Holocene deposits exhibit distinct, predictable and chronologically constrained facies patterns that are quite useful as appropriate modern analogs for interpreting the ancient record. In this study, we examined the sedimentary response of the Po Plain coastal system to short term (millennial scale) relative fluctuations of sea level through high resolution sequence stratigraphic analysis of the Holocene succession.Meters thick parasequences form the building blocks of stratigraphic architecture. Above the Younger Dryas paleosol, a prominent stratigraphic marker that demarcates the transgressive surface, Early Ho locene parasequences (#s 1 3) record alternating periods of rapid flooding and gradual shoaling, and are stacked in a retrogradational pattern that mostly reflects stepped, post glacial eustatic rise. Conversely, Middle to Late Holocene parasequences (#s 4 8) record a complex, pattern of coastal progradation and delta upbuilding that took place following sea level stabilization at highstand, starting at about 7 cal ky BP. The prominent transgressive surface at the base of parasequence 1 correlates with the period of rapid, global sea level rise at the onset of the Holocene (MWP 1B), whereas flooding surfaces associated with parasequences 2 and 3 apparently reflect minor Early Holocene eustatic jumps reported in the literature. Changes in shoreline trajectory, parasequence architecture and lithofacies distribution during the following eustatic highstand had, instead, an overwhelming autogenic component, mostly driven by river avulsions, delta lobe switching, local subsidence and sediment compaction. We document a ~1000 year delayed response of the coastal depositional system to marine incursion, farther inland from the maximum landward position of the shoreline. A dramatic reduction in sediment flux due to fluvial avulsion resulted in marine inundation in back barrier position, whereas coastal progradation was simultaneously taking place basinwards.We demonstrate that the landward equivalents of marine flooding surfaces (parasequence boundaries) may be defined by brackish and freshwater fossil assemblages, and traced for tens of kilometers into the non marine realm. This makes millennial scale parasequences, whether auto or allogenic in origin, much more powerful than systems tracts for mapping detailed extents and volumes of sediment bodies.The Holocene parasequences of the Po coastal plain, with strong age control and a detailed under standing of sea level variation, may provide insight into the driving mechanisms and predictability of successions characterized by similar depositional styles, but with poor age constraint, resulting in more robust interpretations of the ancient record.
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 isdiagenetic 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 isgenuine 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.
Upper Quaternary sequences of the Po Plain (Italy) were used to assess the informative strength and sequence-stratigraphic overprint of quantitative paleoecological patterns. Three densely sampled cores (89 samples, 98 genera, 23,280 specimens), dominated by extant mollusk species with known environmental distributions, were analyzed with detrended correspondence analysis (DCA). The DCA scores, calibrated using extant genera, provided outstanding estimates of bathymetry (؎3 m) and related environmental parameters. Depth-related successions of mollusk associations delineated by using DCA were consistent with independent sequence-stratigraphic interpretations and yielded insights inaccessible via routine techniques (e.g., depth estimates for maximum flooding surfaces). The DCA ordination demonstrates the severity of the sequence-stratigraphic overprint: samples are highly uniform taxonomically during late transgressive systems tracts and highly variable during the following highstand systems tracts. When analyzed across comparable systems tracts, similar species associations repeat during the last and current interglacial cycles, suggesting that Po Plain mollusk associations have remained remarkably stable over the past 125 k.y. The results are consistent with the bathymetric interpretation of the DC axis 1 postulated previously for the Paleozoic fossil record, demonstrate the sequence-stratigraphic overprint of paleoecological patterns predicted by computer modeling, and illustrate the utility of quantitative paleoecological patterns in augmenting sequence-stratigraphic interpretations. Figure 1. Study area map (left inset) and geologic cross section (right) of upper Quaternary deposits of Po Plain (simplified after Amorosi et al., 2004). TST-transgressive systems tract; HST-highstand systems tract; s.l.-sea level; SB-sequence boundary.
To understand the complex stratigraphic response of a coastal depositional system to rapid eustatic rise and sediment inputs, the evolution of the Adriatic coastline and Po River system, during the post‐glacial (Holocene) transgression, was investigated. The landward migration and evolution of a wave‐dominated estuary was mapped, based on an extensive data set comprising 14 boreholes, 28 core descriptions and 308 piezocone tests, chronologically constrained between 11·5 and 7·0 kyr bp by 137 radiocarbon dates. Palaeogeographic maps reveal temporal differences in retrogradational geometries and mechanisms that likely underpin shoreline retreat. The Po estuary initially developed within a shallowly incised valley and then spread onto the interfluves. Between 11·5 and 9·2 kyr bp the Po fluvial system became avulsive/distributive and wetlands developed in topographically depressed areas. The shoreline retreated at a mean rate of ca 10 m year−1, between 9·2 kyr and 7·7 kyr bp, following a stepped trajectory at the centennial scale. After 7·7 kyr bp, bayhead deltas started to prograde and partially filled the estuary. The overall stratigraphic architecture is interpreted to reflect the sedimentary response of the coastal depositional system to the main pulses of early Holocene eustatic rise. The influence of antecedent topography, partly due to local subsidence, was dominant at the time of initial transgression. Basin morphology influenced sediment dispersal and partitioning. Sediment supplied by the Po River was trapped within the estuary, whereas coastal sand bodies at the estuary mouth were fed by alongshore currents and by reworking of older barriers. High‐resolution age control that ties facies evolution to independently constrained eustasy provides direct data to test models of short‐term coastal retreat under conditions of relative sea‐level rise, and makes this case study a useful analogue for the interpretation of ancient marginal‐marine, retrogradational systems where only stratal geometries are available.
The role of antagonistic organismal interactions in the production of long-term macroevolutionary trends has been debated for decades. Some evidence seems to suggest that temporal trends in predation frequency share a common causative mechanism with genus-level diversity, whereas studies on the role of parasites in “shaping” the evolutionary process are rare indeed. Digenean trematodes (Phylum Platyhelminthes) infest molluscs in at least one stage of their complex life cycle. Trematodes leave characteristic oval-shaped pits with raised rims on the interior of their bivalve hosts, and these pits are preserved in the fossil record. Here we survey 11,785 valves from the Pleistocene–Holocene deposits of the Po Plain and from nearby modern coastal environments on the northeast Adriatic coast of Italy. Of these, 205 valves exhibited trematode-induced pits. Trematodes were selective parasites in terms of host taxonomy and host body size. Infestation was restricted to lower shoreface/transition-to-platform paleoenvironments. During the Holocene, individuals from the transgressive systems tract were significantly more likely to be infested than those from highstand systems tracts. Temporal trends in infestation frequency cannot be explained as an ecological/evolutionary phenomenon (e.g., the hypothesis of escalation); instead the trend seems controlled by environmental variation induced by glacio-eustatic sea-level changes and inadequate sampling. Because this interaction appears to be ephemeral, both temporally and spatially, it is not likely that any selective pressure would be continuous over geologic time in this region. Furthermore, these results support the hypothesis that antagonistic interactions are lower in the northern Adriatic Sea in comparison to other midlatitude shallow marine settings.
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