Wolfgang Kiessling

The Pace of Shifting Climate in Marine and Terrestrial Ecosystems

Ecologically relevant measures of contemporary global climate change can predict species distributions and vulnerabilities. Climate change challenges organisms to adapt or move to track changes in environments in space and time. We used two measures of thermal shifts from analyses of global temperatures over the past 50 years to describe the pace of climate change that species should track: the velocity of climate change (geographic shifts of isotherms over time) and the shift in seasonal timing of temperatures. Both measures are higher in the ocean than on land at some latitudes, despite slower ocean warming. These indices give a complex mosaic of predicted range shifts and phenology changes that deviate from simple poleward migration and earlier springs or later falls. They also emphasize potential conservation concerns, because areas of high marine biodiversity often have greater velocities of climate change and seasonal shifts.

The Chicxulub Asteroid Impact and Mass Extinction at the Cretaceous-Paleogene Boundary

The Fall of the Dinosaurs According to the fossil record, the rule of dinosaurs came to an abrupt end ∼65 million years ago, when all nonavian dinosaurs and flying reptiles disappeared. Several possible mechanisms have been suggested for this mass extinction, including a large asteroid impact and major flood volcanism. Schulte et al. (p. 1214) review how the occurrence and global distribution of a global iridium-rich deposit and impact ejecta support the hypothesis that a single asteroid impact at Chicxulub, Mexico, triggered the extinction event. Such an impact would have instantly caused devastating shock waves, a large heat pulse, and tsunamis around the globe. Moreover, the release of high quantities of dust, debris, and gases would have resulted in a prolonged cooling of Earths surface, low light levels, and ocean acidification that would have decimated primary producers including phytoplankton and algae, as well as those species reliant upon them. The Cretaceous-Paleogene boundary ~65.5 million years ago marks one of the three largest mass extinctions in the past 500 million years. The extinction event coincided with a large asteroid impact at Chicxulub, Mexico, and occurred within the time of Deccan flood basalt volcanism in India. Here, we synthesize records of the global stratigraphy across this boundary to assess the proposed causes of the mass extinction. Notably, a single ejecta-rich deposit compositionally linked to the Chicxulub impact is globally distributed at the Cretaceous-Paleogene boundary. The temporal match between the ejecta layer and the onset of the extinctions and the agreement of ecological patterns in the fossil record with modeled environmental perturbations (for example, darkness and cooling) lead us to conclude that the Chicxulub impact triggered the mass extinction.

Phanerozoic trends in the global diversity of marine invertebrates.

It has previously been thought that there was a steep Cretaceous and Cenozoic radiation of marine invertebrates. This pattern can be replicated with a new data set of fossil occurrences representing 3.5 million specimens, but only when older analytical protocols are used. Moreover, analyses that employ sampling standardization and more robust counting methods show a modest rise in diversity with no clear trend after the mid-Cretaceous. Globally, locally, and at both high and low latitudes, diversity was less than twice as high in the Neogene as in the mid-Paleozoic. The ratio of global to local richness has changed little, and a latitudinal diversity gradient was present in the early Paleozoic.

Geographical limits to species-range shifts are suggested by climate velocity

The reorganization of patterns of species diversity driven by anthropogenic climate change, and the consequences for humans, are not yet fully understood or appreciated. Nevertheless, changes in climate conditions are useful for predicting shifts in species distributions at global and local scales. Here we use the velocity of climate change to derive spatial trajectories for climatic niches from 1960 to 2009 (ref. 7) and from 2006 to 2100, and use the properties of these trajectories to infer changes in species distributions. Coastlines act as barriers and locally cooler areas act as attractors for trajectories, creating source and sink areas for local climatic conditions. Climate source areas indicate where locally novel conditions are not connected to areas where similar climates previously occurred, and are thereby inaccessible to climate migrants tracking isotherms: 16% of global surface area for 1960 to 2009, and 34% of ocean for the ‘business as usual’ climate scenario (representative concentration pathway (RCP) 8.5) representing continued use of fossil fuels without mitigation. Climate sink areas are where climate conditions locally disappear, potentially blocking the movement of climate migrants. Sink areas comprise 1.0% of ocean area and 3.6% of land and are prevalent on coasts and high ground. Using this approach to infer shifts in species distributions gives global and regional maps of the expected direction and rate of shifts of climate migrants, and suggests areas of potential loss of species richness.

Paleoreef maps; evaluation of a comprehensive database on Phanerozoic reefs

To get a better understanding of controls on reef development through time, we created a comprehensive database on Phanerozoic reefs. The database currently comprises 2470 reefs and contains information about geographic position/paleoposition, age, reef type, dimensions, environmental setting, paleontological and petrographical features, and reservoir quality of each buildup. Reef data were analyzed in two qualitatively different ways. The first type of analysis was by visualization of paleogeographic reef distribution maps. Five examples (Late Devonian, Early Permian, Late Triassic, Late Jurassic, middle Miocene) are presented to show the potential of paleoreef maps for paleogeographic and paleoclimatological reconstructions. The second type of analysis was a numerical processing of coded reef characteristics to realize major trends in reef evolution and properties of reef carbonates. The analysis of paleolatitudinal reef distributions through time shows pronounced asymmetries in some time slices, probably related to climatic asymmetries rather than controlled by plate tectonic evolution alone. The dominance of particular reef builders through time suggests that there are seven cycles of Phanerozoic reef development. First curves for the Phanerozoic distribution of bioerosion in reefs, bathymetric setting, and debris potential of reefs are presented. The observed pattern in the temporal and spatial distribution of reefs with reservoir quality may assist in hydrocarbon exploration. Statistical tests on the dependencies of reefal reservoir quality suggest that large size, high debris potential, low paleolatitude, high amount of marine aragonite cement, and a platform/shelf edge setting favor reservoir quality. Reefal reservoirs are significantly enhanced in times of high evaporite sedimentation, elevated burial of organic carbon, low oceanic crust production, low atmospheric CO2 content, and cool paleoclimate, as well as when they are present in aragonite oceans.

Patterns of Phanerozoic carbonate platform sedimentation

Carbonate platforms changed substantially in spatial extent, geometry, composition and palaeogeographical distribution through the Phanerozoic. Although reef construction and carbonate platform development are intimately linked today, this was not the case for most of the Phanerozoic. Carbonate production by non-enzymatic precipitation and non-reefal organisms is mostly responsible for this decoupling. Non-reefal carbonate production was especially prolific during times of depressed reef growth, balancing losses in reef carbonate production. Palaeogeographical distribution and spatial extent of Phanerozoic carbonate platforms exhibit trends related to continental drift, evolutionary patterns within carbonate platform biotas, climatic change and, possibly, variations in ocean chemistry. Continental drift moved large Palaeozoic tropical shelf areas into higher latitudes, thereby reducing the potential size of tropical platforms. However, the combined global size of carbonate platforms shows no significant decline through the Phanerozoic, suggesting that availability of tropical shelf areas was not a major control of platform area. This is explained by the limited platform coverage of low-latitude shelves (42% maximum) and occasional high-latitude excursions of platform carbonates. We speculate that reduced tropical shelf area in the icehouse tropics forced the migration of the many carbonate-secreting organisms into higher latitudes and, where terrigenous input was sufficiently low, extensive carbonate platform could develop.

Distribution of Chicxulub ejecta at the Cretaceous-Tertiary boundary

The mineralogical, sedimentological, and geochemical information in a large database on the Cretaceous-Tertiary (K-T) boundary is used to document the distribution of impact debris derived from the Chicxulub crater. The database is coupled with a geographic information system (GIS) allowing the plotting of the information on a latest Cretaceous paleogeographic map. The database will be available in part on the internet in the near future, and contains data from 345 K-T boundary sites worldwide. However, relatively few sites are known in South America, Australia, Africa, and in the high latitudes. Major disturbances of sedimentation, such as massive debris flows, failure of platform margins, or significant erosion of Upper Cretaceous layers, occur throughout the Gulf of Mexico. Mass wasting of material also took place in the western and eastern parts of the Atlantic Ocean. Almost 100 K-T boundary sites analyzed for Ir recorded the positive anomaly; Ir is spread homogeneously throughout the world, but is diluted at proximal sites because of the high volume of sediment that was in suspension in the Gulf of Mexico after the impact. Shocked quartz is more common, and maybe larger in size west of the crater. The main advantage of the database is to provide a convenient method to manage the huge amount of data available in the literature, and to reveal patterns or characteristics of the data. The database can help refine the variables used in mathematical models and documents the origin, transport, and deposition of ejecta during a cratering event.

Reefs as Cradles of Evolution and Sources of Biodiversity in the Phanerozoic

Cradle of Diversity Is the biological diversity of reefs a result of attracting species that originated elsewhere, or are they particularly important as cradles of evolution? Kiessling et al. (p. 196; see the cover) examine a large database of fossil benthic marine organisms dating back to the Cambrian to test these questions. It seems that reefs, even in comparison to other shallow marine environments, were indeed important during the origination of new species, including ones that migrate elsewhere. Analysis of fossil evidence indicates that reefs were disproportionally important in the origination of new species. Large-scale biodiversity gradients among environments and habitats are usually attributed to a complex array of ecological and evolutionary factors. We tested the evolutionary component of such gradients by compiling the environments of the geologically oldest occurrences of marine genera and using sampling standardization to assess if originations tended to be clustered in particular environments. Shallow, tropical environments and carbonate substrates all tend to have harbored high origination rates. Diversity within these environments tended to be preferentially generated in reefs, probably because of their habitat complexity. Reefs were also prolific at exporting diversity to other environments, which might be a consequence of low-diversity habitats being more susceptible to invasions.

Testing the role of biological interactions in the evolution of mid-Mesozoic marine benthic ecosystems

Abstract Evaluating the relative importance of biotic versus abiotic factors in governing macroevolutionary patterns is a central question of paleobiology. Here, we analyzed patterns of changes in global relative abundances and diversity of ecological groups to infer the role of biological interactions as driving evolutionary forces in mid-Mesozoic macrobenthic marine ecosystems. Specifically, we tested the hypothesis of escalation, which states that macroevolutionary patterns were controlled by an increasing pressure exerted by enemies on their victims. Associated with evidence of increasing levels of predation and biogenic sediment reworking (bulldozing) is an increasing representation of predation- and disturbance-resistant groups in the fossil record. In particular, we observe increasing proportions of mobile organisms; a decline of vulnerable epifauna living freely on the substrate; and a trend toward infaunalization of the benthos. These trends were most pronounced in the paleotropics, i.e., the region where biological activity is thought to have been highest. The observation that these changes affected several biotic traits and occurred within independent clades argues against the overriding role of a single key adaptive innovation in causing shifts in ecological abundance. Also, changes in the abiotic environment cannot explain these faunal patterns because of lacking cross-correlations with physico-chemical parameters such as global sea level, climate, and seawater chemistry. We conclude that in marine benthic ecosystems of the mid Mesozoic, enemy-driven evolution, or escalation, was a plausible and important factor.

Ecological, taxonomic, and taphonomic components of the post-Paleozoic increase in sample-level species diversity of marine benthos

Abstract Biological veracity of the sharp diversity increase observed in many analyses of the post-Paleozoic marine fossil record has been debated vigorously in recent years. To assess this question for sample-level (“alpha”) diversity, we used bulk samples of shelly invertebrates, representing three major fossil groups (brachiopods, bivalves, and gastropods), to compare the Jurassic and late Cenozoic sample-level diversity of marine benthos. After restricting the data set to single-bed, whole-fauna, bulk samples (n ≥ 30 specimens) from comparable open marine siliciclastic facies, we were able to retain 427 samples (255 Jurassic and 172 late Cenozoic), with most of those samples originating from our own empirical work. Regardless of the diversity metric applied, the initial results suggest that standardized sample-level species (or genus) diversity, driven by evenness and/or richness of the most common taxa, increased between the Jurassic and late Cenozoic by at least a factor of 1.6. When the data are partitioned into the three dominant higher taxa, it becomes clear that (1) the bivalves, which dominated the samples for both time intervals, increased in sample-level diversity between the Jurassic and the late Cenozoic by a much smaller factor than the total fauna; (2) the removal of brachiopods, which were a noticeable component of the Jurassic samples, did not significantly affect standardized sample-level diversity estimates; and (3) the gastropods, which were rare in the Jurassic but common in many late Cenozoic samples, contributed notably to the increase in sample-level diversity observed between the two time intervals. Parallel to these changes, the samples revealed secular trends in ecological structure, including Jurassic to late Cenozoic increases in proportion of (1) infauna, (2) mobile forms, and (3) non-suspension-feeding organisms. These trends mostly persist when data are restricted to bivalves. Supplementary analyses indicate that these patterns cannot be attributed to sampling heterogeneities in paleolatitudinal range, lithology, or paleoenvironment of deposition. Likewise, when data are restricted to samples dominated by species with originally aragonitic shells, the observed temporal changes persist at a comparable magnitude, suggesting that the pervasive loss of aragonite in the older fossil record is unlikely to have been the primary cause of the observed patterns. The comparable ratio of identified to unidentified species and genera, observed when comparing the Jurassic and late Cenozoic samples, indicates that the relatively poorer (mold/cast) preservation of Jurassic aragonite species also is unlikely to have been responsible for the observed patterns. However, the diagenesis-related taphonomic and methodological artifacts cannot be ruled out as an at least partial contributor to the observed post-Paleozoic changes in diversity, taxonomic composition, and ecology (the outcomes of the three tests of the diagenetic bias available to us are incongruent). The study demonstrates that the post-Paleozoic trends in the sample-level diversity, ecology, and taxonomic structure of common taxa can be replicated across multiple studies. However, the diversity increase estimated here is much less prominent than suggested by many previous analyses. The results also narrow the list of causative explanations down to two testable hypotheses. The first is diagenetic bias—a spurious trend driven by either (a) increasing taphonomic loss of small specimens in the older fossil record or (b) a shift in sampling procedures between predominantly lithified rocks of the Mesozoic and predominately unlithified, and therefore sievable, sediments of the late Cenozoic. The second hypothesis is genuine biological changes—macroevolutionary trends in the structure of marine benthic associations through time, consistent with predictions of several related models such as evolutionary escalation, increased ecospace utilization, and the Mesozoic marine revolution. Future studies should focus on testing these two rival models, a key remaining challenge for identifying the primary causative mechanism for the long-term changes in sample-level diversity, ecology, and taxonomic structure observed in the Phanerozoic marine fossil record.