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NARROW
GeoRef Subject
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all geography including DSDP/ODP Sites and Legs
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Canada
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Arctic Archipelago (1)
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Eastern Canada
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Baffin Island
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Barnes ice cap (1)
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Ontario (8)
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Nunavut
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Baffin Island
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Barnes ice cap (1)
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Western Canada
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Manitoba (1)
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Northwest Territories (1)
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Lake Nipissing (1)
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North America
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Great Lakes
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Lake Superior (1)
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Great Lakes region (1)
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elements, isotopes
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carbon
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C-14 (4)
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isotopes
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radioactive isotopes
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C-14 (4)
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fossils
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Chordata
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Vertebrata
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Tetrapoda
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Mammalia
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Theria
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Eutheria
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Carnivora
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Fissipeda
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Ursidae
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Ursus (1)
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Invertebrata
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Arthropoda
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Mandibulata
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Crustacea
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Ostracoda (1)
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Insecta
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Pterygota
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Neoptera
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Endopterygota
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Coleoptera (3)
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Mollusca (1)
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Protista
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Foraminifera (1)
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microfossils (2)
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palynomorphs
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miospores
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pollen (2)
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Plantae (1)
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geochronology methods
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racemization (1)
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geologic age
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Cenozoic
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Quaternary
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Holocene
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lower Holocene (1)
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Pleistocene
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Lake Agassiz (1)
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upper Pleistocene
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Wisconsinan (2)
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upper Quaternary (1)
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-
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Laurentide ice sheet (1)
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Primary terms
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absolute age (4)
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biogeography (2)
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Canada
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Arctic Archipelago (1)
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Eastern Canada
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Baffin Island
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Barnes ice cap (1)
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Ontario (8)
-
-
Nunavut
-
Baffin Island
-
Barnes ice cap (1)
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-
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Western Canada
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Manitoba (1)
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Northwest Territories (1)
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-
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carbon
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C-14 (4)
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Cenozoic
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Quaternary
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Holocene
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lower Holocene (1)
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Pleistocene
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Lake Agassiz (1)
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upper Pleistocene
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Wisconsinan (2)
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-
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upper Quaternary (1)
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Chordata
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Vertebrata
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Tetrapoda
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Mammalia
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Theria
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Eutheria
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Carnivora
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Fissipeda
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Ursidae
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Ursus (1)
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engineering geology (1)
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geochronology (1)
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geomorphology (1)
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geophysical methods (1)
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glacial geology (3)
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Invertebrata
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Arthropoda
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Mandibulata
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Crustacea
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Ostracoda (1)
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Insecta
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Pterygota
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Neoptera
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Endopterygota
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Coleoptera (3)
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-
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-
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Mollusca (1)
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Protista
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Foraminifera (1)
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-
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isotopes
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radioactive isotopes
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C-14 (4)
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-
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maps (1)
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North America
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Great Lakes
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Lake Superior (1)
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Great Lakes region (1)
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paleoclimatology (6)
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paleoecology (7)
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paleontology (1)
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palynomorphs
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miospores
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pollen (2)
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permafrost (1)
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Plantae (1)
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sediments
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clastic sediments
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till (1)
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peat (1)
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stratigraphy (3)
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sediments
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sediments
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clastic sediments
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till (1)
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peat (1)
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soils
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paleosols (1)
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Holocene paleoclimate and paleoecology determined from fossil Coleoptera at Brampton, Ontario, Canada
Late-glacial climate and ecology of a kettle section at Brampton, Ontario, Canada, as determined from fossil Coleoptera
Age and paleoecological significance of an early postglacial fossil assemblage near Marathon, Ontario, Canada
Paleoecology and age of the Flitaway and Isortoq interglacial deposits, north-central Baffin Island, Northwest Territories, Canada
Plant and insect fossils from Nipissing sediments along the Goulais River, southeastern Lake Superior
Paleoclimatic implications of a Late Wisconsinan insect assemblage from Rostock, southwestern Ontario
Late Wisconsin and early Holocene paleoenvironments of east-central North America based on assemblages of fossil Coleoptera
Abstract The examination of fossil assemblages of Coleoptera (beetles) in North America is a relatively new but rapidly growing research area. This chapter is an attempt to use suites of fossil Coleoptera to establish the nature and timing of different paleoenvironments at the margins of the Laurentide Ice Sheet as it advanced and retreated from the Great Lakes region. Some of the work is synthesized from previous publications, but some important data are from unpublished sites. Before the various sites illustrated in Figure 1 are discussed, certain assumptions must be restated that are implicit in the study of Quaternary insect assemblages. The first of these is that beetle species can be identified by characters that are not always used by neotaxonomists. The latter frequently describe species by using portions of the exoskeleton that are destroyed or scattered following the death of the organism. In many cases a specific determination cannot be made with the available fossil components, but even narrowing the identification to a species group often is sufficient to provide valuable ecological data. The second assumption is that species have not evolved during the Pleistocene. Early in the century a general belief prevailed that intense speciation occurred during periods of glaciation. This was one of the greatest barriers to the development of paleoentomology, and it was not until the work of Henriksen (1933), Lindroth (1948), and Coope (1959, 1968; Coope and others, 1961) that this belief was shown to be fallacious. Beetles recovered from Quaternary deposits can be matched precisely with modern species, although they may occur currently thousands of kilometers away from the fossil locality. Examples of major late Pleistocene geographic shifts are demonstrated in papers by Coope (1973) and Hammond and others (1979). Some general statements can be added to the two basic tenets stated above. Paleoenvironments or paleoclimates are not established by use of individual species, but rather of species assemblages. Inherent is the assumption that we know the full modern distribution of a species (or at least the range limits), and that adequate ecological data are available. We assume that the ecology of the fossil species is the same as that of the modem species, and that little or no physiological change has occurred during this period. Publications commenting on some of the points mentioned above include two excellent summaries by Coope (1970, 1979). North American reviews are provided by Ashworth (1979), Matthews (1977, 1980), Morgan and Morgan (1980a, 1980b), and Morgan and others (1983a).