scholarly journals Fossil mosses: What do they tell us about moss evolution?

2021 ◽  
Vol 43 (1) ◽  
Author(s):  
MICHAEL S. IGNATOV ◽  
ELENA V. MASLOVA

The moss fossil records from the Paleozoic age to the Eocene epoch are reviewed and their putative relationships to extant moss groups discussed. The incomplete preservation and lack of key characters that could define the position of an ancient moss in modern classification remain the problem. Carboniferous records are still impossible to refer to any of the modern moss taxa. Numerous Permian protosphagnalean mosses possess traits that are absent in any extant group and they are therefore treated here as an extinct lineage, whose descendants, if any remain, cannot be recognized among contemporary taxa. Non-protosphagnalean Permian mosses were also fairly diverse, representing morphotypes comparable with Dicranidae and acrocarpous Bryidae, although unequivocal representatives of these subclasses are known only since Cretaceous and Jurassic. Even though Sphagnales is one of two oldest lineages separated from the main trunk of moss phylogenetic tree, it appears in fossil state regularly only since Late Cretaceous, ca. 70 million years ago (Ma), while earlier they were found twice as small leaf fragments from Lower Jurassic (ca. 200 Ma) and Late Ordovician (ca. 455 Ma). Pleurocarpous mosses appear in fossil state near the border between Jurassic and Cretaceous, although most Cretaceous mosses belong to acrocarps. Only in Eocene amber pleurocarps become more numerous than acrocarps. Some Eocene mosses can be assigned to extant families and sometimes genera, although the majority of Eocene pleurocarps are difficult to identify up to the family, as their morphology often allows placement of a particular specimen into several different families.

2012 ◽  
Vol 21 (1) ◽  
pp. 131-144 ◽  
Author(s):  
A.G. Kirejtshuk ◽  
A. Nel

In the paper two new species of the genus Rhyzobius Stephens, 1829 (R. antiquus sp. nov. and R. gratiosus sp. nov.) and one new species of the genus Nephus Mulsant 1846 (N. subcircularis sp. nov. without a certain subgeneric placement) from the Lowermost Eocene amber of Oise are described. A short review of known fossil records of the family Coccinellidae is given.


Zootaxa ◽  
2011 ◽  
Vol 2742 (1) ◽  
pp. 60 ◽  
Author(s):  
DAVID PENNEY ◽  
ANDREW MCNEIL ◽  
DAVID I. GREEN ◽  
ROBERT BRADLEY ◽  
YURI M. MARUSIK ◽  
...  

A new species of the extant spider family Anapidae is described from a fossil mature male in Eocene amber from the Baltic region and tentatively assigned to the genus Balticoroma Wunderlich, 2004. Phase contrast X-ray computed micro-tomography was used to reveal important features that were impossible to view using traditional microscopy. Balticoroma wheateri new species is easily diagnosed from all other anapids by having clypeal extensions that run parallel to the ectal surface of the chelicerae and in having the metatarsus of the first leg highly reduced and modified into what is presumably a y-shaped clasping structure. Although only a single extant anapid species occurs in northern Europe, the family was diverse in the Eocene. The discovery of yet another anapid species in Baltic amber supports the idea that Eocene European forests may have been a hotspot of evolution for this family of spiders.


1997 ◽  
Vol 71 (6) ◽  
pp. 1109-1124 ◽  
Author(s):  
Li Guo-Qing ◽  
Mark V. H. Wilson ◽  
Lance Grande

Review of recently collected material of Eohiodon from North America suggests that there are two valid species, E. rosei (Hussakof) and E. woodroffi Wilson. Eohiodon falcatus Grande is identical to E. woodruffi in known skeletal features and nearly all meristic features and is treated as a junior synonym of the latter. The fossil genus Eohiodon Cavender differs from Hiodon Lesueur, which is known from both fossil and extant species, in numerous meristic and osteological features. The caudal skeleton in Eohiodon is nearly identical to that in Hiodon.The traditionally accepted Notopteroidei, containing Lycopteridae, Hiodontidae, and Notopteridae, is a polypheletic group. The Asian fossil family Lycopteridae is not more closely related to Hiodontidae than it is to other taxa in the Osteoglossomorpha, but is sister to all other Osteoglossomorpha. The Hiodontiformes sensu stricto, including only the family Hiodontidae, is the sister-group of the Osteoglossiformes. This family is not more closely related to notopterids than to other taxa in Osteoglossiformes. The Notopteridae are most closely related to the Mormyroidea; together they and the fossil family Ostariostomidae constitute the sister-group of the Osteoglossoidei.Fossil records of Hiodontiformes sensu stricto and Notopteroidei indicate a widespread pre-Neogene biogeographic range of these freshwater teleosts, suggesting that extinction must have been involved in the Cenozoic evolution of these two osteoglossomorph sublineages.


Zootaxa ◽  
2021 ◽  
Vol 5067 (3) ◽  
pp. 301-351
Author(s):  
GLENN M. SHEA

The modern classification of skinks is based on a nomenclature that dates to the 1970s. However, there are a number of earlier names in the family group that have been overlooked by recent workers. These names are identified and their validity with respect to the International Code of Zoological Nomenclature investigated, along with their type genera. In most cases, use of these names to supplant junior synonyms in modern day use is avoidable by use of the Reversal of Precedence articles of the Code, but the names remain available in case of future divisions at the tribe and subtribe level. Other names are unavailable due to homonymy, either of their type genera or the stems from similar but non-homonymous type genera. However, the name Egerniini is replaced by Tiliquini, due to a limited timespan of use of Egerniini. A new classification of the Family Scincidae is proposed, providing a more extensive use of Code-regulated levels of classification, including tribes and subtribes, and a detailed synonymy provided for each taxonomic unit.  


Check List ◽  
2020 ◽  
Vol 16 (6) ◽  
pp. 1733-1745
Author(s):  
Regigláucia Rodrigues de Oliveira ◽  
Ronison Ferreira de Oliveira ◽  
Hermeson Cassiano de Oliveira ◽  
Denilson Fernandes Peralta ◽  
Gonçalo Mendes da Coceição

Located in southwestern Maranhão, the Parque Nacional da Chapada das Mesas (PNCM), with an extent of about 160,046 ha, is completely inserted in the Cerrado phytogeographic domain. The topography is characterized by a plateau formation consisting of steep hills and medium-altitude mountains with flat tops, which give the PNCM its name. We present an annotated checklist of the mosses that occur in the PNCM. Our checklist includes 26 species of pleurocarpous mosses distributed in 10 families and 22 genera and two species of cladocarpous mosses of the family Orthotrichaceae. The most species-rich families of pleurocarpous mosses were Sematophyllaceae (7 spp.), Pylaisiadelphaceae (6 spp.), and Stereophyllaceae (4 spp.). Eleven species are recorded for the first time from Maranhão and three species are recorded for the first time in the northeast region of Brazil. Taxithelium pluripunctatum (Renauld & Cardot) W.R. Buck and Trichosteleum glaziovii (Hampe) W.R. Buck, are recorded for the first time from Maranhão and the Cerrado phytogeographic domain. Our results expand the knowledge of the Brazilian bryoflora and add distribution data for a number of species in Maranhão and the northeast region.


2020 ◽  
Vol 94 (4) ◽  
pp. 748-757
Author(s):  
Jobst Wendt

AbstractIn contrast to almost all other invertebrate phyla that constructed biomineralized skeletons during the “Cambrian explosion” and maintained them during the entire fossil record, ascidian tunicates evolved this protective and stabilizing advantage only during the Permian, although soft-bodied representatives of this subphylum made their first appearance already in the early Cambrian. It remains enigmatic why these compound calcareous skeletons persisted only until the Late Triassic, subsequently followed by less-rigid internal skeletons from the Lower Jurassic onwards, which consist of scattered isolated spicules only. In addition to recently described aragonitic ascidian exoskeletons from the Permian and Triassic, new discoveries of similar, but colonial ascidian compound endoskeletons in the lower Carnian exhibit a short-living branch of this group, which moreover contain the first indubitable calcareous spicules. The latter are embedded in the solid endoskeleton, which is composed of polygonal aragonitic plates with smooth outer and zigzag lined inner boundaries. They consist of irregular, parallel (orthogonal), or fan-shaped (clinogonal) arrangements of acicular aragonite crystals. The following taxa are described as new: order Cassianomorpha new order with the family Cassianosomidae new family and the genus Toscanisoma new genus with the species T. multipartitum new species and T. triplicatum new species.UUID: http://zoobank.org/03555353-cdab-42e8-8e99-9bfce15fa249


Author(s):  
Wiesław Krzemiński ◽  
Agnieszka Soszyńska-Maj ◽  
Katarzyna Kopeć ◽  
Irena D. Sukatsheva

ABSTRACTThe family Austropanorpidae (Mecoptera) was described by Willmann in 1977 from the Eocene of Australia, based on one genus and species, Austropanorpa australis Riek, 1952. During a restudy of the collection of the Paleontological Institute, Russian Academy of Sciences in Moscow, a second and much older representative of this family was found. This specimen, described as Orthophlebia martynovae Sukatsheva, 1985 from Siberia (Russia), was considered until now to be a member of family Orthophlebiidae. We transfer this species to the Austropanorpidae, extending the age of this family back to the Early Jurassic. An updated diagnoses of the family Austropanorpidae and genus Austropanorpa are presented here.


1938 ◽  
Vol 57 ◽  
pp. 221-227
Author(s):  
James Small

Applying Udny Yule's formulæ (1924) to the Compositæ, Small (1937) found that the average ages in doubling periods (Dp-ages) of the tribes of Compositæ, when plotted against a time-scale, gave points on an exponential curve called the BAT curve. If this curve is characteristic of average families of Angiosperms it should be possible to place the Dp-ages of tribes within other families on this curve as plotted against geological time, and thus obtain an order of geological origin which is quite independent of actual fossil records and which can be checked against any facts known concerning the evolutionary history of the family.


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