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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Contact dermatitis 17 (1987), S. 0 
    ISSN: 1600-0536
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Molecular Phylogenetics and Evolution 3 (1994), S. 365-382 
    ISSN: 1055-7903
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 28 (1985), S. 249-252 
    ISSN: 1432-1041
    Keywords: digoxin ; renal digoxin clearance ; renal function ; chronic congestive heart failure ; atrial fibrillation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary Renal digoxin clearance was compared in patients suffering from atrial fibrillation with well preserved cardiac function (n=9; salt intake ±170 mmol daily) and patients with chronic congestive heart failure (n=10; salt intake 50 mmol daily and maintenance treatment with diuretics). There was no difference between the groups concering digoxin dosage, creatinine clearance, diuresis or sodium excretion in the urine. Digoxin clearance in chronic heart failure proved to be significantly lower than in atrial fibrillation (48±21 vs 71±36 ml·min−1, p〈0.05), and Cdig/Ccreat was similarly reduced at 0.73±0.15 compared to 1.09±0.27 (p〈0.005). Steady state serum digoxin concentration was significantly higher in patients with congestive heart failure (1.44±0.47 vs 0.87±0.33 µg·l−1, p〈0.01). Chronic congestive heart failure is a state with reduced digoxin clearance by the kidney, which could lead to digoxin intoxication not explicable by overdose, reduced renal function or the effect of interacting drugs.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 25 (1983), S. 375-379 
    ISSN: 1432-1041
    Keywords: digoxin ; renal clearance ; natriuresis ; sodium loading ; sodium depletion ; furosemide ; diuretic effect
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary To evaluate the influence of different types of natriuresis on the renal clearance of digoxin (Cldig) and the Cldig/Clcr ratio, studies were performed in which sodium-depleted patients were placed on a moderately high sodium diet for 6 days. In another group natriuresis was evoked by furosemide. In the first study, in 10 patients, there was a 10-fold increase in Na excretion and a small rise in diuresis (V) and Clcr, which was accompanied by an increase in Cldig from 57.5±32, and 60.7±27.3 (duplicate measurements) to 103.9±55.4 (p〈0.01) and 103.8±46.5 ml min−1 (p〈0.01). Cldig/Clcr rose from 0.60±0.24 and 0.61±0.16 to 0.91±0.31 and 0.91±0.21, respectively (bothp〈0.005). Serum digoxin concentration declined from 1.24±0.35 and 1.19±0.40 to 1.02±0.35 and 0.97±0.32 µg/l (bothp〈0.01) during the high sodium diet. In the furosemide — induced natriuresis (6 patients), changes in Na excretion and V were a multiple of those caused by Na loading, but the Cldig/Clcr ratio was not increased. The results are in accordance with the concept of digoxin backdiffusion in the proximal tubules, which is dependent on proximal Na reabsorption. In the more distal segments of the nephron, where the action of furosemide occurs, there does not appear to be any transtubular movement of digoxin.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1438-3888
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The relationship between distributional boundaries and temperature responses of some Northeast American and West European endemic and amphiatlantic rhodophytes was experimentally determined under varying regimes of temperature, light, and daylength. Potentially critical temperatures, derived from open ocean surface summer and winter isotherms, were inferred from distributional data for each of these algae. On the basis of the distributional data the algae fall within the limits of three phytogeographic groups: (1) the Northeast American tropical-to-temperate group; (2) the warm-temperate Mediterranean Atlantic group; and (3) the amphiatlantic tropical-to-warm temperate group. Experimental evidence suggests that the species belonging to the northeast American tropical-to-temperate group(Grinnellia americana, Lomentaria baileyana, andAgardhiella subulata) have their northern boundaries determined by a minimum summer temperature high enough for sufficient growth and/or reproduction. The possible restriction of 2 species (G. americana andL. baileyana) to the tropical margins may be caused by summer lethal temperatures (between 30 and 35 °C) or because the gradual disintegration of the upright thalli at high temperatures (〉30 °C) promotes an ephemeral existence of these algae towards their southern boundaries. Each of the species have a rapid growth and reproductive potential between 15–30 °C with a broad optimum between 20–30 °C. The lower limit of survival of each species was at least 0 °C (tested in short days only). Growth and reproduction data imply that the restrictive distribution of these algae to the Americas may be due to the fact that for adequate growth and/or reproduction water temperatures must exceed 20 °C. At temperatures ≦15 °C reproduction and growth are limited, and the amphiatlantic distribution through Iceland would not be permitted. On the basis of experimental evidence, the species belonging to the warm-temperate Mediterranean Atlantic group(Halurus equisetifolius), Callophyllis laciniata, andHypoglossum woodwardii), have their northern boundaries determined by winter lethal temperatures. Growth ofH. equisetifolius proceeded from 10–25 °C, that ofC. laciniata andH. woodwardii from 5–25 °C, in each case with a narrow range for optimal growth at ca. 15 °C. Tetrasporelings ofH. woodwardii showed limited survival at 0 °C for up to 4 d. For all members of the group tetrasporangia occurred from 10–20 °C. The southern boundary ofH. equisetifolius andC. laciniata is a summer lethal temperature whereas that ofH. woodwardii possibly is a winter growth and reproduction limit. Since each member of this group has a rather narrow growth and survival potential at temperatures 〈5 °C and 〉20 °C, their occurrence in northeast America is unlikely. The (irregular) distribution ofSolieria tenera (amphiatlantic tropical-to-warm temperate) cannot be entirely explained by the experimental data (possibly as a result of taxonomic uncertainties).
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1438-3888
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The temperature responses for growth and survival have been experimentally tested for 6 species of the green algal genusCladophora (Chlorophyceae; Cladophorales) (all isolated from Roscoff, Brittany, France, one also from Connecticut, USA), selected from 4 distribution groups, in order to determine which phase in the annual temperature regime might prevent the spread of a species beyond its present latitudinal range on the N. Atlantic coasts. For five species geographic limits could be specifically defined as due to a growth limit in the growing season or to a lethal limit in the adverse season. These species were: (1)C. coelothrix (Amphiatlantic tropical to warm temperate), with a northern boundary on the European coasts formed by a summer growth limit near the 12°C August isotherm. On the American coasts sea temperatures should allow its occurrence further north. (2)C. vagabunda (Amphiatlantic tropical to temperate), with a northern boundary formed by a summer growth limit near the 15°C August isotherm on both sides of the Atlantic. (3)C. dalmatica, as forC. vagabunda. (4)C. hutchinsiae (Mediterranean-Atlantic warm temperate), with a northern boundary formed by a summer growth limit near the 12°C August isotherm, and possibly also a winter lethal limit near the 6°C February isotherm; and a southern boundary formed by a southern lethal limit near the 26°C August isotherm. It is absent from the warm temperate American coast because its lethal limits, 5° and 30°C, are regularly reached there. (5) Preliminary data forC. rupestris (Amphiatlantic temperate), suggest the southeastern boundary on the African coast to be a summer lethal limit near the 26°C August isotherm; the southwestern boundary on the American coast lies on the 20°C August isotherm. For one species,C. albida, the experimental growth and survival range was wider than expected from its geographic distribution, and reasons to account for this are suggested.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Helgoland marine research 41 (1987), S. 261-272 
    ISSN: 1438-3888
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Indirect evidence of the existence of long-distance dispersal of seaweeds is provided by the fact that mid-oceanic islands of volcanic origin are inhabited by well-developed seaweed floras which could reach these islands only overseas from continental donor areas. For instance, the flora of Tristan da Cunha (S. Atlantic Ocean) was established by long-distance dispersal in less than 1 million years (the approximate age of the island); the seaweed flora of the Faeroes (N. Atlantic Ocean) could be constituted in less than 10,000 years (the end of the Pleistocene ice cover of these islands). There is no evidence for either supporting or discounting the possible role of planktonic stages of seaweeds (spores, propagules, zygotes) in the long-distance dispersal of seaweeds. There is, however, some evidence of long-distance dispersal as floating plants, or as plants attached to floating objects (including floating algae). There are a few examples of “artificial” long-range dispersal by man (possibly on ship hulls, oysters, in ballast water). Long-range dispersal of seaweeds does exist, but it is an exception rather than the rule. If it were the rule, the world’s seaweed floras would show similar latitudinal gradients in species composition in the oceans and on both hemispheres. This is, however, not the case.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Helgoland marine research 42 (1988), S. 339-383 
    ISSN: 1438-3888
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In traditional chlorophytan systems the organizational level was the primary character for the distinction of main groups (classes and orders). For instance, in Fott (1971), the flagellate level corresponds with the Volvocales, the coccoid level with the Chlorococcales, the filamentous level with the Ulotrichales, the siphonocladous level with the Siphonocladales, and the siphonous level with the Bryopsidales. The new system presented here is an elaboration and emendation of recently proposed taxonomies and their underlying phylogenetic hypotheses, and it is mainly based on ultrastructural features which have become available over the last 15 years. The following criteria are used for the distinction of classes and orders: (1) architecture of the flagellate cell (flagellate cells are considered as the depositories of primitive characters); (2) type of mitosis-cytokinesis; (3) place of meiosis in the life history and, consequently, the sexual life history type; (4) organizational level and thallus architecture; (5) habitat type (marine versus feshwater and terrestrial); (6) chloroplast type. The following classes are presented: Prasinophyceae, Chlamydophyceae, Ulvophyceae (orders Codiolales, Ulvales, Cladophorales, Bryopsidales, Dasycladales), Pleurastrophyceae (?), Chlorophyceae s.s. (orders Cylindrocapsales, Oedogoniales, Chaetophorales), Zygnematophyceae, Trentepohliophyceae, Charophyceae (orders Klebsormidiales, Coleochaetales, Charales). The new system no longer reflects the traditional hypothesis of a stepwise evolutionary progression of organizational levels in which the flagellate level represents the most primitive lineage, the coccoid and sarcinoid levels lineages of intermediate derivation, and the filamentous, siphonocladous and siphonous levels the most derived lineages. Instead, it is now hypothesized that these levels have arisen over and over again in different chlorophytan lineages which are primarily characterized by their type of flagellate cell. The flagellate green algal classes Prasinophyceae (with organic body scales) and Chlamydophyceae probably represent bundles of highly conservative lineages that diverged very long ago. Consequently, extant genera and species in these classes can be expected to have emerged long ago. Fossil evidence points to a minimum age of 600 Ma of certain extant Prasinophycean genera, and molecular evidence to a minimum age of 400–500 Ma of a fewChlamydomonas species. On the contrary, the most derived “green algal” lineage, the Angiosperms, can be expected to consist of, on average, much younger genera and species. Fossil evidence points to a minimum age of genera of 5–60 Ma. Lineages of intermediate evolutionary derivation (Ulvophyceae, Chlorophyceae, Charophyceae) can be expected to encompass genera and species of intermediate age. Fossil and (limited) molecular evidence point to a minimum age of 230–70 Ma of extant genera in Bryopsidales, Dasycladales and Cladophorales (Ulvophyceae) and of 250–80 Ma of extant genera in Charales (Charophyceae).
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Helgoland marine research 42 (1988), S. 553-562 
    ISSN: 1438-3888
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Young, crustose plants ofDumontia contorta grown in the laboratory from carpospores were transferred in September 1983 to their natural habitat in Lake Grevelingen (SW Netherlands). The number of upright fronds per crust, length of upright fronds, and diameter of crusts were determined monthly until October 1984 and the presence of tetrasporangia was noted. Although fronds were initiated from crusts throughout the period of short daylengths (〈13 h light per day, i.e. from September to March), the majority of the fronds was initiated in October and November when short daylengths coincided with optimum temperatures for frond initiation (ca 10–20°C). By April, i.e. within 5–6 months, these plants had reached maximum sizes and had become fertile; subsequently, the plants decayed. The successively smaller numbers of fronds that were formed in December and January also reached maximum sizes after ca 5–6 months, i.e. by May and June, but these fronds remained much smaller than the fronds initiated in October–November, possibly because of lower temperatures and light levels at the start of their growth. It is suggested that the fronds have a fixed maturation period (ca 5–6 months) irrespective of their size and the moment of their initiation. Crusts were shown to “oversummer” and to produce new fronds at the onset of shortday conditions in September 1984.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Helgoland marine research 42 (1988), S. 131-132 
    ISSN: 1438-3888
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Type of Medium: Electronic Resource
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