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Contact Name
Ahmadi Riyanto
Contact Email
medpub@litbang.deptan.go.id
Phone
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Journal Mail Official
ahmadi_puslitbangnak@yahoo.com
Editorial Address
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Location
Kota bogor,
Jawa barat
INDONESIA
Jurnal Ilmu Ternak Veteriner
ISSN : 08537380     EISSN : 2252696X     DOI : -
Core Subject : Health,
Aims JITV (Jurnal Ilmu ternak dan Veteriner) or Indonesian Journal of Animal and Veterinary Sciences (IJAVS) aims to publish original research results and reviews on farm tropical animals such as cattle, buffaloes, sheep, goats, pigs, horses, poultry, as well as non domesticated Indonesian endemic animals, such as deers, anoa, babirusa, etc. Scope Indonesian Journal of Animal and Veterinary Sciences . The journal will consider primary research papers from any source if they make an original contribution to the experimental or theoretical understanding and application of theories and methodologies of some aspects of animal science and veterinary
Articles 1,756 Documents
Isolation and number of circulated primordial germ cells (circulated-PGCs) on stages of embryonic development of Gaok chicken Kostaman T; Yusuf TL; Fahrudin M; Setiadi MA
Jurnal Ilmu Ternak dan Veteriner Vol 18, No 1 (2013): MARCH 2013
Publisher : Indonesian Center for Animal Research and Development (ICARD)

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (260.474 KB) | DOI: 10.14334/jitv.v18i1.260

Abstract

Avian primordial germ cell (PGCs) show a unique migration pathway during early development. During the early embryonic development, as soon as the formation of blood vessels, PGCs enter the circulatory system and migrate to the gonadal primordial. The aim of this study was to examine the number of circulated-PGCs from Gaok chicken at different developmental stages of embryo. One hundred fertile eggs were divided into 5 groups and incubated in a portable incubator at 38oC and humidity 60%. Hatching was set according to the embryonic development stage between 14-18. The blood collection was done through the dorsal aorta using micropipette under microscope. The collected blood was grouped based on the embryonic stages and placed on a 1.5 ml eppendorf tube which had been filled with 1.000 µl of Calcium and Magnesium-free phosphate buffered saline (PBS -). The PGCs were then purified using nycodenz density gradient centrifugation. The results showed that the average number of circulated-PGCs per embryo from Gaok chicken were significantly affected by the stage of embryonic development (P < 0.05). The number of circulated-PGCs at stages 14, 15, 16, 17 and 18 were 42.8 ± 8.9, 51.0 ± 5.8, 37.6 ± 5.9, 32.8 ± 3.6 and 32.6 ± 3.2, respectively. However, the number of circulated-PGCs was no different between stage of 17 and 18. At Gaok chicken, the number of circulated-PGCs reach the peak at stage 15, it is recommended that collection of PGCs embryonic chicken from blood circulation was the best on stage 15. This information is useful in efficiency production of germline chimera and to preserve PGCs of other Indonesian native chicken. Key Words: Gaok Chicken, PGCs, Embryonic Development Stages
Relative superiority analysis of Garut lamb and its crossbred Ismeth Inounu; N Hidayati; Subandriyo .; B Tiesnamurti; L.O Nafiu
Jurnal Ilmu Ternak dan Veteriner Vol 8, No 3 (2003): SEPTEMBER 2003
Publisher : Indonesian Center for Animal Research and Development (ICARD)

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (206.994 KB) | DOI: 10.14334/jitv.v8i3.388

Abstract

The objective of the research was to evaluate the relative superiority of Garut lamb and its crosses with St. Croix and Moulton Charollais. The research was conducted at Animal Research Station, Indonesian Research Institute for Animal Production, Bogor, Indonesia. The data used for this paper was collected from 1995 to 2002. The results revealed that individual lamb weight at birth, at weaning, preweaning daily gain, at 6, 9 and 12 months of age of the composite sheep (HG = 50% St. Croix : 50% Garut, MG = 50% M. Charollais : 50% Garut, MHG (MG X HG) dan HMG (HG X MG) = 25% St. Croix : 25% M. Charollais : 50% Garut) were higher than Garut sheep. The relative superiority were 6.7-13.1% for lamb weight at birth, 6.6- 15.6% for lamb weight at weaning, 3.2-20.8% for preweaning daily gain dan 6.2-17.9% for lamb weight at 9 month of age, respectively. The superiority of composite sheep were obtained in good and limited feed condition. Lamb growth parameters were also affected by feed condition, parity, sex, and rearing type.   Key words: Garut, St. Croix, M. Charollais sheep, relative superiority
Effect of exogenous glutathione in medium fertilization to improve blastocyst rates of bovine embryos E Triwulanningsih; P Situmorang; I-G Putu; T Sugiarti; A.M Lubis; D.A Kusumaningrum; W Caroline; R.G Sianturi
Jurnal Ilmu Ternak dan Veteriner Vol 7, No 2 (2002): JUNE 2002
Publisher : Indonesian Center for Animal Research and Development (ICARD)

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (190.218 KB) | DOI: 10.14334/jitv.v7i2.283

Abstract

Glutathione (C10H17N3O6S) is a tripeptide (γ-Glu-Cys-Gly) widespread in living organism. Glutathione (GSH) at the 5 mM concentration increased the motility and fertility of frozen-thawed sperm. Intracellulair glutathione improved the cleavage rate and embryo development to the blastocyst rate. Research on in vitro embryos production through the implementation of GSH during IVF (in vitro fertilization) on embryo development has been conducted at the Laboratorium Reproductive of Physiology, Research Institute for Animal Production. Ovaries of beef cattle as source of oocytes were collected from the slaughterhouse in a thermo flask with 350C PBS as medium and transported to the laboratory. The oocytes were fertilized in vitro with selected motile sperm using Percoll gradient (90 and 45%). Ten COCs (cumulus oocytes complexes) were transfered to 44 μl of fertilization medium (mTALP) was performed with either 0; 0.25; 0.50; 0.75 and 1.00 mM of glutathione as treatment A, B, C, D and E respectively, and inseminated with 2 μl of capacitated sperm and added 2 μl of heparin and 2 μl of PHE (consisting of 20 μM penicillamine, 10 μM hypotaurine, 1 μM epinephrine). Incubation between sperm and oocytes in the 5% CO2 incubator and RH 90% in fertilization media (TALP) for 20 hours. All zygotes were cultured in modification of CR1aa medium up to blastocyst and were fed serum 5 μl/50μl medium on day 6. Results of this experiment showed that the effect of concentration of glutathione (0, 0.25; 0.50; 0.75 and 1.00 mM) on fertilization medium to the percentage of cleavage rates were 69.35 + 29.40; 79.07 + 13.17; 67.88 + 10.65; 98.10 + 3.30 and 82.62 + 24.19% not significant different (P>0.05) among treatments A, B, C, D dan E respectively.The precentages of morula and blastocyst for treatment D were 50.45 + 42.64% and 31.28 + 24.28%; while 36.55 + 24.13% and 17.74 + 17.86% for treatment E respectively. Key words: Glutathione, in vitro fertilization, oocytes, cleavage
Biological value (in vitro and in sacco) of chemically treated feather as rumen by pass protein source W Puastuti; D Yulistiani; I-W Mathius
Jurnal Ilmu Ternak dan Veteriner Vol 9, No 2 (2004): JUNE 2004
Publisher : Indonesian Center for Animal Research and Development (ICARD)

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (189.539 KB) | DOI: 10.14334/jitv.v9i2.412

Abstract

A series of experiments has been conducted to study chemical processing method of feather meal using hydrocloric acid (HCl) and to evaluate the biological values by in vitro and is sacco methods of the hydrolitic feather meal (HBA). Feather meal was hydrolyzed using four levels of HCl concentration (i.e.0, 6, 12 and 24%) in three incubation times (i.e. 2, 4, and 6 days). The hydrolysis reaction was carried out in closed container in the ratio of feather meal and HCl of 2:1 (w/v). In vitro evaluation was conducted to measure dry matter (DM) and organic matter (OM) digestibility, DM solubility, ammonia (NH3) and volatile fatty acid (VFA) content. In sacco to observe the degradation of HBA crude protein. Results of in sacco evaluation in rumen showed that soluble and degraded crude proteins (CP) were significantly only affected by HCl concentration (P<0.01). The rate and the amount of degraded protein in 24 hours inclution in the rumen were affected by the HCl concentration and incubation time of hydrolysis. More amino acid degradation occurred on longer time showed that HCl had quadratic effect (P<0,01) on pH of HBA. However durations of hydrolysis did not significantly affect acidity (P>0.05). In vitro DM and OM digestibilities of HBA increased as the concentration of HCl was increased. The increase of DM digestibility followed the equation Y = -0.0231x3 + 0.7323x2 – 1.5716x + 12.383 (r = 0.994); and the OM digestibility followed the equation Y = -0.0229x3 + 0.7194x2 – 1.0606x + 15.951 (r = 0.993). Time of incubation, on the other hand, did not affect OM and DM digestibilities (P>0.05). DM solubility of HBA was significantly affected by HCl concentration and the length of incubation time (P<0.01). The increase of DM solubility was followed by the increase of NH3 content (P<0.01). The relation between DM solubility and NH3 content followed the equation Y = 0.4365x + 5.4047 (r = 0.966). The increase of DM solubility followed the equation Y = -0.027x3 + 0.9596x2 – 4.8142x + 5.3878 (r = 0.973) and the increase of NH3 content followed the equation Y = -0.0085x3 + 0.3175x2 – 1.4139x + 7.0889 (r = 0.992). Result of in sacco evaluation showed that fraction of crude protein (CP) disolved and fraction of CP degraded in rumen was significantly affected by HCl concentration (P<0.01), while the rate of CP degradation and the amount of fraction degraded during 24 hours in the rumen were affected by the HCl concentration and the durations of hydrolysis (P<0.01)  indicating that more feather meal protein was hydrolized by HCl, therefore weakened or cut the chain of amino acid in the feather protein. Treatment with 12% HCl for 4 days hydrolysis of feather meal resulted in CP fraction degradation during 24 hours incubation in the rumen of 53%, indicating that the potency of CP of HBA as rumen by pass protein was 47%.   Key words: Chicken feather, HCl hydrolysis, digestibility by pass protein
Effect of fermented Banana peel on Broiler Carcass Koni TNI
Jurnal Ilmu Ternak dan Veteriner Vol 18, No 2 (2013): JUNE 2013
Publisher : Indonesian Center for Animal Research and Development (ICARD)

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (143.265 KB) | DOI: 10.14334/jitv.v18i2.315

Abstract

This experiment was conducted to examine effect of inclusion of fermented banana peel by Rhyzopus oligosporus in diets on slaughter weight, carcass weight  and carcass percentage, weight and percentage abdominal fat of broiler. The experiment was done based on Completely Randomized Design with four treatments and four replications and each replication consisted of six chickens. The treatment were R0 = without banana peel fermented, R1 = 5% banana peel fermented, R2 = 10% banana peel fermented, R3 = 15% banana peel fermented. Data of the experiment were analyzed, using ANOVA and then continued with Duncan's Multiple Range Test. Result showed that level of fermented banana peel affected slaughter weight and carcass weight. However carcass persentage, weight and percentage of abdominal fat was not affected by treatment. Banana peel fermented by Rhizopus oligosporus could can be used maximally 10% in broiler ration. Key Words: Banana Peel, Rhyzopus oligosporus, Slaughter Weight, Carcass Weight, Abdominal Fat
Production and purification of Bacillus anthracis protective antigen Simson Tarigan; Rahmat S Adji; Lily Natalia
Jurnal Ilmu Ternak dan Veteriner Vol 10, No 3 (2005): SEPTEMBER 2005
Publisher : Indonesian Center for Animal Research and Development (ICARD)

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (1036.122 KB) | DOI: 10.14334/jitv.v10i3.445

Abstract

Protective antigen (PA) plays crucial roles in the pathogenicity and virulence of Bacillus anthracis. Animals or human immunised with the protein acquire a complete protection against the disease. In addition to vaccine, PA can also be developed into a sensitive diagnostic test for anthrax. The purpose of this study was to produce PA using a culture medium easily obtained, and to develop a simple and effective technique for purification of the protein. To produce PA, B. anthracis Sterne 34F2 strain was first grown on blood agar, then bacterial colonies were suspended and incubated for 2 hours in RPMI-1640 supplemented with NaHCO3 and Tris. Protein components in the culture supernatant were separated consecutively with Phenyl sepharose, Qsepharose and Superdex-200 columns. This order was used in order to simplify and speed up the purification process. The PA contained in the fractions was detected by a dot blot or an ELISA using commercial PA specific antibody. The PA was absorbed strongly by the phenyl sepharose whereas other proteins were absorbed weakly or not absorbed at all. When these PA-containing fractions were loaded into Q-sepharose column, PA was absorbed considerably weaker than contaminated proteins. Although the level of purity obtained from the Q-sepharose column was satisfactory, further separation on Superdex produced an even higher purity. However, on SDS-PAGE analysis, the purified PA was seen as a two-band protein (54.7 and 29.2 kDa) because of nicked proteolysis. On an immunoblot assay, only the 54.7 band was recognised by the PA-specific antibody. Despite the nick proteolysis, the PA purified in this study was considered to retain its biological activities.     Key Words: Bacillus anthracis, Protective Antigen, Protein Purification
The relative superiority of milk production of Garut sheep and its crossbred I Inounu; S Sukmawati; R.R Noor
Jurnal Ilmu Ternak dan Veteriner Vol 11, No 4 (2006): DECEMBER 2006
Publisher : Indonesian Center for Animal Research and Development (ICARD)

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (279.146 KB) | DOI: 10.14334/jitv.v11i4.541

Abstract

Garut sheep (GG) is one of some native sheep that had been well known to the people of West Java. This sheep have some advantages including their ability to produce multiple birth, reach sexual maturity faster and resistant to internal parasite. However, this sheep have also some disadvantages including low milk production, high mortality and low weaning weight. Crossbreeding is one way to improve animal genetic quality. The objective of this study is to evaluate whether the Garut, St.Croix cross (HG), and Moulton Charollais cross (MG) are superior in milk production when compared to Garut sheep. This study was conducted at small ruminant experimental station of Research Institute for Animal production from June to August 2002.  The superiority of the crossed sheep was determined by subtracting the average milk production of the crossed sheep (HG or MG) and Garut sheep and then divided the values by the average milk production of Garut sheep, except for the threeway crosses (MHG and HMG) is calculated from the difference in milk production between the means of threeway crossbred with the means of two parents (MG and HG). The data had been corrected by parity and type of birth.  The General Linear model of SAS was used to calculate the least square means. Average milk production from GG, MG, HG, MHG and HMG ewes in this study were respectivelly 53.41, 59.48, 55.89, 44.87 and 54.66 kg. The relative superiority for milk production of MG and HG were 11% and 5% over Garut sheep respectively and for the threeway crossbred MHG/HMG  was -14% over their parents (MG and HG). Key Words: Milk Production, St.Croix, Moulton Charollais, Garut, Crossing
Inactivation of Bacillus anthracis by Gamma irradiation N. Natalia; A. Priadi; Z. Irawati
Jurnal Ilmu Ternak dan Veteriner Vol 14, No 3 (2009): SEPTEMBER 2009
Publisher : Indonesian Center for Animal Research and Development (ICARD)

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (289.628 KB) | DOI: 10.14334/jitv.v14i3.347

Abstract

The use of Bacillus anthracis as a biological weapon heighlightened awareness of the need for validated methods for the inactivation of B. anthracis spores. Ionizing radiation is capable of causing a variety of chemical changes and biological effects on bacteria which can be due both to direct interactions with critical cell components and to indirect actions on bacteria by molecular entities formed as a result of radiolysis of other molecules in the bacterial cell. This study determined the gamma irradiation dose for inactivating B. anthracis spores and its biological effects on the bacterial characteristics. Gamma irradiation was conducted at the IRKA irradiator at the National Nuclear Energy Agency, Jakarta and cobalt-60 was used as the source of ionizing radiation (capacity of ca. 134,044 Kci). Freeze dried culture of B. anthracis in glass ampoules was irradiated using   variable doses of 30, 20 and 10 KGy. Viability, biochemical and protease enzyme characteristics of B. anthracis were evaluated before and after irradiation.  The ability of B. anthracis to degrade gelatin, haemoglobin and bovine immunoglobulin G was also tested. The results showed that ionizing radiation  was able to inactivate or kill 11,05 x 108 cfu B. anthracis by 95.37%, 99.58% and 99.99 at respective doses of 10, 20 and 30 KGy. Bacterial spores appear to be less susceptible to irradiation than the vegetative cells, because of their specific structure. The survive spores irradiated at 30kGy shows some biochemical characteristic changes. The survivors failed to degrade methyl -D-glucopyranoside and arbutine. The ability of B. anthracis protease to degrade gelatin, haemoglobin and bovine immunoglobulin G was not affected by irradiation. These findings showed that a gamma irradiation at 30 KGy effectively inactivates B. anthracis spores without changing the protease activities. Key words: Gamma Irradiation, B. anthracis Characters, Protease
IBR vaccination program evaluation in Bali cattle using inactive vaccine BHV-1 field isolate with serum netralization test in laboratorium scale Sudarisman .
Jurnal Ilmu Ternak dan Veteriner Vol 6, No 4 (2001): DECEMBER 2001
Publisher : Indonesian Center for Animal Research and Development (ICARD)

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (179.523 KB) | DOI: 10.14334/jitv.v6i4.248

Abstract

Inacctive vaccine has been reported to have some effects on experimental infection using BHV-1 virus. this study was carried out to evaluate the effectivity of inactive BALITVET BHV-1 vaccine in Bali cattle by means of serological test in laboratorium scale. Thirty Bali cattle were divided into four treatment groups. Group I (8 animals) was a control group which didn’t receive any vaccination. Group II (10 animals) was vaccinated once. Group III (9 animals) was vaccinated twice for period of one month and Group IV (3 animals) was cattle which have had clinical pathogenicity test for BHV-1 one year ago. Challenge test was done 1 month after last vaccination with field virus at dose 5 x 108 TCID50. Four animals in control group, 5 animals in group II, 5 animals in group III and 3 animals in group IV were challenged and then all animals were mixed in one big pen. BHV-1 antibody titre evaluation was done by serum netralization test. The results of the study revealed that the cattle mixed together with infected cattle which had clinical signs, showed no significant infection in clinical signs and blood BHV-1 antibody titre. Meanwhile, experimental cattle infected with 5 x 10 8 TCID50 BHV-1 field isolate (i.v.) showed IBR clinical signs. BHV-1 antibody titre were increased 45 days after challenge. Cattle vaccinated 30 days before and challenged with field isolate could defend from the disease (revealed by no clinical signs) show significant BHV-1 antibody titre and have fluctuated titre between vaccinated once and twice. However, cattle vaccinated and mixed with infected cattle, showed no IBR clinical signs and had significant BHV-1antibody titre with different fluctuations. Cattle vaccinated twice, could maintain its high BHV- 1antibody titre as long as 120 days post vaccination compared with cattle vaccinated once with low titre until 120 days post vaccination. Cattle which had patogenicity test one year ago and showed clinical signs, still had high BHV-1 antibody titre after challenge test with dose 5 x 108 TCID50. However the titre were decreasing at 120 day post challenge and the titre were not as high as the cattle received twice vaccination. It can be concluded that IBR vaccination by using field isolate is good in booster method.   Key words: Vaccine evaluation, inactive vaccine, BHV-1, Bali cattle
Comparative study of the productivity of Madura Cattle and Its crossbreed with Limousin in Madura island Farahdilla Kutsiyah; Kusmartono .; Trinil Susilawati
Jurnal Ilmu Ternak dan Veteriner Vol 8, No 2 (2003): JUNE 2003
Publisher : Indonesian Center for Animal Research and Development (ICARD)

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (182.635 KB) | DOI: 10.14334/jitv.v8i2.379

Abstract

Comparative study of the productivity between Madura cattle and crossbreed (Madura x Limousine) was done to identify problem and potential of crossbreed cattle at Madura island. Survey and direct field observation were conducted in Pamekasan. Data were descriptively analyzed or using correlation-regression, and t-test and indicated that service per conception (S/C) and calving rate (CR) of Madura cattle (n=34) and crossbreed (n=38) were 1.464 and 1.986; 58.8 and 52.6% respectively. Average birth weight (n = 17), weaning weight (n = 15) and ADG (average daily gain) pre weaning (n = 15) on calf of Madura cattle were 19.78 ± 1.224 kg; 119.53 ± 9.772 kg; 445 ± 48.53 g/day. Average birth weight (n = 17), weaning weight (n = 14) and ADG pre weaning (n = 14), on calf of crossbreed offspring were 27.60 ± 1.298 kg; 171.47 ± 31.055 kg; 678 ± 146.03 g/day. It is concluded that reproductive performance of Madura cattle was greater than their crossbreed, whereas production performance on calf of crossbreed offspring was greater than calf of Madura cattle. It is suggested that good quality and continuous supply of local feed must be maintained to prevent the negative effect for their growth. Key words: Madura cattle, Limousine cattle, crossbreed, productivity

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