Thallus in the context of "Leprose lichen"

Liverworts are a group of non-vascular land plants forming the division Marchantiophyta (/mɑːrˌkæntiˈɒfətə, -oʊˈfaɪtə/ ). They may also be referred to as hepatics. 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. The division name was derived from the genus name Marchantia, named after his father by French botanist Jean Marchant.

It is estimated that there are about 9000 species of liverwort. Some of the more familiar species grow as a flattened leafless thallus, but most species are leafy with a form very much like a flattened moss. Leafy species can be distinguished from the apparently similar mosses on the basis of a number of features, including their single-celled rhizoids. Leafy liverworts also differ from most (but not all) mosses in that their leaves never have a costa (present in many mosses) and may bear marginal cilia (very rare in mosses). Other differences are not universal for all mosses and liverworts, but the occurrence of leaves arranged in three ranks, the presence of deep lobes or segmented leaves, or a lack of clearly differentiated stem and leaves all point to the plant being a liverwort. Liverworts are distinguished from mosses in having unique complex oil bodies of high refractive index.

Lemnoideae is a subfamily of flowering aquatic plants, known as duckweeds, water lentils, or water lenses. They float on or just beneath the surface of still or slow-moving bodies of fresh water and wetlands. Also known as bayroot, they arose from within the arum or aroid family (Araceae), so often are classified as the subfamily Lemnoideae within the family Araceae. Other classifications, particularly those created prior to the end of the twentieth century, place them as a separate family, Lemnaceae.

These plants have a simple structure, lacking an obvious stem or leaves. The greater part of each plant is a small organized "thallus" or "frond" structure only a few cells thick, often with air pockets (aerenchyma) that allow it to float on or just under the water surface. Depending on the species, each plant may have no root or may have one or more simple rootlets.

The evolution of plants has resulted in a wide range of complexity, from the earliest algal mats of unicellular archaeplastids evolved through endosymbiosis, through multicellular marine and freshwater green algae, to spore-bearing terrestrial bryophytes, lycopods and ferns, and eventually to the complex seed-bearing gymnosperms and angiosperms (flowering plants) of today. While many of the earliest groups continue to thrive, as exemplified by red and green algae in marine environments, more recently derived groups have displaced previously ecologically dominant ones; for example, the ascendance of flowering plants over gymnosperms in terrestrial environments.

There is evidence that cyanobacteria and multicellular thalloid eukaryotes lived in freshwater communities on land as early as 1 billion years ago, and that communities of complex, multicellular photosynthesizing organisms existed on land in the late Precambrian, around 850 million years ago.

Coralline algae are red algae in the order Corallinales, characterized by a thallus containing calcareous deposits within its cell walls, giving it hardness. The colors of these algae are typically some hue of pink, or another shade of red, but some species can be purple, yellow, blue, white, or gray-green. Typically, these algae grow in a crustose manner (encrusting rocks and other hardscape); in the intertidal zone of rocky shorelines, and within coral reefs, these algae appear as an abundance of colorful patches on rock surfaces. Unattached specimens (maerl, rhodoliths) may form relatively smooth compact balls, or forming warty to fruticose thalli.

The red algae belong to the division Rhodophyta, within which the coralline algae form the order Corallinales. There are over 1600 described species of nongeniculate coralline algae. The corallines are presently grouped into two families on the basis of their reproductive structures. Most are marine, though one species lives in freshwater; Pneophyllum cetinaensis.

An archegonium (pl.: archegonia), from the Ancient Greek ἀρχή ("beginning") and γόνος ("offspring"), is a multicellular structure or organ of the gametophyte phase of certain plants, producing and containing the ovum or female gamete. The corresponding male organ is called the antheridium. The archegonium has a long neck canal or venter and a swollen base. Archegonia are typically located on the surface of the plant thallus, although in the hornworts they are embedded.