Middle Ordovician reefs of Norway

The Middle Ordovician reefs of Norway were the first to develop in the western part of the Balto-scandian epicontinental sea and are the earliest coral-stromatoporoid reefs so far reported in Europe. Small patch reefs in the Steinvika Limestone, Langesund-Skien district, consist mainly of algae, echinoderms, corals and stromatoporoids. Bryozoans, molluscs, arthropods and brachiopods are also present. The reefs developed on pelmatozoan-rich substrates and are organically zoned, consisting of a pioneer community of stemmed echinoderms and sheet algae, a high-diversity intermediate community dominated by fasciculate corals and a low diversity climax community of massive corals and stromatoporoids. These communities are interpreted as the seral stages of an autogenic ecological succession. Small patch reefs are also present in the laterally equivalent Mjøsa Limestone, Toten and Nes-Hamar districts. These are organically very similar to those in the Steinvika Limestone and developed in an identical way. A large complex, consisting of several reefs, is also present in the Mjøsa Limestone. Unlike the reefs elsewhere, which developed within shallow inshore areas, this complex developed at the outer edge of the inshore shelf. The outstanding feature of the complex is the main reef forming the offshore limit which is totally dominated by stromatoporoids and lacks a sequential development. This is due to the influence of the harsher environment at the shelf edge.     

Biotic structure and morphology of patch reefs from South China (Ningqiang Formation, Telychian, Llandovery, Silurian)

Summary Ningqiang Formation (late Telychian, Llandovery, Silurian), characterized by nearly 3000 m of shales in tercalated with carbonates, is situated between Ningqiang (S. Shaanxi Province) to Guangyuan (N. Sichuan Province) adjacent to the northwest margin of the Yangtze Platform. The high diversity “Xiushan Fauna”, and abundant reef development, illustrate a relatively warm and persistent shallo marine environment in these early Silurian sediments. The sequence shows reef radiation after recovery from the end Ordovician mass extinction envents. Multiple horizons of reef-building occurred within a relatively short geological interval and resulted in more than 30patch reefs up to 200 m in diameter and 1–50 m vertically, composed of abundant fossils. Reef biota include frame-building corals, stromatoporoids, bryozoans, and microbialites, and reef-associated oranisms such as crinoids, brachiopods, trilobites, gastropods, nautiloids and ostracods. Three reefrelated biotic associations are recognised: a) reefs dominated by framework with crinoids and microbia; b) reefs dominated by only crinoids and microbia; and c) crinoiddomainated facies. Seven representative reef examples illustrate different morphologies and growth styles. A high terrigenous debris input and shallow epicontinental ramp, which lacked obvious topographic variation, were major controls which resulted in rather simple reefs; sedimentation was apparently the main constraint on lateral and vertical extension of reefs, and prevented large-scale reef complexes developing.     

The oldest labechiid stromatoporoids from intraskeletal crypts in lithistid sponge–Calathium reefs

Early Ordovician (early Floian) reefs of South China include lithistid sponge–Calathium reefs with a three‐dimensional skeletal framework. These structures are among the first post‐Cambrian skeletal‐dominated reef structures and provides an opportunity to test how the novel metazoan builders changed the environments and increased topographic complexity within benthic communities. We document the oldest labechiid stromatoporoid (Cystostroma) in a lithistid sponge–Calathium reef of the Hunghuayuan Formation in southeastern Guizhou, South China. These earliest stromatoporoids may have originated in reefs, and we argue that the complex topography created by the hypercalcified sponge Calathium facilitated the emergence of stromatoporoids. Beyond Cystostroma, keratose sponges, Pulchrilamina (hypercalcified sponge) and bryozoans have also inhabited in the micro‐habitats (cavities and hard substrates) provided by Calathium. These findings suggest that ecosystem engineering by Calathium played an important role in the further diversification of reefs during the Ordovician.     

The oldest bryozoan reefs: a unique Early Ordovician skeletal framework construction

Adachi, N., Ezaki, Y. & Liu, J. 2011: The oldest bryozoan reefs: a unique Early Ordovician skeletal framework construction. Lethaia, Vol. 45, pp. 14–23. The oldest bryozoan reefs occur in the Lower Ordovician (late Tremadocian) Fenhsiang Formation of the Three Gorges area, South China. These reefs show a unique type of bryozoan (Nekhorosheviella) framework, and were constructed as follows: the first stage involved colonization by lithistid sponges, which acted as a baffler to trap sediments, providing bryozoans with a stable substrate for attachment. The bryozoans then grew as an encruser on the surfaces of sponges, showing a preferential downwards and lateral growth within the sponge scaffolding to avoid biological and physical disturbance. Finally, these biotic combinations among skeletal organisms formed a rigid, three‐dimensional skeletal framework. This mode of bryozoan growth in association with lithistid sponges is remarkable and unique in its growth direction, and the appearance of such reefs, just prior to the widespread development of skeletal‐dominated reefs as part of the Great Ordovician Biodiversification Event, provides an excellent example of the earliest attempts by skeletal organisms to form frameworks by themselves. This find significantly enhances our understanding of the initial stages of skeletal‐dominated reef evolution and the ensuing development of reefs during the Middle–Late Ordovician. □Bryozoa, Early Ordovician, lithistid sponge, Ordovician radiation, reef.     

Development of algal-foraminiferal-coral reefs in the Lower Carboniferous of Furness, northwest England

Most carbonate buildups of Dinantian age are mud-mounds lacking direct evidence of abundant framework organisms. This contribution describes apparently unique structures containing abundant framebuilding organisms interpreted as true reefs. They occur in the Red Hill Oolite, part of the Carboniferous Limestone succession in the Furness area of northwest England. Reefs were initiated by the attachment of numerous Syringopora colonies to a firm substrate. Encrusting organisms, dominantly the supposed foraminifcr Aphralysia, colonised sediment and corallite surfaces leading to the development of a rigid framework. Thrombolites also assisted in the establishment of bindstone textures. During the later stages of reef growth, Syringopora became less common and its place in the reef was taken by upright, branching growths of solenoporoid algae. Rapid sedimentation and subsidence resulted in reefs with near vertical sides, but little topographic expression on the sea-floor during growth. The occurrence of these reefs cannot be attributed to any single environmental factor but probably resulted from an unusual combination of favourable circumstances. D Calcareous algae, Carboniferous, corals, Dinantian, foraminifera, reefs, thrombolites.     

Paleoecology of Middle Ordovician stromatoporoid mounds in Vermont

Fossiliferous mounds of carbonate mud are a distinctive facies in the middle Chazy Group (Crown Point Formation) at Isle La Motte, Lake Champlain. The mounds are surrounded by bedded calcarenite of spar-cemented pelmatozoan debris. Channels which cut into the mounds during mound growth are filled with the same calcarenite. The mud-free intermound rocks and the mound biota suggest agitated, normal marine shallow-water environments. The principal lime-secreting organisms within the mounds are stromatoporoids, calcareous algae, tabulate corals, sponges, and bryozoans. Each mound is dominated in terms of biomass by one of three groups: stromatoporoids, calcareous algae, and bryozoans. Most of the mound biota first appear at the base of the Crown Point Formation. In the lower Crown Point Formation the organisms increase in number and species. Both changes in the biota are related to periods of shallowing of the Chazy sea which are also reflected in the character of the carbonate sands.     

A late Devonian (Frasnian) coral-bafflestone reef at Houshan in Guilin, South China

Summary Givetian to early Carboniferous sediments of South China are characterized by carbonates. Middle and Late Devonian strata are best developed in the Guilin area. Reefs and organic shoals are recorded by various lithofacies types indicating the existence of an extended carbonate platform and a change of the composition of reef communities in time. Starting in the late Devonian, stromatoporoids and corals were replaced by algae that subsequently played an important role together with stromatoporoids, receptaculitids and fasciculate rugose corals in reef communities. In Houshan, 5 km west of Guilin, a coral-bafflestone reef occurs in the Frasnian strata, situated near an offshore algal-stromatoporoid reef. The coral reef was formed in a back-reef area adjacent to the inner platform margin. The coral-bafflestone reef is unique among the late Devonian reefs of South China with regard to the biotic composition. The reef is composed of fasciculate colonies ofSmithiphyllum guilinense n. sp. embedded within in packstones and wackestones. The height of colonies reaches 1 m. The community is low-diverse. The species ofSmithiphyllum occurring in the Frasnian reef complexes of Guilin exhibit a distinct facies control:Smithiphyllum guilinense occurs in or near to margin facies and formed bafflestone, constituting a coral reef whereasSmithiphyllum occidentale Sorauf, 1972 andSmithiphyllum sp.—characterized by small colonies with thin corallites—are restricted to the back-reef and marginal slope facies. The bush-like coral colonies baffled sediments. Algae and stromatoporoids (mainlyStachyodes) are other reef biota. Reef-dwelling organisms are dominated by brachiopods. The reefs are composed from base to top of five lithofacies types: 1) cryptalgal micrite, 2) peloidal packstone, 3) stromatactis limestone, 4) coral-bafflestone, and 5) pseudopeloidal packstone. The reef complex can be subdivided into back-reef subfacies, reef flat and marginal subfacies, and marginal fore-slope subfacies. The Houshan coral-bafflestone reef is not a barrier reef but a coral patch reef located near the inner margin of a carbonate platform.     

The role of bryozoans in fossil reefs—an example from the Middle Devonian of the Western Sahara

Stenolaemate bryozoans with their stable calcitic skeletons play a significant role in reef building. In the Middle Devonian Sabkhat Lafayrina reef complex (Western Sahara), bryozoans are abundant and diverse. Although they do not form part of the principal framework of reefs, bryozoans are involved significantly in reef growth, especially in the initial stage. In this way, bryozoans are important with respect to initiating reef growth. They contribute greatly to sediment stabilization, making it possible for principal reef builders to grow on hardened and stabilized substrates, and also play sediment-baffling and sediment-filling roles. The aim of this study is to document the diversity of bryozoans in a Middle Devonian reef complex and to estimate their potential for initiation and contribution to reef structures.     

The history of Devonian-Carboniferous reef communities: Extinctions,effects, recovery

Summary Analysis of the taxonomic composition, diversity and guild structure of five “typical” reef and mud mound communities ranging in age from Late Devonian-Early Carboniferous indicates that each of these aspects of community organization changed dramatically in relation to three extinction events. These events include a major or mass extinction at the end of the Frasnian; reef communities were also effected by less drastic end-Givetian and mid-late Famennian extinctions of reef-building higher taxa. Peak Paleozoic generic diversities for reef-building stromatoporoids and rugose corals occurred in the Eifelian-Givetian; reef-building calcareous algal taxa were longranging with peak diversity in the Devonian. These three higher taxa dominated all reef-building guilds (Constructor, Binder, Baffler) in the Frasnian and formed fossil reef communities with balanced guild structures. The extinction of nearly all reef-building stromatoporoids and rugose corals at the end of the Frasnian and the survival of nearly all calcareous algac produced mid-late Famennian reef communities dominated by the Binder Guild. Despite the survival of most calcareous algae and tabulate corals, the mid-late Famennian extinction of all remaining Paleozoic stromatoporoids and nearly all shelf-dwelling Rugosa brought the already diminished Devonian reef-building to a halt. These Devonian extinctions differ from mass extinctions by the absence of a statistically significant drop in taxonomic diversity and by their successional and cumulative effects on reef communities. Tournaisian mud mounds contain communities markedly different from the frame-building communities in Late Devonian and Visean reefs. Mound-building biotas consist of an unusual association dominated by erect, weakly skeletonized members of the Baffler Guild (chiefly fenestrate Bryozoa; Pelmatozoa) and laterally expanded, mud-binding algae/stromatolites and reptant Bryozoa. The initial recovery to reefs with skeletal frameworks in the Visean was largely due to the re-appearance of new species of abundant colonial rugose corals (Constructor Guild) and fenestrate Bryozoa. This Frasnian-Visean evolution in the taxonomic composition and structure of the reef-building guilds is also expressed by abrupt changes in biofacies and petrology of the reef limestones they produced. Thus, “typical” Frasnian reef limestones with balanced guild structures are framestones-boundstones-bafflestones, Famennian reefs are predominantly boundstones, Tournaisian mud mounds are bafflestones and Visean reefs are bafflestones-framestones.     

Paleoecology of a low-diversity silurian community from the tofta beds of Gotland

The Silurian (Wenlockian) Tofta Beds at Galgberget 1, Gotland, Sweden, formed in a protected intertidal setting. Massive fenestral limestone at this locality contains a low diversity community dominated by stromatoporoids, calcareous algae, and ostracods, with less common rugose corals, bryozoans, brachiopods, and trilobites. Abundance of stromatoporoids, which form about 40% of sediment volume, suggests reef-like conditions. The Tofta community differs from typical Silurian reef communities, however, in its low diversity, very limited tiering, and absence of groups such as crionozoans and tabulates. These differences are possibly due to intertidal conditions which precluded upward growth of a mound structure and subjected the community to periodic desication.     

Paleoecologic,temporal, and spatial analysis of early Silurian Reefs of the Chicotte Formation,Anticosti Island,Quebec, Canada

Summary Reefs of the Lower Silurian Chicotte Formation are the largest and most faunally diverse known on Anticosti Island, Quebec. They reach up to 25 m in thickness and 250 m in diameter and are present predominantly at two intervals, forming a lower and upper reef cluster. Remnants of bioherms are represented on the present-day wave-cut terrace as 60 to 100 m diameter, subcircular erosional depressions known as Philip structures or as outcrop. The bioherms were relatively low structures, with approximately 3 to 5 m maximum synoptic relief, some of which developed on hardgrounds and possible paleokarst surfaces of crinoidal wackestone and packstone. Dominant skeletal framework builders and sediment producers within all of the reefs are laminar to low domical stromatoporoids, colonial cerioid and fasciculate rugose corals, colonial tabulate corals, and cryptostome bryozoans. Vertical zonation of reef biota is evident within well-exposed reefs of the lower reef cluster. Three to four stages are recognizable:1) a low-diversity tabulate coral-dominatedpioneering community including large tabulate coral colonies (halysitids and favositids), and few stromatoporoids (clathrodictyids, ecclimadictyids), fasciculate rugosans, large generally monotypic stalked crinoids, and shelly benthos (brachiopods, few ostracodes and trilobites);2) an intermediate- to high-diversity, mixed tabulate coral-stromatoporoid-dominatedreef-core community;3) a slightly lower diversity stromatoporoid-tabulate coral-dominatedclimax community with laminar coenitids and alveolitids; and,4) in a few localities, a capping, low-diversity tabulatecoral-dominated (alveolitid and coenitid), and stromatoporoid-bearing community comprising laminar forms. Amelioration of Early Silurian climates, following Late Ordovician glaciation, allowed gradual reestablishment of extensive shallow-water reef growth, by mainly new and increasingly diverse genera and species of metazoans. Reef development within the Chicotte Formation coincided with global, widespread development of latest Llandovery and earliest Wenlock reefs in subtropical to tropical areas. Chicotte reefs have broad characteristics, in terms of overall biotic composition, vertical successions recognized, and paleogeographic setting, similar to those of equivalent and slightly younger age from intracratonic settings in Baltica (Gotland, Sweden and Estonia) and central and northern Laurentia (Midcontinent, U.S.A.; Hudson Bay, Canada; and North Greenland, Denmark).     

Spatial competition among clonal organisms in extant and selected paleozoic reef communities

Summary Occurrences of densely packed benthic organisms in extant reefs are of two types: 1) live-live interactions, where two living organisms interact, and 2) live-dead associations, where only one is alive and uses the other as a substrate. The latter are common in reef deposits due to biostratinomic feedback, i.e. dense skeletal accumulations provide hard substrates for clonal recruitment, thus facilitating greater frequency of live-dead encounters than in lower biomass level-bottom communities dominated by solitary organisms. Differentiating between these two types in ancient reefs is difficult, often impossible. Most live-live interactions among clones in extant reef communities involve competition for space. Clonal spatial competition is divisible into four types: 1) direct-aggressive: encrusting overgrowth; 2) indirect-passive: depriving neighbors of resources, chiefly sunlight, by growth above them; 3) stand-off: avoidance of competition by organisms adopting positions that avoid or minimize direct polyp/zooid contact; and 4) overwhelming: one clone/ species volumetrically or numerically overwhelms the other, meeting minimal resistance. Despite class-order level differences in taxa, our results indicate that extant analogs, based on the arrangement and distortion of skeletons, are valuable for recognizing live-live interactions in Silurian and Carboniferous reefs and interpreting the types of spatial competition represented. Comparison of overhead (plan) views of live-live coral competition in Polynesian reefs with vertical sections of Silurian and Carboniferous sponge-dominated reefs and biostromes suggests that direct-aggressive competition is more common among extant than among Paleozoic reef-builders. Stand-offs showing clone margin distortion and overwhelming with minor skeletal distortion are most common in our fossil examples and probably relate to the dominance of these reefs by sponges. Success by extant sponges in spatial competition is largely due to allelochemical deterrence which may explain the predominance of stand-off and overwhelming confrontations in fossil sponges rather than tentacle-mesentery based direct aggression among extant corals and bryozoans.     

Diversity,speciation, endemism and extinction in Devonian reef and level-bottom communities,eastern North America

Lower Devonian late Emsian (Bois Blanc and Clear Creek Limestones; Schoharie Formation) level-bottom communities in New York, Michigan and Illinois were moderately cosmopolitan and diverse and dominated by brachiopods and solitary rugose corals. Subsequently (Early Eifelian?), there was an important episode of cratonal patch reef building in New York (Edgecliff Member, Onondaga Limestone), southwestern Ontario (Formosa Reef Limestone, lower Detroit River Group), and the Hudson Bay Lowland (Kwataboahegan Formation) by highly diverse endemic communities. The Edgecliff reefs were built by corals whereas the Formosa and Kwataboahegan reefs were built primarily by stromatoporoids. The strong correlation between high diversity and high endemism during the reef-building episode suggests that these communities contained numberous, small species populations belonging to several major taxa — an example of rapid speciation by geographic isolation and genetic drift.     

Calcified epibionts as palaeoecological tools: examples from the Recent and Pleistocene reefs of Barbados

Calcified epibionts (crustose coralline algae, bryozoans, foraminiferans and serpulid worms) which colinize primary framebuilders of Recent Barbados reefs exhibit a well-defined zonation of species and morphological growth forms in response to environmental factors such as water turbulence and light. Exposed environments are characterized by thick crusts of coralline algae whereas cryptic environments are dominated by thin crusts of algae, bryozoans, foraminiferans and serpulid worms. A model, based on this zonation, was used to decipher the environments of growth and early burial of Pleistocene reefs. Lagoonal corals possess an assemblage of encrusters which document prolonged growth in a uniform environment. Reef crest corals support a mixed succession of shallow water encrusters which record a gradual decrease in light as substrates are smothered by accumulating debris. Sequences such as these represent growth under stable conditions. The model can also be used to interpret sequences formed by catastrophic events and fluctuations in sea level.     

Marine faunal assemblages in the Silurian-Devonian Keyser Limestone of the central Appalachians

Sedimentological analysis of the Keyser Limestone (Upper Silurian - Lower Devonian of the central Appalachians) indicates that its sediments were deposited in a range of marginal and shallow marine environments. Major depositional environments include: tidal flat, lagoon, barrier bar and island, and open marine shelf. Each major environment is represented by a lithofacies which is lithologically and faunally distinct. Tidal flat lithofacies are characterized by eurytopic organisms, including ostracodes, gastropods, stromatoporoids and blue-green algae. Lagoon lithofacies are dominated by bryozoans, brachiopods, ostracodes and stromatoporoids. Barrier lithofacies are characterized by rooted crinoids, encrusting bryozoans and robust brachiopods. Open shelf lithofacies contain a diverse fauna of cystoids, crinoids, bryozoans and brachiopods.
The distributions of faunal assemblages in the Keyser show no simple relationship to either water depth or distance from shore. They are, in general, related to the distributions of depositional environments.
Recurring associations of brachiopod genera were not found in the Keyser. With few exceptions, any genus may be found in any subtidal environment. Abundance of brachiopods is related to the abundance of local hard substrates (usually bryozoans).     

新疆塔里木塔中井区上奥陶统良里塔格组的生物绑结岩

塔里木板块塔中井区上奥陶统凯迪阶良里塔格组灰岩中底栖固着型的钙质微生物、钙藻以及动物苔藓虫、珊瑚、层孔虫,可通过障积、盖覆和粘结等方式形成多种类型的生物绑结岩。对15口井部分岩芯以常用的绑结岩分类方案作岩石学微相分析,并描记底栖固着型生物颗粒的形成特征。菌藻类可在内碎屑表面以包结方式形成粘结岩;钙藻,特别是分枝状钙藻可形成障积岩;层孔虫可被隐藻层纹包结,也可单独形成小型盖覆岩;床板珊瑚格架岩可大量障积生屑和灰泥基质;苔藓虫在动物格架岩比例上占优,可与菌藻类粘结岩互相包结生长,也可独立形成局部小型障积岩。对比巴楚露头区同期藻丘中的绑结岩特征,显示塔中良里塔格组代表晚奥陶世由高生物多样性形成的礁滩复合体生态群落。     

ECOLOGY AND MORPHOLOGY OF RECENT CORAL REEFS

1. The classical ‘coral reef problem’ concerned the geological relationships of reefs as major topographical features; modern coral studies consider reefs both as complex biological systems of high productivity and as geological structures forming a framework for and being modified by coral growth. 2. Deep borings in reefs have conclusively confirmed the general arguments of Darwin, that oceanic reefs developed by progressive subsidence of their foundations. Darwin failed to take account of Pleistocene changes in sea level and their effect on the present surface features of reefs. Daly's alternative ‘glacial control theory’ was based on false assumptions concerning marine erosion rates during glacial periods, but if sea level during the Holocene was higher than at present, as Daly also supposed, the effects on reef features would be profound. 3. Reefs are complex biological systems in tropical seas, dominated by scleractinian corals. Coral faunas are larger and more diverse in the Indo-Pacific than in the Atlantic. Hermatypic corals are restricted to shallow water by the light requirements of their symbiotic algae, but temperature is a major control of worldwide distributions. Temperature, salinity and sediment tolerances of corals are wider than formerly supposed, and corals can survive brief emersion except when it coincides with heavy rainfall. Water turbulence is an important ecological control, but difficult to measure. 4. The trophic status of corals is still unclear, but in spite of their anatomical and physiological specialization as carnivores it is likely that they derive some nutrient substances from zooxanthellae. Suggestions that filamentous algae in coral heads play a major part in the economy of the corals have not been supported by later work, but biomass pyramids constructed on the basis by Odum and Odum remain the only ones available. Most reefs are apparently autotrophic, with 1500–3500 g. Carbon being fixed per m.² per year. 5. Few animals eat corals, which may account for their success. Important predators are fish and the echinoderm Acanthaster. Quantitative estimates of biogenic erosion of organic skeletons on reefs are high. Fish affect not only corals but other invertebrates, algae and marine phanerogams. 6. Corals may be killed by ‘dark water’, intense rain or river floodwaters, earth movements, human interference and especially hurricanes. Reef recovery after hurricanes may take 10–20 years. 7. In addition to fringing, barrier and atoll reefs, intermediate types are recognised. The main types may consist of linear reefs or faros. Smaller lagoon reefs include pinnacles, patches and platforms, and submerged knolls. Complex cellular or mesh reef patterns are also found. 8. Reefs are conspicuously zoned, both laterally in response to changing exposure to waves to form windward and leeward reefs, and transversely, as a result of steep environmental gradients across reef flats from sea to lagoon. Topographic and ecological zones may be characterized by particular coral species, but these vary widely from reef to reef. A major distinction can be made between reefs with and without algal ridges, which are common on open-ocean trade-wind reefs, in the Indo-Pacific, but are absent on Caribbean reefs and on Indo-Pacific reefs in more sheltered waters. gorgonians are common on Caribbean reefs, alcyonaceans in the Indo-Pacific. 9. Much of the difficulty in comparing reefs stems from the lack of uniformity in surveying methods. Problems of describing the complex three-dimensional patterns of organisms on reefs have yet to be solved, and hence little progress has been made in explanation of these patterns. Explanation in terms of simple environmental controls is inadequate. 10. Understanding the distribution of corals is made more difficult both by taxo-nomic problems and by the plasticity of growth form in different situations. 11. Growth of corals and reefs may be estimated by measuring the growth of individual colonies, measuring rates of calcium carbonate deposition in the skeleton, measuring topographic change on the reef and deducing net rates of reef growth from geological evidence. Massive corals may increase in diameter by 1 cm./year, branches of branching corals may increase in length by 10 cm./year. Study of deposition rates shows variation within colonies, between species, in light and dark, and seasonally. Rates of reef growth extrapolated from colony measurements reach 2–5 cm./year, and contrast with figures as low as 0–02 cm/year averaged over 70 million years from borehole data. Both colony growth rates and geological data suggest worldwide variations in rates of reef growth. 12. In spite of clear evidence of long-continued subsidence, present surface features of reefs, often only thinly veneered by modern corals, have been much affected by recent sea level fluctuations. Many slightly raised reefs at 2–10 m. above sea level date at 90–160 thousand years B.P.; there is evidence for a sea level at about the present level at 30–35 thousand years B.P.; and controversy continues over whether sea level has stood higher than the present at any time since the last sea level rise began about 20,000 years ago. Evidence from many reefs suggests a slightly higher sea level in the last 4000 years, but on other reefs such evidence is lacking. 13. Several reef features (submerged terraces, groove-spur systems, algal ridge, reef flat, reef blocks and reef islands) have been interpreted either as relict features dating from a higher sea level in the last 5000 years, or contemporary features developed in response to present processes. In some cases the evidence is equivocal; in others it is clear that diverse features are being grouped together under the same name. If such features are referable to a higher sea level, this may have been of last Interglacial or even Interstadial age rather than Holocene. 14. A reef consists of a rigid framework defining several major depositional environments within and around it. Sediments are of biological, mainly skeletal origin, except in unusual environments such as the Bahama Banks. The characteristics of sediments derived from organisms depend partly on the breakdown patterns of particular skeletons, partly on transportation and sorting processes. Fine sediments may be either detrital, or physicochemical precipitates. 15. Organisms affect sediments after deposition, by disturbance, transportation and probably comminution. Fish and holothurians have been studied in detail. 16. While new theories of coral reefs are proposed from time to time, the need is less for new theories than for standardised procedures to ensure comparability of reef studies and the identification of variations in reefs both on local and regional scales. While reefs as biological systems adjust relatively rapidly to changes, reefs as geological systems adjust much more slowly. Because of the magnitude and recency of Pleistocene fluctuations in sea level, many biological features of reefs are out of phase with inherited geological features, and this had led to much controversy.     

Coral reef encruster communities and carbonate production in cryptic and exposed coral reef habitats along a gradient of terrestrial disturbance

Encrusting calcareous organisms such as bryozoans, crustose coralline algae (CCA), foraminiferans, and serpulid worms are integral components of tropical framework-building reefs. They can contribute calcium carbonate to the reef framework, stabilise the substrate, and promote larval recruitment of other framework-building species (e.g. coral recruits). The percentage cover of encrusting organisms and their rates of carbonate production (g m⁻² year⁻¹) were assessed at four sites within a coastal embayment, along a gradient of riverine influence (high-low). As the orientation and type of substrate is thought to influence recruitment of encrusting organisms, organisms recruiting to both natural (the underside of platy corals) and experimental substrates were assessed. The effect of substrate exposure under different levels of riverine influence was assessed by orientating experimental substrates to mimic cryptic and exposed reef habitats (downwards-facing vs upwards-facing tiles) at each site. Cryptic experimental tiles supported similar encruster assemblages to those recruiting to the underneath (cryptic side) of platy corals, suggesting that tiles can be used as an experimental substrate to assess encruster recruitment in reef systems. Encruster cover, in particular CCA, and carbonate production was significantly higher at low-impact (clear water), high wave energy sites when compared to highly riverine impacted (turbid water), low wave energy sites. Cryptically orientated substrates supported a greater diversity of encrusting organisms, in particular serpulid worms and bryozoans. The inverse relationships observed between riverine inputs and encrusters (total encruster cover and carbonate production) have implications for both the current and future rates and styles of reefal framework production.     

泥质对志留系礁滩生长的抑制作用:黔北桐梓韩家店组的例证

黔北桐梓的戴家沟剖面和狮溪剖面志留系兰多维列统特列奇阶下部的韩家店组出露完好,该组泥岩、粉砂岩中夹有厚度1—3m、直径4—7m的小型点礁。礁核相多具典型的障积格架岩特征,但生长时限短暂,群落分异度低,仅见床板珊瑚、单体四射珊瑚、苔藓虫和海百合茎,礁间为珊瑚、苔藓虫和海百合茎碎片堆积的滩相,伴生丰富的遗迹化石。在陆源碎屑快速沉积的背景下,浑浊海水频繁的富营养化过程限制了礁体纵横向生长和朝高分异度群落发展的可能性。     

A Paleocene coral—algal—sponge reef from southwestern Alabama and the ecology of Early Tertiary reefs

The Late Paleocene Salt Mountain Limestone from southwestern Alabama is a coral-algal-sponge buildup which further characterizes the faunal makeup of early post-Cretaceous reefs. Thin sectioning has disclosed a variety of lithologies, including large foram-algal packstone, algal bindstone, and sponge bafflestone. A low-diversity fauna of massive scleractinian corals caps the sequence, but may be developed intermittently throughout the section as well. The constructional importance of coralline algae and the low diversity of scleractinian corals are characteristic of Paleocene reefs in general. Sponges, however, are virtually unknown in earliest Tertiary sediments. Their abundance in the Salt Mountain demonstrates not only their local contribution to Early Tertiary reefs, but may also reflect an opportunistic response of sponges as reef constructors following the extinction of oligotrophic, rudist-coral reef communities of the Late Cretaceous. □ Paleocene, reef, paleoecology, sponges, extinction.