scholarly journals Indigenous Seeds, Seed Selection and Seed Bank for Sustainable Agriculture

2021 ◽  
Vol 04 (04) ◽  
pp. 13-26
Author(s):  
Bal Krishna Joshi ◽  

Indigenous seeds are grown by the farmers over the years with a strong influence from local natural factors. Such seeds have a higher level of intrapopulation variations and the capacity of buffering the adverse factors. Understanding indigenous seeds along with their diversity are useful to diversify their uses, to assess conservation status, to know the factors making farming areas red zone, and to improve their performance. Selection is the simplest and most common method for the improvement of crop varieties. The variation must be created and maintained to impose selection. Different types of selection can be considered depending on the mode of reproduction of crops. Response to selection and correlated response are estimated to make the selection process more effective. Many different selection approaches can target either developing monomorphic or polymorphic varieties. There are five selection units and can be applied in five crop stages. Farmers’ criteria need to be considered during selection process. Based on the genotypic classes, there are three types of selection namely stabilizing selection, directional selection, and disruptive selection. The most simple and common selection methods are pure lines, mass selection, and class-bulking selection. Orthodox seeds in short, medium, and long-term storage facilities are conserved as a seed bank. Major types are household seed banks, community seed banks, national seeds, natural seed banks, and global seed banks. A seed bank is for assuring the availability of crop diversity for research, study, and production. The common works in seed banks are diversity collection, regeneration, characterization, multiplication, and distribution along with online database management.

1998 ◽  
Vol 76 (7) ◽  
pp. 1188-1197 ◽  
Author(s):  
Heli M. Jutila b. Erkkilä

Seed banks of two seashore meadows were studied on the west coast of Finland (latitude 61°30'-61°33'N, longitude 21°28'-21°41'E). Samples were taken in June to a depth of 10 cm in the geolittoral zone of the grazed and ungrazed transects. The grazed samples were halved lengthwise: one half was grown immediately, the other after cold treatment. One third of the all samples was treated as controls, one third was watered with brackish water, and one third was given a pesticide treatment. Altogether, 13 926 seedlings germinated and 25 species were identified (three annuals, two biennials, and the rest perennials). Most seedlings were perennial monocots, with Juncus gerardii Loisel. the most abundant species. The seed bank was significantly larger and richer in the ungrazed site than in the grazed site. Cold treatment reduced the number of germinating species and seedlings. In the grazed and non-cold-treated samples, the numbers of species and seedlings were highest in the pesticide treatment. In ungrazed samples there were no significant differences among treatments. After the cold treatment, the least number of species and seedlings was produced by the salt-water treatment. Changing brackish water to tap water led to a burst of germination, especially of J. gerardii. The seed bank of the upper geolittoral zone was richer than that of the middle geolittoral. The multivariate classification and ordination groupings are based on the abundances of J. gerardii and Glaux maritima L.; different treatments were not distinguishable. There was a low resemblance between the seed bank and the aboveground vegetation.Key words: seed bank, salinity, pesticide, seashore meadow, cold treatment, vegetation.


1996 ◽  
Vol 36 (3) ◽  
pp. 299 ◽  
Author(s):  
TS Andrews ◽  
RDB Whalley ◽  
CE Jones

Inputs and losses from Giant Parramatta grass [GPG, Sporobolus indicus (L.) R. Br. var. major (Buse) Baaijens] soil seed banks were quantified on the North Coast of New South Wales. Monthly potential seed production and actual seed fall was estimated at Valla during 1991-92. Total potential production was >668 000 seeds/m2 for the season, while seed fall was >146000 seeds/m2. Seed fall >10000 seeds/m2.month was recorded from January until May, with further seed falls recorded in June and July. The impact of seed production on seed banks was assessed by estimating seed banks in the seed production quadrats before and after seed fall. Seed banks in 4 of the 6 sites decreased in year 2, although seed numbers at 1 damp site increased markedly. Defoliation from mid-December until February, April or June prevented seed production, reducing seed banks by 34% over 7 months. Seed banks in undefoliated plots increased by 3300 seeds/m2, although seed fall was estimated at >114 000 seeds/m2. Emergence of GPG seedlings from artificially established and naturally occurring, persistent seed banks was recorded for 3 years from bare and vegetated treatment plots. Sown seeds showed high levels of innate dormancy and only 4% of seeds emerged when sown immediately after collection. Longer storage of seeds after collection resulted in more seedlings emerging. Estimates of persistent seed banks ranged from 1650 to about 21260 seeds/m2. Most seedlings emerged in spring or autumn and this was correlated with rainfall but not with ambient temperatures. Rates of seed bank decline in both bare and vegetated treatment plots was estimated by fitting exponential decay curves to seed bank estimates. Assuming no further seed inputs, it was estimated that it would take about 3 and 5 years, respectively, for seed banks to decline to 150 seeds/m2 in bare and vegetated treatments.


2021 ◽  
Author(s):  
William R. Shoemaker ◽  
Evgeniya Polezhaeva ◽  
Kenzie B. Givens ◽  
Jay T. Lennon

Fluctuations in the availability of resources constrains the growth and reproduction of individuals, which in turn effects the evolution of their respective populations. Many organisms are able to respond to fluctuations by entering a reversible state of reduced metabolic activity, a phenomenon known as dormancy. This pool of dormant individuals (i.e., a seed bank) does not reproduce and is expected to act as an evolutionary buffer, though it is difficult to observe this effect directly over an extended evolutionary timescale. Through genetic manipulation, we analyze the molecular evolutionary dynamics of Bacillus subtilis populations in the presence and absence of a seed bank over 700 days. We find that the ability to enter a dormant state increases the accumulation of genetic diversity over time and alters the trajectory of mutations, findings that are recapitulated using simulations based on a simple mathematical model. While the ability to form a seed bank does not alter the degree of negative selection, we find that it consistently alters the direction of molecular evolution across genes. Together, these results show that the ability to form a seed bank affects the direction and rate of molecular evolution over an extended evolutionary timescale.


Genetics ◽  
1972 ◽  
Vol 72 (1) ◽  
pp. 129-142
Author(s):  
E J Eisen

ABSTRACT Long-term selection for increased 12-day litter weight in two replicate lines (W2, W3) of mice resulted in an apparent selection limit at about 17 generations. Quadratic polynomial and exponential models were fitted to the data in order to estimate the plateaued response and half-life of the selection process. Using the polynomial results, the half-life estimates were 4.5 and 8.6 generations for W2 and W3, respectively. The plateaued responses were 5.1 and 5.8 g which, when expressed in phenotypic standard deviation units, became 1.1 and 1.3. The exponential model provides similar estimates. A negative association between 12-day litter weight and fitness was not considered to be an adequate explanation for the plateau since there was no decrease in fertility of the selected lines. Evidence that exhaustion of genetic variability was not the cause of the plateau came from the immediate response to reverse selection. It was proposed that the plateau may be due to a negative genetic correlation between direct and maternal genetic effects, which would be expected to occur after many generations of selection. There were positive correlated responses in both replicates for adult body weight, which was in agreement with the positive genetic correlation between preweaning and postweaning body weight. The expected positive correlated response for number born was realized in only one of the replicates.


2011 ◽  
Vol 79 (2) ◽  
pp. 157-166 ◽  
Author(s):  
Maciej Wódkiewicz ◽  
Anna Justyna Kwiatkowska-Falińska

Forest seed banks mostly studied in managed forests proved to be small, species poor and not reflecting aboveground species composition. Yet studies conducted in undisturbed communities indicate a different seed bank characteristic. Therefore we aimed at describing soil seed bank in an undisturbed forest in a remnant of European lowland temperate forests, the Białowieża Forest. We compared similarity between the herb layer and seed bank, similarity of seed bank between different patches, and dominance structure of species in the herb layer and in the seed bank of two related oak-hornbeam communities. We report relatively high values of Sorensen species similarity index between herb layer and seed bank of both patches. This suggests higher species similarity of the herb layer and soil seed bank in natural, unmanaged forests represented by both plots than in fragmented communities influenced by man. Although there was a set of core seed bank species present at both plots, yielding high Sorensen species similarity index values, considerable differences between plots in seed bank size and dominance structure of species were found, indicating spatial variability of studied seed bank generated by edaphic conditions. Dominance structure of species in the herb layer was not reflected in the underlying seed bank. This stresses, that natural forest regeneration cannot rely only on the seed bank, although some forest species are capable of forming soil seed banks. While forest seed banks may not reflect vegetation composition of past successional stages, they may inform on history and land use of a specific plot.


2020 ◽  
Vol 1 (4) ◽  
pp. 36-42
Author(s):  
Wubeshet Teshome ◽  
Nesru Temam

Farmers were organized and trained on crop conservation and management, seed selection. Farmers were organized by District Cooperative office with collaboration to EBI for legal entities The key supporter of CSB is District Agricultural office, District Administration office, District youth and women office, District trade office, District land administration office university, NGO and district cooperative office. The members of executive committee are elected every three year by members. Twenty four CSBs have been established, and crop conservation associations are organized and 6 CSBs were under establishment. Twenty one crop type were conserved.


PeerJ ◽  
2019 ◽  
Vol 7 ◽  
pp. e7650 ◽  
Author(s):  
Xian Gu ◽  
Yu Cen ◽  
Liyue Guo ◽  
Caihong Li ◽  
Han Yuan ◽  
...  

The long-term use of herbicides to remove weeds in fallow croplands can impair soil biodiversity, affect the quality of agricultural products, and threaten human health. Consequently, the identification of methods that can effectively limit the weed seed bank and maintain fallow soil fertility without causing soil pollution for the next planting is a critical task. In this study, four weeding treatments were established based on different degrees of disturbance to the topsoil: natural fallow (N), physical clearance (C), deep tillage (D), and sprayed herbicide (H). The changes in the soil weed seed banks, soil nutrients, and soil microbial biomass were carefully investigated. During the fallow period, the C treatment decreased the annual and biennial weed seed bank by 34% against pretreatment, whereas the H treatment did not effectively reduce the weed seed bank. The D treatment had positive effects on the soil fertility, increasing the available nitrogen 108% over that found in the N soil. In addition, a pre-winter deep tillage interfered with the rhizome propagation of perennial weeds. The total biomass of soil bacterial, fungal, and actinomycete in H treatment was the lowest among the four treatments. The biomass of arbuscular mycorrhizal fungi in the N treatment was respectively 42%, 35%, and 91%, higher than that in the C, D, and H treatments. An ecological weeding strategy was proposed based on our findings, which called for exhausting seed banks, blocking seed transmission, and taking advantage of natural opportunities to prevent weed growth for fallow lands. This study could provide a theoretical basis for weed management in fallow fields and organic farming systems.


Author(s):  
Ya-Fei Shi ◽  
Zengru Wang ◽  
Bing-Xin Xu ◽  
Jian-Qiang Huo ◽  
Rui Hu ◽  
...  

Soil seed banks may offer great potential for restoring and maintaining desert ecosystems that have been degraded by climate change and anthropogenic disturbance. However, few studies have explored the annual dynamics in the composition and relative abundance of these soil seed banks. We conducted a long-term observational study to assess the effects of environmental factors (meteorology and microtopography) and aboveground vegetation on the soil seed bank of the Tengger Desert, China. The desert seed bank was dominated by annual herbs. We found that more rainfall in the growing season increased the number of seeds in the soil seed bank, and that quadrats at relatively higher elevations had fewer seeds. The species composition had more similarity in the seed bank than in the aboveground vegetation, though the seed bank and aboveground vegetation did change synchronously due to the rapid propagation of annuals. Together, our findings suggest that the combined effects of environmental factors and plant life forms determine the species composition and size of soil seed banks in deserts. Thus, if degraded desert ecosystems are left to regenerate naturally, the lack of shrub and perennial herb seeds could crucially limit their restoration. Human intervention and management may have to be applied to enhance the seed abundance of longer-lived lifeforms in degraded deserts.


2020 ◽  
Author(s):  
Nathan I. Wisnoski ◽  
Jay T. Lennon

ABSTRACTCoexisting species often exhibit negative frequency dependence due to mechanisms that promote population growth and persistence when rare. These stabilizing mechanisms maintain diversity through interspecific niche differences, but also through life-history strategies like dormancy that buffer dynamics in fluctuating environments. However, there are few tests demonstrating how seed banks contribute to long-term community dynamics and the maintenance of diversity. Using multi-year, high-frequency bacterial community data from a north temperate lake, we documented patterns consistent with stabilizing coexistence, including differential responses of bacterial taxa to environmental conditions and the presence of a seed bank. By maintaining rare taxa over winter periods, the seed bank contributed to recurrent seasonal dynamics. Last, strong negative frequency dependence in rare, but metabolically active, taxa suggested biotic interactions promoted coexistence. Together, our results provide field-based evidence that niche differences and seed banks stabilize bacterial community dynamics and contribute to the maintenance of microbial diversity in nature.


2017 ◽  
Vol 57 (2) ◽  
pp. 165-175 ◽  
Author(s):  
Petra S. Yehnjong ◽  
Michael S. Zavada ◽  
Chris Liu

AbstractSoil seed banks are important to the maintenance and restoration of floras. Extant seed banks exhibit unique characteristics with regard to the distribution of seed size and seed density. Seeds were recovered from the Upper Pennsylvanian Wise Formation in southwest Virginia. Structurally preserved seeds were also examined from coal balls of the Pennsylvanian Pottsville and Allegheny Groups, Ohio. The size distribution of the seeds from the Wise Formation is similar to that of structurally preserved seeds of the Upper Pennsylvanian Pottsville and Allegheny Group coal balls. In contrast, the seed size distributions in extant wetland, grassland, woodland and forest habitats are significantly narrower than that of seeds from the Pennsylvanian seed banks. Larger seeds are less dependent on light for germination, and aid in seedling establishment more than smaller seeds, especially in dense stable forests where disturbance events are rare. Large seed size may contribute to increased seed longevity, which reduces the effect of environmental variability on seed germination and development. The significantly larger size of the Palaeozoic seeds may have imparted an advantage for seedling establishment in the dense Palaeozoic forests. The preponderance of large seeds may be a result of the absence of large seed predators (e.g. herbivorous tetrapods), and may have been an evolutionary strategy to minimize damage to the embryo from a predator population dominated by small invertebrates with chewing or sucking mouthparts. The estimated seed density of 192 seeds/m2in the Palaeozoic seed bank falls within the range of modern seed banks, but at the lower end of modern seed bank densities in a variety of habitats.


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