A behavioural test of the sensitivity of a nocturnal mosquito, Anopheles gambiae, to dim white, red and infra-red light

Abstract. A behavioural test was used to determine the light sensitivity of the nocturnal mosquito Anopheles gambiae Giles s.s. to low intensities of 'white' light (tungsten filament), 'red' light (white light filtered by a darkroom safelight filter) and 'infra-red' light) of two types (white light filtered by a λ>700 nm filter, and light-emitting diodes with λ>900 nm). Mosquitoes were placed in a 20 cm diameter flight-tunnel and their 'optomotor' response to a pattern of stripes moving across their visual field (at 14.5 cm s^-1) was recorded with infra-red-sensitive video. In free-flight, with ample light, the mosquitoes controlled their flight speed and direction in relation to the stripe movement, so that the stripes always appeared to move across their visual field from front to back. They did this by flying either with the moving stripes fast enough to overtake them (19.5 ± 0.7 cm s^-1), or against them more slowly (10.3 ± 0.7 cm s^-1)- The net ground speed of the mosquitoes was thus c. 4–5 cm s^-1. This response was significant down to 10^-5 W m^-2 in 'white' light, and 10^-3 W m^-2 in 'red' light. At light intensities below threshold and in infra-red light, however, they appeared to fly at random with respect to the stripe movement. The assumption commonly made, that mosquitoes do not 'see' in red light, may thus have to be revised.     

Thermal dependence of swimming endurance in juvenile brown trout

The maximum swimming stamina of hatchery reared juvenile brown trout Salmo trutta , swimming against a fixed-velocity water flow of 36·6 cm s^-1 (6·97 L s^-1), was achieved at 16·1° C, and a 90% performance level occurred over a breadth of 7·7° C (12·2–19·9° C). The wide range of temperatures at which swimming performance is close to the maximal capacity could be a consequence of the implications for survival of this function.     

Habitat selection by grayling-II. Preliminary results on larval and juvenile daytime habitats

Larval grayling were found along the shoreline at velocities <20 cm s^-1 depths <40 cm, shear stress <2 dyn m^-2 and over sand and silt. Juveniles were found in the river channel at currents of 20-40 cm s^-1 depths of 40-60 cm and shear stresses of 2-4 dyn m^-2, over gravel and pebbles.     

Circadian rhythms in juvenile american shad, Alosa sapidissima

Swimming activity (in cm s⁻¹) of a school (55 individuals) of young-of-the-year ( total length=110 mm) American shad, Alosa sapidissima , was determined under a variety of photoperiod conditions. These included a normal (ambient), a shifted, and constant-light day. Swimming activity was measured over 4-day periods. During normal days swimming speeds followed periods of about 24 h, with fast speeds (up to 45 cm s⁻¹) and schooling occurring during the photoperiod. Under dark conditions speeds were slower (8 cm s⁻¹) with most fish swimming as individuals. During a shifted day swimming speeds and schooling corresponded to the imposed day. Under constant light (equivalent to bright moonlight) no schooling was evident, and a constant, but slow, swimming speed was observed in each 24-h period. These shad demonstrated an exogenous rhythm with respect to the imposed day length. It is hypothesized that an endogenous circadian rhythm would only be of use to a fish required to hunt or chase its prey. Shad, being plankton feeders, do not chase prey and therefore can exhibit an exogenous circadian rhythm with no detrimental feeding results.     

Dispersion and spatial orientation of Gerris remigis in response to water current: a comparison of pre- and post-diapause adults

ABSTRACT. The movements and orientation of adult Gerris remigis Say (Hemiptera; Gerridae) were examined in an artificial stream to determine the mechanisms by which these stream-dwelling waterstriders compensate for and/or avoid downstream drift, and to compare the movement tendency of pre- and post-diapause adults. G. remigis respond to current by turning to face directly into the current (rotational orientation), intermittently rowing against the current (translational orientation), and moving onto land to avoid the current. These rotational and translational responses enable G. remigis to maintain their positions in currents =S10 cm s^-1. However, avoidance increases with current speed, and few animals are found where currents exceed 10 cm s^-1. These observations correlate well with the observed distribution of adult G. remigis in a natural stream.
Comparisons between life stages reveal that post-diapause adults move more, and are more susceptible to drift than pre-diapause adults. Post-diapause adults also avoid even slight currents (<5 cm s^_1) by seeking land, while pre-diapause adults do not show a significant preference for land until currents exceed 10 cm s^-1. These data suggest that previously reported differences in the movement tendency of pre- and post-diapause adults in the field may reflect physiologically-based behavioural differences between these two life stages rather than merely direct responses to environmental cues.     

The effect of exercise on plasma cortisol and blood sugar levels in the rainbow trout, Salmo gairdnerii Richardson

Preliminary experiments were performed to determine the diurnal variation in cortisol, using trout which had been cannulated three days previously. These results indicated that cortisol levels were reasonably stable between 10.00 and 18.00 hours, thus permitting experimentation during this period without diurnal fluctuations masking the cortisol response. Uncannulated fish were exercised in a flume for 2 h at 1, 2.6 and 5 bl s^-1 and plasma samples taken from groups of five animals at 15, 30, 60 and 120 min after the start of exercise and at 1½, 12 and 24 h after the exercise ceased. The cortisol levels in all cases were elevated after 15 min, but the magnitude of the elevation increased with swimming speed. At 1 bl s^-1 the cortisol levels increased from 76.4 (± 20.4) to 129.2 (± 20.4) ng ml^-1 [mean (± s.d. )]. At 2.6 bl s^-1 the increase was from 72.4 (± 17.1) to 254.4 (± 34.4) ng ml^-1 and at 5 bl s^-1 the increase was from 69.5 (± 27.5) to 326.4 (± 39.0) ng ml^-1. The cortisol levels were stable over the exercise period and all groups recovered to baseline levels after 24 h, though the sample taken 12 h after the termination of exercise was elevated due to regular nocturnal increases in cortisol levels. There were no dramatic changes in blood sugar levels during and after exercise at 1 and 3.2 bl s^-1.     

Some observations on the swimming and feeding of the nauplius larvae of Lepas pectinata (Girripedia: Crustacea)

Limb movements of restrained stage VI nauplii of Lepas pectinata were studied by cine-photography. Outline drawings were made of successive limb positions in both swimming and grooming activity. The antennae appeared to act as leaky paddles performing both propulsion and food gathering. Free-swimming nauplii averaged 120 limb beats min^-1 and a speed of c. 4 mm s^-1. Grooming occurred every 7–20 beats.
It was concluded that lack of streamlining favours filtration at the expense of propulsion. The grooming sequence differs from that of balanid nauplii and is one method of transferring food to the vicinity of the mouth, where sorting and rejection take place prior to ingestion. Fine- and coarse-mesh filters presumably exploit different plankton types. The overall behaviour pattern is well-designed for exploitation of scarce food in the oligotrophic conditions of the ocean-surface habitat.     

Oxygen uptake and heart rate in young Green turtles (Chelonia mydas)

Oxygen uptake. heart rate and breathing frequencies were monitored in yearling Green turtles. Routine fed animals used about 100μ O₂ g live turtle^-1 h^-1 at 25C; this value was not significantly affected by size or short term food deprivation. Starved turtle showed a doubling of oxygen uptake after a satiation meal and heightened uptake persisted for five days. Between 15 and 30C oxygen consumption increased with rising temperature; below 15C there was falling temperature. Vigorous activity increased oxygen uptake to two or three times thr routine fed levels.
Turtles swimming gently at 25C exhibited a heart rate of around 46–48 beats min^-1; this rose to 64–68 beats min^-1 during vigorous and continuous activity. Contrary to expectations profound bradycardia was not seen during diving; even during 10 min dives a rate of 25–28 beats min^-1 was sustained. Significantly lower heart rates were only seen in turtles which were apparently asleep.     

Resistance of a cased caddis larva to accidental entry into the drift: the contribution of active and passive elements

SUMMARY. . 1. The resistance to passive entry into the drift of first to fifth instar larvae of Allogamus auricollis (Pictet, 1834), a case-bearing caddis-fly, was investigated in the laboratory using an artifical stream channel.
2. Dead larvae in their cases were exposed to different current speeds. When the heads of the larvae were directed towards the water flow (frontal position), the current necessary to wash larvae away ranged from 3 cm s^-l (first instars) to 21 cm s^-1 for fifth instars. When the larvae were at right angles to the current (lateral position), these speeds were 2 and 9cm s^-1, respectively. In terms of force (Newtons), this passive resistance to drift ranged from 0.3x10^-6 N (first instar, frontal position) to 307.0x10^-6 N (fifth instar, frontal position). The data obtained in the experiments were in good agreement with values calculated from hydrodynamic equations, using biometric parameters of the larvae.
3. Total resistance to drift was studied by exposing living larvae to different current speeds. The speed just sufficient to wash larvae away ranged from 13 cm s^-1 in the first instar to 27.9 cm s^-1 in the fifth instar (frontal position). In terms of force, the total resistance to drift varied between 5.3x10^-6 N (first instar) and 547.5x10^-6 N (last instar).
4. The difference between total and passive resistance to drift was defined as'active resistance to drift', and is due to the effectiveness of a larva's attachment to the substrate. It ranged from 3.5x10^-6 N (first instar) to 222.8X 10^-6 N (last instar).     

GROWTH OF HETEROSIGMA CARTERAE (RAPHIDOPHYCEAE) ON NITRATE AND AMMONIUM AT THREE PHOTON FLUX DENSITIES: EVIDENCE FOR N STRESS IN NITRATE-GROWING CELLS

The marine alga Heterosigma carterae Hulburt (Raphidophyta) was grown in N-limiting batch cultures using either nitrate or ammonium as the N source, at photon flux densities (PFDs) of 50, 200, and 350 μmol·m^-2·s^-1 in a 12:12 h LD cycle. Carbon content could be estimated from biovolume (μg C = 0.278 × nL; R = 0.98) but not reliably from pigment content. During exponential growth, ammonium-grown cells (in comparison with nitrate-grown cells at the same PFD) attained higher growth rates by at least 20%, contained more N, and had a lower C:N ratio, higher concentrations of intracellular free amino acids, and higher ratios of glutamine: glutamate (Gln: Glu) and asparagine: aspartate (Asn:Asp). Growth was nearly light-saturated on ammonium at 200 μmol·m^-2·s^-1 (cell-specific growth rate of 1.2 d^-1) but probably not saturated in nitrate-grown cells at 350 μmol·m^-2·s^-1. PFD did not affect Gln: Glu or Asn: Asp for a given N source. These results indicate that the nitrate-growing cells were more N-stressed than those using ammonium (which in contrast were relatively C-stressed) and that this organism would show an enhanced competitive advantage against other species when supplied with a transient supply of ammonium rather than nitrate .     

Visually-guided, upwind turning behaviour of free-flying tsetse flies in odour-laden wind: a wind-tunnel study

Abstract. To test the hypothesis that tsetse flies use visual input from the apparent movement of the ground to assess wind direction while in flight, Glossina morsitans morsitans Westwood females were video- recorded in a wind-tunnel as they entered, in cross-wind flight, a broad plume of simulated host odour (C0₂ at c. 0.05%). The tunnel (2.3 times 1.2 m wide) generated winds up to 0.25 m s^-1 and had a strongly patterned floor that could be moved upwind or downwind to increase or decrease the visual input due to wind drift. Flight tracks were analysed for speed, direction relative to the wind, and angle of turn. Mean groundspeeds were c. 1.8 m s^-1. In control measurements in still air (with or without odour) flies turned 50:50 'upwind': 'downwind'. With a 0.25 m s^-1 odour-perme- ated wind, 79% turned upwind, and c. 70% left view flying upwind. When the floor was moved at 0.25 m s^-1 upwind (to mimic the visual input from the ground due to a 0.5 m s_^-1 wind), the strength of this response increased. If instead the floor was moved downwind, faster than the wind speed (to mimic the visual input due to a wind from the opposite direction), 59% turned downwind and c. 70% left view flying downwind, and thus away from the source (though progressing 'upwind' in terms of the visual input from apparent ground pattern movement). Upwind turns were on average significantly larger than downwind turns. It is concluded that tsetse navigate up host odour plumes in flight by responding to the visual flow fields due to their movement over the ground (optomotor anemotaxis), even in weak winds blowing at a fraction of their groundspeed.     

Habitat selection by grayling—I. Spawning habitats

Grayling spawning sites were investigated in two French rivers, the Pollon (1 year) and the Suran (2 years) and described by current velocity, water depth, and substrate composition, completed by an assessment of bottom shear stress with FST-hemispheres. A comparison was made between used and available habitats, the latter being characterized by random sampling of 300 m long (Pollon) and 510 m long (Suran) river sections, both including three riffle/pool sequences. Mean velocities observed on spawning sites did not differ significantly between rivers or years (overall mean 48–9 cm s^-1 S.D. = 11.9, range 25.8–91.7 cm s^-1, n =150). Most water depths ranged from 10 to 40 cm in both rivers, but mean depths were significantly different ( P <0.05). Substratum of spawning grounds was dominated by gravel and pebbles (2–64 mm) in both rivers. Most spawning sites (99%) were characterized by a narrow range of hemispheres (nos 9–13), i.e. a range of shear stress of about 5–16 dyn m^-2. In the Pollon, spawners between spawning acts were found in a resting pool located immediately downstream from the spawning area and characterized by slow-flowing water (mainly <20 cm s^-1) and great depth (mainly >60 cm), with cover provided by overhanging branches and tree roots.     

Is tilting behaviour at low swimming speeds unique to negatively buoyant fish? Observations on steelhead trout,Oncorhynchus mykiss,and bluegill,Lepomis macrochirus

When swimming at low speeds, steelhead trout and bluegill sunfish tilted the body at an angle to the mean swimming direction. Trout swam using continuous body/caudal fin undulation, with a positive (head-up) tilt angle ( 0 , degrees) that decreased with swimming speed ( u , cm s⁻¹) according to: 0 =(164±96).u^{(−1.14±0.41)} (regression coefficients; mean±2 s.e. ). Bluegill swimming gaits were more diverse and negative (head down) tilt angles were usual. Tilt angle was −3·0 ± 0.9° in pectoral fin swimming at speeds of approximately 0.2–1.7 body length s⁻¹ (Ls⁻¹; 3–24 cm s⁻¹), −4.5 ±2.6° during pectoral fin plus body/caudal fin swimming at 1·2–1·7 L s⁻¹ (17–24cm s⁻¹), and −5.0± 1.0° during continuous body/caudal fin swimming at 1.6 and 2.5 L s⁻¹ (22 and 35cm s⁻¹). At higher speeds, bluegill used burst-and-coast swimming for which the tilt angle was 0.1±0.6°. These observations suggest that tilting is a general phenomenon of low speed swimming at which stabilizers lose their effectiveness. Tilting is interpreted as an active compensatory mechanism associated with increased drag and concomitant increased propulsor velocities to provide better stabilizing forces. Increased drag associated with trimming also explains the well-known observation that the relationship between tail-beat frequency and swimming speed does not pass through the origin. Energy dissipated because of the drag increases at low swimming speeds is presumably smaller than that which would occur with unstable swimming.     

A new type of metabolism chamber for the determination of active and postprandial metabolism offish, and consideration of results for coregonid and salmon juveniles

The optomotor reaction of juvenile Coregonus schinzipalea Val. et Cuv. and Salmo salar L. was utilized to develop a circular tube metabolism chamber to measure oxygen consumption and ammonia excretion as a function of swimming speed. The metabolism chamber with a constant water flow assured the maintenance of stable conditions. The unidirectional movement of fish was measured in a circular tube with a single narrowing. The relationships between the swimming speed and oxygen consumption or ammonia excretion described by exponential equations allowed the extrapolation towards the standard metabolism, i.e., zero swimming speed. For a juvenile coregonid (0.1–0.15 g individual weight, 2.6–2.8 cm total length) standard metabolism at 14° C was estimated as 0.65 mg0₂ g⁻¹ h⁻¹ and 17.3 μg N(NH₃)g⁻¹ h⁻¹, whereas for juvenile salmon (136mg individual weight) respective values at 22° C were 0.047mg0₂g⁻¹h⁻¹ and 0.61 μg N(NH₃)g⁻¹ h⁻¹. The feeding test with juvenile salmon was also performed in this circular chamber, and in both energy and nitrogen budgets after a meal the partitioning could be precisely attributed to standard metabolism, active metabolism and specific dynamic action (in the case of oxygen consumption) or postprandial nitrogen increase.
The new metabolism chamber allowed the relationship between metabolism and swimming velocity of juvenile fish with developed rheotactic response. It could be used with adult fish for similar purposes.     

Endurance at intermediate swimming speeds of Atlantic mackerel, Scomber scombrus L., herring, Clupea harengus L., and saithe, Pollachius virens L.

Endurance and swimming speed were measured in mackerel, herring and saithe when they were induced by the optomotor response to swim at prolonged speeds along a 28-m circular track through still water in a 10-m diameter gantry tank. The maximum sustained swimming speed ( U _ms was measured as body lengths per second ( b.l.s ⁻¹) for each species and for saithe of different size groups. Herring with U _ms of 4.06 b.l.s ⁻¹ (25.3 cm, 13.5°C) were the fastest, mackerel U _ms was 3.5 b.l.s ¹ (33 cm, 11.7°C) and saithe (14.4°C) showed a size effect where U _ms at 25 cm was 3.5 b.l.s ¹ and at 50 cm 2.2 b.l.s ¹. When swimming at speeds higher that U _ms, all three species showed reduced endurance as speed increased. How the curved track reduces the swimming speed is discussed.     

The swimming endurance of threespine sticklebacks, Gasterosteus aculeatus L., from the Afon Rheidol, Wales

The endurance of threespine sticklebacks, Gasterosteus aculeatus , swimming with pectoral fin locomotion at 20° C in a laboratory flume was measured. Each trial lasted a maximum of 480 min. At a speed of 4 body lengths per sec (L s⁻¹) all fish were still swimming at the end of the trial, but endurance decreased at higher speeds. At speeds of 5 or 6 L s⁻¹ (20–30 cm s⁻¹) a few fish still maintained labriform locomotion for the 480 min. However, at a speed of 7 L s⁻¹ all fish furled their pectoral fins and used body and caudal fin propulsion but fatigued rapidly. During sustained swimming, fish could cover distances of 6 km or more. No significant differences between males and females were found.     

Movements of ultrasonically tagged brown trout (Sulmo trutta L.) in Lake Constance

In Lake Constance from September 1986 to May 1988 13 adult lake dwelling brown trout ( Sulmo trutta L.) were tagged with ultrasonic transmitters and tracked almost continuously for up to 13 days. Two behaviour types were observed: (a) random movement in locally restricted areas and (b) excursions of up to 40 km distance. Swimming activity during the day was significantly higher than at night in most experiments. In summer swimming depth ranged between 8 and 16 m, and in winter between 0 and 3m. The preferred water temperature was about 14°C in the thermally stratified waterbody. During the experiments mean swimming speed ranged between 0.3 km h⁻¹ (0.1 bodylengths s⁻¹) and 0.9 km h⁻¹ (0.6 bodylengths s⁻¹).     

Analysis of motility parameters from paddlefish and shovelnose sturgeon spermatozoa

Ninety to 100% of paddlefish Polyodon spathula were motile just after transfer into distilled water, with a velocity of 175 μm s^-1, a flagellar beat frequency of 50 Hz and motility lasting 4–6 min. Similarly, 80–95% of shovelnose sturgeon Scaphirhynchus platorynchus spermatozoa were motile immediately when diluted in distilled water, with a velocity of 200 μm s^-1, a flagellar beat frequency of 48 Hz and a period of motility of 2–3 min. In both species, after sperm dilution in a swimming solution composed of 20 mM Tris–HCl (pH 8·2) and 20 mM NaCl, a majority of the samples showed 100% motility of spermatozoa with flagella beat frequency of 50 Hz within the 5 s following activation and a higher velocity than in distilled water. In such a swimming medium, the time of motility was prolonged up to 9 min for paddlefish and 5 min for sturgeon and a lower proportion of sperm cells had damage such as blebs of the flagellar membrane or curling of the flagellar tip, compared with those in distilled water. The shape of the flagellar waves changed during the motility phase, mostly through a restriction at the part of the flagellum most proximal to the head. A rotational movement of whole cells was observed for spermatozoa of both species. There were significant differences in velocity of spermatozoa between swimming media and distilled water and between paddlefish and shovelnose sturgeon.     

Behaviour and performance of juvenile shortnose sturgeon Acipenser brevirostrum at different water velocities

Critical swimming speeds (mean ± s . e .) for juvenile shortnose sturgeon Acipenser brevirostrum were 34·4 cm s⁻¹± 1·7 (2·18 ± 0·09 body lengths, BL s⁻¹). Swimming challenges at 10, 20 and 30 cm s⁻¹ revealed that juvenile A. brevirostrum are relatively poor swimmers, and that the fish did not significantly modify their swimming behaviour, although they spent more time substratum skimming ( i.e. contact with flume floor) at 30 cm s⁻¹ relative to 10 cm s⁻¹. When present, these behavioural responses are probably related to morphological features, such as flattened rostrum, large pectoral fins, flattened body shape and heterocercal tail, and may be important to reduce the costs of swimming.     

The swimming abilities of recently settled post-larvae of Sillaginodes punctata

Sixty-four post-larvae of the King George whiting Sillaginodes punctata were tested in swimming chambers, against one of five flow-through velocities (2, 4, 6, 8 or 10 cm s ⁻¹) for up to a maximum of 120 min. Fish were determined by regression to have an FV₅₀ (50% fatigue velocity) of 6.0 cm s⁻¹. No fish survived the full 120 min at 10 cm s⁻¹. Sixteen individuals were tested in a swimming chamber against a flow-through velocity of 6 cm s ⁻¹ and allowed to swim to exhaustion. Fish swam between 25 and 538 min with a peak at c . 6–8 h. Total swimming time was not correlated with standard length of fish although the size range examined was narrow. Relative to recent studies on the swimming abilities of late-stage larvae of reef fishes, this study indicates that post-larval King George whiting are weak swimmers. The weak swimming ability of post-larval King George whiting is consistent with studies showing passive dispersal and recruitment of this species.