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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of applied ichthyology 15 (1999), S. 0 
    ISSN: 1439-0426
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 2021-05-19
    Description: Aquaculture of sturgeon species and their hybrids is being considered as an important substitution for sturgeon catch due to highly decrease of natural populations, artificial propagation and fingerling release in the sea. In this study, big bester, a new hybrid sturgeon (female beluga × male bester) was produced for the first time in IRAN. Sperm of 7350 ± 1682 kg male bester was used to fertilize the eggs of one 54 kg female Huso huso. The fries of big bester and control trestment of beluga were fed by artificial concentrated food (48-50% protein and 15-17% fat) after egg yolk absorbance, a period of feeding on Artemia and Daphnia. Results showed that rearing and feeding of bester broods was efficient to reach the fish to maturation stage and there is an opportunity to collect qualified ova and sperm from F1 generation. Meanwhile sex determination and maturity assessment of gonads were successfully done via laparoscopy method. The comparison of produced big bester fingerlings with control beluga fingerling showed that the weigth of big bester fingerlings has not significant difference with beluga's (p〈 0.05) at the age up to 2 months.At 3 months of age, beluga fingerlings showed higher weight (p〉0.05), but there are faster growth rate in big bester fingerlings from 3 months of age up to 5 months (p〉 0.05) in comparison with belugs fingerlings. Meanwhile no statistically significant difference was found between length of big bester and beluga fingerlings among any age. The results of current study showed the potential of rearing male bester to produce matured broods and collection of their sperm for big bester production.
    Description: Iranian Fisheries Science Research Institute
    Description: Published
    Keywords: Beluga ; Bester ; Hybridization ; Big bester ; Aquaculture ; Productions
    Repository Name: AquaDocs
    Type: Report , Refereed
    Format: 44pp.
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  • 3
    Publication Date: 2021-05-19
    Description: Considering decrease in total catch of sturgeon & threat of extinction in their stocks, special measures might be adopted. Sperm cryopreservation is one of the suitable methods to prepare bank of frozen gamete for future use in artificial breeding in order to prohibit extinction of sturgeon stocks. This study carried out on 27 male sturgeon during 2001-2004. The investigated sturgeon include 12 male Persian sturgeon (Acipenser persicus), 7 male Acipenser stellatus, 5 male Acipenser nudiventris and 3 male Huso huso. Sperm Collected from spawners in Shahid Beheshti & Shahid Marjani sturgeon rearing & propagation Complex in Rasht & Gorgan. The Sperm which was collected from Shahid Marjani propagation complex placed in the sealed Vessels & transferred by coleman in near zero temperature to cryopreservation laboratory of international sturgeon research institute for further investigation. In this study, the sperm was diluted in ratio 1:1 in two culture media containing dimethyl sulfoxide & glycerol (BC) and the samples stored in 1 ml insulin syringe & 0.5 ml Piot. The diluted sperm froze in a special temperature by automated freezer model 5300 (France IMV). Three phases applied to freeze the samples which are as follow: 1- Begin to freeze from +50c to -100c (30c /min) 2- From 10 0c to 70 0c (20 0c /min) 3- From 70 0c to 130 0c (25 0c /min) After freezing, the samples placed in liquid nitrogen containers with 196 0c temperature. For thawing, the sperm samples took out of liquid nitrogen & placed in water 40 0c. Then motility percent & the sperm quality investigated under 400x microscope. According to the results the mean motility percentage of fresh sperm in Persian sturgeon, Acipenser Stellatus, Acipenser nudiventris and Huso huso was 84, 73.75, 67.5 and 76.66, respectively. The mean percentage of motility in frozen sperm which placed in media containing dimethyl sulfoxide was 32, 37.5, 40 and 20%, respectively. Also, the frozen samples that preserved in BC media (Biociphus) showed 5.2, 75.25, 4.11 and 2.66% motility, respectively. In blank group, the mean fertilization percent of eggs was 90, 72, 71.25 and 90%, respectively. In the treatment group applying frozen sperm in culture media containing dimetlylsulfoxide, the mean fertilization rate was 30, 6.5, 25.39 and 4.75%. Furthermore, no fertilization (0.0%) observed using frozen sperm stored in Biociphus culture media containing glycerol. There was no significant difference in fertilization percent comparing the two storage places (syringe & Piot). According to investigations the culture media containing dimethyl sulfoxide, is a suitable diluter for sturgeon sperm. So, the Cryopreservation technique can be used to preserve the sturgeon sperm for future fertilization & through this way we can prevent extinction of sturgeon stocks.
    Description: Iranian Fisheries Science Research Institute
    Description: Published
    Keywords: Cryopreservation ; Sperm ; Acipenser nudiventris ; Huso huso ; Acipenser stellatus ; Acipenser persicus ; Breeding ; Sturgeon ; Temperature ; Motility ; Fertilization ; Spermatozoa ; Freezing
    Repository Name: AquaDocs
    Type: Report , Refereed
    Format: 53pp.
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  • 4
    Publication Date: 2021-05-19
    Description: In order to introduce a new sturgeon hybrid to aquaculture industry, the possibility of hybrid production by crossing between Siberian and Persian sturgeons and its comparison with its pure parents using morphometric, molecular, cytogenetic and growth performance were conducted. For this purposes eggs and sperms of two pairs of Persian and Siberian sturgeon were collected and reciprocal crosses with 4 treatments were conducted. In treatment 1, Persian sturgeon as control (male and female of Persian sturgeon), treatment 2 (as type I hybrid) from crosses of male Persian sturgeon with eggs of female Siberian sturgeon in treatment 3 (type II hybrid) using crosses between male Siberian sturgeon and female Persian sturgeon and finally treatment 4 by crossing male and female of Siberian sturgeon were used. For each treatment 200 gr. of eggs were fertilized with one ml. of sperm and morphological, meristic parameters of parents and offspring were recorded. For growth comparison of fingerlings of control and hybrids in 3 different phases were measured. In phase (I), larvae rearing from 46 mg. up to 6600 mg. were conducted for a period of 10 weeks. Samples were collected once every two weeks and biological parameters were recorded. In rearing phase II for a period of 330 days, growth comparison were conducted for fish from 6.5 gr. to 750gr. and biological parameter were recorded once every month, where daily growth rate (gr./day), FCR, Specific growth coefficient (percentage per day), increase of body weight, food efficiency and protein efficiency ration were analyzed. In rearing phase (III), from 600 gr. to 2000 gr. for a period of 43 weeks, similar to phase (II) all biological parameters were analyzed, where 26 morphometric and meristic parameters of pure and hybrid parents and offspring were compared both for individual and ratio status of parameters. For genetic analysis and variation between control and hybrid specimens the microsatellite analysis were conducted. For this purposes, genomic DNA were extracted from fin tissues of brood stocks and fingerlings and 10 pairs of specific primers (Afug 56, Afug 63, Afug 241, Afug 229, OX 27, Afug 686, Afug 195, Afug 12, IS 68 and Afug 160) were used. Then PCR Products were electrophoresed on 6% polyacrylamide gel and then were stained with Nitrate silver and alleles were evaluated based on its length (base pair). Cytogenetic analysis and number of chromosome of control fish and hybrid were compared using white blood cell culture method and chromosome spread of parents as well as offspring were prepared by Gimsa staining and were visualized under light microscope. For sexual gonad development, laparoscopic method with light camera (Model M-CAM 1700) were used to differentiate 34 pieces of control and hybrid fish and gonad status of ovary and testis were analyzed. In present investigation the results indicate that, in phase (I) of larvae culture, a significant differences were observed after 10 weeks of feeding (p≤ 0.05) in hybrid and control groups. Maximum growth rate were observed in Siberian sturgeon larvae, followed by type I hybrid, type II hybrid and Persian sturgeon larvae. In phase (II) , growth rate of Persian sturgeon were lower than Siberian sturgeon. For period of 330 days of rearing periods, the control Siberian sturgeon had 1.4gr. weight increment per day, while Persian sturgeon had only1. gr./day. However the hybrid type (I) had an average daily growth of 1.5gr/day and lower growth performance were observed in type II hybrid with daily growth of 1.5 gr./day. In phase (III), growth rates were varied at different age group. The daily growth rate of Siberian sturgeon was 4.5gr/day, while is control Persian sturgeon was 2.6 gr/day. The Siberian sturgeon within 47 weeks of rearing grown from 655 gr. to 2016 gr., however Persian sturgeon for the same period reached from Siberian sturgeon with male’s Persian sturgeon had higher type II hybrid showed opposite results for the same growing period and reached from 640 gr. to 1680 gr. In conclusion of growth performance can be stated that the hybrid from crosses between female Siberian sturgeon with male Persian sturgeon presented highest growth rate in comparison to control hybrid. This excellent achievement can be considered as a big step toward sturgeon aquaculture for meat and Caviar production. In analysis of morphometric characters 26 parameters were investigated which in 18 parameters showed significant differences (p≤ 0.05) which indicate clear distinguish able of hybrid performance in compare with parents where Siberian sturgeon has longer snout compare to Persian sturgeon and its size are intermediate in hybrids. In relative ratio of characters, out of 9 characters totally 7 characters showed significant differences (p≤ 0.05). In molecular analysis using microsatellite primers totally 400 DNA samples of hybrid as well as the control fish were investigated. Totally 784 allele were detected in which 363 alleles were belong to control fish and 421 alleles in hybrid. In this study, 19 alleles with different sizes were observed in hybrids rang from (120bp) in Aox27 primers (400bp) in AFUG229 primers. In comparing of all primers, the primer AFUG160 and AFUG195 with 2 alleles and primer AFUG686 with 7 alleles showed the minimum and maximum allele numbers.The banding patterns were monomorphic in 66 loci of control fish and 65 loci of hybrids, and in 77 loci of control fish and 73 loci of hybrids were diploid in 9 loci of control fish and 12 loci of hybrid fish were tetraploid, in one locus of control samples and 3 hybrid samples were pentaploid and finally within 10 pairs of primers 7 sets were disomic, 3 primers (Afug241, Afug686, Aox27) were tetraploid and 6 primers of (Afug63, Aox27, Afug688, Afug12, Is68, Afug160) showed excellent allele heritability which indicate the high efficiency of microsatellite techniques. In evaluation of the status of gonad development as well as determination of sexual stages laprascopic method indicated that out of 9 samples of Persian sturgeon (4 females and 5 male) were in stage of 2 & 3 gonad development. Out of 8 Siberian sturgeon (4 males+4 females) stage 2, 3, 4 were detected. In 7 gonad samples of hybrid (Female Persian and Male Siberian) totally 5 male and 2 female were observed at stage 3 and 4 gonad development. In analysis of 10 samples of type II hybrid (female Siberian × male Persian) 3 female, 6 males and 1 deformetic were observed. Cytological studies on 30 metaphase palate from 6 fish samples showed that the number of chromosome in hybrid are as same as parents 2n=250±10 where all control and hybrids similar to its parents showed 240 chromosome. In conclusion, It can stated that, this study successfully introduced a new sturgeon hybrid for sturgeon farming both for meat and caviar production. Considering the common name of sturgeon parents used for production this hybrid, we call this hybrid as (Siper) where Si instant for Siberian sturgeon and Per comes from Persian sturgeon.
    Description: Iranian Fisheries Science Research Institute
    Description: Published
    Keywords: Hybrid ; Persian sturgeon ; Siberian sturgeon ; Siper ; Aquaculture ; Acipenser persicus ; Acipenser baerii ; Growth
    Repository Name: AquaDocs
    Type: Report , Refereed
    Format: 133pp.
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  • 5
    Publication Date: 2021-05-19
    Description: Karyotype and number of chromosomes of silver carp (Hypophthalmichthys molitrix) were determined by using tissue-squashing method and gimsa staining. In this experiment 80 larvae and 10 fingerlings (weighting 1-8 g) were examined and totally 30 chromosomal slides were prepared. The obtain results indicated that the number of chromosomes in this species was found 2n=48 (with 88 chromosomal arms). Consist of 6 pairs metacentric (M), 14 pairs submetacentric (SM) and 4 pairs of Acrocentric (A). The karyotype formula can be stated as: (6M + 14SM + 4A).
    Description: Published
    Keywords: Karyotyping ; Chromosome ; Silver Carp ; Hypophthalmichthys molitrix ; Tissue-squashing method ; larvae ; Fingerlings ; Species
    Repository Name: AquaDocs
    Type: Journal Contribution , Refereed
    Format: pp.107-115
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  • 6
    Publication Date: 2021-05-19
    Description: The Caspian Sea trout (Salmo trutta caspius) is distributed in southern basin of the sea and the natural stocks of this fish is critically endangered. The present study was conducted through the breeding seasons of Caspian Sea trout in January 2012. Estimation of sperm male potential was carried on samples collected from a total of 12 male spawners which included 8 samples (caught 3 years ago) and 4 samples (freshly caught). Semen samples were collected after anesthetized with clove powder for 10 minutes at water temperature of 9-9.4 °C. The differences of mean semen volumes, sperm motility time, sperm density and the percentage of sperm motility from freshly caught spawners ( 5.5 ± 3.4 ml , 35.5 ± 8.7 sec , 4.3 ± 0.7 ×109 ml-1 , 32.5 ± 8.5% respectively) were significantly higher than 3 years caught spawners (1.5 ± 0.93 ml, 26.5 ± 12.8 sec , 1.98 ± 1.6 ×109 ml-1 , 25.7 ± 9.7 % respectively) (P 〈 0.05). Also the results showed that there are not significant differences in mean percentage of motility and motility duration between freshly caught sperm from fresh broods and that’s from previously caught (among fresh sperm samples, one, three and eight months of cryopreservation) (P 〉 0.05).
    Description: Iranian Fisheries Science Research Institute
    Description: Published
    Keywords: Sperm cryopreservation ; Percentage of motility ; Sperm bank ; Salmo trutta caspius ; Breeding ; Samples ; Spawners ; Temperature
    Repository Name: AquaDocs
    Type: Report , Refereed
    Format: 31pp.
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  • 7
    Publication Date: 2021-05-19
    Description: Due to high maturation age in sturgeons and lack of morphologic differences between male and female even in brood stocks, sex determination is difficult in these species. In this research with using of AFLP approach and 100 primer combinations, male and female genomic DNA of 20 individuals in Persian sturgeon (Acipenser persicus) and beluga (Huso huso) were investigated. Ligation was carried out with using of MseI and EcoRI, and then adapters were ligated with using of T4 DNA Ligase. Fragments amplification was done through two steps PCR and electrophoresis on denature poly acrylamid and stained by silver staining. Data derived from banding patterns were scored as o (absence) and 1 (Presence). A set of 100 (Eco+3 and Mse+4) primer combinations in A. persicus and H. huso yielded approximately a total of 3771 and 3779 scorable bands, respectively of which 30% in A. persicus and 29.6% in H. huso were polymorphic. The fragments ranged from 50 to 600 bp without revealing any sex specific markers. So we used cDNA-AFLP approach in order to analysis of gene expression in 8 female and 8 male Persian sturgeon gonads. Results revealed two cDNA markers in female gonad (TDF1, TDF2) and they verified with RT-PCR in male and female gonads cDNA. But unfortunately they didn t verify in genomic DNA. According to this research results and previous researches, it seems that sturgeons may have not sex chromosomes or the methods were used couldn t determine them.
    Description: Iranian Fisheries Science Research Institute
    Description: Published
    Keywords: Persian sturgeon ; Beluga ; Sex marker ; AFLP ; cDNA-AFLP ; Investigation ; Identification ; Huso huso ; Acipenser persicus ; Molecular
    Repository Name: AquaDocs
    Type: Report , Refereed
    Format: 112pp.
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  • 8
    Publication Date: 2021-05-19
    Description: The population genetic structure of the Persian sturgeon (Acipenser persicus) in the 2, 3, 4 fisheries regions and Sefidrud River was investigated based on the DNA sequencing method during 2010 – 2013 sturgeon stock assessment in the south Caspian Sea . DNA samples were extracted using ammonium acetate, the quantity of DNA was measured at 260 and 280 nm using spectrophotometry by Nanodrop (ND 1000 model), and the quality was checked by 1% agarose gel electrophoresis. Two sets of mitochondrial gene (D-loop and cytochrom b) after synthesis were used for polymerase chain reaction (PCR). A Neighbor-Joining (NJ) tree was constructed for all haplotypes according to Kimura 2-parameter model using Mega Version 4.0.1, number of haplotypes, haplotype diversity (Hd) and nucleotide diversity and their corresponding variances, genetic divergence overall and between paired populations (Fst) by 10,000 permutations and exact test, the gamma distribution shape parameter for the rate heterogeneity among sites and nucleotide sequence, the historical demographic pattern of A.persicus using neutrality tests and mismatch distribution analysis (D test of Tajima and Fs test of Fu), also the concordance of the observed with the expected distribution under the sudden population model using the Harpending, s raggedness index (Hri) were analysed. All calculations were conducted using ARLEQUIN version 3.11 and DnaSP 4.0. The aligned mtDNA sequences of D-loop and cytochrom b genes were consisted of 500 and 700 base pairs (bp) respectively. 13 and 4 haplotypes were defined, the average haplotype diversity were 0.961 and 0.419, average nucleotide diversity were 0.038 and 0.002, The gamma distribution shape parameter were 0.19 and 0.20 indicating moderate mutation rate heterogeneity among sites in A.persicus. The lowest value of Fst for D-loop gene was calculated between Sefidrud and four fisheries region (-0.002) and the Fst values observed for cytochrom b gene was 0.04 with Nm=5.37 and not statistically significant. The exact test of population differentiation (non-differentiation exact P values) showed significant differences between Sefidrud and other areas (P ≤0.05) for D-loop gene and for cytochrom b gene was nonsignificant (P ≥0.05). The mismatch analysis produced a unimodal distribution of pairwise differences for both genes which was consistent with the sudden population expansion model. Tajima’s D and Fu’s Fs statistics were significantly negative (D= -0.84 and - 0.99, P〉0.01; Fs= -0.220 and -0.079, 〉0.01). ARLEQUIN calculated the value of t as 13.65 and the time since population expansion was estimated to be approximately 1501 years before present based on the mutation rates for the control region and this value for cytochrom b gene t= 0.98 which population expansion time was 7.84 years before present. The results of this study based on D-loop gene showed that population of A.persicus in the Sefidrud River is differ from other studied areas. Therefore fisheries managements of this unique and valuable stock for restocking and conservation of gene pools is strongly recommended.
    Description: Iranian Fisheries Science Research Institute
    Description: Published
    Keywords: Genetic ; Structure ; Sturgeons ; Stock assessment
    Repository Name: AquaDocs
    Type: Report , Refereed
    Format: 69pp.
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  • 9
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    In:  http://aquaticcommons.org/id/eprint/24059 | 18721 | 2018-08-03 07:11:55 | 24059 | Iranian Fisheries Science Research Institute
    Publication Date: 2021-07-15
    Description: Karyotype and number of chromosomes of silver carp (Hypophthalmichthys molitrix) were determined by using tissue-squashing method and gimsa staining. In this experiment 80 larvae and 10 fingerlings (weighting 1-8 g) were examined and totally 30 chromosomal slides were prepared. The obtain results indicated that the number of chromosomes in this species was found 2n=48 (with 88 chromosomal arms). Consist of 6 pairs metacentric (M), 14 pairs submetacentric (SM) and 4 pairs of Acrocentric (A). The karyotype formula can be stated as: (6M + 14SM + 4A).
    Keywords: Biology ; Karyotype ; Chromosome ; Silver Carp ; Hypophthalmichthys molitrix ; Iran
    Repository Name: AquaDocs
    Type: article , TRUE
    Format: application/pdf
    Format: application/pdf
    Format: 107-115
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  • 10
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    Iranian Fisheries Science Research Institute | Tehran, Iran
    In:  http://aquaticcommons.org/id/eprint/25640 | 18721 | 2018-10-14 02:39:07 | 25640 | Iranian Fisheries Science Research Institute
    Publication Date: 2021-07-16
    Description: In this study, 11 male of Caspian trout (Salmo truta caspius) (with mean length and weight 37/8 ± 5/3 cm and 523/3 ± 24/7 respectively) and 23 male of Caspian kutum (Rutilus frisii kutum) (with mean length and weight 36/1 ± 7/1 cm and 631/3 ± 21/6 g respectively) were evaluated. All the fish were good at the initial examination of sexual maturity. After sperm sampling, their quality were tested. In this step, the parameters such as motility, duration of mobility, density, pH and osmolality were measured. After this stage, the sperm samples of Caspian trout in the ratio 1: 3 were diluted with the aqueous solution containing compounds (0.3M Glucose, 10% Methanol, 10% egg yolk) and the freezing process was done manually and the sperm was frozen in liquid nitrogen. The sperm samples of Caspian kutums were diluted (ratio of 1: 3) with two soluble diluent containing compounds (350 mM glucose, 30 mM Tris and 4% Polyethylene glycol) and (350 mM glucose, 30 mM Tris and 2% Glycerol) and were frizzed automatically by Planner Kryo instrument and placed in liquid nitrogen. The sperm samples were thawed 1 to 3 months after the date of first freezing and their quality were assessed by measuring percent and timing motility. The results showed that the obtained semen volume of Caspian trout was more than Caspian kutum. Moreover, percentage of motile sperm, timing motility and sperm density of Caspian trout were higher than those of Caspian kutum but osmolality and pH of Caspian trout were lower than those of Caspian kutum. Over time, the percentage of sperm motility and mobility for both species declined compared with fresh samples. After thawing, percentage of motile sperm and timing motility of Caspian kutum were lower than those factors Caspian trout. The results showed that the sample of Caspian kutum sperm that were diluted by ethylene glycol after thawing and were immotile ll of them. However, the samples were diluted by glycerol, after thawing, were alive and motile. According to the results, it seems very important species differences that must be fully considered in the process of freezing sperm. The use of a single protocol would not be successful in cryopreservation because the reaction of sperm against to chemical agents is variable. Therefore, it is essential to get the right information to protect valuable Caspian fish by using cryopreservation. Further studies on the characteristics of each species, as well as the freezing process take appropriate diluent.
    Keywords: Aquaculture ; Biology ; Iran ; Salmo truta caspius ; Caspian trout ; Rutilus frisii kutum ; Caspian kutum ; Sperm ; Bony fish ; Cryopreservation
    Repository Name: AquaDocs
    Type: monograph
    Format: application/pdf
    Format: application/pdf
    Format: 38
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