scholarly journals After the boring billion and before the freezing millions: evolutionary patterns and innovations in the Tonian Period

2018 ◽  
Vol 2 (2) ◽  
pp. 161-171 ◽  
Author(s):  
Shuhai Xiao ◽  
Qing Tang

The Tonian Period (ca. 1000–720 Ma) follows the ‘boring billion' in the Mesoproterozoic Era and precedes ‘snowball Earth' glaciations in the Cryogenian Period. It represents a critical transition in Earth history. Geochemical data indicate that the Tonian Period may have witnessed a significant increase in atmospheric pO2 levels and a major transition from predominantly sulfidic to ferruginous mid-depth seawaters. Molecular clock estimates suggest that early animals may have diverged in the Tonian Period, raising the intriguing possibility of coupled environmental changes and evolutionary innovations. The co-evolution of life and its environment during the Tonian Period can be tested against the fossil record by examining diversity trends in the Proterozoic and evolutionary innovations in the Tonian. Compilations of Proterozoic microfossils and macrofossils apparently support a Tonian increase in global taxonomic diversity and morphological range relative to the Mesoproterozoic Era, although this is not reflected in assemblage-level diversity patterns. The fossil record suggests that major eukaryote groups (including Opisthokonta, Amoebozoa, Plantae, and SAR) may have diverged and important evolutionary innovations (e.g. multicellularity and cell differentiation in several groups, eukaryovory, eukaryote biomineralization, and heterocystous cyanobacteria) may have arisen by the Tonian Period, but thus far no convincing animal fossils have been found in the Tonian. Tonian paleontology is still in its nascent stage, and it offers many opportunities to explore Earth-life evolution in this critical geological period.

2008 ◽  
Vol 5 (1) ◽  
pp. 253-267 ◽  
Author(s):  
G. Le Hir ◽  
Y. Goddéris ◽  
Y. Donnadieu ◽  
G. Ramstein

Abstract. The Snowball Earth theory initially proposed by Kirschvink (1992) to explain the Neoproterozoic glacial episodes, suggested that the Earth was fully ice-covered at 720 Ma (Sturtian episode) and 640 Ma (Marinoan episode). This succession of extreme climatic crises induced environmental perturbations which are considered as a strong selective pressure on the evolution of life (Hoffman et al., 1998). Using a numerical model of carbon-alkalinity global cycles, we quantify environmental stresses caused by a global glaciation. According to our results, we suggest that during global glaciations, the ocean becomes acidic (pH~6), and undersaturated with respect to carbonate minerals. Moreover the quick transition from ice-house to greenhouse conditions implies an abrupt and large shift of the oceanic surface temperature which causes an extended hypoxia. The intense continental weathering, in the aftermath of the glaciation, deeply affects the seawater composition inducing rapid changes in terms of pH and alkalinity. We also propose a new timing for post glacial perturbations and for the cap carbonates deposition, ~2 Myr instead of 200 kyr as suggested in a previous modelling study. In terms of Precambrian life sustainability, seawater pH modifications appear drastic all along the glaciation, but we suggest that the buffering action of the oceanic crust dissolution avoids a total collapse of biological productivity. But short-lived and large post-glacial perturbations are more critical and may have played the role of an environmental filter proposed in the classic snowball Earth theory. Although the link between environmental changes and life sustainability cannot be modelled accurately, we suggest that only a permissive life (Knoll, 2003) may explain the relative continuity in microfossils diversity observed before, during and after Neoproterozoic glaciation events.


1992 ◽  
Vol 6 ◽  
pp. 60-60
Author(s):  
William A. Clemens

The currently available fossil record suggests, 1) biogeographic differentiation of the Late Cretaceous terrestrial biota and, 2) distinctly different patterns of evolution of terrestrial faunas and floras across the Cretaceous\Tertiary boundary.Discovery in Alaska of dinosaurs and mammals that lived at Late Cretaceous northern high latitudes provides evidence that many groups of terrestrial vertebrates had extensive geographic ranges and faunas were biogeographically differentiated. The Alaskan dinosaurs, represented by individuals that range in size from hatchlings to adults, might have been migratory forms living at high latitudes only during the summer months. In contrast, the small mammals probably were not migratory.Although recent discoveries are expanding our knowledge of the evolution of the terrestrial biota, the fossil record of terrestrial vertebrates during the Cretaceous\Tertiary transition is still heavily biased in favor of the northern Western Interior of North America. Here evolutionary change of the terrestrial fauna did not just involve extinction of lineages, some already decreasing in taxonomic diversity, and survival of many others. Shifts in biogeographic range and immigration of new groups played a significant role in remodeling the terrestrial fauna. The paleobotanical record is more extensive but also is biased with the most detailed record coming from the Western Interior where floral change is characterized as “massive” or “catastrophic” in scope.These conflicting evolutionary patterns are well founded being based on analysis of substantial fossil records. A new program of research directed toward resolution of the apparent paradox tests the hypothesis that at the end of the Cretaceous the terrestrial biota was biogeographically heterogeneous and evolutionary patterns of faunal and floral change in the Western Interior cannot be taken as globally representative.


2021 ◽  
pp. 1-15
Author(s):  
Thomas M. Cullen ◽  
Lindsay Zanno ◽  
Derek W. Larson ◽  
Erinn Todd ◽  
Philip J. Currie ◽  
...  

The Dinosaur Park Formation (DPF) of Alberta, Canada, has produced one of the most diverse dinosaur faunas, with the record favouring large-bodied taxa, in terms of number and completeness of skeletons. Although small theropods are well documented in the assemblage, taxonomic assessments are frequently based on isolated, fragmentary skeletal elements. Here we reassess DPF theropod biodiversity using morphological comparisons, high-resolution biostratigraphy, and morphometric analyses, with a focus on specimens/taxa originally described from isolated material. In addition to clarifying taxic diversity, we test whether DPF theropods preserve faunal zonation/turnover patterns similar to those previously documented for megaherbivores. Frontal bones referred to a therizinosaur (cf. Erlikosaurus), representing among the only skeletal record of the group from the Campanian–Maastrichtian (83–66 Ma) fossil record of North America, plot most closely to troodontids in morphospace, distinct from non-DPF therizinosaurs, a placement supported by a suite of troodontid anatomical frontal characters. Postcranial material referred to cf. Erlikosaurus in North America is also reviewed and found most similar in morphology to caenagnathids, rather than therizinosaurs. Among troodontids, we document considerable morphospace and biostratigraphic overlap between Stenonychosaurus and the recently described Latenivenatrix, as well as a variable distribution of putatively autapomorphic characters, calling the validity of the latter taxon into question. Biostratigraphically, there are no broad-scale patterns of faunal zonation similar to those previously documented in ornithischians from the DPF, with many theropods ranging throughout much of the formation and overlapping extensively, possibly reflecting a lack of sensitivity to environmental changes, or other cryptic ecological or evolutionary factors.


1992 ◽  
Vol 6 ◽  
pp. 174-174 ◽  
Author(s):  
Conrad C. Labandeira

A considerable amount of research has been devoted toward evaluating the impact of the Cretaceous/Tertiary extinction on terrestrial life. This research has focused primarily on terrestrial vertebrates (primarily dinosaurs), marine invertebrates (notably molluscs and foraminifera), and to a lesser extent, terrestrial vascular plants. Terrestrial arthropods, especially insects, have seldomly been investigated, principally because of an alleged depauperate fossil record. Nevertheless, within the past two decades, some of the most productive and taxonomically diverse insect faunas have originated from Cretaceous amber- and compression-fossil deposits from every continent. Whereas it was once thought that the Cretaceous represented an unknown void in the understanding of insect evolution, now it appears that many extant lineages are traceable to Cretaceous precursors.Three approaches are available for determining the extent of the effect of the terminal Cretaceous extinction event on insects. Assessed for the interval from the Early Cretaceous to the Early Paleogene, these approaches are: (1) establishing the secular pattern of familial- and generic-based taxonomic diversity (macroevolution); (2) recognizing the persistence or eradication of specific insect/vascular plant interactions, such as leaf-mining, wood-boring and pollination (behavior); and (3) establishing temporal trends in the range of mouthpart design, as an indicator of faunal disparity or structural diversity (morphology). These three operationally separate but complimentary approaches allow the advantage of using distinct data bases to bear on a common question. The body-fossil record of insects provides primary data for the taxonomic expansion, steady-state, or contraction of insect faunas. The trace-fossil record of those insect interactions that are coevolved with plant hosts reveals the temporal continuity of highly stereotyped and taxonomically obligate behaviors. Both of these are contrasted to an assessment of insectan structural disparity, herein determined from a robust data base of 30 modern insect mouthpart classes that are traced back in geologic time.A preliminary analysis of each of these three approaches indicates broad agreement–namely that insects were not dramatically affected by the terminal Cretaceous extinction event. First, insects experienced only a modest decline in diversity, about 9 percent at the family level. (The generic level is not yet analyzed.) Second, although the data base is limited, there is no indication of the extinction of major leaf-mining, wood-boring, pollinating or other plant-specific behaviors at the end of the Cretaceous. In fact, leaf-mine morphologies for three lepidopteran families with Cretaceous occurrences are apparently indistinguishable from their modern descendants. Last, of the 30 mouthpart classes occurring during the Paleogene, 28 are represented during the Cretaceous. These data provide strong evidence for a largely uninterrupted continuum of insect faunas across the Cretaceous/Tertiary boundary as measured by taxonomic diversity, coevolved behavior, and structural disparity.Because of abundant and often intimate associations between insects and flowering plants, these results are consistent with a gradual and not catastrophic change in terrestrial floras across the Cretaceous/Tertiary boundary. Acceptance of a catastrophic extinction of flowering plants during the terminal Cretaceous would necessitate an unprecedented level of host-switching by coevolved insects on contemporaneous plants. This is unlikely, based on evidence from the prolific literature on modern insect/plant interactions. These studies indicate the ubiquity of obligate insect specificity for various secondary chemicals on many flowering plant species.


2002 ◽  
Vol 8 ◽  
pp. 267-288 ◽  
Author(s):  
Blaire Van Valkenburgh ◽  
Ian Jenkins

Synapsids include modern mammals and their fossil ancestors, the non-mammalian synapsids, or ‘mammal-like reptiles' of old classifications. The synapsid fossil record extends from the Late Carboniferous to the present, a span of nearly 300 million years. However, it can be broken into two distinct phases of diversification, separated by about 150 million years. The first phase extends from the Late Carboniferous to the mid-Triassic, includes the first large land predators on Earth, and is almost entirely non-mammalian. The second phase begins about 65 million years ago after the demise of the dinosaurs, includes only mammals, and extends to the present. In this overview of synapsid predators, we emphasize terrestrial species of large size, and their adaptations for killing and feeding, rather than locomotion. Despite fundamental differences in jaw mechanics and tooth morphology, there are significant parallels in the non-mammalian and mammalian radiations of synapsid predators. Both groups evolve sabertooth forms more than once, and both evolve short-snouted, powerful biting forms. In addition, both the Late Carboniferous—Triassic and Cenozoic phases are characterized by repeated patterns of clade replacement, in which one or a few clades evolve large size and seem to dominate the carnivore guild for several million years, but then decline and are replaced by new taxa. Moreover, within both ancient and Cenozoic predator clades, there are parallel trends over time toward increased body size and hypercarnivory that likely result from a combination of interspecific competition and energetic constraints.


2019 ◽  
Vol 18 (6) ◽  
pp. 575-589 ◽  
Author(s):  
Amanda L. S. Gomes ◽  
Bruno Becker-Kerber ◽  
Gabriel L. Osés ◽  
Gustavo Prado ◽  
Pedro Becker Kerber ◽  
...  

AbstractInvestigations into the existence of life in other parts of the cosmos find strong parallels with studies of the origin and evolution of life on our own planet. In this way, astrobiology and paleobiology are married by their common interest in disentangling the interconnections between life and the surrounding environment. In this way, a cross-point of both sciences is paleometry, which involves a myriad of imaging and geochemical techniques, usually non-destructive, applied to the investigation of the fossil record. In the last decades, paleometry has benefited from an unprecedented technological improvement, thus solving old questions and raising new ones. This advance has been paralleled by conceptual approaches and discoveries fuelled by technological evolution in astrobiological research. In this context, we present some new data and review recent advances on the employment of paleometry to investigations on paleobiology and astrobiology in Brazil in areas such biosignatures in Ediacaran microbial mats, biogenicity tests on enigmatic Ediacaran structures, research on Ediacaran metazoan biomineralization, fossil preservation in Cretaceous insects and fish, and finally the experimental study on the decay of fish to test the effect of distinct types of sediment on soft-tissue preservation, as well as the effects of early diagenesis on fish bone preservation.


2013 ◽  
Vol 61 (3) ◽  
pp. 167 ◽  
Author(s):  
N. Pérez-Harguindeguy ◽  
S. Díaz ◽  
E. Garnier ◽  
S. Lavorel ◽  
H. Poorter ◽  
...  

Plant functional traits are the features (morphological, physiological, phenological) that represent ecological strategies and determine how plants respond to environmental factors, affect other trophic levels and influence ecosystem properties. Variation in plant functional traits, and trait syndromes, has proven useful for tackling many important ecological questions at a range of scales, giving rise to a demand for standardised ways to measure ecologically meaningful plant traits. This line of research has been among the most fruitful avenues for understanding ecological and evolutionary patterns and processes. It also has the potential both to build a predictive set of local, regional and global relationships between plants and environment and to quantify a wide range of natural and human-driven processes, including changes in biodiversity, the impacts of species invasions, alterations in biogeochemical processes and vegetation–atmosphere interactions. The importance of these topics dictates the urgent need for more and better data, and increases the value of standardised protocols for quantifying trait variation of different species, in particular for traits with power to predict plant- and ecosystem-level processes, and for traits that can be measured relatively easily. Updated and expanded from the widely used previous version, this handbook retains the focus on clearly presented, widely applicable, step-by-step recipes, with a minimum of text on theory, and not only includes updated methods for the traits previously covered, but also introduces many new protocols for further traits. This new handbook has a better balance between whole-plant traits, leaf traits, root and stem traits and regenerative traits, and puts particular emphasis on traits important for predicting species’ effects on key ecosystem properties. We hope this new handbook becomes a standard companion in local and global efforts to learn about the responses and impacts of different plant species with respect to environmental changes in the present, past and future.


2015 ◽  
Vol 370 (1684) ◽  
pp. 20150038 ◽  
Author(s):  
Gregory D. Edgecombe ◽  
Xiaoya Ma ◽  
Nicholas J. Strausfeld

Extant panarthropods (euarthropods, onychophorans and tardigrades) are hallmarked by stunning morphological and taxonomic diversity, but their central nervous systems (CNS) are relatively conserved. The timing of divergences of the ground pattern CNS organization of the major panarthropod clades has been poorly constrained because of a scarcity of data from their early fossil record. Although the CNS has been documented in three-dimensional detail in insects from Cenozoic ambers, it is widely assumed that these tissues are too prone to decay to withstand other styles of fossilization or geologically older preservation. However, Cambrian Burgess Shale-type compressions have emerged as sources of fossilized brains and nerve cords. CNS in these Cambrian fossils are preserved as carbon films or as iron oxides/hydroxides after pyrite in association with carbon. Experiments with carcasses compacted in fine-grained sediment depict preservation of neural tissue for a more prolonged temporal window than anticipated by decay experiments in other media. CNS and compound eye characters in exceptionally preserved Cambrian fossils predict divergences of the mandibulate and chelicerate ground patterns by Cambrian Stage 3 ( ca 518 Ma), a dating that is compatible with molecular estimates for these splits.


2018 ◽  
Vol 15 (21) ◽  
pp. 6607-6619 ◽  
Author(s):  
Janet E. Burke ◽  
Willem Renema ◽  
Michael J. Henehan ◽  
Leanne E. Elder ◽  
Catherine V. Davis ◽  
...  

Abstract. The clustering of mitochondria near pores in the test walls of foraminifera suggests that these perforations play a critical role in metabolic gas exchange. As such, pore measurements could provide a novel means of tracking changes in metabolic rate in the fossil record. However, in planktonic foraminifera, variation in average pore area, density, and porosity (the total percentage of a test wall that is open pore space) have been variously attributed to environmental, biological, and taxonomic drivers, complicating such an interpretation. Here we examine the environmental, biological, and evolutionary determinants of pore characteristics in 718 individuals, representing 17 morphospecies of planktonic foraminifera from 6 core tops in the North Atlantic. Using random forest models, we find that porosity is primarily correlated to test surface area, test volume, and habitat temperature, key factors in determining metabolic rates. In order to test if this correlation arose spuriously through the association of cryptic species with distinct biomes, we cultured Globigerinoides ruber in three different temperature conditions, and found that porosity increased with temperature. Crucially, these results show that porosity can be plastic: changing in response to environmental drivers within the lifetime of an individual foraminifer. This demonstrates the potential of porosity as a proxy for foraminiferal metabolic rates, with significance for interpreting geochemical data and the physiology of foraminifera in non-analog environments. It also highlights the importance of phenotypic plasticity (i.e., ecophenotypy) in accounting for some aspects of morphological variation in the modern and fossil record.


Paleobiology ◽  
1994 ◽  
Vol 20 (3) ◽  
pp. 320-344 ◽  
Author(s):  
Mike Foote

It has been argued that many clades originating in the early Paleozoic filled their design space rapidly while still at low taxonomic diversity. Standardization of morphology for analytical purposes facilitates testing of this claim. Here I document evolutionary patterns of morphological disparity in Ordovician-Devonian crinoids, using a set of 75 discrete characters covering the principal features of the crinoid stem, cup, tegmen, and arms. Disparity is measured as the average dissimilarity among species, the range of morphospace occupied, and the number of realized character-state combinations. Comparison with generic richness reveals that the full range of form was essentially attained by the early part of the Caradocian, long before the time of maximal taxonomic diversity. Despite subsequent taxonomic diversification, the variety of crinoid form did not expand appreciably; increased diversity was accommodated by the evolution of variations upon the spectrum of designs established earlier. The data discussed here do not definitively imply specific sources of constraint, but the effective stasis in disparity supports previous arguments that some morphological limits were reached early in crinoid history.


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