Characteristics of the digestive vacuole membrane of the alga-bearing ciliate Paramecium bursaria.
Kodama, Yuuki; Fujishima, Masahiro
2012-07-01
Cells of the ciliate Paramecium bursaria harbor symbiotic Chlorella spp. in their cytoplasm. To establish endosymbiosis with alga-free P. bursaria, symbiotic algae must leave the digestive vacuole (DV) to appear in the cytoplasm by budding of the DV membrane. This budding was induced not only by intact algae but also by boiled or fixed algae. However, this budding was not induced when food bacteria or India ink were ingested into the DVs. These results raise the possibility that P. bursaria can recognize sizes of the contents in the DVs. To elucidate this possibility, microbeads with various diameters were mixed with alga-free P. bursaria and traced their fate. Microbeads with 0.20μm diameter did not induce budding of the DVs. Microbeads with 0.80μm diameter produced DVs of 5-10μm diameter at 3min after mixing; then the DVs fragmented and became vacuoles of 2-5μm diameter until 3h after mixing. Each microbead with a diameter larger than 3.00μm induced budding similarly to symbiotic Chlorella. These observations reveal that induction of DV budding depends on the size of the contents in the DVs. Dynasore, a dynamin inhibitor, greatly inhibited DV budding, suggesting that dynamin might be involved in DV budding. Copyright © 2011 Elsevier GmbH. All rights reserved.
Analysis of laser fluorosensor systems for remote algae detection and quantification
NASA Technical Reports Server (NTRS)
Browell, E. V.
1977-01-01
The development and performance of single- and multiple-wavelength laser fluorosensor systems for use in the remote detection and quantification of algae are discussed. The appropriate equation for the fluorescence power received by a laser fluorosensor system is derived in detail. Experimental development of a single wavelength system and a four wavelength system, which selectively excites the algae contained in the four primary algal color groups, is reviewed, and test results are presented. A comprehensive error analysis is reported which evaluates the uncertainty in the remote determination of the chlorophyll a concentration contained in algae by single- and multiple-wavelength laser fluorosensor systems. Results of the error analysis indicate that the remote quantification of chlorophyll a by a laser fluorosensor system requires optimum excitation wavelength(s), remote measurement of marine attenuation coefficients, and supplemental instrumentation to reduce uncertainties in the algal fluorescence cross sections.
Antiviral Potential of Algae Polysaccharides Isolated from Marine Sources: A Review.
Ahmadi, Azin; Zorofchian Moghadamtousi, Soheil; Abubakar, Sazaly; Zandi, Keivan
2015-01-01
From food to fertilizer, algal derived products are largely employed in assorted industries, including agricultural, biomedical, food, and pharmaceutical industries. Among different chemical compositions isolated from algae, polysaccharides are the most well-established compounds, which were subjected to a variety of studies due to extensive bioactivities. Over the past few decades, the promising results for antiviral potential of algae-derived polysaccharides have advocated them as inordinate candidates for pharmaceutical research. Numerous studies have isolated various algal polysaccharides possessing antiviral activities, including carrageenan, alginate, fucan, laminaran, and naviculan. In addition, different mechanisms of action have been reported for these polysaccharides, such as inhibiting the binding or internalization of virus into the host cells or suppressing DNA replication and protein synthesis. This review strives for compiling previous antiviral studies of algae-derived polysaccharides and their mechanism of action towards their development as natural antiviral agents for future investigations.
Edmundson, Scott J.; Huesemann, Michael H.
2015-10-28
Night biomass loss in photosynthetic algae is an essential parameter that is often overlooked when modeling or optimizing biomass productivities. Night respiration acts as a tax on daily biomass gains and has not been well characterized in the context of biofuel production. We examined the night biomass loss in three algae strains that may have potential for commercial biomass production ( Nannochloropsis salina-CCMP1776, Chlorella sorokiniana-DOE1412, and Picochlorum sp. LANL-WT). Biomass losses were monitored by ash free dry weight (AFDW mg/L -1) and optical density (OD 750) on a thermal-gradient incubator. Night biomass loss rates were highly variable (ranging from -0.006more» to -0.59 day -1), species-specific, and dependent on both culture growth phase prior to the dark period and night pond temperature. In general, the fraction of biomass lost over a 10 hour dark period, which ranged from ca. 1 to 22% in our experiments, was positively correlated with temperature and declined as the culture transitioned from exponential to linear to stationary phase. Furthermore, the dynamics of biomass loss should be taken into consideration in algae strain selection, are critical in predictive modeling of biomass production based on geographic location and can influence the net productivity of photosynthetic cultures used for bio-based fuels or products.«less
DOE Office of Scientific and Technical Information (OSTI.GOV)
Edmundson, Scott J.; Huesemann, Michael H.
Night biomass loss in photosynthetic algae is an essential parameter that is often overlooked when modeling or optimizing biomass productivities. Night respiration acts as a tax on daily biomass gains and has not been well characterized in the context of biofuel production. We examined the night biomass loss in three algae strains that may have potential for commercial biomass production ( Nannochloropsis salina-CCMP1776, Chlorella sorokiniana-DOE1412, and Picochlorum sp. LANL-WT). Biomass losses were monitored by ash free dry weight (AFDW mg/L -1) and optical density (OD 750) on a thermal-gradient incubator. Night biomass loss rates were highly variable (ranging from -0.006more» to -0.59 day -1), species-specific, and dependent on both culture growth phase prior to the dark period and night pond temperature. In general, the fraction of biomass lost over a 10 hour dark period, which ranged from ca. 1 to 22% in our experiments, was positively correlated with temperature and declined as the culture transitioned from exponential to linear to stationary phase. Furthermore, the dynamics of biomass loss should be taken into consideration in algae strain selection, are critical in predictive modeling of biomass production based on geographic location and can influence the net productivity of photosynthetic cultures used for bio-based fuels or products.«less
NASA Astrophysics Data System (ADS)
Novaczek, I.; Lubbers, G. W.; Breeman, A. M.
1990-09-01
Three species of Arctic to cold-temperate amphi-Atlantic algae, all occurring also in the North Pacific, were tested for growth and/or survival at temperatures of -20 to 30°C. When isolates from both western and eastern Atlantic shores were tested side-by-side, it was found that thermal ecotypes may occur in such Arctic algae. Chaetomorpha melagonium was the most eurythermal of the 3 species. Isolates of this alga were alike in temperature tolerance and growth rate but Icelandic plants were more sensitive to the lethal temperature of 25°C than were more southerly isolates from both east and west. With regard to Devaleraea ramentacea, one Canadian isolate grew extraordinarily well at -2 and 0°C, and all tolerated temperatures 2 3°C higher than the lethal limit (18 20°C) of isolates from Europe. Concerning Phycodrys rubens, both eastern and western isolates died at 20°C but European plants tolerated the lethal high temperature longer, were more sensitive to freezing, and attained more rapid growth at optimal temperatures. The intertidal species, C. melagonium and D. ramentacea, both survived freezing at -5 and -20°C, at least for short time periods. C. melagonium was more susceptible than D. ramentacea to desiccation. Patterns of thermal tolerance may provide insight into the evolutionary history of seaweed species.
Patoine, Guillaume; Thakur, Madhav P; Friese, Julia; Nock, Charles; Hönig, Lydia; Haase, Josephine; Scherer-Lorenzen, Michael; Eisenhauer, Nico
2017-11-01
A better understanding of the mechanisms driving litter diversity effects on decomposition is needed to predict how biodiversity losses affect this crucial ecosystem process. In a microcosm study, we investigated the effects of litter functional diversity and two major groups of soil macro-detritivores on the mass loss of tree leaf litter mixtures. Furthermore, we tested the effects of litter trait community means and dissimilarity on litter mass loss for seven traits relevant to decomposition. We expected macro-detritivore effects on litter mass loss to be most pronounced in litter mixtures of high functional diversity. We used 24 leaf mixtures differing in functional diversity, which were composed of litter from four species from a pool of 16 common European tree species. Earthworms, isopods, or a combination of both were added to each litter combination for two months. Litter mass loss was significantly higher in the presence of earthworms than in that of isopods, whereas no synergistic effects of macro-detritivore mixtures were found. The effect of functional diversity of the litter material was highest in the presence of both macro-detritivore groups, supporting the notion that litter diversity effects are most pronounced in the presence of different detritivore species. Species-specific litter mass loss was explained by nutrient content, secondary compound concentration, and structural components. Moreover, dissimilarity in N concentrations increased litter mass loss, probably because detritivores having access to nutritionally diverse food sources. Furthermore, strong competition between the two macro-detritivores for soil surface litter resulted in a decrease of survival of both macro-detritivores. These results show that the effects of litter functional diversity on decomposition are contingent upon the macro-detritivore community and composition. We conclude that the temporal dynamics of litter trait diversity effects and their interaction with
Patoine, Guillaume; Thakur, Madhav P.; Friese, Julia; Nock, Charles; Hönig, Lydia; Haase, Josephine; Scherer-Lorenzen, Michael; Eisenhauer, Nico
2017-01-01
A better understanding of the mechanisms driving litter diversity effects on decomposition is needed to predict how biodiversity losses affect this crucial ecosystem process. In a microcosm study, we investigated the effects of litter functional diversity and two major groups of soil macro-detritivores on the mass loss of tree leaf litter mixtures. Furthermore, we tested the effects of litter trait community means and dissimilarity on litter mass loss for seven traits relevant to decomposition. We expected macro-detritivore effects on litter mass loss to be most pronounced in litter mixtures of high functional diversity. We used 24 leaf mixtures differing in functional diversity, which were composed of litter from four species from a pool of 16 common European tree species. Earthworms, isopods, or a combination of both were added to each litter combination for two months. Litter mass loss was significantly higher in the presence of earthworms than in that of isopods, whereas no synergistic effects of macro-detritivore mixtures were found. The effect of functional diversity of the litter material was highest in the presence of both macro-detritivore groups, supporting the notion that litter diversity effects are most pronounced in the presence of different detritivore species. Species-specific litter mass loss was explained by nutrient content, secondary compound concentration, and structural components. Moreover, dissimilarity in N concentrations increased litter mass loss, probably because detritivores having access to nutritionally diverse food sources. Furthermore, strong competition between the two macro-detritivores for soil surface litter resulted in a decrease of survival of both macro-detritivores. These results show that the effects of litter functional diversity on decomposition are contingent upon the macro-detritivore community and composition. We conclude that the temporal dynamics of litter trait diversity effects and their interaction with
The MACRO detector at Gran Sasso
NASA Astrophysics Data System (ADS)
Ambrosio, M.; Antolini, R.; Assiro, R.; Auriemma, G.; Bakari, D.; Baldini, A.; Barbarino, G. C.; Barbarito, E.; Barish, B. C.; Battistoni, G.; Becherini, Y.; Bellotti, R.; Bemporad, C.; Bernardini, P.; Bilokon, H.; Bisi, V.; Bloise, C.; Bottazzi, E.; Bower, C.; Brigida, M.; Bussino, S.; Cafagna, F.; Calicchio, M.; Campana, D.; Candela, A.; Carboni, M.; Cecchini, S.; Cei, F.; Ceres, A.; Chiarella, V.; Choudhary, B. C.; Coutu, S.; Cozzi, M.; Creti, P.; de Cataldo, G.; Esposti, L. Degli; Dekhissi, H.; de Marzo, C.; de Mitri, I.; Derkaoui, J.; de Vincenzi, M.; di Credico, A.; di Ferdinando, D.; Diotallevi, R.; Erriquez, O.; Favuzzi, C.; Forti, C.; Fusco, P.; Gebhard, M.; Giacomelli, G.; Giacomelli, R.; Giannini, G.; Giglietto, N.; Giorgini, M.; Giuliani, R.; Goretti, M.; Grassi, M.; Grau, H.; Gray, L.; Grillo, A.; Guarino, F.; Gustavino, C.; Habig, A.; Hanson, J.; Hanson, K.; Hawthorne, A.; Heinz, R.; Hong, J. T.; Iarocci, E.; Katsavounidis, E.; Katsavounidis, I.; Kearns, E.; Kim, H.; Kyriazopoulou, S.; Lamanna, E.; Lane, C.; Leone, A.; Levin, D. S.; Lipari, P.; Liu, G.; Liu, R.; Longley, N. P.; Longo, M. J.; Loparco, F.; Maaroufi, F.; Mancarella, G.; Mandrioli, G.; Manzoor, S.; Marrelli, V.; Margiotta, A.; Marini, A.; Martello, D.; Marzari-Chiesa, A.; Mazziotta, M. N.; Michael, D. G.; Mikheyev, S.; Miller, L.; Monacelli, P.; Mongelli, M.; Montaruli, T.; Monteno, M.; Mossbarger, L.; Mufson, S.; Musser, J.; Nicolò, D.; Nolty, R.; Okada, C.; Orsini, M.; Orth, C.; Osteria, G.; Ouchrif, M.; Palamara, O.; Parlati, S.; Patera, V.; Patrizii, L.; Pazzi, R.; Peck, C. W.; Pellizzoni, G.; Perchiazzi, M.; Perrone, L.; Petrakis, J.; Petrera, S.; Pignatano, N.; Pinto, C.; Pistilli, P.; Popa, V.; Rainò, A.; Reynoldson, J.; Ronga, F.; Rrhioua, A.; Sacchetti, A.; Saggese, P.; Satriano, C.; Satta, L.; Scapparone, E.; Scholberg, K.; Sciubba, A.; Serra, P.; Sioli, M.; Sirri, G.; Sitta, M.; Sondergaard, S.; Spinelli, P.; Spinetti, M.; Spurio, M.; Stalio, S.; Steinberg, R.; Stone, J. L.; Sulak, L. R.; Surdo, A.; Tarlè, G.; Togo, V.; Vakili, M.; Valieri, C.; Walter, C. W.; Webb, R.; Zaccheo, N.; MACRO Collaboration
2002-07-01
MACRO was an experiment that ran in the Laboratori Nazionali del Gran Sasso from 1988 to 2000. Its principal goal was to observe magnetic monopoles or set significantly lower experimental flux limits than had been previously available in the velocity range from about β=10 -4 to unity. In addition it made a variety of other observations. Examples are: setting flux limits on other so far unobserved particles such as nuclearites and lightly ionizing particles, searching for WIMP annihilations in the Earth and the Sun and for neutrino bursts from stellar collapses in or near our Galaxy, and making measurements relevant to high energy muon and neutrino astronomy and of the flux of up-going muons as a function of nadir angle showing evidence for neutrino oscillations. The apparatus consisted of three principal types of detectors: liquid scintillator counters, limited streamer tubes, and nuclear track etch detectors. In addition, over part of its area it contained a transition radiation detector. The general design philosophy emphasized redundancy and complementarity. This paper describes the technical aspects of the complete MACRO detector, its operational performance, and the techniques used to calibrate it and verify its proper operation. It supplements a previously published paper which described the first portion of the detector that was built and operated.
The MACRO detector at Gran Sasso
NASA Astrophysics Data System (ADS)
MACRO Collaboration; Ambrosio, M.; Antolini, R.; Assiro, R.; Auriemma, G.; Bakari, D.; Baldini, A.; Barbarino, G. C.; Barbarito, E.; Barish, B. C.; Battistoni, G.; Becherini, Y.; Bellotti, R.; Bemporad, C.; Bernardini, P.; Bilokon, H.; Bisi, V.; Bloise, C.; Bottazzi, E.; Bower, C.; Brigida, M.; Bussino, S.; Cafagna, F.; Calicchio, M.; Campana, D.; Candela, A.; Carboni, M.; Cecchini, S.; Cei, F.; Ceres, A.; Chiarella, V.; Choudhary, B. C.; Coutu, S.; Cozzi, M.; Creti, P.; de Cataldo, G.; degli Esposti, L.; Dekhissi, H.; de Marzo, C.; de Mitri, I.; Derkaoui, J.; de Vincenzi, M.; di Credico, A.; di Ferdinando, D.; Diotallevi, R.; Erriquez, O.; Favuzzi, C.; Forti, C.; Fusco, P.; Gebhard, M.; Giacomelli, G.; Giacomelli, R.; Giannini, G.; Giglietto, N.; Giorgini, M.; Giuliani, R.; Goretti, M.; Grassi, M.; Grau, H.; Gray, L.; Grillo, A.; Guarino, F.; Gustavino, C.; Habig, A.; Hanson, J.; Hanson, K.; Hawthorne, A.; Heinz, R.; Hong, J. T.; Iarocci, E.; Katsavounidis, E.; Katsavounidis, I.; Kearns, E.; Kim, H.; Kyriazopoulou, S.; Lamanna, E.; Lane, C.; Leone, A.; Levin, D. S.; Lipari, P.; Liu, G.; Liu, R.; Longley, N. P.; Longo, M. J.; Loparco, F.; Maaroufi, F.; Mancarella, G.; Mandrioli, G.; Manzoor, S.; Marrelli, V.; Margiotta, A.; Marini, A.; Martello, D.; Marzari-Chiesa, A.; Mazziotta, M. N.; Michael, D. G.; Mikheyev, S.; Miller, L.; Monacelli, P.; Mongelli, M.; Montaruli, T.; Monteno, M.; Mossbarger, L.; Mufson, S.; Musser, J.; Nicolò, D.; Nolty, R.; Okada, C.; Orsini, M.; Orth, C.; Osteria, G.; Ouchrif, M.; Palamara, O.; Parlati, S.; Patera, V.; Patrizii, L.; Pazzi, R.; Peck, C. W.; Pellizzoni, G.; Perchiazzi, M.; Perrone, L.; Petrakis, J.; Petrera, S.; Pignatano, N.; Pinto, C.; Pistilli, P.; Popa, V.; Rainò, A.; Reynoldson, J.; Ronga, F.; Rrhioua, A.; Sacchetti, A.; Saggese, P.; Satriano, C.; Satta, L.; Scapparone, E.; Scholberg, K.; Sciubba, A.; Serra, P.; Sioli, M.; Sirri, G.; Sitta, M.; Sondergaard, S.; Spinelli, P.; Spinetti, M.; Spurio, M.; Stalio, S.; Steinberg, R.; Stone, J. L.; Sulak, L. R.; Surdo, A.; Tarlè, G.; Togo, V.; Vakili, M.; Valieri, C.; Walter, C. W.; Webb, R.; Zaccheo, N.
2002-07-01
MACRO was an experiment that ran in the Laboratori Nazionali del Gran Sasso from 1988 to 2000. Its principal goal was to observe magnetic monopoles or set significantly lower experimental flux limits than had been previously available in the velocity range from about β=10-4 to unity. In addition it made a variety of other observations. Examples are: setting flux limits on other so far unobserved particles such as nuclearites and lightly ionizing particles, searching for WIMP annihilations in the Earth and the Sun and for neutrino bursts from stellar collapses in or near our Galaxy, and making measurements relevant to high energy muon and neutrino astronomy and of the flux of up-going muons as a function of nadir angle showing evidence for neutrino oscillations. The apparatus consisted of three principal types of detectors: liquid scintillator counters, limited streamer tubes, and nuclear track etch detectors. In addition, over part of its area it contained a transition radiation detector. The general design philosophy emphasized redundancy and complementarity. This paper describes the technical aspects of the complete MACRO detector, its operational performance, and the techniques used to calibrate it and verify its proper operation. It supplements a previously published paper which described the first portion of the detector that was built and operated.
Developing New Alternative Energy in Virginia: Bio-Diesel from Algae
DOE Office of Scientific and Technical Information (OSTI.GOV)
Hatcher, Patrick
The overall objective of this study was to select chemical processing equipment, install and operate that equipment to directly convert algae to biodiesel via a reaction patented by Old Dominion University (Pat. No. US 8,080,679B2). This reaction is a high temperature (250- 330{degrees}C) methylation reaction utilizing tetramethylammonium hydroxide (TMAH) to produce biodiesel. As originally envisioned, algal biomass could be treated with TMAH in methanol without the need to separately extract triacylglycerides (TAG). The reactor temperature allows volatilization and condensation of the methyl esters whereas the spent algae solids can be utilized as a high-value fertilizer because they are minimally charred.more» During the course of this work and immediately prior to commencing, we discovered that glycerol, a major by-product of the conventional transesterification reaction for biofuels, is not formed but rather three methoxylated glycerol derivatives are produced. These derivatives are high-value specialty green chemicals that strongly upgrade the economics of the process, rendering this approach as one that now values the biofuel only as a by-product, the main value products being the methoxylated glycerols. A horizontal agitated thin-film evaporator (one square foot heat transfer area) proved effective as the primary reactor facilitating the reaction and vaporization of the products, and subsequent discharge of the spent algae solids that are suitable for supplementing petrochemicalbased fertilizers for agriculture. Because of the size chosen for the reactor, we encountered problems with delivery of the algal feed to the reaction zone, but envision that this problem could easily disappear upon scale-up or can be replaced economically by incorporating an extraction process. The objective for production of biodiesel from algae in quantities that could be tested could not be met, but we implemented use of soybean oil as a surrogate TAG feed to overcome this
Molecular Analyzer for Complex Refractory Organic-Rich Surfaces (MACROS)
NASA Technical Reports Server (NTRS)
Getty, Stephanie A.; Cook, Jamie E.; Balvin, Manuel; Brinckerhoff, William B.; Li, Xiang; Grubisic, Andrej; Cornish, Timothy; Ferrance, Jerome; Southard, Adrian
2017-01-01
The Molecular Analyzer for Complex Refractory Organic-rich Surfaces, MACROS, is a novel instrument package being developed at NASA Goddard Space Flight Center. MACROS enables the in situ characterization of a sample's composition by coupling two powerful techniques into one compact instrument package: (1) laser desorption/ionization time-of-flight mass spectrometry (LDMS) for broad detection of inorganic mineral composition and non-volatile organics, and (2) liquid-phase extraction methods to gently isolate the soluble organic and inorganic fraction of a planetary powder for enrichment and detailed analysis by liquid chromatographic separation coupled to LDMS. The LDMS is capable of positive and negative ion detection, precision mass selection, and fragment analysis. Two modes are included for LDMS: single laser LDMS as the broad survey mode and two step laser mass spectrometry (L2MS). The liquid-phase extraction will be done in a newly designed extraction module (EM) prototype, providing selectivity in the analysis of a complex sample. For the sample collection, a diamond drill front end will be used to collect rock/icy powder. With all these components and capabilities together, MACROS offers a versatile analytical instrument for a mission targeting an icy moon, carbonaceous asteroid, or comet, to fully characterize the surface composition and advance our understanding of the chemical inventory present on that body.
Lipid metabolism and potentials of biofuel and high added-value oil production in red algae.
Sato, Naoki; Moriyama, Takashi; Mori, Natsumi; Toyoshima, Masakazu
2017-04-01
Biomass production is currently explored in microalgae, macroalgae and land plants. Microalgal biofuel development has been performed mostly in green algae. In the Japanese tradition, macrophytic red algae such as Pyropia yezoensis and Gelidium crinale have been utilized as food and industrial materials. Researches on the utilization of unicellular red microalgae such as Cyanidioschyzon merolae and Porphyridium purpureum started only quite recently. Red algae have relatively large plastid genomes harboring more than 200 protein-coding genes that support the biosynthetic capacity of the plastid. Engineering the plastid genome is a unique potential of red microalgae. In addition, large-scale growth facilities of P. purpureum have been developed for industrial production of biofuels. C. merolae has been studied as a model alga for cell and molecular biological analyses with its completely determined genomes and transformation techniques. Its acidic and warm habitat makes it easy to grow this alga axenically in large scales. Its potential as a biofuel producer is recently documented under nitrogen-limited conditions. Metabolic pathways of the accumulation of starch and triacylglycerol and the enzymes involved therein are being elucidated. Engineering these regulatory mechanisms will open a possibility of exploiting the full capability of production of biofuel and high added-value oil. In the present review, we will describe the characteristics and potential of these algae as biotechnological seeds.
Numerical prediction of algae cell mixing feature in raceway ponds using particle tracing methods.
Ali, Haider; Cheema, Taqi A; Yoon, Ho-Sung; Do, Younghae; Park, Cheol W
2015-02-01
In the present study, a novel technique, which involves numerical computation of the mixing length of algae particles in raceway ponds, was used to evaluate the mixing process. A value of mixing length that is higher than the maximum streamwise distance (MSD) of algae cells indicates that the cells experienced an adequate turbulent mixing in the pond. A coupling methodology was adapted to map the pulsating effects of a 2D paddle wheel on a 3D raceway pond in this study. The turbulent mixing was examined based on the computations of mixing length, residence time, and algae cell distribution in the pond. The results revealed that the use of particle tracing methodology is an improved approach to define the mixing phenomenon more effectively. Moreover, the algae cell distribution aided in identifying the degree of mixing in terms of mixing length and residence time. © 2014 Wiley Periodicals, Inc.
Brawley, Susan H.; Blouin, Nicolas A.; Ficko-Blean, Elizabeth; Wheeler, Glen L.; Lohr, Martin; Goodson, Holly V.; Jenkins, Jerry W.; Blaby-Haas, Crysten E.; Helliwell, Katherine E.; Chan, Cheong Xin; Marriage, Tara N.; Klein, Anita S.; Badis, Yacine; Brodie, Juliet; Cao, Yuanyu; Collén, Jonas; Dittami, Simon M.; Gachon, Claire M. M.; Green, Beverley R.; Karpowicz, Steven J.; Kim, Jay W.; Kudahl, Ulrich Johan; Lin, Senjie; Michel, Gurvan; Mittag, Maria; Olson, Bradley J. S. C.; Pangilinan, Jasmyn L.; Peng, Yi; Qiu, Huan; Shu, Shengqiang; Singer, John T.; Sprecher, Brittany N.; Wagner, Volker; Wang, Wenfei; Wang, Zhi-Yong; Yan, Juying; Yarish, Charles; Zäuner-Riek, Simone; Zhuang, Yunyun; Zou, Yong; Lindquist, Erika A.; Grimwood, Jane; Barry, Kerrie W.; Rokhsar, Daniel S.; Schmutz, Jeremy; Stiller, John W.; Grossman, Arthur R.; Prochnik, Simon E.
2017-01-01
Porphyra umbilicalis (laver) belongs to an ancient group of red algae (Bangiophyceae), is harvested for human food, and thrives in the harsh conditions of the upper intertidal zone. Here we present the 87.7-Mbp haploid Porphyra genome (65.8% G + C content, 13,125 gene loci) and elucidate traits that inform our understanding of the biology of red algae as one of the few multicellular eukaryotic lineages. Novel features of the Porphyra genome shared by other red algae relate to the cytoskeleton, calcium signaling, the cell cycle, and stress-tolerance mechanisms including photoprotection. Cytoskeletal motor proteins in Porphyra are restricted to a small set of kinesins that appear to be the only universal cytoskeletal motors within the red algae. Dynein motors are absent, and most red algae, including Porphyra, lack myosin. This surprisingly minimal cytoskeleton offers a potential explanation for why red algal cells and multicellular structures are more limited in size than in most multicellular lineages. Additional discoveries further relating to the stress tolerance of bangiophytes include ancestral enzymes for sulfation of the hydrophilic galactan-rich cell wall, evidence for mannan synthesis that originated before the divergence of green and red algae, and a high capacity for nutrient uptake. Our analyses provide a comprehensive understanding of the red algae, which are both commercially important and have played a major role in the evolution of other algal groups through secondary endosymbioses. PMID:28716924
Brawley, Susan H; Blouin, Nicolas A; Ficko-Blean, Elizabeth; Wheeler, Glen L; Lohr, Martin; Goodson, Holly V; Jenkins, Jerry W; Blaby-Haas, Crysten E; Helliwell, Katherine E; Chan, Cheong Xin; Marriage, Tara N; Bhattacharya, Debashish; Klein, Anita S; Badis, Yacine; Brodie, Juliet; Cao, Yuanyu; Collén, Jonas; Dittami, Simon M; Gachon, Claire M M; Green, Beverley R; Karpowicz, Steven J; Kim, Jay W; Kudahl, Ulrich Johan; Lin, Senjie; Michel, Gurvan; Mittag, Maria; Olson, Bradley J S C; Pangilinan, Jasmyn L; Peng, Yi; Qiu, Huan; Shu, Shengqiang; Singer, John T; Smith, Alison G; Sprecher, Brittany N; Wagner, Volker; Wang, Wenfei; Wang, Zhi-Yong; Yan, Juying; Yarish, Charles; Zäuner-Riek, Simone; Zhuang, Yunyun; Zou, Yong; Lindquist, Erika A; Grimwood, Jane; Barry, Kerrie W; Rokhsar, Daniel S; Schmutz, Jeremy; Stiller, John W; Grossman, Arthur R; Prochnik, Simon E
2017-08-01
Porphyra umbilicalis (laver) belongs to an ancient group of red algae (Bangiophyceae), is harvested for human food, and thrives in the harsh conditions of the upper intertidal zone. Here we present the 87.7-Mbp haploid Porphyra genome (65.8% G + C content, 13,125 gene loci) and elucidate traits that inform our understanding of the biology of red algae as one of the few multicellular eukaryotic lineages. Novel features of the Porphyra genome shared by other red algae relate to the cytoskeleton, calcium signaling, the cell cycle, and stress-tolerance mechanisms including photoprotection. Cytoskeletal motor proteins in Porphyra are restricted to a small set of kinesins that appear to be the only universal cytoskeletal motors within the red algae. Dynein motors are absent, and most red algae, including Porphyra , lack myosin. This surprisingly minimal cytoskeleton offers a potential explanation for why red algal cells and multicellular structures are more limited in size than in most multicellular lineages. Additional discoveries further relating to the stress tolerance of bangiophytes include ancestral enzymes for sulfation of the hydrophilic galactan-rich cell wall, evidence for mannan synthesis that originated before the divergence of green and red algae, and a high capacity for nutrient uptake. Our analyses provide a comprehensive understanding of the red algae, which are both commercially important and have played a major role in the evolution of other algal groups through secondary endosymbioses.
Brawley, Susan H.; Blouin, Nicolas A.; Ficko-Blean, Elizabeth; ...
2017-07-17
Porphyra umbilicalis (laver) belongs to an ancient group of red algae (Bangiophyceae), is harvested for human food, and thrives in the harsh conditions of the upper intertidal zone. Here we present the 87.7-Mbp haploid Porphyra genome (65.8% G + C content, 13,125 gene loci) and elucidate traits that inform our understanding of the biology of red algae as one of the few multicellular eukaryotic lineages. Novel features of the Porphyra genome shared by other red algae relate to the cytoskeleton, calcium signaling, the cell cycle, and stress-tolerance mechanisms including photoprotection. Cytoskeletal motor proteins in Porphyra are restricted to a smallmore» set of kinesins that appear to be the only universal cytoskeletal motors within the red algae. Dynein motors are absent, and most red algae, including Porphyra, lack myosin. This surprisingly minimal cytoskeleton offers a potential explanation for why red algal cells and multicellular structures are more limited in size than in most multicellular lineages. Additional discoveries further relating to the stress tolerance of bangiophytes include ancestral enzymes for sulfation of the hydrophilic galactan-rich cell wall, evidence for mannan synthesis that originated before the divergence of green and red algae, and a high capacity for nutrient uptake. Our analyses provide a comprehensive understanding of the red algae, which are both commercially important and have played a major role in the evolution of other algal groups through secondary endosymbioses.«less
DOE Office of Scientific and Technical Information (OSTI.GOV)
Brawley, Susan H.; Blouin, Nicolas A.; Ficko-Blean, Elizabeth
Porphyra umbilicalis (laver) belongs to an ancient group of red algae (Bangiophyceae), is harvested for human food, and thrives in the harsh conditions of the upper intertidal zone. Here we present the 87.7-Mbp haploid Porphyra genome (65.8% G + C content, 13,125 gene loci) and elucidate traits that inform our understanding of the biology of red algae as one of the few multicellular eukaryotic lineages. Novel features of the Porphyra genome shared by other red algae relate to the cytoskeleton, calcium signaling, the cell cycle, and stress-tolerance mechanisms including photoprotection. Cytoskeletal motor proteins in Porphyra are restricted to a smallmore» set of kinesins that appear to be the only universal cytoskeletal motors within the red algae. Dynein motors are absent, and most red algae, including Porphyra, lack myosin. This surprisingly minimal cytoskeleton offers a potential explanation for why red algal cells and multicellular structures are more limited in size than in most multicellular lineages. Additional discoveries further relating to the stress tolerance of bangiophytes include ancestral enzymes for sulfation of the hydrophilic galactan-rich cell wall, evidence for mannan synthesis that originated before the divergence of green and red algae, and a high capacity for nutrient uptake. Our analyses provide a comprehensive understanding of the red algae, which are both commercially important and have played a major role in the evolution of other algal groups through secondary endosymbioses.«less
The presence of algae mitigates the toxicity of copper-based algaecides to a nontarget organism.
Bishop, West M; Willis, Ben E; Richardson, Robert J; Cope, W Gregory
2018-05-07
Copper-based algaecides are routinely applied to target noxious algal blooms in freshwaters. Standard toxicity testing data with copper suggest that typical concentrations used to control algae can cause deleterious acute impacts to nontarget organisms. These "clean" water experiments lack algae, which are specifically targeted in field applications of algaecides and contain competing ligands. The present research measured the influence of algae on algaecide exposure and subsequent response of the nontarget species Daphnia magna to copper sulfate and an ethanolamine-chelated copper algaecide (Captain®). Significant shifts (p < 0.05) in D. magna 48-h median lethal concentration (LC50) values were found when algae were present in exposures along with a copper salt or a chelated copper formulation. Copper sulfate 48-h LC50 values shifted from 75.3 to 317.8 and 517.8 μg Cu/L, whereas Captain increased from 353.8 to 414.2 and 588.5 μg Cu/L in no algae, 5 × 10 5 , and 5 × 10 6 cells/mL algae treatments, respectively. Larger shifts were measured with copper sulfate exposures, although Captain was less toxic to D. magna in all corresponding treatments. Captain was more effective at controlling Scenedesmus dimorphus at most concentrations, and control was inversely proportional to toxicity to D. magna. Overall, incorporating target competing ligands (i.e., algae) into standard toxicity testing is important for accurate risk assessment, and copper formulation can significantly alter algaecidal efficacy and risks to nontarget organisms. Environ Toxicol Chem 2018;9999:1-11. © 2018 SETAC. © 2018 SETAC.
Diaz-Pulido, Guillermo; Anthony, Kenneth R N; Kline, David I; Dove, Sophie; Hoegh-Guldberg, Ove
2012-02-01
Coralline algae are among the most sensitive calcifying organisms to ocean acidification as a result of increased atmospheric carbon dioxide (pCO2 ). Little is known, however, about the combined impacts of increased pCO2 , ocean acidification, and sea surface temperature on tissue mortality and skeletal dissolution of coralline algae. To address this issue, we conducted factorial manipulative experiments of elevated CO2 and temperature and examined the consequences on tissue survival and skeletal dissolution of the crustose coralline alga (CCA) Porolithon (=Hydrolithon) onkodes (Heydr.) Foslie (Corallinaceae, Rhodophyta) on the southern Great Barrier Reef (GBR), Australia. We observed that warming amplified the negative effects of high pCO2 on the health of the algae: rates of advanced partial mortality of CCA increased from <1% to 9% under high CO2 (from 400 to 1,100 ppm) and exacerbated to 15% under warming conditions (from 26°C to 29°C). Furthermore, the effect of pCO2 on skeletal dissolution strongly depended on temperature. Dissolution of P. onkodes only occurred in the high-pCO2 treatment and was greater in the warm treatment. Enhanced skeletal dissolution was also associated with a significant increase in the abundance of endolithic algae. Our results demonstrate that P. onkodes is particularly sensitive to ocean acidification under warm conditions, suggesting that previous experiments focused on ocean acidification alone have underestimated the impact of future conditions on coralline algae. Given the central role that coralline algae play within coral reefs, these conclusions have serious ramifications for the integrity of coral-reef ecosystems. © 2011 Phycological Society of America.
FAQs
What part of the macro algae is responsible for photosynthesis? ›
Chloroplasts – the organelles responsible for photosynthesis in all higher plants and eukaryotic algae – evolved from Cyanobacteria via endosymbiosis.
What are the characteristics of macro algae? ›Unlike microalgae, they are multicellular class of algae and possess plant-like structural features that grow to large size (50 cm up to 60 m in length). They are typically comprised of a blade or lamina, the stipe, and holdfast for anchoring the entire structure to hard substrates in marine environments.
What are macroscopic algae called? ›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.
What is the difference between algae and macroalgae? ›Microalgae and macroalgae are the two major types of algae based on cellularity. Microalgae are unicellular algal species that may either live singly or in colonies. Macroalgae are multicellular algal species. They are commonly called seaweeds because they can grow profusely at any time.
What are some interesting facts about macroalgae? ›As a result of their photosynthetic activity, marine algae (macroalgae and phytoplankton) are considered to produce between 50% and 75% of the earths oxygen as well as taking up about 25% of the carbon dioxide.
What factors affect photosynthesis in algae? ›The growth and photosynthetic activity of algae are closely tied to the temperature, pH, salinity, and other environmental factors (Yun, Sangheon & Ikkyo, 2010; Fu, 2014).
What are the three main groups of macroalgae? ›Macroalgal species are divided among three large groups that are named according to the colour of their dominant photosynthetic and accessory pigments: red (Rhodophyta), green (Chlorophyta) and brown (Phaephyta). Red algae are the largest and most diverse group, and are extremely important reef-building organisms.
What are the three classification of macro algae? ›Macroalgae are classified into three major groups: brown algae (Phaeophyceae), green algae (Chlorophyta), and red algae (Rhodophyta). As all of the groups contain chlorophyll granules, their characteristic colors are derived from other pigments. Many of the brown algae are referred to simply as kelp.
Why macro algae are difficult to grow? ›Because macroalgae are photosynthetic creatures, they can only grow in the “photic” zone of coastal areas. A photic zone is where enough light enters to allow photosynthesis. To thrive, most macros need medium to intense light.
What does macroalgae need to survive? ›Most macroalgae require medium to strong lighting to thrive. The color of the macroalgae may vary with different light intensities. Some macroalgae can change the pH of the water due to their respiration, so you should regularly monitor your aquarium water quality.
What are the uses of macro algae? ›
Some macroalgae species may serve as bioindicators of the quality of water and some can do bioremediation by bioabsorption and bioaccumulation [4,5,6]. As other vegetables, seaweeds are primary producers, the base of the marine food chain, sustaining several benthic animal communities [7].
What is the most abundant type of macroscopic algae? ›The highest abundance of macroalgae species is Chaetomorpha crassa (26,91%) and the lowest one is Gigartina sp. (0,02%).
What type of algae is best? ›Green coloured algae are the most common type. These indicate good water quality. Green algae are considered as “good” algae but their growth should be kept under control so they won't deprive the fish of nutrients. Some aquarists let green algae thrive to serve as a dietary source for their fish.
What are 3 ways algae are different to plants? ›Algae differ from plants in several ways. They do not have stems or leaves, and their roots are different from plant roots. Algae also do not produce flowers or seeds, as plants do. Like plants, however, algae make their own food through a process called photosynthesis.
What is the difference between macro algae and microalgae? ›Macroalgae (seaweed) are multicellular, large-size algae, visible with the naked eye, while microalgae are microscopic single cells and may be prokaryotic, similar to cyanobacteria (Chloroxybacteria), or eukaryotic, similar to green algae (Chlorophyta).
What are the threats to macroalgae? ›Threats to Macroalgal Diversity: Marine Habitat Destruction and Fragmentation, Pollution and Introduced Species.
What affects the growth of macroalgae? ›The environmental conditions necessary for growing macroalgae vary among species. However, the key variables determining their growth are levels of sunlight, nutrients, salinity, and temperature.
What is the fastest growing macroalgae? ›Chaetomorpha is the most popular and fastest growing macroalgae. It is used to lower nitrates and phosphates, and also to house copepods and other micro fauna. It is most commonly used in refugium but may also be placed directly in the aquarium.
What factors increase algae growth? ›- Levels of nutrients such as phosphorus and nitrogen increase in water. ...
- Deep ocean water rises towards the surface and increases nutrient levels. ...
- Water temperature increases. ...
- Water flow is low and moves slowly, such as during a drought.
Phosphorus and nitrogen are essential to algae production, and these nutrients encourage the growth of algae in waterbodies. Phosphorus is the key nutrient limiting algal growth in the majority of BC lakes.
How much sunlight does algae need? ›
Under what conditions do algae grow best? Algae grow best when they receive 10 -15 hours of sunlight a day and the temperature stays between 60-80° F.
What is the easiest macro algae to grow? ›Chaeto (Chaetomorpha linum) algae is one of the easiest and fastest growing macroalga you can add to your aquarium, making it perfect for beginner aquarists. You can grow it out in your tank or in your sump as long as you offer proper lighting for growth.
What macroalgae is best for nutrient export? ›Caulerpa is a very common algae used in the saltwater aquariums. It is also called Grape algae, Razor algae, and Feather algae which come from its appearance. This algae is great for nutrient export and many fish in the reef aquarium will eat varies types of it.
What nutrients are in macroalgae? ›Although macroalgae are rich in nutritionally important minerals such as iodine, potassium, calcium, magnesium, phosphorus, iron, and zinc, little is known about their bioavailability.
What is the hardiest macro algae? ›Halimeda is one of the hardier and slower growing of the macroalgae. Chaetomorpha Algae, also known as Spaghetti Algae, is an excellent macroalgae for refugiums.
What are 4 common types of algae? ›The main groups of algae found in streams are the green algae (Chlorophyta), red algae (Rhodophyta), blue-green algae (Cyanobacteria) and diatoms (Bacillariophyta).
What are the 7 classification of algae? ›They are Chlorophyceae, Xanthophyceae, Chrysophyceae, Bacillariophyceae, Cryptophyceae, Dinophyceae, Chloromonodineae, Euglinineae, Phaeophyceae, Rhodophyceae and Myxophyceae (Cyanophyceae). The classification is published in his book titled “The Structure and Reproduction of Algae”.
What are 3 limiting factors for algae growth? ›Freshwater algal growth is often limited by the availability of nitrogen (N), phosphorus (P), or both nutrients [3, 4], but human activities are increasing N and P inputs to streams via sources such as wastewater treatment effluent, agricultural runoff, and atmospheric N deposition [5].
Does macro algae need flow? ›Macroalgae growth rates are highly dependent on water parameters, especially with the speed and direction of water flow. If the reef tank system has a lot of fish and high nitrates, the refugium should be stocked with macro that can handle a higher turnover rate.
Does macroalgae need light? ›Like all plants, macroalgae require some minimal amount of light to survive. Their actual rates of growth depend upon the intensity of light that is available to them.
What is the lifespan of a macroalgae? ›
Macroalgae are members of the huge grou aquatic plants know as algae (singular 'alg algae (the primary producers of the plane primitive photosynthetic plants that includ of ). The re e macroalgae have a limited lifespan as fre seaweed drift and they may only li several months.
What spectrum is best for macroalgae? ›Green macroalgae do especially well under full spectrum 6500K lighting because this is a full sunlight spectrum; but also green macroalgae in general will do well under reef spectrum lighting in the higher 10-12,000K range.
Why does my macroalgae keep dying? ›Possibly the number one reason your macroalgae is not growing is because of lack of nutrients. Macroalgae, and all algae, need nutrients to grow and live. Without nitrates and phosphates (which are nutrients in case you didn't know), macroalgae will stop growing and eventually die.
What are the 3 important uses of algae? ›What can you make from algae? Jet fuel, vegan eggs, food colouring and running shoes can all be made from algae. They're even being used on a space mission . We can blend algae with gasoline to make bio-fuel, and we can convert it into bio-diesel and bio jet-fuel.
What are 3 economic uses of algae? ›Algae are used extensively in industries to prepare some products like sugar, soap, cement, rubber blotting paper etc. Algae are used in agriculture to increase soil fertility. For example, Nostoc, Anabena. Some algae are used in the preparation of medicines.
Does macroalgae reduce ammonia? ›Macroalgae remove and consume ammonia and ammonium
This is essential for keeping your tank water clean and healthy.
One type of phytoplankton, Prochlorococcus, releases countless tons of oxygen into the atmosphere. It is so small that millions can fit in a drop of water. Prochlorococcus has achieved fame as perhaps the most abundant photosynthetic organism on the planet.
What is the most abundant algae in the world? ›Red algae are the most numerous of the three seaweed groups with around 5,000 – 5,500 species worldwide and about 1,300 of these occur in Australian waters. They are predominantly benthic and live in all of the world's oceans.
Which algae is most important? ›Red algae are considered as the most important source of many biologically active metabolites in comparison to other algal classes.
What is the most expensive algae? ›World Production of seaweed
The most valuable crop is the red alga Nori (Porphyra species, mainly P.
What is the healthiest algae? ›
Chlorella and spirulina are forms of algae that are highly nutritious and safe to eat for most people. They're associated with many health benefits, including lowered risk factors for heart disease and improved blood sugar management.
What kills algae the best? ›In the same way that baking soda can be a spot treatment for black algae, household borax does the same for blue and green algae. Simply use the borax to scrub away algae that's sticking to your pool walls, then use the brush to dislodge it. Follow up by vacuuming up or scooping out the free-floating algae.
What are 2 ways algae help the environment? ›As autotrophic organisms, algae convert water and carbon dioxide to sugar through the process of photosynthesis. Photosynthesis also generates oxygen as a byproduct, contributing to the survival of fish and other aquatic organisms.
Why is algae better than plants? ›Photosynthetic efficiency is higher in algae than in higher plants, because of a wide range of antenna pigments to harvest more solar energy and a variety of carbon dioxide-concentrating systems to increase carbon dioxide concentration around ribulose-1,5-bisphosphate carboxylase/oxygenase.
What are 6 ways algae can be used? ›Algae fuels are categorized into bio-ethanol, biogas, bio-hydrogen, biodiesel and bio-oil. Algae as a food have been explored for different applications as in production of single cell proteins, pigments, bioactive substances, pharmaceuticals and cosmetics.
Can you eat macro algae? ›Humans have eaten macroalgae, like wakame and nori seaweed, for thousands of years. But recently attention has turned to the nutritional and environmental potential of their microscopic cousins.
What is an example of a macro algae? ›Macroalgae belong to three main phyla: Rhodophyta (red algae), Chlorophyta (green algae), and Phaeophyta (brown algae).
Can you have too much macro algae? ›No such thing as too much macroalgae, as long as you keep nitrates and, less important IME, phosphates at good levels.
Is algae responsible for photosynthesis? ›Algae are a diverse group of predominantly aquatic photosynthetic organisms, including cyanobacteria, green algae and other eukaryotic algae. They account for more than 50% of the photosynthesis that takes place on Earth.
What does algae use for photosynthesis? ›All algae use chlorophyll a to collect photosynthetically active light. Green algae and euglenophytes also use chlorophyll b.
In what part of the cell are the photosynthetic pigments found in algae? ›
All algae contain photosynthetic pigments. These are usually an integral part of the structure of the chloroplast lamellae, but sometimes, as in bluegreen algae, they are homogeneously distributed throughout that part of the protoplasm called the “chromatoplasm.” Pigments are molecules, which absorb light.
What is the main photosynthetic structure of the algae body? ›Each chloroplast contains flattened, membranous sacs, called thylakoids, that contain the photosynthetic light-harvesting pigments, the chlorophylls, carotenoids, and phycobiliproteins (see below Photosynthesis).
Which energy is algae responsible for produce? ›These solar cells utilise the photosynthetic properties of microorganisms such as algae to convert light into electric current that can be used to provide electricity. During photosynthesis, algae produce electrons, some of which are exported outside the cell where they can provide electric current to power devices.
Which algae are best at photosynthesis? ›Among photosynthetic organisms, cyanobacteria and eukaryotic microalgae are the most promising feedstocks for the sustainable production of bulk bio-based materials such as food, feed, fuel and high-value metabolites; moreover, they can be used for wastewater treatments and in mitigation processes for CO2-emissions [3] ...
What type of photosynthesis do most algae perform? ›Plants, algae and cyanobacteria all conduct oxygenic photosynthesis 1,14. That means they require carbon dioxide, water, and sunlight (solar energy is collected by chlorophyll A). Plants and phytoplankton use these three ingredients to produce glucose (sugar) and oxygen.
Which two substances do the algae need for photosynthesis? ›The substances used during photosynthesis are carbon dioxide and water. The substances produced are glucose and oxygen gas. Plants and algae take in carbon dioxide and water from the environment and absorb light energy from the sun. Energy from the sun powers the reaction through which the sugar glucose is produced.
Does algae need oxygen for photosynthesis? ›In photosynthesis, plants and algae use solar energy to take carbon dioxide (CO2) from the air and synthesize sugars. This process produces oxygen as a byproduct, which earth's animals depend on to breathe. However, oxygen impairs the activity of key photosynthetic reactions.
What pigment is common to all algae? ›Hence, chlorophyll a is the pigment that is common to all of the algal classifications.
What are two pigments found in algae? ›Three major classes of photosynthetic pigments occur among the algae: chlorophylls, carotenoids (carotenes and xanthophylls) and phycobilins. The pigments are characteristic of certain algal groups as indicated below.
What are the major pigments present in algae? ›Phaeophyceae or brown algae comprise about 2000 species that are mostly marine. They possess abundant of fucoxanthin pigment along with chlorophyll a and chlorophyll c.
What makes algae not a plant? ›
One of the main characteristics that differentiates macroalgae from plants is their structure. They may appear similar, but the macroalgae do not have specialized organs and tissues, and they are not vascularized. They also do not have the capacity to form a structure with flowers, leaves, roots or a stem.
Does algae have RNA? ›RNA-mediated silencing pathways have been studied in the unicellular green alga Chlamydomonas reinhardtii and used as a reverse genetics tool in a few algal species. However, RNAi mechanisms and their applications remain largely uncharacterized in most algae.
Can algae be used as medicine? ›In the US, they've been sold in supplements since the late 1970s. People use blue-green algae for treating high blood pressure and as a protein supplement. It's also used for high levels of cholesterol or other fats (lipids) in the blood, diabetes, obesity, and many other conditions.