Alkaline Lake: Difference between revisions

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We decided to focus on Lake Magadi in our research for several reasons. There are several alkaline lakes (Lakes Bogoria, Natron, and Magadi) which are all similar to one another. They are all saline and alkaline and similar in scale. Wildlife and microbial diversity are analogous amongst all the lakes. We chose to study Lake Magadi because it is the most studied of the alkaline lakes.
We decided to focus on Lake Magadi in our research for several reasons. There are several alkaline lakes (Lakes Bogoria, Natron, and Magadi) which are all similar to one another. They are all saline and alkaline and similar in scale. Wildlife and microbial diversity are analogous amongst all the lakes. We chose to study Lake Magadi because it is the most studied of the alkaline lakes.


===Where located?===
===Location===
Geological Coordinates:  1° 52′ 0″ S, 36° 16′ 0″ E
Geological Coordinates:  1° 52′ 0″ S, 36° 16′ 0″ E



Revision as of 22:00, 26 August 2008

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Description of Niche

We decided to focus on Lake Magadi in our research for several reasons. There are several alkaline lakes (Lakes Bogoria, Natron, and Magadi) which are all similar to one another. They are all saline and alkaline and similar in scale. Wildlife and microbial diversity are analogous amongst all the lakes. We chose to study Lake Magadi because it is the most studied of the alkaline lakes.

Location

Geological Coordinates: 1° 52′ 0″ S, 36° 16′ 0″ E

Lake Magadi is the southernmost lake in Kenya, and is located in the Rift Valley. The lake is located 2000 feet below sea level forming one of the lowest points in the valley.

Physical Conditions?

Lake Magadi is a saline-alkaline lake. The lake acts as a sink for seasonal streams. Magadi is famous for its cherts from sodium silicate precursors. It has a pH of 10 and alkalinity of 380 mmol L-1. Lake Magadi has a surface area of 100 km2 and a depth that ranges from 1-5 m. Mineral composition consists mostly of trona mixed with halite and either kogarkoite or villaumite, resulting in fluoride concentrations up to 8.7 mg F-.


Physical Conditions of alkaline lakes (including Lake Magadi)

Lake Basin Surface Area (km2) Maximum Depth (m) Salinity and pH Productivity
Lake Natron 930 8.5 35%, 8.5-10.3 High productivity due to algal bacterial OM
Lake Bogoria 160 8.5 35%, 9.8-10.3 High productivity due to algal bacterial OM
Lake Magadi 100 5 >30%, 9.8-10.5 High productivity due to algal bacterial OM

Influence by Adjacent Communities

The high fluoride concentration in Lake Magadi, is strongly related to the weathering of volcanic rocks enriched in fluoride and alkalis which are found in the same area as Lake Magadi. This has affected the local community who have customarily used the chert from Lake Magadi as a meat tenderizer and has inadvertently ingested high levels of fluorine.

Conditions under which the environment changes

Do any of the physical conditions change? Are there chemicals, other organisms, nutrients, etc. that might change the community of your niche.

Who lives there?

Species Description
Habmonas campisalis obligatory alkaliphilic, nitric oxide reducing denitrifier, nitrate denitrifier
Amphibacillus fermentum, Amphibacillus tropicus alkaliphilic, saccharolytic, rod-shaped gram-positive bacteria, resistant to heating and drying. Some form endospres, some don’t. All capable of both aerobic and anaerobic growth. Sodium chloride independent, sodium carbonate dependent. Metabolize glucose, mono- and disaccharides in aerobic mode, while forming formate, ethanol, and acetate when anaerobic.
Halonatronum saccharophilum alkaliphilic, somewhat halophilic, chemoorganotrophic bacterium. Spore-forming, rod-shaped, gram-negative. Obligatorily carbonate- and sodium chloride dependent. Peritrichously flagellated rod. Reduces sulfate ion to hydrogen sulfide. Catabolizes glucose, fructose, sucrose, maltose, starch, glycogen, N-acetyl-D-glucosamine. Glucose fermentation yields formate, acetate, ethanol, H2, and CO2
Haloakaliphilic archaea not much known. Very distant relation to any other archaea (only 76% genetic relationship).
Natronoincola histidinovorans 2 strains (1 sporogenous, 1 asporogenous); moderately haloalkaliphilic, obligatorily anaerobic, fermentative bacteria, motile, gram-positive, depends on sodium ions and bicarbonate. Only utilize two amino acids: histidine and glutamate, forming acetate and ammonium as their products
Tindallia magadii alkaliphilic, obligatorily anaerobic, fermentative, asporogenous, gram-positive. Ferments the amino acids arginine and ornithine, producing acetate, propionine, and ammonia.
Desulfonatronovibrio hydrogenovorans alkaliphilic, sulfate-reducing bacterium, sodium dependent.
Natrionella acetigena extremely haloalkalaphilic, chemoorganotrophic, homoacetogenic bacterium. Obligate anaerobe, motile, gram-negative, spore-forming rod. Dependent on sodium carbonate, chloride ions. Ferments mainly lactate, ethanol, pyruvate, glutamate, and propanol, with acetate as the main and only product.
Spirochaeta alkalica, Spirochaeta Africana, Spirochaeta asiatica mesophilic, anaerobic, saccharolytic, dissipotrophs. They differ in their final glucose metabolic products and proportions of similar products. All ferment glucose, and S. alkalica and S. Africana produce acetate, hydrogen, ethanol, and lactate, with the proportions of each differing between the two. S asiatica is strictly anaerobic, and produces acetate, ethanol, and lactate. S. Africana and alkalica are somewhat aerotolerant.
Natronococcus amylolyticus haloalkalaphilic archaeon, produces alpha-amylase, appears red-orange in clusters

Non-Microbes Present

Lake Magadi is a popular destination for many animals due to the fact that it is situated between Massai Mara and Amboseli National Parks, but very few animals actually have any contact with, or live in, the lake itself. However, the lake is a popular destination for wading birds during the dry season including flamingos, heron, pelicans, and spoonbills. The birds congregate in streams of fresh water that run into the lake because this water brings in large amounts of diverse food. There is only one species of fish that can actually be found in the lake itself. Tilapia grahami, a type of small tilapia, have adapted to live in the harsh conditions of the lake, and are normally found in the lagoons on the lake’s periphery. An abundance of research has been performed on these fish, indicating that the fish have adapted to live in temperatures up to and possibly above 44◦C, a pH varying between 5-11 (though the lake naturally ranges from pH 9-11), low oxygen levels in the water (as low as 1.1 mg O2/L of water), and a salinity concentration up to 4%. These tilapia have many adaptations to survive in this lake, and due to the lakes extreme conditions, little other non-microbial life exists.

Do the microbes that are present interact with each other?

The microbes share substrates and metabolic products, but little else is known.

Do the microbes change their environment?

Do they alter pH, attach to surfaces, secrete anything, etc. etc.

Do the microbes carry out any metabolism that affects their environment?

The proliferation of certain kinds of halophilic archaebacteria, particularly Natronobacteria, causes the salt flats of Lake Magadi to turn a vivid pink color. This type of bacteria grows optimally in pH 9.5 at a very low Mg2+ level (2). What is most unique about Natronobacteria is that they tolerate both halophilic as well as alkaliphilic environments, meaning that they can thrive in both salty and high pH environments (1). They are Gram-negative bacteria, so they have a thin peptidoglycan layer as well as an additional outer membrane that comprises of phospholipids and lipopolysaccharides, which allow for pathogenicity. Natronobacteria are aerobic organisms that require high amounts of salt and nutrients for survival. More specifically, they use complex sugars such as ribose, sucrose, and glucose to fix nitrogen to produce organic compounds that ultimately lead to their growth (3). As the cells of these bacteria proliferate, they synthesize carotenoids, organic pigments that are red/pink in color for this specific type of bacteria. Since Natronobacteria thrive mostly in salty conditions, this pigmentation is seen most frequently in the vast amount of salt flats that surround the lake. This is what gives the lake one of its most famous attributes: an overall blushing appearance.

Current Research

A large amount of current research involving lake Magadi is to try to purify and culture novel forms of bacteria able to live in alkaline lakes. For example, in 2004 eight new strains of denitrifying bacteria were found in a lagoon with a pH of 10 by looking at their 16s rRNA to prove they are in fact eight new strains of a new species, and how related they are to other currently known species. Another more recent project, published in December of 2007, described experiments that isolated a new genus and species of bacteria, Methylohalomonas lacus. Two strains of these bacteria were cultured from the sediment of Lake Magadi and another alkaline lake in the Kulunda Steppe in Altai, Russia by growing bacterial cultures on media containing varying salt concentrations and pH levels, and projects are ongoing to try and find more microbial life with the adapted ability to live in the alkaline conditions of lakes such as lake Magadi.

A third research project involving lake Magadi focused on the Tilapia grahami, the small tilapia described above. There are isolated populations of these fish in lagoons around the edge of the lake, all living in differential volumes of oxygen, pH levels, temperature, and salinity. Once a year, during the flood season, there is the possibility for these isolated populations to come into contact with one another, and researchers are looking at the possible flow of genetic information between these isolated populations, and the adaptations that may have arisen from this isolation/interaction dichotomy by looking at regions of the mitochondrial DNA from six populations of these fish. The evidence suggests a model that does not include gene flow between these populations, though new, more stable DNA sequences are being studied to try and better categorize this isolation.


An abundant amount of current research projects involving Natronobacteria include classifying and isolating different strains of this type of bacteria in other highly saline and alkaline environments. One such type of research was held in the soil of former Lake Texcoco located in valley of Mexico City, Mexico. Using 16S ribosomal RNA gene sequencing, numerous clades coming from the Halobacteriaceae family were found including Natronobacterium (4). This project is still ongoing since there are still species that have yet to be identified in the soil.


Biotechnological Application: Alkaliphiles isolated in soda lakes have been analyzed and used for their various alkali-tolerant enzymes in many industrial processes (5). Because these enzymes have the ability to function at high levels of pH, they are particularly useful in processes that require these extreme conditions. These alkaliphiles are thought to have significant economic potential because their specialized enzymes are already “used in detergent compositions and in leather tanning, and are foreseen to find applications in the food, waste treatment and textile industries; additionally, (they) are potentially useful for biotransformations, especially in the synthesis of pure enantiomers” (5).

References

Sorokin, D.Y. Trotsenko, Y.A. Doronina, N.V. Tourova, T.P. Galinski, D.A. Kolganova, T.V. and Muyzer G. “Methylohalomonas lacus gen. nov., sp. nov. and Methylonatrum kenyense gen. nov., sp. nov., methylotrophic gammaproteobacteria from hypersaline lakes.” Int J Syst Evol Microbiol. December. (2007) Wilson, P.J. Wood, C.M. Walsh, P.J. Bergman, A.N. Bergman, H.L Laurent, P. and White, B.N. “Discordance between genetic structure and morphological, ecological, and physiological adaptation in Lake Magadi tilapia.” Physiol Biochem Zool. July-August. (2004) Boltianskaya, Iu. V. Antipoz, A.N. Kolganova, T.V. Lysenko, A.M. Kostrikina, N.A. and Zhilina, T.N. “Halomonas campisalis, an obligatorily alkaliphilic, nitrous oxide-reducing denitrifier with a Mo-cofactor-lacking nitrate reductase.” Mikrobiologiia. May-June. (2004) Reite, O.B. Maloiy, G.M.O. and Aasehaug, B. “pH, Salinity and Temperature Tolerance of Lake Magadi Tilapia.” Nature. February 1. (1974)


http://www.webkenya.com/eng/safari/magadi.php http://www.ncbi.nlm.nih.gov/pubmed/15315225?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum http://www.ncbi.nlm.nih.gov/pubmed/11785140?ordinalpos=10&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum http://www.ncbi.nlm.nih.gov/pubmed/11338841?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum http://www.ncbi.nlm.nih.gov/pubmed/10357000?ordinalpos=15&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum http://www.ncbi.nlm.nih.gov/pubmed/9688817?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum http://www.ncbi.nlm.nih.gov/pubmed/9662608?ordinalpos=17&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum http://www.ncbi.nlm.nih.gov/pubmed/8995816?ordinalpos=18&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum http://www.ncbi.nlm.nih.gov/pubmed/8661677?ordinalpos=19&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum http://www.ncbi.nlm.nih.gov/pubmed/8573509?ordinalpos=20&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum http://www.ncbi.nlm.nih.gov/pubmed/7547296?ordinalpos=21&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum

1.Nieto, J., Oren, A., and Ventosa ,A. “Biology of Moderately Halophilic Aerobic Bacteria”. Microbiol Mol Biol Rev. 1998. Volume 62. p. 504-544 <http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=98923> 2. Mwatha, W., and Grant, W. “Natronobacterium vacuolata sp. nov., a Haloalkaliphilic Archaeon Isolated from Lake Magadi, Kenya”. International Journal of Systematic Bacteriology. 1993. Volume 3. p. 401-404 <http://ijs.sgmjournals.org/cgi/reprint/43/3/401> 3. Grant W.E., (2006). ALKALINE ENVIRONMENTS AND BIODIVERSITY, in Extremophiles. [Eds. Charles Gerday, and Nicolas Glansdorff], in Encyclopedia of Life Support Systems (EOLSS), Developed under the Auspices of the UNESCO, Eolss Publishers, Oxford, UK. [1] 4. Alcantara-Hernandez, R., Dendooven, L., Enriquez-Aragon, J., Estrada-Alvardo, I., Hernandez-Rodriguez, C., Marsch, R., Neria-Gonzalez, I., and Valenzuela-Encinas, C. “Phylogenetic analysis of the archaeal community in an alkaline-saline soil of the former lake Texcoco (Mexico)”. Extremophiles. 2008. Volume 12. p. 247-54. <http://www.ncbi.nlm.nih.gov/pubmed/18097633?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum> 5. Jones, B. E., Grant, W. D., and Collins, N. C., “Gram-negative alkaliphilic microorganisms.” U.S. Patent 5733767, March 1998.



Edited by [Jonathan Kim, Eugene Vu, Trevor Parry, Daniel Zhou], students of Rachel Larsen