scholarly journals SMALL SHELLY FOSSIL PRESERVATION AND THE ROLE OF EARLY DIAGENETIC REDOX IN THE EARLY TRIASSIC

Palaios ◽  
2018 ◽  
Vol 33 (10) ◽  
pp. 441-450 ◽  
Author(s):  
SARA B. PRUSS ◽  
NICHOLAS J. TOSCA ◽  
COURCELLE STARK
Palaios ◽  
2021 ◽  
Vol 36 (10) ◽  
pp. 326-329
Author(s):  
MARK A. WILSON ◽  
ANNA M. COOKE ◽  
SHELLEY A. JUDGE ◽  
TIMOTHY J. PALMER

ABSTRACT Ooimmuration is here defined as a taphonomic process by which fossils are preserved within ooids. It is a form of lithoimmuration, although depending on the role of microbes in the formation of the ooid cortex, ooimmuration can also be considered a type of bioimmuration. Fossils enclosed within ooids are protected from bioerosion as well as the abrasion common in energetic depositional environments such as ooid shoals. Many taxa in some fossil assemblages may be known only because they were ooimmured. We describe as examples of ooimmuration fossils preserved in an oolite from the Middle Jurassic (Bajocian) Carmel Formation in southwestern Utah.


Palaios ◽  
2019 ◽  
Vol 34 (7) ◽  
pp. 331-348 ◽  
Author(s):  
FILIPE G. VAREJÃO ◽  
LUCAS V. WARREN ◽  
MARCELLO G. SIMÕES ◽  
FRANZ T. FÜRSICH ◽  
SUZANA A. MATOS ◽  
...  

ABSTRACTThe Aptian Crato Konservat-Lagerstätte is renowned for its exceptionally preserved fossils in lacustrine laminated limestones. Although previous works on this site include numerous taxonomic studies, its taphonomy remains a subject of debate. Herein, we present new data on the taphonomy of decapod crustaceans preserved in wrinkle laminites, highlighting the role of microbial mats in enhancing fossil preservation. Our results suggest that benthic microorganisms may have promoted protection and organic mineralization of some of the allochthonous to parautochthonous organic remains within the microbial laminites of the Crato lake. Overall, this work provides the first empirical evidence that the preservational pathways of the fossils in the Crato Konservat-Lagerstätte involved microbial mats.


Paleobiology ◽  
1988 ◽  
Vol 14 (2) ◽  
pp. 139-154 ◽  
Author(s):  
Peter A. Allison

Actualistic experiments have quantified rate of anaerobic decay and associated mineralization around proteinaceous macro-organisms. Carcasses of the polychaete wormNereisand the eumalacostracansNephropsandPalaemonwere buried in airtight glass jars filled with sediment and water from marine, brackish, and lacustrine environments. Over a period of 25 weeks the contents were examined to determine the state of decay and were chemically analyzed to monitor early diagenetic mineralization (two methods for such analysis are reviewed). Decay processes were active in the experimental conditions despite anoxia and had virtually destroyed the carcasses within 25 weeks. However, decay-rate in the sulfate-reducing marine system was greater than in the methanogenic freshwater environments. Petrological and geochemical analyses of the organic remains identified discrete layers of authigenic iron monosulfide (a pyrite precursor) on the surface of the decayingNephropscuticle within weeks of initiating the experiment. Chemical analysis of decomposing flesh showed a marked increase in pore-water calcium content with time.The results clearly show that anoxia is ineffective as a long-term conservation medium in the preservation of soft-bodied fossils. However, decay-induced mineralization can be very rapid so that even a slight reduction in decay rate can lead to improved levels of fossil preservation. Traditionally, stagnation and rapid burial are considered to be the main prerequisites for the preservation of soft-bodied fossils and the formation ofKonservat-Lagerstätten. Clearly these factors are only important in that they promote early diagenetic mineralization. This is the only way to halt information loss through decay.


Geology ◽  
2013 ◽  
Vol 41 (2) ◽  
pp. 123-126 ◽  
Author(s):  
Ines Melendez ◽  
Kliti Grice ◽  
Kate Trinajstic ◽  
Mojgan Ladjavardi ◽  
Paul Greenwood ◽  
...  

2015 ◽  
Vol 282 (1808) ◽  
pp. 20150476 ◽  
Author(s):  
Aodhán D. Butler ◽  
John A. Cunningham ◽  
Graham E. Budd ◽  
Philip C. J. Donoghue

Exceptionally preserved fossils provide major insights into the evolutionary history of life. Microbial activity is thought to play a pivotal role in both the decay of organisms and the preservation of soft tissue in the fossil record, though this has been the subject of very little experimental investigation. To remedy this, we undertook an experimental study of the decay of the brine shrimp Artemia , examining the roles of autolysis, microbial activity, oxygen diffusion and reducing conditions. Our findings indicate that endogenous gut bacteria are the main factor controlling decay. Following gut wall rupture, but prior to cuticle failure, gut-derived microbes spread into the body cavity, consuming tissues and forming biofilms capable of mediating authigenic mineralization, that pseudomorph tissues and structures such as limbs and the haemocoel. These observations explain patterns observed in exceptionally preserved fossil arthropods. For example, guts are preserved relatively frequently, while preservation of other internal anatomy is rare. They also suggest that gut-derived microbes play a key role in the preservation of internal anatomy and that differential preservation between exceptional deposits might be because of factors that control autolysis and microbial activity. The findings also suggest that the evolution of a through gut and its bacterial microflora increased the potential for exceptional fossil preservation in bilaterians, providing one explanation for the extreme rarity of internal preservation in those animals that lack a through gut.


2020 ◽  
Author(s):  
Éva Oravecz ◽  
Gábor Héja ◽  
László Fodor

<p>The Permian to Lowermost Triassic Perkupa Evaporite forms the base of the enigmatic Silica Nappe (uppermost tectonic unit of the Aggtelek Hills, Inner Western Carpathians) and played the role of the main detachment level during the Cretaceous nappe stacking. Regionally, the Silica Nappe is one of the most enigmatic tectonic units of the Alpine-Carpathian area as up until now, it had many unanswered structural problems, like do the three or four different folding directions necessarily suggest multiple folding phases, how to solve the problem of extreme thickness changes in pre-orogenic sediments or why are young-on-older contacts so frequent in the area. Furthermore, several previous studies suggested that there may be salt diapirs rooting in this evaporitic detachment level but their role in the evolution of the Silica Nappe has not been studied in details.</p><p>In this study new approaches were applied in order to explain the abovementioned questions and to understand the deformation of the problematic Aggtelek Mts. Detailed geological mapping and structural analysis resulted in the recognition of extensive salt tectonics in the Inner Western Carpathians. Field results showed that not only simple salt diapirs but also map-scale salt walls were present in the southernmost part of the Silica Nappe. The observed onlap surfaces on the salt flaps and the extreme thickness changes within the Lower Triassic formations suggested that these salt structures originally formed syn-sedimentary with the respect to the Early Triassic sedimentation. Starting probably from the latest Early Triassic, sedimentation occurred in minibasins, the evolution of which was controlled by the continuously growing salt structures. Salt movements were coupled with doming and drag folding along the salt structures that resulted in slumping and syn-sedimentary normal faulting in the sedimentary cover.</p><p>These pre-existing salt structures and normal faults strongly influenced the geometry and kinematics of the subsequent Cretaceous deformation: the majority of shortening was localized at the salt walls and diapirs while the minibasins were left mostly unaffected. When the salt walls were squeezed, secondary salt welds formed that were now mapped as linear rauhwacke zones. Due to further shortening, the welds were reactivated as oblique thrust welds and the minibasin borders evolved into young-on-older thrust contacts. After peeling the effects of evaporite deformation off the Cretaceous shortening, the main tectonic transport direction was estimated to be towards S-SE.</p><p>Consequently, the structural evolution of the Silica Nappe is much more complex than previously thought but many long-standing problems could be explained by considering structural inheritance and bringing pre-orogenic salt tectonics into the interpretation. Nevertheless, the Aggtelek Mts. turned out to be a good area to further study the effects of inherited salt structures on the evolution of fold-and-thrust belts and to draw conclusions on how to separate salt-related folding from regular shortening related structures in poor outcrop conditions.</p><p>The research was supported by the research found NKFIH OTKA 113013 and the ÚNKP-18-2 New National Excellence Program of the Ministry of Human Capacities.</p>


JAMA ◽  
1966 ◽  
Vol 195 (12) ◽  
pp. 1005-1009 ◽  
Author(s):  
D. J. Fernbach
Keyword(s):  

JAMA ◽  
1966 ◽  
Vol 195 (3) ◽  
pp. 167-172 ◽  
Author(s):  
T. E. Van Metre

Paleobiology ◽  
1980 ◽  
Vol 6 (02) ◽  
pp. 146-160 ◽  
Author(s):  
William A. Oliver

The Mesozoic-Cenozoic coral Order Scleractinia has been suggested to have originated or evolved (1) by direct descent from the Paleozoic Order Rugosa or (2) by the development of a skeleton in members of one of the anemone groups that probably have existed throughout Phanerozoic time. In spite of much work on the subject, advocates of the direct descent hypothesis have failed to find convincing evidence of this relationship. Critical points are:(1) Rugosan septal insertion is serial; Scleractinian insertion is cyclic; no intermediate stages have been demonstrated. Apparent intermediates are Scleractinia having bilateral cyclic insertion or teratological Rugosa.(2) There is convincing evidence that the skeletons of many Rugosa were calcitic and none are known to be or to have been aragonitic. In contrast, the skeletons of all living Scleractinia are aragonitic and there is evidence that fossil Scleractinia were aragonitic also. The mineralogic difference is almost certainly due to intrinsic biologic factors.(3) No early Triassic corals of either group are known. This fact is not compelling (by itself) but is important in connection with points 1 and 2, because, given direct descent, both changes took place during this only stage in the history of the two groups in which there are no known corals.


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