Wojciech Krawczyński

New Devonian Microconchids (Tentaculita) from the Holy Cross Mountains, Poland

Abstract Tentaculitoid microconchid tubeworms from Devonian (uppermost Emsian–upper Givetian) deposits of the Holy Cross Mountains, Poland, include three new species from stratigraphically well-constrained lithological units: Polonoconchus skalensis n. gen. n. sp., Palaeoconchus sanctacrucensis n. sp. and Microconchus vinni n. sp. The microconchids inhabited fully marine environments during transgressive pulses, as is evidenced from facies and associated fossils. Polonoconchus skalensis n. gen. n. sp. and Palaeoconchus sanctacrucensis n. sp. inhabited secondary firm- to hard-substrates in deeper-water, soft-bottom environments. They developed planispiral, completely substrate-cemented tubes and planispiral tubes with elevated apertures, which is indicative of environments where sedimentation rate is low but competition for space (by overgrowth) may be high. Microconchus vinni n. sp., on the other hand, developed a helically coiled distal portion of the tube as a response to a high sedimentation rate. As the taxonomic composition of Devonian microconchids is poorly recognized at both regional and global scales, this new material contributes significantly to our understanding of the diversity of these extinct tube-dwelling encrusters.

Middle Jurassic (Bathonian) encrusted oncoids from the Polish Jura, southern Poland

Oncoids from two localities (Ogrodzieniec and Blanowice) of the Polish Jura, southern Poland, have been investigated with respect to their genesis and paleoecology. These oncoids occur within Middle Jurassic (Bathonian) deposits. Those from Ogrodzieniec are large, elliptical, and embedded within a presumably condensed carbonate bed. Those from Blanowice, on the contrary, are significantly smaller, irregular to box-like in shape, and occur within the ore-bearing clays. The oncoids from both localities consist of a distinct carbonate core and laminated cortex that is significantly thicker and better preserved in the Ogrodzieniec oncoids. SEM and optical microscopic investigation of the oncoid cortices revealed the presence of carbonate and silicate layers with web-like structures similar to those occurring in recent cyanobacterial microbialites. Thus, the oncoid cortices investigated may have formed in a photic zone environment with the aid of coccoid and filamentous cyanobacteria. Oxic conditions prevailed during oncoid cortex formation within the siliciclastic setting, which is manifested by low total organic carbon content, high pristane/phytane (Pr/Ph) ratio, and significant predomination of the C31 homohopanes. On the cortices’ surfaces, as well as between particular laminae, various encrusting organisms have been found. The encrusters, dominated by serpulids and bryozoans, are cryptic species that inhabited the undersides and recesses of the oncoids. Their presence on both the upper and lower surfaces of the oncoids indicates that the oncoids were episodically overturned on the seafloor. The much better developed cortex lamination and much higher diversity and abundance of encrusters in the Ogrodzieniec oncoids may point to better trophic conditions prevailing in a shallower marine environment characterized by transparent waters, as opposed to a deeper siliciclastic environment with less transparent waters and probably worse trophic conditions prevailing during formation of the Blanowice oncoids.