In order to examine the effects of crude oil and dispersed crude oil (DCO) on the swimming ability of puffer fish, Takifugu rubripes, the critical swimming speeds (U crit) of fish exposed to different concentrations of water-soluble fraction (WSF) of crude oil and DCO solution were determined in a swimming flume. WSF and DCO significantly affected the U crit of puffer fish (p < 0.05). The U crit of puffer fish exposed to 136 mg L(-1) WSF and 56.4 mg L(-1) DCO decreased 48.7 % and 43.4 %, respectively. DCO was more toxic to puffer fish than WSF. These results suggested that crude oil and chemically dispersed oil could weaken the swimming ability of puffer fish.
The critical swimming speed (U , cm s) of juvenile tiger puffer Takifugu rubripes was determined under different temperatures (15, 21, 25 and 30 °C), salinities (5, 10, 20, 32 and 40), body lengths (3.32, 4.08, 5.06 and 5.74 cm) and starvation days (1, 3, 6 and 9 days). Acute temperature change, body length and starvation significantly influenced the U of tiger puffers, whereas acute salinity change had no significant effect. The U increased as the temperature increased from 15 to 30 °C. The U increased as the body length increased from 3.32 to 5.74 cm, whereas relative critical swimming speed (U', body length s) decreased. The relationship between the body length (l, cm) and U or U' can be described by the quadratic model as U = - 1.4088 l + 16.976 l - 11.64, R = 0.9698 (P< 0.01) or U ' = - 0.1937 l + 0.9504 l + 7.7666, R = 0.9493 (P< 0.01). The U decreased as starvation days increased from 1 to 9 days. Low temperature and starvation can reduce the swimming ability of juvenile tiger puffers. Results can be of value in evaluating the swimming ability of juvenile tiger puffers, understanding ecological processes and improving the population enhancement of tiger puffers.
Background
Supracondylar humeral fractures (SCHFs) are frequent in children, and closed reduction with percutaneous pin fixation remains the standard surgical treatment for displaced SCHFs. Two pinning configurations, medial–lateral crossed entry pinning (MLP) and lateral-only entry pinning (LP), are widely used, but which one is superior to another one is still debatable. This meta-analysis aimed to compare the efficacy and safety of both pinning fixation methods.
Methods
Randomized controlled trials (RCTs) were searched on PubMed, EMBASE, Web of Science, Cochrane library and Google Scholar. Relative risk (RR) and mean difference (MD) with corresponding 95% confidence interval (CI) were calculated for radiographical outcomes, functional outcomes and complications.
Results
A total of 19 RCTs comprising 1297 Gartland type II and type III fractures were included. MLP had a decreased risk of loss of reduction (RR = 0.70, 95%CI 0.52–0.94, P = 0.018) but a higher risk of iatrogenic ulnar nerve injury (RR = 2.21, 95%CI 1.11–4.41, P = 0.024) than LP. However, no significant difference was observed for incidence of ulnar nerve injury if applying a mini-open technique in MLP group (RR = 1.73, 0.47–6.31, P = 0.407). There were no differences between both groups in loss of carrying angle (MD = − 0.12, 95%CI − 0.39 to 0.16), loss of Baumann angle (MD = 0.08, 95%CI − 0.15 to 0.30), excellent grading of Flynn criteria (RR = 1.06, 95%CI 0.99–1.14, P = 0.102) and pin tract infection (RR = 0.92, 95%CI 0.50–1.70).
Conclusions
MLP is more effective in maintaining fixation, while LP is safer with respect to ulnar nerve injury. MLP with a mini-open technique reduces the risk of ulnar nerve lesion and is an effective and safe choice.
To understand the behavior of the large yellow croaker (Larimichthys crocea) in a pen aquaculture setting, three individuals in each of two experimental groups were telemetered in meter scale by four cable-synchronized hydrophones. The ultrasound pinger system was applied to track the motion of six L. crocea for 24 h using two fixation methods, i.e., implanting tags in the abdomen (the in vivo implantation group) and hanging tags on the dorsal fin (the dorsal fin suspension group). Pingers repeated unique 62.5 kHz coded signals at 5 s intervals along with a pressure signal. The results showed that fish tagged with internal pingers took approximately 3 h longer than externally tagged fish to stabilize in their behavior, as measured by depth utilization; the horizontal movements of the test fish were mostly found outside of the fence, where the test fish performed round-trip swimming, with the least probability of appearing near the production platform and more frequent activities in the feeding areas.
The construction of marine ranches can enrich and conserve the fishery resources and improve the marine ecosystem, which helps realize the sustainable utilization of these resources. Sebastes schlegelii is a major breeding and releasing fish species in the marine ranches of North China. Its behavioral characteristics can be understood better by researching its vocalization, which will provide data support for constructing acoustic taming marine ranches with S. schlegelii as the target fish species. However, there are few studies focusing on its sounds and behaviors. Therefore, based on the passive acoustic monitoring technology, the audios of underwater noises made by S. schlegelii were extracted using an AQH hydrophone. The high-definition internet protocol camera was used to monitor the behavior change of S. schlegelii. Then, by collating and replaying the collected audios and videos, the feeding behavior and biological noises of S. schlegelii were matched to analyze their relationship. Results are as follows: (1) The noise of chewing settling granular baits (Φ5.0 mm) has a main frequency band and sound pressure level of 2000~4500 Hz and 96.53 ± 0.65 dB, respectively; in this feeding process, the main frequency band and sound pressure level of the swimming noise are 25~400 Hz and 95.63 ± 0.38 dB, respectively; the values are 500~700 Hz and 97.34 ± 4.91 dB, respectively, for the noise of flapping the water with the tail. (2) The sound signals emitted by S. schlegelii are mostly presented as single pulses during normal habitation or ingestion of baits on the surface of the water tank. However, S. schlegelii will attack and fight against each other when scrambling for baits, during which these signals are presented as continuous pulses. To sum up, the vocalization of S. schlegelii is closely related to feeding activities, and the sounds produced under different behaviors have specific biological significance.
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