Soil Environment

From MicrobeWiki, the student-edited microbiology resource
[15]

Introduction

Early Earth Illustration [14]

Microbial activity, measured in terms of biomass and respiration, reflects the flux of carbon through biotic systems. This page explores the soil environmental and physical factors regulating microbial activity. Microbes are vital to the world's ecosystems, being integral parts of the carbon and nitrogen cycles and affecting plant growth and survival. Microbes, like all other organisms, are affected by a variety of factors and have developed specialized niches.

This quote by Shuhei Ono from the Carnegie Institution's Geophysical Laboratory summarizes the resilience and profound effect of microbes:

“We think that there were microbes in the oceans, before the oxygenated atmosphere, which would have used methane for energy...Oxygen first appeared on the surface of the Earth when microbes developed the capacity to split water molecules to produce O2 using the Sun's energy. This is a bit advanced biochemistry, but we think this biological revolution emerged sometime before 2.7 billion years ago." [8]

Chemical Factors

pH

pH changes in soils is due to both biotic and abiotic processes in the soil. Consuming or releasing H+ through redox reactions and fermentation, and/or from rainfall that leaches bases in soil and thus lowering the pH [1]. The majority of soil microbes thrive in neutral pH (6-7) due to the high availability of most nutrients in this pH range, but there are examples of microbes (especially fungi) that can tolerate pH of 1 to 13 [1]. Some organisms that can tolerate extreme pH include bacteria in Halomonas and Archea Archaeoglobus. Alterations in pH can render essential microbe enzymes inactive and/or denature proteins within the cells and prevent microbial activity from occurring [2]. pH changes can also effect microbes in their access to metals and organics that react differently under varied pH régimes [2].

Oxygen

Oxygen levels dictate the oxidation-reduction reactions that occur and largely what microbial processes occur. In the presence of oxygen, O2 will be used for aerobic respiration, but when concentrations are low other electron acceptors are used (such as sulfur, iron, etc.) [2]. This phenomenon can be seen in flooded soils. Some microbial enzymes require O2, so the level of O2 can regulate the enzymatic activity. Some products of O2 reactions are toxic (such as superoxide radical O2-) and without the proper enzymes to inactivate these toxins microbes are susceptible to harm.

Cation Exchange Capacity (CEC)

The CEC is the total amount of exchangeable cations that a soil can hold at a specific pH [1]. The negatively charged soil particles allow for charged soil microorganisms (due to charged organic molecules) to be attracted or repelled from soil. The ability to be held or repelled from the soil influences the ability of microbes to uphold their presence in the soil. The full understanding of how this mechanism works is not understood yet, but postulated mechanisms include: ion exchange attractions, weak attractive forces, coordination bonding, and hydrogen-bonding. The CEC of the soil also influences the availability of nutrients in the soil for microbial use, as charged nutrient particles also will be held or moved through the soil based on its charge [1].

Physical Factors

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Soil Texture

Soil has the following types of texture:Sand (0.05-2.0 mm) Silt (0.002-0.05mm) Clay ( < 0.002mm)[1].Sands are loose and single-grained (that is, not aggregated together). They feel gritty to the touch and are not sticky. Each individual sand grain is of sufficient size that it can easily be seen and felt. Sands cannot be formed into a cast by squeezing when dry.Clay is the finest textured of all the soil classes. Clay usually forms extremely hard clods or lumps when dry and is extremely sticky and plastic when wet.[4] Soils that are coarse textured are less likely to have a well-defined structure and therefore fewer structured pore space than s soil high in clay content.S. carpocapsae (diameter=25um) move more in fine sandy loam soil than in clay soil.[5]

Soil pores

Soil pores play a major role in water and air movement. Also, soil microorganisms reside in pores. Pore space is largely determined by size and arrangement of aggregates and affects the movement of water, air, and organisms in soil.Soil pore size distribution: Macropores ( >75um) Mesopores ( 30-70um) Micropores ( 5-30um) Ultramicropores (0.1-5um) Crytopores ( <0.1um).The average particle size could be determined by knowing the soil type and the percentage of sand, clay, and silt.

Soil Structure

Aggregation of primary soil particles is a critical determinant of soil structure.Structure is strongly affected by climate, biological activity, density and continuity of surface cover, and soil management practices. Soils that are coarse textured are less likely to have a well-defined structure and therefore fewer structured pore space than s soil high in clay content. Ecological relationships among soil organisms are influenced by soil structure.

Soil water

Soil water is essential for soil microorganisms. Without some water, there is no microbial activity.Soil with large diameter particles (coarse texture) can contain less water than soil with small diameter particles (fine texture).[6]

Temperature

Soil temperature greatly influences the rates of biological, physical, and chemical processes in the soil. Within a limited range, the rates of chemical reactions and biological processes double for every 10 degree increase.Soil temperature governs the rates and directions of soil physical processes and chemical reactions, and influences biological processed. Different pathogen species and strains have different thermal limits for survival, germination and infection.[5]

Soil aggregates

Soil aggregates are groups of soil particles that bind to each other more strongly than to adjacent particles. The space between the aggregates provide pore space for retention and exchange of air and water.Aggregation affects erosion, movement of water, and plant root growth.[7]Polysaccharides produced by soil bacteria and humic substances produced by fungi improve aggregation.

Biological Factors

Soil Fauna

Soil animals are divided into macrofauna (>2 mm, earthworms), mesofauna (0.1-0.2 mm, mites and nematodes), and microfauna (<0.1 mm, protozoa). These eukaryotes have a range of effects on microbial communities:

  • Grazing: Grazing increases decomposition rates, freeing nutrients. Grazing also includes direct consumption of other organisms.
  • Nutrient cycling: Soil fauna is responsible for up to 30% of the total soil mineralizable nitrogen. Additionally, soil fauna can remobilize nutrients as waste products. This allows for increases in microbial growth.
  • Microbial community composition: Other organisms in the community are directly effected through consumption. Some soil fauna feed selectively, consuming certain organisms instead of others. This changes the makeup of the microbial community.

In addition to these direct effects, soil fauna has several indirect effects on microbes. One of these effects is habitat alteration. Earthworms especially alter the soil habitat through the formation of burroughs, which changes gas exchange, water movement, and resource locations. Microorganisms are sensitive to the presence of oxygen in their enviroment, and water is essential for microbial existence. Changes in resource locations may allow for microorganisms to colonize another area. [1]

Organism Interactions

There are several types of interactions between organisms. The table below outlines the positive, negative, and neutral aspects that each organism receives as a result of the interaction. These interactions can create environments that promote or discourage specific microbial growth.

-

Interaction Type

-

Population 1

-

Population 2

-

Example

Mutualism (symbiosis) + + Rhizobia/legumes, mycorrhizal fungi/most plants (Bradyrhizobium), fungi/green algae, fungi/cyanobacteria (Anabaena)
Commensalism + 0 Aerobic oxygen consumption creates an anaerobic environment to support anaerobes
Synergism + + or 0 Flooded soils: fermenters provide carbon and hydrogen gas for methanogens and sulfate

reducers (Desulfosarcina), which in turn reduce toxic effects of acetate and hydrogen gas to fermenters

Amensalism - + or 0 Production of acidic or toxic chemicals
Predation - + Protozoa, nematodes, and slime molds are all major soil predators that consume bacteria
Competition (antagonism) - + Growth rates that allow for utilization of a resource before a competitor
Parasitism - + Viruses

[1, 2]

Bioavailability

Bioavailability is a term that refers to the availability of a soil substrate (both nutrients and toxins) to an organism. The EPA lists this definition of bioavailability:

“The term bioavailability designates the state of that fraction of a chemical that is available for uptake and/or transformation by living organisms. Although associated primarily with ecotoxicology, and usually in reference to organic and metallic pollutants, the term bioavailability is also relevant to native organic material. Thus, the “problem” of bioavailability, has existed for microorganisms far longer than has the presence of xenobiotic chemicals in the environment. Sorption, insolubility, and related processes are largely responsible for controlling bioavailability of many pollutants to microorganisms in soils and sediments” [3].

Bioavailability is of special interest to environmental groups because of it's correlation with bioremediation. A common assumption made when discussing bioavailability is that only what is in solution can be metabolized. There are three major factors that effect bioavailability:

  • Sorption: how a substrate bonds to surfaces, especially charged surfaces such as clay and organic matter.
  • Solubility: the capacity for a substance to dissolve in solution. (Insolubility refers to a substance that is unable to dissolve.)
  • Chemical speciation: some substrates may be less available at certain pH or are less available because of charge [2]

Plant Growth-Promoting Rhizobacteria (PGPR)

Rhizobacteria colonize roots. PGPR bacteria colonization promotes plant growth and seed germination and helps plants resist environmental stresses and diseases. Harmful root colonization is caused by deleterious rhizoshpere microorganisms (DRMO). DRMO bacteria remove water and nutrients from the plant supply. PGPR bacteria are able to promote plant growth by colonizing before and thus preventing the colonization of DRMO. Pseudomonas is a genus containing many PGPR bacteria. Azotobacter and Azospirillum are also PGPR bacteria because of their production of gibberellic and indoleacetic acid, which are plant growth-stimulating hormones. [1]

Relevant Organisms

Acidobacterium capsulatum - it was found in acid mine drainage (AMD)

Acidobacterium capsulatum picture [13]

Sinorhizobium meliloti is isolated from soil, which synthesizes an extracellular polymer that facilitates the transport of such hydrophobic pollutants as polynuclear aromatic hydrocarbons, as well as the toxic metals lead and cadmium in soil.[9]

Some microbial environments are extreme for life. Organisms inhabiting extreme environments are called extremophiles. Extremophilic microorganisms could be found in the harsh environment, such as hot springs, ice covering lake, salty water, and in soils or waters with pH lower than 0 or as high as 12. Those microorganisms can not live without the extreme environment.[10] One of recent discovery is Spirochaeta Americana.

Extreme condition Descriptive term Genus/ species Domain
High temperature Hyperthermophile Pyrolobus fumarii Archaea
Low temperature Psychophile Polaromonas vacuolata Bacteria
Low pH Acidophile Picrophilus oshimae Archaea
High pH Alkaliphile Natronobacterium Archaea
Pressure Barophile Moritella yayanosii Bacteria
Salt Halophile Halobacterium Archaea

Current Research

To find out what is new in the according to the American Academy of Microbiology (AAM) click: http://www.asm.org/Academy/index.asp

An Overview of Extremophiles:

" Prokaryotic extremophiles were the first representatives of life on Earth and they are responsible for the genesis of geological structures during the evolution and creation of all currently known ecosystems. Flexibility of the genome probably allowed life to adapt to a wide spectrum of extreme environments. As a result, modern prokaryotic diversity formed in a framework of physico-chemical factors, and it is composed of: thermophilic, psychrophilic, acidophilic, alkaliphilic, halophilic, barophilic, and radioresistant species. This artificial systematics cannot reflect the multiple actions of different environmental factors since one organism could unite characteristics of several extreme-groups. In this review we show the current status of studies in all fields of extremophiles and summarize the limits of life for different species of microbial extremophiles. We also discuss the finding of extremophiles from unusual places such as soils, and briefly review recent studies of microfossils in meteorites in the context of the significance of microbial extremophiles to Astrobiology." [11]


Molecular Genetics from Michigan State University:

" Bacteria in the phylum Acidobacteria are widely distributed and abundant in soils, but their ecological roles are poorly understood, owing in part to a paucity of cultured representatives. In a molecular survey of acidobacterial diversity at the Michigan State University Kellogg Biological Station Long-Term Ecological Research site, 27% of acidobacterial 16S rRNA gene clones in a never-tilled, successional plant community belonged to subdivision 1, whose relative abundance varied inversely with soil pH. Strains of subdivision 1 were isolated from these never-tilled soils using low-nutrient medium incubated for 3 to 4 weeks under elevated levels of carbon dioxide, which resulted in a slightly acidified medium that matched the pH optima of the strains (between 5 and 6). Colonies were approximately 1 mm in diameter and either white or pink, the latter due to a carotenoid(s) that was synthesized preferentially under 20% instead of 2% oxygen. Strains were gram-negative, aerobic, chemo-organotrophic, nonmotile rods that produced an extracellular matrix. All strains contained either one or two copies of the 16S rRNA encoding gene, which along with a relatively slow doubling time (10 to 15 h at ca. 23°C) is suggestive of an oligotrophic lifestyle. Six of the strains are sufficiently similar to one another, but distinct from previously named Acidobacteria, to warrant creation of a new genus, Terriglobus, with Terriglobus roseus defined as the type species. The physiological and nutritional characteristics of Terriglobus are consistent with its potential widespread distribution in soil." [12]


Andrew D. Cartmill, Luis A. Valdez-Aguilar, Donita L. Bryan and Alejandro Alarcon, Arbuscular mycorrhizal fungi enhance tolerance of vinca to high alkalinity in irrigation water, Scientia HorticulturaeVolume 115, Issue 3, , 1 February 2008, Pages 275-284. (http://www.sciencedirect.com/science/article/B6TC3-4PYRKM2-1/2/64bcf8c9a8286c08606ec95ada501b97)

References

1. Sylvia, D. M., Fuhrmann, J.F., Hartel, P.G., and D.A Zuberer (2005). "Principles and Applications of Soil Microbiology." New Jersey, Pearson Education Inc.

2. Scow, Kate. "Lectures in Soil Microbiology." UC Davis, Winter 2008.

3. EPA (2003). Madsen, E.L. "Report on Bioavailability of Chemical Wastes with Resepect to the Potential for Soil Bioremediation." Washington, D.C., U.S. EPA.

4. http://edis.ifas.ufl.edu/SS169

5. JSTOR: Florida Entomologist Vol.75, No. 4, p.539,1991

6. http://www.newton.dep.anl.gov/askasci/env99/env201.htm

7. http://soils.usda.gov/sqi/publications/files/sq_eig_1.pdf

8. Reuters (2006, March 22). Climate Change And The Rise Of Atmospheric Oxygen. ScienceDaily. Retrieved March 4, 2008 from http://www.sciencedaily.com/releases/2006/03/060322140017.htm

9. Characterization of a Sinorhizobium Isolate and Its Extracellular Polymer Implicated in Pollutant Transport in Soil,2002,Applied and Environmental Microbiology,p. 423-426, Vol. 68, No. 1

10. Michael T. M, John M. M, (2006). "Brock Biology of Microorganisms", Prentice Hall

11. Pikuta, Elena V., Hoover, Richard B. & Tang, Jane (2007). Microbial Extremophiles at the Limits of Life. Critical Reviews in Microbiology, 33 (3), 183-209. Retrieved March 10, 2008, from http://www.informaworld.com/10.1080/10408410701451948

12. Stephanie A Eichorst, John A. Breznak, and Thomas M. Schmidt, Isolation and Characterization of Soil Bacteria that Define ' Terriglobis ' gen. nov., in the Phyllum 'Acidobacteria' Appl. and Env. Microbiology Vol. 73, No. 8, Apr. 2007, p.2708-2717

13.http://images.google.com/imgres?imgurl=http://genome.jgi-psf.org/finished_microbes/images/aciel.jpg&imgrefurl=http://genome.jgi-psf.org/finished_microbes/aciel/&h=200&w=250&sz=28&hl=en&start=1&sig2=6npNlBQae1my_bwz8QsSww&um=1&tbnid=AEMeG-cKT6-3_M:&tbnh=89&tbnw=111&ei=5lvdR-aJPIOUhAOq__W-Cw&prev=/images%3Fq%3DAcidobacterium%2Bcapsulatum%26um%3D1%26hl%3Den%26sa%3DN

14. http://biology.clc.uc.edu/Courses/bio106/origins.htm

15. http://www.cartoonstock.com/lowres/amc0839l.jpg

16. American Society for Microbiology. "Microorganisms One Part Of The Solution To Energy Problem, Says Report." ScienceDaily 17 November 2006. 16 March 2008 <http://www.sciencedaily.com/releases/2006/11/061117023921.htm>.

Edited by students of Kate Scow