scholarly journals The biology and ecology of the liverwort Cephaloziella varians in Antarctica

2009 ◽  
Vol 22 (2) ◽  
pp. 131-143 ◽  
Author(s):  
K.K. Newsham

AbstractThe biology and ecology of Cephaloziella varians, the most widespread and abundant liverwort in Antarctica, are reviewed. A description of the species is given, together with information on its geographical distribution, reproduction, habitats, associated organisms and responses to environmental stresses. Characteristics of its photosynthetic physiology are also presented, including data on oxygen evolution rates and chlorophyll a fluorescence parameters. Substratum and tissue chemistry, water relations and pigments are discussed, along with recent data demonstrating that the dark pigment in the apical leaves of C. varians is the anthocyanidin riccionidin A. Recent studies showing that the ericoid mycorrhizal symbiont Rhizoscyphus ericae is present in the tissues of the plant at a wide range of locations in the maritime and sub-Antarctic are also described. It is evident, from the literature reviewed, that C. varians has several adaptations that enable it to survive in the Antarctic biome, explaining its survival at higher latitudes than any other hepatic. The species’ major adaptations include the synthesis of riccionidin A in apical leaves, enabling efficient heat absorption and protection from photoinhibition, and the presence in stems and rhizoids of fungal hyphae, which are potentially beneficial to the hepatic’s nutrition and possibly also synthesize cryoprotectants.

Polar Biology ◽  
2021 ◽  
Author(s):  
Deborah Bozzato ◽  
Torsten Jakob ◽  
Christian Wilhelm ◽  
Scarlett Trimborn

AbstractIn the Southern Ocean (SO), iron (Fe) limitation strongly inhibits phytoplankton growth and generally decreases their primary productivity. Diatoms are a key component in the carbon (C) cycle, by taking up large amounts of anthropogenic CO2 through the biological carbon pump. In this study, we investigated the effects of Fe availability (no Fe and 4 nM FeCl3 addition) on the physiology of Chaetoceros cf. simplex, an ecologically relevant SO diatom. Our results are the first combining oxygen evolution and uptake rates with particulate organic carbon (POC) build up, pigments, photophysiological parameters and intracellular trace metal (TM) quotas in an Fe-deficient Antarctic diatom. Decreases in both oxygen evolution (through photosynthesis, P) and uptake (respiration, R) coincided with a lowered growth rate of Fe-deficient cells. In addition, cells displayed reduced electron transport rates (ETR) and chlorophyll a (Chla) content, resulting in reduced cellular POC formation. Interestingly, no differences were observed in non-photochemical quenching (NPQ) or in the ratio of gross photosynthesis to respiration (GP:R). Furthermore, TM quotas were measured, which represent an important and rarely quantified parameter in previous studies. Cellular quotas of manganese, zinc, cobalt and copper remained unchanged while Fe quotas of Fe-deficient cells were reduced by 60% compared with High Fe cells. Based on our data, Fe-deficient Chaetoceros cf. simplex cells were able to efficiently acclimate to low Fe conditions, reducing their intracellular Fe concentrations, the number of functional reaction centers of photosystem II (RCII) and photosynthetic rates, thus avoiding light absorption rather than dissipating the energy through NPQ. Our results demonstrate how Chaetoceros cf. simplex can adapt their physiology to lowered assimilatory metabolism by decreasing respiratory losses.


2018 ◽  
Vol MA2018-01 (31) ◽  
pp. 1917-1917
Author(s):  
Dongho Lee ◽  
Kyoung-Shin Choi

Producing hydrogen via solar water splitting using a photoelectrochemical cell (PEC) persists as one of the most exciting research topics in the field of solar fuels. The construction of efficient PECs requires the integration of multiple components including a photoanode, a photocathode, an oxygen evolution catalyst, and a hydrogen evolution catalyst. Therefore, the compatibility and stability of all of these elements in a given operating condition are crucial. When the stability of a semiconductor electrode used as the photoanode or photocathode is limited in an acidic or basic condition which is optimum for the operation of the other components, a thin protective layer has been deposited on the semiconductor surface to prevent its chemical dissolution. Surface coating of a thin and conformal TiO2 layer has been proven to be successful for protecting photoelectrodes since TiO2 is chemically and electrochemically stable in a wide range of pH conditions under both anodic and cathodic conditions. In order to prevent the semiconductor surface from coming into direct contact with the corrosive electrolyte, complete coverage of the photoelectrode with TiO2 is required. At the same time, the TiO2 layer should be thin enough not to interfere with the charge transport properties of the photoelectrode. As a result, atomic layer deposition (ALD) has been the only successful tool used to date to produce an effective protective layer. However, the slow processing time and economic viability of ALD methods motivated us to develop an inexpensive and facile solution-based synthesis method for the deposition of high quality TiO2 coating layers. In this presentation, we report a new electrochemical method to deposit a thin and conformal TiO2 layer on nanoporous BiVO4 that has an intricate, high surface area morphology. BiVO4 is a promising n-type photoanode material with a relatively low bandgap (2.4~2.5 eV). However, its usage has been limited to neutral and mildly basic conditions (pH 5~9) because it is chemically unstable in strongly acidic and basic conditions. Our method allows for the deposition of a 5~6 nm thick TiO2 layer on BiVO4 within 1 min and the resulting BiVO4/TiO2 electrodes exhibit chemical stability in basic solutions (pH 12~13). Sulfite oxidation measurements of BiVO4 and BiVO4/TiO2 electrodes show that the thin TiO2 protective layer does not significantly reduce the hole transfer to the electrolyte. Finally, we demonstrate the photoelectrochemical stability of the BiVO4/TiO2 electrode for photoelectrochemical water oxidation in basic solutions by coupling the BiVO4/TiO2 electrode with appropriate oxygen evolution catalysts.


Author(s):  
D. W. Minter

Abstract A description is provided for Helminthosphaeria stuppea, which is apparently saprobic and able to colonize woody parts of a wide range of plants. Some information on its associated organisms and substrata, habitats, dispersal and transmission, and conservation status is given, along with details of its geographical distribution (North America (USA (California, Colorado, Utah and Washington)), Europe (Austria, Czech Republic, Denmark, France and UK)) and hosts (including Tsuga mertensiana). No reports of negative economic impacts have been found.


Author(s):  

Abstract A new distribution map is provided for Bactrocera papayae Drew & Hancock Diptera: Tephritidae. Attacks a wide range of fleshy fruits and vegetables. Information is given on the geographical distribution in ASIA, Brunei, Christmas Island, Indonesia, Bali, Flores, Java, Kalimantan, Lombok, Sulawesi, Sumbawa, Timor, Malaysia, Sabah, Peninsular Malaysia, Singapore, Thailand, AUSTRALASIA, Australia, Queensland, Indonesia, Irian Jaya, Papua New Guinea.


Author(s):  
J. E. M. Mordue

Abstract A description is provided for Ustilago hypodytes. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: A wide range of grasses, including species of Agropyron (many), Ammophila, Brachypodium, Bromus, Calamagrostis, Diplachne, Distichlis, Elymus (many), Festuca, Glyceria, Hilaria, Hordeum, Haynaldia, Lygeum, Melica, Orysopsis, Panicum, Phalaris, Phleum, Poa (many), Puccinellia, Secale, Sitanion, Sporobolus, Stipa (many), and Trisetum. DISEASE: Stem smut of grasses. GEOGRAPHICAL DISTRIBUTION: Chiefly a temperate species found in Europe (including Denmark, Finland, France, Germany, Hungary, Italy, Romania, Sweden, Switzerland, UK, USSR, Yugoslavia) and North America (Canada, USA) and extending to central and South America (Argentina, Peru, Uruguay), N. Africa (Libya, Morocco, Tunisia), Japan, Australia and New Zealand. TRANSMISSION: Not fully understood, though inoculation experiments have demonstrated that infection occurs in mature vegetative plants (possibly through meristematic tissue), not seeds or flowers (22, 240; 24, 511). Once established, infection is systemic, probably overwintering in the root system and spreading by vegetative multiplication of host plants as well as from plant to plant (24, 511; 19, 720).


Author(s):  
G. M. Waterhouse

Abstract A description is provided for Pythium intermedium. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On a wide range of hosts represented by the following families: Begoniaceae, Bromeliaceae, Chenopodiaceae, Compositae, Coniferae, Cruciferae, Euphorbiaceae, Geraniaceae, Gramineae, Leguminosae, Liliaceae, Linaceae, Moraceae, Onagraceae, Ranunculaceae, Rosaceae, Solanaceae, Ulmaceae, Violaceae; also in the Equisetales and Filicales. DISEASES: Damping-off of seedlings, foot rot and root rot of ornamentals, occasionally of crop plants and trees. GEOGRAPHICAL DISTRIBUTION: Asia (China); Australia & Oceania (Hawaii); Europe (England, Belgium, France, Germany, Holland, Sweden, U.S.S.R.); North America (U.S.A.); South America (Argentina). TRANSMISSION: A common soil inhabitant.


Author(s):  
D. Brayford

Abstract A description is provided for Cylindrocarpon olidum var. olidum. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: Wide range. At IMI there are records on: Asparagus, Camellia, Cocos, Cordylina, Heterodera (nematode), Medicago saliva, Narcissus, Pelargonium, Picea, Pinus, Pyrus, Secale, Solanum.DISEASE: Root rotting. GEOGRAPHICAL DISTRIBUTION: Africa: Ghana, Zimbabwe; Australasia: Australia; Europe: Germany, Great Britain; North America: Canada, Honduras, USA. TRANSMISSION: Soil-borne; slimy spores are probably spread by water.


Author(s):  
C. Booth

Abstract A description is provided for Gibberella fujikuroi var. subglutinans. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On several hosts of economic importance in the Gramineae; also on a wide range of hosts represented by the following families: Amaryllidaceae, Anacardiaceae, Bromeliaceae, Chenopodiaceae, Convolvulaceae, Cruciferae, Iridaceae, Leguminosae, Liliaceae, Malvaceae, Marantaceae, Musaceae, Palmae, Rosaceae, Rutaceae, Sterculiaceae (14: 708; 31: 515; 36: 501; 40: 89 and Herb. IMI). DISEASES: Causes a seedling blight, and root, stalk and kernel rot of maize; also on heads and stalks of sorghum associated with a foot and stem rot, and causing a stem rot and top rot of sugar-cane ('pokkah boeng'). Other records include a wilt of Crotalaria, a heart rot of leaves of banana and Manila hemp, and fruit rot of banana, cacao and pineapple. There appear to be no references to pathogenicity to rice. Also entomogenous on cereal stem borer larvae and other insects (27: 71; 33: 382; 38: 141, 740). GEOGRAPHICAL DISTRIBUTION: Africa (Central African Republic, Congo, Ghana, Ivory Coast, Kenya, Mauritius, Morocco, Reunion, Sierra Leone, South Africa, Southern Rhodesia, Tanganyika, Uganda); Asia (Formosa (Taiwan), Hong Kong, India, Java, Indo-China, Philippines, Syria); Australasia (Hawaii, New South Wales, New Zealand, Victoria); Europe (Czechoslovakia, Germany,? Italy, Poland, Romania); Central America & West Indies (French Antilles, Honduras, Trinidad); North America (Canada, United States); South America (Argentina, Peru). (CMI Map 191). TRANSMISSION: Both seed and soil-borne. Air-borne ascospores produced from perithecia on over-wintered plant debris or on dead stalks of sugar-cane at the beginning of the rainy season are also important sources of infection (30: 344). The pathogen may also be disseminated on pupae and adults of cereal stem borers and their parasites in sugar-cane (33: 382).


Author(s):  
G. M. Waterhouse

Abstract A description is provided for Phytophthora nicotianae var. parasitica. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On a very wide range of host plants comprising 58 families including: avocado, castor, Cinchona spp., citrus, cotton, eggplant, guava, lucerne, papaw, parsley, pineapple, Piper betle, rhubarb, sesame, strawberry, tomato. DISEASES: Damping-off of seedlings (tomato, castor, citrus, cotton); root rot (citrus, avocado, strawberry, lucerne); crown rot (parsley, rhubarb, strawberry, lucerne); brown stem rot of tobacco; stem canker and tip blight of Cinchona spp. ; leaf blight (castor, sesame, pineapple, Piper betle) and fruit rot (citrus, tomato, guava, papaw, eggplant). GEOGRAPHICAL DISTRIBUTION: Africa (Ethiopia, Mali, Madagascar, Mauritius, Morocco, Nigeria, Sierra Leone, Southern Rhodesia, Tanganyika); Asia (Burma, Ceylon, China, Formosa, India, Israel, Japan, Java, Malaya, Philippines); Australia & Oceania (Australia, Hawaii, Tasmania); Europe (Cyprus, France, Germany, Great Britain, Holland, Ireland, Italy, Poland, Portugal, U.S.S.R.); North America (Bermuda, Canada, Mexico, U.S.A.); Central America & West Indies (Costa Rica, Cuba, El Salvador, Guatemala, Jamaica, Montserrat, Puerto Rico, Trinidad);. South America (Argentina, Brazil, British Guiana, Colombia, Paraguay, Peru, Venezuela). TRANSMISSION: Soil-borne, spreading rapidly after heavy rain or where soil remains moist or water-logged (40: 470). Also recorded in drainage water in India and in reservoirs and canals supplying citrus groves in U.S.A. (23: 45; 39: 24). A method for determining a disease potential index in soil using lemon fruit has been described (38: 4). Also present in testas of seeds from diseased citrus fruit which may infect nursery seedbeds (37: 165).


Author(s):  
G. M. Waterhouse

Abstract A description is provided for Pythium aphanidermatum. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. HOSTS: On a wide range of hosts, often similar to those attacked by P. butleri, but inducing different symptoms, represented in the following families: Amaranthaceae, Amaryllidaceae, Araceae, Basellaceae, Bromeliaceae, Cactaceae, Chenopodiaceae, Compositae, Coniferae, Convolvulaceae, Cruciferae, Cucurbitaceae, Euphorbiaceae, Gramineae, Leguminosae, Linaceae, Malvaceae, Moraceae, Passifloraceae, Rosaceae, Solanaceae, Umbelliferae, Violaceae, Vitaceae, Zingiberaceae. DISEASES: Damping-off of various seedlings; 'cottony-leak' of cucurbit fruit in storage; 'cottony blight' of turf grasses; root and stalk rot of maize. Other hosts: tobacco, sugar-beet, sugar-cane, papaw, pineapple, ginger, bean and cotton. GEOGRAPHICAL DISTRIBUTION: Africa (Central African Republic, Fernando, Ghana, Kenya, Malawi, Mali, Nigeria, Sierra Leone, South Africa, Southern Rhodesia, Sudan, Togo, Zambia); Asia (Ceylon, China, Formosa, India, Indonesia, Israel, Japan, Java, Malaya, Philippines, Sumatra); Australasia & Oceania (Australia, Hawaii, New Caledonia); North America (Canada, Mexico); Central America & West Indies (Antilles, Jamaica, Puerto Rico); South America (Argentina, Brazil, Peru, Venezuela); Europe Austria, Cyprus, Czechoslovakia, Great Britain, Greece, Holland, Italy, Poland, U.S.S.R., Yugoslavia). (CMI Map 309) TRANSMISSION: Soil-borne. Eggplant fruit become infected when blossom end is in contact with soil (5: 465). Readily isolated from soil using fresh potato cubes treated with streptomycin and pimaricin as baits (43, 1519; 43, 46) or seedling papaw roots in soil containing papaw tissue (43, 1720). Also recorded as seed-borne on tomato and cucurbits but doubtful whether seed-transmitted (see Noble et al., An Annotated List of Seed-Borne Diseases, 1958, pp. 23, 25, 124).


Sign in / Sign up

Export Citation Format

Share Document