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ANAS ANAS, FARIDA DAMAYANTI, MOHAMAD KADAPI, NONO CARSONO, and SANTIKA SARI
UNS Solo
Abstract. Anas, Damayanti F, Kadapi M, Carsono N, Sari S. 2022. The shifting genetic diversity pattern of Indonesian rice improved varieties from 1943-2019 based on historical pedigree data. Biodiversitas 23: 4649-4656. For rice plants in Indonesia, stagnation in increasing crop yields due to a reduction in genetic diversity is a significant issue. The issue of using the same parents in breeding programs and consumer preferences for a single main variety are among the causes of the narrowing of rice plants' genetic diversity. The purpose of this study is to figure out which ancestors are significant and how the genetic diversity of improved Indonesian rice cultivars has changed over time. Changes in the genetic background of the Indonesian rice gene pool were decided using pedigree analysis by calculating the coefficient of parentage (COP) among varieties. There are 280 ancestors in the rice gene pool. The pedigree map exemplifies the complexities of rice breeding in Indonesia. The four classical ancestors of DGWG, Taichung Native1, China, and Latisail had a noteworthy influence on all irrigated rice plant types (11.22%) and upland rice plant types (8.30%) in the gene pool. The dominance of the phenomenal variety IR64 has been continued by Inpari 32, which is a direct derivative of Ciherang. In the meantime, Inpago9, Luhur 2, and UPLRI ancestors set the foundation for the upland rice plant type. Inpara7 and Inpara9, along with their IRRI-introduced parents (IRRIpara4 and IRRIpara5), had a significant impact on Indonesian tidal rice plants. The A1, Hipa7, and Hipa3 varieties are heavily influenced by the hybrid rice plants of Indonesia.
Nur Asiah, Junianto Junianto, Ayi Yustiati, Sukendi Sukendi, Melta Rini Fahmi, Zainal A. Muchlisin, and Muhamad Kadapi
F1000 Research Ltd
Background: Kelabau (Osteochilus spp.) is a freshwater fish commonly found in the rivers of Riau, Indonesia. Researchers believe that these are Osteochilus kelabau; however, accurate taxonomic determination of these fish in Riau waters has not been made. The purpose of this study was to facilitate the identification of the kelabau based on its morphology and genetics using biometric and cytochrome c oxidase subunit 1 (CO1) analyses, respectively. Methods: Fish samples were collected from the Siak, Kampar and Rokan rivers in Riau Province, Indonesia. The DNA of 90 fish was extracted from the caudal fins using a DNA extraction kit, after which it was amplified using primers Fish-F1 and Fish-R1. Sequencing was conducted by Applied Biosystems Macrogen Korea, and the DNA sequences were then edited and aligned using MEGA v. 7. All samples were BLAST-searched for identification using the National Center for Biotechnology Information and BOLD System. Phylogenetic trees were constructed, and similarity index was calculated using accession numbers AP011385.1 and KC631202.1 in GenBank. Results: Analysis of the consensus barcode sequence for 86 species revealed a high percentage of barcode matches (96%–97% in GenBank and 96.6%–96.76% in the BOLD System). The nucleotide distance between groups of kelabau from the different rivers based on the Kimura 2-parameter model gave the following results: 0.05% between groups from the Siak and Kampar rivers, 0.09% between those from the Siak and Rokan rivers and 0.05% between those from the Kampar and Rokan rivers. The nucleotide distance between the groups in the Siak (0.09%), Kampar (0.00%) and Rokan (0.10%) Rivers indicated that the kelabau in those rivers were related to each other. Conclusions: Based on the results of the research data using CO1 and biometric analyses, the kelabau were confirmed to be O. melanopleurus.
Mochamad Arief Soleh, Mira Ariyanti, Intan Ratna Dewi, Muhamad Kadapi
Faculty of Food and Agriculture, United Arab Emirates University
Under natural conditions, plants are often subjected to waterlogging due to poor soil drainage and or exessive rainfall. This condition leads to reduced maximum quantum yield of photosystem II (fv/fm) under suboptimal growing system. Under well-watered conditions (WW), the fv/fm of ten varieties of sugarcane were maintained at more than 0.78. However, following waterlogging for 4 days and a constant light of 3000 mmolmol-1 for 60s, the fv/fm of ten varieties of sugarcene varied from 0.587 in PS882 (V4) to 0.740 in GMP2 (V9). Meanwhile, under fluctuating light intensity from dark to highlight of 1600 mmolmol-1, the fv/fm of all varieties decreased to below of 0.1 except in the genotype PSJK922 (V5) at 28 DAT (day after treatment) of waterlogging. This difference was then further examined through measurements of stomatal conductance (gs) among the varieties. There was negative correllation between fv/fm and stomatal conductance, high gs was not associated with lower fv/fm. Dendrogam analyses showed the variety of PS881 (V1), PS864 (V3) and Kidang Kencana (KK) were highly sensitive to waterlogging. These results suggest potential screening of plants based on improve fv/fm under abiotic condition.
C. Suherman, A. Nuraini, A.P. Wulandari, and M. Kadapi
IOP Publishing
Kadapi Muhamad, Kaworu Ebana, Shuichi Fukuoka, and Kazutoshi Okuno
Springer Science and Business Media LLC
Morphological traits and two kinds of molecular markers were employed to study the genetic relationships among improved rice (Oryza sativa) varieties of Indonesia since 1943. Dendrograms based on morphological traits and both molecular markers (simple sequence repeats, SSR and single nucleotide polymorphism, SNP) agreed in separating the varieties into two primary groups. Based on the morphological traits, a larger group (>60 %) contains varieties with smaller sizes compared with those in the smaller group (<40 %). SSR and SNP markers revealed that most of the varieties belonged to indica (88; 89 %) and japonica (9; 8 %) subspecies, and 3 % of varieties were not involved in two subspecies. The molecular markers revealed that the genetic diversity (H) stagnated between stage II (1967–1985) and stage III (1986–2003). However, during stage I (1943–1966), H was higher than in the other stages as revealed by SNP markers, while H in stage I was lower than in the other stages as revealed by SSR markers. In this study, the two molecular data sets were positively correlated and positive correlations between the phenotypic and molecular data depended on the kind of molecular marker: SNP had higher Mantel r values than SSRs. Besides, SSR markers seem to be appropriate for pedigree studies, while SNP markers could be used to reveal genomic relationships. These findings were attributable to the different properties of these two different markers. These results suggested that the diversity and differentiation of both the phenotypic and molecular marker variations were probably resulted from the crossing and selection in rice breeding in Indonesia. We suggest that Indonesia needs another strategy to improve new varieties to avoid a reduction in genetic diversity and similarity.
Kadapi Muhamad, Kaworu Ebana, Shuichi Fukuoka, and Kazutoshi Okuno
Springer Science and Business Media LLC
AbstractAnalysis of the
genetic structure of Indonesian Oryza sativa and O. rufipogon using neighbour-joining trees based on single nucleotide polymorphism (SNP) and simple sequence repeat (SSR) markers revealed that O. sativa in Indonesia is separated from O. rufipogon. Accessions of O. sativa in this study were differentiated into two major groups, indica and tropical japonica, excluding some varieties. SSR and SNP markers revealed the high value of differentiation (FST) and genetic distance (D) between indica and tropical japonica and we discovered four loci by SNP markers and one locus by SSR markers that play a role in differentiation between indica and tropical japonica. Interestingly, genetic diversity (H) in O. rufipogon was lower than that in O. sativa, however H in O. rufipogon was the highest and H in tropical japonica was the lowest when O. sativa was divided into two groups. Inbreeding coefficient (Fst) showed evidences that gene flow (Nm) between species and within species might be one of the mechanisms related to the diversification and differentiation of Indonesian rice germplasm by asymmetric pattern between species and within O. sativa as revealed by SSR and SNP markers. In addition, we found evidences on stabilizing selection in Indonesian rice germplasm and they might be the reasons why Indonesian rice germplasm did not differentiate due to source location of landrace. However, we found a weak relation between SSR and SNP markers probably due to highly polymorphic in SSR and the different properties of both markers.