Metacommunity analyses show an increase in ecological specialisation throughout the Ediacaran period

The first animals appear during the late Ediacaran (572 to 541 Ma); an initial diversity increase was followed reduction in diversity, often interpreted as catastrophic mass extinction. We investigate Ediacaran ecosystem structure changes over this time period using the “Elements of Metacommunity Structure” framework to assess whether this diversity reduction in the Nama was likely caused by an external mass extinction, or internal metacommunity restructuring. The oldest metacommunity was characterised by taxa with wide environmental tolerances, and limited specialisation or intertaxa associations. Structuring increased in the second oldest metacommunity, with groups of taxa sharing synchronous responses to environmental gradients, aggregating into distinct communities. This pattern strengthened in the youngest metacommunity, with communities showing strong environmental segregation and depth structure. Thus, metacommunity structure increased in complexity, with increased specialisation and resulting in competitive exclusion, not a catastrophic environmental disaster, leading to diversity loss in the terminal Ediacaran. These results reveal that the complex eco-evolutionary dynamics associated with Cambrian diversification were established in the Ediacaran.

This study shows that the eco-evolutionary dynamics of metazoan diversification known from the Cambrian Period started earlier in the Ediacaran Period with the Avalon assemblage and increased in complexity towards the Phanerozoic as new anatomical innovations appeared, culminating in the “Cambrian Explosion."     

Dickinsonia from the Ediacaran Dengying Formation in the Yangtze Gorges area,South China

Dickinsonia is an iconic fossil of the Ediacara biota (~575–539 Ma). It was previously known from siliciclastic successions of the White Sea assemblage in Australia, Baltica, and possibly India. Here we describe Dickinsonia sp. from the terminal Ediacaran Shibantan Member limestone (ca. 551–543 Ma) of the Dengying Formation in the Yangtze Gorges area of South China. The stratigraphic distribution of Ediacara-type fossils in the Shibantan Member indicates that this biota uniquely preserves both the White Sea and Nama assemblages in stratigraphic succession. The new data presented here suggests that Dickinsonia had wider paleogeographic and paleoenvironmental distributions, implying its strong dispersal capability and environmental tolerance.     

Ediacaran microbial colonies

Enigmatic discoidal fossils are common in Neoproterozoic sedimentary sequences and in the stratigraphic record pre-date the first appearance of diverse Ediacaran fossil assemblages. Termed 'medusoids', these Neoproterozoic discoidal fossils have generally been interpreted as coelenterate-grade organisms implying a radially symmetrical body plan for ancestral eumetazoans. Analysis of exceptionally preserved discoidal fossils from the White Sea area, however, indicates that most of these discoidal forms represent colonial microbes. Localized pyritization, for example, reveals the presence of a conspicuous filamentous substructure in Ediacaria , whereas concentric rings, radial sectors and central structures in Cyclomedusa and Paliella compare directly with Recent microbial colonies growing in a nutritionally heterogeneous environment. At least some Ediacaran discoids can be compared with extant concentric ring-shaped microbial colonies that grow in hypersaline microbial mats. Insofar as most of the remaining record of Ediacaran discoids can be attributed to the holdfast structures of non-radiate modular organisms, there is no support from the fossil record for identifying a radiate ancestry for the Metazoa.     

Infaunal augurs of the Cambrian explosion: An Ediacaran trace fossil assemblage from Nevada,USA

Morphologically complex trace fossils, recording the infaunal activities of bilaterian animals, are common in Phanerozoic successions but rare in the Ediacaran fossil record. Here, we describe a trace fossil assemblage from the lower Dunfee Member of the Deep Spring Formation at Mount Dunfee (Nevada, USA), over 500 m below the Ediacaran–Cambrian boundary. Although millimetric in scale and largely not fabric‐disruptive, the Dunfee assemblage includes complex and sediment‐penetrative trace fossil morphologies that are characteristic of Cambrian deposits. The Dunfee assemblage records one of the oldest documented instances of sediment‐penetrative infaunalization, corroborating previous molecular, ichnologic, and paleoecological data suggesting that crown‐group bilaterians and bilaterian‐style ecologies were present in late Ediacaran shallow marine ecosystems. Moreover, Dunfee trace fossils co‐occur with classic upper Ediacaran tubular body fossils in multiple horizons, indicating that Ediacaran infauna and epifauna coexisted and likely formed stable ecosystems.     

Skeletal Nets of the Ediacaran Fronds

The Ediacara fauna is traditionally regarded as the first complex, diverse and widespread macroscopic life. The uncertainty of systematic position of its members has led to very different views on the early evolution of metazoans. In part, this may be due to a lack of data on sclerotization: a hard skeleton is a part of the archetype of the most taxa known from the fossil record, whereas the Ediacara fauna as a whole is most often considered soft-bodied, which complicates comparison. Here we report the Late Precambrian frond-like fossils (Petalonamae) from the Vendian assemblage of the Southeastern White Sea area (∼555.3 Ma), which show evidence of elaborate skeleton composed of a regular meshwork reinforced by dense longitudinal and circular bands. Judging from the nature of preservation and the dynamics of the environment Ediacaran fronds secreted a relatively rigid but flexible skeleton. The fact that frond-like Petalonamae had a supporting structure similar to that of sponges and cnidarians seems to be a powerful argument in favor of their metazoan affinity. The new observations indicated also that the widespread skeletonization had occurred long before the “Cambrian skeletal revolution”.     

贵州新元古代到寒武纪早期特异埋藏后生生物群及其研究意义

贵州化石丰富,素有古生物王国之称,其中早期特异埋藏后生生物十分发育,由老至新有埃迪卡拉系的瓮安生物群、江口庙河生物群、寒武系第1统的小壳动物群、第2统下部的牛蹄塘生物群及中上部的杷榔动物群、第3统底部的凯里生物群。这些特异埋藏生物群与云南寒武系的澄江动物群、关山生物群及陕南埃迪卡拉系高家山生物群构成了我国早期后生生物的演化链,反映了从动物起源（瓮安生物群）、可疑多门类动物出现（江口庙河生物群）、动物骨骼化（高家山生物群）、生物矿化质和量的变化或骨骼动物爆发性辐射（小壳动物群）及海绵动物辐射（牛蹄塘生物群）再到动物主要门类出现的寒武纪大爆发（澄江动物群）、海洋生物多样化及生态复杂化（凯里生物群）的演化过程。     

Reappraising the early evidence of durophagy and drilling predation in the fossil record: implications for escalation and the Cambrian Explosion

The Cambrian Explosion is arguably the most extreme example of a biological radiation preserved in the fossil record, and studies of Cambrian Lagerstätten have facilitated the exploration of many facets of this key evolutionary event. As predation was a major ecological driver behind the Explosion – particularly the radiation of biomineralising metazoans – the evidence for shell crushing (durophagy), drilling and puncturing predation in the Cambrian (and possibly the Ediacaran) is considered. Examples of durophagous predation on biomineralised taxa other than trilobites are apparently rare, reflecting predator preference, taphonomic and sampling biases, or simply lack of documentation. The oldest known example of durophagy is shell damage on the problematic taxon Mobergella holsti from the early Cambrian (possibly Terreneuvian) of Sweden. Using functional morphology to identify (or perhaps misidentify) durophagous predators is discussed, with emphasis on the toolkit used by Cambrian arthropods, specifically the radiodontan oral cone and the frontal and gnathobasic appendages of various taxa. Records of drill holes and possible puncture holes in Cambrian shells are mostly on brachiopods, but the lack of prey diversity may represent either a true biological signal or a result of various biases. The oldest drilled Cambrian shells occur in a variety of Terreneuvian‐aged taxa, but specimens of the ubiquitous Ediacaran shelly fossil Cloudina also show putative drilling traces. Knowledge on Cambrian shell drillers is sorely lacking and there is little evidence or consensus concerning the taxonomic groups that made the holes, which often leads to the suggestion of an unknown ‘soft bodied driller’. Useful methodologies for deciphering the identities and capabilities of shell drillers are outlined. Evidence for puncture holes in Cambrian shelly taxa is rare. Such holes are more jagged than drill holes and possibly made by a Cambrian ‘puncher’. The Cambrian arthropod Yohoia may have used its frontal appendages in a jack‐knifing manner, similar to Recent stomatopod crustaceans, to strike and puncture shells rapidly. Finally, Cambrian durophagous and shell‐drilling predation is considered in the context of escalation – an evolutionary process that, amongst other scenarios, involves predators (and other ‘enemies’) as the predominant agents of natural selection. The rapid increase in diversity and abundance of biomineralised shells during the early Cambrian is often attributed to escalation: enemies placed selective pressure on prey, forcing phenotypic responses in prey and, by extension, in predator groups over time. Unfortunately, few case studies illustrate long‐term patterns in shelly fossil morphologies that may reflect the influence of predation throughout the Cambrian. More studies on phenotypic change in hard‐shelled lineages are needed to convincingly illustrate escalation and the responses of prey during the Cambrian.     

Middle and Late Cambrian sponge spicules from Hunan, China

Abundant and well-preserved assemblages of disarticulated sponge spicules occur in Middle and Late Cambrian platform carbonates of western Hunan, China. Assemblages recovered from 11 stratigraphic horizons include calcisponges, demosponges, and hexactinellids. Hexactinellida, in particular, are both abundant and diverse in Upper Cambrian carbonates. Comparison with spicule assemblages from Australia indicates that many of these taxa have long stratigraphic ranges, limiting their use in correlation. The morphological diversity of these spicules exceeds that known for living siliceous sponges, supporting the observation that during the Cambrian radiation, sponges, like other metazoans, evolved a variety of architectural forms not observed in later periods. Like conodonts, individual sponges can produce more than one spicule form; thus, an "apparatus genus" concept based on multiple co-occurring elements may eventually prove useful in the biostratigraphic and paleobiological interpretation of disarticulated sponge spicules. Four distinctive forms are recognized as new taxa: Australispongia sinensis new genus and species, Flosculus gracilis new genus and species, Pinnatispongia bengtsoni new genus and species, and Nabaviella paibiensis new species.     

Tubular microfossils from the Ediacaran Weng’an Biota (Doushantuo Formation,South China) are not early animals

The early Ediacaran Weng’an Biota (ca. 609 Ma) of the Doushantuo Formation (Guizhou Province, China) encompasses an abundant and exquisitely preserved assemblage of phosphatic microfossils that have provided unique insight into the origin and early evolution of multicellular eukaryotes. However, the affinities of these early organisms are far from certain, including the tubular microfossils Crassitubulus, Quadratitubus, Ramitubulus, and Sinocyclocylcicus. These taxa have been widely accepted as stem-cnidarians or, alternatively, interpreted as filamentous cyanobacteria, or multicellular algae. We use high-resolution X-ray tomographic microscopy to analyse the structure and development of the four taxa. Our data and analysis allow us to conclude that these four taxa were not biomineralized. Crassitubulus, Quadratitubus, and Sinocyclocylcicus, may be grouped on the basis that they exhibit alternating complete and incomplete cross walls, and bipolar growth; which makes them favourably comparable to filamentous cyanobacteria. In contrast, Ramitubulus exhibits only complete cross walls, unipolar growth and dichotomous branching. These features are difficult to reconcile with a cyanobacterial interpretation. They are, instead, more indicative of multicellular algae-like Cambrian Epiphyton. Thus, the Weng’an tubular microfossils constitute a disparate assemblage of cyanobacteria and algae, but none represents early Ediacaran animals.     

A fungal analog for newfoundland ediacaran fossils?

We propose that some of the more conspicuous Ediacaran fossilsfrom the Avalon Peninsula of Newfoundland, including Aspidella,Charnia, and Charniodiscus, were biologically similar to membersof the Kingdom Fungi. These organisms were multicellular ormultinuclear, lived below the photic zone, could not move ordefoul themselves, did not exhibit taphonomic shrinkage, andwere not transported or moved. Aspidella, in particular, appearsto exhibit indeterminate growth without a maximum size constraint,and appears to show growth zonations similar to modern mycelia.Other fossils from this deposit exhibit a fractal-like growthpattern. Together, these features falsify algal, lichen, andmetazoan interpretations of these fossils, yet reflect characteristicsof modern fungal mycelia. We emphasize that although no MistakenPoint fossil appears to be a metazoan, not all of the MistakenPoint taxa, and not all of the Ediacaran organisms in general,can reasonably be interpreted using a fungal analogy. Furthermore,the hypothesis that these fossils were functionally fungus-likeneed not imply that the organisms were members of the crown-groupFungi. We propose further tests for evaluating both this functionalhypothesis and the phylogenetic hypothesis that these organismswere members of the total-group Fungi.     

First evidence for Cambrian glaciation provided by sections in Avalonian New Brunswick and Ireland: Additional data for Avalon–Gondwana separation by the earliest Palaeozoic

The first evidence for Cambrian glaciation is provided by two successions on the Avalon microcontinent. The middle lowest Cambrian (middle Terreneuvian Series and Fortunian Stage–Stage 2 boundary interval) has an incised sequence boundary overlain by a fluvial lowstand facies and higher, olive green, marine mudstone on Hanford Brook, southern New Brunswick. This succession in the lower Mystery Lake Member of the Chapel Island Formation may be related to melting of an ice sheet in Avalon. The evidence for this interpretation is a muddy diamictite with outsized (up to 10 cm in diameter), Proterozoic marble and basalt clasts that penetrated overlying laminae in the marine mudstone. That eustatic rise was associated with the mudstone deposition is suggested by an approximately coeval rise that deposited sediments with Watsonella crosbyi Zone fossils 650 km away in Avalonian eastern Newfoundland. A sea-level rise within the Watsonella crosbyi Chron, at ca. 535 Ma, may correspond to a unnamed negative ¹³C excursion younger than the basal Cambrian excursion (BACE) and the ZHUCE excursion in Stage 2 of the upper Terreneuvian Series. Cambrian dropstones are now also recognized on the northern (Gander) margin of Avalon in continental slope–rise sedimentary rocks in southeast Ireland. Although their age (Early–Middle Cambrian) is poorly constrained, dropstones in the Booley Bay Formation provide additional evidence for Cambrian glaciation on the Avalon microcontinent. Besides providing the first evidence of Cambrian glaciation, these dropstone deposits emphasize that Avalon was not part of or even latitudinally close to the terminal Ediacaran–Cambrian, tropical carbonate platform successions of West Gondwana.     

Slime travelers: Early evidence of animal mobility and feeding in an organic mat world

Mobility represents a key innovation in the evolution of complex animal life. The ability to move allows for the exploration of new food sources, escapes from unfavorable environmental conditions, enhanced ability to exchange genetic material, and is one of the major reasons for the diversity and success of animal life today. The oldest widely accepted trace fossils of animal mobility are found in Ediacaran‐aged rocks (635–539 Ma). The earliest definitive evidence for movement associated with exploitation of resources for feeding occurs in the White Sea assemblage of the Ediacara Biota—macroscopic, soft‐bodied fossils of Ediacaran age. Here, we evaluate potential support for mobility in dickinsoniomorphs, presenting new data regarding abundant Dickinsonia and associated trace fossils from the Ediacara Member, South Australia. Results quantitatively demonstrate that Dickinsonia was capable of mobility on relatively short, ecological timescales. This organism was bilaterally symmetrical, likely moved via muscular peristalsis, and left trace fossils due to active removal of the organic mat related to feeding. Analogous structures associated with Yorgia indicate that it was also mobile and fed in a similar manner. Morphological evidence suggests that two other modular taxa, Andiva and Spriggina, were able to move but did not feed in a manner that impacted the organic mat. Together, these data suggest that mobility was present in multiple disparate bilaterally symmetrical Ediacaran taxa.     

The origin of the animals and a ‘Savannah’ hypothesis for early bilaterian evolution

The earliest evolution of the animals remains a taxing biological problem, as all extant clades are highly derived and the fossil record is not usually considered to be helpful. The rise of the bilaterian animals recorded in the fossil record, commonly known as the ‘Cambrian explosion’, is one of the most significant moments in evolutionary history, and was an event that transformed first marine and then terrestrial environments. We review the phylogeny of early animals and other opisthokonts, and the affinities of the earliest large complex fossils, the so‐called ‘Ediacaran’ taxa. We conclude, based on a variety of lines of evidence, that their affinities most likely lie in various stem groups to large metazoan groupings; a new grouping, the Apoikozoa, is erected to encompass Metazoa and Choanoflagellata. The earliest reasonable fossil evidence for total‐group bilaterians comes from undisputed complex trace fossils that are younger than about 560 Ma, and these diversify greatly as the Ediacaran–Cambrian boundary is crossed a few million years later. It is generally considered that as the bilaterians diversified after this time, their burrowing behaviour destroyed the cyanobacterial mat‐dominated substrates that the enigmatic Ediacaran taxa were associated with, the so‐called ‘Cambrian substrate revolution’, leading to the loss of almost all Ediacara‐aspect diversity in the Cambrian. Why, though, did the energetically expensive and functionally complex burrowing mode of life so typical of later bilaterians arise? Here we propose a much more positive relationship between late‐Ediacaran ecologies and the rise of the bilaterians, with the largely static Ediacaran taxa acting as points of concentration of organic matter both above and below the sediment surface. The breaking of the uniformity of organic carbon availability would have signalled a decisive shift away from the essentially static and monotonous earlier Ediacaran world into the dynamic and burrowing world of the Cambrian. The Ediacaran biota thus played an enabling role in bilaterian evolution similar to that proposed for the Savannah environment for human evolution and bipedality. Rather than being obliterated by the rise of the bilaterians, the subtle remnants of Ediacara‐style taxa within the Cambrian suggest that they remained significant components of Phanerozoic communities, even though at some point their enabling role for bilaterian evolution was presumably taken over by bilaterians or other metazoans. Bilaterian evolution was thus an essentially benthic event that only later impacted the planktonic environment and the style of organic export to the sea floor.     

The Ediacaran emergence of bilaterians: congruence between the genetic and the geological fossil records

Unravelling the timing of the metazoan radiation is crucial for elucidating the macroevolutionary processes associated with the Cambrian explosion. Because estimates of metazoan divergence times derived from molecular clocks range from quite shallow (Ediacaran) to very deep (Mesoproterozoic), it has been difficult to ascertain whether there is concordance or quite dramatic discordance between the genetic and geological fossil records. Here, we show using a range of molecular clock methods that the major pulse of metazoan divergence times was during the Ediacaran, which is consistent with a synoptic reading of the Ediacaran macrobiota. These estimates are robust to changes in priors, and are returned with or without the inclusion of a palaeontologically derived maximal calibration point. Therefore, the two historical records of life both suggest that although the cradle of Metazoa lies in the Cryogenian, and despite the explosion of ecology that occurs in the Cambrian, it is the emergence of bilaterian taxa in the Ediacaran that sets the tempo and mode of macroevolution for the remainder of geological time.     

Origin and early diversification of the phylum Cnidaria Verrill: major developments in the analysis of the taxon's Proterozoic–Cambrian history

Diploblastic eumetazoans of the phylum Cnidaria originated during the Neoproterozoic Era, possibly during the Cryogenian Period. The oldest known fossil cnidarians occur in strata of Ediacaran age and consist of polypoid forms that were either nonbiomineralizing or weakly so. The oldest possible anthozoans, including the genus Ramitubus, may be related to tabulate corals and occur in the Doushantuo Lagerstätte (upper Doushantuo Formation, South China), the age of which is poorly constrained (approximately 585 Ma?). Conulariid scyphozoans may first appear as early as 635–577 Ma (Lantian Formation, South China). A definite conulariid, most similar to Palaeozoic species assigned to the genus Paraconularia, occurs in association with the possible scyphozoan, Corumbella werneri, in the latest Ediacaran (c. 543 Ma) Tamengo Formation of Brazil. Basal Cambrian (c. 540 Ma) phosphorites in the upper Kuanchuanpu Formation (South China) yield solitary polyps of the oldest probable anthozoan (Eolympia pediculata), which appears to have been a stem hexacorallian. This same formation contains fossils interpreted by some authors as pentaradial cubozoan polyps; however, both the oldest known cubozoans and the oldest hydrozoans, all medusae, may actually occur in the Cambrian (Series 3, c. 505 Ma) Marjum Formation (Utah, USA). Although these recently published palaeontological data tend to corroborate the hypothesis that Cnidaria has a relatively deep Neoproterozoic history, the timing of major internal branching events remains poorly constrained, with, for example, the results of some molecular clock analyses indicating that the two cnidarian subphyla (Anthozoaria and Medusozoa) may have originated as many as one billion years ago. Further progress towards elucidating the evolution and early fossil record of cnidarians may accrue from: (1) an intensive search for phosphatized soft parts in possible anthozoans from the Ediacaran Doushantuo Formation; (2) an expanded search for Ediacaran conulariids; and (3) additional detailed analyses of the taphonomy and preservation of Ediacaran and Cambrian cnidarians, including possible pentaradial cubozoan polyps from the Fortunian upper Kuanchuanpu Formation.     

论中国早寒武世原牙形类和牙形状化石——分类评述和地层意义

原牙形类和牙形状化石是早寒武世微小骨骼化石中非常特征的一个类群。自二十世纪70年代以来,这些齿状的微型磷质骨片化石在中国下寒武统含小壳化石地层中被大量发现,据统计已描述有25属52种。通过文中的评述和讨论,证实其中的一些属种是次异名或属于无效的分类名称,还有一些在归属上尚存在疑问。通过对原牙形类和牙形状化石定义的讨论,将先前指定为原牙形类的13个属进行了分类评述。表明其中的5个属是次异名,还有2个属是未知的节肢动物。其它的12个牙形状化石属中也有5个属是次异名,它们不仅显示了有多种动物亲缘的牙形状形态,而且大多属于绝灭生物,只有Beshtashella和Paraformitchella(=Beshtashella)被指定为软体动物。文中还简要地讨论了大多数属的时空分布,包括3个阶段的原牙形类地层分布,这不仅具有划分对比地层的意义,而且还反映了原牙形类的演化趋势。     

Interpreting the Earliest Metazoan Fossils: What Can We Learn?

SYNOPSIS. The Ediacaran fossils of the latest Precambrian haveat one time or another been grouped with almost every extantkingdom, and also lumped into separate kingdom-level taxa. Thishas often been based on the facile use of a few characters,or on some sort of "overall similarity." This has not been avery fruitful approach; if anything, it has held back understandingof the Ediacaran organisms and of their significance for laterhistory. While many of the simpler forms remain problematic,careful study of the more complex forms gives good reasons toplace at least some of them with the Animalia. A complementaryapproach is to use sources of information such as the distributionof fossils across space, time, and paleoenvironments. The resultsmay feed back into systematic work, allowing us to constructand test more robust hypotheses of these organisms' evolutionaryrelationships.     

The youngest Ediacaran fossils from southern Africa

Discovery of fossils of the Ediacara biota near the top of the Spitzkopf Member at farm Swanpunt extends the known range of these remains in Namibia more than 600 m to near the sub-Cambrian unconformity. The fossiliferous beds occur approximately 100 m above a volcanic ash dated at 543 +/- 1 Ma, and thus may be the youngest Proterozoic Ediacara-type fossils reported anywhere in the world. Fossils are preserved within and on the tops of dm-thick beds of storm-deposited sandstone at two stratigraphic levels; the environment is interpreted as open marine, generally calm but with episodic disruptions by storm waves, and probably within the euphotic zone. The presence of Pteridinium carolinaense (St. Jean), which is also known from the classic sections in Ediacara and the White Sea among others, reinforces evidence from geochronology and chemostratigraphy that the Swartpunt section is terminal Neoproterozoic in age. The new genus and species Swartpuntia germsi is a large, multifoliate frond that exhibits at least three quilted petaloids. Macroscopically, Swartpuntia resembles Pteridinium and Ediacara-type fronds such as Charniodiscus traditionally interpreted as Cnidaria, whereas microscopically it exhibits segmentation that is remarkably similar to that of the putative worm Dickinsonia. Combination of diagnostic characters of these supposedly disparate groups in a single species suggests that many species of quilted Ediacaran organisms were more similar to each other than they were to any modern groups, and provides support for the concept of the "Vendobionta" as a late Neoproterozoic group of mainly multifoliate organisms with a distinctive quilted segmentation.     

寒武纪早期岩家河生物群:研究进展和展望*

埃迪卡拉纪-寒武纪转换时期动物的起源、演化和"寒武纪大爆发"一直是国际古生物学界研究的热点问题,其中寒武纪早期小壳化石群与埃迪卡拉纪化石群和寒武纪早期澄江化石库之间的内在关系是古生物学界研究的难题,其主要原因是寒武纪早期与小壳化石群伴生的宏体动、植物化石的缺乏。发现于峡东地区的寒武纪早期岩家河生物群填补了这一缺失环节,该生物群包含宏体动物、宏观藻类、小壳化石、球形化石(可能的胚胎化石)、微古植物和蓝菌类等化石,部分宏体化石显示了从埃迪卡拉纪向寒武纪过渡色彩。化石保存方式有碳质膜、黄铁矿化、磷酸盐化、硅化。因此对岩家河生物群生物多样性和埋藏学进行综合研究,将可提供纽芬兰世(梅树村期)碳酸盐台地—碳酸盐台地内部的局部凹陷盆地相的一个较完整的生物景观图,对探索"寒武纪大爆发主幕"前夕生物的辐射、演化模式及保存机制具有重要的科学意义。