Last common ancestor in the context of "Cladogram"

Homo erectus (/ˌhoʊmoʊ əˈrɛktəs/ lit. 'upright man') is an extinct species of archaic human from the Pleistocene, spanning nearly 2 million years. It is the first human species to evolve a humanlike body plan and gait, to leave Africa and colonize Asia and Europe, and to wield fire. Some populations of H. erectus were ancestors of later human species, including H. heidelbergensis — the last common ancestor of modern humans, Neanderthals, and Denisovans. As such a widely distributed species both geographically and temporally, H. erectus anatomy varies considerably. Subspecies are sometimes recognized: H. e. erectus, H. e. pekinensis, H. e. soloensis, H. e. ergaster, H. e. georgicus, and H. e. tautavelensis.

The species was first described by Eugène Dubois in 1893 as "Pithecanthropus erectus" using a skullcap, molar, and femur from Java, Indonesia. Further discoveries around East Asia were used to contend that humanity evolved out of Asia. Based on historical race concepts, it was argued that local H. erectus populations evolved directly into local modern human populations (polycentrism) rather than all humanity sharing a single anatomically modern ancestor (monogenism). As the fossil record improved over the mid-to-late 20th century, "Out of Africa" theory and monogenism became the consensus.

Homo antecessor (Latin for 'pioneer man') is an extinct species of archaic human recorded in the Spanish Sierra de Atapuerca, a productive archaeological site, from 1.2 to 0.8 million years ago during the Early Pleistocene. Populations of this species may have been present elsewhere in Western Europe, and were among the first to settle that region of the world, hence the name. The first fossils were found in the Gran Dolina cave in 1994, and the species was formally described in 1997 as the last common ancestor of modern humans and Neanderthals, supplanting the more conventional H. heidelbergensis in this position. H. antecessor has since been reinterpreted as an offshoot from the modern human line, although probably one branching off just before the modern human/Neanderthal split.

Despite being so ancient, the face is unexpectedly similar to that of modern humans rather than other archaic humans—namely in its overall flatness as well as the curving of the cheekbone as it merges into the upper jaw—although these elements are known only from a juvenile specimen. Brain volume could have been 1,000 cc (61 cu in) or more, but no intact braincase has been discovered. This is within the range of variation for modern humans. Stature estimates range from 162.3–186.8 cm (5 ft 4 in – 6 ft 2 in). H. antecessor may have been broad-chested and rather heavy, much like Neanderthals, although the limbs were proportionally long, a trait more frequent in tropical populations. The kneecaps are thin and have poorly developed tendon attachments. The feet indicate H. antecessor walked differently than modern humans.

In biology, a clade (//kleɪd//) (from Ancient Greek κλάδος (kládos) 'branch'), also known as a monophyletic group or natural group, is a group of organisms that is composed of a common ancestor and all of its descendants. Clades are the fundamental unit of cladistics, a modern approach to taxonomy adopted by most biological fields.

The common ancestor may be an individual, a population, or a species (extinct or extant). Clades are nested, one in another, as each branch in turn splits into smaller branches. These splits reflect evolutionary history as populations diverged and evolved independently. Clades are termed monophyletic (Greek: "one clan") groups.

Convergent evolution is the independent evolution of similar features in species of different periods or epochs in time. Convergent evolution creates analogous structures that have similar form or function but were not present in the last common ancestor of those groups. The cladistic term for the same phenomenon is homoplasy. The recurrent evolution of flight is a classic example, as flying insects, birds, pterosaurs, and bats have independently evolved the useful capacity of flight. Functionally similar features that have arisen through convergent evolution are analogous, whereas homologous structures or traits have a common origin but can have dissimilar functions. Bird, bat, and pterosaur wings are analogous structures, but their forelimbs are homologous, sharing an ancestral state despite serving different functions.

The opposite of convergent evolution is divergent evolution, where related species evolve different traits. Convergent evolution is similar to parallel evolution, which occurs when two independent species evolve in the same direction and thus independently acquire similar characteristics; for instance, gliding frogs have evolved in parallel from multiple types of tree frog.

A cladogram (from Greek κλάδος klados "branch" and γραμμα gramma "character") is a diagram used in cladistics to show evolutionary relations (common descent) between groups of organisms. Cladograms are a type (subset) of phylogenetic trees that do not normally show evolutionary time but are required to meet specific criteria defined by cladistics. Like other evolutionary trees, cladograms can be used show actual, hypothesized, or even hypothetical descent. Modern cladograms are most often generated algorithmically through computational phylogenetics using genetic data, typically from DNA sequencing, as part of a molecular systematics approach.

A cladogram uses lines that branch off in different directions ending at a clade, a group of organisms with a last common ancestor. There are many shapes of cladograms but they all have lines that branch off from other lines. The lines can be traced back to where they branch off. These branching off points represent a hypothetical ancestor (not an actual entity) which can be inferred to exhibit the traits shared among the terminal taxa above it. This hypothetical ancestor might then provide clues about the order of evolution of various features, adaptation, and other evolutionary narratives about ancestors.

Homo heidelbergensis is a species of archaic human from the Middle Pleistocene of Europe and Africa, as well as potentially Asia depending on the taxonomic convention used. The species-level classification of Homo during the Middle Pleistocene is controversial, called the "muddle in the middle", owing to the wide anatomical range of variation that populations exhibited during this time. H. heidelbergensis has been regarded as either the last common ancestor of modern humans, Neanderthals, and Denisovans; or as a completely separate lineage.

H. heidelbergensis was described by German anthropologist Otto Schoetensack in 1908 based on a jawbone, Mauer 1, from a sand pit near the village of Mauer — 10 km (6.2 mi) southeast of Heidelberg. It was the oldest identified human fossil in Europe, and Schoetensack described it as an antediluvian race (before the Great Flood) which would eventually evolve into living Europeans. By the mid-20th century, all archaic human taxa were lumped as subspecies of either H. erectus or H. sapiens, with the former evolving into the latter without any coexistence. The species was usually lumped as H. e. heidelbergensis. While its utility was complicated by its definition on a jawbone (which is rarely ever found, and otherwise bears few diagnostic features) British physical anthropologist Chris Stringer revived the species in 1983, redefining it as a Euro-African ancestor of modern humans and Neanderthals using namely Kabwe 1, Petralona 1, Bodo, and Arago. These skulls are united mainly by their supraorbital torus (brow ridge) anatomy.