Patterns of oviposition by Sandia xami (Lepidoptera, Lycaenidae) in relation to food plant apparency

ABSTRACT.

• 1 The butterfly Sandia xami (Reakirt) has a very clumped yearly pattern of oviposition on its food plant Echeveria gibbiflora D.C., and the mean number of eggs per plant is always very low.
• 2 Three features of host plants are highly associated with the probability of being oviposited upon: height of plant; degree of conspicuousness; and degree of isolation from conspecific plants.
• 3 The relative importance of these factors as predictors of the probability of oviposition change according to the time scale considered: height and conspicuousness are more important over short (weekly) time intervals whilst isolation takes precedence over longer (yearly) periods.
• 4 It is hypothesized that the clumped pattern of oviposition is responsible for the low numbers of the butterflies relative to their very abundant food plant.

     

Patterns and causes of morphological population differentiation in the Tenerife skink, Chalcides viridanus

Recent studies indicate that differential selection between mesic and xeric habitats is the most plausible explanation of within-island geographic variation in the Gran Ganarian skink, Chalcides sexlineatus. The island of Tenerife shows mesic/xeric heterogeneity similar to that on Gran Canaria, so we tested the prediction of parallel geographic patterns of morphological population differentiation in the Tenerife skink, Chalcides viridanus. Geographic variation was found to be complex; patterns of differentiation in body dimensions and scalation show evidence of both mosaic and latitudinal facets. Using randomization and regression methods, significant relationships were found between a hypothesized xeric/mesic model of population differentiation and geographic variation in female body dimensions, as well as with substantial proportions of the geographic variation in male and female scalation and, to a lesser extent, body dimensions. Matrix comparisons based on the entire morphological distance matrices show that the patterns of variation are not concordant with an alternative hypothesis of historical secondary contact, or with an isolation-by-distance model. It is argued that a substantial component of the geographic variation in body dimensions and scalation of C. viridanus is due to differential selection along an aridity gradient.     

A CRISPR design for next-generation antimicrobials

Two recent publications have demonstrated how delivering CRISPR nucleases provides a promising solution to the growing problem of bacterial antibiotic resistance.     

The regional variation of aboveground live biomass in old-growth Amazonian forests

The biomass of tropical forests plays an important role in the global carbon cycle, both as a dynamic reservoir of carbon, and as a source of carbon dioxide to the atmosphere in areas undergoing deforestation. However, the absolute magnitude and environmental determinants of tropical forest biomass are still poorly understood. Here, we present a new synthesis and interpolation of the basal area and aboveground live biomass of old‐growth lowland tropical forests across South America, based on data from 227 forest plots, many previously unpublished. Forest biomass was analyzed in terms of two uncorrelated factors: basal area and mean wood density. Basal area is strongly affected by local landscape factors, but is relatively invariant at regional scale in moist tropical forests, and declines significantly at the dry periphery of the forest zone. Mean wood density is inversely correlated with forest dynamics, being lower in the dynamic forests of western Amazonia and high in the slow‐growing forests of eastern Amazonia. The combination of these two factors results in biomass being highest in the moderately seasonal, slow growing forests of central Amazonia and the Guyanas (up to 350 Mg dry weight ha^?1) and declining to 200–250 Mg dry weight ha^?1 at the western, southern and eastern margins. Overall, we estimate the total aboveground live biomass of intact Amazonian rainforests (area 5.76 × 10⁶ km² in 2000) to be 93±23 Pg C, taking into account lianas and small trees. Including dead biomass and belowground biomass would increase this value by approximately 10% and 21%, respectively, but the spatial variation of these additional terms still needs to be quantified.     

Optimization of citric acid treatment for the sequential extraction of fucoidan and alginate from Sargassum latifolium and their potential antioxidant and Fe(III) chelation properties

In this study, citric acid was applied as a safe organic acid for the treatment of the brown macroalga Sargassum latifolium to facilitate the sequential extraction of fucoidan and alginate without cross contamination. Box-Behnken experimental design was used to investigate the effects of citric acid concentration, temperature, and time on fucoidan yield, its fucose and sulfate contents, and molecular weight (MW), while the investigated responses of the sequentially extracted alginate were yield, mannuronic/guluronic acid ratio (M/G) and MW. Under the optimized conditions, the fucoidan yield, fucose content, sulfate content, and MW were 6.55%, 21.01%, 30.92% and 7.12 × 10³ Da, respectively, while alginate yield, M/G, and MW were 28.81%, 0.36, and 1.50 × 10⁵ Da, respectively. The optimized products showed good Fe(III) chelating properties and the iron contents were 509.82 mg g^?1 for fucoidan-Fe and 406.71 ± 5.18 mg g^?1 for alginate-Fe. Under simulated gastrointestinal conditions, fucoidan-Fe and alginate-Fe complexes released 46 and 57% iron, respectively, which are nutritionally relevant amounts. Both fucoidan and alginate showed potent antioxidant properties, but their Fe complexes exhibited a reduced activity. The results of the present study indicated that citric acid could support the basis for an economical biorefinery process for the sequential extraction of fucoidan and alginate. Additionally, these polysaccharides could be good candidates for the preparations of iron supplements.

     

Protective effect of cannabidiol against cadmium hepatotoxicity in rats

The protective effect of cannabidiol, the non-psychoactive component of Cannabis sativa, against liver toxicity induced by a single dose of cadmium chloride (6.5 mg kg^?1 i.p.) was investigated in rats. Cannabidiol treatment (5 mg kg^?1/day, i.p.) was applied for five days starting three days before cadmium administration. Cannabidiol significantly reduced serum alanine aminotransferase, and suppressed hepatic lipid peroxidation, prevented the depletion of reduced glutathione and nitric oxide, and catalase activity, and attenuated the elevation of cadmium level in the liver tissue resulted from cadmium administration. Histopathological examination showed that cadmium-induced liver tissue injury was ameliorated by cannabidiol treatment. Immunohistochemical analysis revealed that cannabidiol significantly decreased the cadmium-induced expression of tumor necrosis factor-α, cyclooxygenase-2, nuclear factor-κB, caspase-3, and caspase-9, and increased the expression of endothelial nitric oxide synthase in liver tissue. It was concluded that cannabidiol may represent a potential option to protect the liver tissue from the detrimental effects of cadmium toxicity.     

Experimental wood addition in streams: effects on organic matter storage and breakdown

1. Channel complexity affects the physical structure, biotic communities and functioning of stream ecosystems. Large wood (LW) is a key element in the creation and maintenance of physically complex stream channels in forested areas. 2. In an attempt to enhance stream habitat quality and ecosystem functioning and to reduce inputs of organic matter to a downstream reservoir, LW was experimentally introduced into four mountain streams in the Basque Country (northern Spain), ranging in channel width from 3 to 13 m. Following a before–after/control–impact (BACI) design, streams were monitored during 1 year prior to wood addition and during 2 years after addition in one control and one experimental reach per stream. 3. Areal cover of benthic organic matter in the entire channel was measured from regular transects and the mass of stored organic matter from random Surber samples. Breakdown of organic matter was assessed in litter bag experiments performed with black alder leaves. When 50% of the initial mass in the bags remained, invertebrates associated with leaf bags were collected. 4. Wood placement produced a 2‐ to 70‐fold increase in the storage of organic matter, especially in thick deposits upstream from wood jams, with values in excess of 2 kg AFDM per m² in the small streams. The accumulation of organic matter produced by wood introduction decreased with increasing stream size. 5. Despite the large increase in the availability of organic matter, litter breakdown rates were unaffected by the experimental reaches, suggesting large increases in the total amount of organic matter consumed at the reach scale. 6. Numbers of invertebrates and shredders per gram of leaf litter did not respond to wood addition. Average body mass of invertebrates associated with leaf litter showed a non‐significant decreasing trend, which might reflect increased recruitment. 7. Although the effects of wood addition can depend on wood stability and stream size, adding LW to restore channel complexity can improve environmental conditions for invertebrate communities and affect stream ecosystem functioning, enhancing the efficiency to use organic matter inputs on a reach scale.     

Chromosome counts in the genus Festuca L. section Festuca (Poaceae) in the Iberian Peninsula

Chromosome numbers have been counted in 102 populations belonging to 34 taxa of Festuca L. section Festuca from the Iberian Peninsula. Four of these taxa have been counted for the first time and another three for the first time from the Iberian Peninsula. Furthermore, the levels of ploidy for another three taxa have been obtained for new populations within their distribution area, and for another 18 taxa the ploidy levels have been confirmed. Five levels of ploidy have been established for this section: diploid, tetraploid, hexaploid, octoploid and decaploid. There are 17 diploid taxa, eight tetraploid, three octoploid, two octoploid and one decaploid. The three remaining taxa represent polyploid complexes (one tetra-hexa-octoploid and two hexa-octoploids).