Kathleen H. Lavoie
University of New Mexico
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Featured researches published by Kathleen H. Lavoie.
Geomicrobiology Journal | 2001
D. Northup; Kathleen H. Lavoie
In this article, we provide a review of geomicrobiological interactions in caves, which are nutrient-limited environments containing a variety of redox interfaces. Interactions of cave microorganisms and mineral environments lead to the dissolution of, or precipitation on, host rock and speleothems (secondary mineral formations). Metabolic processes of sulfur-, iron-, and manganese-oxidizing bacteria can generate considerable acidity, dissolving cave walls and formations. Examples of possible microbially influenced corrosion include corrosion residues (e.g., Lechuguilla and Spider caves, New Mexico, USA), moonmilk from a number of caves (e.g., Spider Cave, New Mexico, and caves in the Italian Alps), and sulfuric acid speleogenesis and cave enlargement (e.g., Movile Cave, Romania, and Cueva de Villa Luz, Mexico). Precipitation processes in caves, as in surface environments, occur through active or passive processes. In caves, microbially induced mineralization is documented in the formation of carbonates, moonmilk, silicates, clays, iron and manganese oxides, sulfur, and saltpeter at scales ranging from the microscopic to landscape biokarst. Suggestions for future research are given to encourage a move from descriptive, qualitative studies to more experimental studies.In this article, we provide a review of geomicrobiological interactions in caves, which are nutrient-limited environments containing a variety of redox interfaces. Interactions of cave microorganisms and mineral environments lead to the dissolution of, or precipitation on, host rock and speleothems (secondary mineral formations). Metabolic processes of sulfur-, iron-, and manganese-oxidizing bacteria can generate considerable acidity, dissolving cave walls and formations. Examples of possible microbially influenced corrosion include corrosion residues (e.g., Lechuguilla and Spider caves, New Mexico, USA), moonmilk from a number of caves (e.g., Spider Cave, New Mexico, and caves in the Italian Alps), and sulfuric acid speleogenesis and cave enlargement (e.g., Movile Cave, Romania, and Cueva de Villa Luz, Mexico). Precipitation processes in caves, as in surface environments, occur through active or passive processes. In caves, microbially induced mineralization is documented in the formation of carbonates, ...
PLOS ONE | 2017
Kathleen H. Lavoie; Ara S. Winter; Kaitlyn J. H. Read; Evan M. Hughes; Michael Spilde; D. Northup
Subsurface habitats harbor novel diversity that has received little attention until recently. Accessible subsurface habitats include lava caves around the world that often support extensive microbial mats on ceilings and walls in a range of colors. Little is known about lava cave microbial diversity and how these subsurface mats differ from microbial communities in overlying surface soils. To investigate these differences, we analyzed bacterial 16S rDNA from 454 pyrosequencing from three colors of microbial mats (tan, white, and yellow) from seven lava caves in Lava Beds National Monument, CA, USA, and compared them with surface soil overlying each cave. The same phyla were represented in both surface soils and cave microbial mats, but the overlap in shared OTUs (operational taxonomic unit) was only 11.2%. Number of entrances per cave and temperature contributed to observed differences in diversity. In terms of species richness, diversity by mat color differed, but not significantly. Actinobacteria dominated in all cave samples, with 39% from caves and 21% from surface soils. Proteobacteria made up 30% of phyla from caves and 36% from surface soil. Other major phyla in caves were Nitrospirae (7%) followed by minor phyla (7%), compared to surface soils with Bacteroidetes (8%) and minor phyla (8%). Many of the most abundant sequences could not be identified to genus, indicating a high degree of novelty. Surface soil samples had more OTUs and greater diversity indices than cave samples. Although surface soil microbes immigrate into underlying caves, the environment selects for microbes able to live in the cave habitats, resulting in very different cave microbial communities. This study is the first comprehensive comparison of bacterial communities in lava caves with the overlying soil community.
Astrobiology | 2001
Penelope J. Boston; Michael Spilde; D. Northup; L.A. Melim; D.S. Soroka; L.G. Kleina; Kathleen H. Lavoie; L.D. Hose; L.M. Mallory; Clifford N. Dahm; Laura J. Crossey; Rachel T. Schelble
Journal of Cave and Karst Studies | 2000
Kathleen H. Lavoie; Susan M. Barns; J.P. Boston; Laura J. Crossey; K.I. Cunnimgham; Clifford N. Dahm; L.M. Mallory; D. Northup
Journal of Cave and Karst Studies | 2007
Kathleen H. Lavoie; Kurt L. Helf; Thomas L. Poulson
Archive | 2005
Kathleen H. Lavoie; D. Northup
Archive | 2010
Kathleen H. Lavoie; Diana E. Northup; Hazel A. Barton
Archive | 2015
Diana E. Northup; Kathleen H. Lavoie
Scientia Discipulorum | 2013
Mohammed Chandoo; Elizabeth Lavoie; Utsav Pandey; Suganthi Thirunavukarasu; Kathleen H. Lavoie; Thomas Wolosz; Kurt L. Helf
Archive | 2002
D. Northup; Penelope J. Boston; Michael Spilde; Rachel T. Schelble; Kathleen H. Lavoie; Alejandra Alvarado Zink