Gelidium

Last updated

Gelidium
Icones of Japanese algae (Pl. CVI) (8006301038).jpg
Gelidium amansii
Scientific classification OOjs UI icon edit-ltr.svg
(unranked): Archaeplastida
Division: Rhodophyta
Class: Florideophyceae
Order: Gelidiales
Family: Gelidiaceae
Genus: Gelidium
J.V. Lamouroux, 1813
Synonyms

AcanthopeltisOkamura, 1892

Gelidium is a genus of thalloid red algae comprising 134 species. Its members are known by a number of common names. [note 1]

Contents

Taxonomy and nomenclature

Gelidiaceae has 159 species, considered to be the largest family in Gelidiales with four major genera: Capreolia, Gelidium, Gelidiophycus, and Ptilophora [1] .

Gelidium was first described by Lamouroux in 1813 and is regarded to be one the genus with the most species. Species diversity has been established by previous studies, whereas, molecular analysis reveals biogeographic relations that concerns its current distribution pattern in oceans. [2]

Identification of species has been a challenge as sexual plants are somewhat difficult to find in nature, therefore, other physiological features are examined instead, such as branching patterns and vegetative traits, but subsequent studies revealed that these are also affected by its development and environmental factors [3] highlighting the need for genetic studies utilizing genetic markers. [2]

Morphology

Specimens can reach around 2–40 cm (0.79–16 in) in size. Branching is irregular, or occurs in rows on either side of the main stem. Gelidium produces tetraspores. Many of the algae in this genus are used to make agar. Chaetangium is a synonym. [4]

Distribution

Gelidium are widely distributed globally, specifically in tropical to temperate regions, but lacking in polar regions. [5] In the ocean, Gelidium can be found inhabiting the intertidal to subtidal zone. [2] Species from the genus require further studies to distinguish boundaries among members, as recent molecular research have shown that there are cryptic, unidentified species assumed to be regionally endemic and isolated but may also be ubiquitous in nature. [2] Some species are common in the Atlantic and Pacific Ocean (G. crinale) while some are confined in North Atlantic waters (G. pussillum) [6] [3] [7] . Reports of G. pussillum occurrence outside of its specified range may be questionable and requires further verification. [2]

Ecology

Gelidiales consists of many species that are economically important as they produce agar while some serve ecologically significant functions such as substrate cover. [5] The growth of Gelidium can primarily be affected by nutrient availability and light. In turn, these factors are also regulated by temperature and water movement, respectively. Santelices (1991) evaluated how eight factors may affect Gelidium productivity, all of which are important in understanding how different interactions correlate to production yield. Some of these factors include seasonality, phenotypic characters, age, reproductive state, and even the source of the algae. [5]

Life history

Gelidium is assumed to follow the Polysiphonia life cycle, with sexual and tetrasporangial generations. [8] Tetrasporangia formation is also known to be affected by temperature and other environmental factors including light, salinity and moisture, [9] although germination rates remain unaffected based on an earlier study. [10]

In 1993, Gelidium robustum in Santa Barbara, California was investigated for 16-months showing tetrasporangial abundance throughout the year, but may not have the ability to germinate despite maximum spore output. [8]

Cultivation and exploitation

An important agarophyte, Gelidium has been cultured in Korea [11] and China [12] since the early 1990s, with some cultivation efforts noted in Europe, specifically in Spain [13] and Portugal. [11] [14] In South Africa, G. pristoides (Turner) has been cultivated in the field while laboratory trials on G. crinale (Turner) and Pterocladiella capillacea (Gmel.) Santelices and Hommersand were tested in Israel. [15] [16]

Gelidium has been found to be over-exploited in Japan, depleting algal beds [17] which in part, affects agar production, pushing the need for even more efforts in cultivation, replacing the practice of harvesting wild Gelidium. [18] In 2017, global data have shown that Norway, China, and Chile are among the countries that lead the overharvesting of seaweeds, mostly kelp. [18] Advances in Gelidium cultivation have been put forth including the use of floaters at sea and marine ponds for free-float technology in cultivation. [19] At its core, environmental factors are needed to be controlled for favorable growth of Gelidium revealing how ponds may be the better option among the set-ups [18] .

Chemical composition

Agar is primarily extracted from Gelidium especially among North African Atlantic and South European species based on specific gel properties with water. In Morocco, Gelidium sesquipidale is known to be harvested during summer time to extract agar used commercially, making the country among the top producers in the world. [20]

Agarocolloids are known to be extracted in algae belonging to the orders Gracilariales and Gelidiales with certain applications in the food and cosmetics. Gelling properties often differ among species, seasons, seaweed age, and substitutions between sulphate esters, among other compounds. Sulphate composition often dictates gel strength, while methyl esters determine gelling and elasticity. [20]

Utilization and management

In Portugal, G. sesquipedale are commonly harvested for agar since the 1960s. [21] Management strategies are yet to be implemented especially among big commercial companies that should be responsible in harvesting the resource, similar to South Africa where the decrease in annual Gelidium landings show how fisher folk shifted to collecting kelp for abalone feeds instead of Gelidium harvesting. [22]

Gelidium as environmental records

Gelidium species have been collected, pressed and maintained in herbaria and personal collections from the 1850s onwards since seaweed collecting became a popular pastime for the middle classes as well as scientists in Europe and North America. [23] These numerous well-documented specimens can provide information beyond taxonomy. [24]

Sensitive measurement of stable nitrogen isotope ratios in Gelidium species collected in southern Monterey Bay between 1878 and 2018 showed a pattern of changes that matched with changes in the California current and provided support for a theory about the end of the local fishing industry. [25] Nitrogen isotope ratios are well established as a measure of nutrient productivity in aquatic ecosystems. The California current runs along coastal California and correlation with information on fish catches indicates that an increase in nutrient-rich cold water is important for fish productivity, notably sardines. [26] The California current has only been measured since 1946. The correlations with the Gelidium nitrogen ratios allowed the California current to be projected back into the nineteenth century and compared with historical records of fish catches. [25] The data matched, notably for the highest sardine catches through the 1930s and then the sudden decrease from 1945 to 1950 that ended the Monterey cannery industry. This information supports the theory that environmental changes as well as overfishing caused the collapse of the local fishery business. More broadly, this suggests that elemental analysis of historical samples of macroalgae can provide evidence of primary productivity processes. The species used included specimens of G. coulteri, G. robustum, G. purpurascens, G. pusillum and G. arborescens collected over a 140-year timespan from the 6 km coastline between Point Pinos, Pacific Grove and Cannery Row, Monterey in California, US. [25]

Species

Notes

  1. Recorded common names are tengusa, makusa, genso, niu mau tsai, japansche scheleiachtige mos, steen-or klipbloem, hay tsay, olus marinus, sajur laut, tschintschau, tschoo-hoae, onikusa, hirakusa, obusa, rødalge-slaegt, gelídeos, punalevä-suku, tokoroten, kanten, tokoro-tengusa, kinukusa, isingglass, hai-ten-gusa, tocoroten, tengusa-agar, limu lo-loa, hai-tengusa, onigusa, oyakusa, kanten weed, goumaocai, hime tengusa, shihua and tanmae.

Related Research Articles

<i>Chondrus crispus</i> Species of edible alga

Chondrus crispus—commonly called Irish moss or carrageenan moss —is a species of red algae which grows abundantly along the rocky parts of the Atlantic coasts of Europe and North America. In its fresh condition it is soft and cartilaginous, varying in color from a greenish-yellow, through red, to a dark purple or purplish-brown. The principal constituent is a mucilaginous body, made of the polysaccharide carrageenan, which constitutes 55% of its dry weight. The organism also consists of nearly 10% dry weight protein and about 15% dry weight mineral matter, and is rich in iodine and sulfur. When softened in water it has a sea-like odour. Because of the abundant cell wall polysaccharides, it will form a jelly when boiled, containing from 20 to 100 times its weight of water.

<i>Caulerpa</i> Genus of seaweeds

Caulerpa is a genus of seaweeds in the family Caulerpaceae. They are unusual because they consist of only one cell with many nuclei, making them among the biggest single cells in the world.

<i>Callophyllis variegata</i> Species of seaweed

Callophyllis variegata, commonly known as carola, is a type of edible seaweed, a member of the genus Callophyllis. Callophyllis variegata occurs in Concepción de Chile and other parts of South America such as Peru, the Falkland Islands, Tierra del Fuego. But also in New Guinea, South Africa, Australia, New Zealand, Alaska, St. Paul Island, Antarctic and subantarctic islands such as the Graham Land, Kerguelen, Macquarie Island, South Georgia, and the South Orkney Islands.

<span class="mw-page-title-main">Florideophyceae</span> Class of algae

Florideophyceae is a class of exclusively multicellular red algae. They were once thought to be the only algae to bear pit connections, but these have since been found in the filamentous stage of the Bangiaceae. They were also thought only to exhibit apical growth, but there are genera known to grow by intercalary growth. Most, but not all, genera have three phases to the life cycle.

<i>Codium</i> Genus of algae

Codium is a genus of edible green macroalgae under the order Bryopsidales. The genus name is derived from a Greek word that pertains to the soft texture of its thallus. One of the foremost experts on Codium taxonomy was Paul Claude Silva at the University of California, Berkeley. P.C. Silva was able to describe 36 species for the genus and in honor of his work on Codium, the species C. silvae was named after the late professor.

<i>Gelidiella</i> Genus of algae

Gelidiella is a genus of red algae. Worldwide there are 22 species of Gelidiella, mostly tropical and subtropical. Gelidiella and Gelidium are now both united into one order Gelidiales.

<span class="mw-page-title-main">Gelidiaceae</span> Family of algae

The Gelidiaceae is a small family of red algae containing eight genera. Many species of this algae are used to make agar.

<span class="mw-page-title-main">Seaweed</span> Macroscopic marine algae

Seaweed, or macroalgae, refers to thousands of species of macroscopic, multicellular, marine algae. The term includes some types of Rhodophyta (red), Phaeophyta (brown) and Chlorophyta (green) macroalgae. Seaweed species such as kelps provide essential nursery habitat for fisheries and other marine species and thus protect food sources; other species, such as planktonic algae, play a vital role in capturing carbon and producing at least 50% of Earth's oxygen.

<span class="mw-page-title-main">Red algae</span> Division of plant life

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.

<span class="mw-page-title-main">Edible seaweed</span> Algae that can be eaten and used for culinary purposes

Edible seaweed, or sea vegetables, are seaweeds that can be eaten and used for culinary purposes. They typically contain high amounts of fiber. They may belong to one of several groups of multicellular algae: the red algae, green algae, and brown algae. Seaweeds are also harvested or cultivated for the extraction of polysaccharides such as alginate, agar and carrageenan, gelatinous substances collectively known as hydrocolloids or phycocolloids. Hydrocolloids have attained commercial significance, especially in food production as food additives. The food industry exploits the gelling, water-retention, emulsifying and other physical properties of these hydrocolloids.

<span class="mw-page-title-main">Ice-ice</span> Disease condition of seaweed

Ice-ice is a disease condition of seaweed. Ice-ice is caused when changes in salinity, ocean temperature and light intensity cause stress to seaweeds, making them produce a "moist organic substance" that attracts bacteria in the water and induces the characteristic "whitening" and hardening of the seaweed's tissues. Bacteria involved include those in the Vibrio-Aeromonas and Cytophaga-Flavobacteria complexes. The bacteria lyse epidermal cells and chloroplasts, turning the seaweed tissue white. The disease is known from seaweeds including Kappaphycus alvarezii and Eucheuma denticulatum, economically important sources of carrageenan. In countries where seaweed is harvested as a crop, ice-ice can wreak havoc on yields. Zamboanga, Philippines, had an outbreak of ice-ice in 2004, and Bali, Indonesia, experienced an outbreak in 2009. A rise in surface sea temperatures of 2–3 degrees Celsius can trigger ice-ice outbreaks.

<span class="mw-page-title-main">Seaweed farming</span> Farming of aquatic seaweed

Seaweed farming or kelp farming is the practice of cultivating and harvesting seaweed. In its simplest form farmers gather from natural beds, while at the other extreme farmers fully control the crop's life cycle.

<i>Kappaphycus</i> Genus of algae

Kappaphycus is a genus of red algae. Species are distributed in the waters of East Africa, Indonesia, Malaysia, Hainan Island, the Philippines, and Micronesia.

<i>Hildenbrandia</i> Genus of algae

Hildenbrandia is a genus of thalloid red alga comprising about 26 species. The slow-growing, non-mineralized thalli take a crustose form. Hildenbrandia reproduces by means of conceptacles and produces tetraspores.

<span class="mw-page-title-main">Aquaculture of giant kelp</span> Cultivation of seaweed

Aquaculture of giant kelp, Macrocystis pyrifera, is the cultivation of kelp for uses such as food, dietary supplements or potash. Giant kelp contains iodine, potassium, other minerals vitamins and carbohydrates.

<i>Hypnea</i> Genus of algae

Hypnea is a genus of red algae, and a well known carrageenophyte.

<span class="mw-page-title-main">Gelidiellaceae</span> Family of algae

The Gelidiellaceae is a small family of red algae containing 5 genera of agarophytes.

<span class="mw-page-title-main">Pterocladiaceae</span> Family of algae

The Pterocladiaceae is a small family of red algae containing 2 genera of agarophytes.

<span class="mw-page-title-main">Gracilariaceae</span> Family of algae

The Gracilariaceae is a small family of red algae containing several genera of agarophytes. It has a world-wide distribution. 24 species are found in China, and 6 species are found in Great Britain and Ireland. It is found in Australia and Chile.

Kathleen "Kay" Margaret Cole was a Canadian phycologist, known as one of the world's leading experts in the cytology of marine algae. In 1998 the Canadian Botanical Society awarded her the George Lawson Medal for lifetime achievement.

References

  1. JAMAS, MAYRA; IHA, CINTIA; C. OLIVEIRA, MARIANA; M. P. B. GUIMARÃES, SILVIA; T. FUJII, MUTUE (2017-07-25). "Morphological and molecular studies on Gelidiaceae and Gelidiellaceae (Gelidiales, Rhodophyta) from Brazil with description of the new species Gelidium calidum". Phytotaxa. 314 (2): 195. doi:10.11646/phytotaxa.314.2.2. ISSN   1179-3163.
  2. 1 2 3 4 5 Boo, Ga Hun; Kim, Kyeong Mi; Nelson, Wendy A.; Riosmena-Rodríguez, Rafael; Yoon, Kyung Ju; Boo, Sung Min (April 2014). "Taxonomy and distribution of selected species of the agarophyte genus Gelidium (Gelidiales, Rhodophyta)". Journal of Applied Phycology. 26 (2): 1243–1251. doi:10.1007/s10811-013-0111-7. ISSN   0921-8971. S2CID   14936519.
  3. 1 2 Freshwater, D. Wilson; Rueness, J. (1994-05-01). "Phylogenetic relationships of some European Gelidium (Gelidiales, Rhodophyta) species, based on rbcL nucleotide sequence analysis". Phycologia. 33 (3): 187–194. doi:10.2216/i0031-8884-33-3-187.1. ISSN   0031-8884.
  4. Tronchin, E. M.; Freshwater, D. W.; Bolton, J. J.; Anderson, R. J. (2002). "A Reassessment and Reclassification of Species in the Genera Onikusa Akatsuka and Suhria J. Agardh ex Endlicher (Gelidiales, Rhodophyta) Based on Molecular and Morphological Data". Botanica Marina. 45 (6): 548–558. doi:10.1515/BOT.2002.058. S2CID   84425094.
  5. 1 2 3 Santelices, B. (1991). Juanes, J. A.; Santelices, B.; McLachlan, J. L. (eds.). "Production ecology of Gelidium". International Workshop on Gelidium. Developments in Hydrobiology. Dordrecht: Springer Netherlands: 31–44. doi:10.1007/978-94-011-3610-5_3. ISBN   978-94-011-3610-5.
  6. Kim, Kyeong-Mi; Boo, Sung-Min (2012). "Phylogenetic relationships and distribution of Gelidium crinale and G. pusillum (Gelidiales, Rhodophyta) using cox1 and rbcL sequences". Algae. 27 (2): 83–94. doi: 10.4490/algae.2012.27.2.083 . ISSN   1226-2617. S2CID   83652614.
  7. Millar, Alan J. K.; Freshwater, D. Wilson (2005-06-30). "Morphology and molecular phylogeny of the marine algal order Gelidiales (Rhodophyta) from New South Wales, including Lord Howe and Norfolk Islands". Australian Systematic Botany. 18 (3): 215–263. doi:10.1071/SB04041. ISSN   1446-5701.
  8. 1 2 Melo, Ricardo A.; Neushul, Michael (1993). Chapman, A. R. O.; Brown, M. T.; Lahaye, M. (eds.). "Life history and reproductive potential of the agarophyte Gelidium robustum in California". Fourteenth International Seaweed Symposium. Developments in Hydrobiology. Dordrecht: Springer Netherlands: 223–229. doi:10.1007/978-94-011-1998-6_27. ISBN   978-94-011-1998-6.
  9. Santelices, Bernabe; G, Bernabé Santelices (1988). Synopsis of Biological Data on the Seaweed Genera Gelidium and Pterocladia (Rhodophyta). Food & Agriculture Org. ISBN   978-92-5-102717-2.
  10. Correa, J.; Avila, M.; Santelices, B. (1985-03-01). "Effects of some environmental factors on growth of sporelings in two species of Gelidium (Rhodophyta)". Aquaculture. 44 (3): 221–227. doi:10.1016/0044-8486(85)90246-7. ISSN   0044-8486.
  11. 1 2 Melo, Ricardo A. (1998-06-01). "Gelidium commercial exploitation: natural resources and cultivation". Journal of Applied Phycology. 10 (3): 303–314. doi:10.1023/A:1008070419158. ISSN   1573-5176. S2CID   32635073.
  12. Fei, X. G.; Huang, L. J. (1991). Juanes, J. A.; Santelices, B.; McLachlan, J. L. (eds.). "Artificial sporeling and field cultivation of Gelidium in China". International Workshop on Gelidium. Developments in Hydrobiology. Dordrecht: Springer Netherlands: 119–124. doi:10.1007/978-94-011-3610-5_11. ISBN   978-94-011-3610-5.
  13. Camba, Juan Antonio Seoane (1997). ""Gelidium sesquipedale" (clem) thuret cultivation in Galicia (Spain)". Lagascalia. 19 (1): 179–186. ISSN   0210-7708.
  14. Salinas, J. M. (1991). Juanes, J. A.; Santelices, B.; McLachlan, J. L. (eds.). "Spray system for re-attachment of Gelidium sesquipedale (Clem.) Born. et Thur. (Gelidiales: Rhodophyta)". International Workshop on Gelidium. Developments in Hydrobiology. Dordrecht: Springer Netherlands: 107–117. doi:10.1007/978-94-011-3610-5_10. ISBN   978-94-011-3610-5.
  15. Boulus, Areen; Spaneir, Ehud; Friedlander, Michael (2007-03-03). "Effect of outdoor conditions on growth rate and chemical composition of Gelidium crinale in culture". Journal of Applied Phycology. 19 (5): 471. doi:10.1007/s10811-007-9158-7. ISSN   1573-5176. S2CID   43030778.
  16. Gal-Or, Sharon; Israel, Alvaro (2004-06-01). "Growth responses ofPterocladiella capillacea(Rhodophyta) in laboratory and outdoor cultivation". Journal of Applied Phycology. 16 (3): 195–202. doi:10.1023/B:JAPH.0000048505.13667.bf. ISSN   1573-5176. S2CID   38064200.
  17. Fujita, D.; Ishikawa, T.; Kodama, S.; Kato, Y.; Notoya, M. (2006-10-01). "Distribution and Recent Reduction of Gelidium Beds in Toyama Bay, Japan". Journal of Applied Phycology. 18 (3): 591–598. doi:10.1007/s10811-006-9060-8. ISSN   1573-5176. S2CID   9864922.
  18. 1 2 3 Buschmann, Alejandro H.; Camus, Carolina; Infante, Javier; Neori, Amir; Israel, Álvaro; Hernández-González, María C.; Pereda, Sandra V.; Gomez-Pinchetti, Juan Luis; Golberg, Alexander; Tadmor-Shalev, Niva; Critchley, Alan T. (2017-10-02). "Seaweed production: overview of the global state of exploitation, farming and emerging research activity". European Journal of Phycology. 52 (4): 391–406. doi:10.1080/09670262.2017.1365175. ISSN   0967-0262. S2CID   53640917.
  19. Friedlander, Michael (2009), Borowitzka, Michael A.; Critchley, Alan T.; Kraan, Stefan; Peters, Akira (eds.), "Advances in cultivation of Gelidiales", Nineteenth International Seaweed Symposium: Proceedings of the 19th International Seaweed Symposium, held in Kobe, Japan, 26–31 March 2007., Developments in Applied Phycology, Dordrecht: Springer Netherlands, vol. 2, pp. 1–6, doi:10.1007/978-1-4020-9619-8_1, ISBN   978-1-4020-9619-8 , retrieved 2022-01-24
  20. 1 2 Mouradi-Givernaud, Aziza; Amina Hassani, Lalla; Givernaud, Thierry; Lemoine, Yves; Benharbet, Oumaima (1999-04-01). "Biology and agar composition of Gelidium sesquipedale harvested along the Atlantic coast of Morocco". Hydrobiologia. 398: 391–395. doi:10.1023/A:1017094231494. ISSN   1573-5117. S2CID   23800143.
  21. Santos, Rui; Duarte, Pedro (1991-03-01). "Marine plant harvest in Portugal". Journal of Applied Phycology. 3 (1): 11. doi:10.1007/BF00003915. ISSN   1573-5176. S2CID   1682347.
  22. Troell, M.; Robertson-Andersson, D.; Anderson, R. J.; Bolton, J. J.; Maneveldt, G.; Halling, C.; Probyn, T. (2006-06-30). "Abalone farming in South Africa: An overview with perspectives on kelp resources, abalone feed, potential for on-farm seaweed production and socio-economic importance". Aquaculture. 257 (1): 266–281. doi:10.1016/j.aquaculture.2006.02.066. hdl: 10566/1005 . ISSN   0044-8486.
  23. Giaimo, Cara. "The Forgotten Victorian Craze for Collecting Seaweed". Atlas Obscura. Retrieved 27 October 2020.
  24. Trethewey, Laura. "What Victorian-era seaweed pressings reveal about our changing seas". The Guardian. Retrieved 27 October 2020.
  25. 1 2 3 Miller, Emily A; Lisin, Susan E; Smith, Celia M; Van Houtan, Kyle S (2020). "Herbaria macroalgae as a proxy for historical upwelling trends in Central California". Proceedings of the Royal Society B. 287 (1929): 20200732. doi: 10.1098/rspb.2020.0732 . PMC   7329038 . PMID   32546101.
  26. Ware, D M; Thompson, R E (1991). "Link between longterm variability in upwelling and fish production in the northeast Pacific Ocean". Can. J. Fish. Aquat. Sci. 48 (12): 2296–2306. doi:10.1139/f91-270 . Retrieved 27 October 2020.