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Journal articles on the topic 'Paleoecology'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Ausich, William I. "Paleoecology Workshop." PALAIOS 7, no. 2 (1992): 239. http://dx.doi.org/10.2307/3514935.

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2

Gavin, Daniel. "PALEOECOLOGY SECTION." Bulletin of the Ecological Society of America 84, no. 4 (2003): 186. http://dx.doi.org/10.1890/0012-9623(2003)84[186b:ps]2.0.co;2.

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3

Shuman, Bryan. "PALEOECOLOGY SECTION." Bulletin of the Ecological Society of America 85, no. 4 (2004): 186–87. http://dx.doi.org/10.1890/0012-9623(2004)85[186b:ps]2.0.co;2.

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4

Booth, Robert. "PALEOECOLOGY SECTION." Bulletin of the Ecological Society of America 86, no. 4 (2005): 263. http://dx.doi.org/10.1890/0012-9623(2005)86[263a:ps]2.0.co;2.

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5

Brugam, Richard. "Paleoecology Section." Bulletin of the Ecological Society of America 89, no. 4 (2008): 368. http://dx.doi.org/10.1890/0012-9623(2008)89[368a:ps]2.0.co;2.

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6

Bottjer, David J. "Bivalve Paleoecology." Notes for a Short Course: Studies in Geology 13 (1985): 122–37. http://dx.doi.org/10.1017/s0271164800001135.

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Bivalves are one of the major macroinvertebrate fossil groups of the Phanerozoic. Bivalves have occupied many aqueous habitats, and in doing this have undergone a steady, relatively unchecked increase in diversity (Figure 1). Thus, bivalves are one of the most useful fossil groups in paleoecology, both for environmental reconstruction as well as for deciphering patterns and processes of evolutionary paleoecology.

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7

Kohn, Alan J. "Gastropod Paleoecology." Notes for a Short Course: Studies in Geology 13 (1985): 174–89. http://dx.doi.org/10.1017/s0271164800001160.

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Paleoecology concerns the life processes and patterns of environmental relationships of groups of ancient organisms during their lifetimes. Two assumptions are fundamental to paleoecological theory: observed patterns in populations, associations, communities and ecosystems represented in the fossil record were imposed by contemporaneous physical and biological environmental factors and their interactions, and at least some past environmental conditions can be discerned from fossil assemblages and their rock matrices.

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8

Ward, Peter D., and Gerd E. G. Westermann. "Cephalopod Paleoecology." Notes for a Short Course: Studies in Geology 13 (1985): 215–29. http://dx.doi.org/10.1017/s0271164800001196.

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Studying the paleoecology of the extinct chambered cephalopods is somewhat analogous to studying a distant landscape through the wrong end of a powerful telescope: we can see very small views of what must have been great panoramic vistas. Two factors have lead to this situation. First, the extant cephalopods still utilizing the phragmocone system of density reduction are at very low standing diversity, while most of the more interesting taxa, such as ammonites and belemnites, are completely extinct. Our functional interpretations of various shell morphologies thus depend heavily on generalizat

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9

Miller, Ranall F. "Chitin paleoecology." Biochemical Systematics and Ecology 19, no. 5 (1991): 401–11. http://dx.doi.org/10.1016/0305-1978(91)90057-7.

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10

Lamsdell, James C., and Curtis R. Congreve. "Phylogenetic paleoecology: macroecology within an evolutionary framework." Paleobiology 47, no. 2 (2021): 171–77. http://dx.doi.org/10.1017/pab.2020.61.

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The burgeoning field of phylogenetic paleoecology (Lamsdell et al. 2017) represents a synthesis of the related but differently focused fields of macroecology (Brown 1995) and macroevolution (Stanley 1975). Through a combination of the data and methods of both disciplines, phylogenetic paleoecology leverages phylogenetic theory and quantitative paleoecology to explain the temporal and spatial variation in species diversity, distribution, and disparity. Phylogenetic paleoecology is ideally situated to elucidate many fundamental issues in evolutionary biology, including the generation of new phen

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11

Webb, Robert H. "Spatial and Temporal Distribution of Radiocarbon Ages on Rodent Middens from the Southwestern United States." Radiocarbon 28, no. 1 (1986): 1–8. http://dx.doi.org/10.1017/s0033822200059981.

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The analysis of rodent middens, principally deposited by packrats (Neotoma sp), has rapidly become the most important paleoecologic and paleoclimatologic tool in the southwestern United States. The recent discovery of rodent middens created by stick-nest rats (Leporillus sp) and rock wallabies (Petrogale sp) in Australia (Green et al, 1983; P S Martin, oral commun, 1984) and by dassie rats (Petromus typicus) in South Africa (L Scott, oral commun, 1984) portends the use of midden analysis in arid regions worldwide. Several recent reviews of southwestern paleoecology (eg, Spaulding et al, 1983)

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12

Winder, Isabelle C. "Early Hominin Paleoecology." Environmental Archaeology 19, no. 2 (2014): 179–80. http://dx.doi.org/10.1179/1461410314z.00000000058.

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13

Erwin, D. H. "Paleoecology: A Redirection." Science 278, no. 5339 (1997): 815–16. http://dx.doi.org/10.1126/science.278.5339.815.

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14

Babin, Claude. "Paleoecology concepts andapplications." Geobios 24, no. 1 (1991): 112. http://dx.doi.org/10.1016/0016-6995(91)80043-y.

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15

Whiteman, C. A. "Paleoecology of Beringia." Quaternary Science Reviews 4, no. 4 (1985): x—xiii. http://dx.doi.org/10.1016/0277-3791(85)90011-3.

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16

Schwörer, Christoph, Brigitta Ammann, Marco Conedera, and Willy Tinner. "Wälder in der Zeitmaschine – Möglichkeiten und Grenzen der Paläoökologie." Schweizerische Zeitschrift fur Forstwesen 170, no. 3 (2019): 117–24. http://dx.doi.org/10.3188/szf.2019.0117.

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Forests in a time machine – possibilities and limits of paleoecology Paleoecology allows the reconstruction of ecological processes that take place on long timescales – for example the vegetation dynamics since the last Ice Age or changes in the species composition of forests due to anthropogenic land use. This can be achieved by analyzing plant remains like pollen, spores, leaves, seeds or charcoal that have been conserved over millennia under low oxygen conditions in the sediment of lakes and mires. In this article, we outline the principals, the limits and the potential of paleoecology. It

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17

Leighton, Lindsey R. "New Directions in the Paleoecology of Paleozoic Brachiopods." Paleontological Society Papers 7 (November 2001): 185–206. http://dx.doi.org/10.1017/s1089332600000966.

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Because of their great abundance, widespread distribution, excellent preservation potential (Foote and Sepkoski, 1999), and a tendency not to disarticulate after death, brachiopods are ideal subjects for paleoecological research involving morphometrics, population analysis, and phylogenetics. Paleoecology is a subdiscipline that demands large data sets and statistical tests, and brachiopods provide the opportunity to create such databases. I fully expect to see brachiopods play a major role in the coming years in studies on the cutting edge of paleoecology. My approach in this chapter is to pr

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18

Kitchell, Jennifer A. "Evolutionary paleoecology: recent contributions to evolutionary theory." Paleobiology 11, no. 1 (1985): 91–104. http://dx.doi.org/10.1017/s0094837300011428.

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In the past decade, evolutionary paleoecology has shifted away from corroborative research of the “me-too-ecology” type toward its proper domain—the evolutionary consequences of ecological properties, roles, and strategies at the individual, population, community, and species levels. The science of evolutionary paleoecology tests for linkage between a species' ecology and its macroevolutionary history. Do the ecological characters of species within clades influence differential rate dynamics, particularly rates of faunal turnover and diversification? Intellectual coequality, once hampered by t

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19

Meldahl, Keith H., J. Robert Dodd, and Robert J. Stanton. "Paleoecology: Concepts and Applications." PALAIOS 6, no. 5 (1991): 511. http://dx.doi.org/10.2307/3514988.

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20

Bottjer, David J. "Evolutionary Paleoecology: Diverse Approaches." PALAIOS 10, no. 1 (1995): 1. http://dx.doi.org/10.2307/3515003.

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21

Miller, William. "Advances in Deepsea Paleoecology." PALAIOS 9, no. 1 (1994): 1. http://dx.doi.org/10.2307/3515073.

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22

Hanson, B. "PALEOECOLOGY: Long-Lasting Consequences." Science 303, no. 5659 (2004): 731a—731. http://dx.doi.org/10.1126/science.303.5659.731a.

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23

Sugden, Andrew M. "Future predictions from paleoecology." Science 361, no. 6405 (2018): 888.13–890. http://dx.doi.org/10.1126/science.361.6405.888-m.

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24

Wang, Yigang, and Gerd E. G. Westermann. "Paleoecology of Triassic ammonoids." Geobios 26 (January 1993): 373–92. http://dx.doi.org/10.1016/s0016-6995(06)80391-8.

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25

Reyment, Richard. "Paleoecology: Concepts and applications." Palaeogeography, Palaeoclimatology, Palaeoecology 91, no. 1-2 (1992): 186–87. http://dx.doi.org/10.1016/0031-0182(92)90044-6.

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26

Napier, Joseph D., Guillaume de Lafontaine, and Melissa L. Chipman. "The Evolution of Paleoecology." Trends in Ecology & Evolution 35, no. 4 (2020): 293–95. http://dx.doi.org/10.1016/j.tree.2019.12.006.

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27

Sugden, A. M. "PALEOECOLOGY: Living in Harmony." Science 295, no. 5554 (2002): 409b—409. http://dx.doi.org/10.1126/science.295.5554.409b.

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28

Jackson, J. B. C. "PALEOECOLOGY: Measuring Past Biodiversity." Science 293, no. 5539 (2001): 2401–4. http://dx.doi.org/10.1126/science.1063789.

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29

Maas, Mary C. "Paleoecology in primate evolution." Evolutionary Anthropology: Issues, News, and Reviews 3, no. 1 (2005): 6–8. http://dx.doi.org/10.1002/evan.1360030105.

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30

Walker, Ian R. "Chironomidae (Diptera) in paleoecology." Quaternary Science Reviews 6, no. 1 (1987): 29–40. http://dx.doi.org/10.1016/0277-3791(87)90014-x.

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31

Terras, Rafael, Mirian Carbonera, Guilherme Budke, and Karla Janaísa Gonçalves Leite. "FAMÍLIA SPINOSAURIDAE (DINOSAURIA: THEROPODA): TAXONOMIA, PALEOBIOGEOGRAFIA E PALEOECOLOGIA (UMA REVISÃO)." PALEONTOLOGIA EM DESTAQUE - Boletim Informativo da Sociedade Brasileira de Paleontologia 37, no. 77 (2023): 14–54. http://dx.doi.org/10.4072/paleodest.2022.37.77.02.

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Spinosauridae family (Dinosauria: Theropoda): taxonomy, paleobiogeography and paleoecology (a revision). Spinosauridae is a family of Tetanuran theropod dinosaurs that was widely distributed during the Early Cretaceous. Here we revised the state of art of the family’s taxonomy, paleobiogeography and paleoecology. We compiled updated diagnosis for the holotypes of the 20 species attributed to the family since 1841, alongside with the different hypotheses related to the family’s paleobiogeography and paleoecology. We also compiled updated diagnosis for a series of indeterminate elements that are

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32

DiMichele, William A., and Robert A. Gastaldo. "Plant Paleoecology in Deep Time1." Annals of the Missouri Botanical Garden 95, no. 1 (2008): 144–98. http://dx.doi.org/10.3417/2007016.

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33

Levin, Lisa A. "Paleoecology and Ecology of Xenophyophores." PALAIOS 9, no. 1 (1994): 32. http://dx.doi.org/10.2307/3515076.

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34

Wooller, Matthew. "Mangrove paleoecology and environmental change." PAGES news 16, no. 1 (2008): 40–41. http://dx.doi.org/10.22498/pages.16.1.40.

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35

Fontana, Sonia L., and Keith D. Bennett. "Quaternary paleoecology: Reconstructing past environments." Past Global Changes Magazine 22, no. 1 (2014): 46. http://dx.doi.org/10.22498/pages.22.1.46.

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36

Fontana, Sonia L., and Keith D. Bennett. "Quaternary paleoecology: Reconstructing past environments." Past Global Change Magazine 23, no. 2 (2015): 77. http://dx.doi.org/10.22498/pages.23.2.77.

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37

Olago, Daniel O., and Eric O. Odada. "Paleoecology of Eastern Africa Mountains." PAGES news 9, no. 3 (2001): 19–21. http://dx.doi.org/10.22498/pages.9.3.19.

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38

Tinner, Willy, and Brigitta Ammann. "Timberline Paleoecology in the Alps." PAGES news 9, no. 3 (2001): 9–11. http://dx.doi.org/10.22498/pages.9.3.9.

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39

Lovejoy, Thomas E. "Paleoecology and the path ahead." Frontiers in Ecology and the Environment 5, no. 9 (2007): 456. http://dx.doi.org/10.1890/1540-9295(2007)5[456:patpa]2.0.co;2.

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40

Shipman, Pat. "Paleoecology of Fort Ternan reconsidered." Journal of Human Evolution 15, no. 3 (1986): 193–204. http://dx.doi.org/10.1016/s0047-2484(86)80045-8.

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41

Ekdale, A. A. "Paleoecology of the marine endobenthos." Palaeogeography, Palaeoclimatology, Palaeoecology 50, no. 1 (1985): 63–81. http://dx.doi.org/10.1016/s0031-0182(85)80006-7.

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42

Olson, Everett C. "Vertebrate paleoecology: A current perspective." Palaeogeography, Palaeoclimatology, Palaeoecology 50, no. 1 (1985): 83–106. http://dx.doi.org/10.1016/s0031-0182(85)80007-9.

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43

Verma, Omkar. "Paleoecology: Past, present and future." Journal of the Geological Society of India 91, no. 1 (2018): 115–16. http://dx.doi.org/10.1007/s12594-018-0843-8.

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44

Miller, William. "Paleoecology of benthic community replacement." Lethaia 19, no. 3 (1986): 225–31. http://dx.doi.org/10.1111/j.1502-3931.1986.tb00735.x.

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45

KOTAKE, NOBUHIRO. "Paleoecology of the Zoophycos producers." Lethaia 22, no. 3 (1989): 327–41. http://dx.doi.org/10.1111/j.1502-3931.1989.tb01349.x.

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46

Heusser, C. J. "Quaternary paleoecology of Fuego-Patagonia." Revista do Instituto Geológico 15, no. 1-2 (1994): 7–26. http://dx.doi.org/10.5935/0100-929x.19940002.

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47

Kumaran, Navnith K. P., and Ruta B. Limaye. "Holocene Palynology and Tropical Paleoecology." Quaternary International 325 (March 2014): 1–2. http://dx.doi.org/10.1016/j.quaint.2014.02.005.

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48

Hughes, Paul. "Paleoecology and the conservation paradox." Landscape Ecology 32, no. 1 (2016): 227–28. http://dx.doi.org/10.1007/s10980-016-0470-y.

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49

Bartlein, P. J., and I. C. Prentice. "Orbital variations, climate and paleoecology." Trends in Ecology & Evolution 4, no. 7 (1989): 195–99. http://dx.doi.org/10.1016/0169-5347(89)90072-4.

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50

McDougall, Kristin. "Micropaleontological Evidence of A Submarine Fan in the Lower Coaledo Formation, Southwestern Oregon, USA." Journal of Foraminiferal Research 53, no. 4 (2023): 311–37. http://dx.doi.org/10.61551/gsjfr.53.4.311.

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Abstract The middle Eocene lower Coaledo Formation was interpreted as ten shoaling upward delta-margin cycles based on sediments and macrofauna. The strata, however, contains deep-water foraminifers. Explanations to resolve this anomaly included reworking, bathymetric range extension, or upward migration of water masses. Paleoecology analysis of foraminifers indicates that the few shelf species are poorly preserved whereas the well-preserved lower bathyal species dominate, and planktic organisms are present. Evidence for reworking, bathymetric range extension, or upward migration of water mass

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