Morning flight behavior of nocturnally migrating birds along the western basin of Lake Erie

Many species of birds that normally migrate during the night have been observed engaging in so‐called morning flights during the early morning. The results of previous studies have supported the hypothesis that one function of morning flights is to compensate for wind drift that birds experienced during the night. Our objective was to further explore this hypothesis in a unique geographic context. We determined the orientation of morning flights along the southern shore of Lake Erie's western basin during the spring migrations of 2016 and 2017. This orientation was then compared to the observed orientation of nocturnal migration. Additionally, the orientation of the birds engaged in morning flights following nights with drifting winds was compared to that of birds following nights with non‐drifting winds. The morning flights of most birds at our observation site were oriented to the west‐northwest, following the southern coast of Lake Erie. Given that nocturnal migration was oriented generally east of north, the orientation of morning flight necessarily reflected compensation for accumulated, seasonal wind drift resulting from prevailingly westerly winds. However, the orientation of morning flights was similar following nights with drifting and non‐drifting winds, suggesting that birds on any given morning were not necessarily re‐orienting as an immediate response to drift that occurred the previous night. Given the topographical characteristics of our observation area, the west‐northwest movement of birds in our study is likely best explained as a more complex interaction that could include some combination of compensation for wind drift, a search for suitable stopover habitat, flying in a direction that minimizes any loss in progressing northward toward the migratory goal, and avoidance of a lake crossing.     

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.     

Starvation of drifting goby larvae due to retention of free embryos in upstream reaches

The embryonic drift pattern of amphidromous Rhinogobius species varies along river courses. It peaks soon after sunset in reaches with gentle gradient on the plains, whereas it occurs throughout the day in steep reaches. Examination of the size of the sagittal otolith and notochord length indicated that the age of embryos drifting in steep reaches varied widely, ranging from 0 to 7 days. Many had exhausted their yolk. We attributed the all-day drift in steep reaches to retention of drifting embryos in slack waters or eddies near the banks. In contrast, most embryos drifting in reaches with gentle gradients were recently-hatched individuals. We estimated that in normal or low river flow most embryos from the upstream reaches perish through starvation before they reach the sea.     

Interspecific differences in drift behaviour between the native <Emphasis Type="Italic">Gammarus pulex</Emphasis> and the exotic <Emphasis Type="Italic">Gammarus roeseli</Emphasis> and possible implications for the invader’s success

“Drifting” is known to subject aquatic invertebrates to intense predation by drift feeding fish. Consequently, interspecific variations in drifting behaviour could lead to differences in predation pressure between coexisting prey species. Predation being an important factor determining the success of invaders, differences in drift patterns could advantage either native or exotic invertebrates through differential predation by native fish predators. The exotic freshwater amphipod (Gammarus roeseli) has now largely colonized Western Europe where it is often found in sympatry with a native species (Gammarus pulex). Here we documented interspecific differences in drifting behaviour that might have favored the invader’s success through differential predation. Benthic and drifting amphipods were sampled three times at the same site to compare the proportion of each species within and between sample types (benthos or drift) across time. Compared with the benthos, where the invader (G. roeseli) was significantly less abundant than the native (G. pulex), G. roeseli was proportionally overrepresented in the drift but displayed a very different drifting pattern. While G. pulex drift rates remained roughly constant over a 24 h period, G. roeseli showed a marked diel periodicity with low diurnal and high nocturnal drift rates. Such drifting behaviour could procure this species with a competitive advantage regarding predation as most drift feeding fish are diurnal. As a result, the native appears more disadvantaged with respect to drift. This may partly explain the ability of G. roeseli to coexist with G. pulex in a habitat more suitable to the native.     

Invertebrate drift in the piedmont part of the Kedrovaya River (Primorsky Krai,Russia) in warm season

Diurnal dynamics of invertebrate drift in the Kedrovaya River (Primorsky Krai, Russia), which flows in the zone of influence of the monsoon climate, has been studied. It has been shown that drifting invertebrates tend to shift from a predominantly daytime drift pattern to a distinguished nocturnal drift pattern during the frost-free period. The ratio of the total number of nighttime migrants to the total number of daytime migrants increased with every subsequent month. It has been proposed that the degree of light contrast between day and night can be significant in the regulation of nocturnal drift intensity.     

Reduced drift activity of two benthic invertebrate species is mediated by infochemicals of benthic fish

Regulating mobility by actively entering the drift under imminent predation risk is an avoidance strategy employed by aquatic macroinvertebrate species that is widely accepted within the scientific community. This response was most evident with respect to diurnal predators that feed in the water column, such as many salmonids. We investigated the role of the nocturnal benthivorous gudgeon [Gobio gobio (L.)] on the drift activity of two macroinvertebrate species known to display this behaviour: Baetis rhodani (PICTET) and Gammarus pulex (L.). Laboratory drift experiments using gudgeon kairomones were conducted with the results determining significant altered activity in the presence of gudgeon kairomones for both macroinvertebrate species. B. rhodani showed reduced drift activity in the kairomone treatment compared to the kairomone-free control, with a distinct nocturnal pattern being observed for both. G. pulex shifted from a similar day/night movement pattern to a nocturnal movement pattern with decreased activity during the day. Reduce activity during the day, whilst maintaining normal activity at night would not reduce the probability of encountering a nocturnal predator under natural conditions and therefore appears to not be a meaningful anti-predator response. To assess the relevance of these findings under natural conditions, we compared the experimental results with drift measurements from field observations. These show a significant reduction in drift activity for G. pulex and slight tendencies for reduced night-time drift for B. rhodani, under seasonal variations. We conclude that the behaviour in response to the physical contact or the hydrodynamic stimuli of nocturnal predators is the most likely explanation for the differences between the results from our laboratory experiment and the field observation. We further discuss that the observed migration patterns might have different species specific consequences for density stabilisation on a population level.     

Drift dynamics of Chironomidae larvae: I. Preliminary results and discussion of importance of mesh size and level of taxonomic identification in resolving Chironomidae diel drift patterns

Diel drift samples utilizing nets with mesh size less than 200 microns were taken in Linesville Creek, Pennsylvania, an eastern deciduous forest stream, and Inlet Run, Wyoming, an alpine snow melt stream. Identification of drifting Chironomidae larvae to lowest level taxonomic categories indicated 51 species or species group categories representing 51.95% of the total insect drift in Linesville Creek and 18 species or species group categories representing 70.47% of the total insect drift in Inlet Run. Orthocladiinae were the predominant larvae in the drift in Linesville Creek, with 19 species comprising 43.84% of the Chironomidae drift. In decreasing abundance were Chironomini (12 species, 40.36% of Chironomidae drift), Tanytarsini (10 species, 8.89%), and Tanypodinae (10 species, 6.91%). By contrast, Diamesinae were the predominant larvae in the drift in Inlet Run, (5 species, 71.43%) followed by Orthocladiinae (10 species, 27.25%), Tanytarsini (2 species, 1.20%), and Podonominae (1 species, 0.12%). Comparison of drift composition with substrate samples and/ or emergence data indicated a close relationship between relative abundance in drift and relative abundance in the benthos. Behavioral drift patterns with nocturnal peaks were seen for 3 species or species groups in Linesville Creek. Four species with diurnal drift peaks were present in Inlet Run. Analysis of the size distribution of drifting larvae indicates that a mesh size as small as 200 microns is required to resolve diel drift patterns. It is postulated that random factors greatly influence the apparent diel drift pattern of Chironomidae when nets with mesh size in excess of 400 microns are employed in drift studies. Conflicting literature reports of behavioral drift for Chironomidae may be due to differing species composition of drifting larvae and net mesh size related artifacts.     

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.     

Fish drift in a Danube sidearm‐system: II. Seasonal and diurnal patterns

Seasonal and diurnal patterns of larval and juvenile fish drift were investigated in the Marchfeldkanal, a man‐made side branch of the Danube River near Vienna, Austria. A clear seasonal pattern with peak densities in mid‐June was found. Species composition varied over time, showed a site specific pattern and was dominated by tubenose goby Proterorhinus marmoratus . Water temperature was the main factor responsible for the increase of drift densities until the median drift date and repeated occurrence of early larval stages in drift indicated repeated spawning for many species. Significant differences in drift densities between different time periods of the day (day, dusk, night and dawn) were found for common bream Abramis brama , barbel Barbus barbus , chub Leuciscus cephalus , tubenose goby and roach Rutilus rutilus . The highest drift rates occurred at night (2200–0400 hours), with 86% of all larvae drifting during the hours of darkness. Fish larvae of different lengths drifting at different phases of the day were found for common bream, bleak Alburnus alburnus and chub, with largest larvae drifting during dusk (chub) and day (bleak and common bream). For bleak, all gudgeon species Gobio spp., tubenose goby, roach and for all cyprinid species combined, one 2 h night sample was found to be sufficient to predict the total 24 h drift.     

Diel,size-differential drift patterns of three macroinvertebrate species in the lower Mississippi River,Louisiana (USA)

We explored macroinvertebrate size-differential drift in the lower Mississippi River (a 9th order system). Because this river system is highly turbid, we hypothesized that visually-dependent vertebrate predators feeding on drifting organisms would be at a disadvantage. Thus, size-differential drift should not occur. For one 24-hour period in both January and April, six drift nets were used to sample surface drift. Nets were emptied once every four hours. Individual intra-ocular distances of three macroinvertebrate species (Hydropsyche orris: Trichoptera, Hexagenia limbata: Ephemeroptera, Macrobrachium ohione: Crustacea) were measured. Percentages of size classes in the drift were determined. In both months, large individuals of H. orris and H. limbata were prevalent in the nocturnal but scarce in the diurnal drift. In January, large M. ohione drifted regardless of time. In April, large M. ohione predominated the nocturnal drift. Our results could not be attributed solely to vertebrate predator avoidance. Other mechanisms such as diel microhabitat migration and current velocity may have accounted for the results.     

An assessment of short-term depletion of stream macroinvertebrate benthos by drift

A study was conducted to determine if emigration of drifting macroinvertebrates from a stream riffle which was blocked for one week from immigration by upstream colonists significantly reduced the abundance of drift collected from the tail of the riffle. The head of a 9 m long riffle of a 2nd order stream in Maryland (USA) was blocked from incoming drift by a 250 m mesh weir. Upstream immigration of invertebrates into the riffle was largely prevented by a partition placed at the tail of the riffle which held the drift nets. Benthos and drift samples were collected from the riffle prior to weir placement and following its removal, and drift was collected at dusk on each day. No difference in drift or in benthic abundance between the beginning and end of the study was observed. This is largely attributed to recruitment of immature insects (primarily hatching of eggs present at the outset), particularly of Dolophilodes distinctus and species of Tanytarsini, from within the riffle. Results suggest that recruitment of riffle species is of sufficient magnitude to more than compensate for short-term riffle depletion due to drift. Samples of drifting and non-drifting (benthic) animals were held without food for 12 h after collection and mortality within each group was determined. The mortality of drifting animals was three-fold that of benthic animals.     

Differential behavioural responses of mayflies from streams with and without fish to trout odour

1. In streams, mayflies (Order Ephemeroptera) are at risk from fish feeding visually in the water column. The effect of fish odour on the behaviour of Baetis bicaudatus from a fishless stream and a trout stream was investigated in four large oval tanks supplied with water from the fishless stream.
2. For each mayfly population, mayfly positioning on the substratum and movement in the water column (drift) were measured during the day and night, over 3 days. Brook trout ( Salvelinus fontinalis ) odour was added to two tanks to test the effect of a threat from fish.
3. Throughout the experiment more mayflies from the trout stream were observed on the substratum surface and in the water column during the night than the day, but the magnitude of night drift was less in tanks with fish odour.
4. Baetis from the fishless stream also displayed a nocturnal periodicity in drift and positioning, but their night-time drift was not affected by the presence of fish odour. On the first day of the experiment, however, more mayflies were observed on the substratum surface and drifting in tanks without fish odour during the day.
5. Sensitivity to fish odour may enable mayflies to alter their behaviour according to the risk of predation from fish.     

Differential behavioural responses of mayflies from streams with and without fish to trout odour

1. In streams, mayflies (Order Ephemeroptera) are at risk from fish feeding visually in the water column. The effect of fish odour on the behaviour of Baetis bicaudatus from a fishless stream and a trout stream was investigated in four large oval tanks supplied with water from the fishless stream.
2. For each mayfly population, mayfly positioning on the substratum and movement in the water column (drift) were measured during the day and night, over 3 days. Brook trout ( Salvelinus fontinalis ) odour was added to two tanks to test the effect of a threat from fish.
3. Throughout the experiment more mayflies from the trout stream were observed on the substratum surface and in the water column during the night than the day, but the magnitude of night drift was less in tanks with fish odour.
4. Baetis from the fishless stream also displayed a nocturnal periodicity in drift and positioning, but their night-time drift was not affected by the presence of fish odour. On the first day of the experiment, however, more mayflies were observed on the substratum surface and drifting in tanks without fish odour during the day.
5. Sensitivity to fish odour may enable mayflies to alter their behaviour according to the risk of predation from fish.     

Size-dependent drift responses of mayflies to experimental hydrologic variation: active predator avoidance or passive hydrodynamic displacement?

Summary Larger nymphs within aquatic insect taxa have been frequently observed to be transported down-stream in the stream drift only at night. Others have hypothesized this pattern results primarily from large nymphs' behavioural avoidance of entering drift during daylight, when size-selective, visually-feeding fish predators are most active. This hypothesis assumes that animals can actively control their entry into the drift, which may not be the case under all flow conditions. We experimentally induced streamflow increases and decreases in adjacent riffles in a hydrologically-stable stream during the daytime to examine whether changes in diel patterns of drift abundance and size-distribution of mayflies were consistent with the hypothesis of active avoidance of diurnal drift. We assessed the likelihood of active vs. passive mechanisms of diurnal drift entry and transport for four taxa that differ with respect to body size, morpho-behavioural attributes, microhabitat use, and general propensity to drift. In each of three seasons, diurnal and nocturnal drift samples were collected in three riffles over two diel cycles. Background drift patterns were established on the first day (no flow manipulation). Six h before sunset on the second day, flow was experimentally increased in one riffle, decreased in the second, and not altered in the third (control). Between-day differences in diurnal and nocturnal drift rate and size composition were then compared among the treatment and reference riffles. Responses of two taxa were consistent with active control over drift entry, transport, or both. For Baetis spp., drift-prone mayflies typically preyed upon by fish, diurnal drift rates immediately increased following both flow reduction and flow elevation in all seasons, but only small individuals comprised the drift. Drift by large individuals was delayed until nighttime. Epeorus longimanus also exhibited significant increases in drift rates following flow reduction and elevation, but responses of this large-bodied species were restricted to nighttime. Drift responses for these two taxa were largely independent of direction of hydrologic change, thus indicating a strong behavioural control over drift. By contrast, numbers and sizes of drifting Paraleptophlebia heteronea and Ephemerella infrequens depended strongly on direction of flow change. Drift rates for both species generally declined after flow reduction and increased after flow elevation. Moreover, after flow elevation, larger individuals often drifted diurnally, a finding consistent with expectations under a passive hydrodynamic model. These experiments indicate that size-dependent mayfly drift reflects not only presumed risk from visual fish predators, but also functional attributes of species such as morphology, behaviour, and microhabitat affiliation, which influence aspects of drift entry and transport under variable hydrologic conditions.     

Diel drift of Chironomidae in a large lowland river (Central Poland)

The diel drift patterns of Chironomidae larvae were investigated in a seventh order section of the Warta River (Central Poland) over two diel cycles during May 1989. Three nets (mesh size 400 m) were installed in a cross section of the Warta River.The estimated drift density was low, but was comparable to that calculated for other large rivers. Spatio-temporal fluctuations in abundance and composition of macroinvertebrate drift, including Chironomidae, were observed with the highest density of drifting macrobenthos recorded near the depositional bank of this river. The ratio benthosdrift indicated differing propensities for of the older instars of a given chironomid taxon to drift. Orthocladiinae larvae were the most abundant subfamily of Chironomidae in drift but not in benthos, reaching up to 73% of the total drifting chironomid larvae. More taxa but fewer individuals (about 20% of the chironomid larvae collected) belonged to the tribe Chironomini, the dominant group in benthos.A major part of chironomid drift collection may represent behavioural drift because the net mesh size used in the Warta River was insufficient to catch the earliest instars (distributional drift). Both at the family and subfamily level chironomid larvae exhibited a distinct nocturnal drift periodicity. Nocturnal periodicity was documented for the dominant species, but due to the low density of many chironomid species, it was impossible to determine their diel drift pattern. Some Chironomidae appeared to be aperiodic.     

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.     

Nocturnal drift of mayfly nymphs as a post-contact antipredator mechanism

1. The predominantly nocturnal constrained drift of stream invertebrates is commonly regarded as a behaviour that avoids encounters with visually foraging fish in the water column. The alternative explanation, that drift peaks are caused by bottom-feeding, nocturnal predators, has rarely been tested.
2. We examined these hypotheses by collecting invertebrate drift in five streams in northern Finland: one with brown trout ( Salmo trutta , a drift-feeding fish), one with alpine bullhead ( Cottus poecilopus , a benthic fish), one with both species, and two fishless streams.
3. Drift by Baetis mayflies was aperiodic or slightly diurnal in both fishless streams on all sampling occasions. In contrast, drift was nocturnal in streams with trout and, to a lesser extent, in the stream with bullhead. Non-dipteran prey drifted mainly nocturnally in all streams with fish, whereas Diptera larvae were less responsive to the presence of fish.
4. In laboratory experiments, bullheads were night-active, causing a much higher frequency of drift by touching Baetis at night than during the day. Thus, increased nocturnal drift may serve to avoid both visual predators (a pre-contact response) and benthic fish (a post-contact response). In streams with bottom-feeding fish, nocturnal drift should be caused by increased drift by night rather than by reduced drift by day.     

The influence of predatory fish on mayfly drift: extrapolating from experiments to nature

1. A knowledge of how individual behaviour affects populations in nature is needed to understand many ecologically important processes, such as the dispersal of larval insects in streams. The influence of chemical cues from drift‐feeding fish on the drift dispersal of mayflies has been documented in small experimental channels (i.e. < 3 m), but their influence on dispersal in natural systems (e.g. 30 m stream reaches) is unclear. 2. Using surveys in 10 Rocky Mountain streams in Western Colorado we examined whether the effects of predatory brook trout (Salvelinus fontinalis) on mayfly drift, that were apparent in stream‐side channels, could also be detected in natural streams. 3. In channel experiments, the drift of Baetis bicaudatus (Baetidae) was more responsive to variation in the concentration of chemical cues from brook trout than that of another mayfly, Epeorus deceptivus (Heptageniidae). The rate of brook trout predation on drifting mayflies of both species in a 2‐m long observation tank was higher during the day (60–75%) but still measurable at night (5–10%). Epeorus individuals released into the water column were more vulnerable to trout predation by both day and night than were Baetis larvae treated similarly. 4. Drift of all mayfly taxa in five fishless streams was aperiodic, whereas their drift was nocturnal in five trout streams. The propensity of mayflies to drift was decreased during the day and increased during the night in trout streams compared with fishless streams. In contrast to the channel experiments, fish biomass and density did not alter the nocturnal nature nor magnitude of mayfly drift in natural streams. 5. In combination, these results indicate that mayflies respond to subtle differences in concentration of fish cues in experimental channels. However, temporal and spatial variation in fish cues available to mayflies in natural streams may have obscured our ability to detect responses at larger scales.     

Behavior of early life intervals of Klamath River green sturgeon, <Emphasis Type="Italic">Acipenser</Emphasis><Emphasis Type="Italic">medirostris</Emphasis>, with a note on body color

We studied ontogenetic behavior, migration, and wintering behavior of young Klamath River green sturgeon, Acipenser medirostris, in the laboratory to provide insight into likely behavior of wild sturgeon. Hatchling free embryos preferred cover but were poor swimmers and could not move farther than a few centimeters to cover. The poor swimming ability and cover preference of hatchlings suggests evolution for habitat selection of females to place eggs in habitat with cover for eggs (and hatchlings), and for egg characteristics (large, dense, and weakly adhesive) to cause rapid sinking into cover without drifting. A day or so after fish developed into larvae (first life interval feeding exogenously), day-12 larvae initiated a 12-day downstream nocturnal migration. A totally nocturnal migration is unlike other Acipenser migrants yet studied. Migrant larvae had a dark-colored body typical of other Acipenser species that migrate as larvae. Tail color was a dark black (black-tail phenotype) only during the early larva period, suggesting a morphological adaptation for migration, foraging, or both. Post-migrant larvae and early juveniles to day 84 foraged diurnally with a nocturnal activity peak. Day 110–181 juveniles moved downstream at night until water temperature decreased to about 8°C, indicating wild juveniles migrate downstream to wintering habitat. Habitat preference of month 9–10 wintering juveniles suggests wild juveniles are in deep pools with low light and some rock structure. Wintering juveniles were only active at night. Initiation and cessation of daily activity was at dusk and dawn during illumination changes of <1.0lx. This sensitivity to illumination has not been found before in sturgeons. During the first 10months of life, nocturnal activity of early life intervals is a dominant feature of migration, foraging, and wintering.     

A comparison of the relative contributions of temporal and spatial variation in the density of drifting invertebrates in a Dorset (U.K.) chalk stream

1. Invertebrate drift is commonly investigated in streams, with the majority of studies focussed on temporal (typically diel) variation. In comparison, few studies have investigated spatial variation in drift and there is little consensus among them. We tested the hypothesis that spatial variation in invertebrate drift is as important as temporal variation. 2. The density of drifting invertebrates in a chalk stream was sampled using an array of nets arranged to determine vertical, lateral and longitudinal variation. Samples were collected at dawn, during the day, at dusk and by night, on four separate monthly occasions. Insecta and Crustacea were analysed separately to identify the effect of differing life history strategies. The density of drifting debris was also recorded, to act as a null model. 3. Time of day and vertical position together explained the majority of the variance in invertebrate drift (79% for Insecta and 97% for Crustacea), with drift densities higher at dusk and night, and nearer the stream bed. Independently, time of day (38%, Insecta; 52%, Crustacea) and vertical position (41%, Insecta; 45%, Crustacea) explained a similar amount of the observed variance. Month explained some of the variance in insect drift (9%) but none for Crustacea. 4. Variation in the density of drifting debris showed little in common with invertebrate drift. There was little variation associated with time of day and only 27% of the observed variation in debris could be explained by the factors investigated here, with month explaining the largest proportion (20%). We suggest the difference in drifting debris and invertebrates provides further evidence for a strong behavioural component in invertebrate drift. 5. Spatial variation in invertebrate drift can be of the same order of magnitude as the much‐described diel temporal variation. The extent of this spatial variation poses problems when attempting to quantify invertebrate drift and we recommend that spatial replication should be incorporated into drift studies.