault, on a steep(25° to 35°), straight slope that exhibits no evidence of slump-ing or landsliding (Robinson, Von Herzen, et al., 1989, p.78).Sediment at this site consists of rubble, breccia, and sandoverlain by foraminiferal ooze. Sediment sections 80 cm and 6m long were recovered at Holes 734B and 734G, respectively.Station 17 of Conrad Cruise 27 is located in a sediment basin(4.5 to 5 km water depth and 10 to 20 km wide) on the eastflank of the Atlantis II Fracture Zone. All samples analyzed inthis study were retrieved from within 150 cm of the sedimentsurface, most commonly from the top 30 cm of the sedimentcolumn (Table 1). Sediment ages, on the basis of calcareousnannofossil biomarkers, are middle Pleistocene (Core 118-732B-1H), Holocene (Core 118-734B-1H), and early Pleis-tocene (Core 118-734G-1H) (Robinson, Von Herzen, et al.,1989). The samples are representative of the range of sedimenttypes encountered in this fracture zone and include calcareous(foraminiferal) ooze, sandy clay, volcanic sand (fine andcoarse), gravel, and volcanic breccia.

METHODSAll samples were washed with distilled water prior to

analysis. Eight samples were split into <62 µm and >62 µmsize fractions. The mud was separated after freeze drying,

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E. VAN DER FLIER-KELLER

Table 1. Location and lithology of sediment samples.

Sample

AFZ4AFZ10AFZ5AFZ11AFZ12AFZ1AFZ2AFZ13AFZ6AFZ7AFZ3AFZ8AFZ9

Lithologicdescription

Volcanic sandGravel and oozeSandy clayGravelCoarse sandForaminiferal oozeForaminiferal oozeFine sandCalcareous oozeForaminiferal oozeVolcanic brecciaCalcareous oozeCalcareous ooze

Core, section

118-732B-1H118-732B-1H118-732B-1H118-732B-1H118-732B-1H118-734B-1H118-734B-1H118-734B-1H118-734G-3H118-734G-3H118-734G-3HRC27-9 17 1RC27-9 17 1

Interval(cm)

18-2485-94

114-117142-146146-150

3-413-1525-28

1-25-6

16-170-55

Percentage

>62 µm

28

7993

128989

11

<62 µm

72

217

8811119999

washing, sonication for 60 s, and wet sieving. The fines werecentrifuged to remove salt, then freeze dried after washing.The sand was collected and dried at 80°C. Weights of thesefractions are listed in Table 1. Where necessary, samples werecrushed to -200-mesh size using a tungsten carbide Bluellerbefore splitting into separate fractions for geochemical andmineralogical analyses. Major and trace elements were ana-lyzed by X-ray fluorescence (XRF). Because of the originalsmall size of a number of the split samples, particularly fromthe finer-grained clay and ooze intervals, the final amount ofmaterial available for geochemical and mineralogical analyseswas small. Where samples were smaller than 0.5 g (minimumsample size for XRF), major and trace elements were ana-lyzed by inductively coupled plasma spectroscopy (ICP) fol-lowing total digestion (samples AFZ 1, 2, 3, 7, 5S, and 6S).REE abundances were determined for these samples usingICP-mass spectrometry (MS). Precision of XRF analyses onthe basis of duplicate measurements range from 0% to 7% formajor elements, except for sodium (Na2O), which was 65%.

Precision of trace-element values ranges from 2% to 14%,except for cobalt (Co), chromium (Cr), vanadium (V), andyttrium (Y), which was 43% to 59%. Co and Cr levels aresignificantly lower in the duplicate samples than in the major-ity of other samples. Mineralogy was determined using X-raydiffraction (XRD). Scans were run on whole-round samples,or where insufficient sample was available, on either the <62or >62 µm fractions. In addition, <2 µm fractions of samplesAFZ8 and AFZ9 were separated and analyzed specifically foridentification of clay minerals, i.e., untreated, following gly-colation, and following heating to 375° and 550°C, respec-tively.

RESULTS AND DISCUSSION

MineralogyQualitative mineral contents of the samples (or sample

splits, as indicated) are given in Table 2. A wide range ofigneous, metamorpnic, and sedimentary minerals is present,

Table 2. Mineralogy of sediment samples, Atlantis II Fracture Zone.

Sample

AFZ4AFZ 10

aAFZ5AFZ 11AFZ 12

bAFZlbAFZ2

AFZ13

aAFZ6

bAFZ7bAFZ3aAFZ8aAFZ9

Se

XXXX

XX

XXXXX

XXX

XXX

XX

XXXXXX

AFZ8 <2 µm

AFZ9

Ch

XX

X

X

XX

Sm

XXX

X

X

X

Ca

XXX

XXXXX

XXX

XXXXXXXXXXXX

Ar

XXXXX

XXX

XXXX

Qt

XXX

X

XXXXXX

XX

Al

XXXXXX

XXXXXXXX

XX

Tr

XXXXX

XXXX

XX

X

X

XXXX

En

XX

XXX

XXX

XXXX

Di

XXXX

XXXXX

An

XXXX

XXXXX XBr

XMgXBrXXMgXIIXBrXXMgXMgXBaXBr

XKaXIIXKaXII

a <62 µm fraction.b >62 µm fraction.XXX = abundant, XX = common, X = trace.Se = Serpentine; Al = Albite; Mg = Magnetite; Ch = Chlorite; Tr = Hornblende; II Illite; Sm = Smectite/Ch;En = Enstatite; Ba = Barite Ca = Calcite; Di = Diopside/Augite; Ar = Aragonite; An = Analcime; Ka = Kaolinite;Qt = Quartz; Br = Brucite.

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GEOCHEMISTRY AND MINERALOGY, ATLANTIS II FRACTURE ZONE

reflecting the contribution from a variety of sources. Smectiteand chlorite are the most common clay minerals; however,traces of illite and kaolinite were determined in samples AFZ8 and AFZ 9 (<2 µm fractions). The latter was identified bythe presence of an XRD peak at approximately 10 Å, and abroad peak at 7.15 Å, which became asymmetrical on glyeo-lation, then disappeared when heated to 550°C and is thoughtto correspond to the presence of poorly crystallized orpartially disordered kaolinite. Mixed-layer smectite-chloritewas identified as a broad peak from 12 to 15 Å, whichexpanded slightly upward on glycolation and collapsed to 10Å when heated (Samples AFZ 8 and AFZ9). Peaks attributedto chlorite occurred at 7.15 and 3.52 Å.

Samples from Hole 732B typically contain plagioclase(albite), amphibole (tremolite or hornblende), clinopyroxene(diopside and/or augite), orthopyroxene (enstatite), serpentine(lizardite and chrysotile), analcime, and commonly smectite/chlorite and chlorite. By contrast, samples from Holes 734Band 734G contain mainly serpentine, calcite, aragonite, am-phibole, orthopyroxene, and chlorite in both the <62 and >62µm fractions. Trace quantities of brucite and magnetite arealso common in these samples. The most restricted mineral-ogy (calcite and quartz, with traces of smectite/chlorite,plagioclase, kaolinite, and illite) occurs in the Conrad 27-9ooze samples. Vertical changes in mineralogy within any onecore may be related primarily to lithology and the size fractionof the sample examined. However, in Hole 732B, similarlithologies show stratigraphic variations in mineralogy. Chlo-rite and smectite abundances decrease with depth, whileserpentine is most abundant in the deepest sample.

Sources of the minerals noted in the fracture-zone sedi-ments include (1) the immediate basement, (2) biogenic com-ponents, and (3) long-distance sediment transport from conti-nental areas and other parts of the ocean.

1. Weathered, altered, and eroded basalt, diabase, andlesser peridotite are the likely primary source rocks at Hole732B, while serpentinized peridotite may be the dominantsource for sediments at Holes 734B and 734G. Mineralsdirectly contributed from this source include primary igneousminerals, in addition to in-situ hydro thermal weathering prod-ucts, such as serpentine, brucite, and magnetite (peridotiteassemblage) and smectite-chlorite, albite, and analcime (ba-salt assemblage). On the basis of mineralogy, the ultramaficcomponent is most important in sediments from Holes 734Band 734G, while minerals present in sediments from Hole732B are mainly derived from basaltic material.

2. Foraminiferal tests are thought to constitute the mainsource for the carbonate minerals. Water depths at Holes732B, 734B, 734G, and Conrad 27-9 are 4878.3, 3670.4,3417.4, and 4500 to 5000 m, respectively (Robinson, VonHerzen, et al., 1989). Local carbonate compensation depth(CCD) has been estimated as 4800 m in this latitudinal zone(Kolla et al., 1976). Some dissolution of nannofossil calcitethus may have occurred in sediments from Cores 118-732B-1H and Conrad 27-9. Minor amounts of calcite may alsobe derived from altered igneous fragments.

3. High levels of kaolinite and quartz were found in theMadagascar Basin compared with other parts of the westernIndian Ocean (Venkatarathnam et al., 1976; Venkatarathnamand Biscaye, 1977). Madagascar has been proposed as a likelysource area for these minerals. It is probable that the kaoliniteand quartz present in the Atlantis II Fracture Zone sedimentsalso derived from Madagascar, possibly by surface or otherocean currents. Chlorite and illite contents are high in thesouthern part of the southwest Indian Ocean-Antarctic region(Venkatarathnam et al., 1976). The presence of these minerals

in the Atlantis II Fracture Zone may indicate derivation fromthe Antarctic region (Rateev et al., 1969) via the Antarcticbottom-water current (AABW). Some smectite may havederived from the Crozier Basin to the east and south by theAABW; however, it most likely was locally formed. Basementand biogenous sources appear to be volumetrically the mostimportant contributers to the fracture-zone sediments, espe-cially as the circulation within the fault and access to majorocean currents would be expected to be low, given theelevated topography, rugged steep slopes, and localized flowof the AABW through the Southwest Indian Ridge (Warren,1978). Where the sediment cover is thin, the basement sourcemay be most important, while in sediment ponds (such as thatfrom which Samples AFZ8 and AFZ9 were taken), the biog-enous and long-distance contributions are higher.

Geochemistry

Results of geochemical analyses are listed in Table 3.Contents of major and trace elements are reported as ana-lyzed, not on a carbonate-free basis. REE results of sixsamples are presented in Table 4. Because of the smallnumbers of samples examined in this study, only generaltrends were observed.

Great variability exists in the contents of both major andtrace elements in the samples. For example, contents ofmagnesium (MgO) vary from 1.25% to 29.95%; calcium(CaO), from 4.57% to 37.20%; Cr, from 28 to 2460 ppm; andnickel (Ni), from 41 to 793 ppm. This variability largelyreflects changes in sediment mineralogy caused by differencesin proportions of igneous and biogenic material. In addition,certain samples have been anomalously enriched in specificelements, for example, lead (Pb) and zinc (Zn) in calcareousooze Sample AFZ7 are enriched by 8 and 11 times the averageof other samples, respectively, and barium (Ba) in calcareousooze Sample AFZ6 is enriched by 25 times the mean for theremaining samples.

On the basis of comparisons with average oceanic pelagicsediment (Chester and Aston, 1976), Atlantis II Fracture Zonesediments are typically enriched in MgO and fall into threedistinct groupings, as follows:

1. Hole 732B: Sediment samples have silica (SiO2) andalumina (A12O3) comparable to oceanic averages; are enrichedin MgO, phosphorous (P2O5), titania (TiO2), iron (Fe2O), andNa2O; and are depleted in manganese (MnO), potassium(K2O), and CaO. Trace elements in these samples are vari-ously enriched (Cr, Ni, V), depleted (Ba, Pb, Zn) and compa-rable (strontium [Sr], Co) to average values in deep-sea clays(Fleet and Kempe, 1974).

2. Holes 734B and 734G: Samples have comparable P2O5values, are enriched in Fe2O3, and are depleted in the remain-ing major elements, compared to average oceanic pelagicsediments. Compared with average trace-element values fordeep-sea clays, Cr, Ni, Sr, and Co are enriched and copper(Cu) is depleted in these samples. The range in Ba, Pb, V, andZn contents is large, and values vary from significantly higherto significantly lower than the average for deep-sea clays.

Conrad RC 27-9 calcareous ooze samples have comparablemajor-element chemistries to average oceanic calcareous pe-lagic sediments, with the exceptions of Na2O and P2O5, andK2O and MnO, which are enriched and depleted, respectively.The majority of trace elements in these two ooze samples areenriched relative to average deep-sea carbonates (Fleet andKempe, 1974); however, Sr is depleted and Pb and V valuesare similar.

147

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E. VAN DER FLIER-KELLER

Table 3. Major and trace element contents of Atlantis II Fracture Zone sediments.

Sample

AFZ4AFZ10AFZ5AFZ11AFZ12AFZ1AFZ2AFZ13AFZ6AFZ7AFZ3AFZ8AFZ9

Sample

AFZ4AFZ10AFZ5AFZ11AFZ12AFZ1AFZ2AFZ13AFZ6AFZ7AFZ3AFZ8AFZ9

SiO2

45.6246.27

a44.4447.5644.03

b23.01b34.6737.05

a27.79b33.19b34.1828.8122.12

Ba

9566

115778

104784917

13122132513161121969

A12O3

11.1513.919.35

14.759.732.012.752.793.973.403.385.514.60

Co

756951437678

1081057175952824

TiO2

1.121.400.911.621.050.080.130.180.290.400.420.370.28

Cr

834493232668

1232107121592460101215661535

4128

Fe2O3

9.329.356.71

10.169.784.106.978.016.378.017.343.432.71

Cu

10356

10561746966294734438276

Percentage

CaO

6.567.87

10.938.944.57

21.7711.907.95

19.0214.2414.4532.5037.20

Mn

17911643196913761445117916061118856

1117114016281294

MgO

11.3511.255.639.32

19.7015.5026.1129.9513.8020.9222.44

1.581.25

K2O

0.630.381.120.380.350.060.070.070.200.110.100.890.74

Na2O

2.752.901.753.292.610.370.350.360.510.730.561.201.46

Parts per million

Ni

463374170258782892

17931533702

11291270

4541

Pb

48152811156647

3126311

522214

Rb

1612

a3659

b4b8

2*9b2b52321

MnO

0.200.210.270.180.170.140.160.110.100.120.130.220.17

Sr

12211032813790

14331629965683507588898

1006

P 2 O 5

0.630.220.210.270.180.140.140.150.180.180.180.220.20

V

174178106224165

103536

20357573819

LOI

8.195.15

a19.384.218.21

b26.95b17.03

14.82a22.10b17.58b17.72

27.0632.06

Y

27252335201315121114101917

Total

97.5298.91

100.7100.68100.3894.13

100.28101.4494.3398.88

100.9103.79102.79

Zn

29380

1049593

23216651

2461457

1315247

Zr

99100

a11410868

b93b 1 2 3

65a80b50b558480

a Based on <62 µm fraction.Based on >62 µm fraction.

Table 4. REE contents of selected sediments, Atlantis II FractureZone.

Element(ppma)

LaCePrNdSmEuGdTbDyHoErTmYbLuLa/YbCe/La

AFZ-1mud

4.179.181.365.421.160.401.550.241.600.381.090.160.910.144.582.20

AFZ-2mud

2.747.501.145.401.340.341.460.312.010.421.250.201.060.152.582.74

AFZ-3mud

4.5810.4

1.636.521.431.341.860.262.150.441.250.171.230.193.722.27

AFZ-7mud

4.599.491.516.681.480.981.840.302.290.481.290.181.210.183.792.07

AFZ-5sand

5.2211.72.37

11.22.621.053.540.594.110.822.540.302.030.302.572.24

AFZ-6sand

2.124.970.853.721.070.491.300.201.440.301.160.120.780.092.722.34

a Size fraction: mud—less than 62 µm; sand—greater than 62 µm.

Compared to active ridge sediments (ARS) (Chester andAston, 1976), Cr and Ni are significantly enriched in allsediments of the Atlantis II Fracture Zone samples, while theremaining transition metals are depleted. Exceptions includeSamples AFZ2 and AFZ13, where Co values are comparableto ARS compositions, and AFZ7, where Zn content is signif-icantly higher. Fe2O3 and MnO contents typical of metal-richhydrothermal sediments were not noted in the Atlantis IIFracture Zone samples, indicating that the enrichments oftrace elements are the result of factors other than hydrother-mal effects.

A number of geochemical studies on sediments from theIndian Ocean have been conducted previously (Bostrom andFisher, 1971 [Indian Ocean]; Cook, 1974 [eastern IndianOcean]; Fleet and Kempe, 1974 [southern Indian Ocean];Pimm, 1974 [Wharton Basin]; McArthur and Elderfield, 1977[Mid-Indian Ocean Ridge and Marie Celeste Fracture Zone]).A single sample from the floor of the Marie Celeste FractureZone provides the closest comparison by tectonic setting.This sample contains significantly more CaCO3 and less SiO2,Fe2O3, MnO, K2O, P2O5, and MgO than the Atlantis IIFracture Zone sediments. TiO2 and A12O3 values are compa-rable to contents in sediments from Holes 734B and 734G, andConrad RC 27-9, while Na2O is enriched. Compared withsediment analyses in other Indian Ocean localities, theAtlantis II Fracture Zone sediments are generally uniformlyenriched in MgO, TiO2, Cr, and Ni, while the patterns forother elements are more variable, depending on sedimentlithology.

Major and trace element contents of <62- and >62-µm splitsof selected samples are shown in Table 5. The <62-µ.m portionsof the samples generally contain higher proportions of Ba, Cu,Pb, Sr, V, Zn, TiO2, and CaO than do the sand-sized fractions ofthe same samples, although there are some reversals of thisrelationship. This reflects a size fractionation to higher concen-trations of carbonate and accessory titanium oxides in the siltand clay fractions. Although deep-sea carbonates and other oozesediments are generally depleted in most trace elements relativeto average deep-sea clays, it has been shown that high levels ofZn, Pb, V, and Sr may be found in calcareous tests (Chester andAston, 1976), possibly associated with iron hydroxide coatingson the test surfaces. In addition, Dymond et al. (1980) showedthat high percentages of Cu, Zn, and Mn in Galapagos carbon-ates were leachable with hydrochloride acetic acid. Elements

148

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GEOCHEMISTRY AND MINERALOGY, ATLANTIS II FRACTURE ZONE

such as Sr, Pb, Zn, and possibly V in the Atlantis II FractureZone sediments thus may represent (at least in part) a biogeniccontribution. The sand fraction of the split samples tends tocontain significantly higher Co, Cr, Ni, Fe2O3, and MgO than themud portion, reflecting a greater proportion of lithogenous orbasement-derived clastic material. This, therefore, indicates apartitioning of elements in the sediments by texture and associ-ated composition.

Source Provinces and LithologyOne of the most important controls on the geochemistry

and mineralogy of sediments in the Atlantis II Fracture Zoneis sediment source and the resultant sediment lithology. Allsediment samples examined in this study have higher MgO,Cr, and Ni contents than average pelagic sediments and otherIndian Ocean sediments. The levels of these elements are inthe ranges documented for ultramafic lithologies (Engel andFisher, 1975). The sediments accumulating in this fracturezone thus are thought to reflect significant contributions fromultramafic source rocks. A local source for much of thismaterial is supported by the thin nature of the sedimentarysequence in most parts of the fracture-zone environment, theserpentinitic and ultramafic composition, and the rubbly,coarse, proximal nature of most of the basal sediments, inaddition to the common exposure of the serpentinitized peri-dotite. Sediment samples from Holes 734B and 734G, becauseof their high MgO (13.8% to 29.95%), Cr, Ni, and Co contents;low A12O3, K2O, Na2O, and rubidium (Rb) contents; andcharacteristic serpentine, brucite, and magnetite mineral as-semblages, reflect the highest contribution from this source.The second identifiable source is basalt, which distinguishesHole 732B sediment samples from the above-mentioned pri-marily serpentinite-derived samples. Hole 732B samples arecharacterized by high SiO2, A12O3, TiO?, Fe2O3, Na2O, V, Y(scattered Cu), and low Sr. Characteristic minerals include

amphibole, and clinopyroxene, and albite, analcime and smec-tite, which are, respectively, typical mafic minerals and theirsubmarine weathering products. These samples thus are influ-enced by basaltic and subsidiary serpentinitic sources, as issuggested by the nature of clasts in the basal sediments ofCore 118-732B-1H (dominated by basalt and diabase at Site732, and specifically phyric basalt at the 135-150 cm interval,and weathered basalt and serpentinite at the 70-95 cm inter-val). The third sediment source is calcareous ooze (in partic-particular, foraminiferal ooze) and diatoms and sponges.Samples that contain a high proportion of calcareous ooze(particularly samples from RC 27-9) exhibit high CaO and Sr,and low SiO2, TiO2, Fe2O3, and Cr. As suggested by results ofthe sample splits, a high proportion of Pb and Zn may also becontributed through the biogenic components. Major mineralphases in these samples are calcite and quartz. In addition,these phases contain traces of kaolinite and illite not observedin other Atlantis II Fracture Zone sediments.

Proportions of the three source materials in the sedimentsmay reflect (1) the thickness of the sediment cover (thinsedimentary sections, for example, less than 2 m, appear tohave higher contents of basement-derived material in thesediment, while in thicker sediment ponds ooze materialappears to dominate, and long-distance transported clay min-erals are more likely to be present), and (2) the nature of thebasement, i.e., serpentinite, gabbro, peridotite, or basalt.Thickness of the sediment cover is probably related to averageseafloor slope, with greatest thicknesses occurring on lowerslopes. Higher slope areas with thinner sediment cover mayalso be more proximal to basement outcrops. The distinctionbetween the three source provinces is illustrated using aternary diagram showing CaO, A12O3, and MgO (Fig. 1). Acertain amount of overlap may occur, where, for example, acalcareous ooze sample like AFZl also includes a significantproportion of ultramafic material.

Table 5. Major and trace element contents of <62 µm and >62 µm splits of selected sediments.

Sample

AFZ5AFZ5SAFZlAFZ1SAFZ2AFZ2SAFZ6AFZ6SAFZlAFZ7SAFZ3AFZ3S

Sample

AFZ5AFZ5SAFZlAFZ1SAFZ2AFZ2SAFZ6AFZ6SAFZlAFZ7SAFZ3AFZ3S

SiO2

44.44

23.01

34.6727.79

33.19

34.18

Ba

158750

150595049

14870300

6420695

6610662

A12O3

9.0110.202.102.013.292.714.093.063.253.423.193.40

Co

5541518575

1107078567751

101

TiO2

0.871.000.120.060.170.130.310.180.400.411.000.35

Cr

140470679

1175128022251016985739

1668715

1636

Fe2O3

6.666.812.594.514.437.166.564.985.558.324.997.63

Cu

102114103608465483694277040

Percentage

CaO

13.005.60

25.6820.7312.6711.8419.6414.4917.0113.9016.7314.17

Mn

229611301155118510201650849905795

1157740

1189

MgO

3.4511.269.75

17.0218.4926.6913.2717.6612.0622.0111.8623.75

K2O

1.400.400.070.060.010.070.240.010.060.120.100.10

Parts per million

Ni

116308477

1002875

1862695752516

1205514

1363

Pb

3218

18036

1104297

33866626711644

Na2O

1.482.440.890.231.110.290.530.310.500.750.780.53

Rb

36

4

89

2

5

MnO

0.320.140.150.140.130.160.100.120.100.120.090.13

Sr

412110

1295147017651619715449763475848556

P 2 O 5

0.250.090.070.160.050.150.210.020.090.190.070.19

V

93140276

4035

2245064566156

Y

25187

149

15127

10141010

Zn

10798

408185208163238308

15101450250116

Zr

114

93

12380

50

55

AFZ5 = less than 62 µm fraction; AFZ5S = greater than 62 µm fraction.

149

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E. VAN DER FLIER-KELLER

CaO

MgO

Figure 1. CaO, A12O3, and MgO ternary diagram showing the sepa-ration of ooze, primarily ultramafic-derived, and primarily basalt-derived sediments.

Rare Earth Elements

Compared to a variety of normal deep-sea sediments (forexample, Shimokawa et al., 1972; Piper, 1974a, 1974b) andsediments from active plate boundaries (Dymond et al., 1980;Ruhlin and Owen, 1986; Kunzendorf et al., 1988), the REEcontents of the Atlantis II Fracture Zone sediments are low.This is most evident for lanthanum (La), neodymium (Nd),samarium (Sm), terbium (Tb), and lutetium (Lu), while levelsof cerium (Ce), europium (Eu), and ytterbium (Yb) are morecomparable to average values for sediments from active plateboundaries. Compared with sediments from the Carlsberg andCentral Indian Ocean ridges (Kunzendorf et al., 1988), La, Ce,Nd, and Sm contents are low, Tb contents are slightly lower,while Eu, Yb, and Lu contents are comparable. Ratios of Lato Yb (degree of fractionation) and Ce to La (redox variation)

10 -

1 -

\ " '

- "Yb

HARS^

-

-

i i i Mill

AMIOR

* % i ! / — ^

m\

• • •

BAFA

\ . m

LLÜ

-

-

-

CeLa

i i i i i i 111

0.1 10

Figure 2. Values of rare earth elements for Atlantis II Fracture Zonesediments plotted onto the characterization scheme of Kunzendorf etal. (1988). HARS = hydrothermally affected ridge sediments, MIOR= Central Indian Ocean Ridge sediments, CR = Carlsberg Ridgesediments, AFZ = Atlantis II Fracture Zone sediments, Area I =deep-sea sediments, Area III = marine basalts and related rocks.

(Kunzendorf et al., 1988) for the Atlantis II Fracture Zonesediments plot in the lower right portion of the sedimentaryfield and in the basalt field (Fig. 2), indicating (1) no evidenceof hydrothermal activity (Marchig et al., 1982; Kunzendorf etal., 1988) in these sediments and (2) the presence of abundantrelatively unfractionated basaltic and other basement mate-rial, particularly in the coarser-grained sediment fractionsexamined.

CONCLUSIONSThe sediments from sites drilled in the Atlantis II Frac-

ture Zone exhibit geochemical characteristics, includinghigh MgO, Cr, and Ni contents, which readily distinguishthem from other deep-sea sediments. Abundant serpentineand the presence of brucite and magnetite, coupled withhighest MgO, Cr, and Ni contents in samples from Holes734B and 734G indicate that significant components of thesesediments are derived from the ultramafic basement. Site732 sediments exhibit volumetrically important contribu-tions from basaltic as well as serpentinitic basement mate-rials, as evidenced by the presence of albite, analcime,primary mafic minerals, smectite-chlorite, and high SiO2,A12O3, TiO2, Fe2O3, V, and Y. A third component of thesediments is the biogenic material, reflected primarily in thepresence of carbonates, high CaO, Sr, and Pb, and Zn incertain samples.

REE values and ratios of La to Yb, and Ce to La indicateno evidence of hydrothermal activity. This is supported by themajor- and trace-element data.

REFERENCES

Bostrom, K., and Fisher, D. E., 1971. Volcanogenic uranium, vana-dium and iron in Indian Ocean sediments. Earth Planet. Sci. Lett.,11:95-98.

Chester, R., and Aston, S. R., 1976. The geochemistry of deep-seasediments. In Riley, J. P., and Chester, R. (Eds.), Chem. Ocean-ogr., 6: London (Academic), 281-390.

Cook, P. J., 1974. Major and trace element geochemistry of sedimentsfrom Deep Sea Drilling Project, Leg 27, Sites 259-263, easternIndian Ocean. In Veevers, J. J., Heirtzler, J. R., et a\.,Init. Repts.DSDP, 27: Washington (U.S. Govt. Printing office), 481-497.

Dymond, J., Corliss, J. B., Cobler, R., Muratli, C. M., Chou, C , andConard, R., 1980. Composition and origin of sediments recoveredby deep drilling of sediment mounds, Galapagos Spreading Center:DSDP Leg 54. In Rosendahl, B. R., Hekinian, R., et al., Init.Repts. DSDP, 54: Washington (U.S. Govt. Printing Office), 377-385.

Engel, C. G., and Fisher, R. L., 1975. Granitic to ultramafic com-plexes of the Indian Ocean ridge system, western Indian Ocean.Geol. Soc. Am. Bull., 86:1553-1578.

Fisher, R. L., and Sclater, J. G., 1983. Tectonic evolution of thesouthwest Indian Ocean since the mid-Cretaceous: plate motionsand stability of the pole of Antartctica/Africa for at least 80Myr.Geophys. J. R. Astron. Soc, 73:553-576.

Fleet, A. J., and Kempe, D.R.C., 1974. Preliminary geochemicalstudies of the sediments from DSDP Leg 26, southern IndianOcean. In Davies, T. A., Luyendyk, B. P., et al., Init. Repts.DSDP, 27: Washington (U.S. Govt. Printing Office), 541-551.

Kolla, V., Be, A.W.H., and Biscaye, P. E., 1976. Calcium carbonatedistribution in the surface sediments of the Indian Ocean. J.Geophys. Res., 81:2605-2616.

Kunzendorf, H., Stoffers, P., and Gwozdz, R., 1988. Regional vari-ations of REE patterns in sediments from active plate boundaries.Mar. Geol., 84:191-199.

Marchig, V., Gundlach, H., Moller, P., and Schley, F., 1982. Somegeochemical indicators for discrimination between diagenetic andhydrothermal metalliferous sediments. Mar. Geol, 50:241-256.

Me Arthur, J. M., and Elderfield, H., 1977. Metal accumulation ratesin sediments from Mid-Indian Ocean Ridge and Marie CelesteFracture Zone. Nature, 266:437-439.

150

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GEOCHEMISTRY AND MINERALOGY, ATLANTIS II FRACTURE ZONE

Pimm, A. C , 1974. Mineralisation and trace element variation indeep-sea pelagic sediments of the Wharton Basin, Indian Ocean.In Von der Borch, C. C , Sclater, J. G., et al., Init. Repts. DSDP,22: Washington (U.S. Govt. Printing Office), 469-476.

Piper, D. Z., 1974a. Rare earth elements in the sedimentary cycle: asummary. Chem. Geol., 14:285-304.

, 1974b. Rare earth elements in ferromanganese nodulesand other marine phases. Geochim. Cosmochim. Acta, 38:1007-1022.

Rateev, M. A., Gorbunova, Z. N., Lisitzin, A. P., and Nosov, G. L.,1969. The distribution of clay minerals in the ocean. Sedimentol-ogy, 13:21-43.

Robinson, P. T., Von Herzen, R. P., et al., 1989. Proc. ODP, Init.Repts., 118: College Station, TX (Ocean Drilling Program).

Ruhlin, D. E., and Owen, R. M., 1986. The rare earth elementgeochemistry of hydrothermal sediments from the east PacificRise: Examination of a seawater scavenging mechanism.Geochim. Cosmochim. Acta, 50:393-400.

Shimokawa, T., Masuda, A., and Izawa, K., 1972. Rare-earth ele-ments in the top samples of cores from the Pacific Ocean floor.Geochem. J., 6:75-81.

Venkatarathnam, Kolla, Henderson, L., and Biscaye, P. E., 1976.Clay mineralogy and sedimentation in the western Indian Ocean.Deep-Sea Res., 23:949-961.

Venkatarathnam, Kolla, and Biscaye, P. E., 1977. Distribution andorigin of quartz in the sediments of the Indian Ocean. J. Sediment.Petrol., 47:642-649.

Warren, B. A., 1978. Bottom water transport through the SouthwestIndian Ridge. Deep-Sea Res., 25:315-321.

Date of initial receipt: 24 August 1989Date of acceptance: 17 April 1990Ms 118B-164

151


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