Modern
lagoonal microbialites of Tikehau and Moorea (
French Polynesia
) : nature, distribution and
lithification processes
Microbialites
are organosedimentary deposits that have accreted as a result of
benthic (prokaryotic or eukaryotic) communities, trapping and
binding detrital sediment and / or forming the locus of mineral
precipitation (Burne & Moore, 1987). Stromatolites (in greek:
stroma, carpet and lithos, stone) represent the best known
type of microbialite.
Microbialites
were part of Earth’s History for more than 3 billion years with
a variable importance. One supposed microbialites excluded from marine environment since Mesozoic. Recent discovery of their
presence during some periods of Quaternary, characterized by
environmental and climatic changes, led to examine their role in
modern environments (Camoin & Montaggioni, 1994).
For
about twenty years microbialites proliferation in modern reefal
settings, subjected to an anthropic stress or not, was highlighted
in many localities (
Bahamas
,
Great Barrier Reef
,
Antilles
…). Rapid blooms of microbial benthic
communities in tropical reefs seem to be linked with environmental
stress periods and/or
climatic events that may have a harmful effect on the development
of coralgal communities
Microbialites
including stromatolitic structures, have been observed in French
Polynesia, from the fringing
reef to the inner flat of the barrier reef of Moorea, a high
island partially exposed to human impact, and in the whole lagoon
of Tikehau atoll (pinnacle slopes and surrounding bottom) (Sprachta,
et al., 1999), in
pristine conditions where no direct human impact evidenced (Sprachta
et al, 2001). Similar specimens of cyanobacterial microbialites
proliferate as well from the back reef zone to the fringing reef
of
Mayotte
(
Comoros
archipelago,
Indian Ocean
) under heavy terrigenous inputs, (Sprachta,
2003).
The study of these modern lagoonal
microbialites was supported by two national programs: “Programme National Récifs Coralliens” (PNRCO) and
“Programme National Environnement Côtier” (PNEC) in
collaboration with CEREGE (Centre Européen de Recherche et
d'Enseignement de Géosciences de l'Environnement, COM (Centre
d’Océanologie de Marseille), Biological Science Center of the University of Boston (USA), Max Planck Institute of marine
microbiology of Bremen (Germany) and Department of
Microbiology of the University of Arizona (USA). Main objectives were the determination of
nature and composition in micro-organisms implied in the formation of
microbialites and evaluation of the importance of
‘microbialite' in biogeochemical cycles of the modern reef
systems.
A-Nature
and
distribution of lagoonal microbialites
Four
morphological types, mainly composed of specific mono populations
of filamentous cyanobacteria were observed (Abed et al,
2003) :
|
1-
decimeter sized
hemispherical domes formed by Phormidium cf crosbyanum
(Tilden), P. sp. TK1, P. hendersonii
(Howe), Schizothrix sp TK.
domes
of Phormidium
crosbyanum |
 |
|
2-
gelatinous masses produced by
Phormidium laysanense (Lemmerman)
|
 |
|
3-
meter-sized microbial mats
mainly made of Hydrocoleum chantharidosmum (Gomont), Hydrocoleum
coccineum (Gomont), Phormidium sp. or Schizothrix sp.
mats
of Hydrocoleum
coccineum |
 |
|
4- hairy
microbialites produced by the cyanobacteria Symploca hydnoïdes (Gomont)
|
 |
Lagoonal
microbialites are able to colonize various sites characterized by
different ecological conditions, such as Tikehau, a semi-closed
atoll with no anthropic pressure; high islands lagoons largely
open on the ocean and locally subjected to an anthropic pressure
such as Moorea; or lagoon subjected to a strong human pressure
like
Mayotte
(Sprachta, 2003).
Light,
nutriments supplies, hydrodynamism and sedimentation are the
specific factors of microbialitic development. Any modification of
these factors led to a variability of density and diversity in the
different types of microbialite along the slopes of pinnacles and
motus. Their settlement and development at a given depth and on a
particular substrate depends on cyanobacterial metabolic needs.
Indeed, filamentous cyanobacteria, can accommodate to a wide range
of ecological conditions thanks to specific physiological
adaptations. Thus, lagoonal
microbialites settle between the surface and 25 m deep, on various
types of substrate (mud, sand, gravels, and coral colonies) and
under extreme conditions of luminosity (Sprachta et al.,
2001; Fig.).

Zonation
of lagoonal microbialites on the slopes of a pinnacle at
Tikehau
(Sprachta et al., 2001).
Proliferation
of marine microbialites has significantly increased during the
last fifteen to twenty years and is obviously facilitated by
natural or human factors, injurious for the coralgal
communities. Progressive disappearance of the coral colonies
leaves a free field to replacement communities such as
microbialites.
B-Lithification
of lagoonal microbialites
|
Initially,
trapping and binding mineral particles strengthen
microbialites and play a significant role in their
formation. These particles mainly bioclastic in origin,
include skeletal fragments of corals, calcareous algae,
forams or cocoliths. |

Microphotograph
of trapped particles among filamentous cyanobacteria |

Close-up showing a cocolith
glued to a decaying cyanobacterial
sheath |
Microbialite
partial lithification results from biochemical reactions
involving
magnesian calcite precipitation mainly in the inner part of the
domes where the decay of cyanobacterial sheaths produce an organic
framework of very thin fibrils (fig.),
(Sprachta et al., 2001).
Detailed
view of a degraded cyanobacterial sheath encrusted by
precipitated carbonates
Biochemical
analyses of organic matter contained within microbialites
highlighted the selection of some compounds towards
intramineral organic matrices. These macromolecules are
characterized by enrichment in aspartic and glutamic acids,
responsible for the chelation of calcium.
The two antagonistic functions of crystal nucleation
and crystal growth inhibition are allotted to these organic
matrices. Specific electric charges of polypeptides and
polysaccharides which compose intramineral organic matrices,
are known to be implied in biomineralization. Acidic
macromolecules, in relation to a b
sheaths structure, initiate the nucleation of micro aggregates
of magnesian calcite to their surface (Weiner & Addadi,
1991).
| The
nucleus growth continues in this alkaline media, saturated
in carbonates (fig.).
In the case of the most hardened microbialites, the
precipitation of concentric layers of calcite around these
nucleii leads to the formation of rhomboedral calcite
crystal around the degraded sheaths (fig.)
(Sprachta, 2003).
|

Cyanobacterial
sheath
heavily incrusted by precipitated
carbonates
bbbbbb |

Precipitation
of rhomboedral
calcite crystal around
decaying cyanobacterial sheaths |
References
Abed
R., Golubic S., Garcia-Pichel F., Camoin G., Sprachta S. (sous
presse) Characterization of microbialithe-forming cyanobacteria in
a tropical lagoon: Tikehau atoll, Tuamotu, French Polynesia.
Journal of Phycology
Burne
R. V., Moore L. S. (1987) Microbialites : Organosedimentary
deposits of benthic microbial communities. Palaios, v. 2, p.
241-254
Camoin G. F., Montaggioni L. F. (1994). High energy
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Sprachta S., Camoin G., Gautret P., Le Campion T., Golubic S.
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Microbialites in a modern lagoonal environment : nature and
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mineralized tissues : controllers of crystal formation.
Trends in Biochemical Sciences v.16, p. 252-256.
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