scholarly journals Late Ordovician deep-water brachiopod fauna from Raheen, Waterford Harbour, Ireland

2017 ◽  
Vol 35 (1) ◽  
pp. 1-18
Author(s):  
Matthew A. Parkes
2005 ◽  
Vol 96 (4) ◽  
pp. 317-325 ◽  
Author(s):  
Yves Candela

ABSTRACTComparisons of the Caradoc assemblages with North American biofacies indicate that the Bardahessiagh Formation was deposited during a transgressive regime, which peaked with the presence of a typical Sericoidea association (member (II)). These diverse and exceptionally preserved faunas lived below the storm-wave base. The assemblages also contained a shallower water brachiopod component typical of transition zone environments or above, which may have been transported during periods of instability. A deep-water regime (BAs 4 to 4–5) through the Rawtheyan occurs with the deposition of the Killey Bridge Formation, which yielded a diverse brachiopod fauna including Bimuria, Chonetoidea and Christiania. The Rawtheyan assemblage also contains a shallower water component. Representatives of the deep-water Proboscisambon assemblage occur in middle parts of the Tirnaskea Formation. This distinctive low-diversity assemblage yields small, thin-shelled brachiopods including Dedzetina, Sericoidea, Protozyga and Proboscisambon. The upper parts of the Tirnaskea Formation yielded the low diversity, shallow water (BA 3) Hirnantia fauna, which is characterised by the presence of Eostropheodonta, which is a key form of the fauna, Dysprosorthis and the absence of Hirnantia. As a whole the changing brachiopod biofacies monitor environmental fluctuations, on part of the Laurentian margin, driven mainly by eustatic and tectonic events.


Lethaia ◽  
2019 ◽  
Vol 53 (3) ◽  
pp. 332-344 ◽  
Author(s):  
Bing Huang ◽  
David A. T. Harper ◽  
Hanghang Zhou ◽  
Jiayu Rong

2017 ◽  
Vol 35 ◽  
pp. 1
Author(s):  
David A.T. Harper ◽  
Matthew A. Parkes ◽  
Zhan Ren-Bin

2009 ◽  
Vol 33 (2) ◽  
pp. 163-183 ◽  
Author(s):  
Zhong-Qiang Chen ◽  
G. R. Shi ◽  
Yongqun Gao ◽  
Jinnan Tong ◽  
Fengqing Yang ◽  
...  

Lethaia ◽  
2006 ◽  
Vol 39 (1) ◽  
pp. 79-90 ◽  
Author(s):  
Z. Q. CHEN ◽  
G. R. SHI ◽  
FENG-QING YANG ◽  
YONG-QUAN GAO ◽  
JINNAN TONG ◽  
...  

2012 ◽  
Vol 149 (6) ◽  
pp. 964-988 ◽  
Author(s):  
ALAN W. OWEN ◽  
DAVID L. BRUTON

AbstractThe trilobite fauna of the upper Ordovician (middle Katian) Pyle Mountain Argillite comprises a mixture of abundant mesopelagic cyclopygids and other pelagic taxa and a benthic fauna dominated by trilobites lacking eyes. Such faunas were widespread in deep water environments around Gondwana and terranes derived from that continent throughout Ordovician time but this is the only known record of such a fauna from North America and thus from Laurentia. It probably reflects a major sea level rise (the ‘Linearis drowning events’) as does the development of coeval cyclopygid-dominated deep water trilobite faunas in terranes that were marginal to Laurentia and are now preserved in Ireland and Scotland. The Pyle Mountain Argillite trilobite fauna occurs with a deep water Foliomena brachiopod fauna and comprises 22 species. Pelagic trilobites (mostly cyclopygids) constitute 36% of the preserved sclerites, and 45% of the fauna is the remains of trilobites lacking eyes, including one new species, Dindymene whittingtoni sp. nov. Three species of cyclopygid are present, belonging in Cyclopyge, Symphysops and Microparia (Heterocyclopyge). Cyclopygids are widely thought to have been stratified in the water column in life and thus their taxonomic diversity reflects the relative depths of the sea-beds on which their remains accumulated. A tabulation of middle and upper Katian cyclopygid-bearing faunas from several palaeoplates and terranes arranged on the basis of increasing numbers of cyclopygid genera allows an assessment of the relative depth ranges of the associated benthic taxa. The Pyle Mountain Argillite fauna lies towards the deeper end of this depth spectrum.


2015 ◽  
Vol 89 (6) ◽  
pp. 1068-1075 ◽  
Author(s):  
Jack W. Kallmeyer ◽  
William I. Ausich

AbstractA new crinoid association reported from the Kope Formation (Katian, Ordovician) of northern Kentucky and southwestern Ohio changes the model for facies distribution of crinoids along an Ordovician onshore-offshore depth gradient. Glyptocrinus nodosus n. sp., Plicodendrocrinus casei (Meek, 1871), Cincinnaticrinus varibrachialis (Warn and Strimple, 1977), and Ectenocrinus simplex (Hall, 1847) are reported from a suspension-feeding assemblage with 26 taxa. This assemblage developed above an argillaceous packstone with most of the fossils preserved in shale. The fauna was comprised principally of secondary epifaunally tiered suspension feeders, deposit feeders, and predators. This is the first reported occurrence of Glyptocrinus Hall, 1847 and Plicodendrocrinus Brower, 1995 from the Kope Formation (lower Cincinnatian), and Glyptocrinus is represented by a new species, G. nodosus. Also, this is the first report of pinnulate camerate crinoids from the deep-water facies of the Kope Formation. Thus, deep-water Cincinnatian crinoid assemblages were comprised of disparids, cladids, and camerates; and the assemblage was characterized by a variety of filtration fan types for acquisition of resources.


Author(s):  
L. M. E. McCobb ◽  
L. E. Popov

ABSTRACTTwo trilobite faunas of Late Ordovician (Katian) age are described from the Mayatas Formation in the Stepnyak region of north-central Kazakhstan. The older, oligotaxic fauna derives from flanks of a carbonate build-up, and is dominated by numerous Sphaerexochus specimens. Amphilichas is also relatively common, with Pliomerina and indeterminate asaphids present as rare components. The overlying unit of siliceous argillites contains a different assemblage, representing the raphiophorid biofacies and comprising seven genera. The poorly preserved fauna is dominated by blind trilobites (a new genus of trinucleid, the three-segmented raphiophorid Pseudampyxina, Malongullia?, Lonchodomas and Arthrorhachis) and at least two species of large-eyed Telephina, suggesting that they occupied the disphotic zone in deep water offshore. A single cranidium of the odontopleurid Primaspis is also present. The trinucleid, Iputaspis stepnyakensis gen. et sp. nov., has an unusual pit arrangement, with E1 and E2 aligned in sulci and all I arcs irregularly arranged. The Atansor area is located within the Stepnyak tectonostratigraphical unit, which probably represented an Ordovician active margin of the Kalmykkol–Kokchetav Microplate. Some of the genera represented in the faunas have affinities with Australia and South China and, also, there is a possible link to European peri-Gondwana.


2017 ◽  
Vol 13 (9) ◽  
pp. 20170400 ◽  
Author(s):  
Seth Finnegan ◽  
Christian M. Ø. Rasmussen ◽  
David A. T. Harper

Mass extinction events are recognized by increases in extinction rate and magnitude and, often, by changes in the selectivity of extinction. When considering the selective fingerprint of a particular event, not all taxon extinctions are equally informative: some would be expected even under a ‘background’ selectivity regime, whereas others would not and thus require special explanation. When evaluating possible drivers for the extinction event, the latter group is of particular interest. Here, we introduce a simple method for identifying these most surprising victims of extinction events by training models on background extinction intervals and using these models to make per-taxon assessments of ‘expected’ risk during the extinction interval. As an example, we examine brachiopod genus extinctions during the Late Ordovician Mass Extinction and show that extinction of genera in the deep-water ‘ Foliomena fauna’ was particularly unexpected given preceding Late Ordovician extinction patterns.


Author(s):  
David A. T. Harper

ABSTRACTDiverse and abundant brachiopod faunas, associated with unstable outer shelf and slope environments, occur through the Upper Ardmillan Group (upper Caradoc–upper Ashgill) in the Girvan district of SW Scotland. Representatives of the deep-water Foliomena fauna occur intermittently throughout the group, appearing in both the Whitehouse and Drummuck subgroups. This distinctive assemblage of small, thin-shelled brachiopods, including Dedzetina, Christiania, Cyclospira and Foliomena itself, first appeared in South China during the early Caradoc but had colonised the Laurentian margins by the late Caradoc. Within the upper Caradoc–lower Ashgill Whitehouse Subgroup, the Foliomena fauna is interbedded with a variety of other less cosmopolitan deep-water assemblages including the Onniella–Skenidioides and Lingulella–Trimurellina associations. Shallower-water environments in the middle Ashgill Lower Drummuck Subgroup hosted the Fardenia–Eopholidostrophia association in sands, and the Christiania-Leptaena association in muds and silts. The remarkable Lady Burn Starfish Beds in the upper part of the group contain a variety of brachiopod-dominated assemblages including the Eochonetes and Plaesiomys-Schizophorella associations, transported from various shelf locations, within a very diverse mid-Ashgill biota. Nevertheless, elements of the Foliomena fauna persisted to near the top of the Drummuck Subgroup, occurring as rare assemblages in more muddy and silty facies. The upper Ashgill High Mains Formation contains abundant elements of the terminal Ordovician Hirnantia fauna including Eostropheodonta, Hindella and Hirnantia itself, but also some taxa more typical of the Laurentian Edgewood Province. As a whole, the changing brachiopod biofacies monitor environmental fluctuations, on part of the Laurentian margin, driven by mainly eustatic and tectonic events.


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