Gorde:
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| Formatua: | Recurso digital |
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Zenodo
2025
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| Gaiak: | |
| Sarrera elektronikoa: | https://doi.org/10.5281/zenodo.15150653 |
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Aurkibidea:
- <p><b>Genus <i>Kiaeroceras</i> Strand, 1934</b></p><p><b>Type species</b></p><p><i>Kiaeroceras frognoyense</i> Strand, 1934, from Frognoyøa island, Ringerike, Norway, “ <i>Trinucleus</i> limestone, (4cβ)” (Strand 1934: 98), SØrbakken Formation, Late Katian; by original designation.</p><p><b>Diagnosis</b></p><p>Orthocones with ovate conch cross section, narrower ventral conch margin; mature body chamber slightly bulbous, with shallow constriction near aperture; aperture with deep and broad hyponomic sinus; sutures with lateral lobes and pronounced ventral saddle; siphuncle close to ventral conch margin, with broadly expanded siphuncular segments, with prominent bullettes. (Adopted from Strand 1934.)</p><p><b>Remarks</b></p><p>The diagnosis of the genus given in Kröger (2013) is imprecise, it is corrected herein and features now the important characters described in Strand (1934). Moreover, the relatively rich Estonian material described herein reveals a few features, not known from type material of the type species. These include the shape and dimensions of the more apical phragmocone parts, variability in conch cross section shape as well as the extent and development of endosiphuncular deposits. Consequently, species are included here, which have conch cross sections with a CHI of nearly 1, although possessing the characteristically narrow margin on the prosiphuncular side. Additionally, the hyponomic sinus which is deep in the type species, does not seem to be deep in all species. Finally, the more complete specimens of this genus reveal that the curvature is endogastric and that the suture develops a lateral lobe during the latest growth stages (compare, e.g., Fig. 34H, and Strand 1934: pl. 9 fig. 4 and pl. 12 fig. 2). The genus is interpreted here sensu lato, to include these deviations from the original diagnosis.</p><p>The genus was placed within the Cyrtogomphoceratidae by Teichert (1964b) and has been compared to <i>Protophragmoceras</i> by Strand (1934). This was based on the presence of heavy endosiphuncular bullettes in the type-material. The new material, described herein, shows that in specimens assigned to <i>Kiaeroceras</i> transitions exist from typical discosorid-like bullettes toward valcouroceratid-like actinosiphonate deposits (see below in description of <i>K</i>. <i>kaebliki</i> sp. nov.).</p><p>Moreover, Strand (1934) described <i>Mixosiphonoceras norvegicum</i> Strand, 1934 from late Katian strata in Norway. The type species of <i>Mixosiphonoceras</i> is mid Silurian in age and the genus is placed within the Brevicoceratidae, which are known otherwise only from the mid Silurian to Devonian. Therefore, it is likely that the Norwegian species represents another <i>Kiaeroceras</i>.</p><p>The presence of actinosiphonate deposits in endogastrically curved <i>Kiaeroceras</i>, in orthocones (<i>Mixosiphonoceras norvegicum</i> Strand, 1934), and in exogastrically curved valcouroceratids suggests either multiple independent origins of this type of endosiphuncular deposit or a close relationship between these taxa. A detailed phylogenetic, or cladistic analysis of the oncocerid-discoserid groups, which could help to solve this open question (suggested also by Pohle <i>et al.</i> 2022) is beyond the scope of this work.</p><p>Below, four species of <i>Kiaeroceras</i> are described in open nomenclature. These are known almost exclusively from their mature body chambers. Their differing sizes and shapes are unique, and they differ from species described in the literature and herein. However, the relatively low number of known specimens of <i>Kiaeroceras</i> does not permit evaluation of the intraspecific and interspecific variability in, e.g., mature body chamber size, and CHI. The possibility therefore exists, that some of these species, represent intraspecific variability.</p>