Abstract. Over time scales of thousands to millions of years, and in the absence of rejuvenating disturbances that initiate primary or early secondary succession, ecosystem properties such as net primary productivity, decomposition, and rates of nutrient cycling undergo substantial declines termed ecosystem retrogression. Retrogression results from the depletion or reduction in the availability of nutrients, and can only be reversed through rejuvenating disturbance that resets the system; this differs from age-related declines in forest productivity that are driven by shorter-term depression of nutrient availability and plant ecophysiological process rates that occur during succession. Here we review and synthesize the findings from studies of long-term chronosequences that include retrogressive stages for systems spanning the boreal, temperate, and subtropical zones. Ecosystem retrogression has been described by ecologists, biogeochemists, geologists, and pedologists, each of which has developed somewhat independent conceptual frameworks; our review seeks to unify this literature in order to better understand the causes and consequences of retrogression. Studies of retrogression have improved our knowledge of how long-term pedogenic changes drive shorter-term biological processes, as well as the consequences of these changes for ecosystem development. Our synthesis also reveals that similar patterns of retrogression (involving reduced soil fertility, predictable shifts in organismic traits, and ecological processes) occur in systems with vastly different climatic regimes, geologic substrates, and vegetation types, even though the timescales and mechanisms driving retrogression may vary greatly among sites. Studies on retrogression also provide evidence that in many regions, high biomass or "climax" forests are often transient, and do not persist indefinitely in the absence of rejuvenating disturbance. Finally, our review highlights that studies on retrogressive chronosequences in contrasting regions provide unparalleled opportunities for developing general principles about the long-term feedbacks between biological communities and pedogenic processes, and how these control ecosystem development.

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Quantifying global patterns of terrestrial nitrogen (N) cycling is central to predicting future patterns of primary productivity, carbon sequestration, nutrient fluxes to aquatic systems, and climate forcing. With limited direct measures of soil N cycling at the global scale, syntheses of the 15N:14N ratio of soil organic matter across climate gradients provide key insights into understanding global patterns of N cycling. In synthesizing data from over 6000 soil samples, we show strong global relationships among soil N isotopes, mean annual temperature (MAT), mean annual precipitation (MAP), and the concentrations of organic carbon and clay in soil. In both hot ecosystems and dry ecosystems, soil organic matter was more enriched in 15N than in corresponding cold ecosystems or wet ecosystems. Below a MAT of 9.8°C, soil δ15N was invariant with MAT. At the global scale, soil organic C concentrations also declined with increasing MAT and decreasing MAP. After standardizing for variation among mineral soils in soil C and clay concentrations, soil δ15N showed no consistent trends across global climate and latitudinal gradients. Our analyses could place new constraints on interpretations of patterns of ecosystem N cycling and global budgets of gaseous N loss.

The conversion of two-thirds of New Zealand's native forests and grasslands to agriculture has followed trends in other developed nations, except that pastoral grazing rather than cropping dominates agriculture. The initial conversion of land to pasture decreased soil acidity and elevated N and P stocks, but caused little change in soil organic C stocks. However, less is known about C and nutrient stock changes during the last two decades under long-term pastoral management. We resampled 31 whole soil profiles in pastures spanning seven soil orders with a latitudinal range of 36-461S, which had originally been sampled 17-30 years ago. We measured total C, total N, and bulk density for each horizon (generally to 1 m) and also reanalyzed archived soil samples of the same horizons for C and N. On average, profiles had lost significant amounts of C (À2.1 kg C m À2 ) and N (À0.18 kg N m À2 ) since initial sampling. Assuming a continuous linear decline in organic matter between sampling dates, significant losses averaged 106 g C m À2 yr À1 (P 5 0.01) and 9.1 g N m À2 yr À1 (P 5 0.002). Removal of C through leaching and erosion appears too small to explain these losses, suggesting losses from respiration exceed the inputs of photosynthate in the soil profile. These results emphasize that resampling soil profiles provide a robust method for detecting soil C changes, and add credence to the suggestion that soil C losses may be occurring in some temperate soil profiles. Further work is required to determine whether these losses are continuing and how losses might be extrapolated across landscapes to determine the implications for New Zealand's national CO 2 emissions and the sustainability of the implied rates of soil N loss.

The Nanjing Declaration on Nitrogen Management, signed in Nanjing in October 2004, calls for national governments to optimize N management by several strategies including assessment of N cycles. Here we develop a first N budget for New Zealand (267,000 km 2 ), at both national and regional scales. The national inputs are estimated to be 36.5 kg/ha, mainly from biological N fixation, but also increasingly from fertilizer application and atmospheric deposition. The outputs are estimated at 40.5 kg/ha. Biological N fixation from legumes in pasture was the most important input in most regions. Exceptions were Auckland, with a large urban population, and the West Coast of the South Island, with large tracts of rain forest. Outputs were distributed in the order leaching>ammonia volatilisation>erosion=produce=denitrification. These outputs are very different from global averages because of the large numbers of grazing animals on pasture. A large loss occurs between the subsoil and the oceans, and further research is needed to identify these pathways. Riverine export of N was generally well correlated with inputs.

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Abstract. Here we present an experimental setup for water stable isotope (δ18O and δD) continuous-flow measurements and provide metrics defining the performance of the setup during a major ice core measurement campaign (Roosevelt Island Climate Evolution; RICE). We also use the metrics to compare alternate systems. Our setup is the first continuous-flow laser spectroscopy system that is using off-axis integrated cavity output spectroscopy (OA-ICOS; analyzer manufactured by Los Gatos Research, LGR) in combination with an evaporation unit to continuously analyze water samples from an ice core. A Water Vapor Isotope Standard Source (WVISS) calibration unit, manufactured by LGR, was modified to (1) enable measurements on several water standards, (2) increase the temporal resolution by reducing the response time and (3) reduce the influence from memory effects. While this setup was designed for the continuous-flow analysis (CFA) of ice cores, it can also continuously analyze other liquid or vapor sources. The custom setups provide a shorter response time (~ 54 and 18 s for 2013 and 2014 setup, respectively) compared to the original WVISS unit (~ 62 s), which is an improvement in measurement resolution. Another improvement compared to the original WVISS is that the custom setups have a reduced memory effect. Stability tests comparing the custom and WVISS setups were performed and Allan deviations (σAllan) were calculated to determine precision at different averaging times. For the custom 2013 setup the precision after integration times of 103 s is 0.060 and 0.070 ‰ for δ18O and δD, respectively. The corresponding σAllan values for the custom 2014 setup are 0.030, 0.060 and 0.043 ‰ for δ18O, δD and δ17O, respectively. For the WVISS setup the precision is 0.035, 0.070 and 0.042 ‰ after 103 s for δ18O, δD and δ17O, respectively. Both the custom setups and WVISS setup are influenced by instrumental drift with δ18O being more drift sensitive than δD. The σAllan values for δ18O are 0.30 and 0.18 ‰ for the custom 2013 and WVISS setup, respectively, after averaging times of 104 s (2.78 h). Using response time tests and stability tests, we show that the custom setups are more responsive (shorter response time), whereas the University of Copenhagen (UC) setup is more stable. More broadly, comparisons of different setups address the challenge of integrating vaporizer/spectrometer isotope measurement systems into a CFA campaign with many other analytical instruments.