Diel changes of larval drift among amphidromous gobies in Japan, especially Rhinogobius brunneus

Larvae of amphidromous gobies migrate to the sea as passive drift. In order to identify the diel drift pattern (DDP) of each species, we conducted 24 hour collections in different sections ofthree rivers. The DDPs ofdifferent species at each sampling station were almost identical, but the DDP of each species varied among stations, depending on the topographical features of water-courses. Downstream migration occurred throughout the day in steep water-courses while it was nocturnal with a peak in number soon after sunset in gentle gradients in the plain and was also nocturnal with a small amount of day time drifting between the two gradients. It is suggested that the larvae drifting from the upper parts of the river in daytime halted their migration in a pool with low flow rate until twilight.     

Incorporating invertebrate predators into theory regarding the timing of invertebrate drift

Theory concerning the timing of lotic invertebrate drift suggests that daytime-feeding fish cause invertebrates to restrict their drift behavior to the nighttime. However, there is growing evidence that the nighttime foraging of invertebrate predators also contributes to the nocturnal timing of drift, though it is unclear whether the nocturnal behavior of invertebrate predators is innate or proximately caused by fish. In two experiments, one conducted in a fish-bearing stream and a second in a fishless stream, we compared the drift patterns of Baetidae (Ephemeroptera) from channels with and without benthic invertebrate predators. We tested whether invertebrate predators affect the timing of drift, either as a proximate cause of nocturnal drift in the fishless stream (diel periodicity) or as a proximate cause of a pre-dawn peak in drift in the fish-bearing stream (nocturnal periodicity). In the fish-bearing stream experiment, a pre-dawn increase of baetid drift occurred independently of invertebrate predators, indicating that invertebrate predators were not the proximate cause of nocturnal periodicity in the stream. In the fishless stream experiment, invertebrate predators caused more baetid drift at night than during the day, indicating that invertebrate predators caused the nocturnal drift pattern we observed in the stream, and that invertebrate predators can influence drift timing independently of fish. Therefore, we suggest that both visually feeding fish and nocturnally foraging benthic predators, when present, affect the timing of invertebrate drift; visually feeding fish by reducing daytime drift, and benthic predators by increasing nighttime drift.     

Under-ice drift of invertebrates in the piedmont part of Kedrovaya River (Primorskii Krai)

According to quantitative indices, the under-ice drift of invertebrates in the piedmont part of the Kedrovaya River (Primorskii Krai) is lower than during the ice-free period. The winter drift is constituted mainly by Diptera and Ephemeroptera. In the warm season, an active drift of hydrobionts is observed only at night; during the freezing-over period, the drift occurs both at night and in the daytime. The number of daytime migrants prevails over organisms drifting at night. The drift of invertebrates is rather low at twilight. The coming of spring thaw and the appearance of gullies leads to an increase in the abundance of animals in the stream. After the ice breaks up in the river, the larvae of Ephemeroptera return to night-drift activity upon the recession of the flood. However, quantitative indices of the daytime drift of other invertebrate groups remains rather high.     

Daytime micro-naps in a nocturnal migrant: an EEG analysis

Many species of typically diurnal songbirds experience sleep loss during the migratory seasons owing to their nocturnal migrations. However, despite substantial loss of sleep, nocturnally migrating songbirds continue to function normally with no observable effect on their behaviour. It is unclear if and how avian migrants compensate for sleep loss. Recent behavioural evidence suggests that some species may compensate for lost night-time sleep with short, uni- and bilateral 'micro-naps' during the day. We provide electrophysiological evidence that short episodes of sleep-like daytime behaviour (approx. 12s) are accompanied by sleep-like changes in brain activity in an avian migrant. Furthermore, we present evidence that part of this physiological brain response manifests itself as unihemispheric sleep, a state during which one brain hemisphere is asleep while the other hemisphere remains essentially awake. Episodes of daytime sleep may represent a potent adaptation to the challenges of avian migration and offer a plausible explanation for the resilience to sleep loss in nocturnal migrants.     

Long-term patterns of invertebrate stream drift in an Australian temperate stream

1. Invertebrate stream drift was sampled bimonthly in the Acheron River, Victoria, Australia, over a period of 18 months. Replicated hourly samples were collected over a 25-h period on each sampling date. A total of 194 taxa were identified in the drift. However, total drift density was dominated by few taxa. 2. Some evidence was obtained for a seasonal pattern in drift: this was most pronounced in relative abundances of individual taxa and the composition of the drift, rather than in total drift densities. Most of the commonly collected taxa reflected the seasonal pattern of total drift. However, some of the common taxa did not. 3. A small number of taxa showed behavioral drift, with a nocturnal increase in drift densities. One species of ‘Baetis’ drifted in high densities over short periods of time around dusk and dawn. It did not drift in higher densities during the night than during the day. The results emphasize the need for drift studies to be more rigorously designed than is typically the case.     

Sleep related O2 desaturation in COPD patients with normoxaemia and mild hypoxyaemia

It is unknown whether daytime features predict oxygenation during sleep in COPD patients with normoxaemia or mild hypoxaemia. In this study our purpose was to evaluate by a pulse oxymeter, nocturnal desaturation in 33 COPD with PaO2 > 60 mmHg and to examine some daytime parameters as possible predictors of nocturnal hypoxaemia. A significant nocturnal desaturation has been defined by spending > or = 30% of total sleep-time with a TSTSaO2 < 90% > 30. According to this criterion we classified our patients in Desaturators (D) and Non Desaturators (ND). Our results showed that 39% of our patients were D and 61% ND. Among anthropometric and respiratory functional data we found that daytime SaO2B (r = 0.74 p < 0.001) daytime PaO2 (r = 0.47 p < 0.01) and daytime PaCO2 (r = 0.45 p < 0.05) were significantly correlated with the nocturnal oxygen desaturation and can predict the presence of sleep related hypoxaemia. In conclusion, our study confirms that a relatively high percentage of COPD patients with normoxaemia or borderline hypoxaemia exhibits significant nocturnal hypoxaemia. Further studies will suggest whether sleep related hypoxaemia deserves nocturnal oxygen therapy.     

Do bird captures reflect migration intensity? – Trapping numbers on an Alpine pass compared with radar counts

A limitation of standardized mist netting for monitoring migration is caused by the lack of knowledge about the relationship between trapped birds and birds flying aloft. Earlier studies related nocturnal radar counts with trapping data of the following day. In this study, we compared for the first time data gathered simultaneously by radar and mist netting, separately for diurnal and nocturnal migration. Trapping numbers were strongly correlated with migratory intensities measured by radar (r>0.6). A multiple regression analysis, including wind speed and wind direction explained 61% of variation in the number of captures. During the night, and particularly with favourable winds, birds flew at higher altitudes and hence escaped the nets to a higher proportion. The number of nocturnal migrants trapped during daytime was well correlated with migratory intensities observed by radar in the preceding night. The diurnal time patterns, however, revealed fundamental differences between trapping counts and radar observations. This was mainly due to increasing and decreasing flight altitudes in the course of the night, and by the limitations of the radar technique that underestimates migratory intensities during the day when birds aggregate in flocks. In relation to the migratory intensity recorded by radar, diurnal migrants are trapped in a much higher proportion than nocturnal migrants. Finally, our results confirm that trapping data from a site hardly used for stopover are well suited to represent the ongoing migration during the day and night.     

Effects of trout on the diel periodicity of drifting in baetid mayflies

Some benthic invertebrates in streams make frequent, short journeys downstream in the water column (=drifting). In most streams there are larger numbers of invertebrates in the drift at night than during the day. We tested the hypothesis that nocturnal drifting is a response to avoid predation from fish that feed in the water column during the day. We surveyed diel patterns of drifting by nymphs of the mayfly Baetis coelestis in several streams containing (n=5) and lacking (n=7) populations of rainbow trout, Oncorhynchus mykiss. Drifting was more nocturnal in the presence of trout (85% of daily drift occurred at night) than in their absence (50% of daily drift occurred at night). This shift in periodicity is due to reduced daytime drifting in streams with trout, because at a given nighttime drift density, the daytime drift density of B. coelestis was lower in streams occupied by trout than in troutless streams. Large size classes of B. coelestis were underrepresented in the daytime drift in trout streams compared to nighttime drift in trout streams, and to both day and night drift in troutless streams. Differences in daytime drift density between streams with and without trout were the result of differences in mayfly drift behaviour among streams because predation rates by trout were too low to significantly reduce densities of drifting B. coelestis. We tested for rapid (over 3 days) phenotypic responses to trout presence by adding trout in cages to three of the troutless streams. Nighttime drifting was unaffected by the addition of trout, but daytime drift densities were reduced by 28% below cages containing trout relative to control cages (lacking trout) placed upstream. Drift responses were measured 15 m downstream of the cages suggesting that mayflies detected trout using chemical cues. Overall, these data support the hypothesis that infrequent daytime drifting is an avoidance response to fish that feed in the water column during the day. Avoidance is more pronounced in large individuals and is, at least partially, a phenotypic response mediated by chemical cues.     

Invertebrate drift in a glacial river and its non-glacial tributary

1. Invertebrate drift was studied in a glacially fed river and a non-glacial tributary in western Norway. Samples were taken during two consecutive 24-h periods in May, July and October 1997. The 3 months are characterized by snowmelt, ice melt and rainfall runoff, respectively. The main glacial river has colder, more turbid water, especially during the period of maximum ice melt during summer.
2. Chironomidae, especially the genus Diamesa , dominated the drift in the main river in May and October, constituting 97 and 99% of total numbers, respectively. Simuliidae, Plecoptera, Ephemeroptera and Trichoptera were the other main components.
3. A comparison of drift and benthos data revealed that the tributary was of little significance for colonization of the main glacial river. Only some additional species in very low numbers were recorded downstream of the confluence.
4. During July significant differences in diel drift pattern of Chironomidae and Simuliidae existed between the glacial and non-glacial reaches. There was a mid-day peak independent of discharge in the glacial river, but this peak was not noted in the tributary. Species of the genus Diamesa appear to be adapted for daytime drift, possibly evolved through the absence of predators and competitors that are typical of rhithral systems where nocturnal drift is more usual.     

A continuous study of the total drift of freshwater shrimps, Gammarus pulex, in a small stony stream in the English Lake District

1. The objective was to determine the major factors affecting the downstream dispersal (drift) of freshwater shrimps, Gammarus pulex. Sample replication and frequency are major problems in the quantification of drift. For the first time, these problems were avoided by sampling the whole stream continuously so that all the shrimps drifting downstream at the sampling point were caught in a net emptied at dusk and dawn in 1966, and every 3 days in 1967. 2. There was no consistent seasonal pattern in drift rates, but a high proportion of annual drift was taken in only a few samples. There was a nocturnal diel pattern of drift with peaks soon after dusk and just before dawn. A power function described the significant (P < 0.001) relationship between drift and flow, and was used to neutralise the dominant effects of flow by standardising total drift over 24 h, nocturnal drift and diurnal drift (drift per 50 m³). These were all significantly (P < 0.001) related to benthos density, but not to date, temperature, or length of the night or day. 3. The relationship between drift values and the independent variables, flow and benthos density, was well described (P < 0.001) by a multiple‐regression model. Adding temperature, date, and/or the length of the night or day did not improve model fit. Variations in flow and benthos density explained 94% of the variation in total drift over 24 h, 97% of the variation in nocturnal drift, but only 44% of the variation in diurnal drift. A power function described (P < 0.001) the relationship between total drift and the volume of water sampled over 3‐day periods in 1967. Flow explained 95% of this drift variation; it was unnecessary to add another variable such as benthos density. 4. The significance of this study is that it avoided the problems associated with the quantification of drift samples. Therefore, the conclusions are more robust than those of many previous studies. A high proportion of the annual drift losses would have been undetected by intermittent sampling. Temperature, season, night or day length had no significant effect on drift densities, and the relationship between drift and benthos densities was proportional, not density dependent. The nocturnal increase in drift could not be interpreted as an antipredator behaviour. The dominance of flow and benthos density was apparent but the quantitative relationships posed further questions, especially those related to drift distances at different velocities.     

Wind conditions experienced during the day predict nocturnal restlessness in a migratory songbird

A variety of methods have been used to study the relationship between wind conditions and departure decisions of migrant birds at stopover sites. These methods are either costly or suffer from inaccuracy in determining whether or not an individual has resumed migration. Here we present a novel and simple approach to studying the relationship between wind conditions and departure likelihood. Northern Wheatears Oenanthe oenanthe caught during stopover were temporarily caged to measure their nocturnal migratory restlessness, which is an accurate proxy for their individual departure likelihood. We then related the degree of nocturnal restlessness to wind conditions prevailing at the time of capture. Confirming the general pattern from previous studies of departure, the intensity of nocturnal migratory restlessness, and hence departure likelihood, increased with increasing wind support towards the migratory goal. This suggests that approximating the propensity to depart by measuring nocturnal migratory restlessness is a reliable way to study the effect that wind conditions experienced during stopover has on the departure decision of migrants. Our study also shows that nocturnal migrants possess the ability to use information gathered during the day for their departure decisions at night. Because measuring migratory restlessness is straightforward and inexpensive, our approach is ideally suited to test hypotheses regarding spatio‐temporal variation in wind selectivity in migrating birds.     

Diel changes in habitat use by dragonflies: Nocturnal roosting site selection by the threatened dragonfly Sympetrum depressiusculum (Odonata: Libellulidae)

Although it is well recognized that insects' habitat use and requirements may change during the season, very little attention has been devoted to diel habitat changes in most insects. In this study, we compared habitat utilization patterns of Sympetrum depressiusculum (Selys, 1841) adult dragonflies between daytime activities and nocturnal roosting. During daytime, we captured and marked adult individuals with fluorescent paint in different habitats. At night, we searched, using UV light, for marked individuals that remained on the habitats. We found that habitat selection for daytime activities and that for nocturnal roosting differed significantly. Adults clearly avoided ponds and their immediate surroundings for nocturnal roosting, whereas this habitat type was frequently utilized for daytime activities. We suggest that nocturnal avoidance of the riparian area is associated with lower temperatures, which adversely affect thermoregulation, and that selection of specific habitats for nocturnal roosting is closely associated with vegetation structure providing stability during windy nights and serving as a suitable shelter. Such habitat properties are found especially on fallow land, a habitat type whose representation in agricultural areas has been gradually decreasing in recent decades.     

Home range of the Japanese fluvial sculpin, Cottus pollux, in relation to nocturnal activity patterns

Patterns of space use related to the activity of individual Japanese fluvial sculpins, Cottus pollux, were examined during the non-breeding season, in the upper reaches of the Inabe River, central Japan. Sculpins appeared more frequently at night than in daytime. Among 31 recaptured sculpins, 30 (96.8%) showed nocturnal activity patterns, there being no fish which exhibited an entirely diurnal activity pattern. Of 21 sculpins captured both in daytime and at night, the most common pattern of space use (n = 14, 66.7%) was that in which the nocturnal home range entirely encompassed the diurnal range. Overall, nocturnal home ranges were significantly larger than diurnal ranges. Active sculpins were rarely found on sand-associated substrata in daytime, but were seen more frequently on such substrata at night.     

Flight by night or day? Optimal daily timing of bird migration

Many migratory bird species fly mainly during the night (nocturnal migrants), others during daytime (diurnal migrants) and still others during both night and day. Need to forage during the day, atmospheric structure, predator avoidance and orientation conditions have been proposed as explanations for the widespread occurrence of nocturnal migration. However, the general principles that determine the basic nocturnal-diurnal variation in flight habits are poorly known. In the present study optimal timing of migratory flights, giving the minimum total duration of the migratory journey, is evaluated in a schematic way in relation to ecological conditions for energy gain in foraging and for energy costs in flight. There exists a strong and fundamental advantage of flying by night because foraging time is maximized and energy deposition can take place on days immediately after and prior to the nocturnal flights. The increase in migration speed by nocturnal compared with diurnal migration will be largest for birds with low flight costs and high energy deposition rates. Diurnal migration will be optimal if it is associated with efficient energy gain immediately after a migratory flight because suitable stopover/foraging places have been located during the flight or if energy losses during flight are substantially reduced by thermal soaring and/or by fly-and-forage migration. A strategy of combined diurnal and nocturnal migration may be optimal when birds migrate across regions with relatively poor conditions for energy deposition (not only severe but also soft barriers). Predictions about variable timing of migratory flights depending on changing foraging and environmental conditions along the migration route may be tested for individual birds by analysing satellite tracking results with respect to daily travel routines in different regions. Documenting and understanding the adaptive variability in daily travel schedules among migrating animals constitute a fascinating challenge for future research.     

THE EFFECT OF DELAYED POPULATION GROWTH ON THE GENETIC DIFFERENTIATION OF LOCAL POPULATIONS SUBJECT TO FREQUENT EXTINCTIONS AND RECOLONIZATIONS

I investigated the effects of delayed population growth on the genetic differentiation among populations subjected to local extinction and recolonization, for two different migration functions; (1) a constant migration rate, and (2) a constant number of migrants. A delayed period of population growth reduces the size of the newly founded populations for one or several generations. Whether this increases differentiation among local populations depends on the actual pattern of migration. With a constant migration rate, fewer migrants move into small populations than into large, thus providing ample opportunity for drift to act within a population. A prolonged period of population growth thus makes the conditions for enhanced differentiation between local populations less restrictive and also inflates the actual levels of differentiation. The effect depends on the relative magnitudes of k_e, the effective number of colonizers and k, the actual number of colonizers. When there is a constant number of migrants into a population per generation, migration into small populations is increased. This increase of migration in small populations counteracts the effects of genetic drift due to small population size. It increases the rate by which populations approach equilibrium, as small populations are swamped by migrants from larger populations closer to genetic equilibrium, and overall levels of differentiation are thus reduced. I also discuss situations for which the results of this paper are relevant.     

Drift and upstream movement in Yuccabine Creek,an Australian tropical stream

Drift and upstream movement were monitored over 14 months in a seasonal upland tropical stream in northeastern Australia. There were distinct seasonal pulses in the drift with variable peak levels in the summer wet season and low more stable levels during the dry season. Drift density ranged from 0.36 to 3.98 animals per m³ (monthly mean = 1.26). There was no correlation between drift density and either benthic density or stream discharge. In the absence of catastrophic drift, drift was dispersive, not depletive in the wet season. A total of 121 taxa were caught in the 14 drift samples. Most taxa had nocturnal maximum drift levels with a peak immediately after sunset, a pattern apparently related to level of light and not temperature. Compensation for drift by upstream-moving nymphs and larvae was least during the wet season and increased during the dry season to a peak of 27% by numbers. Mean compensation was 8.2%. It is suggested that apart from in the wet season when an animal may drift substantial distances, most riffle animals will spend their larval lives in one small stretch of stream.     

Presence of sculpins (Cottus gobio) reduces drift and activity of Gammarus pulex (Amphipoda)

Introduction of sculpins into a stream previously devoid of these predators significantly reduced drift rate of Gammarus pulex. The drift of insect larvae was not affected. High amounts of exudates after implantation of sculpins were probably responsible for the low number of drifting G. pulex specimens. Laboratory experiments confirmed reduced locomotory activity of G. pulex when exposed to caged sculpins, an observation that excludes reduced drift activity as a result only of predation.The average size of drifting G. pulex specimens was larger during the night than during the day. This result is in accordance with the hypothesis that large individuals should, in relation to small ones, turn nocturnal because of greater predation risk during daytime. Presence of sculpins did not alter the size composition of drifting G. pulex.     

Wind drift,compensation, and the use of landmarks by nocturnal bird migrants

In this paper we describe fall nocturnal migration at three localities in eastern New York, one adjacent to the Hudson River, the other two 30 km to the west in a topographically more uniform area. Migrants at both study areas moved southwest in winds not out of the west and were, therefore, seemingly unaffected by the river. In west winds, however, birds away from the river moved south-southeast whereas those in the vicinity of the river flew a track west of south paralleling the river. In addition, a relative increase in the number of migrants along the river compared to away was observed in west winds as birds presumably became concentrated near the river. We conclude that on most autumn nights migrants passing through this area have a preferred track direction toward the southwest and in strong winds from the west and northwest they are drifted. Upon reaching the vicinity of the Hudson River, some birds alter their headings yielding a track direction that closely parallels the river resulting in at least a partial compensation for wind drift. No alternative hypothesis is consistent with all the data.     

Visual ecology: hiding in the dark

The ability of many animals to camouflage themselves against a background is a well-known daytime phenomenon. Now it has even been found to occur at night, highlighting the reality of nocturnal visual predation.     

State-dependent shifts between nocturnal and diurnal activity in salmon

Animal species have usually evolved to be active at a specific time of the daily cycle, and so are either diurnal, nocturnal or crepuscular. However, we show here that the daily timing of activity in juvenile Atlantic salmon is related to the life-history strategy that they have adopted (i.e. the age at which they will migrate to the sea) and their current state (body size/relative nutritional state). Salmon can detect food more easily by day than by night, but the risk of predation is greater. Nocturnal foraging should generally be preferred, but the greater the need for growth, the greater should be the shift towards diurnal activity. In line with this prediction, all fish were predominantly nocturnal, but salmon preparing to migrate to the sea, which would experience size-dependent mortality during the forthcoming migration, were more diurnal than fish of the same age and size that were delaying migration for a further year. Moreover, the proportion of activity by day was negatively correlated with body size within the intending migrants. It has previously been shown that overwinter survival in fish delaying migration is maximized not by growth but by minimizing exposure to predators. As predicted, daytime activity in these fish was correlated with the prior rate of weight loss, fish being more diurnal when their risk of starvation was greater. To our knowledge, these are the first quantitative demonstrations of state-dependent variation in the timing of daily activity.