Macrozamia concinna

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Macrozamia concinna
Scientific classification Red Pencil Icon.png
Kingdom: Plantae
Clade: Tracheophytes
(unranked): Gymnospermae
Division: Cycadophyta
Class: Cycadopsida
Order: Cycadales
Family: Zamiaceae
Genus: Macrozamia
Species:
M. concinna
Binomial name
Macrozamia concinna
D.L. Jones
Macrozamia concinna Dist Map4.png
Occurrence data from AVH

Macrozamia concinna is a part of the plant family, Zamiaceae. It originates from a division of Cycadophyta which encompasses the complete species of cycads. M. concinna is primarily habituated in New South Wales, Australia and maintains a distinct appearance allowing it to be easily identifiable from other cycads. M. concinna also implements a unique method of reproduction to fertilise its offsprings, as opposed to the common method of wind pollination. This difference in reproduction mechanisms has survived throughout the ages of prehistoric cycad species and M. concinna continues to procreate with it.

Contents

The population of M. concinna is under threat from habitat loss associated with urbanisation, potential reproduction failure and loss to fire. [2]

Etymology

M. concinna was named in 1988 by D.L. Jones, classifying the plant after its prim and proper appearance, where it was finally recognised as its own separate species. Prior to its unique classification, it had been categorised as being part of the M. pauli-guilielmi umbrella. [3]

The specific epithet concinna stems from the Latin for neat or elegant in a compact and tidy habitat. [4] The unanimous decision to continue the name has been confirmed with the moniker being used in various publications as well as being identified throughout multiple journals regarding cycads.

History

M. concinna's heritage originates back 280 million years ago during the Permian period, often being cited as one of the oldest living seed organism that still exists within the current geological flora. [5] The occurrence of these plants happened to precede the dominance of dinosaurs, which was estimated to being around 240 million years ago. [6] M. concinna specifically, was discovered to be descended from cycad ferns during the Mesozoic age and have often been referred to as living fossils. [7]

Biology

M. concinna is often characterised as a dwarf cycad that has both male and female varieties that are vicariously covered in leaf bases.

There are often certain characteristics found relating to M. concinna. A description of these cycads sorts them by a variety of leaves unique to each individual plant that pinnate with the possibility of these pinnae dividing themselves down the middle of the leaves to form 2 distinct sides. The florae themselves frequently have darker green fronds with them twisting multiple times at the base. The seeds produced by M. concinna are visually distinguishable with their reddish complexion. M. concinna plant has a usual 1 – 5 fronds in diameter of 50-90 cm long, connected to the stem or the base, which is spirally twisted. The amount of fronds each plant will have in particular bears no resemblance to the habitat but rather is dependent on a product of genetics. [3] The longest frond on the cycad may stretch from 14 to 21 cm long by 4-6 cm wide. [8] The pinnae that stem from the frond usually take on discernible characteristics on M. concinna as opposed to other plants within the Macrozamia Family. The pinnae on M. concinna tend to grow in a spiral 360 degree motion laterally from the stem of the plant. The pinnae may twist several times rather than just once. It may also be that certain pinnae do not twist at all. The plant also has the ability to prorate cones. These cones are usually gender specific with female species having only one cone with dimensions of 13–15 cm long, 7-8 cm in diameter with their seeds being 2.1-2.6 cm long and 1.8-2.4 cm wide. Males are usually identified with having 1-2 cones on a sporadic basis, with the cones being 14-22 cm long with a diameter of 4-4.5cm with spines of 0–1.3cm long. [8]

M. concinna had been previously misclassified for a number of years before D.L. Jones specified its difference to widespread classification. Inadvertently, M. concinna still “relates in varying degrees to each of the other three New South Wale’s cycads possessing multi-twisted stems” ( M. fawcettii , M. flexuosa and M. plurinervia ). It has a close relationship to the larger M. plurinervia, (from which it was segregated) but is more akin in size and general characteristics to M. flexuosa.” [3] This would provide some insight into why it was misclassified in the first place.

In addition to its physical structure, M. concinna's physiological process follows the lineage of gymnosperms, a plant with less complex fertility processes, lacking an ovary or unable to produce fruit. [9] Gymnosperms themselves have been around for 319 million years and are shared between a number of genus's including cycads, ginkgos and conifers. [10] Unfortunately, the continuation of the species is declining with each year as gymnosperms face a higher risk of extinction with over a 40% possibility. [11]

Habitat

M. concinna is endemic to New South Wales and is classified as part of their native flora. They are usually fond of dry areas and can be found in dry eucalyptus forests under a eucalyptus canopy with a medium to dense understory. [8] The sparsely spread species is usually found in habitats containing dry sclerophyll woodlands present through upper hunter valley, north of the Nundle and hanging Rock region, ranging outwards all the way through to around Liverpool plains(CSIRO, 1998). The plants usually prefer slopes at high altitude, with an elevation of 800 metres to 1200 metres. M. concinna has been spotted on several occasions but its most recent spotting has happened to be on hanging rock, at an elevation of approximately 900m. [8]

Reproduction

Cycads in general were initially thought to have utilised wind pollination techniques in order to propagate their seeds into fertility. Only recently, Scientists uncovered the idiosyncratic method that M. concinna utilised to pollinate their seeds.

In addition, M. concinna, along with other cycads are shown to share a mutualistic relationship with insect pollinators called thrips or Cycadothrips chadwiki by their scientific name. [12] Terry, Walter, Moore, Roemer and Hull concluded in their published paper “Odour mediated push pull Pollination in cycads” that “Pollen-laden thrips leave male cycad cones in a single mass during the daily thermogenic phase, when cone temperatures and volatile emissions increase dramatically, thrips are repelled. As thermogenesis declines, total volatile emissions diminish and cones attract thrips, resulting in pollination of female cones.” The heat produced within the cone occurs within the strobili of M. concinna. The generation of heat follows a “cycardian rhythm” which is co-ordinated based on the “size and durability of the strobili.” It is assumed that the strobili contains starch that produces the necessary reactions for thermogenesis to occur. [13] Within M. concinna and other cycads, the resulting heat perpetuated from the strobili to the cone is often characterised with a smell. [14]

This would indicate that depending on the heat given off by the cones, the thrips are able to detect a scent unique to that temperature. When temperatures fluctuates too much, at quick speeds, the thrips are repelled, almost like a push mechanism. When the heat produced by the cone stagnates and the volatility of temperatures reduce, it releases an odour detected by the thrips which attracts them, symbolic of a pull mechanism.

M. concinna is a threatened species according to the IUCN red list and this is due to the particular close extinction of their pollinator thrips. According to the IUCN red list, there are only 1000 – 2500 mature species left in the wild with the population slowly declining in the coming years. [1]


Evolutionary properties

The uniqueness of the M. concinna is that it is part of a genus that is used as an anchor to compare the evolutionary path and characteristics of both gymnosperms and angiosperms. The difference between these 2 plants is that Gymnosperms are characterised as flowerless plants who produce cones and seeds that are not enclosed within an ovary but rather sit on the surface of the plant. [15] In comparison, Angiosperms are vascular plants, commonly distinguished with a root system, stems and flowers. Within angiosperms, the plant encloses the seeds behind the stigma and therefore, reproduction occurs in a completely different mechanisms to gymnosperms. [16] The importance of M. concinna's lineage is that it provides insight into the evolutionary distinctions between both gymnosperms and angiosperms, acting as an intermediary species within its physical and physiological systems. The importance of this distinction has been quoted by famous cycadologist Knut Norstog, in comparing the analysis of cycad history to the interpretation of the rosetta stone, signifying the importance of M. concinna and its origins to understanding the “origins of seed plants and their counterparts." [17]

One method of comparing the evolution of M. concinna as a gymnosperm is to evaluate the branching mechanisms that are utilised within the system. Common ancestry shared with M. concinna indicates that an isotomous branching system has remained pivotal within its heritage. This, in comparison with seed plants indicates a certain evolutionary change that led to a different branching structure to take place. This has been analysed through careful observation to be due to two subsequent evolutionary stages to lead to the formation of the flowering plants branching system. [17]

A further distinction between both M. concinna development stage can be made during a process surrounding the megagametophyte. During the early development phase of the formation of the gametophyte, which is the reproduction organ of plants, the megagametophyte has unrestricted ability to undergo nuclear division to produce a megagametophyte with several nuclei within a single enclosed membrane. This process has been compared to the formation of gametophytes in angiosperms as well, which helps to bridge the connection and lineage that the M. concinna plant belongs to. The distinction which separates the plants from angiosperms is the resulting outcome of these cells. Within plants like M. concinna, gymnosperm reproduction cells are haploids, and the endosperm of angiosperms are triploids. [17] Furthermore, the endosperm are developed post-fertilisation whilst the megagametophyte is mainly completed pre-fertilisation. Therefore, after discussing the findings of the fertilisation process and the reproduction cells within angiosperms and gymnosperms, it was discovered that the differences were down to the time at which both started the reproduction process. The reporductory system was completed in gymnosperms like M. concinna during pollination whilst angiosperm reproductions began when fertilised. [17]

Horticulture

M. concinna is known to possess qualities that thrive in dry areas but also survive cold temperatures through their acclimation to higher latitudes of placement. This results in great difficulty in sporing one within a controlled environment. The rarity of doing so has been noted by various bloggers to being one that is difficult to attain in maturity. Adversely, it is also a plant that lacks the necessary qualities that attracts botanists or plant enthusiast to actively pursue an adult sample. [18]

Related Research Articles

Gametophyte Haploid stage in the life cycle of plants and algae

A gametophyte is one of the two alternating multicellular phases in the life cycles of plants and algae. It is a haploid multicellular organism that develops from a haploid spore that has one set of chromosomes. The gametophyte is the sexual phase in the life cycle of plants and algae. It develops sex organs that produce gametes, haploid sex cells that participate in fertilization to form a diploid zygote which has a double set of chromosomes. Cell division of the zygote results in a new diploid multicellular organism, the second stage in the life cycle known as the sporophyte. The sporophyte can produce haploid spores by meiosis that on germination produce a new generation of gametophytes.

Sporangium Enclosure in which spores are formed

A sporangium is an enclosure in which spores are formed. It can be composed of a single cell or can be multicellular. All plants, fungi, and many other lineages form sporangia at some point in their life cycle. Sporangia can produce spores by mitosis, but in nearly all land plants and many fungi, sporangia are the site of meiosis and produce genetically distinct haploid spores.sporangia (singular-sporangium)

Conifer Division of plants including extinct and current conifers

Conifers are a group of cone-bearing seed plants, a subset of gymnosperms. Scientifically, they make up the division Pinophyta, also known as Coniferophyta or Coniferae. The division contains a single extant class, Pinopsida. All extant conifers are perennial woody plants with secondary growth. The great majority are trees, though a few are shrubs. Examples include cedars, Douglas-firs, cypresses, firs, junipers, kauri, larches, pines, hemlocks, redwoods, spruces, and yews. As of 1998, the division Pinophyta was estimated to contain eight families, 68 genera, and 629 living species.

Cycad Division of naked seeded dioecious plants

Cycads are seed plants that typically have a stout and woody (ligneous) trunk with a crown of large, hard, stiff, evergreen and (usually) pinnate leaves. The species are dioecious, therefore the individual plants of a species are either male or female. Cycads vary in size from having trunks only a few centimeters to several meters tall. They typically grow very slowly and live very long, with some specimens known to be as much as 1,000 years old. Because of their superficial resemblance, they are sometimes mistaken for palms or ferns, but they are not closely related to either group.

Archegonium Organ of the gametophyte of certain plants, producing and containing the ovum

An archegonium, 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.

Gymnosperm Clade of non-flowering, naked-seeded vascular plants

The gymnosperms, also known as Acrogymnospermae, are a group of seed-producing plants that includes conifers, cycads, Ginkgo, and gnetophytes, forming the clade Gymnospermae. The term gymnosperm comes from the composite word in Greek: γυμνόσπερμος, literally meaning 'naked seeds'. The name is based on the unenclosed condition of their seeds. The non-encased condition of their seeds contrasts with the seeds and ovules of flowering plants (angiosperms), which are enclosed within an ovary. Gymnosperm seeds develop either on the surface of scales or leaves, which are often modified to form cones, or solitary as in yew, Torreya, Ginkgo. Gymnosperms show alternation of generations; and have a dominant diploid sporophytic phase, a reduced haploid gametophytic phase which is dependent on the sporophytic phase.

Ovule A small body in seed-bearing plants that consists of the integument(s), nucellus, and embryosac (containing the egg cell) and develops into the seed after fertilization

In seed plants, the ovule is the structure that gives rise to and contains the female reproductive cells. It consists of three parts: the integument, forming its outer layer, the nucellus, and the female gametophyte in its center. The female gametophyte — specifically termed a megagametophyte— is also called the embryo sac in angiosperms. The megagametophyte produces an egg cell for the purpose of fertilization. The ovule is a small structure present in the ovary. It is attached to the placenta by a stalk called a funicle. The funicle provides nourishment to the ovule.

Sporophyll

A sporophyll is a leaf that bears sporangia. Both microphylls and megaphylls can be sporophylls. In heterosporous plants, sporophylls bear either megasporangia and thus are called megasporophylls, or microsporangia and are called microsporophylls. The overlap of the prefixes and roots makes these terms a particularly confusing subset of botanical nomenclature.

Bennettitales Extinct order of seed plants

Bennettitales is an extinct order of seed plants that first appeared in the Permian period and became extinct in most areas toward the end of the Cretaceous. Bennettitales are among the most common Mesozoic seed plants, and had morphologies including shrub and cycad-like forms. The foliage of bennettitaleans is superficially nearly indistinguishable from that of cycads, but they are distinguished from cycads by their more complex flower-like reproductive organs, at least some of which were likely pollinated by insects.

Double fertilization Complex fertilization mechanism of flowering plants

Double fertilization is a complex fertilization mechanism of flowering plants (angiosperms). This process involves the joining of a female gametophyte with two male gametes (sperm). It begins when a pollen grain adheres to the stigma of the carpel, the female reproductive structure of a flower. The pollen grain then takes in moisture and begins to germinate, forming a pollen tube that extends down toward the ovary through the style. The tip of the pollen tube then enters the ovary and penetrates through the micropyle opening in the ovule. The pollen tube proceeds to release the two sperm in the megagametophyte.

<i>Cycas micronesica</i> Species of plant

Cycas micronesica is a type of cycad found in the island of Yap in Micronesia, the Marianas islands of Guam and Rota, and The Republic of Palau. It is commonly known as Federico nut or Fadang in Chamorro. The species, previously lumped with Cycas rumphii or Cycas circinalis, was described in 1994 by Ken Hill. Paleoecological studies have determined that C. micronesica has been present on the island of Guam for about 9,000 years. It is linked with the human degenerative disease Lytico-Bodig disease, which is similar to amyotrophic lateral sclerosis (ALS) through a neurotoxin (BMAA) in the seeds, which were a traditional food source on Guam until the 1960s.

<i>Macrozamia glaucophylla</i>

Macrozamia glaucophylla is a species of cycad from the genus Macrozamia and the family Zamiaceae. Endemic to New South Wales, Australia, this species has features that resembles palms, although both species are taxonomically quite different. The current population trend of Macrozamia glaucophylla is stable with 2,500 to 10,000 mature individuals. The species are found in several habitats including forest and savanna. Ecologically, Macrozamia glaucophylla lives in terrestrial system, a land-based community of organisms where the biotic and abiotic components interact in the given area.

<i>Macrozamia heteromera</i>

Macrozamia heteromera is a species of cycad in the family Zamiaceae initially discovered by Charles Moore in 1858 and is endemic to New South Wales, Australia. It can be found in the north-western region of New South Wales within the Warrumbungle mountains and further south west towards the Coonabarabran district. It is a low trunked cycad usually at a height below 1 metre and can be found in dry sclerophyll woodlands. M. heteromera can be distinguished from the rest of the Macrozamia genus by its mid-green, narrow, usually divided pinnae and divided seedling pinnae.It is a plant that has toxic seeds and leaves, a characteristic common to cycads. However, after proper preparation and procedure, the seeds are fine for consumption.

<i>Macrozamia miquelii</i> Species of cycad

Macrozamia miquelii, is a species of cycad in the plant family Zamiaceae. It is endemic to Queensland and New South Wales in Eastern Australia. Located within sclerophyll forests dominated by eucalyptus trees, the cycad grows on nutrient-poor soils. It is recognised within the Zamiaceae family for its, medium height at 1 m, intermediate size of male and female cones and lighter green leaves compared to other cycads within the plant family of Zamiaceae. The seeds have an orange red sarcotesta which attracts fauna consumption, allowing a mutualistic seed dispersal for the cycad. These seeds are also edible for human consumption if prepared correctly to remove the toxins.

<i>Macrozamia riedlei</i> Species of cycad

Macrozamia riedlei, commonly known as a zamia or zamia palm, is a species of cycad in the plant family Zamiaceae. It is endemic to southwest Australia and often occurs in jarrah forests. It may only attain a height of half a metre or form an above trunk up to two metres with long arching fronds of a similar length. The giant cones amidst the crown of palm-like fronds contain edible seeds surrounded by red sarcotesta. The seeds are consumed by birds and animals, and can be a favoured part of the human diet when prepared correctly. M. riedlei benefits from a close association with bacteria that fix nitrogen, which also produce substances found throughout the plant that are toxic to some animals when consumed. The species is cultivated for ornamental use in urban and domestic environments.

<i>Macrozamia spiralis</i> Species of cycad

Macrozamia spiralis is a species of cycad in the family Zamiaceae. It is endemic to New South Wales in eastern Australia, where it is found in sclerophyll forest on low-nutrient soils. Plants generally lack a trunk and have 2–12 leaves that range up to 100 cm (40 in) in length.

Medullosales Extinct order of Late Carboniferous seed ferns

The Medullosales is an extinct order of pteridospermous seed plants characterised by large ovules with circular cross-section and a vascularised nucellus, complex pollen-organs, stems and rachides with a dissected stele, and frond-like leaves. Their nearest still-living relatives are the cycads.

<i>Encephalartos ghellinckii</i> Species of cycad

Encephalartos ghellinckii Lem. or Drakensberg cycad is endemic to South Africa, and is one of about 70 species found in sub-Saharan Africa. Strongly associated with the Natal Drakensberg, this 3m tall evergreen species is found from the foothills to fairly high altitudes, growing on stream banks, steep grassy slopes and sandstone outcrops. Its preferred habitat lying within grassveld, it has developed resistance to veldfires, and also the intense cold brought on by snow and frost.

<i>Encephalartos whitelockii</i> Species of plant

Encephalartos whitelockii is a species of cycad that is native to Uganda.

<i>Zamia integrifolia</i> Species of cycad

Zamia integrifolia, also known as coontie palm is a small, tough, woody cycad native to the southeastern United States, the Bahamas, Cuba, the Cayman Islands, and Puerto Rico.

References

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