Wotte and Sundberg—Small shelly fossils from the Great Basin
Remarks.—Spicules show a flat base and an almost radial symmetry. Number and arrangement of the rays indicates a systematic affiliation to Chancelloria.
Genus Archiasterella Sdzuy, 1969
Type species.—Archiasterella pentactina Sdzuy, 1969 (p. 134–137, pl. 15, fig. 4–12, 13?, text figs. 2d, 3, 4); Andalusiana cornuta-Termierella sevillana band (lower Cambrian; middle Marianian Stage; correlated with the upper- most Terreneuvuian/Cambrian Stage 2); basin of Guadalcanal, Sierra Morena, southern Spain.
Archiasterella cf. A. hirundo Bengtson in Bengtson et al., 1990 Figure 8.23
Occurrence.—One spicule from the Log Cabin Mine section (LC 1); Delamaran Stage.
Description.—Spicule with 4+0 rays. Specimen strongly recrystallized.
Remarks.—Configuration and arrangement of rays suggests a similarity with A. hirundo Bengtson in Bengtson et al., 1990.
Phylum Echinodermata Klein, 1734 Indeterminate echinoderm ossicles Figure 8.1–8.8
Occurrence.—Several ossicles from the Echo Canyon (E 12, E 15), Log Cabin Mine (LC 6), and Split Mountain (SM 14, SM 15) sections; Dyeran Stage.
Remarks.—Echinoderm ossicles with preserved stereome micro- structure. Morphology ranges from plates, irregular segments, to barrel-shaped segments, typical for eocrinoids and edrioasteroids. However, no assignment to a particular taxon is possible.
Phylum Tardipolypoda Chen and Zhou, 1997 Class Xenusia Dzik and Krumbiegel, 1989
Order Scleronychophora Hou and Bergström, 1995 Family Eoconchariidae Hao and Shu, 1987
Genus Microdictyon Bengtson, Matthews, and Missarzhevsky in Missarzhevsky and Mambetov, 1981
Type species.—Microdictyon effusum Bengtson, Matthews, and Missarzhevsky in Missarzhevsky and Mambetov, 1981 (p. 78, pl. 13, figs. 3, 5); Rhombocorniculum cancellatum Zone, Geres Member, basal Shabakty Formation (lower Cambrian; upper
895
Atdabanian Stage; correlated with the lower Cambrian Series 2); Ushbas River, Malyi (Lesser) Karatau, Kazakhstan (see Mam- betov and Missarzhevsky, 1972).
Microdictyon montezumaensis new species Figure 8.24–8.25
Holotype.—Specimen FG 544/GB/M/5/C8-8 from sample M 5 from the upper Fallotaspis Zone of the Montenegro Member; middle Montezuman Stage; 5mbelow the 127maluminum tag; Montezuma Range section.
Diagnosis.—Microdictyon with simple, smooth nodes.
Description.—One fragment of ~180 μm thickness (Fig. 8.25). Sclerite composed of a dense crystalline layer (capping, sensu Bengtson et al., 1986) forming its surface and the walls/bases of holes, and a coarser crystalline layer hosting the holes (frame- work, sensu Bengtson et al., 1986). Holes surrounded by a prominent ridge (Fig. 8.24, 8.25). Cross-section of holes clearly shows the relationship between holes and ridges, offering a barrel-shaped structure (Fig. 8.25). At the capping, hole dia- meters constricting from ~80 μm to ~50 μm, extending into bulbous cavities (width of 120 μm in their central part) in the framework. Holes surrounded by six regularly arranged weak nodes (Fig. 8.24, 8.25).
Etymology.—Named after Montezuma Range.
Remarks.—The exact determination of Microdictyon species is primarily based on the morphology of the nodes surrounding the holes. A further aspect is the hole diameter and a common basal closure of the holes. The last feature is a typical characteristic of M. effusum (Bengtson et al., 1986, p. 101, fig. 3). However, the absence of such a basal closure in all other described species of Microdictyonmay be an artifact of
preservation.According to the original description, the nodes of M. effusum have a mushroom- like shape, although this and the basal closure are not observable on the figured material (Bengtson et al. in Missarzhevsky and Mambetov, 1981, pl. 13, figs. 3, 5). Bengtson et al. (1986) described a distinct brim and a sub-centrally placed apex for M. effusum. Nodes of our sclerite show no prominent relief (Fig. 8.24, 8.25). However, the good preservation of the surface layer indicates no or only minor erosion, thus excluding a destruction of prominent nodes. Therefore, the gentlemorphology on the sclerite is considered as representing the original shape. Because the structure of the nodes is an essential criterion for species definition, it is necessary to assign this fragment to the new species M. montezumaensis.
Figure 7. Small shelly fossils from the Delamar, Echo Shale, and Combined Metals members of Echo Canyon, Grassy Spring, Groom Range, and Oak Spring Summit sections; Dyeran Stage. (1–6) Pelagiella aff. P. subangulata (Tate, 1892); scale bar = 200μm: (1–3) FG 544/GB/GS/13/A6-8, (1, 2) lateral view, (3) oblique apertural view; (4–6) FG 544/GB/GR/11/A10-14, (4, 5) lateral view, (6) oblique apertural view. (7–12) Helcionellid gen. and sp. indet. 1; note the fine radial lirae in the apical region: (7, 8) FG 544/GB/OS/3/B2-3; scale bar = 500μm; (7) lateral view, (8) apical view; (9, 10) FG 544/GB/OS/3/B2-5; scale bar = 200μm; (9) lateral view, (10) apical view; (11, 12) FG 544/GB/OS/3/B2-4; scale bar = 500μm; (11) lateral view, (12)apical view. (13–16) Helcionellid gen. and sp. indet. 2; scale bar = 500μm; note the well-developed concentric rugae in the apical region: (13, 14) FG 544/GB/OS/3/B2-8, (13) lateral view, (14) apical view; (15, 16) FG 544/ GB/OS/3/B2-9, (15) lateral view, (16) apical view. (17–32) Parkula sp.; scale bars 400μm except for (25, 26, 31, 32)(200μm): (17, 18) FG 544/GB/GS/13/A6-2, (17) dorsal view, (18) oblique view from the aperture; (19, 20) FG 544/GB/E/12/B6-17, (19) dorsal view, (20) oblique view from the aperture; (21, 22) FG 544/GB/ GS/17/A4-14, (21) dorsal view, (22) oblique view from the aperture; (23, 24) FG 544/GB/GS/17/A5-15, (23) dorsal view, (24) oblique view from the aperture; (25, 26) FG 544/GB/E/12/B6-7, (25) dorsal view, (26) oblique view from the aperture; (27, 28) FG 544/GB/GS/17/A5-16, (27) dorsal view, (28) oblique view from the aperture; (29, 30) FG 544/GB/E/10/A3-5, (29) dorsal view, (30) oblique view from the aperture; (31, 32) FG 544/GB/E/10/A3-2, (31) dorsal view, (32) oblique view from the aperture.
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