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Abstract Nitrogen (N) is a key nutrient required by all living organisms for growth and development, but is a limiting resource for many organisms. Organisms that feed on material with low N content, such as wood, might be particularly prone to N limitation. In this study, we investigated the degree to which the xylophagous larvae of the stag beetle Ceruchus piceus (Weber) use associations with N-fixing bacteria to acquire N. We paired acetylene reduction assays by cavity ring-down absorption spectroscopy (ARACAS) with 15N2 incubations to characterize rates of N fixation within C. piceus. Not only did we detect significant N fixation activity within C. piceus larvae, but we calculated a rate that was substantially higher than most previous reports for N fixation in insects. While taking these measurements, we discovered that N fixation within C. piceus can decline rapidly in a lab setting. Consequently, our results demonstrate that previous studies, which commonly keep insects in the lab for long periods of time prior to and during measurement, may have systematically under-reported rates of N fixation in insects. This suggests that within-insect N fixation may contribute more to insect nutrition and ecosystem-scale N budgets than previously thought. 

Allometric equations are often used to estimate plant biomass allocation to different tissue types from easier-to-measure quantities. Biomass allocation, and thus allometric equations, often differs by species and sometimes varies with nutrient availability. We measured biomass components for five nitrogen-fixing tree species ( Robinia pseudoacacia , Gliricidia sepium , Casuarina equisetifolia , Acacia koa , Morella faya ) and three non-fixing tree species ( Betula nigra , Psidium cattleianum , Dodonaea viscosa ) grown in field sites in New York and Hawaii for 4–5 years and subjected to four fertilization treatments. We measured total aboveground, foliar, main stem, secondary stem, and twig biomass in all species, and belowground biomass in Robinia pseudoacacia and Betula nigra , along with basal diameter, height, and canopy dimensions. The individuals spanned a wide size range (<1–16 cm basal diameter; 0.24–8.8 m height). For each biomass component, aboveground biomass, belowground biomass, and total biomass, we determined the following four allometric equations: the most parsimonious (lowest AIC) overall, the most parsimonious without a fertilization effect, the most parsimonious without canopy dimensions, and an equation with basal diameter only. For some species, the most parsimonious overall equation included fertilization effects, but fertilization effects were inconsistent across fertilization treatments. We therefore concluded that fertilization does not clearly affect allometric relationships in these species, size classes, and growth conditions. Our best-fit allometric equations without fertilization effects had the following R 2 values: 0.91–0.99 for aboveground biomass (the range is across species), 0.95 for belowground biomass, 0.80–0.96 for foliar biomass, 0.94–0.99 for main stem biomass, 0.77–0.98 for secondary stem biomass, and 0.88–0.99 for twig biomass. Our equations can be used to estimate overall biomass and biomass of tissue components for these size classes in these species, and our results indicate that soil fertility does not need to be considered when using allometric relationships for these size classes in these species. 

Abstract Nitrogen (N) limitation to net primary production is widespread and influences the responsiveness of ecosystems to many components of global environmental change. Logic and both simple simulation (Vitousek and Fieldin in Biogeochemistry 46: 179–202, 1999) and analytical models (Menge in Ecosystems 14:519–532, 2011) demonstrate that the co-occurrence of losses of N in forms that organisms within an ecosystem cannot control and barriers to biological N fixation (BNF) that keep this process from responding to N deficiency are necessary for the development and persistence of N limitation. Models have focused on the continuous process of leaching losses of dissolved organic N in biologically unavailable forms, but here we use a simple simulation model to show that discontinuous losses of ammonium and nitrate, normally forms of N whose losses organisms can control, can be uncontrollable by organisms and can contribute to N limitation under realistic conditions. These discontinuous losses can be caused by temporal variation in precipitation or by ecosystem-level disturbance like harvest, fire, and windthrow. Temporal variation in precipitation is likely to increase and to become increasingly important in causing N losses as anthropogenic climate change proceeds. We also demonstrate that under the conditions simulated here, differentially intense grazing on N- and P-rich symbiotic N fixers is the most important barrier to the responsiveness of BNF to N deficiency. 

Abstract Symbiotic nitrogen fixation (SNF) is a key ecological process whose impact depends on the strategy of SNF regulation—the degree to which rates of SNF change in response to limitation by N versus other resources. SNF that is obligate or exhibits incomplete downregulation can result in excess N fixation, whereas a facultative SNF strategy does not. We hypothesized that tree‐based SNF strategies differed by latitude (tropical vs. temperate) and symbiotic type (actinorhizal vs. rhizobial). Specifically, we expected tropical rhizobial symbioses to display strongly facultative SNF as an explanation of their success in low‐latitude forests. In this study we used¹⁵N isotope dilution field experiments in New York, Oregon, and Hawaii to determine SNF strategies in six N‐fixing tree symbioses. Nitrogen fertilization with +10 and +15 g N m⁻² year⁻¹for 4–5 years alleviated N limitation in all taxa, paving the way to determine SNF strategies. Contrary to our hypothesis, all six of the symbioses we studied sustained SNF even at high N.Robinia pseudoacacia(temperate rhizobial) fixed 91% of its N (%N_dfa) in controls, compared to 64% and 59% in the +10 and +15 g N m⁻² year⁻¹treatments. ForAlnus rubra(temperate actinorhizal), %N_dfawas 95%, 70%, and 60%. For the tropical species, %N_dfawas 86%, 80%, and 82% forGliricidia sepium(rhizobial); 79%, 69%, and 67% forCasuarina equisetifolia(actinorhizal); 91%, 42%, and 67% forAcacia koa(rhizobial); and 60%, 51%, and 19% forMorella faya(actinorhizal). Fertilization with phosphorus did not stimulate tree growth or SNF. These results suggest that the latitudinal abundance distribution of N‐fixing trees is not caused by a shift in SNF strategy. They also help explain the excess N in many forests where N fixers are common. 

Abstract Fertilized temperate croplands export large amounts of reactive nitrogen (N), which degrades water and air quality and contributes to climate change. Fertilizer use is poised to increase in the tropics, where widespread food insecurity persists and increased agricultural productivity will be needed, but much less is known about the potential consequences of increased tropical N fertilizer application. We conducted a meta‐analysis of tropical field studies of nitrate leaching, nitrous oxide emissions, nitric oxide emissions, and ammonia volatilization totaling more than 1,000 observations. We found that the relationship between N inputs and losses differed little between temperate and tropical croplands, although total nitric oxide losses were higher in the tropics. Among the potential drivers we studied, the N input rate controlled all N losses, but soil texture and water inputs also controlled hydrological N losses. Irrigated systems had significantly higher losses of ammonia, and pasture agroecosystems had higher nitric oxide losses. Tripling of fertilizer N inputs to tropical croplands from 50 to 150 kg N ha⁻¹ year⁻¹would have substantial environmental implications and would lead to increases in nitrate leaching (+30%), nitrous oxide emissions (+30%), nitric oxide (+66%) emissions, and ammonia volatilization (+74%), bringing tropical agricultural nitrate, nitrous oxide, and ammonia losses in line with temperate losses and raising nitric oxide losses above them.