Anthropogenic effects on soil quality of ancient agricultural systems of the American Southwest

Soil studies of ancient agricultural fields contribute to research on long-term human–environmental relationships and land use sustainability. This kind of research is especially applicable in desert landscapes of the American Southwest because: (1) soil formation is slow enough that cultivation effects persist for centuries to millennia; (2) many ancient fields in valley margins have remained uncultivated since they were abandoned, so long-term soil properties reflect ancient agricultural use; and (3) agricultural features (e.g., terraces, rock alignments and rock piles, and irrigation canals) provide clues for identifying and sampling ancient cultivated and uncultivated soils. Surficial remnants of these field systems persist and remain intact in many cases. Soil studies of ancient and modern American Indian agricultural systems across the Southwest indicate that soil changes are highly variable, ranging from degradation (e.g., organic matter/nutrient decline, compaction), to minimal net change, to enhanced soil quality. Soil changes caused by cultivation can be inferred by comparing soils in agricultural fields relative to reference uncultivated areas in similar landscape settings (that is, space-for-time substitution). Soil response trajectories vary for a number of reasons, such as variability in initial ecosystem conditions, diversity in agricultural methods, variability in the mix of crops and cropping intensity, and environmental sensitivity to alteration (varying resistance and resilience). Studies of rock mulch soils indicate enhanced fertility, with elevated organic carbon, nitrogen, and available phosphorus levels, increased infiltration rates and moisture retention, and no evidence of compaction. By contrast, cultivation effects vary widely for terraced soils. Although numerous studies have focused on irrigation canals, irrigated soils have received far less attention. Soil studies of irrigation systems along the Gila and Santa Cruz rivers of Arizona now underway will help fill this research gap.     

Carbon flux and growth in mature deciduous forest trees exposed to elevated CO2

Whether rising atmospheric carbon dioxide (CO2) concentrations will cause forests to grow faster and store more carbon is an open question. Using free air CO2 release in combination with a canopy crane, we found an immediate and sustained enhancement of carbon flux through 35-meter-tall temperate forest trees when exposed to elevated CO2. However, there was no overall stimulation in stem growth and leaf litter production after 4 years. Photosynthetic capacity was not reduced, leaf chemistry changes were minor, and tree species differed in their responses. Although growing vigorously, these trees did not accrete more biomass carbon in stems in response to elevated CO2, thus challenging projections of growth responses derived from tests with smaller trees.     

Hybrid grass-clump dwarfness in wheat: Physiology and genetics

Summary The growth of all grass-clump dwarfs is sensitive to temperature with low temperature giving rise to the grass-clump phenotype and high temperature producing normal phenotype. A continuous temperature of 26°C is required for normal growth of Type 1 dwarfs, a continuous temperature of 21°C is required for normal growth of Ty[e 2 dwarfs and a continuous temperature of 16°C is required for normal growth of Type 3 dwarfs.Genetic studies show that the inheritance of the grass-clump characteristic is due to three complementary dominant genes.The grass-clump growth habit is produced as a result of the temperature sensitivity of the apical meristem. In grass-clump plants low temperature treatment results in the cessation of cell division, DNA synthesis and phospholipid synthesis in the apical meristem. The primary temperature lesion has not been identified. Prolonged low temperature treatment of grass-clump plants results in extensive cell necrosis in a region just below the apical meristem; this cell death results in the permanent inactivation of the apical meristem.Supported in part by the National Research Council of Canada.     

Effects of leaf age and tree size on stomatal and mesophyll limitations to photosynthesis in mountain beech (Nothofagus solandrii var. cliffortiodes)

Mesophyll conductance, g(m), was estimated from measurements of stomatal conductance to carbon dioxide transfer, g(s), photosynthesis, A, and chlorophyll fluorescence for Year 0 (current-year) and Year 1 (1-year-old) fully sunlit leaves from short (2 m tall, 10-year-old) and tall (15 m tall, 120-year-old) Nothofagus solandrii var. cliffortiodes trees growing in adjacent stands. Rates of photosynthesis at saturating irradiance and ambient CO(2) partial pressure, A(satQ), were 25% lower and maximum rates of carboxylation, V(cmax), were 44% lower in Year 1 leaves compared with Year 0 leaves across both tree sizes. Although g(s) and g(m) were not significantly different between Year 0 and Year 1 leaves and g(s) was not significantly different between tree heights, g(m) was significantly (19%) lower for leaves on tall trees compared with leaves on short trees. Overall, V(cmax) was 60% higher when expressed on the basis of CO(2) partial pressure at the chloroplasts, C(c), compared with V(cmax) on the basis of intercellular CO(2) partial pressure, C(i), but this varied with leaf age and tree size. To interpret the relative stomatal and mesophyll limitations to photosynthesis, we used a model of carbon isotopic composition for whole leaves incorporating g(m) effects to generate a surface of 'operating values' of A over the growing season for all leaf classes. Our analysis showed that A was slightly higher for leaves on short compared with tall trees, but lower g(m) apparently reduced actual A substantially compared with A(satQ). Our findings showed that lower rates of photosynthesis in Year 1 leaves compared with Year 0 leaves were attributable more to increased biochemical limitation to photosynthesis in Year 1 leaves than differences in g(m). However, lower A in leaves on tall trees compared with those on short trees could be attributed in part to lower g(m) and higher stomatal, L(s), and mesophyll, L(m), limitations to photosynthesis, consistent with steeper hydraulic gradients in tall trees.     

Identification of resistance gene analogue markers closely linked to wheat powdery mildew resistance gene Pm31

Specific oligonucleotide primers, designed for the sequences of known plant disease resistance genes, were used to amplify resistance gene analogues (RGAs) from wheat genomic DNA. This method was applied in a bulked segregant analysis to screen for the RGA markers linked to the powdery mildew resistance gene Pm31, introgressed into common wheat from wild emmer. Two RGA markers (RGA200 and RGA390) were found to be closely linked to Pm31 and completely co‐segregating with the marker allele of Xpsp3029 linked to Pm31, with a genetic distance of 0.6 cM. These two RGA markers were then integrated into the formerly established microsatellite map of Pm31 region. The result showed the effectiveness of the RGA approach for developing molecular markers linked to disease resistance genes and demonstrated the efficiency of denaturing polyacrylamide‐gel electrophoresis for detecting polymerase chain reaction polymorphism.     

Can supplemental food increase winter survival of a threatened cottontail rabbit?

Populations of New England cottontails (Sylvilagus transitionalis) have declined substantially in recent decades in response to habitat loss and fragmentation. Among some remnant populations, cottontails occupy small patches of thicket habitat where they experience high mortality rates as a consequence of limited food during winter. This limitation causes rabbits to forage away from cover where they are exposed to predators. Although conservation efforts are emerging to reverse the decline of New England cottontails, most are directed toward improving long-term viability by increasing the abundance of suitable habitats. Such efforts do little to improve the short-term survival of remaining cottontails. To address this immediate need, we evaluated the use of supplemental food as an approach to improve overwinter survival rates. We speculated that by positioning feeders in close proximity to escape cover, rabbits would be less vulnerable to predators. We evaluated this approach using eastern cottontails (Sylvilagus floridanus) as a research surrogate because this species is readily available and has similar habitat requirements to New England cottontails. Transmitter-equipped eastern cottontails were randomly assigned to either a fed or unfed group. Remotely-triggered cameras were also used to gauge use of feeders by cottontails and visits by other species. Winter survival rates were substantially greater for fed rabbits (70%) than for unfed rabbits (32%). Cameras revealed that rabbits were the most frequent consumer and that there was only limited carnivore activity near feeders. We conclude that supplemental feeding may improve survival of remaining New England cottontails as efforts to increase habitat availability continue to develop.     

The nature of Solanum × chaucha Juz. et Buk., a triploid cultivated potato of the South American Andes

Summary The variation in Solanum × chaucha Juz. et Buk. (2n=3x=36) was studied using 114 accessions from the Potato Collection maintained by the International Potato Center. These accession represented less than 5% of the collection originally screened for ploidy. Twenty morphological characters of the tubers, inflorescences and leaves were scored. The accessions were grouped into 20 morphotypes on the basis of the tuber characters. Two-qualitative characters, red-anther tip and sky-blue flowers were diagnostic of 4 morphotypes, but the variation of the quantitative characters overlapped among morphotypes, and were of limited value. Electrophoretic separation of tuber proteins in 7.5% polyacrylamide gels generally confirmed the morphotype groupings. It is concluded that each of the morphotypes represents a single genotype, and these are named according to the International Code of Nomenclature for Cultivated Plants. The variation within S. × chaucha apparently has been restricted by its hybrid origin.