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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,
145
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
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
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
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.
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GEOCHEMISTRY AND MINERALOGY, ATLANTIS II FRACTURE ZONE
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Date of initial receipt: 24 August 1989Date of acceptance: 17 April 1990Ms 118B-164
151