Inter- and intra-specific differences in the number of larval instars in British populations of 24 species of stoneflies (Plecoptera)

1. Ontogenetic changes during the life cycle of aquatic insects are important not only in life‐history studies but also in evaluating food‐web structure. They require information on the growth and number of larval instars but such information is lacking for many species, including Plecoptera. Therefore, the chief objectives of the present study were to determine inter‐ and intra‐specific differences in the number of larval instars in British populations of 24 species of stoneflies, to test Dyar’s hypothesis that growth followed a geometric progression, and to synthesise this information with previously published values for four British species. 2. Larvae were reared at constant temperatures in the laboratory from eggs from 63 populations (one to six populations per species). First instars from each population were divided into three batches and each batch was reared at one of three constant temperatures. For each species, the rearing temperature and source population had no significant effect on the mean size of each larval instar. 3. The relationship between the geometric mean length of each instar and instar number was well described by an exponential equation (P < 0.001, r² > 0.9 for all species), thus supporting Dyar’s hypothesis. Only one species, Brachyptera risi, had the same number of instars for males and females (12–13). For the other 15 herbivorous species and the four smaller carnivorous ones, the number of instars was higher for females than males (range 11–16 for males, 12–17 for females). The larger size of the females was due to their additional instars, not a sex difference in growth rates. In contrast, there was a clear growth separation of the sexes after the 9th or 10th instar for the four largest carnivores. The number of larval instars was highest for these four species (range 16–19 for males, 18–23 for females), and females were much larger than males. 4. A multiple regression equation with data from the present and previous studies (n = 27) showed that variability in the mean length of the first instar and the maximum number of larval instars for each species accounted for 88% and 91% of the variability in the mean length of the final instar for males and females, respectively. 5. Values for Plecoptera in other countries were in general agreement with those in the present study, especially in the same families. Two old, but widely quoted, high values are doubtful. The present study and four previous ones provide a sound basis for ontogenetic studies on 28 species of Plecoptera and their role in aquatic ecosystems.     

Hatching time and growth of Nemurellapictetii (Plecoptera: Nemouridae) in the laboratory and a Lake District stream

SUMMARY. 1. Nemurella pictetii Klapæplek took 2 years to complete its life cycle in both the laboratory and a small stream in the English Lake District.
2. Hatching time (days after oviposition for 10%. 50% and 90% of the eggs to hatch) and hatching period (days between dates for 10% and 90% hatched) decreased with increasing water temperature in the laboratory, and the relationships were well described by a power-law. Estimates of the mean time for 50% hatching in the stream varied between 16 and 31 days after oviposition. depending on temperature.
3. Larval instars numbered fifteen for males and seventeen for females with a constant ratio of 1.18 between successive instars (conformed with Dyar's rule). Larval growth was exponential at four constant temperatures in the laboratory; mean instantaneous growth rates were 0.40±0.01% day⁻¹ at 5.9°C, 0.43±0.01% day⁻¹ at 8.2°C, 0.46±0.01% day⁻¹ at 12. 1°C. 0.56±0.02%day⁻¹ at 19.8°C. No larvae survived after instar XI at 19.8°C.
4. Larval growth was exponential in the stream and was scarcely affected by variations in water temperature (range 4.2 -14.0°C); mean growth rates for three year-classes were 0.41±0.02, 0.43±0.08, 0.54±0.05% day⁻¹. Their similarity to laboratory growth rates under optimum conditions suggests that the availability of resources, such as food and space, was not restricting growth in the stream.     

Molecular Mechanisms of Signal Integration in Hypothalamic Neurons

SYNOPSIS. The purpose of this paper is to describe our studiesfocused on the mechanisms by which hypothalamic neurons processmultiple signals and produce an integrated response. We illustrateour research strategy by reviewing our work on two separateneural systems: the hypothalamic paraventricular nucleus (PVN)and the suprachiasmatic nucleus (SCN). We have focused on differentpeptidergic subpopulations within these nuclei to address twoissues. In the PVN, we concentrate on thepopulation of neuronscontaining thyrotropin-releasing hormone (TRH). These neuronsare inhibited by thyroid hormones, but activated by cold exposure.Using a molecular approach, we have demonstrated that theseconflictingsignals simultaneously act on the same population of TRH neurons.This system will continue to be a productive model to studythe mechanisms by which neurons process multiple signals. Inthe SCN, we concentrate on the population of neurons containingvasoactive intestinal peptide (VIP), peptide histidine isoleucine(PHI) and gastrin releasingpeptide (GRP). We have demonstratedthat injection of all three peptides into the SCN of hamstersmimics the phase-delaying effects of light on circadian wheelrunning behavior. In addition, the genes encoding these peptidesexhibit different 24-hour profiles of changes in neurons ofthe SCN. These data support the hypothesis that one mechanismby which these neurons produce an integrated response is bychanging the concentration ratio of co-released peptides.