Abdullah |
2 |
20–75 dB |
exposure to various noise for 15 min |
3 repetitions in each day for 5 days |
noise interferes with prey perceptions of predators |
Akefe |
30 |
100 dB |
exposed to noise, with or not kaempferol + zinc gluconate |
48 days |
noise interferes with oxidative stress |
Amorim |
16 |
104–140 dB re. 1 μPa |
impacts of boat noise exposure in the reproductive success of wild toadfish |
2 weeks |
Noise affected reproductive success by decreasing the likelihood of receiving eggs, the number of live eggs and increasing the number of dead eggs |
Baltzer |
not specified |
120–99 dB re 1 μPa2s |
effects of underwater noise on marine mammals |
1 day |
anchor pipe vibration embedment noise might induce a behavioral reaction (changes in movements) |
Blanchett |
98 |
51.5–66.6 dB |
associations between visitor numbers, noise levels and stress or critical behavior |
12 days |
lack of association between visitor numbers and stress or critical behavior |
Criddle |
24 |
85–115 dB |
NMDA receptor blocker and sound exposure |
4 h + 28 days |
treated animals show lower hyperactivity |
Durbach |
Not specified |
approximately 3 kHz and a nominal source level of 235 dB re 1 µPa |
investigate the effect of sonar activity on movement behaviors |
3–4 days for 3 years |
Faster and more directed movement during sonar exposure; animals were more likely to cease calling during exposure |
Frouin-Mouy |
2 |
94.8–110.2 dB re 1 μPa |
measuring the underwater source levels, behavioral vocal and non-vocal marine mammal signals |
1 month |
noise can interfere communications between group |
Gang |
120 |
mean sound pressure level of 72 dB (A) |
Associations between aircraft noise and cognitive functions |
2 h daily for 4 days |
Changes in spatial recognition memory |
Grunst |
34 pairs |
60 dB |
altered parental behaviors in response to consistent freeway noise and a diverse anthropogenic noise |
2 weeks |
no population-level changes in nestling provisioning behavior during noise but individual differences in noise sensitivity |
Hastie |
5 |
148 dB re 1 µPa |
measuring the relative influence of a sound (silence, pile driving, and a tidal turbine) on decision-making and foraging success in grey seals |
8 days |
Foraging success was significantly reduced (16%–28% lower) when the speaker was located at the Low Density prey patch |
Hubert |
64 |
mean SPLs 128.3 or 119.0 dB re 1 μPa |
exposed seabass to different impulsive sound treatments (pulse level, elevated background level) |
3 sound treatment in each day for 2 days |
upon sound exposure, fishes increased their swimming depth |
Issad |
32 |
80 dB |
Effects of light and noise pollution on body temperature and anxious behavior |
3–4 weeks |
significant decrease in the number of line crossings and time spent in the open field test. |
Koorpivaara |
182 |
not specified |
dexmedetomidine for noise-associated acute anxiety and fear in dogs |
3 months |
noise can caused hyperactivity by locus coerulus’activation |
Landsberg |
24 |
average 83.9 dB |
two treatment groups (DAP and placebo) in response to a thunderstorm recording |
a week |
pheromones reduce anxiety and fear by noise |
Lara |
Not specified |
130 and 150 dB re 1 μPa |
Shipping activity can altered fish’behavior |
5 days |
continuous noise can increase dark avoidance in anxiety-related dark/light preference test and impaired spontaneous alternation behavior |
Leduc |
32 |
45–100 dB |
Noise can reduce the available cognitive processing capacity |
3 weeks |
fish exposed to noise playbacks require additional time to reach this target and reduce exploratory behavior |
Longenecker |
16 |
116 dB |
relationship between tinnitus, hearing loss, hyperactivity and bursting activity post noise trauma |
1 h |
noise increase tinnitus and hyperactivity |
Manukyan |
24 |
91 dB |
monitoring hdl, ldl, cholesterol, cognitive functions post noise exposure |
60 days |
chronic noise altered behavioral activity, delay in movement and orientation, increased anxiety, deficit spatial memory |
Martin |
35 groups (369 individuals) |
60.9–64.4 (low)/64.4–70.5 (medium)/70.5–80 dB re 20 μPa RMS SPL (high) |
Effect of car and boat noise on marine mammals behavior |
1 month |
detriment of vital activities such as resting and nursing that decreased considerably (from 5.9 to 45% decrease) |
Mikolajczak |
40 |
94–104 dB |
effect of noise by wind turbines on the stress parameters (cortisol) |
17 weeks |
lower activity, some disturbing changes in behavior, increased cortisol |
Miller |
43 |
1–4 kHz |
Effect of sonar noise on foraging |
13 h |
whales ceased foraging completely during killer whale and sonar exposures |
Mills |
28/20 |
120–70 dB re 1 μPa2s/Hz |
short-longer effect motorboat-noise playback on the behavior, cortisol, androgens of anemonefish |
30 min/48 h |
in short term, hiding aggression, androgen level increased |
Mulders |
24 |
20–120 dB |
monitoring hyperactivity post noise exposure |
2 weeks |
hyperactivity in the colliculus begins at some time between 4 and 12 h post trauma |
Park |
27/24 |
41.3–57.60 dB |
Effects of wind turbine on frog’s behavior |
2 days |
Call rate increased after 1 h of exposure |
Pellegrini |
122 groups |
180 dB re: 1 lPa V−1
|
Effects of boat noise on foraging |
9 months |
cooperative foraging may potentially be reducedor interrupted by the presence of boats, in response to the number, type and speed, indicating a behavioral change and acoustic masking |
Pirotta |
32 |
50–200 dB re 1 μPa2s/Hz |
How vessel noise influenced foraging behavior |
5 days |
ship noise caused a significant change in whale behavior up to at least 5.2 km away from the vessel. |
Senzaki |
142 species (58,506 nest) |
Not specified |
Effect of light and noise on reproductive success |
14 years |
Closed-habitat, but not open-habitat, birds also tended to experience a decline in clutch size with noise exposure |
Uran |
30 |
95–97 dB SPL |
Monitoring hippocampal-related behavioral alterations |
15–30–45 postnatal day |
moderate intensity can changed hippocampus, with observed behavioral effects |
Van der Knapp |
49–250 |
123–140 dB (re 1 μPa) |
Effect of boat noise on behavior |
6 months |
in presence of boat noise) fishes spent more time in behaviorsconsidered to be a response to predators |
Van der knapp(b) |
14 |
114–138 dB (re 1 μPa) |
Effect of wind turbine on movement behavior of free swimming |
4 months |
cod did not increase their net movementactivity, but moved closer to the scour-bed (i.e., hard substrate), surrounding their nearest turbine, |
Wang |
60 |
60–100 dB |
investigate the effects of ship noise on foraging, vigilance and flight behaviors |
1 month |
As the noise level increased, foraging behavior decreased and vigilance and flight behaviors increased, particularly above 70 dB |
Wieczerzak |
10/11 |
40 Hz |
Investigated neural plasticity in the auditory and prefrontal cortices in the days following noise exposure |
1 month |
noise exposure impaired spatial learning and reference memory |
Williams |
13 |
241 dB re 1 μPa-m |
Investigated reactions to anthropogenic noise by this deep-diving cetacean |
5 years |
movement from surface to depth (descent) was often more gradual for control dives than for noise exposed dives which showed shorter, more rapid ‘directed’ descents |