Asparagopsis armata

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Asparagopsis armata
Two Diplodus vulgaris.JPG
( Diplodus vulgaris ). In the background, Asparagopsis armata
Scientific classification OOjs UI icon edit-ltr.svg
(unranked): Archaeplastida
Division: Rhodophyta
Class: Florideophyceae
Order: Bonnemaisoniales
Family: Bonnemaisoniaceae
Genus: Asparagopsis
Species:
A. armata
Binomial name
Asparagopsis armata
Synonyms

Falkenbergia rufolanosa

Asparagopsis armata is a species of marine red algae, in the family Bonnemaisoniaceae. [1] English name(s) include red harpoon weed. [2] They are multicellular eukaryotic organisms. This species was first described in 1855 by Harvey, [3] an Irish botanist who found the algae on the Western Australian coast. A. armata usually develops on infralittoral rocky bottoms around the seawater surface to around 40m of depth. Marine algae like A. armata are considered "autogenic ecosystem engineers" as they are at the very bottom of the food chain and control resource availability to other organisms in the ecosystem. [4]

Contents

Population distribution

A. armata is a species native to southern Australia and New Zealand (Southern hemisphere) and is thought to have slowly spread to the Northern hemisphere through the Mediterranean sea, as it is highly invasive. It can now also be found along the British Isles to Senegal as well. [5] The first Mediterranean A. armata was reported in Algeria in 1923. When first found, it seemed strange to find A. armata in this location due to the high summer seawater surface temperatures along southern Mediterranean coasts. However, it was later found that the particular cool water temperatures that stay below 25 °C would allow the species to survive locally during the summer. [3]

Morphology

The fully grown A. armata has sparse branches on which long stolons with harpoon-like hooks and erect shoots develop in all directions. The branches, stolons, and shoots ramify over and over again which give A. armata the thallus-like appearance. [3] The ultimate branchlets are filamentous and composed of three cell rows whereas the larger branches consist of a central medullary filament and a gelatinous matrix surrounded by a cortex 3 – 6 cells thick. [6] Gametophytes are terete and are around 200 mm in height. They form dense, pink intertwining clumps. A characteristic feature of this species is barbs, which attach the A. armata to the ocean benthic substrates. [7]

Life cycle

A. armata has a triphasic diplohaplontic heteromorphic life cycle. In this cycle, the three phases include: haploid carposporophyte, gametophyte and diploid zygote. Multiple phases of different morphology and ploidy contribute differently to the expansion potential of A. armata. Gametophytes of this species are microscopic carposoporophytes, which divide into tetrasporophytes that go through meiosis to be developed into the gametophyte.

A. armata has two morphologically different stages of development– the gametophyte stage and the tetrasporophyte stage.

Life cycle of A. armata.png

A. armata goes through haploid and gametophytic phases in a heteromorphic diplo-haplontic life cycle. [3] The A. armata gametophyte grows into adult form and goes through fecundation to produce diploid carposporophyte; which, then, divide into tetrasporophyte that goes through meiosis to be developed into the gametophyte. [8]

Impact of A. armata as an invasive species

The acceleration of marine biological invasions through increasing trade and travel also caused the transportation of A. armata to areas outside of their native range: Southern hemisphere. Once it is established, A. armata could rapidly spread and dominate the invaded environment without the direct intervention of human activity. [9] A. armata releases large amounts of toxic compounds to gain competitive advantage in the surrounding invaded area. [10] The impairment of invertebrates after exposure to this algal exudate is shown by significantly increased lipid  (and other biochemical biomarkers) content in the organisms such as common prawn and marine snail. [10] The critical impact that the exudate of A. armata causes, via secondary metabolites, severely decreases the survival rate of various species in the rock pool native communities. [10]

Halogenated metabolites

As a defense mechanism against its predators, A. armata produce halogenated metabolites that chase away herbivores and prevent biofouling. These halogenated metabolites are stored as a refractile inclusion inside specialized gland cells, and are activated with Bromine.

Gland cells of A. armata can take up to 10% of the algal volume, which is a large portion of the plant. Gland cell walls are thin in order to help the transfer of metabolites to the structures that connect the gland cells to the pericentral cells. These structures are stalk-like and allow the metabolite to move to the algae's surface. [11]

Methane emissions reduction in ruminants

In 2019, following laboratory studies on the effectiveness of Asparagopsis taxiformis in reducing ruminants' enteric methane emissions, a team from the University of California, Davis, demonstrated that a 1% inclusion of Asparagopsis armata in lactating dairy cows' feed resulted in a 67.2% decrease in methane produced. [12]

In 2021, CH4 Global became the first company in the world to be licensed by intellectual property holders FutureFeed to use Asparagopsis got livestock feed, with the aim of significantly reducing enteric methane emissions in ruminants. These licences enable CH4 Global to make methane reduction claims about the Asparagopsis in their product formulations in the New Zealand and Australian markets, [13] where the company has research and production facilities. A. armata is the dominant species of Asparagopsis in New Zealand. [14] CH4 Global worked with New Zealand’s National Institute of Water and Atmospheric Research (NIWA) to close the life cycle of the seaweed, which they accomplished in June of the same year, [15] enabling large quantities of the seaweed to be aquafarmed.

Sea Forest, based in Tasmania, Australia, and also a FutureFeed licensee, has chosen to focus exclusively on A. armata, and has worked with scientists at James Cook University, University of Tasmania, University of Technology Sydney, and University of New South Wales in Australia, and the University of Waikato in New Zealand, to find out how to trigger its reproduction. [16]

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<i>Palmaria palmata</i> Species of edible alga

Palmaria palmata, also called dulse, dillisk or dilsk, red dulse, sea lettuce flakes, or creathnach, is a red alga (Rhodophyta) previously referred to as Rhodymenia palmata. It grows on the northern coasts of the Atlantic and Pacific Oceans. It is a well-known snack food. In Iceland, where it is known as söl[ˈsœːl̥], it has been an important source of dietary fiber throughout the centuries.

Schmitzia hiscockiana is a small, rare, red seaweed or marine alga of the phylum Rhodophyta or red algae. It was discovered and named in 1985.

<i>Polysiphonia</i> Genus of algae

Polysiphonia is a genus of filamentous red algae with about 19 species on the coasts of the British Isles and about 200 species worldwide, including Crete in Greece, Antarctica and Greenland. Its members are known by a number of common names. It is in the order Ceramiales and family Rhodomelaceae.

<span class="mw-page-title-main">Conceptacle</span>

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In algal anatomy, a pit connection is a hole in the septum between two algal cells, and is found only in the red algae − specifically, all orders except the Porphyridiales and haploid Bangiales. They are often stoppered with proteinaceous "pit plugs". By contrast, many fungi contain septal pores − an unrelated phenomenon.

<i>Rhodochorton</i> Genus of algae

Rhodochorton is a genus of filamentous red alga adapted to low light levels. It may form tufts or a thin purple "turf" up to 5 millimetres high. The filaments branch infrequently, usually at the tips.

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Red algae, or Rhodophyta, are one of the oldest groups of eukaryotic algae. The Rhodophyta comprises one of the largest phyla of algae, containing over 7,000 currently recognized species with taxonomic revisions ongoing. The majority of species (6,793) are found in the Florideophyceae (class), and mostly consist of multicellular, marine algae, including many notable seaweeds. Red algae are abundant in marine habitats but relatively rare in freshwaters. Approximately 5% of red algae species occur in freshwater environments, with greater concentrations found in warmer areas. Except for two coastal cave dwelling species in the asexual class Cyanidiophyceae, there are no terrestrial species, which may be due to an evolutionary bottleneck in which the last common ancestor lost about 25% of its core genes and much of its evolutionary plasticity.

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<i>Asparagopsis</i> Genus of algae

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References

  1. Zanolla, M. (2015). "Photosynthetic Plasticity of the Genus Asparagopsis (Bonnemaisoniales, Rhodophyta) in Response to Temperature: Implications for Invasiveness". Biological Invasions. 17 (5): 1341–1353. doi:10.1007/s10530-014-0797-8. S2CID   18279567.
  2. "MarLIN - The Marine Life Information Network - Harpoon weed (Asparagopsis armata)". www.marlin.ac.uk. Retrieved 2022-07-01.
  3. 1 2 3 4 Andreakis, Nikos; Procaccini, Gabriele; Kooistra, Wiebe HCF (2004-08-01). "Asparagopsis taxiformis and Asparagopsis armata (Bonnemaisoniales, Rhodophyta): genetic and morphological identification of Mediterranean populations". European Journal of Phycology. 39 (3): 273–283. doi:10.1080/0967026042000236436. ISSN   0967-0262. S2CID   84044248.
  4. Crooks, J.A. (2002). "Characterizing ecosystem-level consequences of Biological Invasions, the role of ecosystem engineers". Oikos. 97 (2): 153–166. doi:10.1034/j.1600-0706.2002.970201.x.
  5. Dixon, P.S.; Irvine, L.M. (1977). Seaweeds of the British Isles : Vol. 1: Rhodophyta Part 1: Introduction, Nemaliales, Gigartinales. British Museum. ISBN   0-565-00781-5. OCLC   769250096.
  6. Børgesen, Frederik (1913). The marine Algæ of the Danish West Indies. Copenhagen: Printed by B. Luno. doi:10.5962/bhl.title.1314.
  7. "Asparagopsis armata - Invasive Alien Species Fact Sheet for Mediterranean Network of MPAs". Online Database MedMIS IUCN Center for Mediterranean Cooperation.{{cite web}}: CS1 maint: url-status (link)
  8. Guiry, Michael D.; Dawes, Clinton J. (1992-06-25). "Daylength, temperature and nutrient control of tetrasporogenesis in Asparagopsis armata (Rhodophyta)". Journal of Experimental Marine Biology and Ecology. 158 (2): 197–217. doi:10.1016/0022-0981(92)90227-2. ISSN   0022-0981.
  9. Richardson, D. M. (2011). Fifty years of invasion ecology : the legacy of Charles Elton. Chichester, West Sussex: Wiley-Blackwell. ISBN   978-1-4443-3585-9. OCLC   652743661.
  10. 1 2 3 Silva, Carla O.; Novais, Sara C.; Soares, Amadeu M.V.M.; Barata, Carlos; Lemos, Marco F.L. (2020-08-10). "Impacts of The Invasive Seaweed Asparagopsis armata Exudate on Rockpool Invertebrates". doi: 10.20944/preprints202008.0236.v1 .{{cite journal}}: Cite journal requires |journal= (help)
  11. Paul, Nicholas A.; Cole, Louise; Nys, Rocky De; Steinberg, Peter D. (2006). "Ultrastructure of the Gland Cells of the Red Alga Asparagopsis Armata (bonnemaisoniaceae)1". Journal of Phycology. 42 (3): 637–645. doi:10.1111/j.1529-8817.2006.00226.x. ISSN   1529-8817. S2CID   85291068.
  12. Roque, Breanna M.; Salwen, Joan K.; Kinley, Rob; Kebreab, Ermias (October 10, 2019). "Inclusion of Asparagopsis armata in lactating dairy cows' diet reduces enteric methane emission by over 50 percent". Journal of Cleaner Production. 234: 132–138. doi:10.1016/j.jclepro.2019.06.193. S2CID   197795543 via Elsevier Science Direct.
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  15. "Research Collaboration Uncovers Mechanisms To Trigger Spore Release For Asparagopsis Seaweed | Scoop News". www.scoop.co.nz. June 4, 2021. Retrieved 2022-12-05.
  16. Hughes, Lesley (2022-09-02). "From designing clothes to refashioning cow burps: Sam's $40 million career switch". The Sydney Morning Herald. Retrieved 2022-12-05.