scholarly journals A survey of dinosaur diversity by clade, age, place of discovery and year of description

Author(s):  
Michael P Taylor

Dinosaur diversity is analyzed in terms of the number of valid genera within each major clade, Mesozoic age, place of discovery and year of description. Aves (Archaeopteryx + Neornithes) is excluded. Nomina nuda and nomina dubia are not counted. The results show 451 valid dinosaurian genera at the end of 2001, of which 282 are saurischian (112 sauropodomorphs and 170 theropods, including 93 coelurosaurs) and 169 ornithischian, including 11 pachycephalosaurs, 26 ceratopsians, 60 ornithopods, 12 stegosaurs, and 38 ankylosaurs. Thirty-eight genera arose in the Triassic, 124 in the Jurassic, and 289 in the Cretaceous, of which a disproportionately high number — 85 and 47 — are from the Campanian and Maastrichtian. The Kimmeridgian was the most productive age, with an average of 11.18 new genera per million years. The Kimmeridgian saw an unparalleled boom in sauropod diversity, with 20 new sauropod genera arising in its 3.4 million years, an average of one new sauropod every 170,000 years. Asia was the most productive continent with 149 genera, followed by North America (135), Europe (66), South America (52), Africa (39), Australasia (9), and finally Antarctica (1). Just three countries account for more than half of all dinosaur diversity, with 231 genera between them: the U.S.A (105), China (73), and Mongolia (53). The top six countries also include Argentina (44), England (30), and Canada (30), and together provide 335 dinosaur genera, nearly three quarters of the total. The rate of naming new dinosaurs has increased hugely in recent years, with more genera named in the last 19 years than in all the preceding 159 years. The results of these analyses must be interpreted with care, as diversity in ancient ecosystems is perceived through a series of preservational and human filters yielding observed diversity patterns that may be very different from the actual diversity.

2014 ◽  
Author(s):  
Michael P Taylor

Dinosaur diversity is analyzed in terms of the number of valid genera within each major clade, Mesozoic age, place of discovery and year of description. Aves (Archaeopteryx + Neornithes) is excluded. Nomina nuda and nomina dubia are not counted. The results show 451 valid dinosaurian genera at the end of 2001, of which 282 are saurischian (112 sauropodomorphs and 170 theropods, including 93 coelurosaurs) and 169 ornithischian, including 11 pachycephalosaurs, 26 ceratopsians, 60 ornithopods, 12 stegosaurs, and 38 ankylosaurs. Thirty-eight genera arose in the Triassic, 124 in the Jurassic, and 289 in the Cretaceous, of which a disproportionately high number — 85 and 47 — are from the Campanian and Maastrichtian. The Kimmeridgian was the most productive age, with an average of 11.18 new genera per million years. The Kimmeridgian saw an unparalleled boom in sauropod diversity, with 20 new sauropod genera arising in its 3.4 million years, an average of one new sauropod every 170,000 years. Asia was the most productive continent with 149 genera, followed by North America (135), Europe (66), South America (52), Africa (39), Australasia (9), and finally Antarctica (1). Just three countries account for more than half of all dinosaur diversity, with 231 genera between them: the U.S.A (105), China (73), and Mongolia (53). The top six countries also include Argentina (44), England (30), and Canada (30), and together provide 335 dinosaur genera, nearly three quarters of the total. The rate of naming new dinosaurs has increased hugely in recent years, with more genera named in the last 19 years than in all the preceding 159 years. The results of these analyses must be interpreted with care, as diversity in ancient ecosystems is perceived through a series of preservational and human filters yielding observed diversity patterns that may be very different from the actual diversity.


2013 ◽  
Vol 87 (2) ◽  
pp. 254-268 ◽  
Author(s):  
Pavel Gol'din ◽  
Evgenij Zvonok

A new basal basilosaurid cetacean, Basilotritus uheni n. gen. n. sp., comes from the late middle Eocene (Bartonian) of Ukraine. It is the earliest dated record of a cetacean from Eastern Europe. The tympanic bulla of Basilotritus uheni shares basilosaurid synapomorphies but possesses unusual traits inherited from protocetids. Cetaceans related to Basilotritus uheni and referred to as Eocetus or “Eocetus” have been recorded from Africa, Europe, North America and South America. “Eocetus” wardii from North America is recombined as Basilotritus wardii. Platyosphys paulsonii and Platyosphys einori from Ukraine are considered as nomina dubia; specimens prior referred to as Platyosphys sp. are similar or related to Basilotritus. Other records of the Eocene cetaceans from Ukraine and south Russia are identified as Basilotritus or related genera. Early basilosaurids are demonstrated to be a paraphyletic, morphologically and geographically diverse group of the genera that colonized the world ocean as late as in Bartonian age and were probably the ancestors of Neoceti, as well as of more derived basilosaurids.


2010 ◽  
Vol 84 (1) ◽  
pp. 32-50 ◽  
Author(s):  
William I. Ausich ◽  
Thomas W. Kammer

The Batocrinidae was a component of the North America Early Mississippian crinoid fauna and a significant contributor to the global biodiversity spike referred to as the “Age of Crinoids.” All batocrinids are North American, and all but one species are confined to the Tournaisian and Visean. In this contribution, genera are objectively defined on discrete characters, and the generic assignment of all valid species is re-evaluated. A phylogenetic hypothesis is presented for relationships within the Batocrinidae based on parsimony-based analyses and known stratigraphic ranges.Fifteen basic batocrinid architectural designs are recognized as genera, and four new genera are described:Glannearycrinusn. gen.,Gongylocrinusn. gen,Magnuscrinusn. gen., andSimatocrinusn. gen.Batocrinuswas a catch-all genus for any Mississippian camerate with tetragonal first primibrachials and an anal tube; thus, many late 19thcentury species are in need of a modern generic assignment. In this contribution, 61 percent of the 166 currently valid batocrinid species are reassigned to different genera. In addition,Sunwaptacrinusis transferred to the Batocrinidae, six species are transferred out of the Batocrinidae, and five species are designated as nomina dubia.


2017 ◽  
Vol 43 (2) ◽  
pp. 208 ◽  
Author(s):  
Daniele Cristine Hoffmann Schlesener ◽  
Jutiane Wollmann ◽  
Juliano De Bastos Pazini ◽  
Anderson Dionei Grützmacher ◽  
Flávio Roberto Mello Garcia

Drosophila suzukii (Diptera, Drosophilidae) is an exotic species, endemic to Asia and currently a pest to small and stone fruits in several countries of North America and Europe. It was detected in 2013 for the first time in South America, in the south of Brazil. Unlike most drosophilids, this species deserves special attention, because the females are capable of oviposit inside healthy fruits, rendering their sale and export prohibited. Despite the confirmed existence of this species in different states of Brazil, this insect is yet been to be given the pest status. Nevertheless, the mere presence of this species is enough to cause concern to producers of small fruits and to justify further investigation for it’s control, especially chemical control for a possible change in status. Therefore, the goal of this work was to evaluate, in laboratory, mortality of D. suzukii adults and ovicidal effect when exposed to different insecticides registered for species of the Tephritidae and Agromyzidae families in different cultures. The insecticides deltamethrin, dimethoate, spinosad, fenitrothion, phosmet, malathion, methidathion, and zeta-cypermethrin resulted in mortality to 100 % of the subjects three days after the treatment (DAT). Regarding the effects over eggs, it was  established that the insecticides fenitrothion, malathion, and methidathion deemed 100 % of the eggs not viable, followed by phosmet and diflubenzuron, which also caused elevated reduction in the eclosion of larvae two DAT.


1959 ◽  
Vol 37 (2) ◽  
pp. 173-208 ◽  
Author(s):  
Doris Löve ◽  
Pierre Dansereau

The following paper is an evaluation of the taxonomic and ecological status of the genus Xanthium L. A review of its systematics demonstrates that many so-called "species" described on material from Europe actually have their origin in America, except one, X. strumarium s. str., which seems to have a Mediterranean–European center of dispersal. Another conclusion drawn is that Xanthium consists of only two distinct species: X. spinosum L. and X. strumarium L. The former is a relatively stable species, the latter an enormously variable one readily subdivided into a number of minor taxonomic entities.Ecologically, in eastern North America at least, Xanthium is primarily a beach plant, which prefers open habitats and succumbs to crowding. The seeds are most often dispersed by water and wind. It enters easily into ruderal habitats, but only as long as these are open and unshaded.The generalized short-day flowering response in this genus supports our hypothesis that Xanthium has a tropical–subtropical origin, and we feel that it has its center in Central and/or South America, whence it has spread over the continents north and southward.There is no evidence for any sterility barriers separating the entities of X. strumarium, but we feel that an intense inbreeding with an occasional outbreeding is responsible for the enormous variation, often resulting in small, local, but unstable taxa.


2017 ◽  
Vol 104 (11) ◽  
pp. 1717-1728 ◽  
Author(s):  
C. Matt Guilliams ◽  
Kristen E. Hasenstab-Lehman ◽  
Makenzie E. Mabry ◽  
Michael G. Simpson

Author(s):  

Abstract A new distribution map is provided for Peronospora farinosa Kiessl. Hosts: Beet (Beta vulgaris) and other B. spp., Spinach (Spinacia oleracea), Chenopodium spp. Information is given on the geographical distribution in AFRICA, Ethiopia, Kenya, Libya, Morocco, South Africa, Tanzania, Zimbabwe, ASIA, Afghanistan, Burma, China, Hong Kong, India (Northern States) (Uttar Pradesh) (Madhya Pradesh), Iran, Iraq, Israel, Japan, Korea, Lebanon, Mongolia, Nepal, Pakistan, Taiwan, Thailand, Turkey, USSR, AUSTRALASIA & OCEANIA, Australia, New Zealand, EUROPE, Austria, Belgium, Britain, Bulgaria, Cyprus, Czechoslovakia, Denmark, France, Germany, Greece, Hungary, Iceland, Irish Republic, Italy (Sardina), Malta, Netherlands, Norway, Poland, Portugal, Romania, Spain, Sweden, Switzerland, USSR, Yugoslavia, NORTH AMERICA, Canada, Mexico, USA, CENTRAL AMERICA & WEST INDIES, Guatemala, SOUTH AMERICA, Argentina, Bolivia, Brazil (Sao Paulo), Chile, Ecuador, Peru, Uruguay.


Author(s):  

Abstract A new distribution map is provided for Corynebacterium michiganense pv. michiganense (E.F. Smith) Jensen. Hosts: Tomato (Lycopersicon esculentun). Information is given on the geographical distribution in AFRICA, Kenya, Madagascar, Morocco, South Africa, Tunisia, Uganda, Zambia, Zimbabwe, ASIA, China, India (Nagpur), Israel, Japan, Lebanon, Turkey, AUSTRALASIA & OCEANIA, Australia, Hawaii, New Zealand, EUROPE, Austria, Britain, Channel Islands (Jersey), Bulgaria, Germany, Greece, Hungary, Ireland, Italy (incl. Sicily), Norway, Portugal, Romania, Sardinia, Switzerland, USSR (general, Lithuania, W. Siberia and Crimea), Yugoslavia, NORTH AMERICA, Canada, Nova Scotia, Mexico, USA (general), CENTRAL AMERICA & WEST INDIES, Costa Rica, Cuba, Dominica, Dominican Republic, Panama, SOUTH AMERICA, Argentina (Buenos Aires), (Goldenberg), (Mendoza), (Misiones & Rio Negro), Brazil (Sao Paulo), Chile (Santiago), Colombia, Peru.


Author(s):  

Abstract A new distribution map is provided for Phaeoisariopsis bataticola (Cif. & Bruner) M.B. Ellis. Host: sweet potato (Ipomoea spp.). Information is given on the geographical distribution in NORTH AMERICA, USA, Florida, CENTRAL AMERICA & WEST INDIES, Cuba, Dominican Republic, Puerto Rico, SOUTH AMERICA, Venezuela.


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