Paleocene in the context of "Ocean acidification"

A mangrove is a shrub or tree that grows mainly in coastal saline or brackish water. Mangroves grow in an equatorial climate, typically along coastlines and tidal rivers. They have particular adaptations to take in extra oxygen and remove salt, allowing them to tolerate conditions that kill most plants. The term is also used for tropical coastal vegetation consisting of such species. Mangroves are taxonomically diverse due to convergent evolution in several plant families. They occur worldwide in the tropics and subtropics and even some temperate coastal areas, mainly between latitudes 30° N and 30° S, with the greatest mangrove area within 5° of the equator. Mangrove plant families first appeared during the Late Cretaceous to Paleocene epochs and became widely distributed in part due to the movement of tectonic plates. The oldest known fossils of mangrove palm date to 75 million years ago.

Mangroves are salt-tolerant (halophytic) and are adapted to live in harsh coastal conditions. They contain a complex salt filtration system and a complex root system to cope with saltwater immersion and wave action. They are adapted to the low-oxygen conditions of waterlogged mud, but are most likely to thrive in the upper half of the intertidal zone.

Homo sapiens is a distinct species of the hominid family of primates, which also includes all the great apes. Over their evolutionary history, humans gradually developed traits such as bipedalism, dexterity, and complex language, as well as interbreeding with other hominins (a tribe of the African hominid subfamily), indicating that human evolution was not linear but weblike. The study of the origins of humans involves several scientific disciplines, including physical and evolutionary anthropology, paleontology, and genetics; the field is also known by the terms anthropogeny, anthropogenesis, and anthropogony—with the latter two sometimes used to refer to the related subject of hominization.

Primates diverged from other mammals about 85 million years ago (mya), in the Late Cretaceous period, with their earliest fossils appearing over 55 mya, during the Paleocene. Primates produced successive clades leading to the ape superfamily, which gave rise to the hominid and the gibbon families; these diverged some 15–20 mya. African and Asian hominids (including orangutans) diverged about 14 mya. Hominins (including the Australopithecine and Panina subtribes) parted from the Gorillini tribe between 8 and 9 mya; Australopithecine (including the extinct biped ancestors of humans) separated from the Pan genus (containing chimpanzees and bonobos) 4–7 mya. The Homo genus is evidenced by the appearance of H. habilis over 2 mya, while anatomically modern humans emerged in Africa approximately 300,000 years ago.

The Eocene (IPA: /ˈiːəsiːn, ˈiːoʊ-/ EE-ə-seen, EE-oh-) is a geological epoch that lasted from about 56 to 33.9 million years ago (Ma). It is the second epoch of the Paleogene Period in the modern Cenozoic Era. The name "Eocene" comes from Ancient Greek ἠώς (ēṓs), meaning "dawn", and καινός (kainós), meaning "new", and refers to the "dawn" of modern ('new') fauna that appeared during the epoch.

The Eocene spans the time from the end of the Paleocene Epoch to the beginning of the Oligocene Epoch. The start of the Eocene is marked by a brief period in which the concentration of the carbon isotope C in the atmosphere was exceptionally low in comparison with the more common isotope C. The average temperature of Earth at the beginning of the Eocene was about 27 degrees Celsius. The end is set at a major extinction event called the Grande Coupure (the "Great Break" in continuity) or the Eocene–Oligocene extinction event, which may be related to the impact of one or more large bolides in Siberia and in what is now Chesapeake Bay. As with other geologic periods, the strata that define the start and end of the epoch are well identified, though their exact dates are slightly uncertain.

Snakes are elongated limbless reptiles of the suborder Serpentes (/sɜːrˈpɛntiːz/). Cladistically squamates, snakes are ectothermic, amniote vertebrates covered in overlapping scales much like other members of the group. Many species of snakes have skulls with several more joints than their lizard ancestors and relatives, enabling them to swallow prey much larger than their heads (cranial kinesis). To accommodate their narrow bodies, snakes' paired organs (such as kidneys) appear one in front of the other instead of side by side, and most only have one functional lung. Some species retain a pelvic girdle with a pair of vestigial claws on either side of the cloaca. Lizards have independently evolved elongate bodies without limbs or with greatly reduced limbs at least twenty-five times via convergent evolution, leading to many lineages of legless lizards. These resemble snakes, but several common groups of legless lizards have eyelids and external ears, which snakes lack, although this rule is not universal (see Amphisbaenia, Dibamidae, and Pygopodidae).

Living snakes are found on every continent except Antarctica, and on most smaller land masses; exceptions include some large islands, such as Ireland, Iceland, Greenland, and the islands of New Zealand, as well as many small islands of the Atlantic and central Pacific oceans. Additionally, sea snakes are widespread throughout the Indian and Pacific oceans. Around thirty families are currently recognized, comprising about 520 genera and about more than 4,170 species. They range in size from the tiny, 10.4 cm-long (4.1 in) Barbados threadsnake to the reticulated python of 6.95 meters (22.8 ft) in length. The fossil species Titanoboa cerrejonensis was 12.8 meters (42 ft) long. Snakes are thought to have evolved from either burrowing or aquatic lizards, perhaps during the Jurassic period, with the earliest known fossils dating to between 143 and 167 Ma ago. The diversity of modern snakes appeared during the Paleocene epoch (c. 66 to 56 Ma ago, after the Cretaceous–Paleogene extinction event). The oldest preserved descriptions of snakes can be found in the Brooklyn Papyrus.

The Paleogene Period (IPA: /ˈpeɪli.ədʒiːn, -li.oʊ-, ˈpæli-/ PAY-lee-ə-jeen, -⁠lee-oh-, PAL-ee-; also spelled Palaeogene or Palæogene) is a geologic period and system that spans 43 million years from the end of the Cretaceous Period 66 Ma (million years ago) to the beginning of the Neogene Period 23.04 Ma. It is the first period of the Cenozoic Era, the tenth period of the Phanerozoic and is divided into the Paleocene, Eocene, and Oligocene epochs. The earlier term Tertiary Period was used to define the time now covered by the Paleogene Period and subsequent Neogene Period; despite no longer being recognized as a formal stratigraphic term, "Tertiary" still sometimes remains in informal use. Paleogene is often abbreviated "Pg", although the United States Geological Survey uses the abbreviation "Pe" for the Paleogene on the Survey's geologic maps.

Much of the world's modern vertebrate diversity originated in a rapid surge of diversification in the early Paleogene, as survivors of the Cretaceous–Paleogene extinction event took advantage of empty ecological niches left behind by the extinction of the non-avian dinosaurs, pterosaurs, marine reptiles, and primitive fish groups. Mammals continued to diversify from relatively small, simple forms into a highly diverse group ranging from small-bodied forms to very large ones, radiating into multiple orders and colonizing the air and marine ecosystems by the Eocene. Birds, the only surviving group of dinosaurs, quickly diversified from the very few neognath and paleognath clades that survived the extinction event, also radiating into multiple orders, colonizing different ecosystems and achieving an extreme level of morphological diversity. Percomorph fish, the most diverse group of vertebrates today, first appeared near the end of the Cretaceous but saw a very rapid radiation into their modern order and family-level diversity during the Paleogene, achieving a diverse array of morphologies.

The South American land mammal ages (SALMA) establish a geologic timescale for prehistoric South American fauna beginning 64.5 Ma during the Paleocene and continuing through to the Late Pleistocene (0.011 Ma). These periods are referred to as ages, stages, or intervals and were established using geographic place names where fossil materials where obtained.

The basic unit of measurement is the first/last boundary statement. This shows that the first appearance event of one taxon is known to predate the last appearance event of another. If two taxa are found in the same fossil quarry or at the same stratigraphic horizon, then their age-range zones overlap.

The Maastrichtian ( /mɑːˈstrɪktiən/ mahss-TRIK-tee-ən) is, in the International Commission on Stratigraphy (ICS) geologic timescale, the latest age (uppermost stage) of the Late Cretaceous Epoch or Upper Cretaceous Series, the Cretaceous Period or System, and of the Mesozoic Era or Erathem. It spanned the interval from 72.2 to 66 million years ago. The Maastrichtian was preceded by the Campanian and succeeded by the Danian (part of the Paleogene and Paleocene). It is named after the city of Maastricht, the capital and largest city of the Limburg province in the Netherlands.

The Cretaceous–Paleogene extinction event (formerly known as the Cretaceous–Tertiary extinction event) occurred at the end of this age. In this mass extinction, many commonly recognized groups such as non-avian dinosaurs, pterosaurs, plesiosaurs and mosasaurs, as well as many other lesser-known groups, died out. The cause of the extinction is most commonly linked to an asteroid about 10 to 15 kilometres (6.2 to 9.3 mi) wide colliding with Earth, ending the Cretaceous.

The evolution of the horse, a mammal of the family Equidae, occurred over a geologic time scale of 50 million years, transforming the small, dog-sized, forest-dwelling Eohippus into the large, single-toed, modern-day horse. Paleozoologists have been able to piece together a more complete outline of the evolutionary lineage of the modern horse than of any other animal. Much of this evolution took place in North America, where horses originated but became extinct about 10,000 years ago, before being reintroduced in the 15th century.

The horse belongs to the order Perissodactyla (odd-toed ungulates), the members of which share hooved feet and an odd number of toes on each foot, as well as mobile upper lips and a similar tooth structure. This means that horses share a common ancestry with tapirs and rhinoceroses. The perissodactyls arose in the late Paleocene, less than 10 million years after the Cretaceous–Paleogene extinction event. This group of animals appears to have been originally specialized for life in tropical forests, but whereas tapirs and, to some extent, rhinoceroses, retained their jungle specializations, modern horses are adapted to life in the climatic conditions of the steppes, which are drier and much harsher than forests or jungles. Other species of Equus are adapted to a variety of intermediate conditions.

Insular India was an isolated landmass which became the Indian subcontinent. Across the latter stages of the Cretaceous and most of the Paleocene, following the breakup of Gondwana, the Indian subcontinent remained an isolated landmass as the Indian Plate drifted across the Tethys Ocean, forming the Indian Ocean. The process of India's separation from Madagascar first began 88 million years ago, but complete isolation only occurred towards the end of the Maastrichtian, a process that has been suggested to be the creation of the Deccan Traps. Soon after, the land mass moved northward rather quickly, until contact with Asia was established 55 million years ago. Even then, both landmasses did not become fully united until around 35 million years ago, and periods of isolation occurred as recently as 24 million years ago.

Thus, for a period of 53 million years India retained a degree of isolation, 11 of which it was a complete island continent. This allowed its local biota to follow the typical patterns seen in islands and diversify in unique ways, much as in modern Madagascar, its sister landmass. Faunal interchanges with other landmasses, like Africa and Europe (then an archipelago of islands across the Tethys) occurred during this period, and a considerable Asian influence can already be seen long before contact was made. This rendered India rather peculiar as not just an isolated continent but also a "stepping stone" in the dispersal of many animal and plant clades across Africa, Europe, Madagascar, Asia and possibly even Oceania. Still, several "archaic" clades managed to survive. The vast majority of India's terrestrial vertebrate life was wiped out in the Cretaceous-Paleogene extinction event; only 3 extant tetrapod lineages can trace their ancestry to Cretaceous India. Most of India's few other surviving Gondwanan lineages were outcompeted during the Paleogene by newly-arriving lineages. However, plants and invertebrate fauna were less affected.

This is a list of fossil primates—extinct primates for which a fossil record exists. Primates are generally thought to have evolved from a small, unspecialized mammal, which probably fed on insects and fruits. However, the precise source of the primates remains controversial and even their arboreal origin has recently been questioned. As it has been suggested, many other mammal orders are arboreal too, but they have not developed the same characteristics as primates. Nowadays, some well known genera, such as Purgatorius and Plesiadapis, thought to be the most ancient primates for a long time, are not usually considered as such by recent authors, who tend to include them in the new order Plesiadapiformes, within superorder Euarchontoglires. Some, to avoid confusions, employ the unranked term Euprimates, which excludes Plesiadapiformes. That denomination is not used here.

There is an academic debate on the time the first primates appeared. One of the earliest probable primate fossils is the problematic Altiatlasius koulchii, perhaps an Omomyid, but perhaps a non-Primate Plesiadapiform, which lived in Morocco, during the Paleocene, around 60 Ma. However, other studies, including molecular clock studies, have estimated the origin of the primate branch to have been in the mid-Cretaceous period, around 85 Ma, that is to say, in the time previous to the extinction of dinosaurs and the successful mammal radiation. Nevertheless, there seems to be a consensus about the monophyletic origin of the order, although the evidence is not clear.

Carpolestidae is a family of primate-like Plesiadapiformes that were prevalent in North America and Asia from the mid Paleocene through the early Eocene. Typically, they are characterized by two large upper posterior premolars and one large lower posterior premolar. They weighed about 20-150g, and were about the size of a mouse. Though they come from the order, Plesiadapiformes, that may have given rise to the primate order, carpolestids are too specialized and derived to be ancestors of primates.

Historically, the almost twenty species included within the family were thought to have given rise to each other over time in a linear and straightforward manner. Still today it is widely assumed that Elphidotarsius from the mid to late Paleocene gave rise to Carpodaptes which lived in the late Paleocene and subsequently gave rise to Carpolestes from the early Eocene. As a result, they have been used as biostratigraphic indicators in a variety of paleontological digs. However, the phylogenetic picture has been complicated by the discovery in Asia of both ancestral and derived carpolestids in the same stratigraphic layer.

Butterflies are winged insects from the lepidopteran superfamily Papilionoidea, characterised by large, often brightly coloured wings that often fold together when at rest, and a conspicuous, fluttering flight. The oldest butterfly fossils have been dated to the Paleocene, about 56 million years ago, though molecular evidence suggests that they likely originated in the Cretaceous.

Butterflies have a four-stage life cycle, and like other holometabolous insects they undergo complete metamorphosis. Winged adults lay eggs on plant foliage on which their larvae, known as caterpillars, will feed. The caterpillars grow, sometimes very rapidly, and when fully developed, pupate in a chrysalis. When metamorphosis is complete, the pupal skin splits, the adult insect climbs out, expands its wings to dry, and flies off.

Palaeovespa is an extinct genus of wasp in the Vespidae subfamily Vespinae. The genus currently contains eight species: five from the Priabonian stage Florissant Formation in Colorado, United States, two from the middle Eocene Baltic amber deposits of Europe, and one species from the late Paleocene of France.

The subfamily Vespinae contains the largest and best-known groups of eusocial wasps, including true hornets (the genus Vespa), and the "yellowjackets" (genera Dolichovespula and Vespula). The remaining genus, Provespa, is a small, poorly known group of nocturnal wasps from Southeast Asia. One genus, Palaeovespa, has been described in the Paleocene to Eocene fossil records of North America and Europe. Collectively, the group can be found on all continents except Antarctica, and several of these wasps are invasive species, introduced beyond their native ranges, and can be major pests.

The evolutionary history of the primates can be traced back 57-90 million years. One of the oldest known primate-like mammal species, Plesiadapis, came from North America; another, Archicebus, came from China. Other such early primates include Altiatlasius and Algeripithecus, which were found in Northern Africa. Other similar basal primates were widespread in Eurasia and Africa during the tropical conditions of the Paleocene and Eocene.Purgatorius is the genus of the four extinct species believed to be among the earliest example of a primate or a proto-primate, a primatomorph precursor to the Plesiadapiformes, dating to as old as 66 million years ago.

The surviving tropical population of primates, which is seen most completely in the upper Eocene and lowermost Oligocene fossil beds of the Faiyum depression southwest of Cairo, gave rise to all living species—lemurs of Madagascar, lorises of Southeast Asia, galagos or "bush babies" of Africa, and the anthropoids: platyrrhine or New World monkeys, catarrhines or Old World monkeys, and the apes, including Homo sapiens.

Dipteronia is a genus with two living and one extinct species in the soapberry family Sapindaceae. The living species are native to central and southern China. The fossil species has been found in Middle Paleocene to Early Oligocene sediments of North America and China.

In the geologic timescale the Ypresian is the oldest age or lowest stratigraphic stage of the Eocene. It spans the time between 56 and 48.07 Ma, is preceded by the Thanetian Age (part of the Paleocene) and is followed by the Eocene Lutetian Age. The Ypresian is consistent with the Lower Eocene (Early Eocene).

Simoedosaurus is an extinct reptile known from the Paleocene of North America, Europe and western Asia, and a member of the Choristodera, a group of aquatic reptiles that lived in the Northern Hemisphere from the Jurassic to the early Cenozoic.

A second species, S. dakotensis got its own genus, Kosmodraco, in 2022.