NRU :: Browsing by Author "Mukasa, Settumba B."

Browsing by Author "Mukasa, Settumba B."

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Early Withering of Enlarged Ovules in Pollinated Fruits of Bananas (Musa spp.) Suggest Abortion after Fertilization
(Horticulturae, 2022) Waniale, Allan; Mukasa, Settumba B.; Tugume, Arthur K.; Kubiriba, Jerome; Tushemereirwe, Wilberforce K.; Tumuhimbise, Robooni
Sterility in edible bananas is as a result of a long history of anthropogenic-driven selection for sterile genotypes, since seed is not desirable in fruit pulp for human consumption. However, this poses a challenge to conventional genetic improvement by slowing breeding pipelines. In this study, we investigated whether pollen tubes reach all parts of the ovary, the position of fertilized ovule development in fruits, and potential seed set in selected banana genotypes. We selected four cultivars of East African Highland Cooking bananas (EAHBs), a Matooke hybrid ‘222K-1’, improved diploid ‘2905’, and wild bananas ‘Zebrina (G.F.)’ and ‘Calcutta 4’. There was evidence of pollen tubes in the distal, mid and proximal sections of the fruit, irrespective of hand position and genotype. Fertilization, as indicated by an increase in ovule size, happened along the entire length of the fruit but complete development was biased at the distal end in some genotypes. There were some differences in ovule fertilization rates between hands, with distal hands having more ovules and higher ovule fertilization rates. Ovule fertilization happens in bananas but the vast majority aborts, especially at the proximal end of the ovary. Ovule fertilization rates are generally much lower than available ovules.
Genetic Variability and Evolutionary Implications of RNA Silencing Suppressor Genes in RNA1 of Sweet Potato Chlorotic Stunt Virus Isolates Infecting Sweetpotato and Related Wild Species
(PLoS ONE, 2013) Tugume, Arthur K.; Amayo, Robert; Weinheimer, Isabel; Mukasa, Settumba B.; Rubaihayo, Patrick R.; Valkonen, Jari P. T.
The bipartite single-stranded RNA genome of Sweet potato chlorotic stunt virus (SPCSV, genus Crinivirus; Closteroviridae) encodes a Class 1 RNase III (RNase3), a putative hydrophobic protein (p7) and a 22-kDa protein (p22) from genes located in RNA1. RNase3 and p22 suppress RNA silencing, the basal antiviral defence mechanism in plants. RNase3 is sufficient to render sweetpotato (Ipomoea batatas) virus-susceptible and predisposes it to development of severe diseases following infection with unrelated virus. The incidence, strains and gene content of SPCSV infecting wild plant species have not been studied. Methodology/Principal Findings: Thirty SPCSV isolates were characterized from 10 wild Ipomoea species, Hewittia sublobata or Lepistemon owariensis (family Convolvulaceae) in Uganda and compared with 34 local SPCSV isolates infecting sweetpotatoes. All isolates belonged to the East African (EA) strain of SPCSV and contained RNase3 and p7, but p22 was not detected in six isolates. The three genes showed only limited genetic variability and the proteins were under purifying selection. SPCSV isolates lacking p22 synergized with Sweet potato feathery mottle virus (SPFMV, genus potyvirus; Potyviridae) and caused severe symptoms in co-infected sweetpotato plants. One SPCSV isolate enhanced accumulation of SPFMV, but no severe symptoms developed. A new whiteflytransmitted virus (KML33b) encoding an RNase3 homolog (<56% identity to SPCSV RNase3) able to suppresses sense-mediated RNA silencing was detected in I. sinensis. Conclusions/Significance: SPCSV isolates infecting wild species and sweetpotato in Uganda were genetically undifferentiated, suggesting inter-species transmission of SPCSV. Most isolates in Uganda contained p22, unlike SPCSV isolates characterized from other countries and continents. Enhanced accumulation of SPFMV and increased disease severity were found to be uncoupled phenotypic outcomes of RNase3-mediated viral synergism in sweetpotato. A second virus encoding an RNase3-like RNA silencing suppressor was detected. Overall, results provided many novel and important insights into evolutionary biology of SPCSV.
Interactive effects of Potato virus Y and Potato leafroll virus infection on potato yields in Uganda
(Open Agriculture, 2020) Byarugaba, Arinaitwe Abel; Mukasa, Settumba B.; Barekye, Alex; Rubaihayo, Patrick R.
Potatoes are prone to attack by multiple viruses, which contribute greatly to yield and quality decline depending on the cultivar and the virus involved. This study investigated the effect of co-infection involving Potato virus Y (potyvirus) and Potato leafroll Virus (pelero virus) on productivity of five potato cultivars in Uganda and the nature of virus interaction during co-infection process. Variety response to virus infection by PVY, PLRV and co-infection (PVY + PLRV) varied across different varieties. The plants that were infected with PLRV had leaf rolling, stuntedness, leaf distortion, reduction in leaf size and mottling and light yellow mosaics, and in some cases, purple or red margins were observed, while single infection of PVY induced necrosis, leaf rugosity, crinkling, stunting, interveinal necrosis, blotching of the margins, leaf distortion andmottling. When the two viruses were combined during co-infection with PVY + PLRV, the symptoms were characterized by bright blotching and necrotic leaf margins with purpling of the leaf tips and leaf margins, stuntedness and leaf distortions. The virus disease severity was higher under mixed infected plants than single infected plants. The high disease severity culminated in a significant effect on yield, marketable tuber number per plant, plant growth height and plant vigor, which were different across the varieties. Co-infection involving PVY and PLRV caused a reduction in the marketable yield of 95.2% (Kinigi), 94% (Victoria), 89.5 (Rwagume), 45.3% (Royal) and 23.7% (Sifra). Single infection by PLRV caused a reduction in amarketable yield in Victoria (91.8%), Kinigi (84.8%), Rwagume (73.3%), Royal (47.2%) and Sifra 22.1%, while PVY caused a marketable yield reduction in Victoria (87.2%), Rwagume (85.9.7%), Kinigi (85.1%), Royal (37.4%) and Sifra (14.1%). The effects associated with the coinfection of PVY and PLRV were lower than the combined value of the single infections, suggesting that the two viruses were interacting to affect the potato productivity. The high yield loss suggested that effective resistance strategy targeting PVY, PLRV and their combination was required to save the potato industry in Uganda.
Mixed Infections of Four Viruses, the Incidence and Phylogenetic Relationships of Sweet Potato Chlorotic Fleck Virus (Betaflexiviridae) Isolates in Wild Species and Sweetpotatoes in Uganda and Evidence of Distinct Isolates in East Africa
(PLoS ONE, 2016) Tugume, Arthur K.; Mukasa, Settumba B.; Valkonen, Jari P. T.
Viruses infecting wild flora may have a significant negative impact on nearby crops, and vice-versa. Only limited information is available on wild species able to host economically important viruses that infect sweetpotatoes (Ipomoea batatas). In this study, Sweet potato chlorotic fleck virus (SPCFV; Carlavirus, Betaflexiviridae) and Sweet potato chlorotic stunt virus (SPCSV; Crinivirus, Closteroviridae) were surveyed in wild plants of family Convolvulaceae (genera Astripomoea, Ipomoea, Hewittia and Lepistemon) in Uganda. Plants belonging to 26 wild species, including annuals, biannuals and perennials from four agroecological zones, were observed for virus-like symptoms in 2004 and 2007 and sampled for virus testing. SPCFV was detected in 84 (2.9%) of 2864 plants tested from 17 species. SPCSV was detected in 66 (5.4%) of the 1224 plants from 12 species sampled in 2007. Some SPCSV-infected plants were also infected with Sweet potato feathery mottle virus (SPFMV; Potyvirus, Potyviridae; 1.3%), Sweet potato mild mottle virus (SPMMV; Ipomovirus, Potyviridae; 0.5%) or both (0.4%), but none of these three viruses were detected in SPCFV-infected plants. Co-infection of SPFMV with SPMMV was detected in 1.2% of plants sampled. Virus-like symptoms were observed in 367 wild plants (12.8%), of which 42 plants (11.4%) were negative for the viruses tested. Almost all (92.4%) the 419 sweetpotato plants sampled from fields close to the tested wild plants displayed virus-like symptoms, and 87.1% were infected with one or more of the four viruses. Phylogenetic and evolutionary analyses of the 30-proximal genomic region of SPCFV, including the silencing suppressor (NaBP)- and coat protein (CP)-coding regions implicated strong purifying selection on the CP and NaBP, and that the SPCFV strains from East Africa are distinguishable from those from other continents. However, the strains from wild species and sweetpotato were indistinguishable, suggesting reciprocal movement of SPCFV between wild and cultivated Convolvulaceae plants in the field.
Molecular genetic analysis of virus isolates from wild and cultivated plants demonstrates that East Africa is a hotspot for the evolution and diversification of Sweet potato feathery mottle virus
(Molecular ecology, 2010) Tugume, Arthur K.; Cue´ Llar, Wilmer J .; Mukasa, Settumba B.; Valkonen, Jari P. T.
Sweet potato feathery mottle virus (SPFMV, genus Potyvirus) is globally the most common pathogen of cultivated sweet potatoes (Ipomoea batatas; Convolvulaceae). Although more than 150 SPFMV isolates have been sequence-characterized from cultivated sweet potatos across the world, little is known about SPFMV isolates from wild hosts and the evolutionary forces shaping SPFMV population structures. In this study, 46 SPFMV isolates from 14 wild species of genera Ipomoea, Hewittia and Lepistemon (barcoded for the matK gene in this study) and 13 isolates from cultivated sweet potatoes were partially sequenced. Wild plants were infected with the EA, C or O strain, or co-infected with the EA and C strains of SPFMV. In East Africa, SPFMV populations in wild species and sweet potato were genetically undifferentiated, suggesting inter-host transmission of SPFMV. Globally, spatial diversification of the 178 isolates analysed was observed, strain EA being largely geographically restricted to East Africa. Recombination was frequently detected in the 6K2-VPg-NIaPro region of the EA strain, demonstrating a recombination ‘hotspot’. Recombination between strains EA and C was rare, despite their frequent co-infections in wild plants, suggesting purifying selection against strain EA⁄C recombinants. Positive selection was predicted on 17 amino acids distributed over the entire coat protein in the globally distributed strain C, as compared to only four amino acids in the coat protein N-terminus of the EA strain. This selection implies a more recent introduction of the C strain and a higher adaptation of the EA strain to the local ecosystem. Thus, East Africa appears as a hotspot for evolution and diversification of SPFMV.
Multi-Environmental Evaluation of Protein Content and Yield Stability among Tropical Soybean Genotypes Using GGE Biplot Analysis
(Agronomy, 2021) Obua, Tonny; Sserumaga, Julius Pyton; Awio, Bruno; Nganga, Fredrick; Odong, Thomas L.; Tukamuhabwa, Phinehas; Tusiime, Geoffrey; Mukasa, Settumba B.; Nabasirye, Margaret
The yield and protein performance in a soybean genotype result from its interaction with the prevailing environmental conditions. This makes selecting the best genotypes under varied target production environments more complex. This study’s objectives were to determine protein content and protein stability of 30 elite soybean genotypes in major soybean-growing areas of Uganda, assess the yield performance and stability in soybeans and determine the relationship between the protein content and grain yield in soybeans. The genotypes were planted in a randomized complete block design of three replications for six seasons across eight locations in Uganda. Genotype and genotypeby- environment (GGE) biplot analyses classified the test locations into three mega-environments for soybean protein and grain yields. Genotype NII X GC 20.3 had the highest mean protein content of 43.0%, and BSPS 48A-9-2 and BSPS 48A-28 were superior for the mean grain yield (1207 kg ha􀀀1). Bulindi was the most discriminating and representative test environment for soybean yield. A weak and negative correlation (r = 􀀀0.1**, d.f. = 29) was detected between the protein content (%) and yield (kg ha􀀀1). The highest-yielding genotypes BSPS 48A-9-2, BSPS 48A-31, and Nam II GC 44.2 are recommended for further evaluation under farmers’ production conditions for selection and release as new soybean varieties in Uganda.
Prevalence of R Genes for Resistance to Potato Viruses in Uganda Germplasm
(Potato Research, 2021) Byarugaba, Arinaitwe Abel; Mukasa, Settumba B.; Barekye, Alex; Rubaihayo, Patrick R.
The most important potato viruses in Uganda are Potato virus Y (PVY), Potato leaf roll virus (PLRV), Potato virus X (PVX), Potato virus S (PVS), Potato virus A (PVA) and Potato virus M (PVM). Utilization of R genes in breeding for resistance to viruses has not been explored in Uganda due to limited information on the prevalence of R genes in the available genotypes. This study aimed at identifying potato genotypes with R genes for resistance to potato viruses important in Uganda. The study screened 71 potato accessions from the National Potato Breeding Programme at Kachwekano Zonal Agricultural Research and Development Institute for the presence of resistance genes to viruses using diagnostic molecular markers. The results indicated that 21 out of 71 genotypes had resistance markers, of which nine genotypes, NKRN59.58, Derby, Markies, Sifra, 395017.229, Nakpot 5, 20108.5, Royal and 393220.54, had Ryadg gene for PVY resistance and two genotypes, Kimuri and 319919.3, had Rysto gene for resistance to PVY and PVA. Nine genotypes, 395011.2, Markies, Nakpot 5, 20108.5, Sifra, 20157.6, Royal, 2015.8 and Ambition, had the Nbtbr gene for resistance to PVX. In addition, 14 genotypes, 395011.2, Markies, Nakpot 5, Sarpouna, 393220.54, 391046.14, Sarpomira, 395077.12, Sifra, 20157.6, Royal, Ambition, Kimuri and Caruso, had the Nsadg gene conferring resistance to PVS. Four genotypes, Markies, Sifra, Nakpot 5 and Royal, had the Ryadg, Nbtbr and Nsadg genes for combined resistance to PVY, PVX and PVS. The resistant genotypes could be used as parents to introgress resistance genes into susceptible cultivars.
Production of friable embryogenic callus and regeneration of Ugandan farmer-preferred cassava genotypes
(African Journal of Biotechnology, 2015) Apio, Hellen B.; Alicai, Titus; Baguma, Yona; Mukasa, Settumba B.; Bua, Anton; Taylor, Nigel
Generation of embryogenic callus is a key step in genetic engineering of many crop species, including cassava. Protocols for generation of friable embryogenic callus (FEC) have been lacking for Ugandan cassava genotypes, thereby delaying their genetic engineering for agronomic and other desirable traits. The objective of this study was to determine conditions suitable for production and regeneration of FEC in the Ugandan cassava genotypes; Aladu, Bukalasa and Ebwanateraka, and control cultivar 60444. Immature leaf lobe explants were established on Murashige and Skoog (MS) based media for initiation of organized embryogenic callus (OES). To produce FEC, resulting OES were established on Gresshoff and Doy based callus induction media with varying levels of sucrose, maltose, tyrosine, tryptophan, naphthalene acetic acid (NAA) under light and dark conditions. Subsequently, FEC was subcultured to MS-based embryo maturation and embryo regeneration media. All genotypes produced OES. All genotypes produced FEC except Bukalasa. The amino acid tyrosine favoured production of FEC in Aladu and Ebwanatereka, but not in 60444, while 20 g/L of sucrose trigged production of FEC in Aladu and 60444, but 40 g/L of sucrose was superior for Ebwanatereka. Media supplemented with 1 ml/L naphthalene acetic acid NAA facilitated embryo regeneration in Ebwanatereka and 60444, while Aladu responded better to 5 ml/L NAA. Light, tyrosine and sucrose were essential for FEC production in Uganda cultivars while NAA was required for regeneration of somatic embryos. Ability to produce FEC in these genotypes lays a foundation for their improvement through genetic transformation for the desired and agronomic traits.
Recombination and selection pressure in the ipomovirus sweet potato mild mottle virus (Potyviridae) in wild species and cultivated sweetpotato in the centre of evolution in East Africa
(Journal of general virology, 2010) Tugume, Arthur K.; Mukasa, Settumba B.; Kalkkinen, Nisse; Valkonen, Jari P. T.
Sweet potato mild mottle virus (SPMMV) is the type member of the genus Ipomovirus (family Potyviridae). SPMMV occurs in cultivated sweetpotatoes (Ipomoea batatas Lam.; Convolvulaceae) in East Africa, but its natural wild hosts are unknown. In this study, SPMMV was detected in 283 (9.8 %) of the 2864 wild plants (family Convolvulaceae) sampled from different agro-ecological zones of Uganda. The infected plants belonged to 21 species that were previously not known to be natural hosts of SPMMV. The size of the SPMMV coat protein (CP) was determined by Western blot analysis, N-terminal protein sequencing and peptide mass fingerprinting. Data implicated a proteolytic cleavage site, VYVEPH/A, at the NIb/CP junction, resulting in a CP of approximately 35 kDa. Nearly complete sequences of 13 SPMMV isolates were characterized. Phylogenetic analysis of non-recombinant CP-encoding sequences placed five isolates from wild species sampled in the central zone of Uganda into a separate cluster. Recombination events were detected in the 59- and 39-proximal parts of the genome, providing novel evidence of recombination in the genus Ipomovirus. Thirteen amino acids in the N terminus of the P1 protein were under positive selection, whereas purifying selection was implicated for the HC-Pro-, P3-, 6K1- and CP-encoding regions. These data, supported by previous studies on ipomoviruses, provide indications of an evolutionary process in which the P1 proteinase responds to the needs of adaptation.
Seed Set Patterns in East African Cooking Bananas (Musa spp.) are Dependent on Weather Before, During, and After Pollination
(Research Square, 2020) Waniale, Allan; Mukasa, Settumba B.; Tugume, Arthur K.; Tumuhimbise, Robooni; Kubiriba, Jerome; Tushemereirwe, Wilberforce K.; Batte, Michael; Brown, Allan; Swennen, Rony
Seed set in banana (Musa spp.) is influenced by weather but the most critical weather attribute(s) and the critical period are unknown. Such information is of paramount importance to increase seed set for banana breeding programs. Three female fertile East African cooking bananas (EACBs), ‘Enzirabahima’ (AAA), ‘Mshale’ (AA), and ‘Nshonowa’ (AA) were pollinated with the highly male fertile wild banana ‘Calcutta 4’ (AA). At full maturity, bunches were harvested and ripened and seeds extracted from ripe fruit pulp. Seed set was then correlated with weather before, during, and after pollination. Results: Seed set was positively correlated with high temperatures (r=0.172 – 0.488), solar radiation (r=0.181 – 0.282) and negatively correlated with rainfall (r=-0.214 – -0.238) and relative humidity (RH) (r=-0.158 – -0.438) between 75 and 15 days before pollination (DBP). The pattern of weather association was cultivar-dependent with ‘Nshonowa’ having the strongest significant associations. At the time of pollination, high average temperatures were critical for seed set in ‘Enzirabahima’ (r=0.214, P<0.01) while high morning RH was critical for ‘Mshale’ (r=0.299, P<0.01). After pollination, high morning temperatures were associated with seed set (r=0.150 – 0.429) between 15 days to 90 days after pollination (DAP). High average temperatures were negatively correlated with seed set in ‘Mshale’ and ‘Nshonowa’ from 45 DAP to time of harvest (r=-0.208 – -0.344). Coefficients of correlation were generally highest 15 DBP especially for ‘Mshale’ and ‘Nshonowa.’ Principle component analysis showed that average and maximum temperature are the most important variables in the entire data set. Conclusion: Coefficients of correlation were generally less than 0.5 partly as a result of weather involvement in seed set at several floral development stages; before, during, and after pollination. The most critical developmental stage is 15 DBP especially for ‘Mshale’ and ‘Nshonowa’ as they had the high correlation coefficients. Average temperature should be the main focus for seed set increase in banana.
Seed Set Patterns in East African Cooking Bananas are Asymmetric in Bunches and Fruits
(Research Square, 2020) Waniale, Allan; Mukasa, Settumba B.; Tugume, Arthur K.; Tumuhimbise, Robooni; Kubiriba, Jerome; Tushemereirwe, Wilberforce K.; Batte, Michael; Brown, Allan; Swennen, Rony
Low female fertility in bananas is the biggest hurdle for banana breeding. The aim of this study was to determine seed set patterns in East African cooking bananas EACBs to inform future decisions on a more targeted approach of increasing seed set and subsequently banana breeding efficiency. Matooke (AAA) and Mchare (AA) bananas are genetically distinct but belong to the same genetic complex, they referred to as EACBs. Seed set patterns in ‘Enzirabahima’ (AAA), ‘Mshale’ (AA) and ‘Nshonowa’ (AA) all with residual fertility were examined after hand pollination with a highly male fertile wild banana ‘Calcutta 4’ (AA). Results: Seed set in ‘Enzirabahima’ is predominant in distal hands. Mchare cultivars have a slightly more even distribution of seeds in their hands compared to ‘Enzirabahima.’ There is a gradual increase in seed set from proximal to distal hands with a slight drop in the last hand. This pattern is more definite in ‘Enzirabahima’ and ‘Mshale’ while ‘Nshonowa’ has a somewhat inconsistent pattern. There is also a drop in seed set per 100 fruits per hand from small to larger bunches. However, larger bunches have a higher pollination success compared to smaller bunches. They therefor set more seed on 100 fruits per hand and per bunch basis if bunches without seed are accounted for. Pollination success rate increases from smaller to larger bunches of EACBs. Seed set is biased toward the distal third part of fruits of examined EACBs as well tetraploid Matooke hybrid ‘401K-1’ (AAAA) and improved diploid ‘Zebrina’ GF (AA) that were used for comparison. In comparison, in the highly female fertile ‘Calcutta 4,’ seed set is along the entire length of the fruit. Conclusion: Seed set bias in the distal hands and distal end of fruits suggests a systematic mechanism rather than a random occurrence. It is expected that this information will provide a foundation for increased crossbreeding efficiency in bananas.
Seed Set Patterns in East African Highland Cooking Bananas Are Dependent on Weather before, during and after Pollination
(Horticulturae, 2021) Waniale, Allan; Swennen, Rony; Mukasa, Settumba B.; Tugume, Arthur K.; Kubiriba, Jerome; Tushemereirwe, Wilberforce K.; Batte, Michael; Brown, Allan; Tumuhimbise, Robooni
Seed set in banana is influenced by weather, yet the key weather attributes and the critical period of influence are unknown. We therefore investigated the influence of weather during floral development for a better perspective of seed set increase. Three East African highland cooking bananas (EAHBs) were pollinated with pollen fertile wild banana ‘Calcutta 40 . At full maturity, bunches were harvested, ripened, and seeds extracted from fruit pulp. Pearson’s correlation analysis was then conducted between seed set per 100 fruits per bunch and weather attributes at 15-day intervals from 105 days before pollination (DBP) to 120 days after pollination (DAP). Seed set was positively correlated with average temperature (P < 0.05–P < 0.001, r = 0.196–0.487) and negatively correlated with relative humidity (RH) (P < 0.05–P < 0.001, r = 􀀀0.158–􀀀0.438) between 75 DBP and the time of pollination. After pollination, average temperature was negatively correlated with seed set in ‘Mshale’ and ‘Nshonowa’ from 45 to 120 DAP (P < 0.05–P < 0.001, r = 􀀀0.213–􀀀0.340). Correlation coefficients were highest at 15 DBP for ‘Mshale’ and ‘Nshonowa’, whereas for ‘Enzirabahima’, the highest were at the time of pollination. Maximum temperature as revealed by principal component analysis at the time of pollination should be the main focus for seed set increase.
Seed Set Patterns in East African Highland Cooking Bananas Show Asymmetric Distribution in Bunches and Fruits
(Agronomy, 2021) Waniale, Allan; Swennen, Rony; Mukasa, Settumba B.; Tugume, Arthur K.; Kubiriba, Jerome; Tushemereirwe, Wilberforce K.; Batte, Michael; Brown, Allan; Tumuhimbise, Robooni
Low female fertility in bananas is the biggest hurdle for banana breeding. The aim of this study was to determine seed set patterns in East African Highland Cooking bananas (EAHBs) to inform future decisions on a more targeted approach of increasing seed set and subsequently banana-breeding efficiency. Matooke (AAA) and Mchare (AA) bananas are genetically distinct but belong to the same genetic complex, referred to as EAHBs. Seed set patterns in “Enzirabahima” (AAA), “Mshale” (AA), and “Nshonowa” (AA), all with residual fertility, were examined after hand pollination with a highly male fertile wild banana “Calcutta 4” (AA). Seed set in “Enzirabahima” is predominant in distal hands. Mchare cultivars have a slightly more even distribution of seeds in their hands compared to “Enzirabahima”. There is a gradual increase in seed set from proximal to distal hands with a slight drop in the last hand. This pattern is more definite in “Enzirabahima” and “Mshale”, while “Nshonowa” has a somewhat inconsistent pattern. There is also a drop in seed set per 100 fruits per hand from small to larger bunches. However, larger bunches have a higher pollination success compared to smaller bunches. They therefore set more seed on 100 fruits per hand and per bunch basis, if bunches without seed are accounted for. Pollination success rate increases from smaller to larger bunches of EAHBs. Seed set is biased toward the distal third part of fruits of examined EAHBs, as well as tetraploid Matooke hybrid “401K-1” (AAAA), and improved diploid “Zebrina” GF (AA) that were used for comparison. In comparison, in the highly female fertile “Calcutta 4”, seed set is along the entire length of the fruit. Seed set bias in the distal hands and distal end of fruits suggests a systematic mechanism rather than a random occurrence. It is expected that this information will provide a foundation for increased crossbreeding efficiency in bananas.
Use of timelapse photography to determine flower opening time and pattern in banana (Musa spp.) for efficient hand pollination
(Scientific Reports, 2021) Waniale, Allan; Swennen, Rony; Mukasa, Settumba B.; Tugume, Arthur K.; Kubiriba, Jerome; Tushemereirwe, Wilberforce K.; Uwimana, Brigitte; Gram, Gil; Amah, Delphine; Tumuhimbise, Robooni
Sterility and low seed set in bananas is the main challenge to their conventional genetic improvement. The first step to seed set in a banana breeding program depends on pollination at the right time to ensure effective fertilization. This study aimed at determining bract opening time (BOT) to enhance efficient pollination and seed set in bananas. A Nikon D810 digital camera was set-up to take pictures of growing banana inflorescences at five-minute intervals and time-lapse movies were developed at a speed of 30 frames per second to allow real-time monitoring of BOT. Genotypes studied included wild banana (1), Mchare (2), Matooke (4), Matooke hybrid (1), and plantain (1). Events of bract opening initiated by bract lift for female flowers (P < 0.01) started at 16:32 h and at 18:54 h for male flowers. Start of bract rolling was at 18:51 h among female flowers (P < 0.001) and 20:48 h for male flowers. Bracts ended rolling at 02:33 h and 01:16 h for female and flowers respectively (P < 0.05). Total time of bract opening (from lift to end of rolling) for female flowers was significantly longer than that of male flowers (P < 0.001). On average, the number of bracts subtending female flowers opening increased from one on the first day, to between one and four on the fourth day. The number regressed to one bract on day eight before start of opening of bracts subtending male flowers. There was a longer opening interval between bracts subtending female and male flowers constituting spatial and temporal separation. Bract rolling increased from partial to complete rolling from proximal to the distal end of the inflorescence among female flower. On the other hand, bracts subtending male flowers completely rolled. Differences in BOT of genotypes with the same reference time of assessment may be partly responsible for variable fertility. Hand pollination time between 07:00 and 10:00 h is slightly late thus an early feasible time should be tried.

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