letters to nature
784 NATURE | VOL 405 | 15 JUNE 2000 | www.nature.com
jotunitic chilled margins
8,9
. Chilled margins of similar composition
are also found around the Hidra anorthosite body
7
. Batches of
primitive jotunitic magma derived by partial fusion of a ma®c lower
crust of Gothian to post-Gothian age (1,550±1,400 Myr ago) are
therefore the best candidates for parental melts, not only for the
massif-type anorthosites but also for the associated noritic and
ilmenite-rich intrusions in the Rogaland anorthosite province. The
variations in parental magma composition inferred for other
anorthosite provinces probably depend on the exact nature of the
underlying crust.
The Rogaland anorthosites were emplaced post-orogenically
,60 Myr after the latest recorded Sveconorwegian deformation,
coinciding with post-orogenic granitoid magmatism elsewhere in
south Norway and western Sweden. Seismic and gravimetric pro-
®les along the south coast of Norway have shown that Sveconorwe-
gian Moho-ramp tectonics cause the intrusion of crustal tongues
into the contemporary mantle
28
. Melting of these crustal tongues
was recently proposed to account for the anorthosite formation
29
and currently provides us with the most plausible setting for lower
crustal melting and genesis of the parental magmas for the Rogaland
massif-type anorthosites. M
Received 4 January; accepted 25 April 2000.
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(1996).
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Touret, J. L. R.) 39±60 (Reidel, Dordrecht, 1985).
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the origin of Proterozoic (massif) anorthosites and related rocks. J. Petrol. 40, 339±362 (1999).
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anorthosites, Wyoming, USA: Implications for magma chamber processes and the evolution of
magma conduits in Proterozoic anorthosites. Geochim. Cosmochim. Acta 60, 95±107 (1996).
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anorthositic and related magmas. Am. Mineral. 78, 1016±1030 (1993).
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Wyoming: implications for the composition of melts parental to Proterozoic anorthosite. Contrib.
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Cosmochim. Acta 45, 1545±1561 (1981).
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Rogaland, SW Norway: Evidence from marginal rocks for a jotunite parent magma. Lithos 39, 121±
133 (1997).
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me Âridionale). C. R. Acad. Sci. 306, 45±48 (1988).
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Proterozoic of Rogaland/Vest-Agder, SW Norway. Contrib. Mineral. Petrol. 98, 363±373 (1988).
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the Adirondacks, New York, and other massif-type complexes: Summary. Geol. Soc. Am. Bull. 91, 105±
107 (1980).
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type anorthosites. Nature 311, 372±374 (1984).
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Massif, Northeast Poland. Geophys. J. 4, 111±114 (1998).
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Plutonic Suite. J. Geol. 102, 539±558 (1994).
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southern African peridotite xenoliths: Implications for the chemical evolution of subcontinental
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lower crust. Geology 26, 359±362 (1998).
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Cosmochim. Acta 57, 3093±3104.
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339±352.
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isotopic study of ma®c xenoliths from central Arizona. Geology 25, 651±654 (1997).
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formation and age of the lower continental crust. Nature 393, 58±61 (1998).
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Supplementary information is available on Nature's World-Wide Web site
(http://www.nature.com) or as paper copy from the London editorial of®ce of Nature.
Acknowledgements
Financial support for Re±Os isotopic studies at Monash University derive from the
Monash University Research Fund, the Australian Crustal Research Centre, and the
Australian Research Council. The research reported here was supported by the Norwegian
Research Council.
Correspondence and requests for materials should be addressed to H.S.
(e-mail: henrik.schiellerup@geo.ntnu.no).
.................................................................
Unrelated helpers in a social insect
David C. Queller*, Francesca Zacchi*, Rita Cervo², Stefano Turillazzi²,
Michael T. Henshaw*, Lorenzo A. Santorelli² & Joan E. Strassmann*
* Department of Ecology and Evolution, Rice University, PO Box 1892, Houston,
Texas 22251-1892, USA
² Dipartmento di Biologia Animale e Genetica, Universita Á di Firenze,
Via Romana 17, 50125 Florence, Italy
..............................................................................................................................................
High-resolution genetic markers have revolutionized our under-
standing of vertebrate mating systems
1
, but have so far yielded few
comparable surprises about kinship in social insects. Here we use
microsatellite markers to reveal an unexpected and unique social
system in what is probably the best-studied social wasp, Polistes
dominulus. Social insect colonies are nearly always composed of
close relatives
2,3
; therefore, non-reproductive helping behaviour
can be favoured by kin selection, because the helpers aid repro-
ductives who share their genes
4
. In P. dominulus, however, 35%
of foundress nestmates are unrelated and gain no such advan-
tage. The P. dominulus system is unlike all other cases of
unrelated social insects, because one individual has nearly
0
0.2
0.4
0.6
0.8
1.0
Survival
0
100
200
300
Cell number
Polygynous Monogynous
n=54
n=48
Fraction surviving
Number of cells
n=23
n=19
Figure 1 Success of colonies begun by one foundress and multiple foundresses
(monogynous and polygynous, respectively) measured for 1995 colonies through mid-
August, when reproductives are being produced. Polygynous colonies are more
successful both for survival (P , 0.01, test for equality of percentages) and cell number
(P , 0.01, t-test). Relative numbers of monogynous and polygynous colonies in the
survival study are representative of its source population. The cell number data excludes
failed nests and nests rebuilt after predation. Bars show standard error (s.e.).
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