Oldest known Dicoelosia and Epitomyonia,deep water brachiopods from the Beiguoshan Formation (Middle Katian,Upper Ordovician), Shaanxi,north China

Abstract: A diverse brachiopod fauna from a relatively deep water carbonate facies of the Upper Ordovician Beiguoshan Formation (uppermost Caradoc – lower Ashgill, middle Katian) is characterized by small shells and contains the oldest known Dicoelosia and Epitomyonia, two diagnostic taxa of deep water brachiopod palaeocommunities during the Late Ordovician and Silurian. Three new species are recognized: Dicoelosia cordiformis sp. nov., Dicoelosia perbrevis sp. nov. and Epitomyonia fui sp. nov. These pioneer forms of the family Dicoelosiidae show a relatively high degree of morphological plasticity. The shells of Dicoelosia from the Beiguoshan Formation range from the typical slender‐lobed form with a concavoconvex profile to the strongly equibiconvex, fat‐lobed morphotype that was not known previously until the late Silurian. The Beiguoshan dicoelosiids point to an important attribute of the deep water brachiopods: small generalists with high morphological plasticity, which make them ideal candidates as progenitors for the evolution of shallow water brachiopod faunas in shelf and platform depositional environments.     

Unravelling Phanerozoic evolution of radial to rosette trace fossils

Feeding trace fossils, produced by either deposit or detritus feeders and showing radial to rosetted morphology, are all included in the same architectural category. These radial to rosette ichnofossils are widely recorded worldwide throughout the Phanerozoic and have attracted the attention of numerous ichnologists for decades. Construction of a database summarizing occurrences of radial to rosette trace fossils through the Phanerozoic shows that representatives of this category occurred for the first time during the Fortunian, which accounts for the appearance of at least 12% of the total number of ichnogenera in this category. Overall, 32% of all known rosette ichnogenera resulted from the Cambrian Explosion. A second ichnodiversity increase took place (20%) during the Ordovician. Subsequent to the Great Ordovician Biodiversification Event, this architectural category shows minor fluctuations in ichnodiversity resulting in a long‐term plateau. The apparent decline in ichnodiversity by the end of the Cenozoic could reflect a taphonomic artefact resulting from the difficulties of identifying cumulative trace fossils in highly bioturbated modern sediments. Our data set indicates that several radial to rosette ichnogenera (e.g. Arenituba, Dactylophycus, Gyrophyllites, Phoebichnus, Volkichnium) occurred first in shallow‐marine settings and then migrated to either deeper‐water or marginal‐marine environments, while others (e.g. Asterichnus, Cladichnus, Dactyloidites) apparently first occurred in deep‐sea environments and then migrated to shallower waters.     

Cincinnetina,a new Late Ordovician dalmanellid brachiopod from the Cincinnati type area,USA: implications for the evolution and palaeogeography of the epicontinental fauna of Laurentia

Abstract: The most common forms of Late Ordovician dalmanellid brachiopods from the Cincinnatian type area, previously treated as either Dalmanella or Onniella, are assigned to Cincinnetina gen. nov. The new genus differs from Dalmanella and Onniella in having a consistently developed primary medial costa in the dorsal valve, a larger cardinal process that tends to develop a trilobed myophore, strongly differentiated fine and coarse punctae, and sparse aditicules. Cincinnetina can be distinguished from the closely related Paucicrura and Diceromyonia in its smaller trilobed cardinal process (when developed) that does not have a dominant medial lobe and does not extend into the delthyrial cavity of the ventral valve. Globally, Dalmanella and Onniella occur most commonly in deposits of relatively deep‐ or cool‐water palaeoecological settings, whereas in North America, Cincinnetina, Paucicrura and Diceromyonia are found mainly in carbonate‐rich deposits in warm‐water depositional environments, with Cincinnetina and Paucicrura most common in pericratonic settings and Diceromyonia in palaeoequatorial inland seas.     

Trace fossils from arenig flysch sediments of eire and their bearing on the early colonisation of the deep seas

A sequence of Lower Ordovician (Arenig) turbidites in Co. Wexford, Eire, has yielded one of the earliest diverse ichnofaunas yet recorded from deep water sediments comprising: Chondrites, Glockerichnus, Gordia, Helminthopsis, Lorenzinia, Neonereites, Palaeophycus, Paleodictyon, Planolites, Sublorenzinia, Taenidium, Taphrhelminthopsis, Teichichnus and Tomaculum. This ichnofauna is critical in any analysis of the colonisation of the deep seas by trace fossil‐producing animals.

A world‐wide review shows that the earliest trace fossils are mainly from Late Precambrian shelf sea environments, but many more evolved during very rapid diversification in the pre‐trilobite Lower Cambrian.

There was little increase in diversity in shallow water after the Lower Cambrian but a progressive colonisation of the deep ocean took place and this accelerated during the Ordovician, when the main lineages of deep sea trace fossils were established there. Rosetted, patterned, meandering and simple spiral forms evolved in shallow water in the Upper Precambrian and pre‐trilobite Lower Cambrian and only later migrated into the deep sea, whereas complex, closely programmed, spiral traces may have evolved there.     

Probing the deep shelf: a Lagerstätte from the Upper Ordovician of Girvan, southwestern Scotland

A deep‐water Konservat Lagerstätte from the lower Caradoc (Sandbian) at Girvan is dominated by the trilobite Diacanthaspis trippi, the carpoids Anatifopsis n. sp.? and a new genus of ctenocystoid together with the polyplacophoran Solenocaris solenoides and the brachiopod Onniella williamsi. Most of these are multi‐element organisms, with many specimens preserved in an articulated state in finely laminated rocks, indicating minimal disturbance and suggesting that the fauna is largely an in situ association. It contains few of the species known from other deep‐water sites of similar age at Girvan which contain diverse assemblages of trilobites and brachiopods absent from the Lagerstätte. The taphonomy of the site indicates preservation by rapid burial followed by early diagenesis under dysaerobic conditions. It provides a ‘taphonomic window’ on otherwise unknown faunas from distal shelf facies on the Ordovician Laurentian margin, and, moreover, is an important reminder of the hidden biodiversity that resided in thin‐shelled, multi‐element organisms.     

Latest Ordovician brachiopod and trilobite assemblage from Yuhang,northern Zhejiang,East China: a window on Hirnantian deep-water benthos

A moderately diverse brachiopod and trilobite assemblage, the Leangella–Dalmanitina (Songxites) Assemblage, occurs in the upper Yankou Formation (Hirnantian, probably equivalent to the Normalograptus persculptus Biozone) at Shizi Hill, Yuhang, west of Hangzhou, northern Zhejiang, E China. The brachiopods are rare, characterised by minute, thin shells with very small body cavities, preserved in mudstones as moulds. They may have inhabited quiet, deep-water and dysaerobic slope environments with low levels of nutrients, equivalent to Benthic Assemblage 5. Most genera were adapted for life in deep water and either remained there or alternatively migrated into relatively shallower habitats to evade perturbations during the first phase of the end Ordovician extinctions. The slope environments were recolonised from outer shelf and upper slope communities during the early Hirnantian, but isolated biotas may also have survived in deeper-water habitats by reducing their population size and diversity during the crisis. The Leangella–Dalmanitina (Songxites) Assemblage provides an unique Hirnantian window through which we can monitor the changes in the deep-water biofacies following the first phase of the extinctions. Significantly, parts of the deep water marine environment may have survived intact, the end Ordovician extinctions.     

UPPER ORDOVICIAN BRYOZOANS OF THE PIN FORMATION (SPITI VALLEY, NORTHERN INDIA)

Abstract: Twenty‐nine species of bryozoans from the Upper Ordovician–Lower Silurian Pin Formation (Spiti, India) have been identified. Eight of these are new: Trematopora minima, Ulrichostylus bhargavai, Ptilodictya exiliformis, Phaenopora ordinarius, Oanduellina himalayaica, Pesnastylus? vesiculosum, Ralfina? originalis and Pinocladia triangulata. The fossil record and facies analyses of the area investigated indicate shallow‐water conditions within the subtropical–tropical realm. The distribution pattern of fossils among the Ordovician/Silurian succession on the Northern Gondwana shelf and the influence of the Late Ordovician cooling phases on marine organisms are distinctive owing to a dramatic reduction in diversity globally. As far as the bryozoan taxa of Spiti are concerned, only one (Helopora fragilis) of the 29 species was recorded above the Ordovician/Silurian boundary. Observed bryozoan communities are very similar to faunas of Laurentia, the Baltic, Siberia and southern China of early–late Ordovician age.     

Evolution of the Rhynchotrema–Hiscobeccus lineage: implications for the diversification of the Late Ordovician epicontinental brachiopod fauna of Laurentia

Multivariate analysis based on nine biometric characters of 171 Late Ordovician rhynchonellide specimens from nine upper Sandbian–upper Katian localities in North America supports the hypothesis that one of the diagnostic taxa of the North American epicontinental brachiopod fauna, Hiscobeccus, evolved from Rhynchotrema, which lived predominantly in peri‐cratonic settings. The oldest known Hiscobeccus, H. mackenziensis of early Katian age, exhibits transitional characteristics between Rhynchotrema and Hiscobeccus, and it clusters more closely with Rhynchotrema than with younger species of Hiscobeccus of mid–late Katian (Maysvillian–Richmondian) age. Diversification of the Hiscobeccus lineage in epicontinental seas was characterized by drastic increase in shell size, globosity and lamellosity, especially in palaeoequatorially located inland basins. Such morphological trends are interpreted as adaptation to relatively shallow, muddy substrates, moderate water turbulence, relatively low oxygen content and unstable supply of nutrients in generally overheated epicontinental seas with sluggish circulation.     

High‐resolution δ13Corg chemostratigraphy links the Decorah impact structure and Winneshiek Konservat‐Lagerstätte to the Darriwilian (Middle Ordovician) global peak influx of meteorites

The precise age of the Winneshiek Shale, a recently discovered Konservat‐Lagerstätte located in a very unusual depositional setting inside the Decorah impact structure, has remained uncertain in the absence of biostratigraphically highly diagnostic fossils. This chemostratigraphical study, based on δ¹³C_org data from 36 drill core samples through the shale, shows that the age ranges from the upper part of a small unnamed δ¹³C excursion in the Dw1 Stage Slice of the Darriwilian Global Stage to the lower part of the MDICE excursion in Stage Slice Dw2 of the same stage. This Dw1–Dw2 interval has an isotopic age of ~464–467 Ma. The gradational contact between the Winneshiek Shale and the underlying, rapidly deposited, impact breccia indicates minimal time difference between the impact event and the Winneshiek Shale. New age data show that the Decorah impact event was coeval with the early Darriwilian abnormally high influx of micrometeorites and meteorites recorded in sections in Baltoscandia, Russia and China and that the Decorah crater can be included among the unusually large number of meteorite craters formed during Middle and early Late Ordovician time. As is commonly the case in black shale deposits, the partly uniquely preserved Winneshiek Shale crater fauna is impoverished taxonomically and adds numerically relatively little to the conspicuous and much discussed Darriwilian global biodiversification increase.     

Timing of deep‐sea adaptation in dogfish sharks: insights from a supertree of extinct and extant taxa

Klug, S. & Kriwet, J. (2010). Timing of deep‐sea adaptation in dogfish sharks: insights from a supertree of extinct and extant taxa. —Zoologica Scripta, 39, 331–342. Dogfish sharks (Squaliformes) constitute a monophyletic group of predominantly deep‐water neoselachians, but the reasons and timing of their adaptation to this hostile environment remain ambiguous. Late Cretaceous dogfish sharks, which generally would be associated with deep‐water occur predominantly in shallow water environments. Did the end‐Cretaceous mass extinction event that eliminated large numbers of both terrestrial and aquatic taxa and clades including sharks trigger the evolutionary adaptation of present deep‐water dogfish sharks? Here, we construct, date, and analyse a genus‐level phylogeny of extinct and living dogfish sharks to bring a new perspective to this question. For this, eleven partial source trees of dogfish shark interrelationships were merged to create a comprehensive phylogenetic hypothesis. The resulting supertree is the most inclusive estimate of squaliform interrelationships that has been proposed to date containing 23 fossil and extant members of all major groups. ?Eoetmopterus represents the oldest dalatoid. ?Microetmopterus, ?Paraphorosoides, ?Proetmopterus and ?Squaliogaleus are stem‐group dalatoids in which bioluminescence most likely was not developed. According to our analyses, bioluminescence in dogfish sharks was already developed in the early Late Cretaceous indicating that these sharks adapted to deep‐water conditions most likely at about 100 Mya. The advantage of this reconstruction is that the fossil record is used directly for age node estimates rather than employing molecular clock approaches.     

Different distribution patterns of woody species on a slope in relation to vertical root distribution and dynamics of soil moisture profiles

Distribution patterns along a slope and vertical root distribution were compared among seven major woody species in a secondary forest of the warm-temperate zone in central Japan in relation to differences in soil moisture profiles through a growing season among different positions along the slope. Pinus densiflora, Juniperus rigida, Ilex pedunculosa and Lyonia ovalifolia, growing mostly on the upper part of the slope with shallow soil depth had shallower roots. Quercus serrata and Quercus glauca, occurring mostly on the lower slope with deep soil showed deeper rooting. Styrax japonica, mainly restricted to the foot slope, had shallower roots in spite of growing on the deepest soil. These relations can be explained by the soil moisture profile under drought at each position on the slope. On the upper part of the slope and the foot slope, deep rooting brings little advantage in water uptake from the soil due to the total drying of the soil and no period of drying even in the shallow soil, respectively. However, deep rooting is useful on the lower slope where only the deep soil layer keeps moist. This was supported by better diameter growth of a deep-rooting species on deeper soil sites than on shallower soil sites, although a shallow-rooting species showed little difference between them.     

Facies distribution patterns of some marine benthic faunas in early paleozoic platform environments

Worldwide Late Cambrian—Silurian lithofacies patterns indicate that the platforms of that time were sites of accumulation of two essentially different rocks suites: the platform carbonate rocks and the platform terrigenous rocks. Most of the platform rocks accumulated as sediments in shallow marine environments similar to those of the present but far more widely spread.Present-day marine benthic faunas are distributed in depth zones which are primarily controlled by temperature. Faunas tend to occur in substrate-related discrete clusters (communities) within each life zone; similar substrates in different depth zones commonly have different faunal associations. Individual phyletic stocks may encounter environmental optimum or near-optimum conditions in certain areas, that commonly are revealed by an abundance of species and individuals within species in each stock. Environmental optimum conditions depend upon availability of food that may be utilized, modes of feeding of the animals present, water motion, and substrate, among other factors. Organisms in past seas were distributed in patterns similar to those of the present.Carbonate platforms were particularly widespread during the latest Cambrian—Early Ordovician. Intertidal environments spread widely across those platforms during that time and characteristic faunal associations developed in them. Saukiid and related tribolites dominated latest Cambrian carbonate platform intertidal faunas. The Early Ordovician carbonate platform intertidal was dominated by archeogastropod-nautiloid cephalopod faunas. These animals were joined by tabulate corals and certain brachiopods during the latter part of the Ordovician and Silurian as prominent faunal elements in the carbonate platform intertidal—shallow subtidal. Cruziana and related trace fossils, bivalves, and certain tribolites (notably homalonotids and dalmanitids) dominated most terrigenous platform intertidal—shallow subtidal faunas of the Ordovician and Silurian.Articulate brachiopods (primarily orthoids, strophomenoids, and rhynchonelloids) appear to have been relatively prominent during the Early Ordovician in shallow subtidal environments on both carbonate and terrigenous platforms and to have spread down the bathymetric gradient into increasingly deeper subtidal areas of both platforms during the latter part of the Ordovician. Tribolites dominated faunas in relatively moderate to deep subtidal environments on both platforms during the early part of the Ordovician. They were gradually replaced by brachiopods in first the shallower, and later the deeper subtidal as dominant members of the faunas. Brachiopods (primarily pentameroids and spiriferoids) dominated nearly all Silurian warm-water subtidal environments from the shallow subtidal to the edges of the platforms.Platform uplifts in the Middle Ordovician and glacio-eustatic sea-level fluctuations in the Late Ordovician caused environmental changes across the platforms that were accompanied by marked replacements among marine benthic faunas in all environments. The distribution of Ordovician carbonate platforms and glacial deposits suggests that an Ordovician polar region may have been close to present-day equatorial Africa and that Ordovician warm temperate-tropical regions lay close to the present-day North Pole.     

Deepwater broadcast spawning by Montastraea cavernosa, Montastraea franksi, and Diploria strigosa at the Flower Garden Banks, Gulf of Mexico

Broadcast spawning by corals is a tightly synchronized process characterized by co-ordinated gamete release within 30–60 min time windows once per year. In shallow water corals, annual water temperature cycles set the month, lunar periodicity the day, and sunset time the hour of spawning. This tight temporal regulation is critical for achieving high fertilization rates in a pelagic environment. Given the differences in light and temperature that occur with depth and the importance of these parameters in regulating spawn timing, it has been unclear whether deeper coral can respond to the same environmental cues that regulate spawning behaviour in shallower coral. In this report, a remotely operated vehicle was used to monitor coral spawning activity at the Flower Garden Banks at depths from 33 to 45 m. Three species Montastraea cavernosa, Montastraea franksi, and Diploria strigosa were documented spawning within this depth range. All recorded spawning events were within the same temporal windows as shallower conspecifics. These data indicate that deep corals at this location either sense the same environmental parameters, despite local attenuation, or communicate with shallower colonies that can sense such spawning cues.     

Evolution,palaeoecology, and palaeobiogeography of the Late Ordovician–Early Silurian brachiopod Epitomyonia

Epitomyonia is characterized by various types of dorsal ridges, which may be transverse, longitudinal, or highly convoluted and probably served as skeletal supports for lophophores of various complexity. Multivariate analyses suggest that the Epitomyonia-bearing brachiopod associations lived in relatively shallow-water environment in the Late Ordovician, and inhabited mainly deep-water environments in the early Wenlock. The temporal and spatial change in the faunal distribution may be explained by three alternative scenarios: (1) Epitomyonia followed the broad evolutionary trend of the Palaeozoic Evolutionary Fauna to shift from shallow- to deeper-water settings over time; (2) the dicoelosiid communities could not compete with the large-shelled pentameride communities in continental shelf settings during the Early Silurian; or (3) only the shallow-water Epitomyonia died out in the Late Ordovician mass extinction event, whereas some poorly known deep-water Late Ordovician forms survived into the Early Silurian. Epitomyonia paucitropida n. sp. from the lower Whittaker Formation (late Katian) of the Mackenzie Mountains, northwestern Canada, is reported as the first known Ordovician species of Epitomyonia from the palaeocontinent of Laurentia, characterized by a small shell with weak, transverse dorsal ridges that are most primitive for the genus.     

Root metaxylem and architecture phenotypes integrate to regulate water use under drought stress

At the genus and species level, variation in root anatomy and architecture may interact to affect strategies of drought avoidance. To investigate this idea, root anatomy and architecture of the drought‐sensitive common bean (Phaseolus vulgaris) and drought‐adapted tepary bean (Phaseolus acutifolius) were analyzed in relation to water use under terminal drought. Intraspecific variation for metaxylem anatomy and axial conductance was found in the roots of both species. Genotypes with high‐conductance root metaxylem phenotypes acquired and transpired more water per unit leaf area, shoot mass, and root mass than genotypes with low‐conductance metaxylem phenotypes. Interspecific variation in root architecture and root depth was observed where P. acutifolius has a deeper distribution of root length than P. vulgaris. In the deeper‐rooted P. acutifolius, genotypes with high root conductance were better able to exploit deep soil water than genotypes with low root axial conductance. Contrastingly, in the shallower‐rooted P. vulgaris, genotypes with low root axial conductance had improved water status through conservation of soil moisture for sustained water capture later in the season. These results indicate that metaxylem morphology interacts with root system depth to determine a strategy of drought avoidance and illustrate synergism among architectural and anatomical phenotypes for root function.     

Morphofunctional analysis of Svobodaina species (Brachiopoda,Heterorthidae) from south‐western Europe

Geometric morphometric methods applied to the ventral muscle field outline of the various species of Svobodaina from south‐western Europe identify criteria for discriminating among this key cluster of brachiopod species. These data indicate the close relationship between the patterns of the ventral muscle field in the Svobodaina species and the environmental conditions where each inhabited; the fields are better developed in species related to high‐energy environments. For example, S. armoricana, with the smallest diductor scars, would have inhabited the quiet marine environments of the lower offshore or within protected lagoonal settings. S. feisti would have inhabited the upper offshore, a more energetic environment than S. armoricana. Finally, S. havliceki, with the largest diductor scars, would have thrived in the most energetic environments among all the south‐western European Svobodaina species, living just above the fair‐weather wave base in the lower shoreface. The palaeoecological results suggest a distribution of Svobodaina species during the Late Ordovician along an onshore–offshore transect across the shallow marine platforms of the Mediterranean margin of Gondwana. On the other hand, the occurrence in some localities of several species with overlapping ranges or within the same assemblage indicates that the biostratigraphical efficacy of the genus is restricted. Thus, the previously defined taxon‐range biozones characterized by Svobodaina species of the north Gondwanan margin are in need of reassessment. The morphology of Svobodaina may be a considerable aid to environmental analyses rather than to precise biostratigraphical correlations.     

Ordovician trimerellacean brachiopod shell beds

The large, thick-shelled, inarticulate brachiopod Eodinobolus forms many conspicuous deposits of shells in the Upper Ordovician limestones of central western New South Wales. Both in situ and reworked shell beds arc preserved at recurrent intervals through the successions, in similar facies of both transgressivc and regressive phases of deposition. In situ shell beds arc best developed in transgressivc sequences, with up to four generations of shells exhibited in the individual in situ beds. These monotypic and very low diversity shell beds are interpreted as having formed in marginal marine, quiet water conditions: (1) on the fringes of an offshore island (in part the Molong High of the Tasman Orogen), with the island still providing a fairly continuous supply of terrigenous material: and, (2) after submergence of the island, on the resulting terrigenous-free, major offshore Bahamas-like platform. This may imply that the shell beds developed in different salinity regimes. Possibly Eodinobolus was capable of tolerating a wider than normal range of salinity, from slightly brackish through normal marine, even to marginally hypersaline. However, in both settings, Eodinobolus, in its role as the dominant member of the respective pioneer community, colonized similar substrates in the low energy mud zone. This appears to suggest depositional environments most directly analogous to those of Palaeozoic virgianid pentamerides, and perhaps also comparable with some modern marginal marine oyster and mussel-bed occurrences. ?Ordovician, Brachiopoda, Eodinobolus, palaeoecology, facies, shell beds. New South Wales.     

Mechanical strength of shells of selected extant articulate brachiopods: Implications for paleozoic morphologic trends

Dried shells of Terebratalia transversa, Laqueus californianus, Hemithyris psittacea, and T. unguicula and alcohol‐soaked, tissue‐lined shells of Terebratulina retusa, Dallina septigera, Cryphus vitreus, and Liothyrella uva were crushed in an apparatus that facilitated measurement of the force (newtons) against the valves at the instant of fracture. The results revealed that the costate shells of T. transversa and T. retusa were the strongest. Force is correlated with valve thickness, but not with size (length). When normalized for valve thickness, the force required to fracture shells is correlated with shell biconvexity (height/length) among pooled species of dried specimens. Geniculate specimens of T. retusa were not stronger than the intraspecific variants with a constant radius of curvature to their valves.

The percent‐frequency of plicate, spinose, lamellose and rugate genera increase significantly in the successive stages, Caradocian (Late Ordovician) through Famennian (Late Devonian) at the expense of smooth to costellate genera. The percent‐frequency of rectimarginate (central fold lacking) genera also decreases appreciably in this time frame. These morphologic trends, in combination with the experimental crushing data, support the hypothesis that selection favored species with such anti‐predatory adaptations during a time of escalation of shell‐crushing predators.     

The Devonian nekton revolution

Klug, C., Kröger, B., Kiessling, W., Mullins, G.L., Servais, T., Frýda, J., Korn, D. & Turner, S. 2009: The Devonian nekton revolution. Lethaia, 10.1111/j.1502‐3931.2009.00206.x Traditional analyses of Early Phanerozoic marine diversity at the genus level show an explosive radiation of marine life until the Late Ordovician, followed by a phase of erratic decline continuing until the end of the Palaeozoic, whereas a more recent analysis extends the duration of this early radiation into the Devonian. This catch‐all approach hides an evolutionary and ecological key event long after the Ordovician radiation: the rapid occupation of the free water column by animals during the Devonian. Here, we explore the timing of the occupation of the water column in the Palaeozoic and test the hypothesis that ecological escalation led to fundamental evolutionary changes in the mid‐Palaeozoic marine water column. According to our analyses, demersal and nektonic modes of life were probably initially driven by competition in the diversity‐saturated benthic habitats together with the availability of abundant planktonic food. Escalatory feedback then promoted the rapid rise of nekton in the Devonian as suggested by the sequence and tempo of water‐column occupation. □Devonian, diversity, ecology, food webs, nekton, plankton, radiation.     

Island benthic assemblages: With examples from the Late Ordovician of Eastern Australia

The Benthic Assemblage (B.A.) concept, developed by A.J. Boucot two decades ago principally for continental marine margins, is extended to offshore island settings. Characteristics of modern island biotas, including ecological displacement, and the effects of r and K selection, can be identified in Late Ordovician volcanic islands of central New South Wales. Two variants of B.A.1 are represented, a quiet‐water lingulide biofacies, and a rough‐water rhynchonellide biofacies. The quiet‐water Eodinobolus biofacies occupied a B.A.1–2 position, onshore of and sheltered by a Tetradium wave‐baffle (B.A.2). The offshore shelfal high diversity strophomenide biofacies is equivalent to B.A.3. Remnants of periplatformal B.A.4–5 communities are recognised in allochthonous limestone breccias which were displaced downslope into graptolitic B.A.6 sediments. Steeper offshore gradients, typical of islands, laterally compress the B.A. profiles, and also contribute to downslope slumping. Ecological displacement in island environments results in extension of the habitat range of species into adjacent B.A.s. Reefs complicate the usual B.A. profile by introducing distinct sheltered and turbulent water environments. These characteristics may have applicability in interpretation of islands throughout the Palaeozoic record.