Photosynthetically active radiation use efficiency of <Emphasis Type="Italic">Dactylis glomerata</Emphasis> and <Emphasis Type="Italic">Schedonorus phoenix</Emphasis> along a hardwood tree-induced light gradient

Photosynthetically active radiation use efficiency (PARUE) of orchardgrass (Dactylis glomerata L.) and tall fescue (Schedonorus phoenix (Scop.) Holub) was determined. Leaf mass was harvested for canopies at different shade levels when each reached 20 cm height with 5 cm residue for regrowth to simulate grazing. Total incident PAR at each site was summed for the growth period (S-PAR). Values for PARUE were calculated from dried leaf mass divided by S-PAR. The more highly shaded plants reached 20 cm at lower S-PAR. While overall leaf mass decreased linearly with shade induced decreases in S-PAR, PARUE increased exponentially. The coefficients for the equations representing this exponential increase vary for forage species and may represent a useful index for characterizing forage response to silvopastoral systems.     

In vitro culture of immature seed for rapid generation advancement in tomato

The importance of fast-trackt generation advancement in developing superior germplasm has been recognized in breeding of many crop species. To address this issue in tomato, immature seeds were excised from fruit at different maturity stages and transferred to culture medium. The best culture medium was modified full strength Moorashige–Skoog (MS) salts supplemented with 0.1 mg l⁻¹ IAA, 0.5 mg l⁻¹ IBA, 0.5 mg l⁻¹ GA₃ and 2% sucrose. If the excised seeds were able to grow, most showed shoot formation after a week. Seeds extracted as early as 10 days after pollination were successfully cultured provided they were transferred aseptically and without injury. No morphological or physiological changes in regenerated plants and their fruit relative to the parent were detected. Germination from immature seeds of tomato is a simpler alternative to in vitro culture of immature embryos or callus, as it can be undertaken in comparatively less stringent laboratory conditions. Using this approach, five generations can be produced in a year in contrast to a maximum of three generations with conventional methods. This offers an opportunity for rapid generation advancement aimed towards population development when coupled with marker assisted selection in tomato breeding for biotic and abiotic stress tolerance.     

Ascospore release by <Emphasis Type="Italic">Venturia inaequalis</Emphasis> during periods of extended daylight and low temperature at Nordic latitudes

Darkness suppresses ascospore release in Venturia inaequalis, but the impact of light levels during the extended twilight and dusk that typify Nordic spring conditions is poorly understood. Volumetric spore traps were operated at two different locations in Norway over several years. During the season of asocspore release (approximately 1 April to 30 June), on 25 occasions when rain started during night (after 23:00 h and before 04:00 h) and leaves remained wet until at least midnight the following day, the cumulative percentage of spores trapped at sunrise did not exceed 1%, irrespective of temperature. Three hours after sunrise, cumulative ascospore release reached 0.8%, 3.0%, and 8.1% at temperatures of 0 to 5°C, 5 to 10°C, and >10°C, respectively, and 50% release occurred at 11, 9, and 8 h after sunrise. Additional field and laboratory studies indicated that the protracted dawn and dusk of Nordic latitudes, either alone or in combination with low temperatures, does not substantially alter previously reported patterns of ascospore release.     

Implementation of an artificial reaction control in a TaqMan method for PCR detection of <Emphasis Type="Italic">Ralstonia solanacearum</Emphasis> race 3 biovar 2

A previously published TaqMan PCR test for R. solanacearum race 3 biovar 2 was modified to enable both the validation of negative results and the confirmation of positive results in a closed-tube system. Negative results were validated through the use of a reaction control plasmid, designated pRB2C2, which was designed to generate a 94bp product using the same amplimers targeting the primary diagnostic 68bp sequence in R. solanacearum race 3 biovar 2 DNA. SYBR Green was included in the reaction mix to facilitate the identification of post-reaction products using melt peak analysis. The 94bp reaction control had a melt peak temperature of about 90°C, while the diagnostic target amplicon had a melt peak temperature of about 83°C; thus positive results could be easily confirmed and distinguished from the reaction control product. Addition of pRB2C2 at 100 copies per reaction had no effect on the sensitivity of the TaqMan assay for R. solanacearum race 3 biovar 2, and the modified assay successfully detected R. solanacearum race 3 biovar 2 in infected, asymptomatic tomato stems and leaves as well as in potato tubers and stems.     

Gender power in Kenyan dairy: cows,commodities, and commercialization

In Western Kenya, smallholder dairy production is becoming incrementally commercialized through the commodification and sale of milk through formal market channels. While commercialization is often construed as a way to boost rural livelihoods through increased income from milk, emerging evidence suggests that married women are not directly benefiting from formal milk market participation. This critical issue of gender power imbalance has been framed by development interventions in economic efficiency and social justice perspectives, but thus far interventions in the sector have not addressed how underlying social-market mechanisms embedded in gendered ideology influence smallholder engagement in dairy commercialization. Drawing on feminist theories of power and social embeddedness, this study investigates how gendered power relationships materialize and influence formal milk marketing engagement and practices in Western Kenya. Facilitated discussion groups with smallholder farmers revealed the gendered ideologies and norms that ascribe masculinized meaning to cattle, milk, and commercial enterprise. Key informant interviews with commercial dairy management and farmers were used to identify current practices for increasing women’s formal market participation—namely, direct payments to women for milk deliveries. Findings from this study indicate that cattle and formal dairy market participation are imbued with gendered meaning that create legitimacy around men’s privilege over dairy proceeds. Interventions in the sector aimed at addressing gender power imbalances must acknowledge this dynamic, and accept the social trade-offs and gendered costs of dairy commercialization.     

Molecular characterization of two papaya ringspot virus isolates that cause devastating symptoms in Norte de Santander,Colombia

Papaya ringspot virus is an RNA virus that belongs to the genus Potyvirus, family Potyviridae and affects both papaya and cucurbits, causing great economic losses. PRSV isolates are divided into biotypes P and W; both biotypes naturally infect plants in the family Cucurbitaceae, whereas the P type also naturally infects papaya (Carica papaya L). In the present study, we report the full-length genome sequence of two PRSV-P isolates sampled from the Campo Hermoso (PRSV-CH) and Villa del Rosario (PRSV-VR) localities in Norte de Santander, Colombia. The genomes of these PRSV isolates are 10,326 nt in length and have a predicted ORF of 3344 aa. The identity among Colombian PRSV isolates is 96.9% and 97.3% at the nucleotide and deduced amino acid levels, respectively. PRSV isolates from China had the lowest identity at 78.3% and 89.2% (nucleotide-amino acid), whereas the highest identities were detected in PRSV isolates from Mexico, Venezuela and Hawaii. At the polyprotein level, the amino acid composition surrounding the active polyprotein cleavage sites differ in the Colombian PRSV sequences. The predicted cleavage site in P1/HC-Pro is LEQY/N – LEQY/S instead of MEQY/N. Both of the Colombian PRSV isolates have a putative recombination event in the P1 coding region, which is common in all PRSV isolates from the American continent. The new full-length PRSV sequences from Colombia provide a better understanding of the dynamics of papaya ringspot virus infections in papaya in Colombia and worldwide.