Genus

Chondrites Sternberg, 1833

Taxon description

Baucon et al., 2020c

Emended diagnosis: regularly branching tunnel system consisting of a small number of sub-vertical master-shafts, connected to the ancient sediment-water interface, that branches at depth to form a dendritic network. Fill can be active or passive (diagnosis emended after Osgood, 1970; Fürsich, 1974; Fu, 1991; Uchman, 1995; Blissett and Pickerill, 2004; Uchman et al., 2012).

Remarks: Non-radial forms (hypidiomorphic) may be included within the ichnogenus.The tunnels of Chondrites neither touch nor cross each other (Fu, 1991), although some exceptions are reported (Blissett and Pickerill, 2004; Uchman et al., 2012). Branching may occur in a single plane or as three-dimensional forms, and may consist of up to six orders of branching (Fu, 1991). According to Fu (1991), the branching angle may range from 15° to 90° with an average value between 30°- 60°. The burrow fill is typically uniform/structure-less, though there are some rare accounts of meniscate fill (Fu, 1991). Burrow diameter is narrow and varies between burrow systems (1−5 mm according to Fu (1991); 0.1–10 mm according to Savrda and Bottjer, 1991), but it is generally constant within a single system (Fu, 1991; Savrda and Bottjer, 1991). According to Uchman (1999), tunnels are narrower than 0.95 mm.

Fernández & Pazos, 2012

Remarks. Chondrites is ethologically classified as a feeding trace (fodinichnia). It is generally assigned to depositivorous and/or suspensivorous annelids or sipunculids.

Knaust, 2017

Morphology, Fill and Size: Chondrites is one of the most common and widely distributed trace fossils; due to its rootlike appearance it was originally interpreted as a plant fossil.  It consists of tunnel systems possessing a single or a small number of master shafts, presumably open to the surface, which ramifies with depth under acute angle to form a dendritic or root-like system (Osgood 1970; Fu 1991). Most of the burrows show an active fill, sometimes with portions preserving a meniscate structure. The burrows are unlined. The tunnel diameter remains constant in different parts of the burrow and typically is in the range of less than 1 mm to a few millimeters.

Howard & Frey, 1984

Diagnosis: Dendritic, smooth walled, regularly but asymmetrically branched small burrow systems that ordinarily do not interpenetrate or interconnect. Diameter of components within a given system remains more or less constant.

Mángano et al., 2002a

Recent work suggests that Chondrites may represent specialized feeding behavior that involves chemosymbiosis, being interpreted as a sulfide pump (Fu, 1990, Seilacher, 1990; Bromley, 1996). It has been regarded that the Chondrites animal developed adaptations to cope with oxygen-depleted conditions (Bromley & Ekdale, 1984; Savdra, 1992).

Selection of related publications
Hanken, N.-M., Uchman, A., Nielsen, J. K., Olaussen, S., Eggebø, T., Steinsland, R. 2016. Late Ordovician trace fossils from offshore to shallow water mixed siliciclastic and carbonate facies in the Ringerike Area, Oslo Region, Norway. Ichnos 23, 3-4, 189-221. DOI:10.1080/10420940.2016.1199427
Mikuláš R., Dronov, A. 2005. Trace fossils. 6th Baltic Stratigraphical Conference, IGCP 503 Meeting, August 23-25, 2005. Cambrian and Ordovician of St. Petersburg region. Guidebook of the pre-conference field trip, pp. 33-38. St. Petersburg State University, VSEGEI.
Elias, R. J., Nowlan, G. S., Bolton, T. E. 1988. Paleontology of the type section, Fort Garry Member, Red River Formation (Upper Ordovician), southern Manitoba. pp. 341-359.
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Klassificering
Organism groupBiota
Ichnofossil groupIchnofossils
Bioturbation trace fossils
Trackways and scratch imprints
OrderBiformitidae
FamilyArenicolitidae
Arthrophycidae
Asteriacitidae
Rhizocoralliidae
Rosselichnidae
Siphonichnidae
GenusAcanthorhaphe
Aglaspidichnus
Agrichnium
Altichnus
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Speciesaffinis
bollensis
caespitosus
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stellaris
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unrankedTrusheimichnus
References based on distribution