Karen L. Casciotti

Karen L. Casciotti

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Karen L. Casciotti

Department of Earth System Science Stanford University Stanford CA USA

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 July 2001 in Analytical Chemistry
Verified
Journal Article
Closed access
DSD. M. Sigman
D. M. Sigman
KCK. L. Casciotti
K. L. Casciotti
MAM. Andreani
M. Andreani
CBC. Barford
C. Barford
MGM. Galanter
M. Galanter
JBJ. K. Böhlke
J. K. Böhlke

7 September 2002 in Analytical Chemistry
Verified
Journal Article
Closed access
KCK. L. Casciotti
K. L. Casciotti
DSD. M. Sigman
D. M. Sigman
MHM. Galanter Hastings
M. Galanter Hastings
JBJ. K. Böhlke
J. K. Böhlke
AHA. Hilkert
A. Hilkert

27 April 2007 in Science
Verified
Journal Article
Closed access
PDF file
KBKen O. Buesseler
Ken O. Buesseler
CLCarl H. Lamborg
Carl H. Lamborg
PBPhilip W. Boyd
Philip W. Boyd
PLPhoebe J. Lam
Phoebe J. Lam
TTThomas W. Trull
Thomas W. Trull
SWStephanie Wilson
Stephanie Wilson
The oceanic biological pump drives sequestration of carbon dioxide in the deep sea via sinking particles. Rapid biological consumption and remineralization of carbon in the “twilight zone” (depths between the euphotic zone and 1000 meters) reduce the efficiency of sequestration. By using neutrally buoyant sediment traps to sample this chronically understudied realm, we measured a transfer efficiency of sinking particulate organic carbon between 150 and 500 meters of 20 and 50% at two contrasting sites. This large variability in transfer efficiency is poorly represented in biogeochemical models. If applied globally, this is equivalent to a difference in carbon sequestration of more than 3 petagrams of carbon per year.

2 September 2011 in Science
Verified
Journal Article
Closed access
PDF file
ASAlyson E. Santoro
Alyson E. Santoro
CBCarolyn Buchwald
Carolyn Buchwald
MMMatthew R. McIlvin
Matthew R. McIlvin
KCKaren L. Casciotti
Karen L. Casciotti
The ocean is an important global source of nitrous oxide (N2O), a greenhouse gas that contributes to stratospheric ozone destruction. Bacterial nitrification and denitrification are thought to be the primary sources of marine N2O, but the isotopic signatures of N2O produced by these processes are not consistent with the marine contribution to the global N2O budget. Based on enrichment cultures, we report that archaeal ammonia oxidation also produces N2O. Natural-abundance stable isotope measurements indicate that the produced N2O had bulk δ15N and δ18O values higher than observed for ammonia-oxidizing bacteria but similar to the δ15N and δ18O values attributed to the oceanic N2O source to the atmosphere. Our results suggest that ammonia-oxidizing archaea may be largely responsible for the oceanic N2O source.

5 July 2010 in Environmental Microbiology
Verified
Journal Article
Closed access
PDF file
ASAlyson E. Santoro
Alyson E. Santoro
KCKaren L. Casciotti
Karen L. Casciotti
CFChristopher A. Francis
Christopher A. Francis

1 August 2018 in Chemical Geology
Verified
Journal Article
Open access
RSReiner Schlitzer
Reiner Schlitzer
RARobert F. Anderson
Robert F. Anderson
EDElena Masferrer Dodas
Elena Masferrer Dodas
MLMaeve Lohan
Maeve Lohan
WGWalter Geibert
Walter Geibert
CZCheryl Zurbrick
Cheryl Zurbrick