Bryozoa are a phylum of simple, aquatic invertebrate animals, nearly all living in sedentary colonies. Typically about 0.5 millimetres long, they have a special feeding structure called a lophophore, a "crown" of tentacles used for filter feeding. Most marine bryozoans live in tropical waters, but a few are found in oceanic trenches and polar waters. The bryozoans are classified as the marine bryozoans (Stenolaemata), freshwater bryozoans (Phylactolaemata), and mostly-marine bryozoans (Gymnolaemata), a few members of which prefer brackish water. 5,869 living species are known. At least two genera are solitary ; the rest are colonial.
The PaleozoicEra is the first of three geological eras of the Phanerozoic Eon. Beginning 538.8 million years ago (Ma), it succeeds the Neoproterozoic and ends 251.9 Ma at the start of the Mesozoic Era. The Paleozoic is subdivided into six geologic periods :
The Phanerozoic is the current and the latest of the four geologic eons in the Earth's geologic time scale, covering the time period from 538.8 million years ago to the present. It is the eon during which abundant animal and plant life has proliferated, diversified and colonized various niches on the Earth's surface, beginning with the Cambrian period when animals first developed hard shells that can be clearly preserved in the fossil record. The time before the Phanerozoic, collectively called the Precambrian, is now divided into the Hadean, Archaean and Proterozoic eons.
Graptolites are a group of colonial animals, members of the subclass Graptolithina within the class Pterobranchia. These filter-feeding organisms are known chiefly from fossils found from the Middle Cambrian through the Lower Carboniferous (Mississippian). A possible early graptolite, Chaunograptus, is known from the Middle Cambrian. Recent analyses have favored the idea that the living pterobranch Rhabdopleura represents an extant graptolite which diverged from the rest of the group in the Cambrian. Fossil graptolites and Rhabdopleura share a colony structure of interconnected zooids housed in organic tubes (theca) which have a basic structure of stacked half-rings (fuselli). Most extinct graptolites belong to two major orders: the bush-like sessile Dendroidea and the planktonic, free-floating Graptoloidea. These orders most likely evolved from encrusting pterobranchs similar to Rhabdopleura. Due to their widespread abundance, planktonic lifestyle, and well-traced evolutionary trends, graptoloids in particular are useful index fossils for the Ordovician and Silurian periods.
Ammonoids are a group of extinct marine mollusc animals in the subclass Ammonoidea of the class Cephalopoda. These molluscs, commonly referred to as ammonites, are more closely related to living coleoids than they are to shelled nautiloids such as the living Nautilus species. The earliest ammonites appeared during the Devonian, with the last species vanishing during or soon after the Cretaceous–Paleogene extinction event.
Cheilostomatida, also called Cheilostomata, is an order of Bryozoa in the class Gymnolaemata.
Nautiloids are a group of marine cephalopods (Mollusca) which originated in the Late Cambrian and are represented today by the living Nautilus and Allonautilus. Fossil nautiloids are diverse and speciose, with over 2,500 recorded species. They flourished during the early Paleozoic era, when they constituted the main predatory animals. Early in their evolution, nautiloids developed an extraordinary diversity of shell shapes, including coiled morphologies and giant straight-shelled forms (orthocones). Only a handful of rare coiled species, the nautiluses, survive to the present day.
Cyclostomatida, or cyclostomata, are an ancient order of stenolaemate bryozoans which first appeared in the Lower Ordovician. It consists of 7+ suborders, 59+ families, 373+ genera, and 666+ species. The cyclostome bryozoans were dominant in the Mesozoic; since that era, they have decreased. Currently, cyclostomes seldom constitute more than 20% of the species recorded in regional bryozoan faunas.
Taxonomy of commonly fossilised invertebrates is a complex and evolving field that combines both traditional and modern paleozoological terminology. This article aims to provide a comprehensive overview of the various invertebrate taxa that are commonly found in the fossil record, from protists to arthropods. The taxonomy presented here is not intended to be exhaustive but focuses on invertebrates that are either popularly collected as fossils or are extinct. Special notations are used to highlight invertebrate groups that are important as fossils, very abundant in the fossil record, or have a large proportion of extinct species. These notations are explained below for clarity:
Phylactolaemata is a class of the phylum Bryozoa whose members live only in freshwater environments. Like all bryozoans, they filter feed by means of an extensible "crown" of ciliated tentacles called a lophophore, and like nearly all bryozoans, they live in colonies, each of which consists of clones of the founding member. Unlike those of some marine bryozoans, phylactolaemate colonies consist of only one type of zooid, the feeding forms known as autozooids. These are supported by an unmineralized "exoskeleton" made of gelatinous material or protein, secreted by the zooids. The class contains only one extant order, Plumatellida.
Trepostomatida is an extinct order of bryozoans in the class Stenolaemata. Trepostome bryozoans possessed mineralized calcitic skeletons and are frequently fossilized; some of the largest known fossilized bryozoan colonies are branching trepostomes and massive dome-shaped trepostomes. Trepostomes did not have many specialized zooecia beyond ordinary feeding autozooecia. The two main known heteromorphs are exilazooecia and mesozooecia, which had the purpose of maintaining regular spacing between autozooecia.
The geological history of North America comprises the history of geological occurrences and emergence of life in North America during the interval of time spanning from the formation of the Earth through to the emergence of humanity and the start of prehistory. At the start of the Paleozoic era, what is now "North" America was actually in the southern hemisphere. Marine life flourished in the country's many seas, although terrestrial life had not yet evolved. During the latter part of the Paleozoic, seas were largely replaced by swamps home to amphibians and early reptiles. When the continents had assembled into Pangaea drier conditions prevailed. The evolutionary precursors to mammals dominated the country until a mass extinction event ended their reign.
The concept of the three great evolutionary faunas of marine animals from the Cambrian to the present was introduced by Jack Sepkoski in 1981 using factor analysis of the fossil record. An evolutionary fauna typically displays an increase in biodiversity following a logistic curve followed by extinctions.
Cystoporida, also known as Cystoporata or cystoporates, are an extinct order of Paleozoic bryozoans in the class Stenolaemata. Their fossils are found from Ordovician to Triassic strata.
Fenestrata is an extinct order of bryozoan, dating from the Upper Arenig. Most fenestrate bryozoans formed net-like colonies, often in funnel- or fan-shaped forms, with a single layer of zooids facing one direction. The colony shape served as a filter-feeding apparatus that water currents flowed through, with autozooecial apertures only on the side of the colony facing into the current. This colony structure was vulnerable to predators, so some fenestrate bryozoans produced skeletal superstructures, likely to strengthen or protect the colony, and others had protective spines surrounding their autozooecial apertures.
Articulina is an extant suborder of bryozoans in the order Cyclostomatida.
Fenestellidae is a family of bryozoans belonging to the order Fenestrida. The skeleton of its colonies consists of stiff branches that are interconnected by narrower crossbars. The individuals of the colony inhabit one side of the branches in two parallel rows or two at the branch base and three or more rows further up. Zooids can be recognized as small rimmed pores, and in well-preserved specimens the apertures are closed by centrally perforated lids. The front of the branches carries small nodes in a row or zigzag line between the apertures. Branches split from time to time giving the colonies a fan-shape or, in the genus Archimedes, create an mesh in the shape of an Archimedes screw.
Adelophthalmidae is a family of eurypterids, an extinct group of aquatic arthropods. Adelophthalmidae is the only family classified as part of the superfamily Adelophthalmoidea, which in turn is classified within the infraorder Diploperculata in the suborder Eurypterina.
Lichenalia is an extinct genus of cystoporate bryozoan belonging to the family Rhinoporidae. It is known from the Upper Ordovician to the Middle Silurian periods, which spanned from approximately 460 to 430 million years ago. The genus had a cosmopolitan distribution, with fossil specimens found in various regions of the world, including North America, Europe, and Asia.
Palaeostomata is a superorder of extinct stenolaemate bryozoans, including all extinct orders within Stenolaemata and excluding the order Cyclostomata, which is the only extant stenolaemate order. Palaeostomates are sometimes called "stony bryozoans" because they are heavily calcified, making them ideal candidates for fossilization. They are distinct from cyclostomes because they lack calcified exterior walls above the basal lamina and because their zooecial tubes are transected by calcitic partitions, such as diaphragms.
