scholarly journals The Fossil Record of Ray-Finned Fishes (Actinopterygii) in Greece

2021 ◽  
pp. 91-142
Author(s):  
Thodoris Argyriou

AbstractThe nowadays hyper-diverse clade of Actinopterygii (ray-finned bony fishes) is characterized by a long evolutionary history and an extremely rich global fossil record. This work builds upon 170 years of research on the fossil record of this clade in Greece. The taxonomy and spatiotemporal distribution of the ray-finned fish record of Greece are critically revisited and placed in an updated systematic and stratigraphic framework, while some new fossil data and interpretations are also provided. Greece hosts diverse ray-finned fish assemblages, which range in age from Lower Jurassic to Quaternary. Most known assemblages are of Miocene–Pliocene age and of marine affinities. A minimum of 32 families, followed by at least 34 genera and 22 species, have been recognized in Greece. From originally two named genera and seven species, only two fossil species, established on Greek material, are accepted as valid. Additional taxonomic diversity is anticipated, pending detailed investigations. From a taxonomic perspective, previous knowledge lies on preliminary or authoritative assessments of fossils, with many decades-old treatments needing revision. Little is known about Mesozoic–early Cenozoic occurrences or freshwater assemblages. Given the proven potential of the Greek fossil record, this chapter stresses the need for additional exploration and the establishment of permanent, curated collections of fossil fishes in Greek institutions. Directions for future research are discussed.

Paleobiology ◽  
2021 ◽  
pp. 1-11
Author(s):  
Indrė Žliobaitė ◽  
Mikael Fortelius

Abstract We know that the fossil record is incomplete. But how incomplete? Here we very coarsely estimate the completeness of the mammalian record in the Miocene, assuming that the duration of a mammalian species is about 1 Myr and the species diversity has stayed constant and is structurally comparable to the taxonomic diversity today. The overall completeness under these assumptions appears to be around 4%, but there are large differences across taxonomic groups. We find that the fossil record of proboscideans and perissodactyls as we know it for the Miocene must be close to complete, while we might know less than 15% of the species of artiodactyl or carnivore fossil species and only about 1% of primate species of the Miocene. The record of small mammals appears much less complete than that of large mammals.


Paleobiology ◽  
10.1666/12055 ◽  
2014 ◽  
Vol 40 (1) ◽  
pp. 91-101 ◽  
Author(s):  
Andrew J. Alverson

With species found throughout both marine and fresh waters, the diatom order Thalassiosirales is one of the most phylogenetically and ecologically diverse lineages of planktonic diatoms. A clear understanding of the timescale of Thalassiosirales evolution would provide novel insights into the rates and patterns of species diversification associated with major habitat shifts, as well as provide valuable context for understanding the age and evolutionary history of the model species, Cyclotella nana (= Thalassiosira pseudonana). The freshwater fossil record for Thalassiosirales is extensive, well characterized, and generally supportive of a Miocene origin for the major freshwater lineages. The marine record is, by comparison, more sparse and in many cases, unverified. The discovery of freshwater thalassiosiroids in Eocene sediments pushed the freshwater fossil record considerably further back in time, highlighting an apparent gap of some 30 million years. An alternative interpretation is that the Miocene and Eocene reports represent competing hypotheses. In the absence of additional independent and decisive fossil data, I explored the relative plausibility of these two scenarios with Bayesian relaxed molecular clock methods under a range of fossil calibration schemes. Although I found no support for the Eocene fossil dates, the two major freshwater colonization events probably occurred much earlier than previously thought—as early as the Paleocene for Cyclotella, followed by an Eocene origin for the cyclostephanoid lineage. Much of the extant freshwater diversity in both lineages traces back to the Miocene, however, giving the impression of a single Miocene origin. Efforts to infer the timescale of Thalassiosirales evolution more accurately would benefit from a systematic reevaluation of the marine fossil record and formal integration of fossil species into existing phylogenetic hypotheses.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Iwona Kania-Kłosok ◽  
Wiesław Krzemiński ◽  
Antonio Arillo

AbstractFirst record of the genus Helius—long-rostrum cranefly from Maestrazgo Basin (eastern Spain, Iberian Penisula) is documented. Two new fossil species of the genus Helius are described from Cretaceous Spanish amber and compared with other species of the genus known from fossil record with particular references to these known from Cretaceous period. Helius turolensis sp. nov. is described from San Just amber (Lower Cretaceous, upper Albian) Maestrazgo Basin, eastern Spain, and Helius hispanicus sp. nov. is described from Álava amber (Lower Cretaceous, upper Albian), Basque-Cantabrian Basin, northern Spain. The specific body morphology of representatives of the genus Helius preserved in Spanish amber was discussed in relation to the environmental conditions of the Maestrazgo Basin and Basque-Cantabrian Basin in Cretaceous.


2016 ◽  
Vol 371 (1691) ◽  
pp. 20150225 ◽  
Author(s):  
Daniele Silvestro ◽  
Alexander Zizka ◽  
Christine D. Bacon ◽  
Borja Cascales-Miñana ◽  
Nicolas Salamin ◽  
...  

Methods in historical biogeography have revolutionized our ability to infer the evolution of ancestral geographical ranges from phylogenies of extant taxa, the rates of dispersals, and biotic connectivity among areas. However, extant taxa are likely to provide limited and potentially biased information about past biogeographic processes, due to extinction, asymmetrical dispersals and variable connectivity among areas. Fossil data hold considerable information about past distribution of lineages, but suffer from largely incomplete sampling. Here we present a new dispersal–extinction–sampling (DES) model, which estimates biogeographic parameters using fossil occurrences instead of phylogenetic trees. The model estimates dispersal and extinction rates while explicitly accounting for the incompleteness of the fossil record. Rates can vary between areas and through time, thus providing the opportunity to assess complex scenarios of biogeographic evolution. We implement the DES model in a Bayesian framework and demonstrate through simulations that it can accurately infer all the relevant parameters. We demonstrate the use of our model by analysing the Cenozoic fossil record of land plants and inferring dispersal and extinction rates across Eurasia and North America. Our results show that biogeographic range evolution is not a time-homogeneous process, as assumed in most phylogenetic analyses, but varies through time and between areas. In our empirical assessment, this is shown by the striking predominance of plant dispersals from Eurasia into North America during the Eocene climatic cooling, followed by a shift in the opposite direction, and finally, a balance in biotic interchange since the middle Miocene. We conclude by discussing the potential of fossil-based analyses to test biogeographic hypotheses and improve phylogenetic methods in historical biogeography.


2018 ◽  
Vol 49 (4) ◽  
pp. 399-408
Author(s):  
Sara Gamboa ◽  
Vicente M. Ortuño

Limodromus emetikos sp. n. (Coleoptera: Carabidae) is described and illustrated from Baltic amber (Eocene). Based on its morphological features, the new species is considered a sister taxon of the extant Holarctic assimilis species group. Furthermore, the specimen described here could represent a case of stress-triggered regurgitation, which would represent the first fossil record of such a process in beetles.


Author(s):  
Ricardo Paredes

The accuracy on taxonomic determinations of palaeontology collections may have significant consequences in estimations of organism diversity through time. This justifies the need of taxonomic standardization of palaeontological collections. The perception of palaeodiversity through Phanerozoic time has significantly improved since the Sepkoski showed the marine invertebrate taxonomic data in diversity graphs, organized in orders (Sepkoski 1978) and families (Sepkoski 1979, Sepkoski 1984). The visual impact of these graphs engaged palaeontologists into gathering quantitative macroevolution in order to better understand marine palaeodiversity. Alroy et al. (2008) presented a rebuilt diversity curve based on genus-level in a large sample record. These and other statistically sound and standardized datasets of fossil occurrences have combined sources as literature, databases, and museum collections data as a foundation. Integration of these datasets with the entire fossil record based on individual specimens in space and time would be the ideal approach to species-level taxonomy standards determinations. An example showing how this approach may be achieved is the use of initiatives such as the Web-based data facility Palaeontology Database (PdB) which includes a large amount of fossil record data from throughout the world. The major advantage of that is to gather institucional and also private palaeontological collections with taxonomy experts validation. The core of these datasets is the taxon, with the species as the expected most reliable unit. Taxonomy is therefore the discipline enrolled in the process with the taxonomist at the centre of the process. Updated taxonomy is crucial to create reliable datasets and a careful approach should prevent biased data due to under- or overestimation of diversity. Palaeontological museum collections are known to be one of the largest repositories of fossil data. Taxonomic standardization of palaeontology collections in the context of a museum should: Engage taxonomists in revising fossil clades of the museum material; Promote networking and museum researcher peers involved in similar collections activities; Avoid replication of errors in taxonomic determinations (e.g. exclusive use of Web-based databases sources of taxonomy); Use type material to compare with the collection specimens; Critically analyse previous taxonomic determinations on old labels and associated specimen information; Promote the accessibility of the collection to the research community; Emphasize digitisation of specimen catalogue records as well as 2D imaging of the specimens. Engage taxonomists in revising fossil clades of the museum material; Promote networking and museum researcher peers involved in similar collections activities; Avoid replication of errors in taxonomic determinations (e.g. exclusive use of Web-based databases sources of taxonomy); Use type material to compare with the collection specimens; Critically analyse previous taxonomic determinations on old labels and associated specimen information; Promote the accessibility of the collection to the research community; Emphasize digitisation of specimen catalogue records as well as 2D imaging of the specimens. These practices are valuable complements to current methodologies adopted to improve the taxonomy of collections, resulting in more reliable data which further enables museum-based research focusing on palaeodiversity estimations.


Zootaxa ◽  
2016 ◽  
Vol 4200 (2) ◽  
pp. 327 ◽  
Author(s):  
PEDRO S. R. ROMANO

Pelomedusoides is the most diverse clade of side-necked turtles and there is an extensive fossil record (de Broin, 1988; Lapparent de Broin, 2000; Gaffney et al., 2006, 2011) that dates back at least to the Barremian (Lower Cretaceous) (Romano et al., 2014). Its large fossil record evidences a greater diversity in the past, particularly at the end of the Mesozoic, and exhibits a good sampling of species that are represented by skull material (Gaffney et al., 2006, 2011). As a consequence, the most complete and recent phylogenetic hypotheses for this clade (e.g. Romano et al., 2014; Cadena, 2015) are based on matrices comprising a great amount of cranial characters derived largely from Gaffney et al. (2006, 2011). In addition, it is well established that shell characters show a lot of phenotypic plasticity, even in the fossil species (Romano, 2008; Gaffney et al., 2006, 2011). In most cases it consequently is not justified to rely on “diagnostic features” of poorly informative shell-only material for describing a new species. Because of that, most authors remark new morphotypes in the literature when such aberrant specimens are recovered, but do not make any nomenclatural act by proposing a new yet poorly supported species (e.g. Romano et al., 2013; Ferreira & Langer, 2013; Menegazzo et al., 2015). Unfortunately, such a supposedly new bothremydid turtle (Pleurodira: Bothremydidae) from the Early Paleocene of Brazil was recently described based on poorly diagnostic remains (Carvalho et al., 2016; hereafter CGB, for the authors initials) and a correction of this unfounded nomenclatural act is required. In addition I present some comments on shell only material from Brazil in order to guide splitter-taxonomists to stop describing poorly preserved fossil specimens as new species. 


Author(s):  
Javier GONZÁLEZ-DIONIS ◽  
Carolina CASTILLO RUIZ ◽  
Penélope CRUZADO-CABALLERO ◽  
Elena CADAVID-MELERO ◽  
Vicente D. CRESPO

ABSTRACT Bats are one of the most abundant and important mammals in ecosystems. However, their fossil record is scarce and fragile, making them difficult to find. Accordingly, there is no record of this group in the volcanic islands of the mid-Atlantic Ocean apart from the Canary Islands. This paper studies the first bat fossil record of the Canary Islands (Spain). The material studied is found within two Quaternary lava tubes, Cueva de los Verdes on Lanzarote and Cueva Roja on the island of El Hierro. The dental and humeral morphology and biometry are analysed and compared with current specimens. Among our results we highlight the first fossil data of two species endemic to the islands of the mid-Atlantic Ocean, Plecotus teneriffae and Pipistrellus maderensis, the former from the Canary Islands and the latter from the Azores, Madeira and the Canary Islands. We also confirm the presence of Pipistrellus kuhlii in the fossil record of the island of Lanzarote. No differences are observed between the dental morphology of the current and the fossil populations of P. maderensis and Pl. teneriffae. In the case of P. kuhlii, the populations of the Canary Islands and the Iberian Peninsula show differences in the paraconule with respect to the populations from central Europe. Palaeoecological studies of these taxa suggest that these islands presented a similar habitat when the sites were formed to the present-day habitat.


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