Evolutionary patterns in tropical marine reef fish feeding

The majority of tropical reef fishes are acanthopterygians. Most of them are percomorphs and thus are likely monophyletic. In accordance to modern systematics, the primitive types among the latter are large-mouthed suction feeders. Species from advanced families often have biting oral jaws with a reduced number and complexly shaped teeth. Mouth sizes decrease from the primitive towards the advanced reef fishes when ranked according to increasing family numbers (Nelson 1984). To create a functional resource axis, Randall's (1967) and Hobson's (1974) data on tropical reef fish feeding were re-interpreted by ranking food items from mobile to sessile prey. The primitive paracantho pterygian and acanthopterygian reef fishes are large-mouthed, suction-feeding predators on mobile prey. Most of the advanced, small-mouthed species are browsers and grazers, but often feed on mobile prey too. Obligatory specialists (monophagous and unable to switch) seem to be relatively rare among modern reef fishes. The trends stated above indicate a wealth of parallel developments in many advanced families of reef fishes towards small, often biting oral jaws. This parallelism may be the result of comparable regimes of selection pressures in reefs and of the need for newly evolved species to establish themselves within the already existing guilds.     

On adaptation, the assessment of adaptations, and the value of adaptive arguments in phylogenetic reconstruction

Evolutionary adaptation concerns a relative concept and the study of adaptations is directed to structures of individuals. The concept is devoid of any meaning when it is applied to species or populations. Adaptation is not synonymous with fitness or survival but does contribute to both of them. The term adaptation has a dual meaning since it refers both to the process of adaptation and to the state of being adapted. In the process of adaptation the mechanism of natural selection takes a prominent position. But the operation and effectiveness of natural selection are constrained by various limiting factors. Besides that, features may also be the result of nonadaptive evolution and only attain their present adaptive function at a later point in time. Another possibility is that features have at present a function different from the one for which they were initially designed. With respect to the state of being, the study of adaptation attempts to examine whether a particular feature indeed forms an adequate response to selection forces from the environment. Five methods or approaches generally are used to assess the adaptive significance of features, viz. the comparative, correlation, optimization, cladistic, and synthetic approach. Only the last-mentioned approach forms an adequate method since it attempts to establish, by direct analysis, which well-defined selection force exerts its influence on a certain character. The practicing taxonomist is faced with the problem that the data necessary to apply the synthetic method, generally require detailed field studies. Not all evolutionary changes are under the influence of natural selection. The presence of some features may be based on entirely different mechanisms, such as genetic drift, mutational pressure, pleiotropic gene action, allometric growth, or ecophenotypic responses. Various problems inherent to the optimization approach, and several others of practical and theoretical nature, make the morphocline method of the functional and evolutionary morphologists unsuitable as a method for phylogenetic reconstruction.     

Grassland structure in native pastures: links to soil surface condition

Summary When grassland is grazed by livestock, the structure of the sward changes in a patchy manner. With continuous selective grazing there is a mosaic of short and tall patches but as grazing intensifies the area of short‐grazed patch increases until the paddock has a lawn‐like appearance. This mosaic of patch structures can be stable, as short patches tend to attract repeated grazing and tall patches tend to be avoided. Because heavy grazing can detrimentally affect soil and water functions in grassland (ultimately resulting in erosion), we aimed to assess how well the physical structure of the sward reflects soil surface condition. We described four grassland patch structures that were assumed to reflect different levels of present grazing, and to some extent, past grazing pressure. We assessed patch structure and two other grass‐related variables (basal area of a ‘large tussock’ functional group and basal area of all perennial grass) as possible indicators of soil surface condition. Three indices of condition were measured in the field. The infiltration and nutrient cycling index declined progressively across patch structures, consistent with increasing grazing pressure. The stability index was found to be reduced only for the most heavily grazed grass structure (short patches). We found the ‘large tussock’ grass functional group to be a more sensitive indicator of soil surface condition than the group consisting of all perennial grasses. We found no evidence of sudden soil surface condition decline beyond a certain level of grass basal area, that is, there was no evidence of thresholds, rather, incremental loss of condition accompanied grass decline. We are thus not able to further refine an earlier proposed management recommendation ‘Graze conservatively to maintain dominance of large and medium tussock grasses over 60–70% of the native pastures’, except to suggest the use of short patches as a more practical indicator, rephrasing the recommendation as ‘Graze conservatively to allow a maximum of 30% short‐grazed patches in native pastures’.     

BIOSYNTHESIS OF SMALL MOLECULES IN CHLOROPLASTS OF HIGHER PLANTS

1. Chloroplasts of higher plants contain enzymes which permit them to synthesize many kinds of small molecules in addition to carbohydrates. 2. Either aqueous or non-aqueous techniques may be used to isolate chloroplasts. Aqueous methods permit the isolation of chloroplasts showing high rates of photosynthesis; the organelles can be purified by means of density gradients. Non-aqueously isolated chloroplasts cannot photosynthesize, but show good retention of low-molecular-weight substances and soluble enzymes. 3. Whole cells photoassimilating ¹⁴CO₂ show considerable formation of ¹⁴C-labelled amino acids and lipids, but isolated chloroplasts exhibit very poor synthesis of amino acids and lipids from ¹⁴CO₂. 4. Chloroplasts play an important rôle in reducing nitrate to ammonia. There is controversy about the presence in chloroplasts of nitrate reductase and about the mechanism of the light-dependent reduction of nitrate to nitrite; however, it is generally agreed that non-cyclic electron transport directly supports reduction of nitrite to ammonia via a chloroplastic nitrite reductase. 5. Chloroplasts actively assimilate inorganic nitrogen into amino acids. The assimilation reaction is either the reductive amination of α-ketoglutarate to glutamate or the ATP-dependent conversion of glutamate to glutamine. The enzyme glutamate synthase has recently been found to be present in chloroplasts and may play an important function in nitrogen assimilation. 6. Numerous transaminases (aminotransferases) are present in chloroplasts. 7. The source of α-keto-acid precursors of chloroplastic amino acids is unknown. It remains to be established whether chloroplasts import the required keto acids or whether some of them might be generated via an incomplete tricarboxylic-acid cycle located in the chloroplast. 8. Chloroplasts contain characteristically high levels of mono and digalactosyl diglycerides, sulpholipid and phosphatidyl glycerol. They also have large amounts of polyunsaturated fatty acids. 9. Fatty acids are synthesized by the concerted action of fatty-acid synthetase, elongases and desaturases. Two pathways have been implicated for the formation of α-linolenic acid. 10. The galactosyldiglycerides are synthesized by successive galactosylation of diglyceride. The enzymes responsible are probably located in the chloroplastic envelope. 11. The other major chloroplastic acyl lipids (sulpholipid, phosphatidylglycerol and phosphatidylcholine) have not been, as yet, synthesized de novo by means of isolated chloroplast fractions. However, indirect evidence indicates that the first two are probably formed there. 12. Chlorophyllide synthesis involves the formation of δ-aminolaevulinic acid (δALA) followed by conversion of δALA to protoporphyrin IX, which is then transformed into protochlorophyll. 13. Recent evidence favours the view that δALA synthesis is not mediated by δALA synthetase but by another pathway in which δALA can be derived from α-ketoglutarate or glutamate. It has not been established whether this pathway is localized in plastids. 14. Conversion of δALA to protoporphyrin IX is mediated by soluble enzymes of the plastid stroma. Membrane-bound enzymes mediate the conversion of protoporphyrin to protochlorophyll. 15. Carotenoids are synthesized from acetyl C_oA via geranylgeranyl-pyrophosphate and phytoene intermediates. Evidence has been obtained for both neurosporene and lycopene as precursors of the cyclic carotenoids. 16. The overall pathway of carotenoid formation is subject to photoregulation, particularly during the development of the chloroplast. 17. Carotenes are precursors of xanthophylls, the inserted oxygen being derived from molecular oxygen. 18. Chloroplasts may synthesize or interconvert gibberellin hormones.     

Taxonomy and phylogenetics: Some considerations

The relationships between taxonomy and phylogenetics are discussed. It is suggested that they are distinct biological subdisciplines and some consequences of this position are set out.     

Trends in the Evolution of Passively Dispersing Insects and the Feed-back Control in Phylogenesis

In each definite habitat the environmental conditions may change to a degree exceeding the degree of ecological plasticity of the given species; in such cases the population either must become extinct or its representatives must migrate to some new habitats. The lower its ecological plasticity, the greater is the significance of dispersal for the species. Dispersal may be active or passive. In active dispersal the possibility and probability for representatives of population to encounter suitable conditions depend on the perfection of their locomotory organs, organs of orientation in space and on capacity for energy production. Active dispersal requires high differentiation of organs and is consequently performed by the definitive stage of development. In passive dispersal (anemochory, phoresy etc.) the possibility to meet with favourable conditions is ruled out by the laws of random distribution. Therefore, for passively transported species, highest numbers of disseminating individuals and their smallest mass are advantageous. Consequently passive dispersal is performed, 1s a rule, by juvenile stages, whereas for the adults of the passively dispersing species, high sexual production is characteristic, connected with general degeneration of the organs of active life. For Insecta-Pterygota active dispersal by flight is typical. The appearance of adult Pterygota is that of the dispersing organism. The main functions of the adult stage in Pterygota are dispersal and reproduction, whereas those of the larva are feeding and growth. Only the function of active dispersal determines the progressive evolution of the imago in insects. Functions of dispersal and propagation approach each other in the time but the period of dispersal precedes that of reproduction. The wide separation of these functions in time leads to the regressive changes in adult females. Passing of the function of dispersal from the adult stage to passively disseminating larvae leads to regressive changes in the course of ontogenesis and to features of degeneration in adult females. In rather rare instances of passive dispersal of imagines additional means of propagation are developed (parthenogenesis, paedogenesis, polyembryony). Even in those groups of Pterygota where the females are highly degenerate the males do not exhibit any regression in locomotory and sense organs, still being able to fly. This is connected with the role of sexual reproduction for the persistence of characters, of genes. In the same manner as dispersal is a necessary condition for getting individuals of the species into appropriate environment, amphimixis is the premise for every gene, for each character, to meet with a favourable genetic environment. Sexual differences of adult insects reflect the phenotypic differences of gametes. Males ensure the encounter of sexes. Movements of pairing adults are of the same significance for the further persistence of genes, of characters, as the active dispersal flight of insect females is for the survival of individuals, for persistence of the species. Independent movements of spermatozoa in mating animals (especially in those with internal insemination) are of the same importance for genes dispersal as the crawling of first instar larvae (corrective movements) in actively (by flight) dispersing alate insects in the dispersal of a species.     

Some properties of pelargonium flower-break virus

A virus obtained from pelargonium cvs Irene and Paul Crampel appears to differ from any previously reported; although symptomless in most pelargonium cvs tested, it caused colour break in the flowers of two seedling clones. It seems uncommon in pelargoniums. The virus was readily transmitted by inoculation of sap, but not by Myzus persicae with short feeds, by dodder or through seed. It infected only fifteen of 100 species tested in six of thirty-five plant families. Pelargoniums were freed from the virus by heat-treatment. The virus remained infective after 10 min at 85 ^oC, 3 wk at 20 ^oC or 27 wk at 2 ^oC; it was infective at 1/500000 dilution of Nicotiana clevelandii or Chenopodium quinoa sap. Purified preparations were readily made by several methods, and contained isometric particles c. 30 nm diameter. Although a good antigen, the virus was serologically unrelated to any of forty-two isometric viruses. In immunoelectrophoresis, the virus moved as a single antigenic component towards the cathode. It gave a single, specific zone in density-gradient centrifugation, and one moving component (s⁰_{20 w}= 125 S) in analytical centrifugation. The virus contained one protein of mol. wt. c. 41000. The present cryptogram of the virus is (R)/*: */*:S/S:S/*, and the name pelargonium flower-break virus is proposed.     

Investigations on fungicides: XV. The fungitoxicity and systemic antifungal activity of N-(2, 2, 2-trichloro-1-methoxyethyl) formamide and related compounds

The direct and systemic antifungal activity of 100 compounds structurally related to iV-(2, 2, 2-trichloro-i-methoxyethyl)formamide has been measured. Some of the compounds showed either protectant or systemic activity against powdery mildew fungi. Compounds not possessing a terminal formamido group showed little anti-mildew activity and for good systemic activity an alkyloxy or alkylamino side-chain in the molecule appeared to be necessary.     

Comparison of the size selectivity of diamond (PA) and square (PE) mesh codends for deepwater crustacean species in the Antalya Bay, eastern Mediterranean

The aim of this study was to compare selectivity results of currently used 44 mm nominal polyamide (PA) diamond mesh- and alternatively suggested 40 mm nominal polyethylene (PE) square mesh- codends in the deepwater crustacean trawl fishery in the Antalya Bay, eastern Mediterranean. Selectivity experiments were carried out during targeted trawling of four commonly harvested crustacean species: giant red shrimp Aristaeomorpha foliacea , 'blue and red' shrimp Aristeus antennatus , rose shrimp Parapenaeus longirostris , and pandalid shrimp Plesionika martia . A conventional bottom trawl of 600 meshes around the fishing circle was operated onboard a commercial stern trawler between 6 and 18 June 2007. Depth of the fishing area varied between 441 and 630 m. Data were collected using the covered codend technique, and analyzed using a logistic equation with maximum likelihood for individual and pooled hauls. The commercially used trawl codend was unable to release immature crustaceans. Selectivity parameters of the three species of crustaceans were distinctly lower when collected with the polyamide diamond mesh than with the polyethylene square mesh, except in the case of giant red shrimp for which values were similar. However, the present and previous results show that in square mesh codends, mesh sizes must be more than 40 mm in order to keep catches clear of specimens below minimum landing sizes or 50% sexual maturity sizes of crustaceans in the Mediterranean. This study suggests that regulating mesh size by requiring square mesh openings during deep water crustacean trawling of the eastern Mediterranean is essential for the release of immature individuals.     

THE EFFECTS OF SODIUM CHLORIDE ON HIGHER PLANTS

(1) This review concentrates on the effect of sodium chloride on the growth of higher plants, being primarily concerned with relatively high concentrations i.e. 50 mmol 1^-1 and above, though something is also said about those instances when sodium acts as a micronutrient. Emphasis is placed on particular species or genera for which enough information is available to discuss possible mechanisms. (2) Trace amounts of sodium are required for the growth of plants using the C₄ pathway of carbon fixation and may also be important in plants with Crassulacean acid metabolism. (3) The increased growth of Beta vulgaris brought about by sodium chloride can in part be explained by a sparing effect on potassium. However, growth is still increased when sufficient potassium is available. Complementary studies with rubidium indicate that the hormone balance in the plant may be changed. Sodium chloride also increases the level of sucrose in storage roots and allows beet plants to withstand water stress more readily, possibly by increased turgor pressure. (4) Sodium chloride increases production of dry matter in C₄ species of Atriplex under conditions of low relative humidity because water loss is reduced and photo-synthesis hardly affected. (5) Succulence in many plants is stimulated by salinity. The essential basis of the phenomenon is an increased water potential gradient between the leaf and the external medium. In some instances, it is the accumulation of chloride which is important; in others it is the accumulation of cations, when potassium can be as effective as sodium. (6) Salinity reduces the final area achieved by growing leaves. Most of the studies have been made on Phaseolus vulgaris and an important early event is the reduction in the rate of expansion of the epidermal cells and this may be accompanied by a decrease in their number. Reduction of epidermal cell size is a result of water stress; sodium chloride may directly affect cell division, though water stress cannot be ruled out. Whether salinity brings about inhibition of cell division depends upon the calcium content of the medium – a high content is accompanied solely by a reduction in epidermal cell size. (7) Hormones, as yet unspecified, may play an important part in response of a growing leaf to salinity. However, there is no evidence that sodium chloride per se has an effect on hormone balance within the plant. So far, any measured changes in levels of specific hormones can be ascribed to the osmotic effects of the saline medium. (8) Two estimates by flux analysis of cytoplasmic concentration of sodium in plants growing in conditions of high salinity give a value of around 150 mmol 1^-1. There is no similar information for chloride. Other techniques (histochemistry and X-ray micro-probe analysis) give questionable information. (9) There is now extensive information to show that enzymes of halophytes (other than ATPases) do not differ significantly from those of other higher plants with respect to their sensitivity in vitro to sodium chloride. There is a need for further work with respect to the activity of enzymes in the presence of those metabolites which have the highest cytoplasmic concentration. (10) Sodium-stimulated ATPases have been isolated from plant cells but their distribution amongst higher plants is restricted. (11) There are a number of reports of changed metabolism brought about by saline treatments but it is not clear how far the effects of sodium chloride and water stress are confounded. (12) Sodium appears to increase the sucrose levels in sugar beet by an inhibitory effect on product starch-granule-bound ADP-glucose starch synthase. (13) Reversal of a sodium pump located at the plasmalemma might have an effect on cell turgor. (14) Sodium (like other monovalent cations) causes loss of materials from plant cells, possibly through an effect on carrier proteins; calcium prevents this from happening. Calcium also allows plants to grow better in saline conditions by a depression of sodium uptake by and transport within the plant. The properties and composition of the membranes of mesophytes and halophytes need to be compared. (15) A saline medium exerts a major effect on plant growth through water stress to which a halophyte must adapt. As well as this, the cytoplasmic concentration of sodium chloride must be kept lower than the total cellular concentration of the salt. Unless this happens, it is likely that enzymic activity will be reduced due, in some instances, to an unspecific effect of a high concentration of monovalent cations and/or chloride and in other instances to competition between sodium and other cations, specifically potassium, for activation sites on enzymes, e.g. pyruvate kinase. (16) Further work is required to separate the osmotic effects from the specific effect of sodium chloride after it has entered the plant. As well as this, it has become clear that more information is needed about the mineral nutrition of halophytes.