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Suto, Itsuki; Kawamura, Keita; Hagimoto, Shinta; Teraishi, Akihito; Tanaka, Yuichiro (2012): Marine diatoms in deep sea sediments [dataset publication series]. PANGAEA, https://doi.org/10.1594/PANGAEA.811973, Supplement to: Suto, I et al. (2012): Changes in upwelling mechanisms drove the evolution of marine organisms. Palaeogeography, Palaeoclimatology, Palaeoecology, 339-341, 39-51, https://doi.org/10.1016/j.palaeo.2012.04.014

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Abstract:
Long-term evolution is thought to take opportunities that arise as a consequence of mass extinction (as argued, for example, by Gould, 2002) and the following biotic recovery, but there is absolutely no evidence for this being the case. However, our study shows that eutrophication by oceanic mixing also played a part in the enhancement of several evolutionary events amongst marine organisms, and these results could indicate that the rates of oceanic biodiversification may be slowed if upwelling becomes weakened by future global warming. This paper defines three distinct evolutionary events of resting spores of the marine diatom genus Chaetoceros, to reconstruct past upwelling through the analysis of several DSDP, ODP and land-based successions from the North, South and equatorial Pacific as well as the Atlantic Ocean during the past 40 million years. The Atlantic Chaetoceros Explosion (ACE) event occurred across the E/O boundary in the North Atlantic, and is characterized by resting spore diversification that occurred as a consequence of the onset of upwelling following changes in thermohaline circulation through global cooling in the early Oligocene. Pacific Chaetoceros Explosion events-1 and -2 (PACE-1 and PACE-2) are characterized by relatively higher occurrences of iron input following the Himalayan uplift and aridification at 8.5 Ma and ca. 2.5 Ma in the North Pacific region. These events not only enhanced the diversification and increased abundance of primary producers, including that of Chaetoceros, other diatoms and seaweeds, but also stimulated the evolution of zooplankton and larger predators, such as copepods and marine mammals, which ate these phytoplankton and plants. Current thinking suggests new evolutionary niches open up after a mass extinction, but our study finds that eutrophication can also stimulate evolutionary diversification. Moreover, in the opposite fashion, our results show that as thermohaline circulation abates, global warming progresses and the ocean surface becomes warmer, many marine organisms will be affected by the environmental degradation.
Coverage:
Median Latitude: 33.099517 * Median Longitude: 26.385957 * South-bound Latitude: -11.266500 * West-bound Longitude: -117.900000 * North-bound Latitude: 78.385400 * East-bound Longitude: 145.557800
Date/Time Start: 1974-08-14T00:00:00 * Date/Time End: 1993-08-15T13:06:00
Size:
12 datasets

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Datasets listed in this publication series

  1. Suto, I; Kawamura, K; Hagimoto, S et al. (2012): (Table 1) Occurrences of fossil Chaetoceros resting spore species in DSDP Hole 38-338. https://doi.org/10.1594/PANGAEA.811927
  2. Suto, I; Kawamura, K; Hagimoto, S et al. (2012): (Table 2) Occurrences of fossil Chaetoceros resting spore species in DSDP Hole 41-366. https://doi.org/10.1594/PANGAEA.811934
  3. Suto, I; Kawamura, K; Hagimoto, S et al. (2012): (Table 2) Occurrences of diatoms species in DSDP Hole 41-366. https://doi.org/10.1594/PANGAEA.811935
  4. Suto, I; Kawamura, K; Hagimoto, S et al. (2012): (Table 3) Occurrences of fossil Chaetoceros resting spore species in DSDP Hole 41-369A. https://doi.org/10.1594/PANGAEA.811940
  5. Suto, I; Kawamura, K; Hagimoto, S et al. (2012): (Table 3) Occurrences of diatoms species in DSDP Hole 41-369A. https://doi.org/10.1594/PANGAEA.811939
  6. Suto, I; Kawamura, K; Hagimoto, S et al. (2012): (Table 5) Occurrences of fossil Chaetoceros resting spore species in DSDP Hole 56-436. https://doi.org/10.1594/PANGAEA.811945
  7. Suto, I; Kawamura, K; Hagimoto, S et al. (2012): (Table 6) Occurrences of fossil Chaetoceros resting spore species in DSDP Hole 57-438A. https://doi.org/10.1594/PANGAEA.811965
  8. Suto, I; Kawamura, K; Hagimoto, S et al. (2012): (Table 7) Occurrences of fossil Chaetoceros resting spore species in DSDP Hole 87-584. https://doi.org/10.1594/PANGAEA.811967
  9. Suto, I; Kawamura, K; Hagimoto, S et al. (2012): (Table 8) Occurrences of fossil Chaetoceros resting spore species in ODP Hole 112-682A. https://doi.org/10.1594/PANGAEA.811968
  10. Suto, I; Kawamura, K; Hagimoto, S et al. (2012): (Table 4) Occurrences of fossil Chaetoceros resting spore species in ODP Site 151-908. https://doi.org/10.1594/PANGAEA.811941
  11. Suto, I; Kawamura, K; Hagimoto, S et al. (2012): (Table 9) Occurrences of fossil Chaetoceros resting spore species from Chokubetsu and Atsunai Formations distributed in southeastern Hokkaido, Japan. https://doi.org/10.1594/PANGAEA.811969
  12. Suto, I; Kawamura, K; Hagimoto, S et al. (2012): (Table 10) Occurrences of fossil Chaetoceros resting spore species from the Newport Beach Section. https://doi.org/10.1594/PANGAEA.811972