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GeoRef Categories
Era and Period
Epoch and Age
Book Series
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Calcarina spengleri
ON THE IDENTITY OF CALCARINA SPENGLERI (GMELIN 1791)
Distribution of Calcarina spengleri (Gmelin) and Calcarina mayori Cushm...
Global distribution of Calcarina spengleri (Gmelin), Calcarina mayori C...
BENTHIC FORAMINIFERA OF THE FAMILY CALCARINIDAE FROM GREEN ISLAND REEF, GREAT BARRIER REEF PROVINCE
Diversity and Distribution of Living Larger Benthic Foraminifera from Coral Reef Environments, South Andaman Island, India
Comparisons of apertures of the simple trochospiral calcarinids. 1 Neorot...
Scale bars = 00 μm, that for fig. 1 applies to figs. 1–8 and that for fig. ...
Scale bars = 200 μm, that for fig. 1 applies to figs. 1–4, 6–13, that for f...
Scale bars of figure 1–4, 9 represent 0.5 mm, scale bars of figure 5–8, ...
Scale bars represent 0.5 mm unless stated otherwise. 1–7 & 9–18 scannin...
The Effects of Time-Averaging and Taphonomy on the Identification of Reefal Sub-Environments using Larger Foraminifera: Apo Reef, Mindoro, Philippines
NEOROTALIA LEEUWINENSIS : A NEW SPECIES OF CALCARINID FORAMINIFERA LIVING AT THE SOUTHERN EXTREME OF THEIR BIOGEOGRAPHICAL RANGE, SOUTHWEST AUSTRALIA
REEF FORAMINIFERA AS BIOINDICATORS OF CORAL REEF HEALTH: LOW ISLES REEF, NORTHERN GREAT BARRIER REEF, AUSTRALIA
EPIPHYTIC FORAMINIFERAL ASSEMBLAGES ON MACROALGAE IN REEFAL ENVIRONMENTS OF NEW CALEDONIA
Arthur Earland: the foraminiferal slide collection and correspondence at the University of St Andrews, Scotland
Sedimentary Belts in Lagoon of Kapingamarangi Atoll
Growth and Fecundity of Marginopora Vertebralis and Amphistegina Lobifera in Laboratory Culture
BENTHIC FORAMINIFERA IN A LARGE INDO-PACIFIC CORAL REEF AQUARIUM
Biological Evolution of Southeast Asian Carbonates, Based on Their Microfossil Content
A new compilation of data suggests aragonitic coral reefs were already common in Southeast Asia by the mid-Oligocene. A gradual change from calcite to aragonite seas through the Oligocene and early Miocene appears to be related to a gradual expansion of the importance of scleractinia, along with green algae and mollusks, and an associated decline in the abundance of calcitic larger foraminifera. The larger foraminifera had been important rock-forming bioclasts in the early part of the early Miocene, but were a minor component of carbonate faunas by the end of the middle Miocene. This gradual decline in abundance included a few extinction events that reduced diversity, and these extinctions appear to correlate with periods of tectonic change. The K-selection evolutionary pressure impacted carbonate facies, but foraminifera maintained their taxonomic diversity until the abrupt faunal extinctions. Changes in sea-surface temperature, or the regional change from seasonal to ever-wet climate, do not appear to have impacted larger foraminiferal diversity or caused extinctions, only modified their latitudinal range. Some extinction events can be recognized across the whole Tethys Ocean, as can some of the times of tectonic activity and possible climate change. These correlations tentatively point to a link between large-scale changes in plate motion, oceanography, and foraminiferal extinctions. In contrast, the change from seasonal to ever-wet conditions around the Oligo–Miocene boundary around the South China Sea does not appear to have been caused by a wider tectonic event, and this event does not impact larger foraminifera diversity. A combined tectonic unconformity and mass extinction of larger foraminifera in middle middle Miocene times might have been due to the plate tectonic constriction of a throughflow between the Pacific and Indian Oceans.