Species diversity in the Phanerozoic: a tabulation

Paleobiology ◽  
1976 ◽  
Vol 2 (4) ◽  
pp. 279-288 ◽  
Author(s):  
David M. Raup

On the basis of about 70,000 species citations in the Zoological Record, it is estimated that about 190,000 fossil invertebrate species were described and named through 1970. The true figure may be higher because of incompleteness of the Zoological Record or lower because the estimate does not account for synonymy.About 70% of the species were described from USSR, Europe, and North America. About 42% are Paleozoic, 28% Mesozoic, and 30% Cenozoic. In the Cambrian part of the sample, 75% of the species are trilobites. In the Mesozoic and Cenozoic, about 70% are either molluscs or protozoans.When the data are normalized for absolute time, diversity (species per million years) shows a Paleozoic high in the Devonian which is approximately four-tenths of the Cenozoic level.

Paleobiology ◽  
1978 ◽  
Vol 4 (3) ◽  
pp. 367-372 ◽  
Author(s):  
Carl F. Koch

The published fossil record has significant bias in favor of common and biostratigraphically important taxa when compared with data obtained from a thorough examination of several hundred collections from the Western Interior of North America. Overall species diversity is underestimated by a factor of 3 to 4, and bivalve and gastropod diversity by a factor of 5. The proportion of bivalves increased from 40 to 56% of the fauna, and the proportion of ammonites decreased from 28 to 18%. Thirteen published reports listed 65 species from 203 reported occurrences. Data from all sources showed 170 species for 1050 occurrences. By using abundance data and assuming a log-normal distribution, as many as 200 fossilizable mollusc species may have inhabited the Western Interior during the uppermost biozone of the Cenomanian. The importance of this study is that it quantifies the bias in the published fossil record relative to the potential fossil record for an unusually well studied interval of geologic time. The bias would be greater for less well studied strata.


Zootaxa ◽  
2012 ◽  
Vol 3193 (1) ◽  
pp. 1 ◽  
Author(s):  
DIANA M. PERCY ◽  
ALESSANDRA RUNG ◽  
MARK S. HODDLE

A revised checklist to the species of Psylloidea (Hemiptera) from California is presented, with information on host plantdata, distributions, introduced and pest species, parasites, parasitoids, and predators, and biological control programs. Thelist includes 164 species, of which six are newly recorded. In total, this comprises a 26% increase in the number of speciesrecorded for California since the last published checklist in 1988. Choricymoza Bliven is a new synonym of PhylloplectaRiley, and 10 species previously in Euphalerus Schwarz are recombined under Nyctiphalerus Bliven. California has therichest native psyllid fauna in North America, and the influence of climatic and floristic diversity on this diversificationis considered. Key words: biogeography, host plant, jumping plant lice, species diversity, pest species.


1992 ◽  
Vol 6 ◽  
pp. 295-295
Author(s):  
Garland R. Upchurch

The Cretaceous rise of flowering plants marked an important transition in the modernization of terrestrial ecosystems. Well documented is the diversification of angiosperm pollen during the mid-Cretaceous and the migration of angiosperms from low latitudes to middle and high latitudes during the Barremian to Cenomanian. Global compilations of “species” diversity indicate a rapid rise in angiosperm diversity during the Albian to Cenomanian. This rise parallels a decline in the species diversity of archaic pteridophytes and the gymnosperm orders Cycadales, Bennettitales, Ginkgoales, Czekanowskiales, and Caytoniales. Late Cretaceous floras show more gradual trends in species diversity than mid-Cretaceous floras.Megafloral reconstructions of vegetation and climate for North America and other continents indicate warm temperatures in coastal regions of middle to high latitudes. Cretaceous biomes, however, often cannot be compared closely with Recent biomes. During much of the Cretaceous, conifers and other gymnosperms shared dominance with angiosperms in tropical and subtropical vegetation, unlike the Recent. During the Late Cretaceous, tropical rainforest was areally restricted. The few known leaf megafloras from equatorial regions indicate subhumid, rather than rainforest, conditions. Desert and semi-desert were widespread at lower latitudes and are documented by the occurrence of evaporite minerals in China, Africa, Spain, Mexico, and South America. Mid-latitude vegetation consisted of open-canopy broadleaved and coniferous evergreen woodlands that existed under subhumid conditions and low seasonality. High-latitude vegetation of the Northern Hemisphere consisted of coniferous and broadleaved deciduous forest, rather than boreal forest and tundra. High-latitude vegetation from coastal regions of the Southern Hemisphere consisted of evergreen conifers and angiosperms. Rainforest conditions appear to have been largely restricted to polar latitudes.Data on relative abundance, though often incomplete, indicate that angiosperms became ecologically important in tropical to warm subtropical broadleaved evergreen forests and woodlands by the Cenomanian. However, their rise to dominance took longer in other biomes. Conifers formed an important component of many Late Cretaceous biomes, and the persistence of archaic gymnosperms was strongly influenced by climate. Deciduous Ginkgoales, Czekanowskiales, Bennettitales, and Caytoniales are rare to absent in Late Cretaceous megafloras from warm subtropical to tropical climates, but they persist in megafloras from cooler climates. Archaic conifers such as Frenelopsis occur in megafloras representing low-latitude desert and semi-desert, but they are generally absent in more humid assemblages. Within mid-latitude broadleaved and coniferous evergreen woodland from North America, conifers show evidence for co-dominance with angiosperms into the early Maastrichtian. However, this co-dominance appears to have ended by latest Maastrichtian, which implies that vegetational reorganization occurred during the last few million years of the Cretaceous in North America.


Pedobiologia ◽  
2006 ◽  
Vol 50 (1) ◽  
pp. 61-68 ◽  
Author(s):  
Sophie Rochefort ◽  
Fernand Therrien ◽  
David J. Shetlar ◽  
Jacques Brodeur

2013 ◽  
Vol 17 (1) ◽  
pp. 129-141 ◽  
Author(s):  
Viktoria Wagner ◽  
Toby Spribille ◽  
Stefan Abrahamczyk ◽  
Erwin Bergmeier

2020 ◽  
Vol 119 (2) ◽  
pp. 567-585 ◽  
Author(s):  
Arseny A. Makarikov ◽  
Kurt E. Galbreath ◽  
Ralph P. Eckerlin ◽  
Eric P. Hoberg

Paleobiology ◽  
1976 ◽  
Vol 2 (4) ◽  
pp. 289-297 ◽  
Author(s):  
David M. Raup

Species diversity among fossil invertebrates of the Phanerozoic is highly correlated with volume and area of sedimentary rocks. The correlations are statistically significant at the 1% level. The relationship holds even in regions (such as Canada) where the area and volume of rock do not increase through time. These results are interpreted as indicating that the apparent number of species is strongly dependent on sampling and that many of the changes in diversity seen in the Phanerozoic are artifactual. Consequently, there is no compelling evidence for a general increase in the number of invertebrate species from Paleozoic to Recent. This conclusion applies primarily to marine organisms. Diversity may have been in dynamic equilibrium throughout much of this time.A few intervals of the Phanerozoic have consistently fewer invertebrate species than would be predicted from the amount of sedimentary rock available for study. The Silurian, Permian, and Cretaceous stand out in this regard. This may result either from lower than normal diversity during these periods or from an unusual abundance of unfossiliferous rocks (evaporites, red beds, etc.).


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