Professor
Fields of Interest
Biography
Evolution of Grasses and Assembly of Grassland Ecosystems
Grasslands cover more than 40% of the continents and vitally influences global climate, geochemical cycling, and the animals (including humans!) that depend on them. Given the central role that the grasses (Poaceae) play on Earth today, we ask:
- When/where did Poaceae originate and diversify, and how did it reach its current, world-wide distribution?
- When did grasses able to cope with the open, arid conditions typical of today's grasslands evolve—and when did grasslands start spreading? What drove these changes?
- How and why have grasslands changed through evolutionary time, and how have they influenced faunas and faunal evolution?
- How did grasses themselves respond to the spread of open, grass-dominated habitats through changes in dispersal mode and defense?
We document the evolutionary history of Poaceae and the assembly of grassland ecosystems in multiple regions on different continents (North and South America, Eurasia, Africa) to better understand the unique paths and common factors that have shaped the formation of the grassy biome.
Biotic Responses to Climate Change in Deep-Time
Paleontologists have a unique opportunity to study how plants and animals have responded to major environmental changes over long timescales (104-106 years), providing information that can potentially improve predictions for future ecosystem change. Environmental changes of interest include changes in climate, atmospheric CO2 levels, disturbance (e.g. fire regime). We wonder:
- How are major global climatic events manifested at the local-regional level and how does vegetation respond?
- What can geographic variation in climatic alteration and biotic responses tell us about major drivers and global impacts during these events?
- What role do plants play in faunal responses during environmental change?
- To what extent does ecosystem history influence how vegetation responds to environmental change?
In collaboration with geochemists, geologists and vertebrate palentologists, we address these questions for several major Earth events (e.g., Eocene-Oligocene cooling, middle Miocene warming, end-Cretaceous warming and cooling) on different continents (North and South America, India).
Evolution and Functional Role of Silica in Land Plant
Plants have had to ‘deal’ with silica in their environment since they emerged on land some 450 million years ago. Today, many plants appear to benefit from incorporating Si/silica in their tissues for several reasons, ranging from enhanced protection against parasites and heavy metal poisoning, to mechanical support and herbivore deterrence. To better understand how and why plants accumulate silica in their bodies we ask:
- When did plants start actively accumulating silica in their tissues? Did it happen more than once?
- Did certain groups (e.g., grasses) enhance their silica content relative to others for functional (adaptive) reasons, such as structural support or herbivore defense?
- How have the amounts and shapes of silica bodies evolved across Poaceae? Can we use this shape variation to better track specific grass lineages or to better understand ecological change in the fossil record?
Using phylogenetic comparative methods, modern experiments, and 2D/3D morphometric analyses of silica bodies in both modern and fossil plants, we tackle these questions by reconstructing phylogenetic patterns of silica levels and phytolith shape across land plants in general, and grasses specifically.
Evolutionary Ecology of Plant Communities in the Late Cretaceous-Paleocene
Plant communities underwent major changes in the Late Cretaceous and Paleocene. Flowering plants (angiosperms), although taxonomically diverse, transitioned from being marginal in many ecosystems to becoming ecological dominants, as they are today. The end-Cretaceous saw environmental changes (e.g. Deccan volcanism, warming/cooling), and a major faunal collapse culminating in the extinction of dinosaurs and other animals at the Cretaceous-Paleogene (K-Pg) boundary. In light of these ecosystem transformations, we wonder:
- What ecological role did angiosperms play in ecosystems before they rose to dominance in North America?
- How did plant communities in northeastern Montana and India respond to environmental change leading up to and across the K-Pg boundary?
- What part, if any, did vegetation (change) have in the collapse of Late Cretaceous faunas and foodwebs?
In collaboration with other paleobotanists, neo-ecologists, vertebrate paleontologists (in particular the Wilson lab and colleagues), geologists, and geochemists, we use plant macrofossils and microfossils to reconstruct plant ecological strategies, vegetation types, and environments through time and space during this critical time.
2007 Postdoctoral Fellow, National Museum of Natural History, Smithsonian Institution, Washington, DC
2004-2006 Postdoctoral Fellow, Swedish Museum of Natural History, Stockholm, Sweden
2003 Ph.D., Department of Integrative Biology, University of California, Berkeley
1997 B.A., M.Sc., Department of Geology, Lund University, Sweden
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Selected Research
- Unexpectedly large phytolith C sequestration potential in global terrestrial ecosystems, Strömberg C A E, Song Z, and Liu H, Nature (9999)
- Light environment and epidermal cell morphology in grasses, Dunn R E, Strömberg C A E, and Le T -Y, International Journal of Plant Sciences (9999)
- Large contribution of forests to carbon sink through continental silicate weathering, Strömberg C A E, Li B, Song Z, Liu H, Wang H, Strong P J, and Xu C, Environmental Science & Technology (9999)
- Regional-scale variability in the spread of grasslands in the late Miocene, Strömberg C A E, Chen S T, Smith S Y, and Sheldon N D, Palaeogeography, Palaeoclimatology, Palaeoecology (9999)
- Quasi-static Eocene-Oligocene climate in Patagonia promotes slow faunal evolution and mid-Cenozoic global cooling, Dunn R E, Strömberg C A E, Madden R H, Kohn M J, Carlini A A, Evans S, and Palacios A, Palaeogeography, Palaeoclimatology, Palaeoecology (9999)
- Reconstruction of the recent ethnological and environmental history of the mountainous area of the Catalan Coast (Iberian Peninsula), using macro- and micro-contents from ovicaprine animal dung, Strömberg C A E, Panades i Blas X, Bartolomé i Filella J, Soriano i Tomàs I, Buckland P, Serieyssol K K, Bach i Plaza J, Arillo Aranda A, Lozar F, Stevenson T, and Chamorro i Lorenzo L, Environmental Archaeology (9999)
- Climate, dust, and fire across the Eocene-Oligocene Transition, Patagonia, Dunn R E, Strömberg C A E, Madden R H, Kohn M J, Carlini A A, Selkin P A, Boyle J, and Davies-Vollum K S, Geology (9998)
- Functions of Phytoliths in Vascular Plants: An Evolutionary Perspective, Strömberg C A E, Di Stilio VS, and Song Z, Functional Ecology, 05/2016 (2016)
- Linked canopy, climate and faunal evolution in the Cenozoic of Patagonia, Dunn R E, Strömberg C A E, Madden R H, Kohn M J, and Carlini A A, Science, Volume 347, Issue 6219, p.258-261 (2015)
- Biogeographically distinct controls on C3 and C4 grass distributions: merging community and physiological ecology, Strömberg C A E, Osborne C P, Griffith D M, Anderson T M, Forrestel E J, and Still C J, Global Ecology and Biogeography (2014)
- The Vasa Park flora, King County, Washington, USA – a window into the late Miocene of the Pacific Northwest, Dillhoff R M, Dillhoff T A, Strömberg C A E, and Jijina A P, Paleobotany and Biogrography, A Festschrift for Alan Graham in His 80th Year, p.64-97, St. Louis, Missouri, Missouri Botanical Garden Press (2014)
- Bivalve network reveals latitudinal selectivity gradient at the end-Cretaceous mass extinction., Wilson G P, Bergstrom C T, Strömberg C A E, Ward P D, Sidor C A, Vilhena D A, Harris E B, and Maliska M E, Scientific Reports, Volume 3, p.doi:10.1038/srep01790 (2013)
- Evolution of grasses and grassland ecosystems, Strömberg C A E, Annual Reviews of Earth and Planetary Sciences, Volume 39, p.517-544 (2011)
- The Neogene transition from C3 to C4 grasslands in North America: Stable carbon isotope ratios of fossil phytoliths, Strömberg C A E, McInerney F A, and White J W C, Paleobiology, 2011, Volume 37, p.23-49 (2011)
- The Origins of C-4 Grasslands: Integrating Evolutionary and Ecosystem Science, Strömberg C A E, Edwards E J, Osborne C P, Smith S A, and Consortium Grasses C4, Science, 2010, Volume 328, Issue 5978, p.587-591 (2010)
- Cenozoic paleobotany of the John Day Basin, central Oregon, O’Connor J E, Dorsey R J, Madin I P, Dillhoff R M, Dillhoff T A, Dunn R E, Myers J A, and Strömberg C A E, Volcanoes to Vineyards: Geologic Field Trips through the Dynamic Landscape of the Pacific Northwest, 2009, p.135–164 (2009)
- Methodological concerns for analysis of phytolith assemblages: Does count size matter?, Strömberg C A E, Quaternary International, 2009, Volume 193, p.124–140 (2009)
- The spread of grass-dominated habitats in Turkey and surrounding areas during the Cenozoic: phytolith evidence, Strömberg C A E, Friis E M, Werdelin L, and Saraç G, Palaeogeography, Palaeoclimatology, Palaeoecology, 2007, Volume 250, p.18-49 (2007)
- Palaeoecology of an Early-Middle Miocene lake in China: preliminary interpretations based on phytoliths from the Shanwang Basin, Strömberg C A E, Friis E M, Liang Ming-Mei, Werdelin L, and Zhang Yu-liang, Vertebrata PalAsiatica, 2007, Volume 45, Issue 2, p.145-160 (2007)
- The evolution of hypsodonty in equids: testing a hypothesis of adaptation, Strömberg C A E, Paleobiology, 2006, Volume 32, Issue 2, p.236-258 (2006)
- Dinosaur coprolites and the early evolution of grasses and grazers, Strömberg C A E, Prasad V, Alimohammadian H, and Sahni A, Science, 2005, Volume 310, p.1177-1180 (2005)
- Decoupled taxonomic radiation and ecological expansion of open-habitat grasses in the Cenozoic of North America, Strömberg C A E, Proceedings of the National Academy of Sciences of the Unites States of America, 2005, Volume 102, Issue 34, p.11980-11984 (2005)
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