Bibliothek

Notizen: We studied reproductive traits in nine anadromous brown trout, Salmo trutta L., populations in seven Norwegian rivers. Within populations we found a positive significant correlation between fish length and fecundity in all populations, and between fish length and egg diameter in five populations. There were significant differences in these relationships between populations from different rivers, and between populations from different locations within rivers. When adjusted for variation in fish length, mean fecundity and mean egg diameter showed a negative significant correlation among populations. The ratio of gonadal weight to somatic weight (gonadosomatic index) varied significantly among populations but was not associated with variation in fish length. Comparatively few large eggs were found in brown trout populations co-existing with several other fish species.

Notizen: SUMMARY. The composition of bulk (wet and dry) precipitation in 1975 and 1976 was similar to that found 22 years previously. In 1975, mean values for nine precipitation samplers at one site (Wraymires) ranged from pH 4.3 to 4.5; similar values were obtained in 1976. Samplers covered with fine-mesh plastic gauze caught substantially more Ca2+ and K+ than open samplers, but pH and SO2-4+ NO3- concentrations were similar in open and covered samplers. In precipitation, c. 50% of H+ was balanced by NO3- and c. 50% by SOi; 80% of the SO2-4 was balanced by Ca2+ and Mg2+.Conccntrations of major cations (H+, Na+, K+,Ca2+, Mg2+) and anions (CI-, NO3- SO2-4 and alkalinity [Alk—largely HCO3-]) in upland water- bodies were similar to those found in precipitation, but pH levels were generally higher and above 6.0 m some tarns. At lower altitudes, on base-rich roeks and soils, Ca2+ and Alk become dominant. Results of a survey of lakes and tarns in 1974–78 are compared with a survey in 1953–56 and published data (chiefly for pH and Alk) for 1947–50, 1932 and 1928. Comparisons are also made with other measurements of Alk in three productive lakes (Blelham Tarn, Esthwaite Water and Windermere) for 1936–39 and 1945–80. Winter levels of NO3-N, PO4-P and Si are given for these lakes; although the first two have increased during the late 1960s and the 1970s there has been no significant change in the last. NO3- and probably some SO2-4. In productive lakes a substantial (c. 50%) rise in mean Alk occurred during the late 1960s and the 1970s, possibly related to increased winter levels of NO3-N and PO4-P derived from sewage and fertilizers. In this period the maximum pH levels reached in summer were notably high, sometimes exceeding pH 10. The rise in Alk, conductivity and pH of surface waters is influenced by climatic factors (a decade of drier years), sewage input and biological productivity within the lakes.Considerable seasonal fluctuations in the concentrations of major ions, a characteristic feature of surface waters in the English Lake District, are illustrated and some implications for cation-anion balance briefly discussed. Mid-winter concentrations are usually high forNa+, K+, Cl-. NO3-and low for Ca2+, Mg2+, Alk. SO2-4.Alkalinity. pH and conductivity of Lake District tarns and lakes show no signs of acidification during the period 1928–80. On the contrary, productive lakes have become more alkaline and some unproductive low-alkalinity (〈 100 μ-equiv. 1-1) lakes also show signs of alkalization, with increased mean concentrations of Na+. Ca2+ and Mg2+, balanced by Alk.

Notizen: SUMMARY. 1. The factors influencing the seasonal and inter-annual variations in the numbers of Daphnia hyalina in Esthwaite Water between 1956 and 1972 are analysed. Esthwaite Water has always been eutrophic. but the phosphorus and nitrogen loadings to the lake increased significantly in the mid 1960s.2. Qualitatively, the phytoplankton and zooplankton populations in the lake changed relatively little during the period of study. Quantitatively, however, eutrophic species of algae became more abundant and the numbers of Eudiaptomus declined as the numbers of Daphnia increased.3. The seasonal dynamics of the Daphnia was governed partly by the seasonal temperature cycle, and partly by the periodicity of edible algae. The birth rate of the Daphnia was constrained by temperature from January to April and from October to December. At other times their rate of increase was governed by the relative abundance of edible and inedible algae.4. Edible and inedible species of algae tended 10 appear in a recurring annual sequence. Diatoms such as Asterionella were abundant in the spring, the early summer phytoplankton was dominated by edible flagellates, but inedible algae such as Aphanizomenon and Microcystis become dominant later in the year.5. Daphnia could only reproduce in late summer when there were periodic regrowths of edible algae. Such regrowths were most likely to occur when there had been some entrainment of deep nutrients by episodic wind mixing. Calm weather encouraged the growth of blue-green algae that effectively‘blocked’the development of the Daphnia for the remainder of the summer.6. The factors that controlled the seasonal dynamics of the Daphnia also influenced the average number recorded in a particular year. The average number of Daphnia increased in the early sixties when Cryptomonas was abundant and decreased in the late sixties when blooms of Aphanizomenon appeared in mid summer. Detailed analyses showed that a similar increase in the numbers of Aphanizometion had occurred in the late fifties. The critical factor throughout was the prolonged period of calm resulting in stable stratification.7. This ‘weather’ effect was highlighted by comparing de-trended timeseries of Daphnia and Aphanizometion numbers with a simple measure of thermocline stability. De-trending removed the superimposed effects of progressive enrichment and revealed a 10-year cycle of thermocline stability that matched the temperature cycle recently reported in Windermere, These cycles are related to the movement of weather systems in the Atlantic so could change if the pattern of atmospheric circulation is altered by global warming.8. The possible effects of climate change on Daphnia dynamics are discussed in relation to the findings in Esthwaite Water.

Notizen: SUMMARY. 1. The abundance and species composition of the phytoplankton of Grasmere were monitored over a 12-year period following the commissioning of a small sewage treatment works, upstream of the lake.2. Although Grasmere has been subject to increased phosphorus-loading and has quickly developed many features associated with eutrophication, the composition of its plankton has retained the characteristics of a mesotrophic, soft-water lake: a vernal diatom maximum, generally dominated by Asterionella, is followed by summer growths of nanoplanktonic species, of various colonial Chlorophyceae, before a substantial return to Asterionella-dominance in the autumn. In cooler summers there have been episodes of renewed diatom growth. followed by truncated recapitulations of the essential summer sequence. Anabaena solitaria was relatively common in drier summers when dissolved inorganic nitrogen fell to low concentrations, although many of the ‘larger’ algal species associated with stratified eutrophic lakes (Aphanizomenon, Microcystis, Ceratium spp.) have failed to become abundant in Grasmere.3. Mean biomass levels (as indicated by chlorophyll concentration) have increased in response to the enrichment, though they do not conform well with most chlorophyll/phosphorus regression-models.4. The key factor resisting a more complete transition to a typical eutrophic plankton appears to be the efficiency of episodic flushing of the lake during periods of high fluvial discharge sustained by heavy rainfall over the extensive, mountainous catchment. The probabilities that these limnological conditions might fail to deter the development of ‘nuisance’ blooms are briefly assessed.

Notizen: Recent studies suggest that the nucleus pontis caudalis (nPontc) plays a role in patterning mastication through interactions with the adjacent lateral tegmentum. In this study, we used in vitro intracellular recording and staining to describe the basic membrane properties and morphology of nPontc neurones and to further explore interactions with adjacent structures, using coronal sections of the brainstem of 78 rats, aged 9–28 days. Neurones were large, with dendrites that spread in all directions, and about 64% fired tonically even in the absence of synaptic inputs. Tonic neurones were predominant in the centre of the nucleus. Electrical stimulation of all regions of the nPontc produced mixed excitatory and inhibitory effects on interneurones of lateral tegmental nuclei. Focal inactivation of the dorsal nPontc with injections of tetrodotoxin also had mixed effects on the spontaneous firing of both interneurones and motoneurones but similar injections in the ventral nPontc produced mostly increases of firing. Sixty-five percent of nPontc neurones received synaptic inputs from the lateral tegmental areas and most of these (68%) were excitatory and mediated by glutamatergic receptors. Inhibitory postsynaptic potentials were mediated by GABAA or glycinergic receptors. Although most responses occurred at relatively long latencies (〉 2 ms), they could follow relatively high-frequency stimulation (〉 50 Hz). Excitatory and inhibitory connections between ipsi- and contralateral nPontc neurones were also documented, which could contribute to bilateral coordination of jaw movements. This study provides evidence that the nPontc exerts both tonic and phasic influences on the premotor components of the masticatory central pattern generator.

Notizen: Primary afferent neurons innervating muscle spindles in jaw-closing muscles have cell bodies in the trigeminal mesencephalic nucleus (NVmes) that are electrically coupled and receive synapses. Each stem axon gives rise to a peripheral branch and a descending central branch. It was previously shown that some spikes generated by constant muscle stretch fail to enter the soma during fictive mastication. The present study examines whether the central axon is similarly controlled. These axons were functionally identified in anaesthetized and paralysed rabbits, and tonic afferent firing was elicited by muscle stretch. For the purpose of comparison, responses were recorded extracellularly both from the somatic region and from the central axon in the lateral brainstem. Two types of fictive masticatory movement patterns were induced by repetitive stimulation of the masticatory cortex and monitored from the trigeminal motor nucleus. Field potentials generated by spike-triggered averaging of action potentials from the spindle afferents were employed to determine their postsynaptic effects on jaw-closing motoneurons. Tonic firing of 32% NVmes units was inhibited during the jaw-opening phase, but spike frequency during closing was almost equal to the control rate during both types of fictive mastication. A similar inhibition occurred during opening in 83% of the units recorded along the central branch. However, firing frequency in these was significantly increased during closing in 94%, probably because of the addition of antidromic action potentials generated by presynaptic depolarization of terminals of the central branch. These additional spikes do not reach the soma, but do appear to excite motoneurons. The data also show that the duration and/or frequency of firing during the bursts varied from one pattern of fictive mastication to another. We conclude that the central axons of trigeminal muscle spindle afferents are functionally decoupled from their stem axons during the jaw-closing phase of mastication. During this phase, it appears that antidromic impulses in the central axons provide one of the inputs from the masticatory central pattern generator (CPG) to trigeminal motoneurons.

Notizen: The trigeminal principal sensory nucleus (NVsnpr) contains both trigemino-thalamic neurons and interneurons projecting to the reticular formation and brainstem motor nuclei. Here we describe the inputs and patterns of firing of NVsnpr neurons during fictive mastication in anaesthetized and paralysed rabbits to determine the role that NVsnpr may play in patterning mastication. Of the 272 neurons recorded in NVsnpr, 107 changed their firing patterns during repetitive stimulation of the left or right sensorimotor cortex to induce fictive mastication. Thirty increased their firing tonically. Seventy-seven became rhythmically active, but only 31 fired in phase with mastication. The others discharged in bursts at more than twice the frequency of trigeminal motoneurons. Most rhythmic masticatory neurons were concentrated in the dorsal part, and those which fired during the jaw closing phase of the cycle were confined to the anterior pole of the nucleus. Most of these cells had inputs from muscle spindle afferents, whereas most of those firing during jaw opening had inputs from periodontal receptors. Non-masticatory rhythmical neurons had receptive fields on the lips and face. The majority of rhythmical masticatory units were modulated during fictive mastication evoked by both the left and right cortices and only four changed their phase of firing when switching from one cortex to the other. When coupled with the finding that NVsnpr neurons exhibit spontaneous bursting in vitro[Sandler et al. (1998) Neuroscience, 83, 891], the results described here suggest that neurons of dorsal NVsnpr may form the core of the central pattern generator for mastication.

Notizen: Neurons of the dorsal nucleus reticularis pontis caudalis (nPontc) fire rhythmically during fictive mastication, while neurons of the ventral half tend to fire tonically (Westberg et al., 2001). This paper describes the changes in the pattern of rhythmical mastication elicited by stimulation of the sensorimotor cortex during inhibition or excitation of neurons in this nucleus and adjacent parts of nucleus reticularis gigantocellularis (Rgc) in the anaesthetized rabbit. Masticatory movements and electromyographic (EMG) activity of the masseter and digastric muscles produced by cortical stimulation were recorded before, during and after injections of a local anaesthetic (lidocaine) or excitatory amino acid N-methyl-d-aspartate (NMDA) into nPontc and Rgc through a microsyringe with attached microelectrode to record neuronal activity. Lidocaine inhibited local neurons and modified the motor program, and the effects varied with the site of injection. Most injections into the ventral half of nPontc increased cycle duration, digastric burst duration and burst area. The action of lidocaine in dorsal nPontc was more variable, although burst duration and area were often decreased. The effects on the muscle activity were always bilateral. Lidocaine block of the rostromedial part of Rgc had no effect on movements or on EMGs. Injections of NMDA excited local neurons and when injected into ventral nPontc, it completely blocked mastication. Dorsal injections either had no effect or increased cycle frequency, while decreasing burst duration and area. No increases in EMG burst duration or area were observed with NMDA. Our findings suggest that neurons of ventral nPontc tonically inhibit other parts of the central pattern generator during mastication, while dorsal neurons have mixed effects. We incorporated these findings into a new model of the masticatory central pattern generator.

Notizen: In this study, we describe functional characteristics of neurons forming networks generating oral ingestive motor behaviours. Neurons in medial reticular nuclei on the right side of the brainstem between the trigeminal and hypoglossal motor nuclei were recorded in anaesthetized and paralysed rabbits during two types of masticatory-like motor patterns induced by electrical stimulation of the left (contralateral) or right (ipsilateral) cortical masticatory areas. Sixty-seven neurons in nucleus reticularis pontis caudalis (nPontc), nucleus reticularis parvocellularis (nParv), and nucleus reticularis gigantocellularis (Rgc) were studied. These were classified as phasic or tonic depending on their firing pattern during the fictive jaw movement cycle. Phasic neurons located in the dorsal part of nPontc were active during the jaw opening phase, whilst those in dorsal nParv tended to fire during the closing phase. In most neurons, burst duration and firing frequency changed between the two motor patterns, but there was little change in phase of firing. Tonic units were mainly recorded in the ventral half of nPontc, and at the junction between Rgc and caudal nParv. Cortical inputs with short latency from the contralateral masticatory area were more frequent in phasic (82%) than tonic (44%) neurons, whilst inputs from the ipsilateral cortex were equal in the two subgroups (57% and 56%). Phasic neurons had significantly shorter mean contralateral than ipsilateral cortical latencies, whilst there was no difference among tonic neurons. Intra- and perioral primary afferent inputs activated both types of neurons at oligo-synaptic latencies. Our results show that subpopulations of neurons in medial reticular nuclei extending from the caudal part of the trigeminal motor nucleus to the rostral third of the hypoglossal motor nucleus are active during the fictive masticatory motor behaviour. Unlike masticatory neurons in the lateral tegmentum, the medial subpopulations are spatially organized according to discharge pattern.