The Search for Biomarkers and Microbial Fossils in Antarctic Rock Microhabitats

The survival of lithobiontic microbial communities in Antarctica's extreme cold, dry environment is conditioned by changes in external climatic conditions that can lead to the death of these microorganisms. In the present study, granite samples from maritime Antarctica and sandstone from the Antarctic continental desert were collected with the aim of searching for biomarkers and microbial fossils at the microscopic level of observation. The results reveal the presence of inorganic biomarkers in the form of physicochemical bioweathering mineral patterns, and inorganic deposits such as calcium oxalates and silica. The presence of fossilised algae and other microorganisms within the sandstone rock was also confirmed. Identifying the internal cell structure within the fossilised cells is proposed as a new criterion for the biogenicity of biomorphs.     

矿物电子能量协同微生物胞外电子传递与生长代谢

矿物是无机自然界吸收与转化能量的重要载体,其与微生物的胞外电子传递过程体现出矿物电子能量对微生物生长代谢与能量获取方式的影响。根据电子来源与产生途径,以往研究表明矿物中变价元素原子最外层或次外层价电子与半导体矿物导带上的光电子是微生物可以利用的两种不同胞外电子能量形式,其产生及传递方式与微生物胞外电子传递的电子载体密切相关。在协同微生物胞外电子传递过程中,矿物不同电子能量形式之间既有相似性亦存在着差异。反过来,微生物胞内-胞外电子传递途径也影响对矿物电子能量的吸收与获取,进而对微生物生长代谢等生命活动产生影响。本文在阐述矿物不同电子能量形式产生机制及其参与生物化学反应的共性和差异性特征基础上,综述了微生物获取矿物电子能量所需的不同电子载体类型与传递途径,探讨了矿物不同电子能量形式对微生物生长代谢等生命活动的影响,展望了自然条件下微生物利用矿物电子能量调节其生命活动、调控元素与能量循环的新方式。     

Fossilization of Acidophilic Microorganisms

This study examines fossil microorganisms found in iron-rich deposits in an extreme acidic environment, the Tinto River in SW Spain. Both electron microscopy (SEM and TEM) and non-destructive in situ microanalytical techniques (EDS, EMP and XPS) were used to determine the role of permineralization and encrustation in preserving microorganisms forming biofilms in the sediments. Unicellular algae were preserved by silica permineralization of their cell walls. Bacterial biofilms were preserved as molds by epicellular deposition of schwertmannite around them. In the case of fungi and filamentous algae, we observed permineralization of cell structures by schwertmannite in the sediments. The extracellular polymeric matrix around the cells was also preserved through permineralization of the fibrillar component. The process of permineralization and deposition of iron-rich precipitates present in the acidic waters of Rio Tinto served to preserve many microfossils in an oxidizing environment, in which organic compounds would not normally be expected to persist. Studies of microbial fossil formation mechanisms in modern extreme environments should focus on defining criteria to identify inorganic traces of microbial life in past environments on Earth or other planets.     

Distribution of Microfossils Within Polymetallic Nodules: Biogenic Clusters Within Manganese Layers

Biomineralization is the process by which living organisms or organic matrices produced by them initiate and structure deposition of inorganic polymers/minerals. Deep-sea polymetallic nodules and crusts have recently been recognized as biominerals that are formed around bio-seeds; these deposits are of economic value. A detailed understanding of their formation will contribute to their sustainable exploitation in the future. Polymetallic nodules grow concentrically around discrete nuclei that have recently been described as bio-seeds formed from microorganisms, diatoms, or coccoliths. In the present study, polymetallic nodules from the Clarion-Clipperton Zone have been analyzed. It is described that the approximately 5-cm large polymetallic nodules are composed of micronodules (size of 100–450 μm) that aggregated to nests (2–3 mm). High-resolution scanning electron microscopy (HR-SEM) and high-resolution energy dispersive X-ray (HR-EDX) spectroscopic analyses revealed that the micronodules are composed of discrete layers of Mn and Fe. Imprints of microorganisms/microbe-like assemblies are found in the Mn-rich regions of the micronodules. HR-SEM/EDX analyses confirmed that these microorganisms are surrounded by a Mn-rich environment. These findings strongly suggest that those organisms acted as bio-seeds that allowed the deposition of Mn(IV) minerals which in turn helped Fe minerals to associate. Hence, these data support the concept that the growth of the polymetallic nodules starts as a biomineral and is completed by genuine mineralic depositions. It is expected that these data will contribute to the development of strategies for a sustainable exploitation of the polymetallic nodules.     

Mineral Precipitation by Epilithic Biofilms in the Speed River, Ontario, Canada

Epilithic microbial communities, ubiquitously found in biofilms on submerged granite, limestone, and sandstone, as well as on the concrete support pillars of bridges, were examined in the Speed River, Ontario, Canada. Transmission electron microscopy showed that attached bacteria (on all substrata) were highly mineralized, ranging from Fe-rich capsular material to fine-grained (<1 μm) authigenic (primary) mineral precipitates. The authigenic grains exhibited a wide range of morphologies, from amorphous gel-like phases to crystalline structures. Energy-dispersive X-ray spectroscopy indicated that the most abundant mineral associated with epilithic bacteria was a complex (Fe, Al) silicate of variable composition. The gel-like phases were similar in composition to a chamositic clay, whereas the crystalline structures were more siliceous and had compositions between those of glauconite and kaolinite. The consistent formation of (Fe, Al) silicates by all bacterial populations, regardless of substratum lithology, implies that biomineralization was a surface process associated with the anionic nature of the cell wall. The adsorption of dissolved constituents from the aqueous environment contributed significantly to the mineral formation process. In this regard, it appears that epilithic microbial biofilms dominate the reactivity of the rock-water interface and may determine the type of minerals formed, which will ultimately become part of the riverbed sediment. Because rivers typically contain high concentrations of dissolved iron, silicon, and aluminum, these findings provide a unique insight into biogeochemical activities that are potentially widespread in natural waters.     

An Acidophilic Bacterial-Archaeal-Fungal Ecosystem Linked to Formation of Ferruginous Crusts and Stalactites

The presence of specialized microbial associations between populations of chemoautotrophic bacteria and archaea with ascomycetous fungi was observed inside stalactite-shaped mineral formations in a highly acidic cave environment. Metagenomic, chemical and electron microscopy analyses were used to investigate the relevance of these microbial ecosystems in the formation of stalactites. Ferric hydroxide produced by acidophilic bacteria and archaea was shown to be deposited onto fungal hyphae, resulting in complex mineralized stalactite-shaped structures. Thus, both archaeal-bacterial and fungal members of the ecosystem were shown to play an active role in the formation of stalactites.     

Comparative activity and functional ecology of permafrost soils and lithic niches in a hyper‐arid polar desert

Permafrost in the high elevation McMurdo Dry Valleys of Antarctica ranks among the driest and coldest on Earth. Permafrost soils appear to be largely inhospitable to active microbial life, but sandstone lithic microhabitats contain a trophically simple but functional cryptoendolithic community. We used metagenomic sequencing and activity assays to examine the functional capacity of permafrost soils and cryptoendolithic communities in University Valley, one of the most extreme regions in the Dry Valleys. We found metagenomic evidence that cryptoendolithic microorganisms are adapted to the harsh environment and capable of metabolic activity at in situ temperatures, possessing a suite of stress response and nutrient cycling genes to fix carbon under the fluctuating conditions that the sandstone rock would experience during the summer months. We additionally identified genes involved in microbial competition and cooperation within the cryptoendolithic habitat. In contrast, permafrost soils have a lower richness of stress response genes, and instead the metagenome is enriched in genes involved with dormancy and sporulation. The permafrost soils also have a large presence of phage genes and genes involved in the recycling of cellular material. Our results underlie two different habitability conditions under extreme cold and dryness: the permafrost soil which is enriched in traits which emphasize survival and dormancy, rather than growth and activity; and the cryptoendolithic environment that selects for organisms capable of growth under extremely oligotrophic, arid and cold conditions. This study represents the first metagenomic interrogation of Antarctic permafrost and polar cryptoendolithic microbial communities.     

Microbial Silicification in Sinters from Two Terrestrial Hot Springs in the Uzon Caldera,Kamchatka, Russia

Silicification of microbial communities is the most pervasive form of mineralization in two terrestrial hot springs in the Uzon Caldera. X-ray diffraction and electron microscopy reveal a diverse sinter mineral assemblage dominated by opal-A with accessory sulfur, sulfides, alunite group minerals, oxides, and oxyhydroxides. Aluminum laminations (reported for the first time) noted in one deposit may slow opal-A transformational rates enabling mineralized microbial remnants to exist longer in the rock record. Although preservation of microbial forms decreases over time, the collective mineral assemblage and patterning suggests that they are the most persistent lines of evidence of life in the geologic record.     

Iron-Rich Diagenetic Minerals are Biomarkers of Microbial Activity in Antarctic Rocks

The cold, dry ecosystems of Antarctica have been shown to harbor traces left behind by microbial activity within certain types of rocks, but only two indirect biomarkers of cryptoendolithic activity in the Antarctic cold desert zone have been described to date. These are the geophysical and geochemical bioweathering patterns macroscopically observed in sandstone rock. Here we show that in this extreme environment, minerals are biologically transformed, and as a result, Fe-rich diagenetic minerals in the form of iron hydroxide nanocrystals and biogenic clays are deposited around chasmoendolithic hyphae and bacterial cells. Thus, when microbial life decays, these characteristic neocrystalized minerals act as distinct biomarkers of previous endolithic activity. The ability to recognize these traces may have potential astrobiological implications because the Antarctic Ross Desert is considered a terrestrial analogue of a possible ecosystem on early Mars.     

3‐D analysis of bacterial cell‐(iron)mineral aggregates formed during Fe(II) oxidation by the nitrate‐reducing Acidovorax sp. strain BoFeN1 using complementary microscopy tomography approaches

The formation of cell‐(iron)mineral aggregates as a consequence of bacterial iron oxidation is an environmentally widespread process with a number of implications for processes such as sorption and coprecipitation of contaminants and nutrients. Whereas the overall appearance of such aggregates is easily accessible using 2‐D microscopy techniques, the 3‐D and internal structure remain obscure. In this study, we examined the 3‐D structure of cell‐(iron)mineral aggregates formed during Fe(II) oxidation by the nitrate‐reducing Acidovorax sp. strain BoFeN1 using a combination of advanced 3‐D microscopy techniques. We obtained 3‐D structural and chemical information on different cellular encrustation patterns at high spatial resolution (4–200 nm, depending on the method): more specifically, (1) cells free of iron minerals, (2) periplasm filled with iron minerals, (3) spike‐ or platelet‐shaped iron mineral structures, (4) bulky structures on the cell surface, (5) extracellular iron mineral shell structures, (6) cells with iron mineral filled cytoplasm, and (7) agglomerations of extracellular globular structures. In addition to structural information, chemical nanotomography suggests a dominant role of extracellular polymeric substances (EPS) in controlling the formation of cell‐(iron)mineral aggregates. Furthermore, samples in their hydrated state showed cell‐(iron)mineral aggregates in pristine conditions free of preparation (i.e., drying/dehydration) artifacts. All these results were obtained using 3‐D microscopy techniques such as focused ion beam (FIB)/scanning electron microscopy (SEM) tomography, transmission electron microscopy (TEM) tomography, scanning transmission (soft) X‐ray microscopy (STXM) tomography, and confocal laser scanning microscopy (CLSM). It turned out that, due to the various different contrast mechanisms of the individual approaches, and due to the required sample preparation steps, only the combination of these techniques was able to provide a comprehensive understanding of structure and composition of the various Fe‐precipitates and their association with bacterial cells and EPS.     

土壤矿物与微生物相互作用的机理及其环境效应

土壤矿物与微生物相互作用是地球表层系统中重要的生态过程.微生物或生物分子与矿物间的吸附(粘附)是两者相互作用的基础.吸附(粘附)是一个由分子间力、静电力、疏水作用力、氢键和空间位阻效应等多种作用力或作用因素共同决定、影响的物理化学过程.因此,微生物和矿物的表面性质如表面电荷、疏水性和它们所处的环境条件如pH、电解质浓度、温度等,都影响着矿物-微生物吸附(粘附)过程.微生物细胞或酶可吸附于矿物表面,其结果是细胞代谢或酶活性会发生明显变化,并进一步影响土壤中诸多相关的生态、环境过程.结合4种典型的初始吸附理论:表面自由能热力学理论、DLVO理论、吸附等温线理论和表面复合物理论及本课题组近年来的研究成果,对土壤矿物与微生物相互作用的类型、机理、作用力和现代研究技术等方面的最新研究进展进行了较为全面的论述,对土壤矿物-微生物相互作用的环境效应进行了讨论,并就该领域今后研究工作的特点及应关注的问题进行了展望.     

陕西西乡寒武纪幸运期宽川铺生物群网格状微体化石埋藏学与生物属性研究*

磷酸盐化保存是软躯体化石特异埋藏的一个重要途径, 而微生物在软躯体磷酸盐化过程中可能发挥了重要作用。前人通过埋藏学实验发现, 微生物会在动物胚胎等软躯体组织内部快速滋生, 充填生物体内部空间, 以微生物假形的方式复制了生物体的原始形态。但化石的磷酸盐化过程是否与埋藏学实验模拟的过程一致, 目前仍有争议。本次研究在寒武纪早期宽川铺生物群中发现了一类网格状微体化石。此类化石的保存状态可以根据其中丝状微生物滋生的程度分为三种类型, 它们展示了生物从死亡到微生物侵入、滋生, 最后被磷酸盐化的全过程。这些标本显示, 微生物假形在生物软组织磷酸盐化过程中扮演了重要角色, 但并不是化石磷酸盐化的必由之路, 尤其是当生物体具有矿化硬骨骼或者几丁质软骨骼等抗腐性较强的结构时。此类标本多以不完整保存的残片为主, 正反两面结构一致, 具有典型列状排列的近圆形与哑铃形网孔。由于化石结构简单, 生物学性状较少, 因此它们的亲缘关系尚不明确, 是一类需要继续研究的疑难化石。     

Initial pedogenesis in a topsoil crust 3 years after construction of an artificial catchment in Brandenburg, NE Germany

Cyanobacteria and green algae present in biological soil crusts are able to colonize mineral substrates even under extreme environmental conditions. As pioneer organisms, they play a key role during the first phases of habitat colonization. A characteristic crust was sampled 3 years after installation of the artificial water catchment “Chicken creek”, thus representing an early successional stage of ecosystem development. Mean annual rainfall and temperature were 559 mm and 9.3°C, respectively. We combined scanning electron microscopy (SEM/EDX) and infrared (FTIR) microscopy to study the contact zone of algal and cyanobacterial mucilage with soil minerals in an undisturbed biological soil crust and in the subjacent sandy substrate. The crust was characterized by an approximately 50 μm thick surface layer, where microorganisms resided and where mineral deposition was trapped, and by an approximately 2.5 mm thick lower crust where mineral particles were stabilized by organo-mineral structures. SEM/EDX microscopy was used to determine the spatial distribution of elements, organic compounds and minerals were identified using FTIR microscopy and X-ray diffraction (XRD). The concentration of organic carbon in the crust was about twice as much as in the parent material. Depletion of Fe, Al and Mn in the lower crust and in the subjacent 5 mm compared to the geological substrate was observed. This could be interpreted as the initial phase of podzolization. Existence of bridging structures between mineral particles of the lower crust, containing phyllosilicates, Fe compounds and organic matter (OM), may indicate the formation of organo-mineral associations. pH decreased from 8.1 in the original substrate to 5.1 on the crust surface 3 years after construction, pointing to rapid weathering of carbonates. Weathering of silicates could not be detected.     

Biofilm formation on the surface of monazite and xenotime during bioleaching

Microbial attachment and biofilm formation is a ubiquitous behaviour of microorganisms and is the most crucial prerequisite of contact bioleaching. Monazite and xenotime are two commercially exploitable minerals containing rare earth elements (REEs). Bioleaching using phosphate solubilizing microorganisms is a green biotechnological approach for the extraction of REEs. In this study, microbial attachment and biofilm formation of Klebsiella aerogenes ATCC 13048 on the surface of these minerals were investigated using confocal laser scanning microscopy (CLSM) and scanning electron microscopy (SEM). In a batch culture system, K. aerogenes was able to attach and form biofilms on the surface of three phosphate minerals. The microscopy records showed three distinctive stages of biofilm development for K. aerogenes commencing with initial attachment to the surface occurring in the first minutes of microbial inoculation. This was followed by colonization of the surface and formation of a mature biofilm as the second distinguishable stage, with progression to dispersion as the final stage. The biofilm had a thin-layer structure. The colonization and biofilm formation were localized toward physical surface imperfections such as cracks, pits, grooves and dents. In comparison to monazite and xenotime crystals, a higher proportion of the surface of the high-grade monazite ore was covered by biofilm which could be due to its higher surface roughness. No selective attachment or colonization toward specific mineralogy or chemical composition of the minerals was detected. Finally, in contrast to abiotic leaching of control samples, microbial activity resulted in extensive microbial erosion on the high-grade monazite ore.     

Bone mineralization proceeds through intracellular calcium phosphate loaded vesicles: a cryo-electron microscopy study

Bone is the most widespread mineralized tissue in vertebrates and its formation is orchestrated by specialized cells - the osteoblasts. Crystalline carbonated hydroxyapatite, an inorganic calcium phosphate mineral, constitutes a substantial fraction of mature bone tissue. Yet key aspects of the mineral formation mechanism, transport pathways and deposition in the extracellular matrix remain unidentified. Using cryo-electron microscopy on native frozen-hydrated tissues we show that during mineralization of developing mouse calvaria and long bones, bone-lining cells concentrate membrane-bound mineral granules within intracellular vesicles. Elemental analysis and electron diffraction show that the intracellular mineral granules consist of disordered calcium phosphate, a highly metastable phase and a potential precursor of carbonated hydroxyapatite. The intracellular mineral contains considerably less calcium than expected for synthetic amorphous calcium phosphate, suggesting the presence of a cellular mechanism by which phosphate entities are first formed and thereafter gradually sequester calcium within the vesicles. We thus demonstrate that in vivo osteoblasts actively produce disordered mineral packets within intracellular vesicles for mineralization of the extracellular developing bone tissue. The use of a highly disordered precursor mineral phase that later crystallizes within an extracellular matrix is a strategy employed in the formation of fish fin bones and by various invertebrate phyla. This therefore appears to be a widespread strategy used by many animal phyla, including vertebrates.     

Vitamin C-sulfate inhibits mineralization in chondrocyte cultures: a caveat.

Differentiating chick limb-bud mesenchymal cell micro-mass cultures routinely mineralize in the presence of 10% fetal calf serum, antibiotics, 4 mM inorganic phosphate (or 2.5 mM beta-glycerophosphate), 0.3 mg/ml glutamine and either 25 microg/ml vitamin C or 5-12 microg/ml vitamin C-sulfate. The failure of these cultures to produce a mineralized matrix (assessed by electron microscopy, 45Ca uptake and Fourier transform infrared microscopy) led to the evaluation of each of these additives. We report here that the "stable" vitamin C-sulfate (ascorbic acid-2-sulfate) causes increased sulfate incorporation into the cartilage matrix. Furthermore, the release of sulfate from the vitamin C derivative appears to be responsible for the inhibition of mineral deposition, as demonstrated in cultures with equimolar amounts of vitamin C and sodium sulfate.     

New approaches to the study of Antarctic lithobiontic microorganisms and their inorganic traces,and their application in the detection of life in Martian rocks

Microbial life in the harsh conditions of Antarctica's cold desert may be considered an analogue of potential life on early Mars. In order to explore the development and survival of this epilithic and endolithic form of microbial life, our most sophisticated, state-of-the-art visualization technologies have to be used to their full potential. The study of any ecosystem requires a knowledge of its components and the processes that take place within it. If we are to understand the structure and function of each component of the microecosystems that inhabit lithic substrates, we need to be able to quantify and identify the microorganisms present in each lithobiontic ecological niche and to accurately characterize the mineralogical features of these hidden microhabitats. Once we have established the techniques that will allow us to observe and identify these microorganisms and mineral substrates in situ, and have confirmed the presence of water, the following questions can be addressed: How are the microorganisms organized in the fissures or cavities? Which microorganisms are present and how many are there? Additional questions that logically follow include: What are the existing water relationships in the microhabitat and what effects do the microorganisms have on the mineral composition? Mechanical and chemical changes in minerals and mineralization of microbial cells can give rise to physical and/or chemical traces (biomarkers) and to microbial fossil formation. In this report, we describe the detection of chains of magnetite within the Martian meteorite ALH84001, as an example of the potential use of SEM-BSE in the search for plausible traces of life on early Mars. Electronic Publication     

Nitrogen deposition promotes the production of new fungal residues but retards the decomposition of old residues in forest soil fractions

Atmospheric nitrogen (N) deposition has frequently been observed to increase soil carbon (C) storage in forests, but the underlying mechanisms still remain unclear. Changes in microbial community composition and substrate use are hypothesized to be one of the key mechanisms affected by N inputs. Here, we investigated the effects of N deposition on amino sugars, which are used as biomarkers for fungal‐ and bacterial‐derived microbial residues in soil. We made use of a 4‐year combined CO₂ enrichment and N deposition experiment in model forest ecosystems, providing a distinct ¹³C signal for ‘new’ and ‘old’ C in soil organic matter and microbial residues measured in density and particle‐size fractions of soils. Our hypothesis was that N deposition decreases the amount of fungal residues in soils, with the new microbial residues being more strongly affected than old residues. The soil fractionation showed that organic matter and microbial residues are mainly stabilized by association with soil minerals in the heavy and fine fractions. Moreover, the bacterial residues are relatively enriched at mineral surfaces compared to fungal residues. The ¹³C tracing indicated a greater formation of fungal residues compared to bacterial residues after 4 years of experiment. In contradiction to our hypotheses, N deposition significantly increased the amount of new fungal residues in bulk soil and decreased the decomposition of old microbial residues associated with soil minerals. The preservation of old microbial residues could be due to decreased N limitation of microorganisms and therefore a reduced dependence on organic N sources. This mechanism might be especially important in fine heavy fractions with low C/N ratios, where microbial residues are effectively protected from decomposition by association with soil minerals.     

Extracellular Electron Transfer Between Birnessite and Electrochemically Active Bacteria Community from Red Soil in Hainan,China

The interplay between electrochemically active microorganisms (EAMs) and adjacent minerals universally occurs in natural environments, in which soil is an extremely typical and active one. We stimulated the extracellular electron transfer (EET) process between the bacterial community and birnessite in red soil (collected from Hainan, China) by constructing a microbial fuel cell equipped with synthetic birnessite cathode. Compared to graphite-cathode, the cell voltage of birnessite-cathode was increased by 22% when loading a 1000 Ω-resistance, indicating the EET between microbes and birnessite. Eleven genera of EAMs in red soil were confirmed through 16S rRNA analysis. Neither palpable novel mineral formation nor change of birnessite crystallinity was observed after reaction by Raman and SEM. As oxygen pumped into cathode chamber was the terminal electron acceptor, birnessite principally performed as an intermediate of holistic electron transfer process to favor the cathodic oxygen reduction.     

Amelogenin-Collagen Interactions Regulate Calcium Phosphate Mineralization in Vitro

Collagen and amelogenin are two major extracellular organic matrix proteins of dentin and enamel, the mineralized tissues comprising a tooth crown. They both are present at the dentin-enamel boundary (DEB), a remarkably robust interface holding dentin and enamel together. It is believed that interactions of dentin and enamel protein assemblies regulate growth and structural organization of mineral crystals at the DEB, leading to a continuum at the molecular level between dentin and enamel organic and mineral phases. To gain insight into the mechanisms of the DEB formation and structural basis of its mechanical resiliency we have studied the interactions between collagen fibrils, amelogenin assemblies, and forming mineral in vitro, using electron microscopy. Our data indicate that collagen fibrils guide assembly of amelogenin into elongated chain or filament-like structures oriented along the long axes of the fibrils. We also show that the interactions between collagen fibrils and amelogenin-calcium phosphate mineral complexes lead to oriented deposition of elongated amorphous mineral particles along the fibril axes, triggering mineralization of the bulk of collagen fibril. The resulting structure was similar to the mineralized collagen fibrils found at the DEB, with arrays of smaller well organized crystals inside the collagen fibrils and bundles of larger crystals on the outside of the fibrils. These data suggest that interactions between collagen and amelogenin might play an important role in the formation of the DEB providing structural continuity between dentin and enamel.