Lake restoration by reducing external phosphorus loading: the influence of sediment phosphorus release

SUMMARY. 1. This review considers the factors which determine the recovery of eutrophic lakes following a reduction in the external phosphorus loading.
2 The mean phosphorus content of a lake should decrease roughly in proportion to the reduction in phosphorus input. Where the lake phosphorus concentration does not decrease as predicted, then the release of phosphorus from the sediment is implicated.
3. The current understanding of the processes by which sediment phosphorus is mobilized and transported into the photic zone is described. The extent to which phosphorus release can maintain lake phosphorus concentrations following the reduction in external loading is influenced by: lake morphometry, flushing rate, sediment type, trophic state and history of enrichment.
4. A reduction in the phytoplankton biomass of a lake is dependent upon the size of the decrease in lake phosphorus concentration and the degree to which phosphorus limits primary production. The importance of phosphorus in limiting phytoplankton production tends to decrease with increasing lake trophic status.
5. Improvements in the condition of highly eutrophic lakes require very large reductions in external phosphorus loading, whereas in mildly enriched lakes moderate changes in the supply of phosphorus have noticeable effects on phytoplankton biomass.     

Long- and short-term effects of decreased sink demand on carbohydrate levels and photosynthesis in wheat leaves

Wheat (Triticum aestivum L.) ears were removed to investigate long-term regulation of photosynthesis by sink demand at ambient CO₂ and 22 °C. The CO₂ level was also increased to 660 μmol mol^?1 and temperature was lowered to 5 °C to examine short-term responses of photosynthesis to low sink demand. Sink removal inhibited photosynthesis and increased leaf levels of glucose, fructose and ribulose-1, 5-bisphosphate (RuBP), and the glucose-6-phosphate (G6P)/fructose-6-phosphate (F6P) and RuBP/3-phosphoglycerate (PGA) ratios under growth conditions, but had no effect on the activity and activation state of ribulose-1, 5-bisphosphate carboxylase oxygenase (Rubisco) either under growth or short-term conditions, suggesting an inhibition of photosynthesis by decreased in vivo catalysis of Rubisco. Photosynthesis increased similarly in eared and earless shoots after a rise in CO₂ concentration, and the ratio of triose-phosphates (glyceraldehyde 3-phosphate and dihydroxyacetone phosphate, TP) to PGA was similar or higher for removed than intact ears, suggesting that feedback inhibition of photosynthesis was not caused by a limitation of ATP synthesis in chloroplasts. Under short-term conditions (660 μmol mol^?1 CO₂, 5 °C), TP and RuBP levels and the TP/PGA and TP/RuBP ratios were increased by sink removal, indicating an additional limitation of photosynthesis by the rate of RuBP regeneration.     

Maize streak virus: an old and complex 'emerging' pathogen

Maize streak virus (MSV; Genus Mastrevirus, Family Geminiviridae) occurs throughout Africa, where it causes what is probably the most serious viral crop disease on the continent. It is obligately transmitted by as many as six leafhopper species in the Genus Cicadulina, but mainly by C. mbila Naudé and C. storeyi. In addition to maize, it can infect over 80 other species in the Family Poaceae. Whereas 11 strains of MSV are currently known, only the MSV‐A strain is known to cause economically significant streak disease in maize. Severe maize streak disease (MSD) manifests as pronounced, continuous parallel chlorotic streaks on leaves, with severe stunting of the affected plant and, usuallly, a failure to produce complete cobs or seed. Natural resistance to MSV in maize, and/or maize infections caused by non‐maize‐adapted MSV strains, can result in narrow, interrupted streaks and no obvious yield losses. MSV epidemiology is primarily governed by environmental influences on its vector species, resulting in erratic epidemics every 3–10 years. Even in epidemic years, disease incidences can vary from a few infected plants per field, with little associated yield loss, to 100% infection rates and complete yield loss. Taxonomy: The only virus species known to cause MSD is MSV, the type member of the Genus Mastrevirus in the Family Geminiviridae. In addition to the MSV‐A strain, which causes the most severe form of streak disease in maize, 10 other MSV strains (MSV‐B to MSV‐K) are known to infect barley, wheat, oats, rye, sugarcane, millet and many wild, mostly annual, grass species. Seven other mastrevirus species, many with host and geographical ranges partially overlapping those of MSV, appear to infect primarily perennial grasses. Physical properties: MSV and all related grass mastreviruses have single‐component, circular, single‐stranded DNA genomes of approximately 2700 bases, encapsidated in 22 × 38‐nm geminate particles comprising two incomplete T = 1 icosahedra, with 22 pentameric capsomers composed of a single 32‐kDa capsid protein. Particles are generally stable in buffers of pH 4–8. Disease symptoms: In infected maize plants, streak disease initially manifests as minute, pale, circular spots on the lowest exposed portion of the youngest leaves. The only leaves that develop symptoms are those formed after infection, with older leaves remaining healthy. As the disease progresses, newer leaves emerge containing streaks up to several millimetres in length along the leaf veins, with primary veins being less affected than secondary or tertiary veins. The streaks are often fused laterally, appearing as narrow, broken, chlorotic stripes, which may extend over the entire length of severely affected leaves. Lesion colour generally varies from white to yellow, with some virus strains causing red pigmentation on maize leaves and abnormal shoot and flower bunching in grasses. Reduced photosynthesis and increased respiration usually lead to a reduction in leaf length and plant height; thus, maize plants infected at an early stage become severely stunted, producing undersized, misshapen cobs or giving no yield at all. Yield loss in susceptible maize is directly related to the time of infection: infected seedlings produce no yield or are killed, whereas plants infected at later times are proportionately less affected. Disease control: Disease avoidance can be practised by only planting maize during the early season when viral inoculum loads are lowest. Leafhopper vectors can also be controlled with insecticides such as carbofuran. However, the development and use of streak‐resistant cultivars is probably the most effective and economically viable means of preventing streak epidemics. Naturally occurring tolerance to MSV (meaning that, although plants become systemically infected, they do not suffer serious yield losses) has been found, which has primarily been attributed to a single gene, msv‐1. However, other MSV resistance genes also exist and improved resistance has been achieved by concentrating these within individual maize genotypes. Whereas true MSV immunity (meaning that plants cannot be symptomatically infected by the virus) has been achieved in lines that include multiple small‐effect resistance genes together with msv‐1, it has proven difficult to transfer this immunity into commercial maize genotypes. An alternative resistance strategy using genetic engineering is currently being investigated in South Africa. Useful websites: 〈 http://www.mcb.uct.ac.za/MSV/mastrevirus.htm 〉; 〈 http://www.danforthcenter.org/iltab/geminiviridae/geminiaccess/mastrevirus/Mastrevirus.htm 〉.     

The fate of beryllium compounds in the rat

Beryllium was injected intravenously into rats. When administered as ionic solution or as citrate complex, nearly half of the injected quantity was excreted and most of the remaining beryllium was retained in the bones.     

Characterization of Two Sibling Species of the Genus Stylonychia (Ciliata,Hypotricha): S. mytilus Ehrenberg, 1838 and S. lemnae n. sp. I. Morphology and Reproductive Behavior1

All Stylonychia mytilus-like ciliates which were collected and sent to us during the last 20 years belonged either to S. mytilus or to a new species, S. lemnae, which is described here. The only morphological differences are the shape and the size. Stylonychia mytilus that have been starved for one day average 300 μm in length, and S. lemnae starved for a day are 230 μm long. The occurrence of mating types is described.     

Why are Biennials so Few?: Hart's Results Revisited

Abstract Hart (1977) constructed a model to explain the rarity of biennials in the North American flora. However, Hart's model is inadequate, because: 1) biennials were not compared with annuals, 2) facultative biennials were not included, and 3) the range of general perennial life histories was not considered. Revision of Hart's model shows that strict and facultative biennials are rare, because they compete most successfully against annuals and general perennial life histories only in a narrow range of juvenile and adult survivorship values.