Micromorphology of marine invertebrate trace fossils and their ethological and ichnotaxonomic implications

• Autores: Fernández, Diana Elizabeth; Gutiérrez, Carolina; Arambarric, Gabriel Agustín; Comerio, Marcos; Cuitiño, José Ignacio; Giachetti, Luciana María; Taylor, Colin; Pazos, Pablo Jose
• Año de publicación: 2024
• Idioma: inglés
• Tipo de recurso: documento de conferencia
• Materia: MARINE INVERTEBRATE; TRACE FOSSILS; MICROMORPHOLOGY; ETHOLOGY
• Institución: Consejo Nacional de Investigaciones Científicas y Técnicas

It is common for proposed paleobiological models for specific ichnotaxa to blend or associate concepts related to trace fossil production, basic feeding strategy, and biological affinities of the producers. These models persist in the literature as a whole, hindering the separation of partial interpretations (e.g., detailed interpretation of only the feeding strategy, or only the potential tracemaker) achievable through microscale studies of exceptionally preserved samples. Additionally, analyzing numerous specimens of the same ichnotaxon at different scales allows discussion of established ichnotaxobases due to the morphological variety involved, with the intention that morphologically based diagnoses present inferences about the tracemaker [¹]. Micromorphological studies on current and fossil insect traces have yielded excellent results regarding producer behavior and biological affinity, along with ichnotaxonomic implications [2]. However, micromorphological studies on trace fossils produced by marine invertebrates with this scope are much scarcer, and include techniques such as petrography, scanning electron microscopy (SEM), X-ray microcomputed tomography, etc. [3-10]. These studies provide insights into the trace fossil production mode, potential tracemakers, substrate modification, and their consequences. For instance, in the case of Nereites MacLeay, some microscale features of analyzed specimens supported a construction differing from the typical worm-like organism model, aligning with other previous ideas, and also suggested an interpretation of an arthropod as tracemaker, a concept explored in previous neoichnological studies [6]. In the case of Bolonia Meunier, backfilling structures were interpreted as produced by the aboral and lateral spines of irregular echinoids, which worked together to compact the sediment anteroposteriorly and moved alternatively [10]. Here we present new results from the same line of research, describing and discussing the internal structure of examples of two other iconic ichnotaxa: Ophiomorpha Lundgren and Dictyodora Weiss. Exceptionally preserved examples of Ophiomorpha from Patagonian units (the Lower Cretaceous Agrio Formation and the Miocene Gaiman and Puerto Madryn formations), and of Dictyodora from the Silurian Gala Group (Scotland), were serially thin-sectioned. Transverse (vertical) and parallel (horizontal) to the bedding plane, or longitudinal and transverse to the main axis (depending on the ichnotaxon) sections were analyzed following previously used methods [3,6,10].Ophiomorpha is one of the most globally recognized ichnogenera in marine deposits of various depths and age. Its ichnospecies are primarily classified based on pellet morphology. Ophiomorpha irregulaire Frey et al. exhibits conical or outwardly acute pellets with non-uniform sizes. The validity of this pellet morphology as diagnostic for O. irregulaire has been debated due to the possibility that these pellets are filled with sand-sized grains, enveloped by a layer of mud and organic material, and the conical appearance may result from an incomplete muddy rim [4,11]. This is supported by our results from Lower Cretaceous Ophiomorpha, where walls with coating rich in clays and organic matter bear pellets that appear flame-like but under microscopic analysis show reoriented grains that allow to infer their original spherical shape (Fig. 1A). Also, two types of organic matter were detected within the wall: discrete, dense organic particles of terrigenous affinity (mostly phytoclasts), and amorphous organic matter, mixed with the inorganic matrix. The presence of fermentation chambers [11] in some sectors is not disregarded. Additionally, the Miocene Ophiomorpha-rich deposits, described as composed by O. nodosa Lundgren, are now thought to include O. nodosa and O. borneensis Keij in intergradation, with a dominance of the latter. This implies the tracemaker was able to produce both type of pellets. The characteristic bilobed morphology of the pellets and its regular distribution is confirmed by what is observed in cross-section (Fig. 1B): the semi-spherical reworking by the tracemaker continues inside the wall, reinforcing the idea that these are originally bilobed pellets and not a taphonomical artifact. This material allows to speculate that O. borneensis might be more common than it is currently represented in the literature.Dictyodora Weiss is a three-dimensional complex trace fossil characteristic of marine Paleozoic deposits recorded since the middle Cambrian. Its micromorphology under optical microscope has been illustrated [12,13] or very briefly described [14,15]; only one study illustrated part of the trace fossil under SEM [16]. Our preliminary results on Silurian samples include a thorough description of the internal structure of the area where the structures referred to as spreite and basal burrow interconnect (Fig. 1C-D). In vertical cross-sections it is observed that the lowermost part of the spreite is surrounded by the uppermost and medial part of the basal burrow, in contrast with previous interpretations [17-19], allowing to discuss one of the possible interpretations of the spreite-producing structure as rigid [17]. The tripartite morphology of the basal burrow occasionally seen in samples [17,18] could be explained by this interconnection (Fig. 1D), supporting the necessity of a future diagnosis amendment [18]. More such studies are needed to challenge aspects of paleobiological/ethological models without necessarily completely discarding all ideas within them, and to discuss ichnotaxobases that do not depend but might rely on functional morphology.
Fil: Fernández, Diana Elizabeth. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Estudios Andinos "Don Pablo Groeber". Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Estudios Andinos "Don Pablo Groeber"; Argentina
Fil: Gutiérrez, Carolina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Estudios Andinos "Don Pablo Groeber". Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Estudios Andinos "Don Pablo Groeber"; Argentina
Fil: Arambarric, Gabriel Agustín. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Departamento de Ciencias Geológicas; Argentina
Fil: Comerio, Marcos. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Estudios Andinos "Don Pablo Groeber". Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Estudios Andinos "Don Pablo Groeber"; Argentina
Fil: Cuitiño, José Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Centro Nacional Patagónico. Instituto Patagónico de Geología y Paleontología; Argentina
Fil: Giachetti, Luciana María. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Centro Nacional Patagónico. Instituto Patagónico de Geología y Paleontología; Argentina
Fil: Taylor, Colin. University Of Aberdeeen; Reino Unido
Fil: Pazos, Pablo Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Estudios Andinos "Don Pablo Groeber". Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Estudios Andinos "Don Pablo Groeber"; Argentina
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