17 research outputs found
The First Findings on the Differences in Complete Blood Count Between Diploid and Triploid Tench, Tinca tinca L.
Effect of Long-term Therapeutic Bath in Malachite Green on Common Carp (Cyprinus carpio L.)
Molecular cytogenetic differentiation of paralogs of Hox paralogs in duplicated and re-diploidized genome of the North American paddlefish (Polyodon spathula)
A Model Approach to Distinguish Diploid and Triploid Fish by Means of Computer-assisted Image Analysis
Indirect manifestation of cormorant (
The damage to fisheries caused by cormorant predation pressure consists of losses due to direct predation and subsequent indirect losses elicited by cormorant feeding activities resulting in fish wounding and stress. Healed wounds reduce the commercial value of afflicted fish and stress may impact fish body and health condition. Fulton´s condition coefficient (FCC) was calculated for wounded and healthy two-year old carp originating from five South Moravian (Czech Republic) fishponds. Significant (P = 0.0011) differences in FCC (mean ± s.d.), were found between non-wounded (1.48 ± 0.11, n = 19) and wounded mirror common carp, Cyprinus carpio (1.33 ± 0.14, n = 19). However no differences (P > 0.05) were recorded in scaly common carp between non-wounded (FCC 1.41 ± 0.25, n = 33) and wounded (FCC 1.46 ± 0.47, n = 33) fish of the same age and size category. A computer assisted image analysis was applied to describe the extent of such injuries. In the case of two-year old mirror, scaly and bighead carp (Aristichthys nobilis), signs of serious injuries (necroses) were recorded on 1.93, 0.89 and 1.61% of body surface, respectively. Fish with deep wounds and scars, often accompanied with progressive necroses, were subject to parasitological examination. The percentage of wounded fish from total fish harvested was evaluated as ranging between < 1 and 47.4% in five ponds under study
Indirect manifestation of cormorant (Phalacrocorax carbo sinensis (L.)) predation on pond fish stock
The damage to fisheries caused by cormorant predation pressure consists of losses due to direct predation and subsequent indirect losses elicited by cormorant feeding activities resulting in fish wounding and stress. Healed wounds reduce the commercial value of afflicted fish and stress may impact fish body and health condition. Fulton´s condition coefficient (FCC) was calculated for wounded and healthy two-year old carp originating from five South Moravian (Czech Republic) fishponds. Significant (P = 0.0011) differences in FCC (mean ± s.d.), were found between non-wounded (1.48 ± 0.11, n = 19) and wounded mirror common carp, Cyprinus carpio (1.33 ± 0.14, n = 19). However no differences (P > 0.05) were recorded in scaly common carp between non-wounded (FCC 1.41 ± 0.25, n = 33) and wounded (FCC 1.46 ± 0.47, n = 33) fish of the same age and size category. A computer assisted image analysis was applied to describe the extent of such injuries. In the case of two-year old mirror, scaly and bighead carp (Aristichthys nobilis), signs of serious injuries (necroses) were recorded on 1.93, 0.89 and 1.61% of body surface, respectively. Fish with deep wounds and scars, often accompanied with progressive necroses, were subject to parasitological examination. The percentage of wounded fish from total fish harvested was evaluated as ranging between < 1 and 47.4% in five ponds under study
Nitrite Intoxication of Common Carp (Cyprinus carpio L.) at Different Water Temperatures
Common carp (Cyprinus carpio L.) were exposed to nitrite (1.45 mmol l-1 NO2-) for 48 hours at 14 °C and 20 °C, in order to investigate the mechanism of nitrite poisoning at these water temperatures. The effect of nitrite exposure on fish was assessed on selected haematological and biochemical indicators of the blood. Moreover, nitrite accumulation in the blood, liver and muscle was measured. Nitrite exposure produced high levels of methaemoglobin (88.2 ± 3.3% and 92.9 ± 6.1%) at both water temperatures compared with controls (0.3 ± 0.6% and 2.6 ± 3.0%). High fish mortality occurred in experimental groups (30% and 51%) compared with controls (0%). Nitrite exposure also resulted in an accumulation of nitrite in the fish body. The highest nitrite levels developed in the blood plasma, followed by the liver and muscle, respectively. Carp concentrated nitrite in the blood plasma and tissues to markedly higher levels at higher temperature (20 °C). The plasma nitrite concentrations (10.5 ± 1.9 mmol l-1) were in this case more than 7 times higher than the environmental one. At lower temperature (14 °C), plasma nitrite concentration reached 5.0 ± 1.5 mmol l-1. In either event, plasma K+ levels increased and Cl- levels and osmolality remained unchanged. Plasma Na+ levels slightly decreased at the higher temperature. Nitriteexposed fish showed lower haematocrit values (PCV) at both experimental temperatures compared with controls. At 20 °C, the blood haematocrit decrease (0.20 ± 0.02 l l-1) was accompanied by a low erythrocyte count (1.05 ± 0.12 1012 l-1) and by a low haemoglobin level (51 ± 11 g l-1). At the lower temperature (14 °C), the haematocrit decrease (0.25 ± 0.02 l l-1) was caused by a low mean corpuscular volume (167 ± 27 fl). No significant changes were observed in the mean corpuscular haemoglobin (MCH), mean corpuscular haemoglobin concentration (MCHC), or selected erythrocyte dimensions (major axis, minor axis and aspect ratio)