Modern microbialites in Pavilion Lake, BC, provide an analog for ancient non-stromatolitic microbialites that formed from in situ mineralization. Because Pavilion microbialites are mineralizing under the influence of microbial communities, they provide insights into how biological processes influence microbialite microfabrics and mesostructures. Hemispherical nodules and micrite-microbial crusts are two mesostructures within Pavilion microbialites that are directly associated with photosynthetic communities. Both filamentous cyanobacteria in hemispherical nodules and branching filamentous green algae in micrite-microbial crusts were associated with calcite precipitation at microbialite surfaces and with characteristic microfabrics in the lithified microbialite. Hemispherical nodules formed at microbialite surfaces when calcite precipitated around filamentous cyanobacteria with a radial growth habit. The radial filament pattern was preserved within the microbialite to varying degrees. Some subsurface nodules contained well-defined filaments, whereas others contained only dispersed organic inclusions. Variation in filament preservation is interpreted to reflect differences in timing and amount of carbonate precipitation relative to heterotrophic decay, with more defined filaments reflecting greater lithification prior to degradation than more diffuse filaments. Micrite-microbial crusts produce the second suite of microfabrics and form in association with filamentous green algae oriented perpendicular to the microbialite surface. Some crusts include calcified filaments, whereas others contained voids that reflect the filamentous community in shape, size, and distribution. Pavilion microbialites demonstrate that microfabric variation can reflect differences in lithification processes and microbial metabolisms as well as microbial community morphology and organization. Even when the morphology of individual filaments or cells is not well preserved, the microbial growth habit can be captured in mesoscale microbialite structures. These results suggest that when petrographic preservation is extremely good, ancient microbialite growth structures and microfabrics can be interpreted in the context of variation in community organization, community composition, and lithification history. Even in the absence of distinct microbial microfabrics, mesostructures can capture microbial community morphology.

Treatment with the antigranulocyte monoclonal antibody (MAb) RB6-8C5 increased the severity of infection in mice intragastrically inoculated with Listeria monocytogenes. Most MAb RB6-8C5-treated mice died when inoculated intragastrically with as few as 4 ؋ 10 4 L. monocytogenes bacteria, whereas most control mice survived intragastric inoculation with 4 ؋ 10 8 L. monocytogenes bacteria. The increased severity of infection in MAb RB6-8C5-treated mice appeared to result from listerial multiplication in the spleen and liver rather than from local proliferation in the intestinal tract or mesenteric lymph nodes.

Thrombolites are a common component of carbonate buildups throughout the Phanerozoic. Although they are usually described as microbialites with an internally clotted texture, a wide range of thrombolite textures have been observed and attributed to diverse processes, leading to difficulty interpreting thrombolites as a group. Interpreting thrombolitic textures in terms of ancient ecosystems requires understanding of diverse processes, specifically those due to microbial growth and metazoan activity. Many of these processes are reflected in thrombolites in the Cambrian Carrara, Bonanza King, Highland Peak and Nopah formations, Great Basin, California, USA; they comprise eight thrombolite classes based on variable arrangements and combinations of depositional and diagenetic components. Four thrombolite classes (hemispherical microdigitate, bushy, coalescent columnar and massive fenestrated) contain distinct mesoscale microbial growth structures that can be distinguished from surrounding detrital sediments and diagenetic features. By contrast, mottled thrombolites have mesostructures that dominantly reflect post‐depositional processes, including bioturbation. Mottled thrombolites are not bioturbated stromatolites, but rather formed from disruption of an originally clotted growth structure. Three thrombolite classes (arborescent digitate, amoeboid and massive) contain more cryptic textures. All eight of the thrombolite classes in this study formed in similar Cambrian depositional environments (marine passive margin). Overall, this suite of thrombolites demonstrates that thrombolites are diverse, in both internal fabrics and origin, and that clotted and patchy microbialite fabrics form from a range of processes. The diversity of textures and their origins demonstrate that thrombolites should not be used to interpret a particular ecological, evolutionary or environmental shift without first identifying the microbial growth structure and distinguishing it from other depositional, post‐depositional and diagenetic components. Furthermore, thrombolites are fundamentally different from stromatolites and dendrolites in which the laminae and dendroids reflect a primary growth structure, because clotted textures in thrombolites do not always reflect a primary microbial growth structure.

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