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The effects of flowline length evolution on chemistry–δ 18O profiles from Penny Ice Cap, Baffin Island, Canada

Published online by Cambridge University Press:  14 September 2017

David A. Fisher
Affiliation:
Terrain Sciences Division, Geological Survey of Canada, 601 Booth Street, Ottawa, Ontario K1A 0E8, Canada E-mail: fisher@nrcan.gc.ca
Roy M. Koerner
Affiliation:
Terrain Sciences Division, Geological Survey of Canada, 601 Booth Street, Ottawa, Ontario K1A 0E8, Canada E-mail: fisher@nrcan.gc.ca
Gregory A. Zielinski
Affiliation:
Climate Studies Center, University ofMaine, Institute for Quaternary Studies, Orono, ME 04469-5790, U.S.A.
Cameron P. Wake
Affiliation:
Glacier Research Group, Morse Hall, University of New Hampshire, Durham, NH 03824-3525, U.S.A.
Christian M. Zdanowicz
Affiliation:
Terrain Sciences Division, Geological Survey of Canada, 601 Booth Street, Ottawa, Ontario K1A 0E8, Canada E-mail: fisher@nrcan.gc.ca
Jocelyne C. Bourgeois
Affiliation:
Terrain Sciences Division, Geological Survey of Canada, 601 Booth Street, Ottawa, Ontario K1A 0E8, Canada E-mail: fisher@nrcan.gc.ca
Paul A. Mayewski
Affiliation:
Climate Studies Center, University ofMaine, Institute for Quaternary Studies, Orono, ME 04469-5790, U.S.A.
Nancy Grummet
Affiliation:
School of Earth Sciences, Stanford, Braun Hall Building 320, 45 Serra Mall, Stanford, CA 94305-2115, U.S.A.
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Abstract

The isotopic and chemical signatures for ice-age and Holocene ice from Summit, Greenland, and Penny Ice Cap, Baffin Island, Canada, are compared. the usual pattern of low δ 18O, high Ca2+ and high Cl– is presented in the Summit records, but Penny Ice Cap has lower than present Cl– in its ice-age ice. A simple extension of the Hansson model (Hansson, 1994) is developed and used to simulate these signatures. the low ice-age Cl– from Penny Ice Cap is explained by having the ice-age ice originating many thousands of km inland near the centre of the Laurentide ice sheet and much further from the marine sources. Summit’s flowlines all start close to the present site. the Penny Ice Cap early-Holocene δ 18O’s had to be corrected to offset the Laurentide meltwater distortion. the analysis suggests that presently the Summit and Penny Ice Cap marine impurity originates about 500 km away, and that presently Penny Ice Cap receives a significant amount of local continental impurity.

Information

Type
Research Article
Copyright
Copyright © the Author(s) [year] 2002
Figure 0

Fig. 1Map of the reconstructed ice cover over North America at the Last Glacial Maximum (from Fisher and others, 1985) assuming the bed under Hudson Bay is not deforming. the present positions of the Laurentide remnant ice caps, Penny and Barnes, are indicated by a “P”and “B”, respectively, and the longest possible flowline to them is shown as the thick gray dashed line joining them to the Keewatin flow centre denoted “KK”. the position of the Summit (Greenland) cores is marked “S”. Summit is already virtually at the top of the flowline. A flowline from Summit to the west coast of Greenland (Pâkitsoq, “PS”) (Reeh and others, 1991) is marked for comparison. Since there is not very much lateral room for expansion of the Greenland ice, the Summit flowline origins must always have been close to the present position.

Figure 1

Fig. 2Summit ice-core records: (a) δ 18O from the GRIP core (Johnsen and others, 1997); (b) Ca2+concentration (ppb) (mass) in GISP2 core (Mayewski and others, 1997); (c) Cl–concentration (ppb) in GISP2 ice core; (d) NH4+ concentration (ppb) in GISP2 core.

Figure 2

Fig. 3Penny Ice Cap ice-core records: (a) δ 18O (Fisher and others, 1998); (b) Ca2+ concentration (ppb) (mass) (Fisher and others, 1998); (c) Cl– concentration (ppb); (d) NH4+ concentration (ppb).

Figure 3

Fig. 4Cartoon of the Hansson model, relating ice-core geochemical concentration and flux to water-cycle variables and impurity-specific variables. There are two broad input categories of impurity: marine and continental. Asterisks indicate present values.

Figure 4

Fig. 5The past accumulation rate A with respect to present and the Hansson model variable n/k , where n is the relative transit time, for a given type of impurity and k is the relative survival time, Asterisks indicate present values. (a) Measured values for the GRIP core (Dahl-Jensen, 1993); (b) inferred values for the Penny Ice Cap core using the same A – δ 18O relationship.

Figure 5

Fig. 6A cartoon explaining the extension to the Hansson model. X is the average model distance from source to the start of the flowline. X can be changed either by moving the impurity source or by moving the start of the flowline. for Summit the start of the flowline can at most be a few tens of km from the present drill site. for Penny Ice Cap the Late-glacial flowlines could be 2000 km from the present site (see Fig. 1). X* is the present distance.

Figure 6

Fig. 7Penny Ice Cap chlorine vs uncorrected δ 18O for early-Holocene and ice-age ice. the early-Holocene δ 18O values have probably been affected by meltwater from the wasting Laurentide ice cap and consequently need correcting. for corrected version of this figure see Figure 8b.

Figure 7

Fig. 8Measured and modeled relationship between marine-impurity Cl– and δ 18O for Penny Ice Cap and Summit ice cores. (a) the Summit core results can be fitted best with no significant difference in path length (DIST = 1) and a modern marine transit time 2.7 times the survival time for the injected salts. the Summit marine-impurity concentration in glacial times is 5–10 times the present value. (b) the Penny Ice Cap core results need significantly longer flowlines during the Late-glacial in order to model the lower marine salts during glacial times (i.e. DIST = 5). the modern marine-salt transit time is as above, which is reasonable. Glacial marine concentrations are lower than modern values, which is unique and the starting observation for this whole extension.

Figure 8

Fig. 9Measured and modeled relationship between continental-impurity Ca2+ and δ 18O for Penny Ice Cap and Summit ice cores. (a) the Summit core results can be fitted best with no significant difference in path length (DIST1 = ) and a modern continental transit time 5 times the survival time for the injected impurity. the Summit marine-impurity concentration in glacial times is 30–100 times the present value. (b) the Penny Ice Cap core results need significantly longer flowlines during the Late-glacial in order to model the somewhat higher continental impurity during glacial times (i.e. DIST = 2.5). the modern continental impurity transit time is close to that from Summit, i.e. 1.75– 5 times the modern survival time. Glacial continental concentrations are 2–15 times higher than modern values. That the value of DIST is 5 for marine salts and 2.5 for continental impurities is to be expected, because the marine sources, being closer at present, will become relatively much further away from a remote flowline start than a source already very far away (see Fig. 6).