scholarly journals Ostracods had colonized estuaries by the late Silurian

2021 ◽  
Vol 17 (12) ◽  
Author(s):  
Anna McGairy ◽  
Toshifumi Komatsu ◽  
Mark Williams ◽  
Thomas H. P. Harvey ◽  
C. Giles Miller ◽  
...  

The fossil record of terrestrialization documents notable shifts in the environmental and physiological tolerances of many animal and plant groups. However, for certain significant components of modern freshwater and terrestrial environments, the transition out of marine settings remains largely unconstrained. Ostracod crustaceans occupy an exceptional range of modern aquatic environments and are invaluable palaeoenvironmental indicators in the fossil record. However, pre-Carboniferous records of supposed non-marine and marginal marine ostracods are sparse, and the timing of their marine to non-marine transition has proven elusive. Here, we reassess the early environmental history of ostracods in light of new assemblages from the late Silurian of Vietnam. Two, low diversity but distinct ostracod assemblages are associated with estuarine deposits. This occurrence is consistent with previous incidental reports of ostracods occupying marginal and brackish settings through the late Silurian and Devonian. Therefore, ostracods were pioneering the occupation of marginal marine and estuarine settings 60 Myr before the Carboniferous and they were a component of the early phase of transition from marine to non-marine environments.

2012 ◽  
Vol 279 (1737) ◽  
pp. 2323-2329 ◽  
Author(s):  
Greta Carrete Vega ◽  
John J. Wiens

The most dramatic gradient in global biodiversity is between marine and terrestrial environments. Terrestrial environments contain approximately 75–85% of all estimated species, but occupy only 30 per cent of the Earth's surface (and only approx. 1–10% by volume), whereas marine environments occupy a larger area and volume, but have a smaller fraction of Earth's estimated diversity. Many hypotheses have been proposed to explain this disparity, but there have been few large-scale quantitative tests. Here, we analyse patterns of diversity in actinopterygian (ray-finned) fishes, the most species-rich clade of marine vertebrates, containing 96 per cent of fish species. Despite the much greater area and productivity of marine environments, actinopterygian richness is similar in freshwater and marine habitats (15 150 versus 14 740 species). Net diversification rates (speciation–extinction) are similar in predominantly freshwater and saltwater clades. Both habitats are dominated by two hyperdiverse but relatively recent clades (Ostariophysi and Percomorpha). Remarkably, trait reconstructions (for both living and fossil taxa) suggest that all extant marine actinopterygians were derived from a freshwater ancestor, indicating a role for ancient extinction in explaining low marine richness. Finally, by analysing an entirely aquatic group, we are able to better sort among potential hypotheses for explaining the paradoxically low diversity of marine environments.


Author(s):  
Shibani Bose

The rhinoceros has received scant attention in wildlife histories as against the iconic status enjoyed by elephants, cheetahs, and lions. This is particularly true in the context of ancient India. Against this backdrop, this chapter chronicles the much-neglected saga of the rhinoceros in ancient India based on its first appearance in the fossil record, its presence in archaeological contexts in the form of bones and visual representations till its appearance in the literary texts of the period. The narrative helps us map the geographical retreat of the animal to its present-day havens. The details of this retreat are integral to understanding aspects of the environmental history of ancient India.


2019 ◽  
Author(s):  
Fabiany Herrera ◽  
Mónica R. Carvalho ◽  
Scott L. Wing ◽  
Carlos Jaramillo ◽  
Patrick S. Herendeen

Leguminosae are one of the most diverse flowering-plant groups today, but the evolutionary history of the family remains obscure because of the scarce early fossil record, particularly from lowland tropics. Here, we report ~500 compression or impression specimens with distinctive legume features collected from the Cerrejón and Bogotá Formations, Middle to Late Paleocene of Colombia. The specimens were segregated into eight fruit and six leaf morphotypes. Two bipinnate leaf morphotypes are confidently placed in the Caesalpinioideae and are the earliest record of this subfamily. Two of the fruit morphotypes are placed in the Detarioideae and Dialioideae. All other fruit and leaf morphotypes show similarities with more than one subfamily or their affinities remain uncertain. The abundant fossil fruits and leaves described here show that Leguminosae was the most important component of the earliest rainforests in northern South America c. 60–58 million years ago.


2003 ◽  
Vol 9 ◽  
pp. 181-202 ◽  
Author(s):  
David J. Horne

Ostracodes are ecologically diverse at the present day, inhabiting marine, nonmarine and (semi)terrestrial environments. Modern benthic faunas are dominated by Podocopa (marine and nonmarine Podocopida, marine Platycopida, and extremely rare marine Palaeocopida), while the Myodocopa (Myodocopida and Halocyprida) are diverse in the marine pelagic realm, as well as having many nektobenthic taxa. Their excellent fossil record facilitates reconstructions of their phylogenetic relationships and ecological adaptations throughout their Phanerozoic history. The earliest known ostracodes are of Ordovician age, when representatives of the extant orders Podocopida, Platycopida and Palaeocopida were already present, together with (possible) early Myodocopa and extinct orders such as the Leperditicopida. Cambrian bivalved arthropods such as bradoriids and phosphatocopids are no longer regarded as Ostracoda.Ordovician ostracodes were predominantly marine meiobenthos, diversifying into depth-related assemblages dominated by palaeocopids. The beginnings of podocopan radiations in marginal marine environments (brackish and hypersaline waters) are seen in the Silurian, as is an ecological shift of nektobenthic myodocopans to form the first pelagic ostracode faunas. Of the diverse marine Paleozoic palaeocopids, only a single lineage, the puncioids, survived beyond the Permian and today live interstitially in high-energy shallow marine environments. Post-Paleozoic marine benthic ostracode faunas are dominated by cytheroidean podocopids which gave rise to several radiations in the Mesozoic and Cenozoic. The healdiid metacopines (podocopans), of Devonian origins, enjoyed a marine radiation in the Triassic and Early Jurassic and then became extinct. Marine platycopids were also significant components of Mesozoic marine faunas and are relatively diverse in warm, shallow carbonate environments today.Suggestions that the first freshwater ostracodes were Devonian leperditicopids are controversial; undoubted nonmarine / freshwater radiations developed during the Early Carboniferous, including darwinuloidean and carbonitoidean podocopids and possibly some platycopids, together with cytheroidean podocopids (limnocytherids) in the Late Carboniferous. Of these only the darwinuloideans and limnocytherids survived the end-Permian extinctions and are still found in modern nonmarine waters; however, the dominant freshwater ostracodes today are the cypridoidean podocopids, whose radiation began in the Triassic and attained explosive proportions in the Late Jurassic - Early Cretaceous (although there are controversial suggestions of Paleozoic origins for this group). In addition to the limnocytherids there have been several other, separate invasions of nonmarine waters by cytheroidean podocopids, notably the cytherideids and the commensal entocytherids. Radiations in damp terrestrial environments have been initiated by both marine and nonmarine groups, but such invasions lack a recognized fossil record; (semi)terrestrial cypridoideans and darwinuloideans may represent Late Mesozoic radiations, while the Terrestricytheroidea, with marine affinities, may be much older, possibly Late Paleozoic in origin.


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