16-hour Photoperiod Research Articles

First Report of Charcoal Rot Caused by Macrophomina phaseolina on Hemp in Croatia.

The production of industrial hemp (Cannabis sativa) has had a sharp increase in the past five years in Croatia (Mihelcic 2017). Production has been in constant increase, from 1560 ha in 2015 to 2476 ha in 2019 (PAAFRD). In August 2019, numerous (~1.5%) premature wilted hemp plants (cultivar Fibranova) were observed in commercial fields in Vladislavci (45.4646950° N, 18.5674770° E), around Osijek, Croatia. Diseased plants showed symptoms of chlorosis, rapidly wilting, necrosis and prematurely dying. The stalk of diseased plants was completely desiccated, while internal tissues were spongy and fluffy. Near the soil line, discoloration of the stalk with small spherical to oblong black microsclerotia was detected. Roots were necrotic with brown-gray areas. Twenty root and crown segments of the infected plants (2- to 3-mm long pieces) were surface sterilized with 2% NaOCl for 5 min, rinsed three times with sterile distilled water, and plated on potato dextrose agar (PDA, pH 6.2) media, containing 250 mg per liter of chloramphenicol to inhibit bacterial growth (Zveibil and Freeman 2005). The culture plates were incubated at 28 ± 2°C for 7 days in the dark and purified to obtain a pure culture that produces numerous, dark, hard, ovoidal-shaped sclerotia, averaging 140 x 52 μm (n=50). The single sclerotium isolate produced flat light to dark gray colonies with entire margins. Based on field symptoms, colony and microsclerotia morphology, the fungus was identified as Macrophomina phaseolina (Tassi) Goid (Marquez et al. 2021). Total DNA from the isolate was extracted with Extract-N-Amp Plant PCR Kit (Sigma-Aldrich Co., USA). To confirm morphological identification, part of the TEF 1-alpha gene region was amplified using EF1-728F (Carbone and Kohn 1999) and EF2 (O'Donell et al. 1998). The sequence of the isolate MP1 (212 bp - GenBank accession no. OQ389757), showed 100% nucleotide sequence identity to the reference sequence of M. phaseolina GenBank sequence MG434668 (Casano et al. 2018). Eighteen hemp plants (cv. Fibranova) were sown in six plastic pots (three hemp plants per pot) for the pathogenicity test. Ten-day-old M. phaseolina culture (isolate MP1) was used for inoculum preparation. Each pot of one-week-old plant was irrigated with 100 ml of a microsclerotia suspension (105 microsclerotia/ml)(Abied et al. 2018). Plants were held at 28°C and 70% relative humidity in a growth chamber (aralab, Fitoclima 10.000 HP) with a 16-hour photoperiod. Pots with control plants were irrigated with the same amount of sterile distilled water. Ten weeks after inoculation percentage of wilted plants was 77.78%. In the control variant all plants were healthy. M. phaseolina was reisolated from inoculated plants and morphologically identified. With the liberalization of the law, hemp production in Croatia is increasing, which could result in general disease problems and the disease caused by M. phaseolina. Charcoal rot will be expressed in years with dry and warm summers (Lodha and Mawar 2020), and relatively short, cool, rainy winters (Nevo et al. 2012), which has become common in the last decade in Croatia. To our knowledge, this is the first report of M. phaseolina on hemp in Croatia. The authors declare no conflict of interest.

First report of Robbsia andropogonis causing bacterial leaf spot of bougainvilleas in Taiwan.

Bougainvilleas (Bougainvillea spp.) are popular ornamentals commonly grown as bushes, vines, or trees worldwide (Kobayashi et al. 2007). Leaf spot symptoms were observed on a bougainvillea hedge located in North District, Taichung, Taiwan during August of 2022. The lesions were brown, necrotic and had yellow halos (Fig. S1). All the plants at the location showed similar symptoms. Leaf samples were collected from five plants and symptomatic tissues were minced in 10 mM MgCl2. The samples were streaked onto nutrient agar (NA) and after culturing at 28°C for 2 days, small, round, creamy white colonies were consistently isolated from all the samples. A total of five strains (BA1 to BA5) were obtained; each of them was isolated from a different plant. All five strains induced hypersensitive response in tobacco leaves. Amplification and sequencing of the isolated strains' 16S rDNA using primers 27F and 1492R (Lane 1991) revealed that all five strains shared identical sequences (GenBank accession no. OQ053015) with Robbsia andropogonis LMG 2129T (formerly Burkholderia andropogonis and Pseudomonas andropogonis; GenBank accession no. NR104960; 1,393/1,393 bp). Further testing of BA1 to BA5's DNA samples using the pathogen's species-specific primers Pf (5'-AAGTCGAACGGTAACAGGGA-3') and Pr (5'-AAAGGATATTAGCCCTCGCC-3'; Bagsic et al. 1995) successfully amplified the expected 410-bp amplicon in all five samples; the sequences of the PCR products completely matched to those of BA1 to BA5's 16S rDNA. Strains BA1 to BA5 also tested negative for arginine dihydrolase and oxidase activity, and failed to grow at 40°C, all of which are consistent with descriptions of R. andropogonis (Schaad et al. 2001). Pathogenicity of the isolated bacteria was confirmed by spray inoculation. Three representative strains, BA1 to BA3, were used for the assay. Bacterial colonies were scraped from NA plates and suspended in 10 mM MgCl2 added with 0.02% Silwet L-77. The concentrations of the suspensions were adjusted to 4.4-5.8 x 108 cfu/ml. The suspensions were sprayed onto three-month-old, cutting-propagated bougainvillea plants (to runoff). Controls were treated with bacteria-free solutions. Three plants were used for each treatment group (and the controls). The plants were placed in a growth chamber (27/25°C, day/night; 14-hour photoperiod) and bagged for three days. Within 20 days post inoculation, brown, necrotic lesions resembling those observed in the sampling site were observed on all inoculated plants, but not on the controls. One strain was re-isolated for each treatment group and the re-isolated strains all shared the same colony morphology and 16S rDNA sequence with BA1 to BA5. Additional PCR testing of these re-isolated strains using Pf and Pr also produced the expected amplicon. This is the first formal report of R. andropogonis affecting bougainvilleas in Taiwan. The pathogen has been reported causing diseases of betel palm (Areca catechu), corn and sorghum in Taiwan (Hseu et al. 2007; Hsu et al. 1991), some of which are economically important (Lisowicz 2000; Navi et al. 2002). As such, infected bougainvilleas could potentially serve as an inoculum source for these diseases.

First Report of Corynespora cassiicola Causing Leaf Spot on Jasminum nudiflorum in China.

Winter jasmine (Jasminum nudiflorum Lindl.), a trailing, deciduous shrub, is widely used as an ornamental plant. Its flowers and leaves also has great medicinal value for treatment of inflammatory swelling, purulent eruptions, bruises and traumatic bleeding (Takenaka et al. 2002). In October 2022, leaf spot symptoms were observed on J. nudiflorum distributed in Meiling Scenic Spot (28.78°N, 115.83°E) and Jiangxi Agricultural University (28.75°N, 115.83°E), Nanchang, Jiangxi Province, China. In a week-long series of investigations, the incidences of disease could range up to 25%. Initially, the symptoms of the lesions were small yellow circular spots (0.5 to 1.8 mm), and gradually developing irregular spots (2.8 to 4.0 mm) with grayish white central parts, a dark brown inner ring, and outer yellow halo. To identify the pathogen, sixty symptomatic leaves from fifteen different plants were collected, of which twelve were randomly selected, cut into 4-mm2 pieces, and surface sterilized with 75% ethanol for 30s followed by 5% NaClO for 1 min, rinsed four times with sterile water, and then placed on potato dextrose agar (PDA) medium at 25 °C in the dark for 5 to 7 days. Six isolates with similar morphological characteristics were obtained. Aerial mycelium was vigorous, downy and exhibited white to grayish-green coloration. Conidia were solitary or catenate, pale brown, obclavate to cylindrical, apex obtuse, one to 11 pseudosepta, 24.9 to 125.7 × 7.9 to 12.9 μm (n = 50). Morphological characteristics matched Corynespora cassiicola (Ellis 1971). For molecular identification, two representative isolates (HJAUP C001 and HJAUP C002) were selected for genomic DNA extraction, and the ITS, TUB2 and TEF1-α gene were amplified, using the primer ITS4/ITS5 (White et al. 1990), Bt2a/Bt2b (Lousie and Donaldson 1995) and EF1-728F/EF-986R (Carbone and Kohn 1999), respectively. The sequenced loci (GenBank accession nos. ITS: OP957070, OP957065; TUB2: OP981639, OP981640; TEF1-α: OP981637, OP981638) of the isolates were 100, 99 and 98% similar to the corresponding sequences of C. cassiicola strains (GenBank accession nos. OP593304, MW961419, MW961421, respectively). Phylogenetic analyses of combined ITS and TEF1-α sequences was performed using maximum-likelihood method in MEGA 7.0 (Kuma et al. 2016). The result showed that our isolates (HJAUP C001 and HJAUP C002) clustered with four strains of C. cassiicola at 99% bootstrap values in the bootstrap test (1000 replicates). Based on the morpho-molecular approach, the isolates were identified as C. cassiicola. The pathogenicity of one representative strain (HJAUP C001) was tested by inoculating the wounded leaves of six healthy J. nudiflorum plants under natural condition. Three leaves from each of three plants were punctured with flamed needles and sprayed with a conidial suspension (1 × 106 conidia/ml), and three wounded leaves from each of other three plants were inoculated with mycelial plugs (5 × 5 mm3). Mock inoculations were used as controls with sterile water and PDA plugs on three leaves each, respectively. Leaves from all treatments were incubated in a greenhouse at high relative humidity, 25°C, and 12-hour photoperiod. After one week, all wounded inoculated leaves appeared similar symptoms as described above, whereas the mock inoculated leaves were still healthy. Similar isolates with grayish white and vigorous aerial mycelium were reisolated from inoculated and symptomatic leaves and identified as C. cassiicola by DNA sequencing, fulfilling Koch's postulates. It has been reported that C. cassiicola can cause leaf spots on numerous plant species (Tsai et al. 2015; Lu et al. 2019; Farr and Crossman 2023). However, to our knowledge, this is the first report of C. cassiicola causing leaf spots on J. nudiflorum in China. This finding aids in protection of J. nudiflorum, a medicinal and ornamental plant with high economic value.

Long-term CO2 Enrichment Increases Biomass but Results in Rapid Physiological Acclimation of Petunia and Pansy

Although crops often respond immediately to enriched CO2 concentrations (e.g., increased photosynthesis), this initial response is often not sustained throughout production, thus reducing the benefit of this input. For horticulture species, the timing and extent of these acclimation responses are still widely uncertain. Therefore, the objective of this research was to determine species-specific acclimation responses to elevated CO2 concentrations for pansy (Viola ×wittrockiana ‘Matrix Blue Blotch Improved’) and petunia (Petunia ×hybrida ‘Dreams Midnight’). Seedlings were transplanted to 11.5-cm pots and placed in growth chambers with air temperature, relative humidity, and radiation intensity setpoints of 21 °C, 55%, and 250 μmol⋅m−2⋅s−1, respectively. Carbon dioxide treatments were established using the two growth chambers with setpoints of either 400 (ambient) or 1000 μmol⋅mol−1 (elevated) maintained during a 16-hour photoperiod. In addition to data collected through destructive harvest, the rate of photosynthesis (A) in response to increasing internal leaf CO2 concentration (A-Ci) and at the operating CO2 concentration (A-Ca) were measured weekly with a portable leaf photosynthesis system at saturating [A-Ci (1000 μmol⋅m−2⋅s−1)] or production [A-Ca (250 μmol⋅m−2⋅s−1)] radiation intensities. For both pansy and petunia, elevated CO2 produced greater total shoot dry mass than ambient CO2 after 4 weeks. However, the decreased maximum rate of photosynthetic electron transport, maximum rate of Rubisco carboxylase, and triose phosphate utilization rate of both species were also observed under elevated CO2. Similarly, A measured at 400 and 1000 μmol⋅mol−1 was reduced for both pansy and petunia grown under the elevated compared with ambient CO2 concentration based on A-Ca responses after 7 days, indicating quick physiological acclimation to this input. These results provide information regarding the timing and extent of physiological acclimation in response to elevated CO2 concentrations. However, because of physiological acclimation potentially occurring within 7 days of treatment initiation, additional research is necessary to develop species-specific recommendations for controlled environment production.

First report of Neofusicoccum ribis causing stem blight and dieback of blueberry (Vaccinium corymbosum) in Michigan.

In July 2020, a 3-year-old 'Envoy' northern highbush blueberry bush (Vaccinium corymbosum L.) from a commercial farm in Van Buren County, Michigan was submitted to the Plant & Pest Diagnostics laboratory at Michigan State University. Field disease assessments across the 2-acre planting were an incidence of 2-5% and a severity of 50-100%. Symptoms included red shoot flagging and dead shoots retaining dry leaves, shoots with light green leaves and necrotic margins, and brown-black cankers at the base of the symptomatic shoots. Shoot sections displaying wood discoloration were surface disinfested by dipping in 95% ethanol and flame sterilized. The internal discolored tissues (0.5 cm2) were plated onto 1% ampicillin and streptomycin, quarter-strength potato dextrose agar (PDA) and incubated at room temperature until fungal colonies were observed. A fungus with rapid growth, developing white and then dark gray mycelium, resembling species in the family Botryosphaeriaceae was isolated and subcultured. After DNA extraction and amplification, sequences of three loci were obtained: the internal transcribed spacer (ITS) region, β-tubulin (Bt), and elongation factor 1-α (EF1) using primer pairs ITS1/ITS4, Bt2a/Bt2b, and EF1-728/EF1-986R, respectively (Slippers et al. 2004). The sequences showed 100% identity with Genbank numbers KF766205 (ITS region, 562 bp - OP588109), MT592721 (Bt, 436 bp - OP585548), and MT592229 (EF1, 306 bp - OP585547) of N. ribis (Slippers et al. 2013, Zhang et al. 2021). Sequences were identified using PopSet 1995604550 (Zhang et al. 2021). Pathogenicity was tested on 2-year-old 'Blueray' blueberries. Five plants, 3 shoots per plant (n = 15) were surface-sterilized with a 3% bleach solution by rinsing, wounded with razor blades using a scratching method in 'X' patterns across the length of the wound, and then inoculated using mycelium plugs (5 mm) from 7-day old cultures grown on full-strength PDA. Plugs were crushed and spread onto the wound and the wound was wrapped with parafilm. Control plant shoots (n = 9) were mock inoculated using sterile PDA plugs. Plants were maintained in the greenhouse at 23°C under a 14-hour photoperiod and imaged at 0-, 7-, and 12-days post inoculation (dpi). Symptoms began developing within 7 dpi. At 12 dpi, 9 of 15 inoculated shoots began displaying leaf necrosis and deep red or brown stem discoloration 6 cm above and below the wound, while controls remained healthy. Fungi morphologically identical to the original isolate were reisolated from sections taken from 2.5, 6.3, and 7 cm above and below the inoculation site. Species identity was confirmed by sequencing as described above. Neofusicoccum species are widespread and commonly associated with canker and dieback symptoms of blueberries (Flor et al. 2022). To our knowledge, this is the first report of stem blight and dieback caused by N. ribis in Michigan blueberry production. The species N. parvum and N. ribis have been reported on southern highbush blueberries in California (Koike et al. 2014) and Florida (Wright and Harmon 2010), but neither has been reported on blueberry in Michigan. Accurate diagnoses of Botryosphaeria fungal species in blueberries is critical for effective disease control and yield loss reduction.

First Report of Myrtle Rust Caused by Austropuccinia psidii on Eugenia myrcianthes in Brazil.

The Eugenia myrcianthes fruit can be consumed in natural or processed form (jellies and juices) (Infante et al., 2016). In 2019, in the UTFPR, Dois Vizinhos city, Paraná State - Brazil, yellow uredinias epiphyllous were observed on the tissue surface (leaves, stems, flowers, and fruit) of twenty-one trees of E. myrcianthes, which resembled structures typical of Myrtaceae rust. All colonized tissues showed necrotic lesions that varied in size and shape, causing death, especially in fruit. In the orchard, the fungus affects 50% to 95% yield. Fruit (10) and leaves (20) with symptoms were collected from 11 trees from different positions in the orchard. Infected tissues were incubated (25°C and 12-hour photoperiod) for 7 days to induce sporulation. The epiphyllous uredinia, united in small groups with hyaline and globose urediniospores were observed and presented equinulate ornaments and germinated pores in the subequatorial and inordinate positions (De Pieri, 2012; Cummins; Hiratsuka, 2003) (mean 14.00 μm × 21.12 μm, n = 30) similar to the morphological characteristics of the Austropuccinia genus described by Young (2019). The identification of 10 samples (fruit and leaf) of the pathogen taken from infected parts of the trees was confirmed. For molecular identification, the internal transcribed spacer (ITS) region was amplified by polymerase chain reaction (White et al. 1990) and sequenced. Phylogenetic analyses using Bayesian inference grouped the strain from Eugenia myrcianthes with the epitype species of Austropuccinia psidii (Beenken, 2017), with a high posterior probability (0.99). The sequences of one representative strain (Emg1) were submitted to GenBank (OM948983). For pathogenicity tests, three healthy branches containing 20 leaves were sprayed with 3.0 mL of urediniospores suspension (105) of Emg1 and covered with a plastic bag in the orchard (25ºC). Sterile distilled water was used as a control. Three replications (pathogen and control) were performed on different trees. After 6 days, symptoms appeared and their morphological features were similar to those previously reported. Control branches did not present fungal growth. The inoculation test was repeated again, confirming symptoms such as uredinia and urediniospores, characteristic of the disease. This is the first report of the incidence of A. psidii infection in E. myrcianthes trees in Brazil, causing rust, necrosis, and senescence in fruit, leaves, flowers, and stems. The rust on E. myrcianthes causes destructive damage to yield, as the pathogen causes fruit to rot and drop prematurely.

The role of growth regulators in the ontogenesis of plants of potato cancer differentiators in vitro culture

Goal. To study impact of growing regulators on morphometric indexes and potato cultivar-differentiators productivity in culture in vitro.
 Methods. The studies conducted in the Laboratory of Biotechnology for Agricultural Crops of Ukrainian Plant Quarantine Research Station Institute of Plant Protection of NAAS. Murashige-Skoog (MS) nutrient medium was used with the addition of different concentrations of Epin-maxi growth regulators (MS — control; MS + Epin-maxi r., (2,4-epibrassinolide, 0.012 g/l); MS + Epin-maxi, 0.025 g/l) and Poteitin (MS — control; MS + Poteitin w.s., (2,6-dimethylpyridine-1-oxide with succinic acid, 0.15 mg/l); MS + Poteitin, 0.3 mg/l) on different varieties of potato cancer of different ripeness groups (Schedryk — early, Slovyanka — medium-ripe). Plants grew in terms of cultivation room during 16-hour photoperiod a light intensity of 2000—2500 lux, temperature 22—25°C and humidity of 60—80%. The grafting conducted in quantity 25 plants with three times experiment repeating.
 Results. The morphogenesis optimal indexes received during their put into the nutritious medium MS + Epin-maxi 0.025 g/l and MS + Poteytin 0.3 mg/l. The plants’ height of variety Schedryk increased on 21st day of growing on 4.9—25.2 mm, in control (65.2 mm) and internodes number increased 0.4—0.9 pcs in control (5.2 pcs.). The plant’s height increased of variety Slovyanka in variants with stimulators was more than on 12.1—28.4 mm and the internodes number increased 0.5—1.1 pcs. The root-forming increase determined in all experiments variants: roots quantity — on 2.6—3.4 pcs., their length was 25.6—29.8 mm, the average microtubers weight was in 1.4—1.6 times higher, the mictotubers weight increase on 1 plant in 1.6—1.9 times, the quantity of microtubers on one plants in 1.6—1.8 times in comparison with control.
 Conclusions. The optimal indexes of morphometric parameters and potato cultivar-differentiators productivity on culture in vitro received in variants of research with Epin-maxi 0.025 g/l and Poteytin 0.3 mg/l. These stimulators, when added to the nutrient medium, contributed to an increase in plant height, the number of internodes, root formation (number of roots and their length), average mass of microtubers, mass and number of microtubers per plant.

Light Spectra Have Minimal Effects on Rooting and Vegetative Growth Responses of Clonal Cannabis Cuttings

Until recently, most clonal cannabis (Cannabis sativa) has been propagated using fluorescent lights. Transitioning to light-emitting diodes (LEDs) may be a viable alternative to fluorescent lighting, enabling cultivators to provide specific spectrum treatments to enhance rooting while also saving energy. Vegetative stem cuttings of ‘Gelato-27’, ‘Grace’, and ‘Meridian’ were rooted for 15 days under various combinations of blue (B), red (R), ultraviolet-A (UVA) LEDs, phosphor-converted white (W) LEDs, and a fluorescent (F) control treatment, each with a canopy-level photosynthetic photon flux density (PPFD) of 200 µmol·m−2·s−1 and 16-hour photoperiod. The photon flux ratios of blue (B; 400–500 nm) and red (R; 600–700 nm) narrowband LED treatment combinations were (1) BR, fixed spectrum of B15:R85; (2) B, B75:R25 on day 0–2 followed by B15:R85 on day 2–14; (3) B+UVA, B75:R25 on day 0–2 followed by B15:R85 on day 2–14 plus 15 µmol·m−2·s−1 of UVA on day 7–14; (4) B50, B15:R85 on day 0–7 followed by B50:R50 on day 7–14. The W and F treatments both had static spectra. After the propagation period (i.e., plug stage), a portion of the cuttings under each treatment × cultivar combination were destructively harvested and the remainder were transplanted and grown vegetatively for an additional 21 days (i.e., transplant stage) under a PPFD of ≈275 µmol·m−2·s−1 from ceramic metal halide fixtures and then destructively harvested. Although there were no spectrum treatment effects on the percentage of cuttings that rooted, root index values were higher in cuttings grown under B+UVA vs. F. Further, relative root dry weights of plugs from the B, B+UVA, B50, and F treatments were higher than the W treatment. At the end of the plug stage, there were no spectrum treatment effects on the chlorophyll content index, cuttings grown under the B treatment had thicker stems compared with BR and W treatments, and cuttings grown under the F treatment exhibited the lowest percentage of new aboveground growth. None of the aforementioned spectrum treatment effects from the propagation stage persisted post-transplant. The use of LEDs is a promising, energy-efficient alternative to fluorescent lighting for cannabis propagation and B-enhanced spectrum treatments appear to enhance the rooting performance of clonal cannabis cuttings.

气候变化对北京常见树种春季萌芽的影响——基于控制实验研究

PDF HTML阅读 XML下载 导出引用 引用提醒 气候变化对北京常见树种春季萌芽的影响——基于控制实验研究 DOI: 10.5846/stxb202112183591 作者: 作者单位: 作者简介: 通讯作者: 中图分类号: 基金项目: 国家杰出青年基金项目（42025101）；高等学校学科创新引智计划项目（B18006） Effects of climate change on spring budburst of typical tree species in Beijing based on manipulative experiments Author: Affiliation: Fund Project: 摘要 | 图/表 | 访问统计 | 参考文献 | 相似文献 | 引证文献 | 资源附件 | 文章评论 摘要:气候变化对植物物候产生了重要影响，春季萌芽时间的变化不仅会通过改变植物的光合作用影响碳汇能力，还会通过改变群落内的种间关系影响生态系统结构和功能。因此，掌握群落内不同树种春季萌芽对气候变化的响应对于深刻理解物候时间位分化、认识陆地生态系统碳水循环和能量平衡具有重要意义。为提高春季物候模型的预测精度，阐明气候变化对不同树种春季萌芽的影响，以鹅耳枥（Carpinus turczaninowii）、黑桦（Betula dahurica）、华北落叶松（Larix principis-rupprechtii）、糠椴（Tilia mandshurica）和元宝枫（Acer truncatum）5个温带森林的典型树种为研究对象，通过剪枝实验分析了冬季冷激、春季温度和光周期对枝条春季萌芽时间的影响。结果表明，温度升高和冷激增加显著提前了所有树种的春季萌芽时间，从5℃到20℃，春季萌芽时间平均提前了54.5 d；在较高的冷激条件下，春季萌芽时间平均缩短了17.8 d；光周期对各树种春季萌芽时间均没有显著影响，8 h和16 h光周期条件下各树种平均萌芽时间分别为30.3和30.5 d。此外，随着温度升高，5个树种萌芽时间间隔显著缩短，这主要是由于温度升高萌芽热量需求降低导致的，冷激对树种间萌芽时间间隔无显著影响。在气候变暖背景下，森林群落中不同树种萌芽时间间隔将显著缩短，进而影响物候时间生态位分化，导致种间竞争加剧。研究阐明了气候变化对温带阔叶树种春季萌芽及其时间间隔的影响，为气候变化条件下森林生态系统群落动态及森林可持续经营与管理策略的制定提供了理论支撑。 Abstract:Climate change has caused substantial effects on plant phenology over the past decades. Shifts in spring budburst not only affect carbon sink capacity by changing plants' photosynthesis but also influence the structure and function of the ecosystem by altering the relationship between species within the forest community. Understanding how spring budburst of different species respond to climate change is thus essential to improve our knowledge of phenological temporal niche differentiation, carbon and water cycles, as well as the energy balance of terrestrial ecosystems. In order to improve the ability of the spring phenology model and the influence underlying the responses of spring budburst to climate change, we selected five typical temperate tree species in Beijing, i.e. Carpinus turczaninowii, Betula dahurica, Larix principis-rupprechtii, Tilia mandshurica, and Acer truncatum, to test the effects of winter chilling, spring temperature and photoperiod on spring budburst by using twig cutting experiment. We found that photoperiod had no significant effect on spring budburst while increasing spring temperature and winter chilling significantly advanced budburst date. From 5℃ to 20℃, the budburst was advanced by 54.5 days on average, and it was shortened under high chilling conditions by about 17.8 days. The photoperiod had no significant effect on the budburst of each tree species. The average budburst of tree species was 30.3 and 30.5 days under the condition of 8 hours and 16 hours of photoperiod, respectively. In addition, the time interval of budburst between the five tree species was significantly shortened with the spring warming, which might be caused by the heating requirements of budburst under different temperature treatments, which was mainly caused by the decrease of heat requirement for budburst with the increase of temperature, and the chilling had no significant effect on their time interval. Under the background of climate change, the budburst and time interval of budburst between tree species is likely to largely shorten, which would change the differentiation of temporal niche, leading to the increased inter-species competition. This study clarifies the impact of climate change on the budburst and time interval of temperate broad-leaved tree species and provides theoretical support for the formulation of forest ecosystem community dynamics and forest sustainable operation and management strategies under the condition of climate change. 参考文献 相似文献 引证文献

First report of Phytophthora pluvialis causing needle lesions on Pinus pinea in New Zealand

During routine surveillance in October 2020, needle lesions and necrosis were observed in two 42-year-old stone pines (Pinus pinea) situated in an amenity planting within an infected Pinus radiata plantation in Nelson, New Zealand. Symptoms were widespread across the foliage of infected trees and samples were sent to Scion's Forest Health Reference Laboratory. Approximately fifteen needles displaying yellow and red bands (Fig. 1) tested positive for Phytophthora using a Phytophthora ImmunoStrip® (Agdia, USA), and PCR and subsequent DNA sequencing with Ypap2F/Ypap2R primers (McDougal et al., 2021), indicated Phytophthora pluvialis. A Phytophthora species was isolated from diseased tissue. Morphological characteristics were consistent with those described by Reeser et al. (2013) for P. pluvialis. This identification was confirmed by sequencing the internal transcribed spacer region (White et al., 1990). The isolate was deposited in the National Forest Culture Collection (NZFS 5280) and symptomatic needles were lodged into the National Forest Mycological Herbarium (NZFRI 5931). Foliage symptoms caused by P. pluvialis on other conifers, including Pinus radiata, Pseudotsuga menziesii and Tsuga heterophylla, typically express as distinct khaki/red lesions and black resinous bands (Dick et al., 2014), rather than the yellow and red bands observed on the stone pines (Fig. 2). Pathogenicity testing was done by inoculating stone pine needles with P. pluvialis zoospores using a needle dip assay according to Dick et al. (2014). Stone pine needles from young healthy seedlings were placed in sterile pond water inoculated with P. pluvialis zoospores and incubated in darkness at 17°C for 24 hours. Control needles were placed in sterile pond water. Needles were then lain on moist paper towels in a sealed tray and incubated at 17°C at a 14-hour photoperiod. After ten days, olive/yellow lesions were observed on needles (Fig. 3). These lesions were lighter than those observed on field samples, however, this is common in detached needle assays of other species, such as P. pluvialis infection of Pinus radiata (Dick et al., 2014). Sporangia were observed near the lesion margin of needles (Fig. 4). Sections of symptomatic needles were surface sterilised and plated onto a Phytophthora-selective media (10% carrot agar + ampicillin, pimaricin, rifampicin, nystatin and hymexazol). The resultant cultures displayed morphological features of P. pluvialis, fulfilling Koch's postulates (Fig. 5). Control needles remained healthy (Fig. 3). To our knowledge, this is the first report of P. pluvialis causing needle disease on stone pine. Stone pine is an economically important species due to the production of high value pine nuts and timber. Although stone pine accounts for a small proportion (<1%) of New Zealand's forests, continued monitoring is recommended to assess the impact of disease on the growth and yield of these plantations. Forest Growers Levy Trust funded surveillance and diagnosis through the Forest Biosecurity Surveillance system.

The seed germination properties of two hyperaccumulator plant species with the potential for Ni agromining

The aim of this study is to investigate the effect of different nickel concentrations and light in combination with storage conditions and storage time on the seed germination ability of two serpentine-endemic nickel hyperaccumulating species (Bornmuellera emarginata and B. tymphaea). The seeds of both species were collected from natural populations in the Pindus Mountain range, Greece in early July and stored in a refrigerator (4?C) and in laboratory conditions (22?C). The seeds were exposed to a range of nickel concentrations typical of non-ultramafic-ultramafic gradient in two light environments (12 h photoperiod and continuous darkness). The nickel concentration only had a significant effect on B. emarginata, decreasing its seed germination rate with increasing Ni concentrations. The storage temperature significantly affected the germination percentage of both species and it was higher at 4?C compared to 22?C. A higher germination rate (&gt; 60%) was observed for 5-8-month-old seeds, but both species generally showed significantly higher germination rates in the tests conducted seven months after seed ripening in the field. A higher germination rate was observed in a 12-hour photoperiod than in continuous darkness only for B. tymphaea. This study provides guidelines on the germination capacity of two obligate nickel hyperaccumulators with a potential for use in agromining systems.

Effects of Different Culture Media Compositions on In Vitro Micropropagation from Paradox Walnut Rootstock Nodes

The aim of this study is to establish an effective protocol for in vitro micropropagation from node explants of the 'Paradox' (Juglans regia x J. hindsii) rootstock. In the first stage of the study, the node explants were cultured in semi-solid media after being exposed to different sterilization methods. The most effective sterilization method was observed as ST2 with the lowest darkening rate (4 %). According to the results, SP4 medium provided the highest number of shoots per unit explant (1.05 shoots/explant) and 100 % shoot formation, SP2 medium provided the best mean shoot length (1.6 cm) and the mean number of nodes per unit explant (7.95 nodes/explant). Best root induction was provided from ½ Modified MS medium containing 4 mg/L IBA with 30 g/L sucrose. For root induction explants were retained under dark conditions for 7 days at 24±2oC. In order to ensure root formation and elongation, shoot explants with root induction cultured in a 16-hour photoperiod (3500 lux) for 21 days in different nutrient media containing 2.4 mg/L Gelrite, hormone-free and mixed with vermiculite (1:1 v/v) and was rooting rate is 45.45 % in ¼DFe medium.

Развитие свекловичной тли (Aphis fabae Scop.) в зависимости от различных фотопериодических условий

Among the sucking pests of sugar beet crops in Azerbaijan, black bean aphid (Aphis fabae Sсop.), which occurs on beet seedlings from the moment of development of true leaves, causes significant damage. Based on this, the task of our study was to study the main life processes of beet aphids depending on photoperiodic conditions. The work was carried out in the Laboratory of Ecology and Physiology of Insects and the Center for Applied Zoology of Azerbaijan National Academy of Science in 2013–2019. The experiments were carried out in special photo thermostats with automatic control of temperature and light. The results obtained show that the light factor is of secondary importance for the duration of the larval, reproductive periods and for the entire development cycle compared to temperature. It should be noted that winged forms (about 50%) appear in aphid colonies during a 12-hour photoperiod at a temperature of 17 °C. Under the conditions of Azerbaijan, such photoperiod is observed at the end of March and at the beginning of October, when aphids migrate from primary to intermediate plants and vice versa in autumn (early October) from intermediate to primary. The length of the day established in the experiments, which causes the appearance of winged forms, is consistent with the phenology of this species.

USE OF UNICONAZOLE IN GROWTH REGULATION AND BIOCHEMICAL CHANGES IN MAIZE

The current paper evaluated the incubation time, and doses of Uniconazole (UCZ) applied to maize seeds to verify the plants’ response at different phenological stages. MSG1001 hybrid seeds were treated with UCZ (0, 50, and 100 mg.kg-1 of seed) with different incubation times (IT – 1 min and 12 h). In the lab experiment, the treated seeds were displaced in rolls of the previously moistened Germitest paper and incubated for a week in a BOD chamber at 25ºC with a 12-hour photoperiod. In the greenhouse experiments, sowing was carried out in pots with sand, and supplementary irrigation was applied for ten days. In the field experiment, sowing was performed with 0.5 m spacing between rows in densities of 75,000 and 65,000 plants.ha-1. In the BOD and the greenhouse, the design of both experiments was entirely randomized in a double-factor scheme (IT x UCZ). A randomized block design in a triple-factor scheme (IT x UCZ x Population) was used in the field experiment. Seed treatment with UCZ did not promote germination inhibition. The concentration of 100 mg UCZ kg-1 of seed in the 12-hour IT resulted in a more significant accumulation of root mass in seedlings after one week in the BOD. In the greenhouse, plants in the V1 stage presented longer shoot lengths for the treatments that received UCZ. Incubation time influenced root length, and IT = 12 h at a concentration of 50 mg UCZ kg-1 of seed was more efficient than IT = 1 min. Application of 100 mg UCZ kg-1 of seed was more effective for accumulating chlorophylls A and B in IT = 1 min. In the field, seeds treated with UCZ changed plants for female flowering and the number of green leaves below the ear. The population of 75,000 plants.ha-1 was more productive, with UCZ contributing to the hybrid’s yield. Incubation of the seeds with 50 or 100 mg UCZ kg-1 of seed in IT = 1 min contributed to more productivity than IT = 12 h. The grains’ starch content increased with the application of UCZ at a dose of 100 mg kg-1 of seed, and the starch percentage was modified according to population density and incubation time.

Confirmation report of Bacterial Leaf Streak disease of rice caused by Xanthomonas oryzae pv. oryzicola in Senegal.

Xanthomonas oryzae pv. X. oryzicola (Xoc), the causal agent of Bacterial Leaf Streak (BLS), is considered as one of the most important emerging pathogens of rice in Africa. This disease is estimated as responsible of 20 to 30% yield loss (Sileshi et Gebeyehu 2021) and has been characterized in several west African countries including Mali and Burkina Faso since 2003 and more recently in Ivory Coast (Wonni et al. 2014, Diallo et al. 2021). Presence of BLS symptoms in Senegal were reported by Trinh in 1980 but, to our knowledge, BLS occurrence has never been validated further and no strain of Xoc have ever been isolated from Senegalese rice fields. Xoc is transmitted by seeds which contribute to its spread through the rice trade (Sileshi et Gebeyehu 2021). To confirm Trinh's observations, we surveyed rice fields between 2014 and 2016 in eight different regions where rice is produced in Senegal. Typical disease symptoms characterized by yellow-brown to black translucent leaf streaks sometimes along with exudates, were detected in fields of several regions and collected. Leaf pieces were successively sanitized, rinsed in sterile water, and symptomatic fragments were ground using the Qiagen Tissue Lyser System (QIAGEN, Courtaboeuf, France). The leaf powder was diluted in 1.5 ml of sterile water and incubated for 30 minutes at room temperature. Ten μl of the suspension was streaked on semi-selective PSA medium and incubated at 28°C for 3 to 7 days. Characteristic round, convex, mucous, straw-yellow Xoc candidate colonies were purified from six individual leaf samples from three distinct sites in the northern Senegal River Valley. To confirm their identity, isolated strains were tested for pathogenicity and molecular characterization. All isolates were subjected to the multiplex PCR developed for the identification of X. oryzae pathovars (Lang et al., 2010) and revealed the same PCR profile (two amplicons of 324 and 691 base pairs) similar to that of the Xoc reference strain BLS256. Leaves of 5-week-old plants of O. sativa cv. Kitaake were infiltrated with a needleless syringe containing a bacterial suspension set at an optical density of 0.5. Upon seven days of incubation under greenhouse conditions (27 ± 1°C with a 12-hour photoperiod), all infiltrated spots (2 spots on 3 plants per isolate) developed water-soaked lesions similar to those caused by control strain BLS256, except when leaves were infiltrated with water. Symptomatic leaf tissues were ground and plated on PSA medium, resulting in colonies with typical Xanthomonas morphology that were diagnosed as Xoc by multiplex PCR typing, thus fulfilling Koch's postulate. At last, four of the isolates were subjected to gyrB sequencing upon PCR amplification using the universal primers XgyrB1F and XgyrB1R (Young et al., 2008). Analysis of 780bp partial gyrB sequences of strains S18-3-4, S23-1-12, S52-1-4 and S52-1-10 highlighted 100% identity with the gyrB sequence of strain BLS256 (Acc. No. CP003057). To our knowledge, this is the first report of BLS in Senegal which is supported by molecular characterization methods. This study validates the presence of BLS in Senegal and will serve as a basis for future efforts of rice breeding for locally adapted resistance. More studies are needed to clarify the spatial distribution and prevalence of BLS in Senegal as rice cultivation is expanding rapidly in the country.

Germination Response of Three Florida Panhandle Coastal Dune Plants to Salinity

Campbell-Martínez, G.E.; Thetford, M., and Miller, D., 2022. Germination response of three florida panhandle coastal dune plants to salinity. Journal of Coastal Research, 38(3), 585–591. Coconut Creek (Florida), ISSN 0749-0208. Coastal dunes and their ecosystem services are threatened by human pressures warranting active restoration. Understanding dune plant germination responses to salinity is important when considering plant species and direct seeding locations for coastal dune restoration projects. The germination response of three Florida panhandle native coastal dune plant species to various salinity concentrations (0%, 0.25%, 0.50%, 0.75%, and 1% weight per volume) were tested. Species included were coastalplain honeycombhead (Balduina angustifolia (Pursh)B.L.Rob.), coastalsand frostweed (Crocanthemum arenicola (Chapm.)Barnhart), and squareflower (Paronychia erecta (Chapm.)Shinners). Seeds were germinated within germination boxes, placed in growth chambers under species-specific temperatures with a daily 12-hour photoperiod, and monitored weekly for 4 weeks. Germination responses to salinity were species-specific. Coastalplain honeycombhead had intermediate salt tolerance (highest germination at 0%–0.50% salinity), coastalsand frostweed was the least salt tolerant (highest germination at 0%–0.25% salinity), and squareflower was the most salt tolerant species in respect to germination (high germination across all salinities). Germination was delayed for all species at the highest salinity concentrations (0.75%–1%). However, for all three species, at least one-third of all seeds (>39%) at all salinity concentrations germinated by week 4. Results suggest germination for seeds of these species is possible in saline conditions documented within coastal areas before and after hurricane overwash. Future dune restoration studies for these species should test direct seeding of these plants under field conditions.

Фотопериодическая регуляция образования крылатых форм у свекловичной тли (Aphis fabae Scopoli, 1763)

The study of the process of migration in aphids has great practical importance. Thus, the aphids pass from one plant to another by these morphs and feed there and maintain their population by growing. The literature information on the research of the photoperiodic reactions in aphids is sufficient. However, the seasonal adaptation characteristics of sugar beet aphids have not been studied up to date in Azerbaijan. For this reason, the study of an impact of photoperiod on the emergence of winged ones in the population of black bean aphid is one of the important issues. During the study of reaction of individuals fed in the same routine against the photoperiod in the next generations, it has been defined that short photoperiod is more observed in the following generations. It seems that the information collected from the former generations is directly passed to the next generations. The results show that the continuous breeding of these species by means of parthenogenesis is only available in the long day (14, 16, 18, 24 hours) routine. However, the winged individuals prevail in the short photoperiods. The preference of winged individuals in 24 hours of photoperiod rather than others (14–18 hours) is probably related to the physiological changes occurs in them.

First Report of Brown Leaf Spot of Rice (Oryza sativa) Caused by Bipolaris sorokiniana in Pakistan.

Brown leaf spot of rice is one of the major seed-borne diseases and can diminish grain production up to 52% (Barnwal et al. 2013). In 2018, infected leaf samples showing the typical symptoms of brown spots were collected from the vicinity of the University of Agriculture, Faisalabad (31°26'10.3"N 73°03'35.1"E). The symptoms were brown-dark spots, with gray-light gray or brown centers surrounded by dark margins and with chlorotic halos and of oval or cylindrical shapes (5 to 9 mm in diameter). Disease incidence averaged 61% across the seven fields observed. Leaves were collected from the seven infected fields and symptomatic leaf tissues of 5 mm2 were excised from representative necrotic spots in each. These tissues were surface disinfected with 70% ethanol, rinsed with sterile distilled water (SDW), dried by blotting on paper, and placed on potato dextrose agar medium. For pathogen growth, the plates were placed at 25oC (±2oC) with a 12-hour photoperiod for 5 days. Five samples from each of the infected fields were taken for pathogen isolation and among them ten isolates were sub-cultured and purified by using the single spore method. The resulting fungal colonies were fluffy and ranged in color from grayish black/black to light brown. Fifteen conidia were measured that are olivaceous-brown to dark brown in color, elliptical to oblong with narrow (tapered) ends, with 3-10 septa and 35.6-65.4 µm in length x 13.1-25.7 µm in width. Conidiophores were yellowish-brown, geniculate, and solitary (Pratt 2003). For molecular studies, rDNA of the internal transcribed spacer (ITS) region, translation elongation factor (tef), RNA polymerase II second largest subunit (rpb2) and glyceraldehyde-3-phosphate dehydrogenase (gpd) gene were amplified by using the primers ITS1F/ITS4R (White et al. 1990), EF1-983F/EF1-2218R (Rehner and Buckley 2005), 5F2/7CR (O'Donnell et al. 2007), and GPD1/GPD2 (Berbee et al. 1999) respectively. The sequence of all the amplified gene regions of one SUL-1 isolate was deposited into GenBank with accession numbers MN314844 (ITS), MN326866 (tef), MN990457 (rpb2) and MN990456 (gpd). BLASTn queries of the obtained sequences (ITS, tef, rpb2 and gpd) showed 99-100% homology with the corresponding nucleotide sequences of B. sorokiniana (GenBank accession nos. GU480767, MF490855, LT715652 and MK558818 respectively). To fulfill the Koch's postulates, twenty rice plants (cv. Basmati-385) were sprayed at 2 to 3 leaf stages by using the two representative isolates with a spore suspension of 105 spores/ml. SDW was sprayed on ten control plants. The plants were covered with polyethylene bags to keep the moisture contents and incubated at 25oC (±2oC) for 7 days. After a week, same symptoms as those described above were observed. In the repeated experiment, B. sorokiniana was re-isolated from the infected rice leaves and confirmed morphologically; fulfill the Koch's postulates. With grave worry, the other species of the genus Bipolaris (B. oryzae, and B. victoriae) have also been found to the cause brown leaf spot of rice (Motlagh and Kaviani 2008). To our knowledge, this is the first report of Bipolaris sorokiniana causing brown leaf spot of rice in Pakistan. Because rice is highly consumable grain in Pakistan, so the rapid spread of this disease in the rice farming areas is of a serious concern.

First Report of Phyllosticta capitalensis Causing Black Freckle Disease on Rubus chingii in China.

Rubus chingii is used as an important traditional Chinese medicine, and belongs to the family Rosaceae. The fruit has multiple pharmacological activities, including antioxidant, anti-inflammatory, and improving cognitive impairment (Na Han et al. 2012). In June 2019, a new fungal infection was observed on the leaves of R. chingii in Qiandongnan Miao and Dong Autonomous Prefecture, Guizhou Province, China, forming small lesions with reddish-brown edges along leaf veins. Over 500 plants were surveyed, and nearly 20% of the plants were symptomatic. The diseased plants grew poorly and appeared stunted, and severely affected plants died. Five symptomatic leaves were randomly collected from the field and washed with tap water and distilled water successively. The edges of infected leaf tissue were cut into small pieces (4 to 5 mm2), surface sterilized with 70% ethanol for 30 s and 0.1% HgCl2 for 1 minute, and then rinsed three times in sterile distilled water (Chen et al. 2016). The same fungus was isolated from 41 pieces. The hyphae of a representative isolate were gray, the colony surface was granular, the edges were uneven and white, and the culture turned black over time with black spherical conidia. Conidia were nearly elliptical, unicellular, and each with a hyaline, unstable apical appendage, 3 to 10 µm long. The size of conidia was 10 to 18 μm in length and 4 to 8 μm in width. These morphological characteristics are consistent with those described for the fungus Phyllosticta capitalensis. (Wikee et al. 2013). For an accurate identification, genomic DNA of a representative isolate of the pathogen was extracted to amplify the internal transcribed spacer (ITS) region, the transcription elongation factor (tefa-1), and actin (ACT) genes with the ITS1/ITS4, EF1-728F/EF1-986R, and ACT-512F/ACT-783R (Cheng, L. L. ,et al. 2019), respectively. The ITS, tefa-1 and actin gene sequences were deposited in GenBank and assigned accession numbers MW308365, MW714380 and MW714381, respectively. BLAST search analysis of GenBank (NCBI) showed that the sequences had 100% similarity with those of Phyllosticta capitalensis (GenBank accession no. ITS, MN548091; tefa-1, MN958711; and ACT, MN565575). The pathogenicity of Phyllosticta capitalensis was verified using six healthy detached leaves from healthy R. chingii plants around 40 cm tall. A total of nine plants were used, and three leaves from each plant were artificially inoculated. Each wound was inoculated with conidial suspension (106 mL-1), while the control leaves were coated by sterile water. All the treated plants were covered with plastic bags for 2 days, incubated at 28ºC and 85% relative humidity, with a 12-hour photoperiod. After 15 days following inoculation, the injured leaves showed similar symptoms to the above-mentioned lesions, while the control and uninjured leaves were still healthy. P. capitalensis were reisolated from inoculated leaves, fulfilling Koch's postulates. P. capitalensis is an endophyte, widely distributed in various host plants in China. (Lu, J. M, et al. 2016). To the best of our known, this is the first report of black freckle disease caused by P. capitalensis on Rubus chingii in China. P. capitalensis is a destructive plant pathogen with an unusually broad host range and our findings will be useful for its management and for further research. The author(s) declare no conflict of interest.

Features of long-term preservation of Azhurnaya and Bergamotnaya mint cultivars in an in vitro collection

Mint represents a valuable medicinal and essential oil plant widely used in pharmacology, perfumery, cosmetics, and food industry. In order to maintain collections of cultivars and valuable samples, as well as to carry out breeding, the application of biotechnology appears to be promising for in vitro preservation of plant objects under the conditions of slow growth at low positive temperatures. The present study is focused on the morphometric parameters and genetic stability of the explants of two mint cultivars during their in vitro preservation at 4–6 ºС for a year without illumination. Meristems with two leaf primordia were cultivated on a nutrient medium in a culture room at 26 ºС and illumination of 2–3 klx with a 16-hour photoperiod. Microshoots developing from meristems were divided into single-node stem segments to be used as explants for deposition. After a year of deposition at 4–6 ºС without illumination, the number of viable explants in the Azhurnaya and Bergamotnaya cultivars was established to be 56.5 and 85.7%, respectively. The explants under study were characterized by the development of up to 2.5 shoots up to 13.2 mm long and rhizogenesis with a frequency of up to 52.3%. Following the deposition, microshoots were cut and transferred to a culture room to resume growth. After two subcultivations, viability (100%), morphometric parameters of microshoots, and multiplication index (up to 5.5–7.3) were fully restored. The ISSR-analysis performed according to four studied DNA markers revealed the microshoots of these cultivars to be completely identical to the original plants after in vitro preservation. The conducted studies proved the effectiveness of the conditions used for in vitro preservation of mint explants and confirmed the explant genetic stability after a year of deposition at 4–6 ºС.