Gene flow among different teosinte taxa and into the domesticated maize gene pool

Maize (Zea mays L. ssp. mays) was domesticated from one wild species ancestor, the Balsas teosinte (Zea mays ssp. parviglumis) about 9000 years ago. Higher levels of gene diversity are found in teosinte taxa compared to maize, following domestication and selection bottlenecks. Diversity in maize can be increased via gene flow from teosinte, which has certainly occurred from various taxa, but the rate of flow from different teosinte taxa and the final impact on maize evolution has been difficult to measure. One hundred populations from six Zea taxa, both domesticated (maize) and wild (teosinte), including domesticated landraces from Asia, Africa, and the Americas, were genotyped with 17 SSR markers using 15 individuals per population. Overall levels of diversity were high, and populations could be distinguished based on markers. Relationships between populations followed most published reports, or can now help resolve previously conflicting reports. Gene flow into maize from different teosinte groups, and gene flow between different teosintes, was estimated. Evidence for contributions from the Balsas teosintes and from Chalco teosintes (Z. mays ssp. mexicana) to the maize gene pool was found, as well as from Chalco into ssp. mexicana race ??Durango?? and Z. mays ssp. huehuetenengensis. These contributions are almost certainly the result of post-domestication (and ongoing) exchanges. This information must give more impetus to in situ conservation of teosinte species, and use of these teosintes to continue to direct the evolution of maize, especially in response to new diseases, insect pests, and other biotic and abiotic stresses.     

Lindane Biodegradation by Defined Consortia of Indigenous Streptomyces Strains

The current study aimed to compare lindane degradation by pure and mixed cultures of Streptomyces sp. Cell-free extracts were assayed for potentiating dechlorinase activity and, based on these results, consortia of two to six microorganisms were assayed for their growth on and degradation of lindane. Furthermore, the role of bacterial consortia of lindane-degrading strains was examined in lindane decontamination soil assays. Four actinobacteria, previously isolated from a pesticide-contaminated area, were selected because of their tolerance to lindane and their ability to use the pesticide as sole carbon source. These strains as well as Streptomyces sp. M7 and Streptomyces coelicolor A3 were used to study specific dechlorinase activity (SDA) and lindane removal in mixed cultures. Pure cultures presented SDA in the presence of 1.66 mg L^-1 lindane as carbon source. SDA was improved by certain mixed cultures until 12 times compared with pure cultures. Mixed cultures with two, three, and four strains showed maximum lindane removal of 46% to 68%, whereas combinations of five and six strains did not efficiently remove the pesticide from the culture medium. The Streptomyces sp. A2, A5, M7, and A11 consortium presented the lowest ratio between residual lindane concentration and SDA and could be a promising tool for lindane biodegradation.     

Applying a Lagrangian dispersion analysis to infer carbon dioxide and latent heat fluxes in a corn canopy

Warland and Thurtell (2000) proposed an analytical dispersion Lagrangian analysis (hereafter WT analysis) to relate the mean scalar concentration field to source profiles inside the canopy. The first objective of this study was to evaluate the performance of the WT analysis with existing turbulence statistics parameterizations in a corn canopy, by comparing its inferred net ecosystem CO₂ exchange (NEE) and latent heat flux (λE) with eddy covariance measurements. The second objective was to assess the performance of the WT analysis to infer the soil CO₂ flux. Four parameterizations of turbulence statistics were used to estimate Lagrangian time scale (T_L) and standard deviation of vertical wind velocity (σ_w) profiles. The estimated T_L and σ_w profiles were then corrected for atmospheric stability conditions. The field experiment was carried out in a corn field from August to October 2007 and 2008. Profiles of water vapour and CO₂ mixing ratios were measured using a multiport sampling system connected to an infrared gas analyzer. Wind velocity within and above the canopy and eddy covariance measurements over the canopy were taken. The soil respiration, estimated using the WT analysis, was compared to estimates obtained by an empirical model. WT analysis fluxes showed good correlation (R² = 0.77-0.88) with NEE and λE obtained by the eddy covariance technique, but overestimated net fluxes, especially when corrections for atmospheric stability were applied. The optimization of T_L and σ_w profiles using in-canopy turbulence measurements improved the agreement between measured and modeled NEE and λE. Inferred soil CO₂ fluxes were underestimated and were poorly correlated (R² = 0.02-0.01) with estimates obtained using an empirical model based on soil temperature. This poor performance in estimating the soil respiration is likely caused by the decoupling between inside and above canopy flows.     

Digit innervation of the thoracic limb of Criollo horses: Anatomical description and consequences to perineural blocks

Criollo horse breeding is an important economic activity in South America. Because of their athletic performance, these animals tend to show great incidence of musculoskeletal disorders, many of them diagnosed by means of perineural blocks. However, incorrect interpretation of these blocks may be due to anatomical differences in nerve distribution. The objective of this study was to describe the innervation of the digit region of thoracic limbs in Criollo horses, in order to improve the interpretation of tests for claudication diagnosis based on nerve block. Thirty thoracic limbs from Criollo horses were dissected. It could be observed that in 90% of the limbs, dorsal branches of the palmar nerve originated proximally to the proximal sesamoid bone. In 93% of the cases, the palmar digital nerve and the dorsal branches communicated; in 87% of the cases, communication between branches of the dorsal branch was observed; and in 27% (8/30) of the limbs, the palmar metacarpal nerve and the dorsal branch presented communications. None of the specimens showed complete symmetry in the distribution of nerves in contralateral limbs. The high frequency of communication between the nerves may be a particularity of the Criollo breed that may interfere with the interpretation of perineural blocks. Based on the anatomical position, it may be inferred that divergent results in Criollo horses may occur when abaxial sesamoid nerve block is used. Palmar digital nerve block may be less influenced by these variations, provided it is performed as distal as possible from the ungular cartilage.     

Detection and characterization of Shiga toxin-producing Escherichia coli in captive non-domestic mammals

Shiga toxin producing-Escherichia coli (STEC) is an important emerging pathogen, and ruminants are recognized as their main natural reservoir. The aim of this work was to establish the frequency of STEC in non-domestic mammals of the Zoo and Botanical Garden of La Plata City, Argentina, and to pheno-genotypically characterize STEC isolates. By polymerase chain reaction (PCR), Shiga toxin (stx) gene sequences were detected in 50.8% of 65 fecal samples. Twenty-five STEC strains were isolated from 38.5% of the Zoo's animals. Ten species of order Cetartiodactyla and one species of order Rodentia were recognized as new STEC carriers. STEC strains belonged to 7 different serotypes including new serotypes O12:H25 and O13:H6. Serotype O146:H28, previously associated with human infections, represented 24% of STEC isolates. The most frequent Shiga toxin identified were type 1c and type 2c. Nineteen strains were positive for iha gene, 8 strains were positive for ehxA gene. Moreover, all strains were positive for lpfAO113 and negative for rfbO157, eae, saa, lpfAO157/OI-141, lpfAO157/OI-154, efa1, and toxB genes. Results obtained by XbaI-pulsed-field gel electrophoresis (XbaI-PFGE) confirmed the transmission of STEC strains among different animal species and suborders. In addition, we observed a potential association between STEC-harboring animal and factors such as belonging to order Cetartiodactyla, living in a pit, and belonging to a non-autochthonous species. This is the first work developed with zoological mammals and STEC in Argentina.     

Response of wheat and oat seedlings to root-applied diclofop-methyl and 2,4-dichlorophenoxyacetic acid

Roots of wheat and oat seedlings were treated with diclofop-methyl (methyl 2-[4-(2′,4′-dichlorophenoxy)phenoxy]propanoate) in a specially designed Plexiglas treatment apparatus. Diclofopmethyl severely inhibited the root growth of susceptible oat seedlings but roots of resistant wheat seedlings were unaffected. Diclofop-methyl at 0.3 μM reduced the growth of oat roots to 50% of the control. Direct contact between diclofop-methyl and the inhibited root zone was necessary for growth inhibition since other parts of the seedling (roots and shoots) isolated from contact with diclofop-methyl solution by a physical barrier were unaffected. Diclofop (2-[4-(2′,4′-dichlorophenoxy)phenoxy]propionic acid), the free acid metabolite of diclofop-methyl, was somewhat more phytotoxic than the parent compound. The herbicide, 2,4-dichlorophenoxyacetic acid (2,4-D), which engenders auxin responses, slightly enhanced the inhibition of oat root growth by diclofop-methyl. The primary wheat metabolite, ring-hydroxylated diclofop, was nonphytotoxic to oat root growth, whereas the acetylated derivative of the primary water-soluble oat metabolite (neutral glucose ester of diclofop) inhibited oat root growth to the same extent as diclofop-methyl. These results support the hypothesis that the basis for selectivity between resistant wheat and susceptible oat is the metabolism of diclofop-methyl by aryl hydroxylation and conjugation but not glucose ester conjugation. Translocation is also not an important factor in the phytotoxic activity of diclofop-methyl.