
Natalie Cápiro
· Assistant ProfessorVerifiedCornell University · Biological and Environmental Engineering
Active 2006–2025
About
Professor Natalie Cápiro is the Principal Investigator of the Cápiro Research Group at Cornell University. Her research focuses on environmental microbiology, bioremediation, and the fate and transport of groundwater contaminants. She leads a team that investigates microbial processes and their applications to environmental cleanup and management, contributing to the understanding and development of bioremediation strategies for contaminated groundwater. Her work is situated within the Department of Biological and Environmental Engineering at Cornell University, where she advances knowledge in environmental microbiology and sustainable remediation techniques.
Research topics
- Environmental chemistry
- Chemistry
- Organic chemistry
- Ecology
- Chemical engineering
- Engineering
- Polymer chemistry
- Chromatography
- Biology
Selected publications
Sorption-Desorption Processes Contributing to Natural Attenuation of Trichloroethene in Porous Media
SSRN Electronic Journal · 2025-01-01
preprintOpen accessJournal of Hazardous Materials · 2025-05-05 · 2 citations
articleACS ES&T Water · 2025-06-11 · 10 citations
articleSenior authorCorrespondingDespite widespread detection of perfluorooctane sulfonamide (FOSA) in the environment, its potential for biotransformation by native soil microorganisms and the resulting impacts on microbial communities remain poorly understood. This study examined the biotransformation of FOSA over 308 days in microcosms prepared with two soils, a historically per- and polyfluoroalkyl substances (PFAS)-contaminated soil and a PFAS-free agricultural soil. Indigenous microorganisms in both soils were able to biotransform FOSA with half-lives ranging from 203.0 to 335.1 days. Perfluorooctanesulfonate (PFOS) was the primary biotransformation product, with a molar yield of 21.6 ± 5.2 mol% in the historically PFAS-contaminated soil and 29.5 ± 3.8 mol% in the initially PFAS-free soil. Microbial community analysis revealed that members of the phyla Cyanobacteria and Bacteroidota, as well as the genus Afipia, exhibited greater tolerance to elevated concentrations of FOSA and/or its biotransformation products. Metagenomic predictions using Tax4Fun2 identified functional genes related to amino acid metabolism, sulfur metabolism, and the two-component system, which may be linked to FOSA exposure and/or its biotransformation. These findings highlight the role of biotransformation processes in shaping the environmental fate of FOSA and PFOS, and offer insights into the capacity of native soil microbial communities to transform FOSA and related perfluorooctane sulfonamide derivatives.
Sorption-desorption processes contributing to natural attenuation of trichloroethene in porous media
Journal of Contaminant Hydrology · 2025-06-19 · 2 citations
articleWater Research · 2025-06-10 · 4 citations
articleSenior authorCorrespondingQuantifying biolipid (rhamnolipid) effects on the aggregation behavior of engineered nanoparticles
Environmental Science Nano · 2025-01-01 · 1 citations
articleOpen accessRhamnolipids (mono/diRL) govern iron oxide nanoparticle stability in water as a function of particle surface charge, RL type and concentration, and ionic strength, resulting in complex stabilization processes including non-DLVO behavior.
SSRN Electronic Journal · 2025-01-01
preprintOpen accessSenior authorEnvironmental Science & Technology · 2024-12-10 · 23 citations
articleSenior authorCorrespondingThe environmental fate of per- and polyfluoroalkyl substances (PFAS) in aqueous film-forming foams (AFFFs), especially those synthesized by electrochemical fluorination (ECF) processes, remains largely unknown. This study evaluated the transformation of AFFF-derived ECF-based precursors in aerobic soil microcosms amended with a historically used AFFF formulation (3M Light WaterTM). Fifteen classes of PFAS, including AFFF components and transformation products, were identified or tentatively identified by suspect screening/nontargeted analysis (SSA/NTA) throughout a 308-day incubation. This study demonstrates that AFFF-derived ECF-based precursors serve as sources of perfluoroalkane sulfonamides (FASAs) and perfluoroalkyl acids (PFAAs), which are commonly detected at AFFF-impacted sites. Temporal sampling provided evidence for biotransformation of multiple precursors including tri- or dimethyl ammonio propyl perfluoroalkane sulfonamides. Additionally, the environmental stability (i.e., resistance to transformation) of ECF-based precursors was found to depend upon structural characteristics, including perfluoroalkyl chain length, presence of sulfonamide or carboxamide groups, and functional groups (e.g., a branch of carboxyalkyl group) attached to the nitrogen atoms. These findings provide insights into the transformation pathways of AFFF-derived PFAS and other structurally similar ECF-based PFAS, which will support the management and remediation of PFAS contamination at legacy AFFF-impacted sites.
Environmental Science & Technology · 2024-04-19 · 38 citations
articleSenior authorCorrespondingMicrobial transformation of per- and polyfluoroalkyl substances (PFAS), including fluorotelomer-derived PFAS, by native microbial communities in the environment has been widely documented. However, few studies have identified the key microorganisms and their roles during the PFAS biotransformation processes. This study was undertaken to gain more insight into the structure and function of soil microbial communities that are relevant to PFAS biotransformation. We collected 16S rRNA gene sequencing data from 8:2 fluorotelomer alcohol and 6:2 fluorotelomer sulfonate biotransformation studies conducted in soil microcosms under various redox conditions. Through co-occurrence network analysis, several genera, including Variovorax, Rhodococcus, and Cupriavidus, were found to likely play important roles in the biotransformation of fluorotelomers. Additionally, a metagenomic prediction approach (PICRUSt2) identified functional genes, including 6-oxocyclohex-1-ene-carbonyl-CoA hydrolase, cyclohexa-1,5-dienecarbonyl-CoA hydratase, and a fluoride-proton antiporter gene, that may be involved in defluorination. This study pioneers the application of these bioinformatics tools in the analysis of PFAS biotransformation-related sequencing data. Our findings serve as a foundational reference for investigating enzymatic mechanisms of microbial defluorination that may facilitate the development of efficient microbial consortia and/or pure microbial strains for PFAS biotransformation.
The Science of The Total Environment · 2024-02-06 · 22 citations
article
Frequent coauthors
- 120 shared
Kurt D. Pennell
Providence College
- 56 shared
Tyler F. Marcet
Tufts University
- 54 shared
William G. Rixey
- 49 shared
Neil R. Thomson
- 49 shared
Aldrich Lahvis
Ecolyse (United States)
- 49 shared
Paul Johnson
University of Michigan–Ann Arbor
- 49 shared
Carol J. Ptacek
University of Waterloo
- 49 shared
Matthew J. Thomasson
University of Hull
Labs
Education
Ph.D.
Cornell University
M.S.
Tufts University
B.S.
Auburn University
Awards & honors
- Association of Environmental Engineering and Science Profess…
- SERDP Environmental Restoration Project of the Year 2012
- Eleanor and Mills Bennett Fellowship in Hydrology, Rice Univ…
- NSF Distinguished Sci. & Engr. Fellow of the Alliances for G…
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