Cretaceous mycelia preserving fungal polysaccharides: taphonomic and paleoecological potential of microorganisms preserved in fossil resins

• Autores: M. Speranza, Carmen Ascaso, Xavier Delclòs Martínez, E. Peñalver
• Localización: Geologica acta: an international earth science journal, ISSN 1695-6133, Vol. 13, Nº. 4, 2015, págs. 363-385
• Idioma: catalán
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• Resumen

  • The cortices of pieces of Cretaceous amber around the world sometimes are constituted by networks of filamentous structures. Based on their morphological characteristics, such structures have previously been classified in different microorganismal groups. The correct interpretation, however, is of great importance to establish the conditions of the resin’s burial in the forest litters, and can provide important clues regarding the ecology and environmental conditions of Cretaceous resinous forests. Because these networks of filamentous structures present typical fungal morphological features we conducted a study in order to resolve their origin. The cortices of several pieces of Cretaceous amber from Spain were examined using light and scanning electron microscopy, energy dispersive X-ray spectroscopy, and confocal laser scanning microscopy. This is the first time that Calcofluor white and wheat germ agglutinin conjugated with fluorescein isothiocyanate have been employed as fungal markers in amber, and their use enabled us to detect preserved polysaccharides in the filamentous structures using confocal laser scanning microscopy. These results provide the first and oldest record of ß-1,3 and ß-1,4-linked polysaccharides, and specifically N-acetylglucosamine residues from chitin in a fossil fungus preserved in amber, and to demonstrate that the networks of filamentous structures are mycelia composed of profuse hyphae of a resinicolous fungus. This type of mycelium constitutes one of the largest fungal fossil records known. A similar fungal colonization pattern was observed in extant kauri resin from New Zealand. Using taphonomic data, it is demonstrate that the cortices originated during the Cretaceous due to fungal growth in non-solidified resin. The fossil diagenetic degradation sequence of the fungal hyphae and the surrounding amber is described. This degradation changed the microscopic appearance of the hyphae; thus, some of the previously indicated taxonomic features of this microorganism may actually be fossil diagenetic artifacts. The paleoecological implications with regard to fungal trophic requirements and forest environmental conditions are discussed.