The behaviour of the iconic ichnogenus Chondrites is re-evaluated based on review of existing literature and analysis of novel data (macroscopic, thin section and ESEM-EDX observations; CT-scans and resin peels of modern analogues; computer-controlled serial grinding; morphometric analysis and theoretical morphology). The bedding plane expression of Chondrites is well-constrained by morphometry:(1) the angle of dichotomy formed by a pair of adjacent branches is typically between 30° and 56° (interquartile range; mean: 47°); (2) branching order isbetween 1 and 9; (3) branches are, on average, 9 times longer than wide. In the third dimension, downward branching is dominant but bundled shafts and upward branching may be present.The size of Chondritesincreased markedly from the Late Jurassic to theLate Cretaceous, suggesting that the tracemakers became larger and larger. Microfabric analysis of Chondrites shows active fill or, alternatively, passive fill of empty tunnels by currents or clay percolation, a new mechanism proposed herein. The tracemakers built Chondritesto obtain food: (1) vermiform deposit feeders produced Chondritesfor searching for food in the sediment (fodinichnion); (2) asymbiotic bivalves built Chondritesfor cultivating and directly ingesting bacteria (agrichnion);(3) chemosymbiotic bivalves produced Chondritesto provide symbionts with chemical agents (chemichnion) Chondriteswas modified through the life of the tracemaker or it represented a part of the producer’s lifespan. Chondrites —and its modern tracemaker(s) —is associated with a range of marine settings, including well-oxygenated, dysoxic and space-limited (nucleocave) environments. As such, Chondrites is regarded as an extremotolerant ichnotaxon.
Andrea Baucon, M.B. (2020). Ethology of the trace fossil Chondrites: form, function and environment. EARTH-SCIENCE REVIEWS, 202, 102989-103025 [10.1016/j.earscirev.2019.102989].
Ethology of the trace fossil Chondrites: form, function and environment
Barbara CavalazziWriting – Original Draft Preparation
;
2020
Abstract
The behaviour of the iconic ichnogenus Chondrites is re-evaluated based on review of existing literature and analysis of novel data (macroscopic, thin section and ESEM-EDX observations; CT-scans and resin peels of modern analogues; computer-controlled serial grinding; morphometric analysis and theoretical morphology). The bedding plane expression of Chondrites is well-constrained by morphometry:(1) the angle of dichotomy formed by a pair of adjacent branches is typically between 30° and 56° (interquartile range; mean: 47°); (2) branching order isbetween 1 and 9; (3) branches are, on average, 9 times longer than wide. In the third dimension, downward branching is dominant but bundled shafts and upward branching may be present.The size of Chondritesincreased markedly from the Late Jurassic to theLate Cretaceous, suggesting that the tracemakers became larger and larger. Microfabric analysis of Chondrites shows active fill or, alternatively, passive fill of empty tunnels by currents or clay percolation, a new mechanism proposed herein. The tracemakers built Chondritesto obtain food: (1) vermiform deposit feeders produced Chondritesfor searching for food in the sediment (fodinichnion); (2) asymbiotic bivalves built Chondritesfor cultivating and directly ingesting bacteria (agrichnion);(3) chemosymbiotic bivalves produced Chondritesto provide symbionts with chemical agents (chemichnion) Chondriteswas modified through the life of the tracemaker or it represented a part of the producer’s lifespan. Chondrites —and its modern tracemaker(s) —is associated with a range of marine settings, including well-oxygenated, dysoxic and space-limited (nucleocave) environments. As such, Chondrites is regarded as an extremotolerant ichnotaxon.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.