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64 results for “Mytilus galloprovincialis”
Geographical distribution of the Mediterranean mussel Mytilus galloprovincialis Lamarck, 1819 in the Sea of Japan. in The extension of the distributional range of an invasive mussel, Mytilus galloprovincialis (Bivalvia: Mytilidae) in the Sea of Japan
Geographical distribution of the Mediterranean mussel Mytilus galloprovincialis Lamarck, 1819 in the Sea of Japan.
Fig. 4 in The dual impact of Ostreopsis cf. ovata on Mytilus galloprovincialis and Paracentrotus lividus: Toxin accumulation and pathological aspects Abstract
Fig. 4: Health status of sea urchins (avg±SDV, n = 4 animals) exposed to Ostreopsis cf. ovata (strain D483) for five days at different cell densities. Health index 1 corresponds to all four sea urchins alive after five days of exposure, 0 to all sea urchins dead in four days, intermediate values to different degrees of damage such as spine folded, partial and total spine loss and death in five days.
Fig. 6 in The dual impact of Ostreopsis cf. ovata on Mytilus galloprovincialis and Paracentrotus lividus: Toxin accumulation and pathological aspects Abstract
Fig. 6: Sea-urchin health status (avg±SDV, n = 4) after exposure to whole Ostreopsis cf. ovata cultures (strain 00APS0810-S1) or toxins extracted from cultures of the same cell density.
Fig. 2 in The dual impact of Ostreopsis cf. ovata on Mytilus galloprovincialis and Paracentrotus lividus: Toxin accumulation and pathological aspects Abstract
Fig. 2: Feeding of Mytilus galloprovincialis on Ostreopsis cf. ovata in a 72 h experiment. Weight-normalised ingested cells (avg±SDV) at different time intervals. Fresh microalgal cultures (2.17±0.23·103 cells ml-1) were provided every 24 h. Of the 10 animals of each replicate, 7-8 died at the beginning of the second day while the survivors were toxic (Table 1).
Fig. 5 in The dual impact of Ostreopsis cf. ovata on Mytilus galloprovincialis and Paracentrotus lividus: Toxin accumulation and pathological aspects Abstract
Fig. 5: Sea urchin health status (avg±SDV, n = 4) upon exposure to entire or sonicated Ostreopsis cf. ovata cultures (strain D483) of the same initial cell density.
Fig. 3 in The dual impact of Ostreopsis cf. ovata on Mytilus galloprovincialis and Paracentrotus lividus: Toxin accumulation and pathological aspects Abstract
Fig. 3: Feeding of Paracentrotus lividus (avg±SDV, n = 15) on Ostreopsis cf. ovata epiphytic on the red alga Asparagopsis taxiformis in five experiments lasting five days each. Experiment 4b was performed with the same animals as 4a, which were given a second stock of seaweeds after a two- day interval. Macroalgae (55-131 g) were completely eaten in all cases. Four additional experiments at low epiphytic cell density (<3.4·103 cells g-1) are not represented. Asterisks indicate the experiments in which sea urchins were weakly toxic at the mouse bioassay (Supplementary Material, Table S2).
Fig. 1 in The dual impact of Ostreopsis cf. ovata on Mytilus galloprovincialis and Paracentrotus lividus: Toxin accumulation and pathological aspects Abstract
Fig. 1: Feeding of Mytilus galloprovincialis in six 24 h experiments with animals of different sizes exposed to different Ostreopsis cf. ovata cell concentrations. A) Mussel wet weight (WW) and O. cf. ovata cell density at the beginning of each experiment (avg±SDV). B) Weight-normalised ingested cells (avg±SDV). The asterisks indicate experiments in which some or all replicates were toxic to the mouse bioassay (Supplementary Material, Table S1).
Рис. 2. Схема станΔартных промеров раковины Δвустворчатых моΛΛюсков по А. А. Зютину: L — ΔΛина раковины; H — тоΛщина раковины; D — ширина / выпукΛость Fig. 2. Scheme of bivalve mollusk shell standard measurements: L — shell length; H — shell thickness; D — width / convexity (according to A. A. Zyutin) in Morphometric characteristics of Black Sea mussels Mytilus galloprovincialis Lam. as biomarkers of the anthropogenic impact on the Black Sea coastal biocenoses in tourist destinations
Рис. 2. Схема станΔартных промеров раковины Δвустворчатых моΛΛюсков по А. А. Зютину: L — ΔΛина раковины; H — тоΛщина раковины; D — ширина / выпукΛость Fig. 2. Scheme of bivalve mollusk shell standard measurements: L — shell length; H — shell thickness; D — width / convexity (according to A. A. Zyutin)
Рис. 1. Схема распоΛожения станций отбора проб (сервис ЯнΔекс.Карты) Fig. 1. Location of the sampling stations (source: Yandex.Maps) in Morphometric characteristics of Black Sea mussels Mytilus galloprovincialis Lam. as biomarkers of the anthropogenic impact on the Black Sea coastal biocenoses in tourist destinations
Рис. 1. Схема распоΛожения станций отбора проб (сервис ЯнΔекс.Карты) Fig. 1. Location of the sampling stations (source: Yandex.Maps)
Рис. 3. Ливневый сток, прохоΔящий через территорию муниципаΛьного пΛяжа «Маяк» (фото авторов) Fig. 3. Stormwater runoff passing through the territory of "Mayak" municipal beach (photo by the authors) in Morphometric characteristics of Black Sea mussels Mytilus galloprovincialis Lam. as biomarkers of the anthropogenic impact on the Black Sea coastal biocenoses in tourist destinations
Рис. 3. Ливневый сток, прохоΔящий через территорию муниципаΛьного пΛяжа «Маяк» (фото авторов) Fig. 3. Stormwater runoff passing through the territory of "Mayak" municipal beach (photo by the authors)
FIG. 6 in Морфометрические особенности личинок мидии Mytilus galloprovincialis (Lamarck, 1819) (Bivalvia: Mytilidae) в онтогенеЗе
FIG. 6. Graphs of the correlations: (A) height (H, µm) vs. length (L, µm) of the larval shell, (B) hinge edge length (l, µm) vs. length of Mytilus galloprovincialis larval shells in ontogenesis
РИС. 7. Спектры ЭнергодисперсионноЙ рентгеновскоЙ спектроскопии (ЭДС(х)) лигамента Замкового краЯ (обоЗначено стрелками) левоЙ (A, A1) и правоЙ (B, B1) створок раковины личинок мидии Mytilus galloprovincialis на стадии великонхи с "глаЗком". in Морфометрические особенности личинок мидии Mytilus galloprovincialis (Lamarck, 1819) (Bivalvia: Mytilidae) в онтогенеЗе
РИС. 7. Спектры ЭнергодисперсионноЙ рентгеновскоЙ спектроскопии (ЭДС(х)) лигамента Замкового краЯ (обоЗначено стрелками) левоЙ (A, A1) и правоЙ (B, B1) створок раковины личинок мидии Mytilus galloprovincialis на стадии великонхи с "глаЗком".
FIG. 3 in Морфометрические особенности личинок мидии Mytilus galloprovincialis (Lamarck, 1819) (Bivalvia: Mytilidae) в онтогенеЗе
FIG. 3. Larvae of the mussel Mytilus galloprovincialis at the veliger stage (A = 134.0 µm, B = 143.0 µm, C = 164.0 µm). Scale: 30 µm. A1, B1, C1 demonstrate SEM images of the hinge edge of the veliger shell: (a) left valve, (b) right valve (see description in text).
РИС. 1. Личинки мидии Mytilus galloprovincialis на стадиЯх: A – стерробластулы (стрелками обоЗначены три рЯда ресничек) и B – трохофоры (стрелкоЙ обоЗначены реснички апикального султанчика). МасШтаб: 15 мкм. FIG. 1. Larvae of the mussel Mytilus galloprovincialis at two different stages: (A) –sterroblastula (arrows indicate three rows of cilia) and (B) – trochophore (the arrow indicates cilia of the parietal plume). Scale: 15 µm. in Морфометрические особенности личинок мидии Mytilus galloprovincialis (Lamarck, 1819) (Bivalvia: Mytilidae) в онтогенеЗе
РИС. 1. Личинки мидии Mytilus galloprovincialis на стадиЯх: A – стерробластулы (стрелками обоЗначены три рЯда ресничек) и B – трохофоры (стрелкоЙ обоЗначены реснички апикального султанчика). МасШтаб: 15 мкм. FIG. 1. Larvae of the mussel Mytilus galloprovincialis at two different stages: (A) –sterroblastula (arrows indicate three rows of cilia) and (B) – trochophore (the arrow indicates cilia of the parietal plume). Scale: 15 µm.
РИС. 4. Личинки мидии Mytilus galloprovincialis на стадии великонхи (A – 190,0 мкм; B – 221,0 мкм; C – 253,0 мкм). МасШтаб: 30 мкм. A1; B1; C1 – СЭМ-иЗображениЯ Замкового краЯ раковины личинок на стадии великонхи: a – леваЯ створка; b – праваЯ створка. (Описание в тексте). in Морфометрические особенности личинок мидии Mytilus galloprovincialis (Lamarck, 1819) (Bivalvia: Mytilidae) в онтогенеЗе
РИС. 4. Личинки мидии Mytilus galloprovincialis на стадии великонхи (A – 190,0 мкм; B – 221,0 мкм; C – 253,0 мкм). МасШтаб: 30 мкм. A1; B1; C1 – СЭМ-иЗображениЯ Замкового краЯ раковины личинок на стадии великонхи: a – леваЯ створка; b – праваЯ створка. (Описание в тексте).
Figure 2 in First report of some parasites from Mediterranean mussel, Mytilus galloprovincialis Lamarck, 1819, collected from the Black Sea coast at Sinop
Figure 2. Parasites of M. galloprovincialis: A. Nematopsis legeri, B. Peniculistoma mytili, C. Urastoma cyprinae, D. Parvatrema duboisi, E. Polydora ciliata, F. burrow (Λ) on the inner side of mussel shell.
Figure 3 in Short-time salinity fluctuations are strong activators of oxidative stress in Mediterranean mussel (Mytilus galloprovincialis)
Figure 3. Short-time salinity fluctuations promote ROS formation in hemocytes. Mussels were acclimated to high (24 - 40 ‰, HS) and low (6-14 ‰, LS) environmental salinity. ROS levels were analyzed based on flow cytometric measurement of fluorescence levels of hemocytes stained with DCF-DA. Bars indicate mean±SE. Results were considered significant when p<0.05 by Mann-Whitney test (n=10).
Figure 5 in Short-time salinity fluctuations are strong activators of oxidative stress in Mediterranean mussel (Mytilus galloprovincialis)
Figure 5. Activity of the antioxidant enzymes in gills of mussels following exposure to short-time salinity fluctuations. Activity of SOD (a), Activity of CAT (b). Mussels were acclimated to high (24-40‰, HS) and low (6-14 ‰, LS) environmental salinity. The control group was held at 18‰. Each bar represents the mean value from 10 samples with the standard error. Results were considered significant when p<0.05 by Mann-Whitney test (n=10). (p <0.05).
Figure 2 in Short-time salinity fluctuations are strong activators of oxidative stress in Mediterranean mussel (Mytilus galloprovincialis)
Figure 2. Mortality of mussels exposed to short-time salinity fluctuations. The diagram shows the percentage of dead mussels acclimated to high (24-40 ‰, HS) and low (6-14‰, LS) environmental salinity. The control group was held at 18 ‰. Bars indicate mean±SE (n=10).
Figure 2 in Sex inversion in cultivated mussels Mytilus galloprovincialis Lam. (Crimea, Black Sea) under influence of external environmental factors
Figure 2. Sex inversion in females of the cultivated mussel M. galloprovincialis after a one-month-long laboratory experiment and three-months-long conditioning at the mussel-and-oyster farm, 2016–2017.
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