Abstract
More than 100 volcanic necks in central Scania (southern Sweden) are the product of Jurassic continental rift-related mafic alkaline magmatism at the southwest margin of the Baltic Shield. They are mainly basanites, with rarer melanephelinites. Both rock groups display overlapping primitive Mg-numbers, Cr and Ni contents, steep chondrite-normalized rare earth element patterns (LaN /YbN = 17–27) and an overall enrichment in incompatible elements. However, the melanephelinites are more alkaline and have stronger high field strength element enrichment than the basanites. The existence of distinct primary magmas is also indicated by heterogeneity in highly incompatible element ratios (e.g. Zr/Nb, La/Nb). Trace element modelling indicates that the magmas were generated by comparably low degrees of melting of a heterogeneous mantle source. Such a source can best be explained by a metasomatic overprint of the mantle lithosphere by percolating evolved melts. The former existence of such alkaline trace element-enriched melts can be demonstrated by inversion of the trace element content of green-core clinopyroxenes and anorthoclase which occur as xenocrysts in the melanephelinites and are interpreted as being derived from crystallization of evolved mantle melts. Jurassic magmatic activity in Scania was coeval with the generation of nephelinites in the nearby Egersund Basin (Norwegian North Sea). Both Scanian and North Sea alkaline magmas share similar trace element characteristics. Mantle enrichment processes at the southwest margin of the Baltic Shield and the North Sea Basin generated trace element signatures similar to those of ocean island basalts (e.g. low Zr/Nb and La/Nb) but there are no indications of plume activity during the Mesozoic in this area. On the contrary, the short duration of rifting, absence of extensive lithospheric thinning, and low magma volumes argue against a Mesozoic mantle plume. It seems likely that the metasomatic imprint resulted from the earlier Permo-Carboniferous rifting episode which affected the entire study area and clearly was accompanied by plume activity (Ernst and Buchan in American Geophysical Union, pp 297–337, 1997). Renewed rifting in Jurassic times triggered decompression melting in the volatile-enriched lithospheric mantle and the alkaline melts generated inherited the earlier “stored” plume signature.
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Acknowledgements
This study is part of my diploma thesis completed at the Institute of Geological Sciences, University of Greifswald. Karsten Obst and Zoltan Solyom are thanked for logistical support and for resurrecting the study of Mesozoic volcanism in southern Scandinavia. George Jenner, Dejan Prelevic, Stephen Foley, Dorrit Jacob and Gerhard Wörner are thanked for helpful discussions. The final version of the manuscript has greatly benefited from thoughtful reviews and editorial advice from Hilary Downes, Lotte Larsen and Jochen Hoefs. Jürgen Eidam helped with the XRF analysis in Greifswald and Ulrich Siewers enabled the solution ICP-MS work in Hannover. Special thanks to Dorrit Jacob who ably assisted with the LAM-ICP-MS work in Greifswald. Stephen Foley financially supported the electron microprobe analyses in Göttingen, which were ably assisted by Andreas Kronz. A travel grant for field work was provided by DAAD (Germany).
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Appendix
Appendix
Analytical techniques
Mineral chemistry
Mineral compositions were obtained using a JEOL JXA 8900 RL electron microprobe at the University of Göttingen. Operating voltage for silicates was 15 kV and the probe current was 15 nA. Opaque oxides were measured with 15 kV and 20 nA. The beam diameter varied between 1 and 10 μm dependent on both size and content of volatile elements in the crystal of interest. All the data were reduced with a CITZAF procedure (Armstrong 1995).
In-situ trace element analyses were performed with a laser ablation microprobe (LAM) in Greifswald which consists of a Q-switched Nd-YAG Merchantek UP-213 laser ablation system coupled to an Agilent 7500cs ICP-MS. Ablated material was carried in a continuous stream of argon to the ICP-MS. Mineral analyses were made using the frequency quadrupled laser output with a UV wavelength of 213 nm at a repetition rate of 10 Hz. Energy densities of 10 J/cm2 were adjusted and relatively large ablation craters were drilled (95 μm) to get sufficient signal for accurate quantification of a wide range of trace elements. Detection limits were calculated for individual analyses and approach values below 1 ppb. Calcium was used as an internal standard, with concentrations independently determined by electron microprobe analysis. The SRM NIST 612 and BCR2-G glasses were measured as international reference materials.
Whole-rock geochemistry
Major and selected trace elements were determined by X-ray fluorescence (XRF) spectrometry on fused discs at the University of Greifswald. A sequential wavelength-dispersive Philips PW2404 X-ray spectrometer was equipped with a single goniometer based measuring channel, covering the complete measuring range. Some samples were additionally analyzed by XRF in Lund and results agree within analytical error for all major elements. An in-house standard and international reference materials (BCR2 and BHVO1) have also been incorporated in our measurements. In addition, Fe+2/+3 was determined for selected samples by standard titration techniques in Lund. A wide range of trace elements and REE were measured by ICP-MS at the Federal Institute for Geosciences and Natural Resources in Hannover. Powders were dissolved in teflon bombs using a HF/HNO3 mixture (5 and 2 ml, respectively) and heated up to 170°C under pressure for 12 h. After slow cooling and further addition of HNO3 (2 ml) the digestions were evaporated to near dryness. The samples were taken up in 1 ml HNO3 and 1 ml HCl followed by dilution with 20–30 ml high purity H2O and heated again up to 170°C. Following cooling, samples were diluted to exactly 100 g using more water and Re and Rh were added as internal standards. These resulting solutions were analyzed on a Perkin–Elmer Elan 5000 inductively coupled plasma mass spectrometer using a cross-flow nebulizer. Calibration was achieved using matrix-matched international reference materials.
Comparison of trace elements determined by both the XRF and ICP-MS techniques (i.e. Ce, Y, Zr) was excellent and indicated no dissolution problems for the ICP-MS work. Typical estimates of precision and accuracy for these techniques are given in Jenner (1996).
Sample list
Sample list for Mesozoic mafic alkaline rocks from Scania
Sample ID | Rock type | Facies | Northinga | Eastinga | Location |
---|---|---|---|---|---|
CJBG 1 | Basanite | Glassy | 61990 | 13560 | Lillö |
CJBG 2 | Basanite | Microcrystalline | 62039 | 13598 | Anneklev (Klevahill) |
CJBG 3 | Basanite | Microcrystalline | 62077 | 13556 | Ulfsberg (Bjäret) |
CJBG 4 | Melanephelinite | Microcrystalline | 62095 | 13569 | Hästhallarna |
CJBG 6 | Basanite | Glassy | 62104 | 13661 | Gunnarp (center) |
CJBG 7 | Basanite | Glassy | 62102 | 13663 | Gunnarp (south) |
CJBG 8 | Basanite | Glassy | 62090 | 13670 | Ebbarp |
CJBG 12 | Basanite | Glassy | 62115 | 13675 | Snababerg |
CJBG 13 | Basanite | Glassy | 62109 | 13681 | Skoghus |
CJBG 14 | Basanite | Glassy | 62098 | 13679 | Bolmarehus (Spragebjär) |
CJBG 15 | Basanite | Glassy | 62106 | 13682 | Lönnebjär |
CJBG 16 | Basanite | Glassy | 62106 | 13684 | Lönnebjär |
CJBG 18 | Basanite | Microcrystalline | 62129 | 13668 | Sösdala |
CJBG 19 | Basanite | Glassy | 62120 | 13663 | Sösdala (Eáof Ella) |
CJBG 20 | Basanite | Glassy | 62087 | 13573 | Stenkilstorp |
CJBG 21 | Melanephelinite | Microcrystalline | 62096 | 13567 | Hästhallarna |
CJBG 22 | Melanephelinite | Microcrystalline | 62097 | 13568 | Hästhallarna |
CJBG 23 | Basanite | Microcrystalline | 62119 | 13581 | Knösen |
CJBG 24 | Melanephelinite | Microcrystalline | 62159 | 13607 | Hagstad (Hagstadbjär) |
CJBG 25 | Melanephelinite | Glassy | 62160 | 13610 | Hagstad (Lilla Hagstad) |
CJBG 26 | Basanite | Microcrystalline | 62098 | 13512 | Allarpsberg |
CJBG 27 | Basanite | Glassy | 62127 | 13554 | Säte |
CJBG 32 | Melanephelinite | Microcrystalline | 62121 | 13460 | Jällabjär |
CJBG 33 | Melanephelinite | Microcrystalline | 62118 | 13460 | Jällabjär |
CJBG 34 | Melanephelinite | Microcrystalline | 62113 | 13488 | Billinge II |
CJBG 35 | Melanephelinite | Microcrystalline | 62118 | 13483 | Eneskogens gårdsgard |
CJBG 37 | Basanite | Microcrystalline | 62131 | 13455 | Randsliderna |
CJBG 38 | Melanephelinite | Glassy | 62123 | 13462 | Jällabjär |
CJBG 39 | Basanite | Microcrystalline | 62204 | 13445 | Juskushall |
CJBG 40 | Basanite | Glassy | 62220 | 13461 | Storaryd |
CJBG 41 | Basanite | Microcrystalline | 62198 | 13376 | Bonnarp |
CJBG 42 | Basanite | Microcrystalline | 62140 | 13417 | Rallate |
CJBG 43 | Melanephelinite | Microcrystalline | 61976 | 13581 | Bosjökloster |
CJBG 44 | Melanephelinite | Microcrystalline | 62099 | 13567 | Hästhallarna |
CJBG 45 | Basanite | Microcrystalline | 62211 | 13714 | Espet |
CJBG 52 | Basanite | Microcrystalline | 62094 | 13696 | Lunden |
CJBG 54 | Basanite | Microcrystalline | 62171 | 13586 | Holma |
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Tappe, S. Mesozoic mafic alkaline magmatism of southern Scandinavia. Contrib Mineral Petrol 148, 312–334 (2004). https://doi.org/10.1007/s00410-004-0606-y
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DOI: https://doi.org/10.1007/s00410-004-0606-y