Dicranoloma billardierei | |
---|---|
Scientific classification | |
Kingdom: | Plantae |
Division: | Bryophyta |
Class: | Bryopsida |
Subclass: | Dicranidae |
Order: | Dicranales |
Family: | Dicranaceae |
Genus: | Dicranoloma |
Species: | D. billardierei |
Binomial name | |
Dicranoloma billardierei (Brid.) Paris | |
Distribution Map From Atlas of Living Australia [1] |
Dicranoloma billardierei is a species of bryophyte in the genus Dicranoloma . [2] This moss is extremely common in wet rainforest habitats. [3] In the field, Dicranoloma billardierei, is often confused with Dicranoloma robustum and Dicranoloma fasciatum . [2] However, the short and obtuse nature of the leaves make this moss normally very distinctive.
Dicranoloma billardierei is a lustrous green or gold brown coloured plant that mostly forms cushions up to 80 cm (31 in) in diameter. [4] [2] The stems are branched by innovation and forking. The cross section has 3 to 4 layers of cortical cells and a central stand, with rhizoids in the leaf axils. [4] [2] The leaves are often twisted at the apex, falcate or erect spreading when fresh. [4] [2] The leaves are serrate or entire above and entire below with planes at margins. [4] [2] The mid laminal cells are elongate and irregular with elongate cells extending to apex. [4] [2] The border is well defined and extends from alar group to serrations. The cells that the base of the leaf are usually longer. [4] [2] The costa is narrow and wide in the middle of the leaf with the abaxial surface bearing short spines. [4] There is normally one setae per perichaetium, the capsules are exserted and strongly curved. The operculum is curved and the calyptra is cucullate and smooth. [4] [2] Dicranoloma billarderi is very similar to Dicranoloma robustum but can be distinguished by the more untidy look of the leaves as well as the leaves generally being smaller. [4] [2] Dicranoloma billardierei is almost always paler and less yellow then Dicranoloma robustum. [2] [4] The cushions and stems, which are much branched and visible within the leaves, stems are often prostrate and the short leaves make this moss very distinctive. [4] The obtuse nature of the leaves is readily observed under a hand lens and this can be distinctive of this species. [4] [2] Dicranoloma billardierei can also be confused with Dicranoloma fasciatum. However Dicranoloma billardierei will have serrate upper leaf margins compared to the spinose serrate margins of Dicranoloma fasciatum.
Dicranoloma billardierei lives in epiphytic and terrestrial environments. Generally growing on logs, stumps, exposed roots, soil or on rock. [4] [2] In terrestrial environments it is often found in well drained sites in a variety of forest and shrub types. [4] [2] It occurs in mixed broad leaf or southern beech forest on the forest floor and in New Zealand is often found within manuka scrub environments. [4] [2] This moss often forms a mosaic with Dicranoloma robustum and is found any from sea level up to approximately 1,250 m (4,100 ft). [4] [2]
Dicranoloma billardierei normally consists of a main stem with multiple lateral branches and commonly at each apex a perichaetium was present. [5] This perichaetium is a cluster of leaves surrounding the sex organs of the moss and forming an enveloping sheath. [5] Archegonial, the female sex organs in plants, development began later then the male sex organ of plants, the antheridia. [5] Maturation in archegonia takes around three months compared to antheridia which is about six to seven months. [5] Maturation in antheridia means the sex organs are full size as the leaves surrounding the organs are ‘bulging’. Once fertilization of an archegonium occurs any further development is inhibited. [5] As the haploid gamete fuse, the male gamete from the antheridium fertilizes the female, which results in a diploid spore forming plant forming known as sporophyte. [5]
The internal of fertilization is between two and three months for Dicranoloma billardierei. [5] These sporophytes increase their seta length and capsule size from march to July. [5] By early spring the sporophytes have reached the operculum intact stage and sporophytes begin to rapidly develop. [5] Once spore dispersal completes, the seta is the only evidence left of the sporophyte as the capsules disperse. [5] Sporophyte maturation in Dicranoloma billardierei takes approximately twenty months. [5] Compared to other species such as Dicranoloma menziesii, Dicranoloma billardierei produces relatively small abundance of sporophyte colonies. [5] Sporophytes do not resume development until spores from the previous season have been released. [5] This is because sporophytes rely on gametophyte during the early developmental stages. Waiting for the previous years spores to be released reduces the demand of the gametophyte for nutrition. [5]
Dicranoloma billardierei had a seasonal pattern of sporophyte development and gametangial, the production of gametes in an organ or cell, development occurs multiple times throughout the year with some irregularity. [5] This may a result of unpredictable conditions in the environment of the mosses. [5] Gametophtyes in this species are able to support new sporophytes even with capsules from the previous year, as the sporophytes produce some of their own energy requirements. [5] Dicranoloma billardierei antheridia development tends to occur later than other species like Dicranoloma menziesii and this may be because Dicranoloma billardierei typically occurs in decaying logs and in cool hallows that are protected by overhanging fronds. [5] Reproductive cycle events may be influenced by environmental factors such as rainfall, light and temperature. They are also likely to be genetically controlled. [5]
There are a wide variety of invertebrates associated with mosses and the moist environment they provide. [6] Mosses conduct water externally, they are ectohydric, and also absorb water through much of their surface. [6] They are also able to retain water for long time periods. In moss species such as Dicranoloma, water retention and uptake is enhanced through a covering of rhizoids on the stems and is also liked to growth form. Forms of life will also affect water retention. [6] Invertebrates communities play an important role in the biodiversity within an ecosystem and in mosses. Mosses provide invertebrates camouflage, protection, shelter, food and a place to deposit their eggs. [6] Mosses also benefits from the presence of invertebrates as these organisms may assist in sperm dispersal. [6] Invertebrates such as mites are common on the stems of Dicranoloma, as well as species of Gastropa , Thysanoptera , and Coleoptera all of which feed on the moss. [6] The remains of bacteria, algae, or dead and decaying material found within moss also likely provides a food sources for some species. [6]
Alternation of generations is the predominant type of life cycle in plants and algae. In plants both phases are multicellular: the haploid sexual phase – the gametophyte – alternates with a diploid asexual phase – the sporophyte.
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.
A sporophyte is the diploid multicellular stage in the life cycle of a plant or alga which produces asexual spores. This stage alternates with a multicellular haploid gametophyte phase.
Fissidens adianthoides, the maidenhair pocketmoss, is a moss in the family Fissidentaceae. It was first collected by Hedwig in 1801.
A prothallus, or prothallium, is usually the gametophyte stage in the life of a fern or other pteridophyte. Occasionally the term is also used to describe the young gametophyte of a liverwort or peat moss as well. In lichens it refers to the region of the thallus that is free of algae.
Plant reproduction is the production of new offspring in plants, which can be accomplished by sexual or asexual reproduction. Sexual reproduction produces offspring by the fusion of gametes, resulting in offspring genetically different from either parent. Asexual reproduction produces new individuals without the fusion of gametes, resulting in clonal plants that are genetically identical to the parent plant and each other, unless mutations occur.
This page provides a glossary of plant morphology. Botanists and other biologists who study plant morphology use a number of different terms to classify and identify plant organs and parts that can be observed using no more than a handheld magnifying lens. This page provides help in understanding the numerous other pages describing plants by their various taxa. The accompanying page—Plant morphology—provides an overview of the science of the external form of plants. There is also an alphabetical list: Glossary of botanical terms. In contrast, this page deals with botanical terms in a systematic manner, with some illustrations, and organized by plant anatomy and function in plant physiology.
Aulacomnium palustre, the bog groove-moss or ribbed bog moss, is a moss that is nearly cosmopolitan in distribution. It occurs in North America, Hispaniola, Venezuela, Eurasia, and New Zealand. In North America, it occurs across southern arctic, subboreal, and boreal regions from Alaska and British Columbia to Greenland and Quebec. Documentation of ribbed bog moss's distribution in the contiguous United States is probably incomplete. It is reported sporadically south to Washington, Wyoming, Georgia, and Virginia.
Sexual reproduction is a type of reproduction that involves a complex life cycle in which a gamete with a single set of chromosomes combines with another gamete to produce a zygote that develops into an organism composed of cells with two sets of chromosomes (diploid). This is typical in animals, though the number of chromosome sets and how that number changes in sexual reproduction varies, especially among plants, fungi, and other eukaryotes.
Polytrichum juniperinum, commonly known as juniper haircap or juniper polytrichum moss, is an evergreen and perennial species of moss that is widely distributed, growing on every continent including Antarctica.
Splachnaceae is a family of mosses, containing around 70 species in 6 genera. Around half of those species are entomophilous, using insects to disperse their spores, a characteristic found in no other seedless land plants.
Pogonatum urnigerum is a species of moss in the family Polytrichaceae, commonly called urn haircap. The name comes from "urna" meaning "urn" and "gerere" meaning "to bear" which is believed to be a reference made towards the plant's wide-mouthed capsule. It can be found on gravelly banks or similar habitats and can be identified by the blue tinge to the overall green colour. The stem of this moss is wine red and it has rhizoids that keep the moss anchored to substrates. It is an acrocarpous moss that grows vertically with an archegonium borne at the top of each fertilized female gametophyte shoot which develops an erect sporophyte.
Climacium dendroides, also known as tree climacium moss, belongs in the order Hypnales and family Climaciaceae, in class Bryopsida and subclass Bryidae. It is identified as a "tree moss" due to its distinctive morphological features, and has four species identified across the Northern Hemisphere. The species name "dendroides" describes the tree-like morphology of the plant, and its genus name came from the structure of the perforations of peristome teeth. This plant was identified by Weber and Mohr in 1804. They often have stems that are around 2-10 cm tall and growing in the form of patches, looking like small palm-trees. They have yellow-green branches at the tip of stems. The leaves are around 2.5-3 mm long, with rounder stem leaves and pointier branch leaves. Their sporophytes are only abundant in late winter and early spring, and appears as a red-brown shoot with long stalk and cylindrical capsules.
Polytrichum strictum, commonly known as bog haircap moss or strict haircap, is an evergreen and perennial species of moss native to Sphagnum bogs and other moist habitats in temperate climates. It has a circumboreal distribution, and is also found in South America and Antarctica.
Fissidens limbatus commonly known as Herzog's pocket-moss, is a moss in the family Fissidentaceae. This species is found growing in high elevations in tropical America in addition to the US, Mexico and Canada. Montagne first collected F. crispus in 1838.
Andreaea rupestris is a species of moss in the class Andreaeopsida, are commonly referred to as the "lantern mosses" due to the appearance of their dehisced sporangia. It is typically found on smooth, acidic, exposed rock in the Northern hemisphere. It exhibits the common features of the genus Andreaea such as being acrocarpous, having dark pigmentation, lacking a seta, and bearing 4 lines of dehiscence in its mature sporangia, but can be further identified upon careful examination of its gametophytic leaves which have an ovate base to a more blunt apex compared to other similar species.
Syntrichia latifolia, formerly Tortula latifolia, and commonly known as water screw-moss, is a species of moss belonging to the family Pottiaceae. Syntrichia species differ from members of Tortula due to synapomorphic leaf qualities, such as different basal and distal cells, as well as different costal cross sections where Tortula has an abaxial epidermis and Syntrichia lacks one.
Polytrichastrum formosum, commonly known as the bank haircap moss, is a species of moss belonging to the family Polytrichaceae.