1355:
1031:
1312:
1371:
1020:
469:
create a ‘ragged’ appearance for some fossils, akin to an inverted stack of bowls or plates with sharp lower edges and smoothly curved upper edges. This is one example of how stromatoporoid growth forms can vary somewhat through the animal's lifespan. A single species can acquire a taller, narrower form to survive high sedimentation rates, while acquiring a flatter and more stable form to survive in energetic shallow waters. Some stromatoporoids appear to grow intermittently in a ‘ragged’ style even without sediment burial, as indicated by an abundance of encrusters under the overhanging 'shelves'.
1040:
1343:
1328:
976:
forms. Under this interpretation, the
Devonian extinctions merely prompted stromatoporoids to abandon mineralization until the Jurassic, explaining their lack of fossils between the two time intervals. Most paleontologists disagree with this idea, since Paleozoic and Mesozoic ‘stromatoporoids’ differ in several key aspects. In contrast to true Paleozoic stromatoporoids, Mesozoic species have recognizable spicules and a more complex microstructure within the laminae and pillars which make up the skeleton. Mesozoic ‘stromatoporoids’ are a
397:
135:
1206:
161:
1011:
454:
895:(Late Devonian mass extinction). Diversity loss prior to the Kellwasser event was likely a factor of both falling origination rates and slightly elevated extinction rates. Other groups presented unexpected patterns: the formerly rare amphiporids reached their highest diversity in the Frasnian, while labechiids staged a remarkable comeback in the
329:. Two or three of these orders appeared in the Ordovician while the rest evolved in the Silurian. They rediversified subsequent to mass extinctions at the end of the Ordovician and Silurian, but a more profound decline began in the Late Devonian. With a few putative exceptions, they apparently died out during the
1169:, meaning that they inhabited shaded spaces and cavities. These hidden areas could be found in gaps between the base of the stromatoporoid and its substrate, or on the underside of shelf-like projections. Displaced or toppled sponges had the potential to host cryptic encrusters on any part of the skeleton.
479:
Domical – Dome- or mound-shaped, with a curved surface developing both outwards and upwards from a broad base. Domes occupy a spectrum from low (height less than half of the base's diameter) to high (height up to double the diameter). Some high domical species taper significantly, acquiring a conical
380:. Internally, the astrorhizae diverge as independent tapering tubes that intersect smaller open spaces within the skeletal frame. Astrorhizae are generally equated with the exhalant canals of other sponges, while the mamelons help to channel waste water away from the surface. This mechanism works via
662:
Like many fossil invertebrates, stromatoporoids have long been regarded as an enigmatic group with an uncertain relationship to modern taxa. For much of their history of study, stromatoporoid fossils could only be observed externally or through natural cross-sections. Several hypotheses developed in
1266:
A persistent question for stromatoporoid ecology is how they were able to compete with corals in shallow, brightly lit areas. One hypothesis is that heavy laminar growth forms were more resistant to damage from waves and storms, yet laminar stromatoporoids were equally common in deep or undisturbed
1099:
at intermediate depths, away from muddier basins or saltier shallows. The predominant species were usually laminar or low domical in form. High domical species and other complex forms only developed in calmer settings, where there is little risk of toppling. In a stable environment, stromatoporoids
874:
and throughout the
Silurian, while clathrodictyids and actinostromatids diversified substantially. The other four stromatoporoid orders (Amphiporida, Stromatoporellida, Stromatoporida, and Syringostromatida) also originated in the Silurian, though they remained fairly subdued compared to the three
259:
Externally, some species have raised bumps (mamelons) and star-shaped crevices (astrorhizae), which together help vent exhalant water away from the living surface. Internally, stromatoporoids have a mesh-like skeletal system combining extensive horizontal layers (laminae), vertical rods (pillars),
886:
stage. Clathrodictyids, stromatoporellids, stromatoporids, and syringostromatids benefited the most from this renewal of biodiversity. The arrival of the Late
Devonian disrupted this apex of stromatoporoid evolution. Syringostromatids were the first to be affected, virtually disappearing from the
468:
Stromatoporoids can show a variety of growth forms, with low domes or plates as the most common varieties. Whenever an influx of sediment buries the edge of the skeleton, the buried portion ceases growing while the exposed central portion expands outwards to cover the sediment once more. This can
1299:
overlap with corals to an extent. If one assumes that latilaminae (growth interruptions parallel to laminae) are annual (like tree rings), stromatoporoid growth rates can reach 2 to 10 mm per year, equivalent to corals and much higher than modern calcareous sponges. On the other hand, most
975:
Over 60 valid genera of small hypermineralized
Mesozoic sponges have been described as stromatoporoids based on their anatomical similarity to stromatoporids, actinostromatids, clathrodictyids, or syringostromatids. One hypothesis suggests a direct line of descent between Paleozoic and Mesozoic
813:
stage (about mid-way through the Middle
Ordovician). They were low-profile hypercalcified sponges which were similar to stromatoporoids in many respects, with one key difference: pulchrilaminids had spine-like projections (probably homologous with spicules) between the laminae of the skeleton.
408:
was likely only present at the outer surface of the stromatoporoid skeleton. By volume, the majority of the organism was a dead mesh of internal cavities and support structures. Since most stromatoporoid fossils are only visible in vertical or horizontal cross-section, the internal form of the
1086:
which congregated into closely packed patches. They were adaptable and could thrive at a variety of depths, light levels, and fluctuating sea level regimes. In these regards, they were more similar to corals than to modern calcareous sponges, which generally occupy a narrow selection of rocky
413:, layers arranged transversely (parallel to the living surface of the sponge). Laminae have an intermediate width and spacing (on average around four per millimeter) relative to other layers with the same orientation. Significantly thinner layers, when present, are termed
365:. Most were ambitopic (occupying soft substrate such as mud or sand for most of their life), though some were encrusting (concreted onto hard substrates such as rocks or other organisms). The base was stabilized by a crust-like layer covered with concentric wrinkles. The
842:
Labechiids were by far the most diverse stromatoporoids of the
Ordovician, and some paleontologists have even ventured to reconstruct lines of descent in this preliminary stage of stromatoporoid evolution. The next order to appear were the Clathrodictyida, in the early
1354:
709:, immediately reinvigorated the hypothesis that stromatoporoids were sponges. Moreover, closer investigations of stromatoporoid fossils were able to determine that an individual mound represents a single animal, rather than a colonial congregation of
1287:
algae which live within their cells. Zooxanthellae additionally assist the corals’ biochemical processes, allowing for expeditious growth rates. No equivalent organisms are known in modern sponges, though some demosponges do host a high volume of
720:
Proponents of the sponge hypothesis admitted that sclerosponges and stromatoporoids were not identical in structure; for example, sclerosponges have spicules while true
Paleozoic stromatoporoids do not. Several other enigmatic calcareous fossils
260:
and boxy spaces (galleries), along with other features. The most common growth forms range from laminar (flattened) to domical (dome-shaped). Spheroidal, finger-like, or tree-like species also occur, though they are rare in most environments.
1090:
Unlike corals, stromatoporoids usually settled on soft substrates, so their ‘reefs’ occupied only a single level rather than a multi-tiered vertical framework of built-up skeletons. Flat, horizontally-extensive ‘reefs’ are formally known as
1189:’ all occupied the cryptic niche. The rim of the hidden areas hosted the greatest diversity of encrusters, most of which were filter feeders reliant on a current to feed. More exposed areas were also encrusted by corals (both tabulate and
821:
stage (the latter part of the Early
Ordovician), but abrupt diversification was delayed until the mid-to-late Darriwilian stage, simultaneous with the disappearance of pulchrilaminids. The oldest stromatoporoid ‘reefs’ are known from the
1370:
853:. Though less diverse than their labechiid relatives, Ordovician clathrodictyids were widespread and locally abundant in some areas. The third stromatoporoid order, Actinostromatida, may have originated in the Late Ordovician or the
517:
Irregular – A composite form without an easily characterized shape. Both vertical and horizontal growth habits may be apparent in a single skeleton, with domes, platforms, and columns interspersed throughout the development of the
486:
Columnar – Cylindrical, tall (height more than double the diameter) and trunk-like, without branches. In many cases the outer wall of the column is reinforced with laminar outgrowths. One example of a columnar stromatoporoid is
425:, cylindrical rods oriented longitudinally (i.e., perpendicular to the laminae). Laminae and pillars are often straight and internally solid, but they can exhibit distinctive textures and distortions in some subgroups.
697:
in particular has a thinly encrusting layered skeleton, augmented by internal rods, external knobs, and radiating nutrient canals. These features were equated with pillars, mamelons, and astrorhizae, respectively.
440:
are longitudinal walls which demarcate maze-like corridors, as visible in a transverse cross-section through the skeleton. Stacked dome-shaped pockets, known as cysts, are defined by large convex plates, known as
1300:
stromatoporoid growth forms emphasized stability and horizontal breadth rather than a vertical ‘race for sunlight’, as exhibited by sessile organisms which rely on photosynthesis, such as land plants and corals.
1311:
1411:
Da Silva, A. C.; Kershaw, S.; Boulvain, F. (2011). "Stromatoporoid palaeoecology in the
Frasnian (Upper Devonian) Belgian platform, and its applications in interpretation of carbonate platform environments".
476:
Laminar – Sheet- or plate-shaped, with a broad base and a thin, flat skeleton expanding outwards along the substrate. Sheet-like forms with a slightly thicker profile are sometimes labelled 'tabular'.
432:. In life the galleries would have been filled with seawater, while in fossils the spaces are filled by recrystallized calcite. The galleries may be supplemented by very fine curved plates, termed
713:. Among the strongest evidence for sponge affinities was the degree of similarity between astrorhizae and exhalant canals, which were easier to homologize than the more integrated canal system of
817:
The first stromatoporoids to evolve belonged to the order
Labechiida, which rapidly acquired worldwide diversity in the Middle Ordovician. The oldest reported labechiid species is from the
384:, which states that flow pressure increases as speed decreases, such as when the flow is redirected by a vertical barrier. The surface may also be covered with even smaller bumps known as
1095:. Stromatoporoid reefs had fairly low diversity, with only a few species making up the majority of an assemblage by volume. The most diverse stromatoporoid assemblages were biostromes on
733:’) have been reclassified as sponges thanks to this new information. The sponge hypothesis quickly met widespread acceptance, with a few detractors. Up until the 1990s, some Soviet and
891:
stage. Actinostromatids, stromatoporellids, and stromatoporids were next in line, with their diversity and reef extent collapsing at the end of the Frasnian in accordance with the
1245:, a type of tube-building tabulate coral. Stromatoporoid fossils with syringoporid burrows are so common that some historical sources have misclassified them as a distinct genus,
847:
stage of the Late Ordovician. It has been suggested that clathrodictyids are descended from labechiids, as part of an evolutionary lineage starting at the Siberian species
514:
Digitolaminar – A composite form combining both digitate and laminar characteristics. Finger-like projections are superimposed onto one or more flat plate-like platforms.
962:
1327:
1342:
899:
stage, acquiring levels of diversity not seen since the Ordovician. This would not last, as stromatoporoids appear to have been completely extinguished during the
2629:"Rise of clathrodictyid stromatoporoids during the Great Ordovician Biodiversification Event: insights from the Upper Ordovician Xiazhen Formation of South China"
1100:
could grow to very large sizes exceeding several meters in width or height. The largest singular stromatoporoid fossil ever reported is a 30-meter (98 feet) wide
1722:
Smith 1932 in the Early Carboniferous of England; affinity, palaeogeographic position and implications for the geological history of stromatoporoid-type sponges"
337:
sponges have been classified as stromatoporoids, but they are likely unrelated to the Paleozoic radiation, thus making 'stromatoporoids' (in the broad sense) a
1211:
827:
767:
640:
633:
579:
567:
388:. In contrast to mamelons, papillae are simply external extensions of internal pillars, rather than stacked deflections of the skeleton's outer surface.
1773:
911:
Putative post-Devonian stromatoporoid fossils have been reported, though their referral to the group is rather ambiguous. A supposed labechiid species (
1216:
543:
802:
726:
555:
409:
skeleton is usually the most important region for the purpose of species differentiation. In all species, the most conspicuous internal features are
2584:
Khromych, V. G. (2010-06-01). "Evolution of Stromatoporoidea in the Ordovician–Silurian epicontinental basin of the Siberian Platform and Taimyr".
1134:
626:
619:
573:
3017:
1249:. Syringoporids were able to grow at the same rate as their host in order to prevent being overgrown. Other tabulate corals, rugosan corals, and
648:
612:
605:
494:
1102:
931:
859:
849:
791:
598:
591:
1772:
Ezaki, Yoichi; Masui, Mitsuru; Nagai, Koichi; Webb, Gregory E.; Shimizu, Koki; Sugama, Shota; Adachi, Natsuko; Sugiyama, Tetsuo (2024-08-13).
1295:
Several lines of evidence suggest a mixotrophic lifestyle for stromatoporoids, though none are unambiguous. Their ratios of oxygen and carbon
1166:
780:
775:
786:
3088:
941:
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the 19th and 20th centuries based on this limited set of data. A few authors suggested that stromatoporoids were sponges or relatives of
913:
489:
1997:
665:
1153:. Raised bioherms would have been strengthened by microbial carbonate and other reef-building organisms living between the sponges.
797:
A more probable set of stromatoporoid ancestors evolved in the Ordovician. These forerunners or close relatives are grouped in the
2150:"Chapter 12 (part): Stromatoporida, Syringostromatida, Amphiporida, and genera with uncertain affinities: Systematic Descriptions"
758:
The first unambiguous stromatoporoids appeared in the Ordovician, but superficially similar organisms have been reported from the
1999:
Late Ordovician and Early Silurian stromatoporoid sponges from Anticosti Island, eastern CanadaCrossing the O/S mass extinction
274:. Some stromatoporoid species are useful as environmental proxies, since their form and distribution can help approximate the
2936:
2928:
2875:
2867:
2837:
2829:
2752:
2744:
2710:
2702:
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2273:
2265:
2167:
2159:
2121:
2113:
2081:
2073:
2015:
1933:
1925:
1889:
1881:
1841:
1833:
1697:
1689:
925:. Some sources consider this species to be based on misinterpreted coral fragments, while others certify its legitimacy as a
534:
400:
Side view of a stromatoporoid showing laminae, pillars, and galleries. From the Columbus Limestone (Middle Devonian) of Ohio.
794:’) acquired mesh-like encrusting skeletons with a set of internal rods and domes similar to those of early stromatoporoids.
2628:
2546:
1774:"Post-Devonian re-emergence and demise of stromatoporoids as major reef-builders on a Carboniferous Panthalassan seamount"
3083:
369:
has historically been termed an epitheca or peritheca, names used for a similar attachment layer in sessile cnidarians.
244:. Stromatoporoids were among the most abundant and important reef-builders of their time, living close together in flat
3093:
1117:
Despite their preference for soft flat sediment, stromatoporoids occasionally contributed to built-up skeletal mounds (
1125:-margin stromatoporoid bioherms are particularly well-developed in the Devonian. Notable examples can be found in the
3063:
1951:"Biomechanical analysis of passive flow of stromatoporoids — morphologic, paleoecologic, and systematic implications"
882:
Stromatoporoids recovered strongly in the Early and Middle Devonian, reaching their overall maximum diversity in the
2891:
Mistiaen, B. (1994). "Skeletal density: Implications for development and extinction of Palaeozoic stromatoporoids".
871:
457:
A vertical cross-section through a domical stromatoporoid, showing stacked 'ragged' growth. From the Silurian of
2256:"Chapter 8 (part): Morphological Affinities of the Paleozoic Stromatoporoidea to Other Fossil and Recent Groups"
1263:
are also common endosymbionts, though they apparently only took root in the skeleton after the sponge had died.
3073:
953:) of Russia, has tentatively been identified as a clathrodictyid. Labechiid-like fossils are abundant in early
774:
sponges with low growth habits and porous internal domes comparable to cyst plates. In addition, some colonial
17:
2931:. Boulder, Colorado; Lawrence, Kansas: Geological Society of America; University of Kansas. pp. 631–651.
2870:. Boulder, Colorado; Lawrence, Kansas: Geological Society of America; University of Kansas. pp. 193–208.
2832:. Boulder, Colorado; Lawrence, Kansas: Geological Society of America; University of Kansas. pp. 307–310.
2793:
2747:. Boulder, Colorado; Lawrence, Kansas: Geological Society of America; University of Kansas. pp. 599–612.
2705:. Boulder, Colorado; Lawrence, Kansas: Geological Society of America; University of Kansas. pp. 593–597.
2521:. Boulder, Colorado; Lawrence, Kansas: Geological Society of America; University of Kansas. pp. 575–592.
2268:. Boulder, Colorado; Lawrence, Kansas: Geological Society of America; University of Kansas. pp. 543–549.
2162:. Boulder, Colorado; Lawrence, Kansas: Geological Society of America; University of Kansas. pp. 781–836.
2116:. Boulder, Colorado; Lawrence, Kansas: Geological Society of America; University of Kansas. pp. 769–779.
2076:. Boulder, Colorado; Lawrence, Kansas: Geological Society of America; University of Kansas. pp. 709–754.
1928:. Boulder, Colorado; Lawrence, Kansas: Geological Society of America; University of Kansas. pp. 551–573.
1884:. Boulder, Colorado; Lawrence, Kansas: Geological Society of America; University of Kansas. pp. 487–520.
1836:. Boulder, Colorado; Lawrence, Kansas: Geological Society of America; University of Kansas. pp. 421–486.
1692:. Boulder, Colorado; Lawrence, Kansas: Geological Society of America; University of Kansas. pp. 755–768.
2959:
160:
1618:"The global Hangenberg Crisis (Devonian–Carboniferous transition): review of a first-order mass extinction"
1165:, organisms which attach or encrust onto the outer surface of the skeleton. Most encrusting organisms were
673:). However, for much of their history the mainstream interpretation was that stromotoporoids were colonial
1376:
A magnified cross-section of a stromatoporoid, showing internal laminae, pillars, and galleries. From the
2769:
737:
specialists continued to regard stromatoporoids as cnidarians or cyanobacterial accumulations akin to
701:
In 1970, several living sponges were found to possess a calcareous skeletal framework very similar to
3078:
3068:
3058:
939:, but this is another case of poor preservation and uncertain identity. Finally, the calcitic sponge
875:
older groups. Silurian stromatoporoids would face a second round of extinction in the late Silurian (
2820:"Chapter 5 (part): A List of Upper Paleozoic–Mesozoic Stromatoporoid-like Genera; and Excluded Taxa"
3008:
2918:
2857:
2819:
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2692:
2508:
2255:
2149:
2103:
2063:
1915:
1871:
1823:
1679:
381:
275:
1030:
317:). They are now classified as sponges in the phylum Porifera, based on their similarity to modern
1019:
954:
950:
3035:
2970:
2364:
2032:
361:. Like other sponges, they grow outwards and upwards from a single base attached firmly to the
2858:"Chapter 3 (part): Introduction to Post-Devonian Hypercalcified Sponges (Stromatoporoid Type)"
2290:
1950:
508:
Digitate – Hand-shaped, with finger-like columns clustered together above a broad shared base.
345:
sponges have been identified as stromatoporoids with a somewhat greater degree of confidence.
3030:
2954:
2627:
Jeon, Juwan; Liang, Kun; Kershaw, Stephen; Park, Jino; Lee, Mirinae; Zhang, Yuandong (2022).
1460:"Endobiotic Rugosan Symbionts in Stromatoporoids from the Sheinwoodian (Silurian) of Baltica"
1253:
fossils have been found wedged between growth zones within the stromatoporoid skeleton. Worm
436:. Some species have more complex skeletons with broader pockets beyond the narrow galleries.
2432:
2188:"A new species of the primitive stromatoporoid Cystostroma from the Ordovician of East Asia"
372:
In many species, the upper surface of the skeleton is ornamented with small mounds known as
282:
both within and outside their skeletons. Some studies have argued that stromatoporoids were
3022:
2922:
2861:
2823:
2781:
2738:
2696:
2640:
2593:
2512:
2444:
2302:
2259:
2199:
2153:
2107:
2067:
1962:
1919:
1875:
1827:
1733:
1683:
1629:
1581:
1533:
1471:
1421:
1296:
1107:
763:
511:
Dendroid – Bush-shaped, with a thicket of narrow columns branching away from a narrow base.
1570:"Earliest known rugosan-stromatoporoid symbiosis from the Llandovery of Estonia (Baltica)"
8:
1377:
1268:
867:’ between the ancestral labechiids and their presumed descendants, the actinostromatids.
864:
362:
287:
2785:
2644:
2597:
2448:
2390:
2306:
2203:
1966:
1737:
1633:
1585:
1537:
1475:
1425:
988:). Sponges in this category are understudied and many proposed genera have proven to be
2664:
2476:
2345:
2314:
2223:
1974:
1653:
1494:
1459:
1437:
1096:
1039:
831:
253:
155:
143:
483:
Bulbous – Bulb-shaped, with a narrow base widening upwards into a semi-spherical mass.
376:. A few species may supplement the mamelons with radiating cracks or grooves known as
298:
corals. Though this hypothesis is plausible, circumstantial evidence is inconclusive.
2932:
2871:
2833:
2797:
2748:
2706:
2668:
2656:
2609:
2566:
2522:
2468:
2460:
2406:
2318:
2269:
2227:
2215:
2187:
2163:
2117:
2077:
2011:
1978:
1929:
1885:
1837:
1789:
1751:
1693:
1657:
1645:
1617:
1569:
1521:
1499:
1441:
1433:
1122:
1051:
985:
229:
2547:"100 Million Years of Reef Prosperity and Collapse: Ordovician to Devonian Interval"
2480:
2789:
2648:
2601:
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2398:
2310:
2207:
2186:
Jeon, Juwan; Li, Qijian; Oh, Jae-Ryong; Choh, Suk-Joo; Lee, Dong-Jin (2019-08-01).
2003:
1970:
1781:
1741:
1637:
1589:
1541:
1489:
1479:
1429:
1318:
900:
892:
854:
498:
405:
330:
41:
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1348:
A stromatoporoid as seen from below, showing the basal layer. From Gotland, Sweden
2402:
1593:
1545:
1484:
1230:
1071:
710:
326:
147:
1048:
Dense stromatoporoid biostromes and other assemblages, from top left clockwise:
396:
2993:
1746:
1717:
1361:
1284:
1242:
759:
584:
358:
301:
Prior to the 1970s, stromatoporoids were most frequently equated with colonial
291:
241:
134:
126:. Mesozoic identifications are likely unrelated to the main Paleozoic radiation
2605:
2562:
2211:
1205:
3052:
2801:
2660:
2613:
2570:
2464:
2322:
2219:
1982:
1793:
1755:
1649:
1289:
1280:
1162:
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1083:
926:
876:
771:
722:
342:
233:
123:
85:
49:
2955:
University of California, Berkeley 2019 museum blog post on Stromatoporoidea
2336:
Stearn, Colin W. (1980). "Classification of the Paleozoic Stromatoporoids".
1237:
Like many modern or prehistoric reef-builders, stromatoporoids were host to
2472:
2365:"Stromatoporoid stromatolites; new insight into evolution of cyanobacteria"
1916:"Chapter 8 (part): Functional Morphology of the Paleozoic Stromatoporoidea"
1616:
Kaiser, Sandra Isabella; Aretz, Markus; Becker, Ralph Thomas (2016-01-01).
1503:
1272:
1238:
1221:
1010:
989:
946:
738:
734:
706:
670:
428:
The cubical open spaces among the laminae and pillar meshwork are known as
338:
318:
295:
2770:"Effect of the Frasnian-Famennian extinction event on the stromatoporoids"
2031:
Stearn, Colin W.; Webby, Barry D.; Nestor, Heldur; Stock, Carl W. (1999).
2007:
453:
3002:
2735:"Chapter 9 (part): Extinction Patterns of the Paleozoic Stromatoporoidea"
1872:"Chapter 8 (part): Internal Morphology of the Paleozoic Stromatoporoidea"
1194:
966:
823:
810:
806:
742:
683:
549:
310:
225:
60:
2652:
1267:
waters. Another hypothesis argues that stromatoporoids benefited from a
879:), which reduced the number of genera back to Middle Ordovician levels.
263:
Stromatoporoids competed and coexisted with other reef-builders such as
2349:
1567:
1271:(mutually beneficial) relationship with endosymbiotic microbes. Modern
1259:
1254:
1182:
981:
958:
561:
105:
70:
2693:"Chapter 9 (part): Diversity Trends of the Paleozoic Stromatoporoidea"
2033:"Revised classification and terminology of Palaeozoic stromatoporoids"
1161:
As hard sessile objects, stromatoporoids were used as a substrate for
2509:"Chapter 9 (part): Early Evolution of the Paleozoic Stromatoporoidea"
1785:
1276:
1241:, organisms living fully within the skeleton. The most abundant were
1186:
1130:
1092:
977:
896:
730:
689:
314:
283:
279:
245:
172:
110:
53:
2964:
2397:, Berlin, Heidelberg: Springer Berlin Heidelberg, pp. 230–241,
1641:
1336:, as seen externally. From the Silurian of Saaremaa Island, Estonia.
918:
2987:
2919:"Chapter 10 (part): Paleoecology of the Paleozoic Stromatoporoidea"
1226:
1174:
969:
936:
888:
883:
678:
674:
334:
306:
302:
264:
100:
95:
80:
75:
65:
1824:"Chapter 7: External Morphology of the Paleozoic Stromatoporoidea"
1121:) with successive waves of burial and recolonization or regrowth.
1178:
1170:
1150:
1146:
1138:
1118:
1065:
922:
458:
354:
278:
of sedimentary strata. They hosted a diverse fauna of encrusting
249:
237:
115:
90:
1519:
1190:
844:
818:
502:
462:
404:
By comparison to modern sponges with a similar anatomy, living
268:
192:
182:
142:
Top view of a stromatoporoid with prominent mamelons. From the
45:
2291:"The relationship of the stromatoporoids to the sclerosponges"
2104:"Chapter 11 (part): Actinostromatida: Systematic Descriptions"
857:(early Silurian). The precise timing depends on the status of
1680:"Chapter 11 (part): Clathrodictyida: Systematic Descriptions"
1250:
1142:
980:
group, with different species referable to the Demospongiae (
809:
stage (near the end of the Early Ordovician) up to the early
705:
and stromatoporoids. The modern sponges, collectively termed
271:
221:
2433:"Modern Cyanobacterial Analogs of Paleozoic Stromatoporoids"
903:(end-Devonian mass extinction) at the end of the Famennian.
1317:
Stromatoporoids exposed from below on an outcrop. From the
1111:
1055:
1522:"Symbiotic endobiont biofacies in the Silurian of Baltica"
2794:
10.1130/0091-7613(1987)15<677:EOTFEE>2.0.CO;2
1563:
1561:
1087:
habitats with high nutrient supply and low light levels.
2064:"Chapter 11 (part): Labechiida: Systematic Descriptions"
1410:
863:, a Late Ordovician Estonian genus often considered a ‘
333:
at the end of the Devonian. A number of hypercalcified
2960:
Digital Atlas of Ancient Life page on Stromatoporoidea
2030:
1568:
Vinn, O; Wilson, M.A.; Toom, U.; Mõtus, M.-A. (2015).
1558:
1515:
1513:
236:. They can be characterized by their densely layered
2626:
2391:"Evidences for Cyanophyte Origin of Stromatoporoids"
1082:
Like modern corals, stromatoporoids were gregarious
929:
stromatoporoid. Fossils of the Ordovician labechiid
1771:
1457:
1360:A stromatoporoid with prominent mamelons. From the
766:rather than true forerunners. One example were the
421:. Another universal type of internal structure are
1996:Nestor, Heldur; Copper, Paul; Stock, Carl (2010).
1510:
935:have been reported from sediments as young as the
2431:Kaźmierczak, Józef; Kempe, Stephan (1990-11-30).
1995:
1948:
1615:
1574:Palaeogeography, Palaeoclimatology, Palaeoecology
1526:Palaeogeography, Palaeoclimatology, Palaeoecology
1453:
1451:
3050:
2430:
1949:Boyajian, George E.; Labarbera, Michael (1987).
1622:Geological Society, London, Special Publications
1279:, deriving energy from both tiny prey items and
906:
353:Stromatoporoids are robust sponges with a dense
1397:Stock, C.W. 2001, Stromatoporoidea, 1926–2000:
1391:
1156:
1715:
1448:
417:, while thickened irregular plates are termed
2924:Part E, Porifera (Revised). Volumes 4 & 5
2863:Part E, Porifera (Revised). Volumes 4 & 5
2825:Part E, Porifera (Revised). Volumes 4 & 5
2740:Part E, Porifera (Revised). Volumes 4 & 5
2698:Part E, Porifera (Revised). Volumes 4 & 5
2514:Part E, Porifera (Revised). Volumes 4 & 5
2389:Kaźmierczak, J. (1981), Monty, Claude (ed.),
2261:Part E, Porifera (Revised). Volumes 4 & 5
2155:Part E, Porifera (Revised). Volumes 4 & 5
2109:Part E, Porifera (Revised). Volumes 4 & 5
2069:Part E, Porifera (Revised). Volumes 4 & 5
1921:Part E, Porifera (Revised). Volumes 4 & 5
1877:Part E, Porifera (Revised). Volumes 4 & 5
1829:Part E, Porifera (Revised). Volumes 4 & 5
1685:Part E, Porifera (Revised). Volumes 4 & 5
1520:Vinn, O.; Wilson, M.A.; Mõtus, M.-A. (2014).
2185:
1821:
1716:Kershaw, Stephen; Sendino, Consuelo (2020).
2817:
2388:
2362:
1404:
1321:(Pridoli – Lower Devonian) of Pennsylvania
870:Labechiid diversity contracted during the
133:
2818:Stearn, Colin W.; Stock, Carl W. (2015).
1745:
1493:
1483:
837:
2890:
2583:
1215:, a domical stromatoporoid in the order
1204:
805:. Pulchrilaminids existed from the late
452:
395:
2916:
1225:) is visible at the top left. From the
1000:
14:
3051:
2893:Courier Forschungsinstitut Senckenberg
2851:
2849:
2813:
2811:
2767:
2732:
2728:
2726:
2724:
2722:
2690:
2686:
2684:
2682:
2680:
2678:
2544:
2540:
2538:
2335:
2288:
2253:
2249:
2247:
2245:
2243:
2241:
2239:
2237:
2181:
2179:
2147:
1913:
1869:
1677:
677:, most closely related to mineralized
391:
2969:
2968:
2929:Treatise on Invertebrate Paleontology
2912:
2910:
2908:
2906:
2868:Treatise on Invertebrate Paleontology
2830:Treatise on Invertebrate Paleontology
2745:Treatise on Invertebrate Paleontology
2703:Treatise on Invertebrate Paleontology
2519:Treatise on Invertebrate Paleontology
2506:
2502:
2500:
2498:
2496:
2494:
2492:
2490:
2266:Treatise on Invertebrate Paleontology
2160:Treatise on Invertebrate Paleontology
2143:
2141:
2139:
2137:
2135:
2133:
2114:Treatise on Invertebrate Paleontology
2101:
2097:
2095:
2093:
2074:Treatise on Invertebrate Paleontology
2061:
2057:
2055:
2053:
1926:Treatise on Invertebrate Paleontology
1909:
1907:
1905:
1903:
1901:
1882:Treatise on Invertebrate Paleontology
1865:
1863:
1861:
1859:
1857:
1855:
1853:
1834:Treatise on Invertebrate Paleontology
1817:
1815:
1813:
1811:
1809:
1807:
1805:
1803:
1767:
1765:
1711:
1709:
1690:Treatise on Invertebrate Paleontology
535:Treatise on Invertebrate Paleontology
472:Stromatoporoid growth forms include:
228:common in the fossil record from the
2855:
1673:
1671:
1669:
1667:
1611:
1609:
2846:
2808:
2719:
2675:
2535:
2234:
2176:
24:
3089:Early Ordovician first appearances
2903:
2551:The Paleontological Society Papers
2487:
2315:10.1111/j.1502-3931.1972.tb00868.x
2130:
2090:
2050:
1975:10.1111/j.1502-3931.1987.tb02041.x
1898:
1850:
1800:
1762:
1706:
887:fossil record at the start of the
532:From Stearn et al. (1999) and The
321:. True Paleozoic stromatoporoids (
25:
3105:
2948:
1822:Webby, B.D.; Kershaw, S. (2015).
1664:
1606:
1061:'Lahnmarmor' (Devonian, Germany);
826:of eastern North America and the
762:. These are most likely cases of
522:
341:group if they are included. Some
1434:10.1111/j.1475-4983.2011.01037.x
1369:
1353:
1341:
1326:
1310:
1200:
1038:
1029:
1018:
1009:
159:
58:
2884:
2761:
2620:
2577:
2424:
2382:
2356:
2329:
2282:
2024:
2002:. Canadian Science Publishing.
1989:
1942:
995:
872:Late Ordovician mass extinction
448:
2586:Russian Geology and Geophysics
1458:Vinn, O; Mõtus, M.-A. (2014).
753:
122:Possible persistence into the
13:
1:
2457:10.1126/science.250.4985.1244
2372:Acta Palaeontologica Polonica
2040:Acta Palaeontologica Polonica
1385:
1364:(Middle Devonian) of Michigan
907:Post-Devonian identifications
657:
348:
309:(which also includes corals,
2921:. In Selden, Paul A. (ed.).
2860:. In Selden, Paul A. (ed.).
2822:. In Selden, Paul A. (ed.).
2737:. In Selden, Paul A. (ed.).
2695:. In Selden, Paul A. (ed.).
2511:. In Selden, Paul A. (ed.).
2403:10.1007/978-3-642-67913-1_17
2258:. In Selden, Paul A. (ed.).
2152:. In Selden, Paul A. (ed.).
2106:. In Selder, Paul A. (ed.).
2066:. In Selden, Paul A. (ed.).
1918:. In Selden, Paul A. (ed.).
1874:. In Selden, Paul A. (ed.).
1826:. In Selden, Paul A. (ed.).
1682:. In Selden, Paul A. (ed.).
1594:10.1016/j.palaeo.2015.04.023
1546:10.1016/j.palaeo.2014.03.041
1485:10.1371/journal.pone.0090197
1209:A vertical cross-section of
1193:), crinoids, bryozoans, and
1157:Ectosymbionts and encrusters
748:
497:from the Late Ordovician of
7:
2363:Kaźmierczak, Jozef (1980).
1219:. An endosymbiotic boring (
527:
210:Nicholson & Murie, 1878
10:
3110:
3084:Prehistoric animal classes
1747:10.1186/s42501-020-00077-7
1726:Journal of Palaeogeography
1303:
1185:, and clusters of coiled ‘
1064:unspecified (unspecified,
294:algae), similar to modern
3094:Late Devonian extinctions
2977:
2917:Kershaw, Stephen (2015).
2768:Stearn, Colin W. (1987).
2733:Stearn, Colin W. (2015).
2691:Stearn, Colin W. (2015).
2606:10.1016/j.rgg.2010.05.009
2563:10.1017/S1089332600002424
2395:Phanerozoic Stromatolites
2289:Stearn, Colin W. (1972).
2254:Stearn, Colin W. (2015).
2212:10.1007/s12303-018-0063-7
2148:Stearn, Colin W. (2015).
1914:Stearn, Colin W. (2015).
1870:Stearn, Colin W. (2015).
965:in Japan, representing a
156:Scientific classification
154:
141:
132:
34:
3064:Ordovician invertebrates
1292:within their skeletons.
1074:(Late Devonian, Alberta)
963:Akiyoshi Limestone Group
276:depositional environment
27:Extinct clade of sponges
2633:Journal of Paleontology
2338:Journal of Paleontology
2102:Stock, Carl W. (2015).
1678:Nestor, Heldur (2015).
1399:Journal of Paleontology
961:) reef deposits of the
1401:, v. 75, p. 1079–1089.
1234:
1106:from the Frasnian-age
838:Diversity through time
465:
401:
3074:Late Devonian animals
3031:Paleobiology Database
2856:Wood, Rachel (2015).
2545:Copper, Paul (2011).
2008:10.1139/9780660199306
1380:(Devonian) of Montana
1208:
1103:Actinostroma expansum
456:
399:
382:Bernoulli's principle
2507:Webby, B.D. (2015).
2062:Webby, B.D. (2015).
1108:Shell Rock Formation
1001:Stromatoporoid reefs
917:) is known from the
764:convergent evolution
2786:1987Geo....15..677S
2653:10.1017/jpa.2022.36
2645:2022JPal...96.1285J
2598:2010RuGG...51..684K
2449:1990Sci...250.1244K
2443:(4985): 1244–1248.
2307:1972Letha...5..369S
2204:2019GescJ..23..547J
2192:Geosciences Journal
1967:1987Letha..20..223B
1738:2020JPalG...9...29K
1720:Labechia carbonaria
1634:2016GSLSP.423..387K
1586:2015PPP...431....1V
1538:2014PPP...404...24V
1476:2014PLoSO...990197V
1470:(2): 9(2): e90197.
1426:2011Palgy..54..883D
1378:Jefferson Formation
1334:Densastroma pexisum
1212:Densastroma pexisum
1097:carbonate platforms
914:Labechia carbonaria
850:Priscastroma gemini
828:Machiakou Formation
768:Kazachstanicyathida
392:Internal structures
254:carbonate platforms
1235:
986:calcareous sponges
641:Pseudostromatopora
466:
402:
325:) encompass seven
290:relationship with
240:skeletons lacking
144:Columbus Limestone
3046:
3045:
2971:Taxon identifiers
2938:978-0-9903621-2-8
2877:978-0-9903621-2-8
2839:978-0-9903621-2-8
2754:978-0-9903621-2-8
2712:978-0-9903621-2-8
2528:978-0-9903621-2-8
2412:978-3-642-67915-5
2275:978-0-9903621-2-8
2169:978-0-9903621-2-8
2123:978-0-9903621-2-8
2083:978-0-9903621-2-8
2017:978-0-660-19930-6
1935:978-0-9903621-2-8
1891:978-0-9903621-2-8
1843:978-0-9903621-2-8
1699:978-0-9903621-2-8
1052:Arnheim Formation
634:Pseudactinostroma
580:Syringostromatida
568:Stromatoporellida
357:skeleton lacking
252:on soft tropical
230:Middle Ordovician
215:
214:
211:
127:
16:(Redirected from
3101:
3079:Silurian animals
3069:Devonian animals
3059:Stromatoporoidea
3039:
3038:
3026:
3025:
3013:
3012:
3011:
2998:
2997:
2996:
2979:Stromatoporoidea
2966:
2965:
2943:
2942:
2914:
2901:
2900:
2888:
2882:
2881:
2853:
2844:
2843:
2815:
2806:
2805:
2765:
2759:
2758:
2730:
2717:
2716:
2688:
2673:
2672:
2639:(6): 1285–1317.
2624:
2618:
2617:
2581:
2575:
2574:
2542:
2533:
2532:
2504:
2485:
2484:
2428:
2422:
2421:
2420:
2419:
2386:
2380:
2379:
2369:
2360:
2354:
2353:
2333:
2327:
2326:
2286:
2280:
2279:
2251:
2232:
2231:
2183:
2174:
2173:
2145:
2128:
2127:
2099:
2088:
2087:
2059:
2048:
2047:
2037:
2028:
2022:
2021:
1993:
1987:
1986:
1946:
1940:
1939:
1911:
1896:
1895:
1867:
1848:
1847:
1819:
1798:
1797:
1786:10.1130/G52420.1
1769:
1760:
1759:
1749:
1713:
1704:
1703:
1675:
1662:
1661:
1613:
1604:
1603:
1601:
1600:
1565:
1556:
1555:
1553:
1552:
1517:
1508:
1507:
1497:
1487:
1455:
1446:
1445:
1408:
1402:
1395:
1373:
1357:
1345:
1330:
1319:Keyser Formation
1314:
1217:Actinostromatida
1042:
1033:
1022:
1013:
984:) and Calcarea (
901:Hangenberg event
893:Kellwasser event
855:Llandovery Epoch
544:Actinostromatida
499:Anticosti Island
331:Hangenberg event
218:Stromatoporoidea
209:
206:Stromatoporoidea
204:
164:
163:
137:
121:
120:
57:
42:Early Ordovician
38:Temporal range:
35:Stromatoporoidea
32:
31:
21:
3109:
3108:
3104:
3103:
3102:
3100:
3099:
3098:
3049:
3048:
3047:
3042:
3034:
3029:
3021:
3016:
3007:
3006:
3001:
2992:
2991:
2986:
2973:
2951:
2946:
2939:
2915:
2904:
2889:
2885:
2878:
2854:
2847:
2840:
2816:
2809:
2766:
2762:
2755:
2731:
2720:
2713:
2689:
2676:
2625:
2621:
2582:
2578:
2543:
2536:
2529:
2505:
2488:
2429:
2425:
2417:
2415:
2413:
2387:
2383:
2367:
2361:
2357:
2334:
2330:
2287:
2283:
2276:
2252:
2235:
2184:
2177:
2170:
2146:
2131:
2124:
2100:
2091:
2084:
2060:
2051:
2035:
2029:
2025:
2018:
1994:
1990:
1947:
1943:
1936:
1912:
1899:
1892:
1868:
1851:
1844:
1820:
1801:
1770:
1763:
1714:
1707:
1700:
1676:
1665:
1642:10.1144/SP423.9
1614:
1607:
1598:
1596:
1566:
1559:
1550:
1548:
1518:
1511:
1456:
1449:
1409:
1405:
1396:
1392:
1388:
1381:
1374:
1365:
1358:
1349:
1346:
1337:
1331:
1322:
1315:
1306:
1231:Saaremaa Island
1203:
1175:tabulate corals
1159:
1149:, and southern
1080:
1079:
1078:
1077:
1072:Cairn Formation
1045:
1044:
1043:
1035:
1034:
1025:
1024:
1023:
1015:
1014:
1003:
998:
909:
840:
803:Pulchrilaminida
756:
751:
723:archaeocyathids
669:(an encrusting
660:
556:Clathrodictyida
530:
525:
493:, a very large
451:
394:
351:
208:
202:
158:
148:Middle Devonian
128:
119:
118:
113:
108:
103:
98:
93:
88:
83:
78:
73:
68:
63:
40:
39:
36:
28:
23:
22:
15:
12:
11:
5:
3107:
3097:
3096:
3091:
3086:
3081:
3076:
3071:
3066:
3061:
3044:
3043:
3041:
3040:
3027:
3014:
3009:Stromatoporida
2999:
2983:
2981:
2975:
2974:
2963:
2962:
2957:
2950:
2949:External links
2947:
2945:
2944:
2937:
2902:
2883:
2876:
2845:
2838:
2807:
2760:
2753:
2718:
2711:
2674:
2619:
2592:(6): 684–693.
2576:
2534:
2527:
2486:
2423:
2411:
2381:
2355:
2344:(5): 881–902.
2328:
2301:(4): 369–388.
2281:
2274:
2233:
2198:(4): 547–556.
2175:
2168:
2129:
2122:
2089:
2082:
2049:
2023:
2016:
1988:
1961:(3): 223–229.
1941:
1934:
1897:
1890:
1849:
1842:
1799:
1761:
1705:
1698:
1663:
1628:(1): 387–437.
1605:
1557:
1509:
1447:
1403:
1389:
1387:
1384:
1383:
1382:
1375:
1368:
1366:
1362:Traverse Group
1359:
1352:
1350:
1347:
1340:
1338:
1332:
1325:
1323:
1316:
1309:
1305:
1302:
1285:photosynthetic
1202:
1199:
1158:
1155:
1135:Miette Complex
1084:filter feeders
1076:
1075:
1069:
1062:
1059:
1047:
1046:
1037:
1036:
1028:
1027:
1026:
1017:
1016:
1008:
1007:
1006:
1005:
1004:
1002:
999:
997:
994:
908:
905:
839:
836:
799:incertae sedis
770:, an order of
760:Early Cambrian
755:
752:
750:
747:
727:disjectoporids
659:
656:
655:
654:
653:
652:
645:
637:
630:
627:Praeidiostroma
623:
620:Perplexostroma
616:
609:
602:
595:
585:incertae sedis
582:
576:
574:Stromatoporida
570:
564:
558:
552:
546:
529:
526:
524:
523:Classification
521:
520:
519:
515:
512:
509:
506:
484:
481:
477:
450:
447:
393:
390:
350:
347:
305:in the phylum
292:photosynthetic
286:(engaged in a
220:is an extinct
213:
212:
200:
196:
195:
190:
186:
185:
180:
176:
175:
170:
166:
165:
152:
151:
139:
138:
130:
129:
114:
109:
104:
99:
94:
89:
84:
79:
74:
69:
64:
59:
37:
26:
18:Stromatoporoid
9:
6:
4:
3:
2:
3106:
3095:
3092:
3090:
3087:
3085:
3082:
3080:
3077:
3075:
3072:
3070:
3067:
3065:
3062:
3060:
3057:
3056:
3054:
3037:
3032:
3028:
3024:
3019:
3015:
3010:
3004:
3000:
2995:
2989:
2985:
2984:
2982:
2980:
2976:
2972:
2967:
2961:
2958:
2956:
2953:
2952:
2940:
2934:
2930:
2926:
2925:
2920:
2913:
2911:
2909:
2907:
2898:
2894:
2887:
2879:
2873:
2869:
2865:
2864:
2859:
2852:
2850:
2841:
2835:
2831:
2827:
2826:
2821:
2814:
2812:
2803:
2799:
2795:
2791:
2787:
2783:
2779:
2775:
2771:
2764:
2756:
2750:
2746:
2742:
2741:
2736:
2729:
2727:
2725:
2723:
2714:
2708:
2704:
2700:
2699:
2694:
2687:
2685:
2683:
2681:
2679:
2670:
2666:
2662:
2658:
2654:
2650:
2646:
2642:
2638:
2634:
2630:
2623:
2615:
2611:
2607:
2603:
2599:
2595:
2591:
2587:
2580:
2572:
2568:
2564:
2560:
2556:
2552:
2548:
2541:
2539:
2530:
2524:
2520:
2516:
2515:
2510:
2503:
2501:
2499:
2497:
2495:
2493:
2491:
2482:
2478:
2474:
2470:
2466:
2462:
2458:
2454:
2450:
2446:
2442:
2438:
2434:
2427:
2414:
2408:
2404:
2400:
2396:
2392:
2385:
2378:(2): 243–253.
2377:
2373:
2366:
2359:
2351:
2347:
2343:
2339:
2332:
2324:
2320:
2316:
2312:
2308:
2304:
2300:
2296:
2292:
2285:
2277:
2271:
2267:
2263:
2262:
2257:
2250:
2248:
2246:
2244:
2242:
2240:
2238:
2229:
2225:
2221:
2217:
2213:
2209:
2205:
2201:
2197:
2193:
2189:
2182:
2180:
2171:
2165:
2161:
2157:
2156:
2151:
2144:
2142:
2140:
2138:
2136:
2134:
2125:
2119:
2115:
2111:
2110:
2105:
2098:
2096:
2094:
2085:
2079:
2075:
2071:
2070:
2065:
2058:
2056:
2054:
2045:
2041:
2034:
2027:
2019:
2013:
2009:
2005:
2001:
2000:
1992:
1984:
1980:
1976:
1972:
1968:
1964:
1960:
1956:
1952:
1945:
1937:
1931:
1927:
1923:
1922:
1917:
1910:
1908:
1906:
1904:
1902:
1893:
1887:
1883:
1879:
1878:
1873:
1866:
1864:
1862:
1860:
1858:
1856:
1854:
1845:
1839:
1835:
1831:
1830:
1825:
1818:
1816:
1814:
1812:
1810:
1808:
1806:
1804:
1795:
1791:
1787:
1783:
1779:
1775:
1768:
1766:
1757:
1753:
1748:
1743:
1739:
1735:
1731:
1727:
1723:
1721:
1712:
1710:
1701:
1695:
1691:
1687:
1686:
1681:
1674:
1672:
1670:
1668:
1659:
1655:
1651:
1647:
1643:
1639:
1635:
1631:
1627:
1623:
1619:
1612:
1610:
1595:
1591:
1587:
1583:
1579:
1575:
1571:
1564:
1562:
1547:
1543:
1539:
1535:
1531:
1527:
1523:
1516:
1514:
1505:
1501:
1496:
1491:
1486:
1481:
1477:
1473:
1469:
1465:
1461:
1454:
1452:
1443:
1439:
1435:
1431:
1427:
1423:
1419:
1415:
1414:Palaeontology
1407:
1400:
1394:
1390:
1379:
1372:
1367:
1363:
1356:
1351:
1344:
1339:
1335:
1329:
1324:
1320:
1313:
1308:
1307:
1301:
1298:
1293:
1291:
1290:cyanobacteria
1286:
1282:
1281:zooxanthellae
1278:
1274:
1273:scleractinian
1270:
1264:
1262:
1261:
1256:
1252:
1248:
1244:
1243:syringoporids
1240:
1239:endosymbionts
1232:
1228:
1224:
1223:
1218:
1214:
1213:
1207:
1201:Endosymbionts
1198:
1196:
1195:tentaculitids
1192:
1188:
1184:
1180:
1176:
1172:
1168:
1164:
1163:ectosymbionts
1154:
1152:
1148:
1144:
1140:
1136:
1132:
1128:
1127:Canning Basin
1124:
1120:
1115:
1113:
1109:
1105:
1104:
1098:
1094:
1088:
1085:
1073:
1070:
1067:
1063:
1060:
1057:
1054:(Ordovician,
1053:
1050:
1049:
1041:
1032:
1021:
1012:
993:
991:
987:
983:
979:
973:
971:
968:
964:
960:
956:
955:Pennsylvanian
952:
951:Mississippian
949:stage (upper
948:
944:
943:
938:
934:
933:
928:
927:Carboniferous
924:
920:
916:
915:
904:
902:
898:
894:
890:
885:
880:
878:
877:Pridoli Epoch
873:
868:
866:
862:
861:
856:
852:
851:
846:
835:
833:
829:
825:
820:
815:
812:
808:
804:
801:sponge order
800:
795:
793:
789:
788:
783:
782:
777:
773:
769:
765:
761:
746:
744:
740:
739:stromatolites
736:
732:
728:
724:
718:
716:
712:
708:
707:sclerosponges
704:
699:
696:
692:
691:
686:
685:
680:
676:
672:
668:
667:
651:
650:
649:Taymyrostroma
646:
644:
642:
638:
636:
635:
631:
629:
628:
624:
622:
621:
617:
615:
614:
613:Paschkoviella
610:
608:
607:
606:Lamellistroma
603:
601:
600:
596:
594:
593:
589:
588:
586:
583:
581:
577:
575:
571:
569:
565:
563:
559:
557:
553:
551:
547:
545:
541:
540:
539:
537:
536:
516:
513:
510:
507:
504:
500:
496:
492:
491:
485:
482:
478:
475:
474:
473:
470:
464:
460:
455:
446:
444:
439:
435:
431:
426:
424:
420:
416:
412:
407:
398:
389:
387:
383:
379:
375:
370:
368:
364:
360:
356:
346:
344:
343:Carboniferous
340:
336:
332:
328:
324:
323:sensu stricto
320:
319:sclerosponges
316:
312:
308:
304:
299:
297:
296:scleractinian
293:
289:
285:
281:
277:
273:
270:
266:
261:
257:
255:
251:
247:
243:
239:
235:
234:Late Devonian
231:
227:
223:
219:
207:
201:
198:
197:
194:
191:
188:
187:
184:
181:
178:
177:
174:
171:
168:
167:
162:
157:
153:
149:
145:
140:
136:
131:
125:
124:Carboniferous
117:
112:
107:
102:
97:
92:
87:
82:
77:
72:
67:
62:
55:
51:
50:Late Devonian
47:
43:
33:
30:
19:
2978:
2923:
2896:
2892:
2886:
2862:
2824:
2777:
2773:
2763:
2739:
2697:
2636:
2632:
2622:
2589:
2585:
2579:
2554:
2550:
2513:
2440:
2436:
2426:
2416:, retrieved
2394:
2384:
2375:
2371:
2358:
2341:
2337:
2331:
2298:
2294:
2284:
2260:
2195:
2191:
2154:
2108:
2068:
2043:
2039:
2026:
1998:
1991:
1958:
1954:
1944:
1920:
1876:
1828:
1777:
1729:
1725:
1719:
1684:
1625:
1621:
1597:. Retrieved
1577:
1573:
1549:. Retrieved
1529:
1525:
1467:
1463:
1417:
1413:
1406:
1398:
1393:
1333:
1294:
1265:
1258:
1246:
1236:
1222:Osprioneides
1220:
1210:
1167:cryptobionts
1160:
1116:
1101:
1089:
1081:
996:Paleoecology
978:polyphyletic
974:
967:Panthalassan
947:Serpukhovian
940:
932:Lophiostroma
930:
912:
910:
881:
869:
865:missing link
860:Plumatalinia
858:
848:
841:
816:
798:
796:
785:
779:
776:coralomorphs
772:archaeocyath
757:
743:thrombolites
735:Eastern Bloc
719:
714:
702:
700:
694:
688:
682:
671:foraminifera
664:
661:
647:
639:
632:
625:
618:
611:
604:
599:Eostachyodes
597:
592:Clavidictyon
590:
533:
531:
488:
471:
467:
449:Growth forms
442:
437:
434:dissepiments
433:
429:
427:
422:
419:pachystromes
418:
415:microlaminae
414:
410:
403:
385:
377:
373:
371:
366:
352:
339:polyphyletic
322:
311:sea anemones
300:
262:
258:
248:or elevated
217:
216:
205:
29:
3003:Wikispecies
1420:(4): 1–23.
1275:corals are
1269:mutualistic
1183:brachiopods
982:demosponges
945:, from the
832:North China
824:Chazy Group
811:Darriwilian
807:Tremadocian
792:khasaktiids
790:, and the ‘
781:Maldeotaina
754:Origination
715:Hydractinia
703:Hydractinia
695:Hydractinia
684:Hydractinia
550:Amphiporida
495:aulaceratid
443:cyst plates
438:Pachysteles
378:astrorhizae
367:basal layer
288:mutualistic
226:sea sponges
150:) of Ohio.
3053:Categories
2899:: 319–327.
2780:(7): 677.
2418:2023-08-10
2046:(1): 1–70.
1599:2015-06-18
1551:2014-06-11
1386:References
1277:mixotrophs
1260:Trypanites
1233:, Estonia.
1187:spirorbids
1145:Region of
1093:biostromes
959:Bashkirian
787:Yaworipora
778:or algae (
731:chaetetids
679:hydrozoans
675:cnidarians
658:Affinities
562:Labechiida
349:Morphology
303:hydrozoans
284:mixotrophs
246:biostromes
2802:0091-7613
2669:250002512
2661:0022-3360
2614:1068-7971
2571:1089-3326
2557:: 15–32.
2465:0036-8075
2323:0024-1164
2228:133783450
2220:1598-7477
1983:0024-1164
1794:0091-7613
1756:2524-4507
1732:(1): 29.
1658:131270834
1650:0305-8719
1532:: 24–29.
1442:128455331
1247:Caunopora
1171:Bryozoans
1131:Australia
942:Kyklopora
921:stage of
897:Famennian
749:Evolution
690:Millepora
430:galleries
363:substrate
315:jellyfish
280:symbionts
179:Kingdom:
173:Eukaryota
54:Famennian
2994:Q2116140
2988:Wikidata
2481:22220321
2473:17829211
1504:24587277
1464:PLOS ONE
1297:isotopes
1257:such as
1227:Silurian
1179:crinoids
1119:bioherms
970:seamount
937:Triassic
889:Frasnian
884:Eifelian
681:such as
528:Taxonomy
490:Aulacera
386:papillae
374:mamelons
359:spicules
335:Mesozoic
307:Cnidaria
265:tabulate
250:bioherms
242:spicules
193:Porifera
189:Phylum:
183:Animalia
169:Domain:
2782:Bibcode
2774:Geology
2641:Bibcode
2594:Bibcode
2445:Bibcode
2437:Science
2350:1304354
2303:Bibcode
2295:Lethaia
2200:Bibcode
1963:Bibcode
1955:Lethaia
1778:Geology
1734:Bibcode
1630:Bibcode
1582:Bibcode
1580:: 1–5.
1534:Bibcode
1495:3934990
1472:Bibcode
1422:Bibcode
1304:Gallery
1255:borings
1151:Belgium
1147:Germany
1139:Alberta
1066:Estonia
990:dubious
923:England
666:Gypsina
518:sponge.
459:Gotland
423:pillars
411:laminae
355:calcite
238:calcite
232:to the
199:Class:
3036:105325
2935:
2874:
2836:
2800:
2751:
2709:
2667:
2659:
2612:
2569:
2525:
2479:
2471:
2463:
2409:
2348:
2321:
2272:
2226:
2218:
2166:
2120:
2080:
2014:
1981:
1932:
1888:
1840:
1792:
1754:
1696:
1656:
1648:
1502:
1492:
1440:
1191:rugose
1141:, the
1133:, the
919:Viséan
845:Katian
819:Floian
711:polyps
578:Order
572:Order
566:Order
560:Order
554:Order
548:Order
542:Order
503:Quebec
480:shape.
463:Sweden
406:tissue
327:orders
313:, and
272:corals
269:rugose
46:Floian
3018:IRMNG
2665:S2CID
2477:S2CID
2368:(PDF)
2346:JSTOR
2224:S2CID
2036:(PDF)
1654:S2CID
1438:S2CID
1251:algal
1143:Eifel
1123:Shelf
222:clade
3023:1460
2933:ISBN
2872:ISBN
2834:ISBN
2798:ISSN
2749:ISBN
2707:ISBN
2657:ISSN
2610:ISSN
2567:ISSN
2523:ISBN
2469:PMID
2461:ISSN
2407:ISBN
2319:ISSN
2270:ISBN
2216:ISSN
2164:ISBN
2118:ISBN
2078:ISBN
2012:ISBN
1979:ISSN
1930:ISBN
1886:ISBN
1838:ISBN
1790:ISSN
1752:ISSN
1694:ISBN
1646:ISSN
1500:PMID
1112:Iowa
1056:Ohio
687:and
267:and
61:PreꞒ
2897:172
2790:doi
2649:doi
2602:doi
2559:doi
2453:doi
2441:250
2399:doi
2311:doi
2208:doi
2004:doi
1971:doi
1782:doi
1742:doi
1638:doi
1626:423
1590:doi
1542:doi
1530:404
1490:PMC
1480:doi
1430:doi
1229:of
1137:of
1129:of
1110:of
830:of
741:or
729:, ‘
224:of
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