Type species

Pywackia baileyi Landing in Landing et al., Reference Landing, English and Keppie2010 from the upper Cambrian Cordylodus andresi Biozone, Tiñu Formation (lower Yudachica Member) near Río Salinas, Oaxaca State, Mexico (only known occurrence). Type specimen: NYSM 13515 (Landing et al., Reference Landing, English and Keppie2010, fig. 2K) from sample Tu-4.95.

Diagnosis

Cylindrical to spindle-formed, stem-like, nonbifurcating colonies of linear to helically emplaced polygonal modules, constructed entirely of thin walls (no axial core, modular or skeletal). Mature primary modules have imperforate vertical walls that are longitudinally crenulated (growth bands) and locally thickened at colony exteriors, club-like in section. The skeletal microstructure of all walls is porous, with radiating pillars in layers that are bilaterally symmetrical with arcs peaking at the medial wall. Most walls also have enveloping, exterior, massive skeletal layers that can also be present as symmetrical growth checks in wall tips. Medial layers are not present in walls. Skeletal composition was either phosphatic or calcareous (calcite/aragonite), completely replaced by a phosphate mineral.

Complete colonies display three developmental zones. The distal end is rounded, with modules budding in a linear to helical arrangement, with immature modules that are oval to polygonal, with slightly convex to straight to weakly concave sides. The colony propagates through budding at the distal margin but does not grow indefinitely. In the middle primary region, modules grow radially from the axis and are typically six-sided with a flared, broadly elliptical to circular opening. Vertical lateral walls are smooth and imperforate but often display growth bands (crenulations on module walls with varying degrees of development). Short median ridges present in the base of some modules are a by-product of budding new modules from a basal wall. Irregularly placed partitions of short, vertical skeletal walls are present in some primary modules but are not regularly placed as deterministic partitions (e.g., not septa or diaphragms). Early growth stages (immature) modules are present at budding zones of secondary budding, but no polymorphs were observed.

Proximal colony end is attenuated, spike-like, flat to triangular in cross section, with very immature, elongated modules present, too shallow to house polyps. In a number of specimens, protomodules (elongate with incipient lateral walls, e.g., Landing et al., Reference Landing, Antcliffe, Brasier and English2015, figs. 1.4, 2.2, 4) extend proximally, well beyond the lowermost, first complete module. This suggests proximal growth during later development in larger colonies. Neither colony axis nor walls are thickened in the proximal zone. Holdfasts are absent; pointed proximal end might have stuck into soft sediment.

Diagnosis emended from Landing et al. (Reference Landing, English and Keppie2010, Reference Landing, Antcliffe, Brasier and English2015).

Remarks

Landing et al. (Reference Landing, English and Keppie2010, Reference Landing, Antcliffe, Brasier and English2015) recognized 14-hedron budding as an important characteristic of Pywackia. We did not find this a practical feature for specimen description.

Diagenetic alteration is common on the interior of walls, resulting in pervasive bands of silica, iron minerals, or recrystallized phosphate mineral. Altered interior walls can be misinterpreted as medial walls, but they are clearly variable in placement and not systematically medial.

Colony, module shape, and budding

A line of support for Pywackia as a cnidarian is the overall radial (spindle, rod) shape of the colony (Williams, Reference Williams2011, fig. 1 for colony shape in Pennatulacea). Colonies are composed entirely of thin walls, with no region of skeletal thickening or presence of axial modules or bundles (Fig. 2.1). The structure is reminiscent of radial, unfolded, thin geometric paper, such as that found in holiday table decorations (Supplemental Fig. 2.4).

Modules grow in two directions. They are budded at the rounded distal end, extending the colony through elongation (Fig. 2.2). No Pywackia specimens are exceptionally long (maximum 40 mm; Taylor et al., Reference Taylor, Berning and Wilson2013), so their size is not entirely indeterminant. In contrast, mature specimens bud frontally, away from the colony axis (Fig. 1.6B). This implies that the soft parts (polyps) have a determinant size (~0.30 mm) and life cycle. Basal thickening then thinning of walls indicates mature Pywackia colonies that exhibit secondary (frontal) budding (Supplemental Fig. 1.1). However, secondary budding occurs only after considerable extension of the primary module with narrow growth bands (Fig. 2.6). The advantage is unclear for secondary frontal budding versus simple extension of the modules through incremental growth.

Modules are generally six-sided with six adjacent neighbors but typically bud in series of four to six, although three to seven sides with corresponding neighbors are not uncommon (Taylor et al., Reference Taylor, Berning and Wilson2013). Modules are longer than wide, 0.27–0.59 mm × 0.15–0.38 mm, and at least 0.33 mm in depth (Taylor et al., Reference Taylor, Berning and Wilson2013). At the proximal end of the branch, modules taper and are long (> 1.25 mm; Fig. 2.3; Taylor et al., Reference Taylor, Berning and Wilson2013). Module walls vary between 10 and 20 μm in total thickness, with the outer, massive layer to 5 μm thick (Fig. 1.7, 1.8; Taylor et al., Reference Taylor, Berning and Wilson2013, fig. 2.10, 2.11).

New modules are formed by budding from previous walls, often just prior to termination of the previous wall, as expected in the modular patterns of corals (Rosen, Reference Rosen1986, p. 127, fig. 2). In Pywackia, this results in a ‘Y-shape’ with a small ridge (keel) of the previous wall (Fig. 1.2, hypothetical, new, blue walls centered on keel). Modules open ‘up,’ away from the axis, generally with the largest area at the terminus (Figs. 1.1, 2.1, 2.2). Exteriors of walls have regularly spaced crenulations that parallel the opening (Fig. 2.1, 2.5, 2.6). Their origin deserves further evaluation, but they could represent incremental growth bands.

Pywackia skeletal composition

The original skeletal composition of Pywackia remains unclear and has been proposed to be: (1) originally calcitic, diagenetically altered to a phosphate mineral; (2) as original skeletal phosphatic mineral; or (3) either (1) or (2) plus diagenetic silicate and iron oxide minerals (Landing et al., Reference Landing, English and Keppie2010, Reference Landing, Antcliffe, Brasier and English2015; Taylor et al., Reference Taylor, Berning and Wilson2013). Based on extensive Energy Dispersive Spectroscopy (EDS), well-preserved regions within colonies display detailed, primary skeletal microstructure (see section below, Fig. 1.7B, 1.8), which are now 100% phosphate mineral. However, most specimens are preserved as a combination of a phosphate mineral, especially the more-resistant, massive exterior walls, often with a core of diagenetically altered interior walls (Fig. 2.7).

Results from EDS performed at multiple target sites on two specimens (NYSM 5702, E5074) are summarized in Table 1, for data in three groups: (1) interior porous layers, (2) massive blocky layers at sites that did not appear to be altered (i.e., clear microstructure), and (3) diagenetically altered zones (primary microstructure obscured). The ‘unaltered microstructure’ is nearly 100% phosphatic mineral (Table 1), whereas the altered regions are silicate or iron oxides (Table 1).

Table 1.

Summary of Energy Dispersive Spectrum (EDS) analysis from three microskeleton types, from multiple Pywackia colonies/sections. All values expressed as %.

Additional support for a skeleton originally of a phosphate mineral is that no residual calcium (carbonate) was detected in any of the EDS analyses (Fig. 1.6–1.8). Thus, if skeletons are secondary phosphate mineral, the replacement process was truly 100% complete at the microskeletal level. Therefore, although not definitive, we retain the hypothesis that the skeleton of Pywackia was originally and entirely a phosphatic mineral. However, support for complete calcite to phosphatic diagenetic replacement is that the Tiñu Formation hosts abundant and diverse fauna of phosphatized specimens (Landing et al., Reference Landing, Westrop and Keppie2007).

The uncertain original skeletal composition of Pywackia does not affect its assignment to the phylum Cnidaria. Replacement of a carbonate mineral (calcite, aragonite, or a mixture) conforms with the calcareous skeletons for the majority of cnidarian coral groups, including Pywackia candidates of tabulates and octocorals (Sorauf, Reference Sorauf1996). Alternatively, a primary phosphatic skeleton raises the need for comparisons with conulariids and other cnidarian groups with incipient phosphatic skeletonization (Vinn, Reference Vinn2022).

Other potential processes of preservation for Tiñu Pywackia were investigated but dismissed due to topological and microstructural constraints. These included replacement of organic tissue, steinkerns of either original void spaces or moldic skeletons, or early diagenetic overgrowth (mineralized crust) of either skeleton or tissue.

Pywackia skeletal microstructure

The skeletal microstructure of Pywackia (Fig. 1.4–1.8) provides the strongest support for a cnidarian assignment. Like many cnidarian groups, e.g., corals and conulariids (Leggat et al., Reference Leggat, Camp, Suggett, Heron and Fordyce2019, p. 2727, fig. 3I, J; Van Iten et al., Reference Van Iten, Mironenko and Vinn2022, fig. 4a–d), Pywackia has a porous primary skeleton (Fig. 1.8). This is not the same as the void cells of Taylor et al. (Reference Taylor, Berning and Wilson2013, fig. 2.10, 2.11), which are a product of diagenesis (see Fig. 1.8 [primary pores] vs. Fig. 2.7 [diagenetic voids]). The pores result from a radiating growth of small pillars connected by lateral layers (Fig. 1.4, 1.7, 1.8). When preserved, this structure forms the interior of all walls in Pywackia (Fig. 1.5–1.8). The exterior layer of most body walls has a massive layer of resistant phosphate mineral of variable thickness (Fig. 1.5–1.8). It is unclear whether this massive wall is primary or secondary, because it thins in places, represented by pillars and porous structure (Fig. 1.7A). Massive skeletal wall is also present internally (Fig. 1.6B), where it wraps around the end of an earlier growing tip. In some specimens, this growth alternates with interior pillar and porous skeleton, representing a number of growth checks (Fig. 1.6).

It is possible that the massive phosphatic skeleton could be secondary to, and independent of, the interior porous, pillar skeleton (i.e., a diagenetic result of alteration of the portion of the porous interior). We reject this interpretation because of the internal growth checks but acknowledge that the massive layers are not constant in thickness and can even be absent in places.

Medial wall layers have been described as common in some specimens (Supplemental Fig. 2.3, 2.9, 2.10), but these laminar mineral bodies (silica and iron) commonly form in cracks of Pywackia walls (Fig. 1.5B). Although approximately medial in some specimens, these mineralized zones cut across specimens (Fig. 1.7B). Thus, although walls are bilaterally symmetrical in the lateral section, Pywackia has no biologically derived medial layers.

Microstructure comparison to other cnidarians

The skeletons of conulariids are phosphatic, composed of carbonate apatite (Ford et al., Reference Ford, Van Iten and Clark2016). Their composition is similar to that of Pywackia. If Pywackia also had a skeleton of a primary phosphate mineral, comparisons to the conulariid group are in order. The periderm of Conularia Miller in J. Sowerby, Reference Sowerby1820 and Paraconularia Sinclair, Reference Sinclair1940 (Ford et al., Reference Ford, Van Iten and Clark2016) consists of extremely thin (1–3 μm) more or less distinct, alternating organic-rich and organic-poor microlamellae that are generally parallel to the outer surface of periderm. Interestingly, the organic-rich microlamellae are cross-connected by thread-like pillars of organic material originally embedded in apatite (Ford et al., Reference Ford, Van Iten and Clark2016), although this organic pillar architecture is quite opposite to what we see in Pywackia in which pillars have mineral composition (Fig. 3.5).

The microlamellae of conulariids can be pierced by microscopic circular pores ranging from ~5–10 μm in diameter (Fig. 3.9), which can be quite numerous in some cases (Van Iten et al., Reference Van Iten, De Moraes Leme, Coelho Rodrigues and Guimarães Simões2005a, Reference Van Iten, Vyhlasova, Zhu and Yib). These pores, which extend through no more than two or three microlamellae, are of unknown origin. They might be primary microstructural features, or they might be microborings or microbioclaustrations, which could have been produced by parasitic or pathogenic microbes or fungi (Van Iten et al., Reference Van Iten, Vyhlasova, Zhu and Yi2005b). However, these pores are circular shafts in conulariid phosphatic laminae and are thus quite different in shape from the pores between pillars in Pywackia.

Another supposed cnidarian related to conulariids, Sphenothallus Hall, Reference Hall1847, also has a phosphatic skeleton composed of apatite (Vinn and Kirsimäe, Reference Vinn and Kirsimäe2014; Vinn and Mironenko, Reference Vinn and Mironenko2021). The skeleton of Sphenothallus has a microlamellar structure (Fig. 3.4) but one that is different from Pywackia because its phosphatic lamellae are massive and devoid of any pores.

There is a restricted number of modern studies available on the microstructure of Paleozoic tabulate and rugose corals (Coronado et al., Reference Coronado, Pérez-Huerta and Rodríguez2013, Reference Coronado, Perez-Huerta and Rodriguez2015, Reference Coronado, Pérez-Huerta and Rodríguez2016; Coronado and Rodríguez, Reference Coronado and Rodriguez2016). Resources such as Flügel (Reference Flügel2004) provide rich information for fossil identification at the petrographic scale but limited guidance for the details of skeletal microstructure.

Three principal kinds of calcite crystals occur in syringoporids, i.e., lamellae, fibers, and granules (Rodríguez et al., Reference Rodríguez, Pérez-Huerta and Coronado2014). Lamellae and microlamellae are flat crystals that resemble scales or shields (Rodríguez et al., Reference Rodríguez, Pérez-Huerta and Coronado2014; Fig. 3.7), which can be compared with lateral layers that connect pillars in Pywackia. Fibers are also common in the microstructure of tabulate corals and somewhat resemble pillars in the structure of Pywackia. Tabulate fibers are elongate crystals with irregular morphology, but in some cases, they are barrel-shaped or tabular, depending on their situation in the skeleton (Coronado et al., Reference Coronado, Perez-Huerta and Rodriguez2015). The granules in tabulates are equidimensional crystals, with indentations to their edges, flake morphologies, and irregular distribution (see Coronado et al., Reference Coronado, Perez-Huerta and Rodriguez2015, fig. 6C). The granules could be analog to the massive phosphatic structure of Pywackia.

In rugose corals, the different bricks that compose the microstructure are lamellae, fibers, and granules (Coronado et al., Reference Coronado, Pérez-Huerta and Rodríguez2016) (Fig. 3.8). Similar to tabulate corals, they can be compared with structural elements of Pywackia in the same way as the analogous structural elements of tabulates that were compared above.

Enigmatic anabaritids are usually referred to the Cnidaria. The phosphate replicated tubes of early Cambrian anabaritids have walls that consist of fibers (Kouchinsky and Bengtson, Reference Kouchinsky and Bengtson2002), reflecting an original aragonitic fabric. In anabaritids, bundles of fibers are arranged in growth lamellae, and the latter form an angle of at least 45° with the inner tube wall. The architecture of growth lamellae in anabaritids (Kouchinsky and Bengtson, Reference Kouchinsky and Bengtson2002) is different from that of Pywackia, but the fibers (Fig. 3.6) can roughly be compared with pillars in the structure of Pywackia.

Assignment to a cnidarian subgroup

Based on the overall morphology (module and colonies), we acknowledge similarities with certain tabulate corals (e.g., Landing et al., Reference Landing, English and Keppie2010, Reference Landing, Antcliffe, Brasier and English2015). Landing et al. (Reference Landing, English and Keppie2010) dismissed tabulate coral affinities for Pywackia based on the absence of intermodule pores.

Colony forms and module shapes of the single modern genus Lituaria Valenciennes in Milne Edwards and Haime, Reference Milne Edwards and Haime1850 (very narrow pennatulacean octocoral known as a sea-pencil) are strikingly similar to those of Pywackia (Fig. 3.3; Taylor et al., Reference Taylor, Berning and Wilson2013). The term ‘sea-pen’ is used widely for the pennatulacean group of octocorals, whereas use of the term ‘sea-pencil’ is restricted to the genus Lituaria (Fig. 3.3; Taylor et al., Reference Taylor, Berning and Wilson2013, and avocational SCUBA divers in Singapore, e.g., http://www.wildsingapore.com/wildfacts/cnidaria/others/pennatulacea/pencil.htm). Direct comparison of Pywackia and Lituaria (Fig. 3.1, 3.2) reveals that their sizes are clearly different and there is a nearly 400 Myr time gap between Pywackia and the first appearance of pennatulaceans (Taylor et al., Reference Taylor, Berning and Wilson2013). In addition, neither tabulate nor octocoral skeletal microstructure is similar to that of Pywackia (see Coronado et al., Reference Coronado, Pérez-Huerta and Rodríguez2013).

Our data support assignment of Pywackia to the phylum Cnidaria. Although specimens share morphologies or compositional similarities with several cnidarian groups (tabulate corals, conulariids, and octocorals), we view Pywackia as a member of a rare, independent, and unnamed cnidarian group. Pywackia's latest Cambrian age places it at the cusp of the Ordovician Biodiversity Event (Servais et al., Reference Servais, Harper, Munnecke, Owen and Sheehan2009), which includes the first occurrences of some other cnidarian groups (Elias et al., Reference Elias, Lee and Pratt2021). A phylogeny for modern cnidarians was provided by Kayal et al. (Reference Kayal, Bentlage, Sabrina Pankey, Ohdera, Medina, Plachetzki, Collins and Ryan2018). Although this phylogeny does not include extinct taxa, it provides a context for comparison. We believe that Pywackia is not so much in phylogenetic alignment with one of these traditional cnidarian groups, but rather a reminder of convergent evolution reinventing forms and features within the Bauplan of Cnidaria.

Absence of axial zooecia

Landing et al. (Reference Landing, English and Keppie2010, Reference Landing, Antcliffe, Brasier and English2015) compared the morphological features of Pywackia to those of rhabdomesine cryptostome, stenolaemate bryozoans, exclusive of other, related forms. They emphasized the presence of axial zooids in Pywackia as evidence for a cryptostome bryozoan affinity, a feature not well developed in other Paleozoic bryozoan groups. Taylor et al. (Reference Taylor, Berning and Wilson2013) could not identify ‘axial zooecia’ in any of their or Landing et al.'s (Reference Landing, English and Keppie2010) SEM images of the colony exterior and fragmental sections. Based on cut, polished, transverse and longitudinal sections (Figs. 1.2, 1.3, 2.4, 2.6; Supplemental Figs. 1.1, 2.1, 2.6), no axial modules (zooecia) were seen in Pywaxia, but rather the ‘central axis’ of the colony is constructed of thin walls of essentially back-to-back modules. Thus, the longitudinal axis consists of a weakly defined zone of thin primary walls (Fig. 2.2, 2.4, 2.6; Supplemental Fig. 2.1, 2.6).

Absence of polymorphs (nanozooecia)

Landing et al. (Reference Landing, English and Keppie2010, figs. 2e, f, 3c; Reference Landing, Antcliffe, Brasier and English2015, fig. 1.2, 1.3) called on the presence of polymorphs (nanozooids) as support for bryozoan affinity. We agree with Taylor et al. (Reference Taylor, Berning and Wilson2013) that these structures likely represent immature modules, budded during the beginning of a second generation of growth (Fig. 1.9), rather than discrete polymorphs of a determinate size. This interpretation is supported by their presence in mature colonies, primarily in the zone of secondary growth (budding).

Body symmetry and basal ‘bilobed keels.’—Another line of evidence used by Landing et al. (Reference Landing, English and Keppie2010, fig. 2K, L; Reference Landing, Antcliffe, Brasier and English2015, fig. 1.9, 1.10) to support a bryozoan affinity is the presence of ‘bilobed keels’—small, proximodistal ridges on the base of some modules. They argued that these indicate bilateral rather than radially symmetrical soft parts of the animal polyp. Taylor et al. (Reference Taylor, Berning and Wilson2013) demonstrated that such longitudinal basal keels are not a mainstay of stenolaemate bryozoan morphology. Our examination of keels and module walls shows that the presence of keels is not ubiquitous in all modules or even colonies; in fact, the presence of bilobed keels is relatively rare in Pywackia. In transverse sections, we saw two laterally budding walls for the new module, arising from either side of the previous wall, but just before its end (tip). The combination of these form a broad ‘Y’ (Fig. 1.2, blue lines). Thus, a keel is a nonobligate extension of the previous wall into the newly budded module.

Wall microstructure and composition

Most stenolaemate bryozoans have bilaminar walls, back-to-back lamellar crystals, which sometimes are centered on a medial granular wall (Hageman, Reference Hageman1991, figs. 1–4; Ma et al., Reference Ma, Taylor and Xia2014). Stenolaemate bryozoan skeletal microstructures are well documented (see Boardman, Reference Boardman and Robison1983; Hickey, Reference Hickey1987) and are therefore not illustrated here; for a review using contemporary imaging techniques, see Grenier et al. (Reference Grenier, Griesshaber, Schmahl and Checa2023).

The walls of Pywackia are porous, with annulated pillars and do not show lamellar crystals of stenolaemate bryozoans. Landing et al. (Reference Landing, English and Keppie2010, Reference Landing, Antcliffe, Brasier and English2015) described Pywackia skeletal microstructure as ‘granular or granular prismatic’ based on high magnification of naturally polished Pywackia walls (Landing et al., Reference Landing, Antcliffe, Brasier and English2015, fig. 1.7). They argued that some Paleozoic stenolaemates have granular or granular prismatic microstructure, which is true, but is not exclusive in any group, and when present, typically forms a small and predictable portion of the colony (e.g., core of fenestrates). Granular walls are present in early esthonioporine stenolaemate bryozoans (Ma et al., Reference Ma, Taylor and Xia2014), but even in these cases, questions remain about primary versus diagenetic origins of the granular skeleton (Ma et al., Reference Ma, Taylor and Xia2014). In the SEM view of microstructure (Fig. 1.5–1.8; Supplemental Fig. 1.10–1.12), Pywackia clearly displays porous, annulated pillars, with structured (layered, radiating) porous space, which is unknown in stenolaemate bryozoans.

We agree with Taylor et al. (Reference Taylor, Berning and Wilson2013) that the original skeletal composition is equivocal. The phosphatic state of the fossils does not affect cnidarian versus bryozoan versus other interpretations.

Within module partitions

Landing et al. (Reference Landing, English and Keppie2010, fig. 2G, H; Reference Landing, Antcliffe, Brasier and English2015, figs. 1.6, 1.8, 2.1, 2.2) emphasized the presence of thin diaphragms (partitions across the module) and low hemiphragms (partial partitions of the module) as support for a bryozoan interpretation. We agree with the Taylor et al. (Reference Taylor, Berning and Wilson2013) argument that the placement of these structures in Pywackia is far more irregular than that seen in cryptostome (Paleozoic) bryozoan species.

Module shape and size

Landing et al. (Reference Landing, English and Keppie2010, Reference Landing, Antcliffe, Brasier and English2015) described Pywackia modules in the terminology of bryozoans (e.g., autozooecia with apertures). Taylor et al. (Reference Taylor, Berning and Wilson2013), however, pointed out that the modules are cup-shaped, slightly flaring to the surface. Modules are not tubular or cylindrical as are the cryptostome bryozoans described by Landing et al. (Reference Landing, English and Keppie2010). As a result, Pywackia does not have apertures in the sense of cryptostome bryozoans. Landing et al. (Reference Landing, Antcliffe, Brasier and English2015, fig. 2.2) claimed that Pywackia modules are not ‘cup-like’ but are in fact elongate. This was based on interpretation of what we consider to be module walls but was considered by them as diaphragms (e.g., module walls versus partitions).

Absence of frontal walls

Landing et al. (Reference Landing, Antcliffe, Brasier and English2015, fig. 2.1) argued that weak frontal walls were originally present but were uniformly lost to abrasion. We did not find any evidence for frontal walls. Our observations suggest that of the ~150 Pywackia specimens studied, none had frontal walls removed/eroded and that no illustrated specimens to date represent eroded interiors. Although many specimens examined are eroded/abraded, we also observed many exterior surfaces with growing tips and edges that preserve the outermost wall (Fig. 1.2, 1.3, 1.6; Supplemental Fig. 1.1, 1.4, 1.6); they are not abraded and show no sign of a missing frontal wall. Although the size of the modules was not specified in the original paper (Landing et al., Reference Landing, English and Keppie2010), the submillimeter diameters (0.15–0.59 mm; Landing et al., Reference Landing, Antcliffe, Brasier and English2015) are consistent with a bryozoan affinity (Taylor and Waeschenbach, Reference Taylor and Waeschenbach2015).

Other Cambrian Bryozoa candidates

It is not a goal of this paper to evaluate other contenders for Cambrian bryozoan status, but recent publications demonstrate contemporary interest in the topic. Zhang et al. (Reference Zhang, Zhang, Ma, Taylor and Strotz2021) described evidence for apparently soft-bodied, early Cambrian Bryozoa from the Xiaoshiba Lagerstätte in China (Cambrian Age 3). This interpretation of these phosphatic specimens has been challenged by Yang et al. (Reference Yang, Lan, Zhang and Smith2023) who suggested that the Xiaoshiba specimens are dasyclad algae and not bryozoans. Pruss et al. (Reference Pruss, Leeser, Smith, Zhuravlev and Taylor2022) recently described mineralized bryomorph specimens from the Harkless Formation, Nevada (Cambrian Age 4), which they suggest are palaeostomate bryozoans. These specimens are phosphatic but are consistent with possible replacement of calcite (Pruss et al., Reference Pruss, Leeser, Smith, Zhuravlev and Taylor2022). Further study, combined with existing evidence could well confirm the promise of the Harkless bryomorph fossils as the earliest mineralized Bryozoa.