scholarly journals The evolution of diversity in ancient ecosystems: a review

1998 ◽  
Vol 353 (1366) ◽  
pp. 327-345 ◽  
Author(s):  
S. Conway Morris
Keyword(s):  
Fossil Record ◽  
Molecular Data ◽  
Cambrian Explosion ◽  
Mass Extinctions ◽  
Geological Time ◽  
Biological Communities ◽  
History Of ◽  
Lag Times ◽  
Extinction Events ◽  
Ancient Ecosystems

On a perfect planet, such as might be acceptable to a physicist, one might predict that from its origin the diversity of life would grow exponentially until the carrying capacity, however defined, was reached. The fossil record of the Earth, however, tells a very different story. One of the most striking aspects of this record is the apparent evolutionary longueur, marked by the Precambrian record of prokaryotes and primitive eukaryotes, although our estimates of microbial diversity may be seriously incomplete. Subsequently there were various dramatic increases in diversity, including the Cambrian ‘explosion’ and the radiation of Palaeozoic–style faunas in the Ordovician. The causes of these events are far from resolved. It has also long been appreciated that the history of diversity has been punctuated by important extinctions. The subtleties and nuances of extinction as well as the survival of particular clades have to date, however, received rather too little attention, and there is still a tendency towards blanket assertions rather than a dissection of these extraordinary events. In addition, some but perhaps not all mass extinctions are characterized by long lag–times of recovery, which may reflect the slowing waning of extrinsic forcing factors or alternatively the incoherence associated with biological reassembly of stable ecosystems. The intervening periods between the identified mass extinctions may be less stable and benign than popularly thought, and in particular the frequency of extraterrestrial impacts leads to predictions of recurrent disturbance on timescales significantly shorter than the intervals separating the largest extinction events. Even at times of quietude it is far from clear whether biological communities enjoy stability and interlocked stasis or are dynamically reconstituted at regular intervals. Finally, can we yet rely on the present depictions of the rise and falls in the levels of ancient diversity? Existing data is almost entirely based on Linnean taxa, and the application of phylogenetic systematics to this problem is still in its infancy. Not only that, but even more intriguingly the pronounced divergence in estimates of origination times of groups as diverse as angiosperms, diatoms and mammals in terms of the fossil record as against molecular data point to the possibilities of protracted intervals of geological time with a cryptic diversity. If this is correct, and there are alternative explanations, then some of the mystery of adaptive radiations may be dispelled, in as much as the assembly of key features in the stem groups could be placed in a gradualistic framework of local adaptive response punctuated by intervals of opportunity.

scholarly journals Sediment core fossils in ancient Lake Ohrid: testing for faunal change in molluscs since the Last Interglacial period

2010 ◽  
Vol 7 (3) ◽  
pp. 3969-3999 ◽  
Author(s):  
C. Albrecht ◽  
H. Vogel ◽  
T. Hauffe ◽  
T. Wilke
Keyword(s):  
Sediment Core ◽  
Fossil Record ◽  
Interglacial Period ◽  
Ancient Lake ◽  
Last Interglacial ◽  
Lake Ohrid ◽  
Last Interglacial Period ◽  
History Of ◽  
Extinction Events ◽  
Mollusc Shells

Abstract. Ancient Lake Ohrid is probably of early Pleistocene or Pliocene origin and amongst the few lakes in the world harboring an outstanding degree of endemic biodiversity. Although there is a long history of evolutionary research in Lake Ohrid, particularly on molluscs, a mollusc fossil record has been missing up to date. For the first time, gastropod and bivalve fossils are reported from the basal, calcareous part of a 2.6 m long sediment succession (core Co1200) from the north-eastern part of Lake Ohrid. Electron spin resonance (ESR) dating of mollusc shells from the same stratigraphic level yielded an age of 130±28 ka. Lithofacies III sediments, i.e. a subdivision of the stratigraphic unit comprising the basal succession of core Co1200 between 181.5–263 cm appeared solid, grayish-white, and consisted almost entirely of silt-sized endogenic calcite (CaCO3>70%) and intact and broken mollusc shells. Here we compare the faunal composition of the thanatocoenosis with recent mollusc associations in Lake Ohrid. A total of 13 mollusc species (9 gastropod and 4 bivalve species) could be identified within Lithofacies III sediments. The value of sediment core fossils for reconstructing palaeoenvironmental settings was evaluated. The agreement between sediment and palaeontological proxies was tested. The combined findings of the ecological study and the sediment characteristics suggest deposition in a shallow water environment during the Last Interglacial period. We tested for major faunal changes since the Last Interglacial period and searched for signs of extinction events. The fossil fauna exclusively included species also found in the present fauna, i.e. no extinction events are evident for this site since the Last Interglacial. The thanatocoenosis showed the highest similarity with recent Intermediate Layer (5–25 m) mollusc assemblages. The demonstrated existence of a mollusc fossil record in Lake Ohrid sediment cores also has great significance for future deep drilling projects. It can be hoped that a more far reaching mollusc fossil record will then be obtained, enabling insight into the early evolutionary history of Lake Ohrid.

scholarly journals The origins of modern biodiversity on land

2010 ◽  
Vol 365 (1558) ◽  
pp. 3667-3679 ◽  
Author(s):  
Michael J. Benton
Keyword(s):  
Regional Scale ◽  
Global Scale ◽  
Scale Model ◽  
Time Range ◽  
Geological Time ◽  
New Methods ◽  
Evolution Of Life ◽  
History Of ◽  
Extinction Events ◽  
Mass Extinction Events

Comparative studies of large phylogenies of living and extinct groups have shown that most biodiversity arises from a small number of highly species-rich clades. To understand biodiversity, it is important to examine the history of these clades on geological time scales. This is part of a distinct ‘phylogenetic expansion’ view of macroevolution, and contrasts with the alternative, non-phylogenetic ‘equilibrium’ approach to the history of biodiversity. The latter viewpoint focuses on density-dependent models in which all life is described by a single global-scale model, and a case is made here that this approach may be less successful at representing the shape of the evolution of life than the phylogenetic expansion approach. The terrestrial fossil record is patchy, but is adequate for coarse-scale studies of groups such as vertebrates that possess fossilizable hard parts. New methods in phylogenetic analysis, morphometrics and the study of exceptional biotas allow new approaches. Models for diversity regulation through time range from the entirely biotic to the entirely physical, with many intermediates. Tetrapod diversity has risen as a result of the expansion of ecospace, rather than niche subdivision or regional-scale endemicity resulting from continental break-up. Tetrapod communities on land have been remarkably stable and have changed only when there was a revolution in floras (such as the demise of the Carboniferous coal forests, or the Cretaceous radiation of angiosperms) or following particularly severe mass extinction events, such as that at the end of the Permian.

In search of possible causes of mass extinctions

2004 ◽  
Author(s):  
Tony Hallam
Keyword(s):  
Science Fiction ◽  
High Rate ◽  
Mass Extinctions ◽  
Geological Time ◽  
Steven Spielberg ◽  
Geological Past ◽  
History Of ◽  
The Subject ◽  
Cretaceous Period ◽  
Land Vertebrates

When the subject of extinctions in the geological past comes up, nearly everyone’s thoughts turn to dinosaurs. It may well be true that these long-extinct beasts mean more to most children than the vast majority of living creatures. One could even go so far as to paraphrase Voltaire and maintain that if dinosaurs had never existed it would have been necessary to invent them, if only as a metaphor for obsolescence. To refer to a particular machine as a dinosaur would certainly do nothing for its market value. The irony is that the metaphor is now itself obsolete. The modern scientific view of dinosaurs differs immensely from the old one of lumbering, inefficient creatures tottering to their final decline. Their success as dominant land vertebrates through 165 million years of the Earth’s history is, indeed, now mainly regarded with wonder and even admiration. If, as is generally thought, the dinosaurs were killed off by an asteroid at the end of the Cretaceous, that is something for which no organism could possibly have been prepared by normal Darwinian natural selection. The final demise of the dinosaurs would then have been the result, not of bad genes, but of bad luck, to use the laconic words of Dave Raup. In contemplating the history of the dinosaurs it is necessary to rectify one widespread misconception. Outside scientific circles the view is widely held that the dinosaurs lived for a huge slice of geological time little disturbed by their environment until the final apocalypse. This is a serious misconception. The dinosaurs suffered quite a high evolutionary turnover rate, and this implies a high rate of extinction throughout their history. Jurassic dinosaurs, dominated by giant sauropods, stegosaurs, and the top carnivore Allosaurus, are quite different from those of the Cretaceous period, which are characterized by diverse hadrosaurs, ceratopsians, and Tyrannosaurus. Michael Crichton’s science-fiction novel Jurassic Park, made famous by the Steven Spielberg movies, features dinosaurs that are mainly from the Cretaceous, probably because velociraptors and Tyrannosaurus could provide more drama.

3. Extinction in the past

2019 ◽  
pp. 33-50
Author(s):  
Paul B. Wignall
Keyword(s):  
Fossil Record ◽  
The Past ◽  
Extinction Rates ◽  
History Of ◽  
Extinction Events

Despite the less-than-perfect nature of the fossil record, it still provides a unique window on the history of life, and reveals that there have been dramatic fluctuations in extinction intensities since complex life evolved around 600 million years ago. ‘Extinction in the past’ considers Jack Sepkoski’s database compiled in the 1980s, and his series of highly informative charts showing both diversity and extinction rates since the start of the Cambrian Period 541 million years ago. The calculation of extinction rates and the improved dating of extinction events are discussed, along with the extinction trends that can be observed. Fossils also provide valuable evidence on the nature of selection during extinction.

Community Replacement Pathways: What Do Fossil Sequences Reveal About Marine Ecosystem Transitions?

1990 ◽  
Vol 5 ◽  
pp. 262-272
Author(s):  
William Miller
Keyword(s):  
Fossil Record ◽  
Large Scale ◽  
Marine Ecosystem ◽  
Small Scale ◽  
Data Sets ◽  
Mass Extinctions ◽  
Ultimate Cause ◽  
Long Time ◽  
History Of ◽  
Time And Energy

Paleontologists have lavished much time and energy on description and explanation of large-scale patterns in the fossil record (e.g., mass extinctions, histories of monophyletic taxa, deployment of major biogeographic units), while paying comparatively little attention to biologic patterns preserved only in local stratigraphic sequences. Interpretation of the large-scale patterns will always be seen as the chief justification for the science of paleontology, but solving problems framed by long time spans and large areas is rife with tenuous inference and patterns are prone to varied interpretation by different investigators using virtually the same data sets (as in the controversy over ultimate cause of the terminal Cretaceous extinctions). In other words, the large-scale patterns in the history of life are the true philosophical property of paleontology, but there will always be serious problems in attempting to resolve processes that transpired over millions to hundreds-of-millions of years and encompassed vast areas of seafloor or landscape. By contrast, less spectacular and more commonplace changes in local habitats (often related to larger-scale events and cycles) and attendant biologic responses are closer to our direct experience of the living world and should be easier to interpret unequivocally. These small-scale responses are reflected in the fossil record at the scale of local outcrops.

Ontogeny in the fossil record: diversification of body plans and the evolution of “aberrant” symmetry in Paleozoic echinoderms

Paleobiology ◽  
2007 ◽  
Vol 33 (1) ◽  
pp. 149-163 ◽  
Author(s):  
Colin D. Sumrall ◽  
Gregory A. Wray
Keyword(s):  
Great Reduction ◽  
Fossil Record ◽  
Evolutionary History ◽  
Total Loss ◽  
Cambrian Explosion ◽  
Growth Stages ◽  
Ecological Constraints ◽  
Fivefold Symmetry ◽  
Primary Body ◽  
History Of

Echinoderms have long been characterized by the presence of ambulacra that exhibit pentaradiate symmetry and define five primary body axes. In reality, truly pentaradial ambulacral symmetry is a condition derived only once in the evolutionary history of echinoderms and is restricted to eleutherozoans, the clade that contains most living echinoderm species. In contrast, early echinoderms have a bilaterally symmetrical 2-1-2 arrangement, with three ambulacra radiating from the mouth. Branching of the two side ambulacra during ontogeny produces the five adult rays. During the Cambrian Explosion and Ordovician Radiation, some 30 clades of echinoderms evolved, many of which have aberrant ambulacral systems with one to four rays. Unfortunately, no underlying model has emerged that explains ambulacral homologies among disparate forms. Here we show that most Paleozoic echinoderms are characterized by uniquely identifiable ambulacra that develop in three distinct postlarval stages. Nearly all “aberrant” echinoderm morphologies can be explained by the paedomorphic ambulacra reduction (PAR) model through the loss of some combination of these growth stages during ontogeny. Superficially similar patterns of ambulacral reduction in distantly related clades have resulted from the parallel loss of homologous ambulacra during ontogeny. Pseudo-fivefold symmetry seen in Blastoidea and the true fivefold symmetry seen in Eleutherozoa result from great reduction and total loss, respectively, of the 2–1–2 symmetry early in ontogeny. These ambulacral variations suggest that both developmental and ecological constraints affect the evolution of novel echinoderm body plans.

scholarly journals Diversification events and the effects of mass extinctions on Crocodyliformes evolutionary history

2015 ◽  
Vol 2 (5) ◽  
pp. 140385 ◽  
Author(s):  
Mario Bronzati ◽  
Felipe C. Montefeltro ◽  
Max C. Langer
Keyword(s):  
Mass Extinction ◽  
Fossil Record ◽  
Evolutionary History ◽  
Continuous Process ◽  
Mass Extinctions ◽  
Terrestrial Habitats ◽  
History Of ◽  
The Rich ◽  
A Minor ◽  
Diversification Event

The rich fossil record of Crocodyliformes shows a much greater diversity in the past than today in terms of morphological disparity and occupation of niches. We conducted topology-based analyses seeking diversification shifts along the evolutionary history of the group. Our results support previous studies, indicating an initial radiation of the group following the Triassic/Jurassic mass extinction, here assumed to be related to the diversification of terrestrial protosuchians, marine thalattosuchians and semi-aquatic lineages within Neosuchia. During the Cretaceous, notosuchians embodied a second diversification event in terrestrial habitats and eusuchian lineages started diversifying before the end of the Mesozoic. Our results also support previous arguments for a minor impact of the Cretaceous/Palaeogene mass extinction on the evolutionary history of the group. This argument is not only based on the information from the fossil record, which shows basal groups surviving the mass extinction and the decline of other Mesozoic lineages before the event, but also by the diversification event encompassing only the alligatoroids in the earliest period after the extinction. Our results also indicate that, instead of a continuous process through time, Crocodyliformes diversification was patchy, with events restricted to specific subgroups in particular environments and time intervals.

The biology of mass extinction: a palaeontological view

1989 ◽  
Vol 325 (1228) ◽  
pp. 357-368 ◽  
Keyword(s):  
Mass Extinction ◽  
Large Scale ◽  
Individual Species ◽  
Ecological Groups ◽  
Mass Extinctions ◽  
Geological Time ◽  
Evolutionary Patterns ◽  
Data Set ◽  
High Species Richness ◽  
Extinction Events

Extinctions are not biologically random: certain taxa or functional/ecological groups are more extinction-prone than others. Analysis of molluscan survivorship patterns for the end-Cretaceous mass extinctions suggests that some traits that tend to confer extinction resistance during times of normal (‘background’) levels of extinction are ineffectual during mass extinction. For genera, high species-richness and possession of widespread individual species imparted extinction-resistance during background times but not during the mass extinction, when overall distribution of the genus was an important factor. Reanalysis of Hoffman’s (1986) data ( Neues Jb. Geol. Palaont. Abh. 172, 219) on European bivalves, and preliminary analysis of a new northern European data set, reveals a similar change in survivorship rules, as do data scattered among other taxa and extinction events. Thus taxa and adaptations can be lost not because they were poorly adapted by the standards of the background processes that constitute the bulk of geological time, but because they lacked - or were not linked to - the organismic, species-level or clade-level traits favoured under mass-extinction conditions. Mass extinctions can break the hegemony of species-rich, well-adapted clades and thereby permit radiation of taxa that had previously been minor faunal elements; no net increase in the adaptation of the biota need ensue. Although some large-scale evolutionary trends transcend mass extinctions, post-extinction evolutionary pathways are often channelled in directions not predictable from evolutionary patterns during background times.

scholarly journals A geological history of reflecting optics

2005 ◽  
Vol 2 (2) ◽  
pp. 1-17 ◽  
Author(s):  
Andrew Richard Parker
Keyword(s):  
Photonic Crystals ◽  
Self Assembly ◽  
Fossil Record ◽  
Selection Pressure ◽  
New Records ◽  
Optical Devices ◽  
Geological History ◽  
Geological Time ◽  
History Of ◽  
Optical Reflectors

Optical reflectors in animals are diverse and ancient. The first image-forming eye appeared around 543 million years ago. This introduced vision as a selection pressure in the evolution of animals, and consequently the evolution of adapted optical devices. The earliest known optical reflectors—diffraction gratings—are 515 Myr old. The subsequent fossil record preserves multilayer reflectors, including liquid crystals and mirrors, ‘white’ and ‘blue’ scattering structures, antireflective surfaces and the very latest addition to optical physics—photonic crystals. The aim of this article is to reveal the diversity of reflecting optics in nature, introducing the first appearance of some reflector types as they appear in the fossil record as it stands (which includes many new records) and backdating others in geological time through evolutionary analyses. This article also reveals the commercial potential for these optical devices, in terms of lessons from their nano-level designs and the possible emulation of their engineering processes—molecular self-assembly.

scholarly journals The fossil history of pseudoscorpions (Arachnida: Pseudoscorpiones)

Fossil Record ◽  
2017 ◽  
Vol 20 (2) ◽  
pp. 215-238 ◽  
Author(s):  
Danilo Harms ◽  
Jason A. Dunlop
Keyword(s):  
Fossil Record ◽  
Baltic Amber ◽  
Tree Bark ◽  
Valid Species ◽  
Morphological Reconstruction ◽  
Morphological Stasis ◽  
History Of ◽  
Extinction Events ◽  
Phylogenetic Affinities

Abstract. Pseudoscorpions, given their resemblance to scorpions, have attracted human attention since the time of Aristotle, although they are much smaller and lack the sting and elongated tail. These arachnids have a long evolutionary history but their origins and phylogenetic affinities are still being debated. Here, we summarise their fossil record based on a comprehensive review of the literature and data contained in other sources. Pseudoscorpions are one of the oldest colonisers of the land, with fossils known since the Middle Devonian (ca. 390 Ma). The only arachnid orders with an older fossil record are scorpions, harvestmen and acariform mites, plus two extinct groups. Pseudoscorpions do not fossilise easily, and records from the Mesozoic and Cenozoic consist almost exclusively of amber inclusions. Most Mesozoic fossils come from Archingeay and Burmese ambers (Late Cretaceous) and those from the Cenozoic are primarily from Eocene Baltic amber, although additional fossils from, for example, Miocene Dominican and Mexican ambers, are known. Overall, 16 of the 26 families of living pseudoscorpions have been documented from fossils and 49 currently valid species are recognised in the literature. Pseudoscorpions represent a case of morphological stasis and even the Devonian fossils look rather modern. Indeed, most amber fossils are comparable to Recent groups despite a major gap in the fossil record of almost 250 Myr. Baltic amber inclusions indicate palaeofauna inhabiting much warmer climates than today and point to climatic shifts in central Europe since the Eocene. They also indicate that some groups (e.g. Feaellidae and Pseudogarypidae) had much wider Eocene distributions. Their present-day occurrence is relictual and highlights past extinction events. Faunas from younger tropical amber deposits (e.g. Dominican and Mexican amber) are comparable to Recent ones. Generally, there is a strong bias in the amber record towards groups that live under tree bark, whereas those from litter habitats are underrepresented. We also discuss challenges in interpreting fossils: their cryptic morphology warranting novel techniques of morphological reconstruction, the massive gap in the fossil record between the Palaeozoic and Mesozoic, and problems with the classification of (historically) old amber material. Finally, we discuss aspects of the palaeoecology and biology of the fossils compared with the Recent fauna, such as phoresy.

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