THE BIOLOGY OF LETTUCE ROOT APHID

Lettuce root aphid, Pemphigus bursarius L., is a pest which sometimes causes considerable and widespread damage to crops of summer lettuce.
Its favourite primary host is Lombardy poplar. On hatching in spring, from eggs that have overwintered on this host, the fundatrices cause the development of hollow, flask-shaped galls on the leaf petioles. A fundatrix becomes enclosed within a gall, where it matures, and gives rise to between 100 and 250 young. These fundatrigeniae are all potential alatae and on developing wings leave the gall and migrate to lettuce and other secondary hosts; they reproduce rapidly.
Lettuce sown between mid-April and the end of May is most severely attacked, while lettuce sown in July escapes attack. The alternative secondary hosts belong to the Compositae, subfam. Liguliflorae, and although lettuce is preferred by the fundatrigeniae, Lapsana communis L. and Sonchus asper (L.) Hill often have big colonies of Pemphigus bursarius on their roots. The size of the mature apterae varies between hosts and is largest on lettuce and Sonchus asper.
All winged alienicolae are sexuparae and fly back to poplar. Thus alternative secondary hosts are not reservoirs for lettuce-infesting alatae.
The sexuparae begin appearing on lettuce from about the last week in August. They generally come up to the soil surface and settle around the 'collar' of the host plant, to mature and develop wings. Having flown back to the primary host, the sexuparae seek out crevices in the bark where they produce arostrate sexuales. The ovipara contains one egg, and after mating she crawls as far into the bark crevice as possible and oviposits.     

Codon bias and plasticity in immunoglobulins

Immunoglobulin genes experience Darwinian evolution twice. In addition to the germline evolution all genes experience, immunoglobulins are subjected, upon exposure to antigen, to somatic hypermutation. This is accompanied by selection for high affinity to the eliciting antigen and frequently results in a significant increase in the specificity of the responding population. The hypermutation mechanism displays a strong sequence specificity. Thus arises the opportunity to manipulate codon bias in a site-specific manner so as to direct hypermutation to those parts of the gene that encode the antigen-binding portions of the molecule and away from those that encode the structurally conserved regions. This segregation of mutability would clearly be advantageous; it would enhance the generation of potentially useful variants while keeping mutational loss to acceptably low levels. But it is not clear that the advantage gained would be large enough to produce a measurable effect within the background stochasticity of the evolutionary process. I have performed a pair of statistical tests to determine whether site- specific codon bias in human immunoglobulin genes is correlated with the sequence specificity of the somatic mutation mechanism. The sequence specificity of the mutator was determined by analysis of a database of published immunoglobulin intron sequences that had experienced somatic mutation but not selection. The site-specific codon bias was determined by analysis of published sequences of human germline immunoglobulin V genes. Both tests strongly suggest that evolution has acted to enhance the plasticity of immunoglobulin genes under somatic hypermutation.      

ANTIFUNGAL ACTION OF STREPTOMYCIN-COPPER CHELATE AGAINST PHYTOPHTHORA INFESTANS ON TOMATO (LYCOPERSICON ESCULENTUM)

The antifungal protection afforded by streptomycin-copper chelate in vivo in greenhouse tests against Phytophthora infestans on tomato was found to be of the order of six times greater than that of streptomycin sulphate. The copper chelate also showed much greater resistance to simulated rainfall. Similar tests showed that streptomycin-copper chelate (in terms of streptomycin content) was from 2 1/2 to 5 times more effective as an antifungal prophylactic spray than zinc ethylene-bis(dithiocarbamate) (zineb), and some fifty times more active than copper oxychloride formulated as a commercial 50% wettable powder. These three materials showed roughly similar resistance to weathering by 'rainfall' and it was assumed therefore that 250 i.u./ml. streptomycin as streptomycin-copper chelate might be expected to give the same degree of protection against Phytophthora infestans in the field as would the usual field rates of usage of zineb and copper oxychloride.     

Biochemical, physiological and morphological variation in unarmed hymenolepids (Eucestoda: Cyclophyllidae)

The genus Hymenolepis contains a number of unarmed species. These frequently possess similar morphologies and are difficult to discriminate using the traditional method of comparative morphology. A parasite of the long-tailed field mouse, Apodemus sylvaticus in northeast Ireland, resembles the widespread H. diminuta which is usually a parasite of the rat. Analysis of general and specific proteins of the adults in A. sylvaticus , laboratory mice and rats suggests that the parasite found in the former host and H. diminuta are genetically distinct, though more closely allied than either is to H. nana, H. citelli and H. microstoma . Experimental analysis of the growth and expulsion of the Irish material and H. diminuta from SPF C57 laboratory mice, rats and wild caught A. sylvaticus suggests that there are behavioural and physiological differences in these taxa. Both are expelled from C57 mice though the hymenolepid from Irish A. sylvaticus persists for 3 days more than those of H. diminuta . The former prospers better in rats than H. diminuta in A. sylvaticus . Detailed comparison of the gross morphology of cysticercoid and adult H. diminuta and the Irish hymenolepid reveals differences in size rather than qualitative attributes. The occurrence of H. diminuta in A. sylvaticus is discussed. It is concluded that the hymenolepid recovered from Irish A. sylvaticus differs sufficiently from H. diminuta to warrant species status and that it has adapted to the alimentary canal of A. sylvaticus . This cestode material is described under the name of H. hibernia sp. nov.     

The effect of ocean acidification on symbiont photorespiration and productivity in Acropora formosa

Ocean acidification is expected to lower the net accretion of coral reefs yet little is known about its effect on coral photophysiology. This study investigated the effect of increasing CO₂ on photosynthetic capacity and photoprotection in Acropora formosa. The photoprotective role of photorespiration within dinoflagellates (genus Symbiodinium) has largely been overlooked due to focus on the presence of a carbon‐concentrating mechanism despite the evolutionary persistence of a Form II Rubisco. The photorespiratory fixation of oxygen produces phosphoglycolate that would otherwise inhibit carbon fixation though the Calvin cycle if it were not converted to glycolate by phosphoglycolate phosphatase (PGPase). Glycolate is then either excreted or dealt with by enzymes in the photorespiratory glycolate and/or glycerate pathways adding to the pool of carbon fixed in photosynthesis. We found that CO₂ enrichment led to enhanced photoacclimation (increased chlorophyll a per cell) to the subsaturating light levels. Light‐enhanced dark respiration per cell and xanthophyll de‐epoxidation increased, with resultant decreases in photosynthetic capacity (P_nmax) per chlorophyll. The conservative CO₂ emission scenario (A1B; 600–790 ppm) led to a 38% increase in the P_nmax per cell whereas the ‘business‐as‐usual’ scenario (A1F1; 1160–1500 ppm) led to a 45% reduction in PGPase expression and no change in P_nmax per cell. These findings support an important functional role for PGPase in dinoflagellates that is potentially compromised under CO₂ enrichment.