Apricot is considered an ecologically and economically important tree species of the stone-fruit crops that is widely grown in temperate regions of the world. Very few studies on apricot genetic diversity assessment have been carried out from the regions of Kashmir and Ladakh. In this backdrop, the present study was carried out to analyse the genetic diversity and population structure of 120 apricot genotypes collected from both the regions using 21 SSR markers. A total of 52 alleles were amplified with average values of marker index (MI) = 0.7084, resolving power (RP) = 2.8690, polymorphism information content (PIC) = 0.3132, Na = 2.317, Ne = 1.720, I = 0.572, Ho = 0.284, He = 0.360 and an average polymorphism of 91.2% per assay indicating high level of genetic diversity. The neighbour-joining (NJ) dendrogram generated three main clusters among selected apricot genotypes independent of their geographical locations. Interestingly, the result of the dendrogram coincides with the results of structure analysis which showed that the 120 apricot genotypes could be assigned to three (K = 3) sub-populations and the grouping of genotypes did not follow their geographical location suggesting that they share the same genetic pool. Moreover, analysis of molecular variance showed that 73% of the variation was attributed to differences within the individuals, 25% among individuals while only 2% of the variation was observed among the populations. The present study represents the most comprehensive analysis of the genetic diversity and population structure of apricot genotypes in Kashmir and Ladakh regions of India.

Understanding existing levels of genetic variability of camel populations is capital for conservation activities. This study aims to provide information on the genetic diversity of four dromedary populations, including Guerzni, Harcha, Khouari and Marmouri. Blood samples from 227 individuals belonging to the aforementioned populations were obtained and genotyped by 16 microsatellite markers. A total of 215 alleles were observed, with the mean number of alleles per locus being 13.4 ± 6.26. All loci were polymorphic in the studied populations. The average expected heterozygosity varied from a maximum of 0.748 ± 0.122 in Guerzni population to a minimum of 0.702 ± 0.128 in Harcha population; Guerzni population showed the highest value of observed heterozygosity (0.699 ± 0.088), whereas Harcha population the lowest (0.646 ± 0.130). Mean estimates of F-statistics obtained over loci were FIS = 0.0726, FIT = 0.0876 and FST = 0.0162. The lowest genetic distance was obtained between Guerzni and Khouari (0.023), and the highest genetic distance between Harcha and Marmouri (0.251). The neighbour-joining phylogenetic tree showed two groups of populations indicating a cluster of Guerzni, Khouari and Marmouri, and a clear isolation of Harcha. The genetic distances, the factorial correspondence analysis, the analysis of genetic structure and the phylogenetic tree between populations revealed significant differences between Harcha and other populations, and a high similarity between Guerzni, Khouari and Marmouri. It is concluded from this study that the camel genetic resources studied are well diversified. However, the herd management, especially the random selection of breeding animals, can increase the level of genetic mixing between different populations, mainly among Guerzni, Khouari and Marmouri, that live in the same habitat and grazing area.

Characterization and genetic diversities among members of a species are fundamental to their improvement and conservation. This study was conducted to characterize and estimate genetic diversity in the ecotypes of the locally adapted Muscovy duck in Nigeria using blood proteins (haemoglobin, transferrin and albumin) and enzyme (carbonic anhydrase) markers. Blood samples collected from 20, 40 and 20 adult Muscovy ducks sampled randomly from the Rain Forest, Derived Savanna and Guinea Savanna ecotypes, respectively, were typed for blood proteins and enzyme polymorphism with cellulose acetate paper. Genetic variability in the studied population was accessed using heterozygosity (H), effective number of allele (ne) and polymorphism (percent P). All the 13 allelic variants expressed at the four loci were expressed in the Derived Savanna ecotype but 12 each in the Rain Forest and Guinea Savanna ecotypes. Results showed that all the four loci were polymorphic (100 percent) and the estimated heterozygosity among them was similar (0.424–0.481). Similarity in the estimated genetic variability parameters among ecotypes indicate that the sub-populations understudy was under similar evolutionary forces and there were no appreciable differences among them.

Konkan Kanyal goats are medium-sized animals reared for meat purpose. They are predominantly black in colour with white markings in a specific pattern and are found in the Kudal, Sawantwadi, Dodamarg, Malvan and Vengurle Talukas of Sindhudurg district of Konkan region of Maharashtra state. The mean body weight ranges from 30 kg in adult females to 35 kg in males. The age at first kidding, kidding interval and twinning of these goats is 546 days, 240 days and 35 percent respectively. The average daily milk yield and lactation yield were found to be 0.6 and 69 kg, respectively. Characterization of Konkan Kanyal goats was carried out using a panel of 25 microsatellite markers. The genomic DNA of 50 unrelated goats was isolated and PCR amplified under standardized PCR conditions. The amplified DNA was used for genotyping by the automated DNA Sequencer ABI 3730. The analysis of data revealed that the effective number of alleles ranged from 1.17 to 8.94 and the number of observed alleles ranged from 5 to 19. A total of 255 alleles were observed with a mean of 10.2 alleles/locus. The observed heterozygosity ranged from 0.13 to 0.95, while the expected heterozygosity ranged from 0.14 to 0.89, indicating the heterogeneous nature of the population distributed in the breeding tract. The mean polymorphism content was 0.79. The qualitative graphical method based on the allele frequency spectra detected no shift in the frequency distribution of alleles and a normal L-shaped curve was observed where the alleles with the lowest frequencies were found to be most abundant. Based on the phenotypic and genetic variability, Konkan Kanyal goats appear to be distinct from other goats of Maharashtra state.

Thrips are small insects (0.5–3.0 mm) with distinct habits and life histories characterized by haplodiploid sex determination. In general, low levels of genetic diversity have been reported in haplodiploid insects, although most reports focus on the order Hymenoptera. Therefore, we used RAPD markers to evaluate the structure and both inter- and intra-population genetic variability of Gynaikothrips uzeli (Thysanoptera: Phlaeothripidae). Six populations, three from Paraná state, southern Brazil, and three from Bahia, northeastern Brazil, were studied. Similarly to other haplodiploid insects, the genetic diversity of G. uzeli was reduced. This result is putatively related to the haplodiploid sex determination system, which yields little genetic variation, and to ecological traits of the studied species, such as the low dispersal abilities and life mode in leaf galls. All individuals were homogeneously clustered in their respective collection sites, forming two main groups in which populations from similar environments were more closely related. The analyzed populations were highly structured, and the genetic variation was higher among than within populations.

Mussel culture relies on the mussel self-attachment capacity through byssus production. By doing so, no cages or containment devices are needed. It has been previously suggested that thread production requires a non-negligible part of the energy expenditure in blue mussels Mytilus edulis. Therefore our work investigates the relationships between byssal thread production, mussels energetic reserves and phospholipids profiles in the foot. The relationship between thread production and heterozygosity was also examined. The study was realized in a small lagoon of the Îles-de-la-Madeleine, southern Gulf of St. Lawrence, Canada, on four sampling dates between June and September encompassing the pre- to post-spawning periods. Our results show a significant relationship between the thread numbers and attachment strength. However, no correlations were found between energy reserves, phospholipids composition of the foot or heterozygosity level and byssal production. Our results suggest that mussels in suspension culture in this lagoon were not energy-limited so that the energy reserves did not influence the byssal thread production.

Although numerous studies on vertebrates suggest that inbreeding reduces their resistance against parasites and pathogens, studies in insects have found contradictory evidence. In this study we tested the effect of 1 generation of brother–sister mating (inbreeding) on potential and realized immune responses and other life-history traits in Tenebrio molitor. We found that inbreeding reduced adult mass, pre-adult survival and increased development time, suggesting that inbreeding reduced the condition of the adults and thus potentially made them more susceptible to physiological stress. However, we found no significant effect of inbreeding on the potential immune response (encapsulation response), but inbreeding reduced the realized immune response (resistance against the entomopathogenic fungi, Beauveria bassiana). There was a significant family effect on encapsulation response, but no family effect on the resistance against the entomopathogenic fungi. Given that this latter trait showed significant inbreeding depression and that the sample size for the family-effect analysis was small it is likely that the lack of a significant family effect is due to reduced statistical power, rather than the lack of a heritable basis to the trait. Our study highlights the importance of using pathogens and parasites in immunoecological studies.

Extensive research has been conducted on the characterization of hundreds of date palm (Phoenix dactylifera L.) cultivars worldwide. However, the population genetics of date palms has never been studied. In this study, we collected 200 individuals from 19 populations of different geographical locations in Sudan. The collection sites were grouped according to the type of dates (date palm fruits) that dominates in the area. Ten microsatellite markers were used to investigate the genetic diversity within and among populations and the correlation between the genetic and geographical distances. The tested microsatellite markers showed a high level of polymorphism. A total of 261 alleles were detected at the ten loci. The overall mean value of fixation indices equalled − 0.163, which shows the presence of excess heterozygosity. However, the χ2 tests conducted for every locus in each population indicated no significant deviation from the Hardy–Weinberg equilibrium. The analyses of molecular variance exhibited that about 95% of the total genetic variation existed within populations, while significant differentiation within the type groups could be detected. Although significant isolation by distance (r2 = 0.552, P < 0.05) was detected by a Mantel test, it seems that the spatial effect has become complicated as a result from the exchange and introduction of different kinds of plant materials by date palm growers and traders, as well as seed dispersal. This complexity was clearly apparent in the weak clustering relationships among most of the tested populations.

The molecular genetic characteristics were evaluated, and the genetic effects of marker loci on heterosis of three traits (birth weight, BWT; average daily gain, ADG; and feed and meat ratio, FMR) were analysed in the experimental pig populations: Yorkshire (Y, n=34), Landrace (L, n=46) and Meishan (M, n=55); Yorkshire×Landrace (YL, n=32) and its reciprocal (LY, n=36), Yorkshire×Meishan (YM, n=82) and its reciprocal (MY, n=47), by 39 microsatellite markers selected from pig chromosomes SSC4, 6, 7, 8 and 13. The results indicated that observed alleles ranged from 2 to 6, average 4.13, observed heterozygosity varied from 0.39 (Y) to 0.58 (YM+MY) and average polymorphism information content (PIC) varied from 0.33 (Y) to 0.5 (YM). There were two loci (sw2155 and sw1037) at which the alleles were fixed in Y and L, and there were three loci (sw2409, sw2454 and sw1691) at which the alleles were fixed in M. The results from heterozygosity and kinship analysis revealed an intrinsic genetic relationship among the seven populations. Furthermore, the results on genetic effect analysis indicate that several marker loci had a significant effect on heterosis of the three traits in the two different F1 crossbred populations (P⩽0.01), for example s0161, swr1130 and sw1856 for BWT, sw1856 and swr2036 for ADG, and sw1302 and swr2036 for FMR. The significant marker loci implied a deep genetic relationship between molecular marker loci and heterosis.

Allozyme electrophoresis was used to assess genetic variability and differentiation in 22 populations of Gressittacantha terranova Wise (Hexapoda, Collembola) from a coastal area of Victoria Land between the Mariner Glacier and the Nansen Ice Sheet. Allelic frequencies were determined at five enzyme loci: Phi, Pgm, Hk, Mpi and Mdh. Levels of variability, estimated as rates of heterozygosity, were higher than those calculated for the same loci in taxonomically related and non-related species of non-Antarctic Collembola. Thus, in spite of the ecological simplicity of Antarctic terrestrial ecosystems, G. terranova is characterized by high levels of genetic variability, and the 22 populations could be divided into three geogaphic groups, separated by the Aviator and Campbell glaciers. Genetic differentaton reflects the geographic arrangement of the populations, suggesting that the glaciers are effective barriers to gene flow, and that the patchy distribution of collembolan species in Antarctica has the potential to induce, in the long term, microspeciation processes. Interestingly, detectable genetic differentiation was observed between six populations collected at Edmonson Point, even though these are very close to each other, indicating the impact of geographic isolation even within short distances. The only exception to the congruence between genetic and geographic structuring was provided by the population of Apostrophe Island, for which a recent introduction with individuals coming from southern populations is suggested.

Models of host–parasite co-evolution suggest that parasites can exert frequency-dependent selection on their hosts, favouring rare alleles that confer resistance against widespread parasites and thus contributing to the maintenance of genetic variation, at some loci at least. If parasites are important in maintaining variation at many loci, then host species incurring a high prevalence of parasite infections should exhibit greater levels of genetic variation than host species incurring a lower prevalence. Using data from electrophoretic studies and from field surveys of haematozoan infections, we constructed a dataset including 103 species of North American and European birds to test this prediction. After controlling for sampling effort and phylogenetic influences, we found no relationship between parasite prevalence and either heterozygosity or polymorphism. These results do not support a role for parasites in the overall maintenance of genetic variation via frequency-dependent selection.

Multiple, selectively neutral genetic markers are the most appropriate tools for analysis of parasite population structure and epidemiology, but yet existing methods for characterization of malaria field samples utilize a limited number of antigen encoding genes, which appear to be under strong selection. We describe protocols for characterization of 12 microsatellite markers from finger-prick blood samples infected with Plasmodium falciparum. A two-step, heminested strategy was used to amplify all loci, and products were visualized by fluorescent end-labelling of internal primers. This procedure allows amplification from low levels of template, while eliminating the problem of spurious products due to primer carry over from the primary round of PCR. The loci can be conveniently multiplexed, while accurate sizing and quantification of PCR products can be automated using the GENOTYPER software. The primers do not amplify co-infecting malaria species such as P. vivax and P. malariae. To demonstrate the utility of these markers, we characterized 57 infected finger-prick blood samples from the village of Mebat in Papua New Guinea for all 12 loci, and all samples were genotyped a second time to measure reproducibility. Numbers of alleles per locus range from 4 to 10 in this population, while heterozygosities range from 0·21 to 0·87. Reproducibility (measured as concordance between predominant alleles detected in replicate samples) ranged from 92 to 98% for the 12 loci. The composition of PCR products from infections containing multiple malaria clones could also be defined using strict criteria and scored in a highly repeatable manner.

Phylogenetic relationships of 31 pomacanthid species representing all genera were investigated by horizontal starch gel electrophoresis. Nei's genetic distances (D) were calculated and dendrograms constructed from allozyme variation in 23 loci. The average D value was 0.03 between conspecific colour variants, 0.40 between congeneric subgenera, and 1.27 between confamilial genera. From the dendrograms the following were revealed: (1) the generic status of Apolemichthys arcuatus and Holacanthus venustus, as well as the generic and subgeneric status of Centropyge multifasciata were confirmed; (2) the subgeneric status of Xiphypops was confirmed; (3) Pygoplites diacanthus was found to be closely related to members of the subgenus Pomacanthus; (4) Pomacanthus zonipectus was found to be biochemically distinct from its con-subgeners; (5) the genera Pomacanthus and Holacanthus are more closely related than currently thought; (6) the Genicanthus species might warrant a subfamily of their own.

The electrophoretic variation of four enzymes of wild Anopheles pharoensis in Mwea Irrigation Scheme, Kenya, was studied between 1987 and 1988. The enzyme loci examined were aldehyde oxidase, a-glycerophosphate dehydrogenase, β-hydroxyacid dehydrogenase and lactate dehydrogenase. All the loci examined were dimorphic. A mean heterozygosity (H) of 0.341 was obtained, which is comparable to values for other mosquito species. The allelic frequencies were in genetic disequilibrium compared to Hardy-Weinberg predictions. It is proposed that there may be more than one species in the taxon Anopheles pharoensis.

This paper is about the total number of individuals who are heterozygotic for a specified allele, before it is either lost or fixed. The exact distribution is found for small populations, and two limiting processes are investigated.