Mosses are small, non-vascular flowerless plants in the taxonomic division Bryophytasensu stricto. Bryophyta may also refer to the parent group bryophytes, which comprise liverworts, mosses, and hornworts. Mosses typically form dense green clumps or mats, often in damp or shady locations. The individual plants are usually composed of simple leaves that are generally only one cell thick, attached to a stem that may be branched or unbranched and has only a limited role in conducting water and nutrients. Although some species have conducting tissues, these are generally poorly developed and structurally different from similar tissue found in vascular plants. Mosses do not have seeds and after fertilisation develop sporophytes with unbranched stalks topped with single capsules containing spores. They are typically 0.2–10 cm (0.1–3.9 in) tall, though some species are much larger. Dawsonia, the tallest moss in the world, can grow to 50 cm (20 in) in height. There are approximately 12,000 species.
Bryophytes are a group of land plants, sometimes treated as a taxonomic division, that contains three groups of non-vascular land plants (embryophytes): the liverworts, hornworts and mosses. In the strict sense, Bryophyta consists of the mosses only. Bryophytes are characteristically limited in size and prefer moist habitats although they can survive in drier environments. The bryophytes consist of about 20,000 plant species. Bryophytes produce enclosed reproductive structures, but they do not produce flowers or seeds. They reproduce sexually by spores and asexually by fragmentation or the production of gemmae. Though bryophytes were considered a paraphyletic group in recent years, almost all of the most recent phylogenetic evidence supports the monophyly of this group, as originally classified by Wilhelm Schimper in 1879. The term bryophyte comes from Ancient Greek βρύον (brúon) 'tree moss, liverwort', and φυτόν (phutón) 'plant'.
The embryophytes are a clade of plants, also known as Embryophyta or land plants. They are the most familiar group of photoautotrophs that make up the vegetation on Earth's dry lands and wetlands. Embryophytes have a common ancestor with green algae, having emerged within the Phragmoplastophyta clade of freshwater charophyte green algae as a sister taxon of Charophyceae, Coleochaetophyceae and Zygnematophyceae. Embryophytes consist of the bryophytes and the polysporangiophytes. Living embryophytes include hornworts, liverworts, mosses, lycophytes, ferns, gymnosperms and angiosperms. Embryophytes have diplobiontic life cycles.
The Marchantiophyta are a division of non-vascular land plants commonly referred to as hepatics or liverworts. Like mosses and hornworts, they have a gametophyte-dominant life cycle, in which cells of the plant carry only a single set of genetic information.
Hornworts are a group of non-vascular Embryophytes constituting the division Anthocerotophyta. The common name refers to the elongated horn-like structure, which is the sporophyte. As in mosses and liverworts, hornworts have a gametophyte-dominant life cycle, in which cells of the plant carry only a single set of genetic information; the flattened, green plant body of a hornwort is the gametophyte stage of the plant.
Streptophyta, informally the streptophytes, is a clade of plants. The composition of the clade varies considerably between authors, but the definition employed here includes land plants and all green algae except the Chlorophyta and the more basal Prasinodermophyta.
Marchantiales is an order of thallose liverworts that includes species like Marchantia polymorpha, a widespread plant often found beside rivers, and Lunularia cruciata, a common and often troublesome weed in moist, temperate gardens and greenhouses.
Neodiapsida is a clade, or major branch, of the reptilian family tree, typically defined as including all diapsids apart from some early primitive types known as the araeoscelidians. Modern reptiles and birds belong to the neodiapsid subclade Sauria.
Viridiplantae constitute a clade of eukaryotic organisms that comprises approximately 450,000–500,000 species that play important roles in both terrestrial and aquatic ecosystems. They include the green algae, which are primarily aquatic, and the land plants (embryophytes), which emerged from within them. Green algae traditionally excludes the land plants, rendering them a paraphyletic group. However it is accurate to think of land plants as a kind of alga. Since the realization that the embryophytes emerged from within the green algae, some authors are starting to include them. They have cells with cellulose in their cell walls, and primary chloroplasts derived from endosymbiosis with cyanobacteria that contain chlorophylls a and b and lack phycobilins. Corroborating this, a basal phagotroph archaeplastida group has been found in the Rhodelphydia.
The Dionycha are a clade of spiders (Araneomorphae:Entelegynae), characterized by the possession of two tarsal claws with tufts of hairs (setae) beside them, which produce strong adhesion, enabling some species to climb glass. The circumscription of the group has varied widely; a 2021 analysis resulted in about 20 families, including Salticidae, Gnaphosidae, and Clubionidae.
28S ribosomal RNA is the structural ribosomal RNA (rRNA) for the large subunit (LSU) of eukaryotic cytoplasmic ribosomes, and thus one of the basic components of all eukaryotic cells. It has a size of 25S in plants and 28S in mammals, hence the alias of 25S–28S rRNA.
Diplocynodon is an extinct genus of alligatoroid crocodilian that lived during the Paleocene to Middle Miocene in Europe. Some species may have reached lengths of 3 metres (9.8 ft), while others probably did not exceed 1 metre (3.3 ft). They are almost exclusively found in freshwater environments. The various species are thought to have been opportunistic aquatic predators.
Alligatoroidea is one of three superfamilies of crocodylians, the other two being Crocodyloidea and Gavialoidea. Alligatoroidea evolved in the Late Cretaceous period, and consists of the alligators and caimans, as well as extinct members more closely related to the alligators than the two other groups.
Navajosuchus is an extinct genus of alligatorine crocodylian. Its fossils have been found in the Paleocene-age Nacimiento Formation of the San Juan Basin, New Mexico. It was named in 1942 by Charles C. Mook, and the original type species was N. novomexicanus. N. novomexicanus was based on AMNH 5186, a partial skull collected in 1913. Later research showed that Navajosuchus novomexicanus was the same as the earlier-named Allognathosuchus mooki. However, A. mooki does not belong to the genus Allognathosuchus, and so the name of the crocodilian becomes Navajosuchus mooki. Under whichever name is used, this animal would have been a generalized predator of the Nacimiento floodplains. It was the most common Nacimiento Formation crocodilian, found in both the Puercan and Torrejonian faunal assemblages.
Arambourgia is an extinct monotypic genus of alligatorine crocodylian from Europe. It was named in 1905 as Allognathosuchus gaudryi. It was made a separate genus Arambourgia in 1940. This was synonymized with Allognathosuchus haupti in 1990, but later reassigned as its own genus once again in 2004. Arambourgia was likely to have been part of an early dispersal event of alligatorines from North America to Europe during the Eocene epoch. Arambourgia had non-serrated teeth and a deep orienirostral snout, unlike the flatter snouts of most other alligatorids.
Brachychampsa is an extinct genus of alligatoroid, possibly a basal caiman. Specimens have been reported from New Mexico, Colorado, Wyoming, Montana, North and South Dakota, New Jersey, and Saskatchewan, though only those from Montana, Utah, and New Mexico are based on material sufficient to justify the referral. One specimen has been reported from the Darbasa Formation of Kazakhstan, although the species status is indeterminate for the fossil. The genus first appeared during the late Campanian stage of the Late Cretaceous and became extinct during the late Maastrichtian stage of the Cretaceous. Brachychampsa is distinguished by an enlarged fifth maxillary tooth in the upper jaw.
Saurornitholestinae is a subfamily of the theropod group Dromaeosauridae. The saurornitholestines currently include three monotypic genera: Atrociraptor marshalli, Bambiraptor feinbergi, and Saurornitholestes langstoni. All are medium-sized dromaeosaurs from the Late Cretaceous of western North America. The group was originally recognized by Longrich and Currie as the sister taxon to a clade formed by the Dromaeosaurinae and Velociraptorinae. However, not all phylogenetic analyses recover this group and/or with the same proposed genera.
The Phasianinae are a subfamily of the pheasant family (Phasianidae) of landfowl, the order Galliformes. The subfamily includes true pheasants, tragopans, grouse, turkey and similar birds. Although this subfamily was considered monophyletic and separated from the partridges, francolins, and Old World quails (Perdicinae) till the early 1990s, molecular phylogenies have shown that this placement is paraphyletic. For example, some partridges (genus Perdix) are more closely affiliated to pheasants, whereas Old World quails and partridges from the genus Alectoris are closer to junglefowls. There are two clades in the Phasianinae: the erectile clade and the non-erectile clades. Both clades are believed to have diverged during the early Oligocene, about 30 million years ago.
The ginger-families or ginger group or Core Zingiberales is a terminal clade in the order Zingiberales (Monocotyledoneae) that comprises Zingiberaceae, Costaceae, Marantaceae and Cannaceae. Their shared synapomorphy of a single fertile anther and four or five highly modified staminodia differentiate them from the basal paraphyletic assemblage of the "banana-families".
Vermiviatum covidum is a species of predatory land flatworm, found in France and Italy. The Holotype specimen is MNHN JL351B.
