scholarly journals Coordinated shifts to non-planktotrophic development in spatangoid echinoids during the Late Cretaceous

2009 ◽  
Vol 5 (5) ◽  
pp. 647-650 ◽  
Author(s):  
John A. Cunningham ◽  
Charlotte H. Jeffery Abt
Keyword(s):  
Larval Development ◽  
Late Cretaceous ◽  
Fossil Record ◽  
Evolutionary History ◽  
Sea Urchins ◽  
Geological History ◽  
Extrinsic Factors ◽  
Genus Level ◽  
History Of ◽  
Widespread Interest

Despite widespread interest in the interplay between evolutionary and developmental processes, we still know relatively little about the evolutionary history of larval development. Many clades exhibit multiple shifts from planktotrophic (feeding) to non-planktotrophic (non-feeding) larval development. An important question is whether these switches are scattered randomly through geological history or are concentrated in particular intervals of time. This issue is addressed using the Cretaceous spatangoid sea urchins, which are unusual in that larval strategy can be determined unambiguously from abundantly fossilized adult tests. Using a genus-level phylogeny, we identify five clades of non-planktotrophic taxa, each of which first appears in the fossil record in the Campanian or Maastrichtian (the final two Cretaceous stages). No examples of non-planktotrophy have been identified in any of the earlier stages of the Cretaceous. This strongly suggests that shifts to non-planktotrophic development are clustered in certain episodes of geological history, and this, in turn, implies that extrinsic factors operating at these times are responsible for driving shifts in developmental strategy.

The skeletal morphology of the solemydid turtleNaomichelys speciosafrom the Early Cretaceous of Texas

2014 ◽  
Vol 88 (6) ◽  
pp. 1257-1287 ◽  
Author(s):  
Walter G. Joyce ◽  
Juliana Sterli ◽  
Sandra D. Chapman
Keyword(s):  
North America ◽  
Late Cretaceous ◽  
Lower Cretaceous ◽  
Fossil Record ◽  
Posterior Margin ◽  
Late Jurassic ◽  
Evolutionary History ◽  
Ventral View ◽  
Skeletal Morphology ◽  
History Of

The fossil record of solemydid turtles is primarily based on isolated fragments collected from Late Jurassic to Late Cretaceous sediments throughout North America and Europe and little is therefore known about the morphology and evolutionary history of the group. We here provide a detailed description of the only known near-complete solemydid skeleton, which was collected from the Lower Cretaceous (Aptian–Albian) Antlers Formation of Texas during the mid-twentieth century, but essentially remains undescribed to date. Though comparison is limited, the skeleton is referred toNaomichelys speciosa, which is based on an isolated entoplastron from the Lower Cretaceous (Aptian–Albian) Kootenai (Cloverly) Formation of Montana. The absence of temporal emarginations, contribution of the jugals to the orbits, and a clear subdivision of the middle and inner cavities, and the presence of elongate postorbitals, posteriorly expanded squamosals, a triangular fossa at the posterior margin of the squamosals, an additional pair of tubercula basioccipitale that is formed by the pterygoids, foramina pro ramo nervi vidiani (VII) that are visible in ventral view, shell sculpturing consisting of high tubercles, a large entoplastron with entoplastral scute, V-shaped anterior peripherals, and limb osteoderms with tubercular sculpture diagnoseNaomichelys speciosaas a representative of Solemydidae. The full visibility of the parabasisphenoid complex in ventral view, the presence of an expanded symphyseal shelf, and the unusual ventromedial folding of the coronoid process are the primary characteristics that distinguishNaomichelys speciosafrom the near-coeval European taxonHelochelydra nopcsai.

scholarly journals Late Cretaceous domatia reveal the antiquity of plant–mite mutualisms in flowering plants

2019 ◽  
Vol 15 (11) ◽  
pp. 20190657 ◽  
Author(s):  
S. Augusta Maccracken ◽  
Ian M. Miller ◽  
Conrad C. Labandeira
Keyword(s):  
Late Cretaceous ◽  
Fossil Record ◽  
Evolutionary History ◽  
Upper Cretaceous ◽  
Flowering Plants ◽  
Predaceous Mites ◽  
First Occurrence ◽  
History Of ◽  
Living Species ◽  
Cenozoic Era

Mite houses, or acarodomatia, are found on the leaves of over 2000 living species of flowering plants today. These structures facilitate tri-trophic interactions between the host plant, its fungi or herbivore adversaries, and fungivorous or predaceous mites by providing shelter for the mite consumers. Previously, the oldest acarodomatia were described on a Cenozoic Era fossil leaf dating to 49 Myr in age. Here, we report the first occurrence of Mesozoic Era acarodomatia in the fossil record from leaves discovered in the Upper Cretaceous Kaiparowits Formation (76.6–74.5 Ma) in southern UT, USA. This discovery extends the origin of acarodomatia by greater than 25 Myr, and the antiquity of this plant–mite mutualism provides important constraints for the evolutionary history of acarodomatia on angiosperms.

Stomatopod predation on fossil gastropods from the Plio-Pleistocene of Florida

1991 ◽  
Vol 65 (03) ◽  
pp. 355-360 ◽  
Author(s):  
Dana H. Geary ◽  
Warren D. Allmon ◽  
Marjorie L. Reaka-Kudla
Keyword(s):  
Shallow Water ◽  
Fossil Record ◽  
Evolutionary History ◽  
Considerable Importance ◽  
Geological History ◽  
Benthic Assemblages ◽  
History Of ◽  
Fossil Gastropods

Stomatopods (mantis shrimps) are important predators in Recent tropical shallow-water communities. Despite a long geological history, they are poorly preserved as fossils, and traces of their predation have never been identified from the fossil record. Here we report on Plio-Pleistocene gastropods (mostly Strombus) from Florida with distinctive holes “punched” into their body whorls. The similarity of these holes to holes punched into live gastropods by Gonadactylus implicates gonodactyloid stomatopods as the predators that made them. Recent gonodactyloids break gastropod shells as thick and thicker than those of the Plio-Pleistocene strombids that were punched. Because our data underestimate the incidence of stomatopod predation, the frequency of holes in these strombids (8–13 percent) suggests that stomatopod predation may be of considerable importance in the ecological and evolutionary history of tropical benthic assemblages.

A fossil record of land plant origins from charophyte algae

Science ◽  
2021 ◽  
Vol 373 (6556) ◽  
pp. 792-796 ◽  
Author(s):  
Paul K. Strother ◽  
Clinton Foster
Keyword(s):  
Fossil Record ◽  
Evolutionary History ◽  
Phylogenetic Signal ◽  
Land Plant ◽  
Fossil Plants ◽  
Fossil Plant ◽  
Molecular Phylogenetic ◽  
History Of ◽  
Time Gap ◽  
Evolutionary Continuity

Molecular time trees indicating that embryophytes originated around 500 million years ago (Ma) during the Cambrian are at odds with the record of fossil plants, which first appear in the mid-Silurian almost 80 million years later. This time gap has been attributed to a missing fossil plant record, but that attribution belies the case for fossil spores. Here, we describe a Tremadocian (Early Ordovician, about 480 Ma) assemblage with elements of both Cambrian and younger embryophyte spores that provides a new level of evolutionary continuity between embryophytes and their algal ancestors. This finding suggests that the molecular phylogenetic signal retains a latent evolutionary history of the acquisition of the embryophytic developmental genome, a history that perhaps began during Ediacaran-Cambrian time but was not completed until the mid-Silurian (about 430 Ma).

scholarly journals Experimental degradation of helicoidal photonic nanostructures in scarab beetles (Coleoptera: Scarabaeidae): implications for the identification of circularly polarizing cuticle in the fossil record

2018 ◽  
Vol 15 (148) ◽  
pp. 20180560 ◽  
Author(s):  
Giliane P. Odin ◽  
Maria E. McNamara ◽  
Hans Arwin ◽  
Kenneth Järrendahl
Keyword(s):  
Uric Acid ◽  
Fossil Record ◽  
Evolutionary History ◽  
Polarized Light ◽  
Circularly Polarized Light ◽  
Circularly Polarized ◽  
Alkaline Conditions ◽  
History Of ◽  
Diagenetic History ◽  
Scarab Beetles

Scarab beetles (Coleoptera: Scarabaeidae) can exhibit striking colours produced by pigments and/or nanostructures. The latter include helicoidal (Bouligand) structures that can generate circularly polarized light. These have a cryptic evolutionary history in part because fossil examples are unknown. This suggests either a real biological signal, i.e. that Bouligand structures did not evolve until recently, or a taphonomic signal, i.e. that conditions during the fossilization process were not conducive to their preservation. We address this issue by experimentally degrading circularly polarizing cuticle of modern scarab beetles to test the relative roles of decay, maturation and taxonomy in controlling preservation. The results reveal that Bouligand structures have the potential to survive fossilization, but preservation is controlled by taxonomy and the diagenetic history of specimens. Further, cuticle of specific genus ( Chrysina ) is particularly decay-prone in alkaline conditions; this may relate to the presence of certain compounds, e.g. uric acid, in the cuticle of these taxa.

Systematics and biogeography of the “Metacryphaeus group” Calmoniidae (Trilobita, Devonian), with comments on adaptive radiations and the geological history of the Malvinokaffric Realm

1993 ◽  
Vol 67 (4) ◽  
pp. 549-570 ◽  
Author(s):  
Bruce S. Lieberman
Keyword(s):  
New Species ◽  
South African ◽  
Evolutionary History ◽  
Geological History ◽  
Parsimony Analysis ◽  
Evolutionary Patterns ◽  
The Family ◽  
History Of ◽  
Adaptive Radiations ◽  
Rapid Diversification

Phylogenetic parsimony analysis was used to classify the Siegenian–Eifelian “Metacryphaeus group” of the family Calmoniidae. Thirty-eight exoskeletal characters for 16 taxa produced a shortest-length cladogram with a consistency index of 0.49. A classification based on retrieving the structure of this cladogram recognizes nine genera: Typhloniscus Salter, Plesioconvexa n. gen., Punillaspis Baldis and Longobucco, Eldredgeia n. gen., Clarkeaspis n. gen., Malvinocooperella n. gen., Wolfartaspis Cooper, Plesiomalvinella Lieberman, Edgecombe, and Eldredge (used to represent the malvinellid clade), and Metacryphaeus Reed. The malvinellid clade is most closely related to a revised monophyletic Metacryphaeus. Typhloniscus is the basal member of the “Metacryphaeus group,” and the monotypic Wolfartaspis is sister to the clade containing the malvinellids and Metacryphaeus. Six new species are diagnosed: Punillaspis n. sp. A, “Clarkeaspis” gouldi, Clarkeaspis padillaensis, Malvinocooperella pregiganteus, Metacryphaeus curvigena, and Metacryphaeus branisai. Primitively, this group has South African and Andean affinities, and its evolutionary history suggests rapid diversification. In addition, evolutionary patterns in this group, and the distribution of character reversals, call into question certain notions about the nature of adaptive radiations. The distributions of taxa may answer questions about the number of marine transgressive/regressive cycles in the Emsian–Eifelian of the Malvinokaffric Realm.

scholarly journals A comparative atlas of the skull osteology of European lizards (Reptilia: Squamata)

2019 ◽  
Vol 187 (3) ◽  
pp. 829-928 ◽  
Author(s):  
Andrea Villa ◽  
Massimo Delfino
Keyword(s):  
Fossil Record ◽  
Evolutionary History ◽  
European Species ◽  
History Of ◽  
Diagnostic Key ◽  
Single Bone ◽  
Fossil Lizards ◽  
Bone Remains ◽  
Comparative Osteology ◽  
Broad Scale

Abstract The fossil record provides evidence of a long evolutionary history of European lizards. Since fossil lizards are regularly represented by bone remains, the knowledge of the origins of extant taxa and their distribution in time and space is hindered by the fact that their comparative osteology is not yet completely and adequately known. In spite of a rising interest in this topic since the end of the 20th century, a gap in our knowledge is still evident. We here report the first broad-scale comparative osteological analysis of the skulls of extant European lizards, highlighting significant differences that can be used in identification. This comparative study, including as many European species as possible, leads to the creation of a detailed diagnostic key for each single bone. Also, our data significantly improve the recognizability of extant European non-snake squamates, with 54% of the current diversity to be recognized based on the new results contra the previously estimated 31%. This recognizability is expected to further increase in the future, with new studies focusing on species that are either missing or poorly represented here, or applying promising advanced methodologies.

Theoretical diversity of the marine biosphere

Paleobiology ◽  
2010 ◽  
Vol 36 (1) ◽  
pp. 1-15 ◽  
Author(s):  
Michał Kowalewski ◽  
Seth Finnegan
Keyword(s):  
Empirical Data ◽  
Fossil Record ◽  
Empirical Studies ◽  
Geological History ◽  
Empirical Knowledge ◽  
Primary Target ◽  
History Of ◽  
Global Biodiversity ◽  
Theoretical Considerations ◽  
Marine Biosphere

In considering the history of biodiversity paleontologists have focused on exploratory investigations of empirical data derived from the fossil record. Starting with the pioneering work of Philips (1860), and continuing at an increasing pace through today, this inductive approach has dominated diversity research. In contrast, deductive theoretical considerations that focus on the expected history of biodiversity, and develop independently of empirical knowledge, have remained under-explored. Appreciating the need for a nomothetic paleobiology (Gould 1980), we here reconsider the history of biodiversity, using deductive models constrained by a few, self-evident parameters. This analysis centers on the marine fossil record, the primary target of most previous empirical studies on the geological history of global biodiversity (e.g., Valentine 1969; Raup 1972, 1976; Sepkoski et al. 1981; Alroy et al. 2008).

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.

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