Variability of in-channel sediment storage in a river draining highly erodible areas (the Isábena,Ebro Basin)

Purpose

In-channel sediment storage is a fundamental component of a river basin’s sediment budget. Sediment remains stored until a competent flow re-suspends and transfers it downstream. The objectives of this paper are: (1) to quantify in-channel sediment storage and its spatial and temporal dynamics in the River Isábena, a mesoscale mountainous catchment draining highly erodible areas (badlands) in the south central Pyrenees (Ebro basin) and (2) to analyse changes in storage in the mainstem channel in relation to sediment yield from the main tributaries.

Materials and methods

In-channel sediment storage was measured seasonally (from winter 2011 to winter 2012) at 14 mainstem cross-sections using a re-suspension cylinder. A minimum of three locations were sampled at each section, and two levels of agitation were applied. Samples allowed determination of the amount of sediment accumulated per unit surface area at a given point in the river; estimates of the total storage in the bed of the mainstem Isábena were derived from these data. In addition, main five tributaries were monitored for discharge and suspended sediment transport.

Results and discussion

Results show an annual sedimentary cycle, with the sediment being produced in badlands during winter, transferred to the main channel during spring, stored in the river during summer and, finally, exported out of the basin by the autumn floods. Marked spatial variability was observed; sections located immediately downstream from the main tributaries (i.e. mainly Villacarli) generally held larger amounts of sediment in the bed. Runoff and sediment inputs from the tributaries were the most important factors determining sediment storage and its spatial and temporal dynamics. The overall sediment yield of the Isábena was much higher than the in-channel sediment storage, despite the large amounts stored in the channel.

Conclusions

This finding corroborates a previous published hypothesis that fine sediment in the drainage network has a mean residence time of the order of 1 year and that the basin’s delivery ratio exceeds 90 %; both of these characteristics can be related to the high connectivity between production areas (badlands) and the river network, and to the role of baseflows allowing continuous export of sediment from the catchment.     

Improvement of degraded physical attributes of a saline-sodic soil as influenced by phytoremediation and soil conditioners

This study aimed to evaluate the use of phytoremediation and soil conditioners in the recovery of physical attributes of a saline-sodic Fluvic Neossol in Brazil Northeast. The applied treatments were: Atriplex nummularia L., as phytoremediation plant, due to its ability to extract salts from the soil; organic conditioners, such as bovine and sheep manure; gypsum and polymer, as chemical conditioners. Samples with preserved structure were collected at the time of the experiment installation and 18 months after in the layers 0–10 cm and 10–30 cm. The analyzed attributes were: water dispersed clay, dispersion index, bulk density, penetration resistance, soil porosity, and saturated hydraulic conductivity. The use of sheep manure, gypsum and polymer promoted an increase in saturated hydraulic conductivity in the 0–10 cm layer from 4.51 to 16.37 cm day^?1, 11.26 to 23.95 cm day^?1 and 7.24 to 22.77 cm day^?1, respectively. Gypsum increased the macroporosity in the superficial layer by 42.6%. Atriplex and polymer were more efficient at reducing soil penetration resistance. The polymer was more efficient at improving the physical properties. However, it is necessary to consider phytoremediation with Atriplex as a more sustainable alternative that can still be used as complementary fodder in animal feed.     

Antibacterial and antioxidant activities of essential oils isolated from Thymbra capitata L. (Cav.) andOriganum vulgare L

Antilisterial activities of Thymbra capitata and Origanum vulgare essential oils were tested against 41 strains of Listeria monocytogenes. The oil of T. capitata was mainly constituted by one component, carvacrol (79%), whereas for O. vulgare three components constituted 70% of the oil, namely, thymol (33%), gamma-terpinene (26%), and p-cymene (11%). T. capitata essential oil had a significantly higher antilisterial activity in comparison to O. vulgare oil and chloramphenicol. No significant differences in L. monocytogenes susceptibilities to the essential oils tested were registered. The minimum inhibitory concentration values of T. capitata essential oil and of carvacrol were quite similar, ranging between 0.05 and 0.2 microL/mL. Antioxidant activity was also tested, the essential oil of T. capitata showing significantly higher antioxidant activity than that of O. vulgare. Use of T. capitata and O. vulgare essential oils can constitute a powerful tool in the control of L. monocytogenes in food and other industries.     

Effect of the fungicide imazalil on hepatic microsomal cytochrome P-450 and cytochrome P-450 dependent activities in the Bobwhite quail (Colinus virginianus)

Bobwhite quails were treated with imazalil for 8 weeks. The fungicide was given admixed in the food at 0, 100, 300, 500 and 1000 mg kg^?1. Even at the highest dose tested, imazalil did not affect the liver weight or the hepatic microsomal protein content. In treated quails, no significant induction of cytochrome P-450 or NADPH-cytochrome c-reductase activity was observed. Furthermore, imazalil did not induce or inhibit 7-ethoxyresorufin or 7-ethoxycoumarin O-deethylase in quail microsomes. Only a slight but significant increase by 35% and 49% in aniline hydroxylase activity was measured for the 500- and 1000-mg kg^?1 dose levels, respectively. After a drug-free period of one week, aniline hydroxylase activity returned to control values, indicating that the effect was fully reversible. It is concluded that imazalil does not induce or inhibit drug-metabolizing enzymes in the quail, even at doses which exceed by far the maximum levels currently used to dress seed under field conditions (100 mg kg^?1).     

Biochar as a strategy to manage plant diseases caused by pathogens inhabiting the soil: a critical review

Phytoparasitica - The current agricultural scenario faces a range of challenges, with phytosanitary ones being paramount. In most cases, plant diseases are treated with chemicals; however, they...     

Bioactivity of extracts and isolated compounds from Vitex polygama (Verbenaceae) and Siphoneugena densiflora (Myrtaceae) against Spodoptera frugiperda (Lepidoptera: Noctuidae)

The effects of crude extracts, fractions and isolated compounds from Vitex polygama Cham. and Siphoneugena densiflora Berg were evaluated on the development of Spodoptera frugiperda JE Smith, a destructive insect pest of corn and several other crops. The extracts and fractions were incorporated into an artificial diet at 1 mg g(-1) and offered to the insect during its larval stage. Length and viability of larval and pupal stages as well as pupal weight were assessed. Isolated compounds were tested through superficial contamination of the diet at 0.1 mg g(-1). Weight and viability of ten-day-old larvae were determined. Methanolic and hydroalcoholic S. densiflora extracts caused 100% larval mortality, while leaf and fruit hydroalcoholic extracts from V. polygama were the most active. Among the isolated compounds, flavonoids presented the best insecticidal results, and tannins the best larval growth inhibition.     

Phenolic composition in grape (Vitis vinifera L. cv. Malbec) ripened with different solar UV-B radiation levels by capillary zone electrophoresis

The responses of Vitis vinifera L. cv. Malbec to different solar ultraviolet-B radiation (UV-B) levels were assessed in two contrasting situations, under sunlight with full UV-B (+UV-B) and filtered UV-B (-UV-B), in three different locations at 500, 1000, and 1500 m above sea level (asl). To evaluate the effects of radiation, a simple, accurate, and rapid method for the separation and simultaneous determination of representative phenolic compounds in grape berry skins by capillary zone electrophoresis was developed. Separation was carried out in less than 20 min with 20 mM sodium tetraborate buffer containing 30% methanol, pH 9.00. The procedure is fast and reliable, and extracted grape berry skins can be directly analyzed without prior sample cleanup procedure. Berry skins from the +UV-B treatment at 1500 m asl showed the highest levels of total polyphenols anthocyanins, and resveratrol, compared with the -UV-B treatment at this altitude.     

Species-specific DNA markers for identification of two root-knot nematodes of coffee: Meloidogyne arabicida and M. izalcoensis

Seven root-knot nematodes (RKN), including Meloidogyne exigua, M. incognita, M. paranaensis, M. enterolobii, M. arabicida, M. izalcoensis and M. arenaria are major pathogens of coffee crop in the Americas. Species-specific primers for their identification have been developed for five of them and constitute a fast and reliable method of identification. Here we report a PCR-based assay for specific detection of M. arabicida and M. izalcoensis. Random Amplified Polymorphic DNA fragments specific for these two species were converted into sequence characterized amplified region (SCAR) markers. PCR amplification using the SCAR primers produced a specific fragment of 300 bp and 670 bp for M. arabicida and M. izalcoensis, respectively, which were absent in other coffee-associated Meloidogyne spp. tested. SCAR primers also allowed successful amplification of DNA from single second-stage juveniles (J2), males and females. In addition, these primers were able to unambiguously detect the target species in nematode suspensions extracted from soil and roots samples, in different isolates of the same species or when used in multiplex PCR reactions containing mixtures of species. These results demonstrated the effectiveness of these SCAR markers and their multiplex use with those previously developed for M. exigua, M. incognita, M. paranaensis, M. enterolobii and M. arenaria constitute an essential detection tool. This diagnostic kit will contribute for specific J2 identification of the major RKN infecting coffee from field samples in the Americas.