Quick
Search: 
 
advanced search
 GSW Home    GeoRef Home    My GSW Alerts    Contact GSW    About GSW    Journals List    Help 
American Mineralogist Don't get GSW? Talk to your librarian.
JOURNAL HOME HELP CONTACT PUBLISHER SUBSCRIBE ARCHIVE SEARCH TABLE OF CONTENTS

American Mineralogist; November 2003; v. 88; no. 11-12; p. 1879-1888
© 2003 Mineralogical Society of America
This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (8)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Garvie, L. A.J.
Right arrow Search for Related Content
GeoRef
Right arrow GeoRef Citation

Decay-induced biomineralization of the saguaro cactus (Carnegiea gigantea)

Laurence A.J. Garvie*

Department of Geological Sciences, Arizona State University, Tempe, Arizona 85287-1404, U.S.A.

Correspondence: * E-mail: lgarvie{at}asu.edu

The saguaro, Carnegiea gigantea (Englemann), is a columnar cactus that grows to 15 m tall and weighs up to several tons, of which 85 to 90% of the mass is water. Roughly 18% of the dry mass consists of the biomineral weddellite (CaC2O4·2H2O). The C in the weddellite derives from atmospheric CO2 via photosynthesis. A mature saguaro can contain on the order of 1 x 105 g of weddellite. The weddellite crystals occur as aggregates up to 1 mm wide. After the death of the saguaro, a series of minerals crystallize in the rotting flesh. These minerals form from elements released from the decay of the cactus by microorganisms and thus is a type of biologically induced mineralization. During the initial stages of decay, authigenic Mg- and Ca-bearing minerals crystallize from elements released by the putrefying flesh and include lansfordite (MgCO3·5H2O), nesquehonite (MgCO3·3H2O), several polymorphs of MgC2O4·2H2O including glushinskite, monohydrocalcite (CaCO3·H2O), calcite, vaterite, and several unidentified Mg-bearing phases. As the saguaro decays, the soft, water-rich pith shrinks, but the ribs and skin remain intact, producing warm, moist pockets within the dead saguaro. Abundant, glassy lansfordite crystals to 1 mm in diameter grow in these pockets during the cooler winter months. Further decay leaves a dried hollow shell covered by the saguaro skin, inside of which nesquehonite and monohydrocalcite crystallize. Lansfordite and nesquehonite are unstable in the desert and rapidly amorphize after exposure to the atmosphere. Magnesium oxalates are locally abundant in the decayed flesh and occur as crystals up to 1.5 mm in length. The common occurrence of fungal hyphae on the glushinskite suggests that it forms as a result of the reaction between oxalic acid released by fungi and the Mg-rich solutions of the rotting saguaro. During the final stages of decay, the pith consists of a pale-brown to tan-colored sand of weddellite and its transformation product monohydrocalcite. This sand lithifies to porous sponge-like masses during the final stages of saguaro decay. This monohydrocalcite further alters to calcite. The {delta}13CVPDB of the monohydrocalcite and calcite after weddellite range from –1.65 to + 0.76{per thousand}. The calcite is subsequently solubilized and remobilized, precipitating as caliche in the desert soil, or redistributed by wind. In arid environments, the desert fauna metabolize the atmospheric C bound in the organic matter to CO2. In contrast, decay of the saguaro adds atmospheric C to the soil as inorganic C via the transformation of the biomineral weddellite to calcite. In areas with high saguaro density, it is estimated that up to 2.4 g/m2/yr of calcite can be added to the desert from the decayed cacti. This inorganic C has geologically long soil residence times, thus effectively sequestering the atmospheric C.




This article has been cited by other articles:


Home page
American MineralogistHome page
I. P. Swainson
The effect of the hedenbergitic substitution on the compressibility of jadeite
American Mineralogist, July 1, 2008; 93(7): 1014 - 1018.
[Abstract] [Full Text] [PDF]


Home page
Journal of Sedimentary ResearchHome page
K. Dahl and B. Buchardt
Monohydrocalcite in the Arctic Ikka Fjord, SW Greenland: First Reported Marine Occurrence
Journal of Sedimentary Research, March 1, 2006; 76(3): 460 - 471.
[Abstract] [Full Text] [PDF]


Home page
Mineral MagHome page
D. A. C. Manning, E. Lopez-Capel, and S. Barker
Seeing soil carbon: use of thermal analysis in the characterization of soil C reservoirs of differing stability
Mineralogical Magazine, August 1, 2005; 69(4): 425 - 435.
[Abstract] [Full Text] [PDF]




JOURNAL HOME HELP CONTACT PUBLISHER SUBSCRIBE ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2008 by Mineralogical Society of America