Effects of emergence phenology, taxa tolerances and taxonomic resolution on the use of the Chironomid Pupal Exuvial Technique in river biomonitoring

1. We studied chironomid communities of four rivers in south‐eastern Finland, differing in their water quality, during summer 2004 using the Chironomid Pupal Exuvial Technique, CPET. The aims of the study were to (i) test the adequacy of the generic‐level identification in the CPET method, (ii) define the emergence patterns of chironomid taxa classified as intolerant to organic pollution, (iii) assess the tolerance levels of intolerant chironomids and (iv) identify taxa most indicative of good water quality. 2. Procrustean rotation analysis indicated very strong concordance between the ordinations using either species or genus‐level data, suggesting that generic‐level identification of chironomids is adequate for biomonitoring based on CPET. However, when only a few taxa occur in great numbers, it may be advisable to identify these to the species level, especially if these taxa are important indicators of the impact in question. 3. The detection of a particular species may require accurate timing of sampling, whereas a species‐rich genus might be detected throughout a season. Given that the emergence of chironomid species may vary from year‐to‐year and between sampling sites, community differences detected at the species level may be related to between‐site variation in species’ emergence patterns rather than true differences in species composition. 4. Indicator species analysis (IndVal) showed that the distribution and abundance of intolerant chironomid taxa differed strongly among the studied rivers. Some of the intolerant taxa were restricted to unimpacted conditions, whereas others occurred mainly in impacted rivers. Thus, the indicator status of some genera (e.g. Eukiefferiella, Parametriocnemus, Stempellinella and Tvetenia) needs reassessment.     

Occurrence of Multiple Forms of {alpha}-Amylase and Absence of Starch Phosphorylase in Soya Bean Seeds

Soya bean cultivars ‘Altona’ and ‘Chestnut’have active but quite low levels of -amylase. Activity was assayedwith specific substrates, oxidized amylose and ß-limitdextrin, which were resistant to attack by ß-amylase.During seed development -amylase activity increased to a maximumin both cultivars and then declined towards maturity. Matureand germinating seeds retain low activities of -amylase. Gelelectrophoresis separated the -amylase activity into six majorbands which occurred in both cultivars. The isozyme patternwas quite similar for developing, mature and germinating seed.although the relative proportion of activity in the variousbands changed somewhat. Starch phosphorylase was not detectedin any soya bean seed samples tested, but good activity wasfound in potato tuber extracts used as a control. Mixing experimentsusing soya bean and potato extracts indicated there were noinhibiting factors in soya bean seed extracts. Soya bean seedextracts probably do not contain starch phosphorylase. Glycine max (L.), Merr, soya bean, -amylase, isozymes, phosphorylase     

Starch Deposition and Carbohydrase Activities in Developing and Germinating Soya Bean Seeds

Immature soya bean seeds accumulate starch as a transient reservematerial which is utilized later in development. Germinatingseeds also accumulate starch reserves, probably as a resultof gluconeogenesis from storage lipid. Developing beans showa rapid increase in ß-amylase activity which continuesinto early germination before declining. Distribution of ß-amylaseactivity is not consistent with its supposed role in starchdegradation. Soya bean seeds also contain -amylase and -glucosidaseactivities which could be responsible for starch mobilization. Glycine max (L.) Merr., soya bean, starch, carbohydrase, amylase, -glucosidase     

Seed Maturation in Soybeans (Glycine max L. Merr.) is Independent of Seed Mass and of the Parent Plant, Yet is Necessary for Production of Viable Seeds

Freshly harvested seeds of soybean (Glycine max L. Merr.) orseeds shelled, then dried, were non-viable. Seeds dried in intactpods, even when only 17% of normal size, matured into viableseeds and produced healthy plants. These seeds maintained activityof various enzymes but gained little soluble protein while air-dryingin intact pods. There was a qualitative change in seed proteinsassociated with maturation. Seeds matured in intact pods havea greater proportion of protein as slow-moving bands and havecompletely lost one fast-moving band compared with seeds shelledbefore drying. Seed maturation is a distinct phase of seed production,is independent of the parent plant, and can be imposed on theseed at many stages of development.     

Impact of leaf damage on growth of mountain birch shoots

Canopies of heterophyllous trees expand by production of long shoots. We have previously shown in mountain birch ( Betula pubescens ssp. czerepanovii ) that damage to internode leaves within long shoots does not impede shoot growth, indicating that long-shoot elongation occurs by means of external resources. To study to what extent leaves other than true long-shoot leaves are necessary for the normal growth of mountain birch long shoots, we simulated herbivore damage to the two basal leaves of shoots (which flush simultaneously with short-shoot leaves) and the short-shoot leaves nearest to the long shoot within the branch. Damage to the two basal long-shoot leaves significantly reduced long-shoot growth. Additional damage to short-shoot leaves, situated proximally to the long shoot, did not retard long-shoot growth any more than damage to basal leaves alone. To determine the extent to which short-shoot leaves within a large branch are responsible for the pooled long-shoot production of the branch, we clipped differing proportions of short-shoot leaves from such branches. We found small but significant reduction in the pooled length of the long shoots of the branch, presumably indicating a limited role in long-shoot elongation of current photosynthates within the branch. Our experiments indicate that long shoots are not independent modular units in their carbon economy.     

Systematic within-tree variation in mountain birch leaf quality for a geometrid, Epirrita autumnata

Abstract.

• 1 We studied within-tree variation in leaf quality of the mountain birch, Betula pubescens ssp. tortuosa, for larvae of the autumnal moth, Epirrita autumnata.
• 2 The purpose of the study was to determine the possible occurrence of systematic differences in larval growth on short shoot leaves (i.e. leaves of the same age): among leaves facing in different compass directions, between leaves of lower and upper branches, among leaves on different positions within a branch and among leaves of different sizes within a short shoot. We also measured larval growth between short shoot and long shoot leaves (i.e. between leaves of different age).
• 3 The larvae grew best on leaves on the north side of trees and most poorly on south side leaves, the east and west sides being intermediate. Leaves from the upper branches supported larval growth better than leaves from the lower ones. The larvae grew better on the smallest leaf of each short shoot and were able to utilize it more efficiently than the two larger leaves. Short shoot leaves from the basal and middle parts of the upper branches of the trees were of better quality for the larvae than short shoot leaves from the tip part of the branches. The larval growth rate did not differ between short shoot and long shoot leaves. In general, within-tree variation in the larval growth rate was lower than variation among different trees.
• 4 Damage to leaves can decrease leaf quality for herbivores in the same year (rapidly inducible responses) or the following year(s) (delayed inducible responses). Our results show that systematic within-tree variation in larval growth can be as great as the effects of rapidly inducible responses and that variation among individual trees can be as great as the mean effects of delayed inducible responses.

     

Moisture Loss as a Prerequisite for Seedling Growth in Soybean Seeds (Glycine max L. Merr.)

Rosenberg, L. A. and Rinne, R. W. 1986. Moisture loss as a prerequisitefor seedling growth in soybeanseeds (Glycine max L. Merr.).—J.exp. Bot. 37: 1663–1674. As soybean seeds [Glycine max (L.) Merr.] develop, they undergoa change in seed moisture. When excised prematurely from thepod and planted, seeds do not exhibit seedling growth until63 d after flowering (DAF) when the seed moisture has fallenbelow 60%. In contrast, seed germination (radicle protrusion)can occur when seeds as young as 35 DAF (68–79% moisture)are excised, but this germination docs not lead to comparableseedling growth frequencies unless seeds are first given a moistureloss treatment to artificially reduce their moisture below 60%.A moisture loss treatment applied at 35 DAF thus enables seedto undergo the transition from germination (cell expansion)to seedling growth (cell division and expansion) to the extentthat treated immature seed have a vigour index comparable toseeds matured on the plant (100%). The pattern of protein synthesisin vivo was examined in 35 DAF seed using [³⁵S]-methionine incorporation.When moisture loss treatment was applied for 24 h to 35 DAFseeds, seeds synthesized several new polypeptides when comparedwith untreated seeds at the same developmental stage. The sameseed samples showed 0% seedling growth in the absence of moistureloss treatment and 80% seedling growth when the treatment hadbeen applied. Moisture loss from soybean seeds appears to bea prerequisite for the synthesis of new proteins which may bepart of the metabolic process or processes that allow the soybeanseed to undergo the transition from seed germination to seedlinggrowth. Key words: Moisture loss, germination/growth, soybean     

Changes in Seed Constituents During Germination and Seedling Growth of Precociously Matured Soybean Seeds(Glycine max)

During 7 d of precocious maturation of soybean seed (Glycinemax), the starch content declined and soluble sugar levels increasedin patterns similar to natural seed dehydration and maturation.Total seed protein content and total seed dry weight increasedwhereas oil content remained relatively unchanged. Overall,the proportions of the constituents in precociously maturedseeds were comparable to naturally mature seeds. Precociouslymatured soybean seeds showed much the same germination and seedlinggrowth frequency patterns as naturally matured seeds. Duringgermination and seedling growth of precociously matured seeds,starch, soluble sugar, protein and oil levels followed patternssimilar to naturally mature, germinating seeds and seedlings.Therefore, precocious maturation may be used as a model systemto investigate the control of the physiological and biochemicalevents occurring during seed maturation which lead to germinationand subsequently, seedling growth. Glycine max (L.) Merr., soybean, cotyledons, maturation, germination/seedling growth     

Experimental tests of the role of predation in the population dynamics of voles and lemmings

• 1 Reasons for fluctuating populations of small mammals have been intensively investigated since the early days of modern ecology. Particular interest has been taken in vole populations exhibiting multiannual oscillations. Much empirical and theoretical work has been accomplished to find out the key factor(s) driving these population cycles and many reviews have been written about the results.
• 2 One of the most plausible processes for explaining regular fluctuations in small mammals is predation. Here I review the existing literature on the experimental studies of the role of predation in vole population dynamics in the hope that a critical examination of these studies will help researchers improve the design of future experiments.
• 3 Most predation manipulations have been done in exclosures, but there are also studies that have attempted to reduce or increase predator numbers in non‐fenced areas, islands and enclosures.
• 4 As the number of experimental studies has increased, their quality in terms of replication, use of controls and realistic spatial and temporal scales has also improved.
• 5 Most studies have found population‐level effects of predator manipulations on prey populations. The effects have varied from very weak to very strong, reflecting dissimilar experimental designs and the great variety of predator–prey interactions among different kinds of species in different landscapes. Most of these studies show that predation limits population growth of voles, and in some circumstances even regulate vole population fluctuations, but none of them clearly demonstrates that predation consistently changes fluctuation patterns of voles.
• 6 To be able to assess more reliably the true role of predation on (cyclic) population fluctuations of voles, more competent experiments are still needed not only over the geographical range of cyclic population dynamics, but also in areas of weakly or non‐cyclic populations of voles.