11th ICRS Abstract book - Nova Southeastern University

11th ICRS Abstract book - Nova Southeastern University 11th ICRS Abstract book - Nova Southeastern University

24.12.2012 Views

Oral Mini-Symposium 2: Biotic Response to Ancient Environmental Change in Indo-Pacific Coral Reefs 2-1 Hopping Hotspots: Global Shifts in Marine Biodiversity Willem RENEMA* 1 , David BELLWOOD 2 , John PANDOLFI 3 , JC BRAGA 4 , K BROMFIELD 3 , R HALL 5 , KG JOHNSON 6 , Peter LUNT 7 , CP MEYER 8 , L MCMONAGLE 9 , RJ MORLEY 10 , A. O'DEA 11 , John TODD 6 , FP WESSELINGH 12 , MEJ WILSON 13 1 Nationaal Natuurhistorisch Museum Naturalis, Leiden, Netherlands, 2 2School of Marine and Tropical Biology, JCU, Townsville, Australia, 3 Centre for Marine Studies, Brisbane, Australia, 4 Universidad de Granada, Granada, Spain, 5 SE Asia Research Group, London, United Kingdom, 6 NHM, London, United Kingdom, 7 Murphy Oil, Kuala Lumpur, Malaysia, 8 UC Berkeley, San Francisco, CA, 9 University of Durham, Durham, United Kingdom, 10 Palynova, Cambridge, United Kingdom, 11 STRI, Panama, Panama, 12 NNM Naturalis, Leiden, Netherlands, 13 Curtin University, Perth, Australia Hotspots are a dominant feature of global biodiversity patterns. Many coral reef groups reach their greatest diversity here . Recent fossil and molecular evidence reveal at least three marine biodiversity hotspots during the past 50 million years. These hotspots have moved across almost half the globe, with their timing and locations coinciding with major tectonic events. The birth and death of successive hotspots highlights the link between environmental change and biodiversity patterns. The molecular and fossil evidence from a range of taxa rejects the notion of Pleistocene origins of the modern marine IAA fauna and flora, and point to the presence of a high diversity of extinct and extant lineages from at least the Miocene onwards. Fossil data further establish that the IAA has not always been the centre of marine biodiversity, but that earlier ‘centers of marine biodiversity’ occurred in at least two additional places during the past 50 Million years. The future of modern biodiversity hotspots can now be placed in a historical context. 2-2 Evolution Of Carbonate Factories For The Last 100 Million Years Based On Investigations On Shallow-Water Carbonate Deposits On Seamounts in The Northwestern Pacific Ocean Yasufumi IRYU* 1 , Hideko TAKAYANAGI 1 , Tsutomu YAMADA 1 , Motoyoshi ODA 1 , Tokiyuki SATO 2 , Shun CHIYONOBU 1 , Akira NISHIMURA 3 , Tsutomu NAKAZAWA 3 , Satoshi SHIOKAWA 4 1 Institute of Geology and Paleontology, Graduate School of Science, Tohoku University, Sendai, Japan, 2 Institute of Applied Earth Sciences, Faculty of Engineering and Resource Science, Akita University, Akita, Japan, 3 AIST (Advanced Industrial Science and Technology ), Tsukuba, Japan, 4 JOGMEC (Japan Oil, Gas and Metals National Corporation), Kawasaki, Japan Evolution of carbonate factories for the last 100 million years were delineated by investigating lithology, biotic and abiotic compositions, and depositional ages of shallow-water carbonates collected from 25 sites on 21 seamounts in 6 sea areas (Amami Plateau, Daito Ridge, Oki-Daito Ridge, Urdaneta Plateau, Kyushu-Palau Ridge, and Ogasawara Plateau) in the northwestern Pacific Ocean. There are significant differences among Cretaceous, Eocene, and Oligocene to Pleistocene shallow-water carbonates. The shallow-water carbonate deposits examined in the present study can be roughly divided into three types based on their composition: Cretaceous, Eocene, and Oligocene to Pleistocene types. The Cretaceous type is characterized by abundant occurrence of rudists, microencrusters, solenoporacean algae, and calcareous sponges. The Eocene type includes shallow-water carbonates predominated by Halimeda or nummulitid and discocyclinid larger foraminifers. The Oligocene to Pleistocene type includes abundant corals, nongeniculate and geniculate coralline algae, and miogypsinid, lepidocyclinid, and amphisteginid larger foraminifers. These indicate that carbonate factories comparable with modern coral reefs were initiated in the Oligocene, which corresponds to the timing of the transition from Calcite II to Aragonite III. These changes in the composition of the shallowwater carbonates from the Cretaceous onward is in accordance with those shown in previous studies, which have been considered to reflect a shift in seawater chemistry. Our investigation shows that large amounts of shallow-water carbonates were deposited on the seamounts in Oligocene, although it was a relatively cool period in the Cenozoic. Whereas Early Miocene shallow-water carbonates are limited, although it was a relatively warm period. These suggest that deposition of shallow-water carbonates on seamounts in the northwestern Pacific Ocean was not necessarily controlled by climatic conditions but related with volcanism and tectonics which served foundations for reef/carbonate-platform formation. 2-3 The Influence Of Global And Regional Environmental Change On Cenozoic Carbonates in The Indo-Pacific Moyra WILSON* 1 1 Applied Geology, Curtin University, Perth, Australia The SE Asian carbonate record allows insight into the poorly known response of equatorial marine systems to regional and global change during the Cenozoic. There is a marked change from larger benthic foraminifera to corals as dominant producers in SE Asia around the Oligo- Miocene boundary. The Early Miocene acme of coral development in SE Asia lags Oligocene coral development in the Caribbean and Mediterranean. Changing CO2, oceanography, nutrient input and precipitation patterns are inferred to be the main cause of this lag. Moderate, although falling level of CO2, Ca 2+ and Ca\Mg when combined with the reduced salinities in humid equatorial waters probably all contributed to reduced aragonite saturation hindering reefal development compared with warm more arid regions during the Oligocene. By the Early Miocene, atmospheric CO2 levels had fallen to pre-industrial levels. Although this was a relative arid phase globally, in SE Asia palynological evidence indicates the Early Miocene experienced everwet, but more stable and less seasonal conditions than periods before or after. Tectonic convergence truncated deep through-flow of cool nutrient-rich currents from the Pacific to Indian Ocean around the beginning of the Miocene, thereby directly, and perhaps indirectly (though less seasonal conditions) reducing nutrients. Aragonitic reefs were promoted where previously the waters had been more acidic, more mesotrophic, more turbid, and less aragonite saturated. Extensive reefal development resulted in an order of magnitude expansion of shallow carbonate areas through buildups and pinnacle reefs in the Early Miocene. Tectonics via increased habitat partitioning and reducing distances to other coral-rich regions may also have contributed to enhanced reefal development. Implications of this study are that with anthropogenically induced environmental changes it will be the diverse reefs of SE Asia that are likely to be amongst the first and hardest hit as oceanic aragonite saturation decreases and terrestrial nutrient runoff increases. 2-4 Scleractinian Coral Diversity in The Oligocene Of Sabah, Borneo. Laura MCMONAGLE* 1,2 1 Earth Sciences, Durham University, Durham, United Kingdom, 2 Palaeontology, Natural History Museum, London, London, United Kingdom The modern Indo-West Pacific is characterised by the highest global species diversity in reefcorals and associated biota, but the origins and long-term history of this important biodiversity hotspot remain poorly studied, with most work on the corals derived from collections made in the late 19th Century. The extant biota may have appeared during a diversification event that took place slightly before the Oligocene-Miocene boundary, marked by a change in the style of carbonate deposition in the region. This may also have coincided with a reduction in the deepwater throughflow between the Pacific and Indian Oceans and marine incursions in the area. To better constrain the timing, magnitude, and environmental context for this diversification, a previously undescribed reef-coral fauna has been documented from extensive new collections taken from Oligocene patch-reef facies in the Gomantong Formation of Sabah, Malaysia. Study of nannofossil assemblages suggests that sections range from biozone NP23 (Early Oligocene) to NP25 (Late Oligocene), with the majority falling within nannofossil zone NP24 (late Early to early Late Oligocene). This study has more than doubled the number of coral species previously known from the Oligocene of Borneo, and suggests that the apparent paucity of Paleogene corals from SE Asia could be a result of sampling bias, rather than true lack of diversity. These results show that coral diversification was already underway by the Early Oligocene, rather than occurring at the Oligocene/Miocene boundary. This would indicate that if changes in the Indonesian Throughflow caused increased diversification, then these changes occurred earlier than has so far been suggested. Alternatively it could mean that other factors controlled reefcoral diversification in the Indo-West Pacific during the Oligocene. 9

Oral Mini-Symposium 2: Biotic Response to Ancient Environmental Change in Indo-Pacific Coral Reefs 2-5 Differential response of Southeast Asian and Caribbean reef ecosystems to global environmental change during the Oligocene/Miocene Transition Kenneth JOHNSON* 1 1 Palaeontology Department, Natural History Museum London, London, United Kingdom The paleoceanographic record contains several intervals during the Cenozoic in which apparently rapid global change in the open ocean also had effects on tropical coastal marine ecosystems. One example is the Oligocene/Miocene transition (OMT) that occurred approximately 25-20 Ma. This interval is associated with the termination of a Late Oligocene warm interval by a 'snap' glaciation and development of a stable globallycooler climate phase during the Early Miocene. These changes are contemporaneous with the initial constriction of deep water connections across the Indonesian Throughflow as Australia collided with Eurasia. A database of specimen-based occurrences of reef corals was assembled from both new and existing collections to document the history of coral diversity and the regional extent of reef development in the Caribbean and Southeast Asia during the OMT. All specimens were examined to verify taxonomic identifications and collections were placed within a consistent stratigraphic framework. During the Late Oligocene there was widespread reef building by a moderately diverse biota in the Caribbean. Both diversity and the extent of reef building had crashed by the Early Miocene in response to increased regional surface productivity. In contrast, there was little reef building and low diversity of reef builders in the Late Oligocene of SE Asia. Instead both reef-building and reef-coral diversity in the region increased during the OMT. Therefore, the effects of global change caused a decline in reef-coral diversity and reef-building in the Caribbean but an increase in reef building and radiation of reef-corals in Southeast Asia. The fact that regional biotic responses were out of phase in Southeast Asia and the Caribbean indicates that the ecological signal of global environmental change is modulated by local to regional-scale biotic and oceanographic history. 2-6 Indo-Pacific Coral Growth Forms Through The Miocene To The Pliocene Kate BROMFIELD* 1 , John PANDOLFI 1 1 University of Queensland, Brisbane, Australia One of the most intriguing questions for the evolution of the modern Indo-Pacific coral reef fauna is the antiquity of modern branching-dominated coral assemblages. The Miocene (21-6 Ma) of the Indo-Pacific is a period of pronounced first occurrences of reef coral species, and a complete reorganisation of coral communities has been proposed; from a Miocene fauna dominated by massive growth forms, to reef domination by corals with branching morphologies in the Pliocene. Many genera of modern reef corals (order Scleractinia), are thought to date from the early Pliocene (5.6-3.2 Ma), around 5.3 Ma. This study tested the Miocene/Pliocene growth form transition hypothesis from uplifted reefs at three sites along a longitudinal gradient: Vanua Balavu (16.9-6.7 Ma) in Fiji; New Britain (14.8-12.3 Ma) in Papua New Guinea; and Selayar (5.8-1.4 Ma) in Indonesia. The collection includes 121 coral species, fifteen of which are new, though now extinct. The highest percentage (25%) of newly recorded, extinct species occurred in the late Pliocene (5.8-3.4 Ma) reef deposits of Selayar. Newly described extinct species from the Miocene deposits of Fiji and Papua New Guinea averages 6%. The data shows no significant change in either the relative abundance or the presence versus absence of growth forms among the three sites and times. Miocene assemblages contained 27% abundance of branching individuals and the Pliocene contained 23%. This challenges the premise that reefs underwent a transition from those dominated by massive forms to those dominated by branching forms during this period. However, our study corroborates the previously proposed model of an origination event in reefal corals in the early Pliocene. 2-7 Biodiversity And Biogeography Of Mollusca During The Cenozoic: A Database Approach To The Assessment Of Spatial Patterns And Their Relationship To Global Environmental Change Austin HENDY* 1 1 Geology and Geophysics, Yale University, New Haven, CT A focal point in the Phanerozoic trajectory of global biodiversity has been its apparent rapid increase since the end-Cretaceous extinction. The interval stimulates additional interest through the availability of chronologically well-constrained information on changing global paleoenvironments. This knowledge aids understanding of how the Cenozoic diversification of marine invertebrate faunas was influenced by developing global paleogeography, major tectonic shifts, and related climatic transitions. An extensive dataset (http://paleodb.org) of fossil molluscan occurrences permits analysis of how spatial components of global biodiversity vary through the Cenozoic, specifically how faunas are partitioned biogeographically and how these biogeographic units relate to one another. On a global scale, sampling-standardized diversity appears to have increased at most only 50% over the course of the Eocene-Pleistocene, showing small drops during the Early Oligocene and a slight decline since the Middle Miocene. Nevertheless, there is remarkable stage-to-stage independence in the shape of diversity curves at the regional scale, reflecting both regionally distinct environmental controls and variable data quality, related to reduced sample size. A multivariate analysis of global biogeography reveals that provinciality has increased only slightly during this interval, peaking in the Plio-Pleistocene, although this patterns is strongly influence by spatial sampling intensity. A strengthening latitudinal gradient of diversity is observed through the Neogene, reflecting an increased in not only tropical diversity but also a decline in the richness of faunas from temperate and polar latitudes. Fluctuations in regional endemism and biogeographic similarity between regions appear related to the opening and closing of major oceanic gateways. Nevertheless some aspects of global and regional diversity patterns reflect Cenozoic-scale climatic transitions, expressed by an Early Oligocene decline. The influence of deteriorating global climate through the Neogene appears to be offset by a steepening latitudinal diversity gradient and an associated increased late Neogene provinciality. 2-8 Molluscan Biodiversity in Shallow Carbonate Platforms (Indonesia) Frank WESSELINGH* 1 1 Geology, Naturalis, Leiden, Netherlands A pilot study into the spatial distribution of mollusc taxa in the shallow carbonate platform, the Spermonde Archipelago (Sulawesi, Indonesia) is presented. The very high species numbers and the unresolved taxonomical status of the far majority of these mollusc species should cripple such a documentation. However, by using taxa groups with an as low as possible taxonomic rank, very clear distribution patterns and associations are found. This study shows that molluscan associations probably are a very good tool for study of communities, facies and biodiversity in ancient carbonate platform settings as well. 10

Oral Mini-Symposium 2: Biotic Response to Ancient Environmental Change in Indo-Pacific Coral Reefs<br />

2-5<br />

Differential response of Southeast Asian and Caribbean reef ecosystems to global<br />

environmental change during the Oligocene/Miocene Transition<br />

Kenneth JOHNSON* 1<br />

1 Palaeontology Department, Natural History Museum London, London, United Kingdom<br />

The paleoceanographic record contains several intervals during the Cenozoic in which<br />

apparently rapid global change in the open ocean also had effects on tropical coastal<br />

marine ecosystems. One example is the Oligocene/Miocene transition (OMT) that<br />

occurred approximately 25-20 Ma. This interval is associated with the termination of a<br />

Late Oligocene warm interval by a 'snap' glaciation and development of a stable globallycooler<br />

climate phase during the Early Miocene. These changes are contemporaneous with<br />

the initial constriction of deep water connections across the Indonesian Throughflow as<br />

Australia collided with Eurasia. A database of specimen-based occurrences of reef corals<br />

was assembled from both new and existing collections to document the history of coral<br />

diversity and the regional extent of reef development in the Caribbean and Southeast Asia<br />

during the OMT. All specimens were examined to verify taxonomic identifications and<br />

collections were placed within a consistent stratigraphic framework. During the Late<br />

Oligocene there was widespread reef building by a moderately diverse biota in the<br />

Caribbean. Both diversity and the extent of reef building had crashed by the Early<br />

Miocene in response to increased regional surface productivity. In contrast, there was<br />

little reef building and low diversity of reef builders in the Late Oligocene of SE Asia.<br />

Instead both reef-building and reef-coral diversity in the region increased during the<br />

OMT. Therefore, the effects of global change caused a decline in reef-coral diversity and<br />

reef-building in the Caribbean but an increase in reef building and radiation of reef-corals<br />

in Southeast Asia. The fact that regional biotic responses were out of phase in Southeast<br />

Asia and the Caribbean indicates that the ecological signal of global environmental<br />

change is modulated by local to regional-scale biotic and oceanographic history.<br />

2-6<br />

Indo-Pacific Coral Growth Forms Through The Miocene To The Pliocene<br />

Kate BROMFIELD* 1 , John PANDOLFI 1<br />

1 <strong>University</strong> of Queensland, Brisbane, Australia<br />

One of the most intriguing questions for the evolution of the modern Indo-Pacific coral<br />

reef fauna is the antiquity of modern branching-dominated coral assemblages. The<br />

Miocene (21-6 Ma) of the Indo-Pacific is a period of pronounced first occurrences of reef<br />

coral species, and a complete reorganisation of coral communities has been proposed;<br />

from a Miocene fauna dominated by massive growth forms, to reef domination by corals<br />

with branching morphologies in the Pliocene. Many genera of modern reef corals (order<br />

Scleractinia), are thought to date from the early Pliocene (5.6-3.2 Ma), around 5.3 Ma.<br />

This study tested the Miocene/Pliocene growth form transition hypothesis from uplifted<br />

reefs at three sites along a longitudinal gradient: Vanua Balavu (16.9-6.7 Ma) in Fiji;<br />

New Britain (14.8-12.3 Ma) in Papua New Guinea; and Selayar (5.8-1.4 Ma) in<br />

Indonesia.<br />

The collection includes 121 coral species, fifteen of which are new, though now extinct.<br />

The highest percentage (25%) of newly recorded, extinct species occurred in the late<br />

Pliocene (5.8-3.4 Ma) reef deposits of Selayar. Newly described extinct species from the<br />

Miocene deposits of Fiji and Papua New Guinea averages 6%. The data shows no<br />

significant change in either the relative abundance or the presence versus absence of<br />

growth forms among the three sites and times. Miocene assemblages contained 27%<br />

abundance of branching individuals and the Pliocene contained 23%. This challenges the<br />

premise that reefs underwent a transition from those dominated by massive forms to<br />

those dominated by branching forms during this period. However, our study corroborates<br />

the previously proposed model of an origination event in reefal corals in the early<br />

Pliocene.<br />

2-7<br />

Biodiversity And Biogeography Of Mollusca During The Cenozoic: A Database Approach<br />

To The Assessment Of Spatial Patterns And Their Relationship To Global Environmental<br />

Change<br />

Austin HENDY* 1<br />

1 Geology and Geophysics, Yale <strong>University</strong>, New Haven, CT<br />

A focal point in the Phanerozoic trajectory of global biodiversity has been its apparent rapid<br />

increase since the end-Cretaceous extinction. The interval stimulates additional interest through<br />

the availability of chronologically well-constrained information on changing global<br />

paleoenvironments. This knowledge aids understanding of how the Cenozoic diversification of<br />

marine invertebrate faunas was influenced by developing global paleogeography, major tectonic<br />

shifts, and related climatic transitions.<br />

An extensive dataset (http://paleodb.org) of fossil molluscan occurrences permits analysis of<br />

how spatial components of global biodiversity vary through the Cenozoic, specifically how<br />

faunas are partitioned biogeographically and how these biogeographic units relate to one<br />

another. On a global scale, sampling-standardized diversity appears to have increased at most<br />

only 50% over the course of the Eocene-Pleistocene, showing small drops during the Early<br />

Oligocene and a slight decline since the Middle Miocene. Nevertheless, there is remarkable<br />

stage-to-stage independence in the shape of diversity curves at the regional scale, reflecting<br />

both regionally distinct environmental controls and variable data quality, related to reduced<br />

sample size. A multivariate analysis of global biogeography reveals that provinciality has<br />

increased only slightly during this interval, peaking in the Plio-Pleistocene, although this<br />

patterns is strongly influence by spatial sampling intensity. A strengthening latitudinal gradient<br />

of diversity is observed through the Neogene, reflecting an increased in not only tropical<br />

diversity but also a decline in the richness of faunas from temperate and polar latitudes.<br />

Fluctuations in regional endemism and biogeographic similarity between regions appear related<br />

to the opening and closing of major oceanic gateways. Nevertheless some aspects of global and<br />

regional diversity patterns reflect Cenozoic-scale climatic transitions, expressed by an Early<br />

Oligocene decline. The influence of deteriorating global climate through the Neogene appears<br />

to be offset by a steepening latitudinal diversity gradient and an associated increased late<br />

Neogene provinciality.<br />

2-8<br />

Molluscan Biodiversity in Shallow Carbonate Platforms (Indonesia)<br />

Frank WESSELINGH* 1<br />

1 Geology, Naturalis, Leiden, Netherlands<br />

A pilot study into the spatial distribution of mollusc taxa in the shallow carbonate platform, the<br />

Spermonde Archipelago (Sulawesi, Indonesia) is presented. The very high species numbers and<br />

the unresolved taxonomical status of the far majority of these mollusc species should cripple<br />

such a documentation. However, by using taxa groups with an as low as possible taxonomic<br />

rank, very clear distribution patterns and associations are found. This study shows that<br />

molluscan associations probably are a very good tool for study of communities, facies and<br />

biodiversity in ancient carbonate platform settings as well.<br />

10

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