Comparison of N losses (NO − 3, N 2O, NO) from surface applied, injected or amended (DCD) pig slurry of an irrigated soil in a Mediterranean climate

Nitrous oxide (N ₂O), nitric oxide (NO), denitrification losses and NO^–₃ leaching from an irrigated sward were quantified under Mediterranean conditions. The effect of injected pig slurry (IPS) with and without the nitrification inhibitor dicyandiamide (DCD) was evaluated and also compared with that of a surface pig slurry application (SPS) and a control treatment (Control) without fertiliser. After application, fluxes of NO and N ₂O peaked from SPS (3.06 mg NO-N m ^–2 d ^–1 and 108 mg N ₂O-N m ^–2 d ^–1) and IPS (3.50 mg NO-N m ^–2 d ^–1 and 105 mg N ₂O-N m ^–2 d ^–1). However, when irrigation was applied, N ₂O and NO emissions declined. The total N ₂O and denitrification losses were slightly large from IPS than from SPS, although the differences were not significant (P < 0.05). Emission of NO was not affected by the method of pig slurry application. DCD inhibited nitrification during the first 20–30 days and reduced N ₂O and NO emissions from pig slurry by at least 46% and 37%, respectively. Considering the 215 days following pig slurry application, the emission factor of N ₂O based on N fertiliser was 1.60% (SPS), 2.95% (IPS), and 0.50% (IPS + DCD). The emission factor for NO was 0.14% (SPS), 0.12% (IPS), and 0.02% (IPS + DCD). Environmental conditions of the crop favoured the denitrification process as the most important source of N ₂O during the experimental period. The differences in the denitrification rate between treatments could be explained by the pattern of water soluble carbon (WSC), that was the highest value in injected pig slurry (with and without DCD). Due to low drainage (5% of water applied), leaching losses of NO₃^– were lower than those of denitrification from the upper soil layer (0–10 cm) in all treatments and especially with IPS + DCD, where the nitrification inhibitor was very efficient in reducing leaching losses.     

Environmental controls on nitric oxide emission from northern Chihuahuan desert soils

A survey of nitric oxide (NO) emission from Chihuahuan desert soils found mean NO fluxes <0.1 ng NO-N cm^–2h^–1 during the dry season. These fluxes were at thelower end of the range reported for temperate grassland and woodlandecosystems. NO fluxes from wet or watered soils were higher(0.1–35 ng NO-N cm^–2 h^–1).Watering of black grama grassland soils produced an initial pulse of 12ng cm^–2 h^–1 (12-h after 1-cm watering)with high fluxes sustained over 4 days with repeated watering. Initialpulses from shrubland soils were lower (maximum 5 ngcm^–2 h^–1), and fluxes declined withrepeated watering. Repeated watering of creosotebush soils depleted thesoil NH ₄ ⁺ pool, and NO emissions weredirectly related to soil NH ₄ ⁺ concentrationsat the end of the experiment. In watered andNH ₄ ⁺ -fertilized creosotebush soils, NO fluxeswere positively related to potential net nitrification rates.NH ₄ ⁺ -fertilization boosted the initial NOpulse 15 times in the shrubland and 5 times in black grama grasslandrelative to watered controls. These experimental results point towardgreater substrate limitation in shrublands. In this desert basin, NOemission averaged 0.12 kg N ha^–1 y^–1in untreated soil and 0.76 kg N ha^–1y^–1 in watered soil. We multiplied these averages bythe distribution of grassland and shrubland vegetation within a58,600-ha area of the Jornada del Muerto basin to estimate regionallosses of 0.15–0.38 kg NO-N ha^–1y^–1 for this area of the Chihuahuan desert.     

How widespread is woody plant encroachment in temperate Australia? Changes in woody vegetation cover in lowland woodland and coastal ecosystems in Victoria from 1989 to 2005

Aim Encroachment or densification by woody plants affects natural ecosystems around the world. Many studies have reported encroachment in temperate Australia, particularly in coastal ecosystems and grassy woodlands. However, the degree to which published studies reflect broad-scale changes is unknown because most studies intentionally sampled areas with conspicuous densification. We aimed to estimate changes in woody vegetation cover within lowland grassy woodland and coastal ecosystems in Victoria from 1989 to 2005 to determine whether published reports of recent encroachment are representative of broad-scale ecosystem changes. Location All lowland grassy woodland and coastal ecosystems (c. 6.11 × 10⁵ ha) in Victoria, Australia. Four major ecosystems were analysed: Plains woodlands, Herb-rich woodlands, Riverine woodlands and Coastal vegetation. Methods Changes in woody vegetation cover from 1989 to 2005 were assessed based on state-wide vegetation maps and Landsat analyses of woody vegetation cover conducted by the Australian Greenhouse Office’s National Carbon Accounting System. The results show changes in woody cover within mapped patches of native vegetation, rather than changes in the extent of woody vegetation resulting from clearing and revegetation. Results When pooled across all ecosystems, woody vegetation increased by 18,730 ha from 1989 to 2005. Woody cover within Riverine woodlands and within Plains woodlands each increased by >7000 ha. At the patch scale, the mean percentage cover of woody vegetation in each polygon increased by >5% in all four ecosystems: Riverine woodlands (+9.2% on average), Herb-rich woodlands (+7.6%), Plains woodlands (+6.7%) and Coastal vegetation (+5.9%). Regression models relating degree of encroachment to geographic and climatic variables were extremely weak (r² ≤ 0.026), indicating that most variation occurred at local scales rather than across broad geographic gradients. Main conclusions At the scale of observation, woody vegetation cover increased in all lowland woodland and coastal ecosystems over the 16-year period. Thus, published examples of encroachment in selected coastal and woodland patches do appear to reflect widespread increases in woody vegetation cover in these ecosystems. This densification appears to be associated with changes in land management rather than with post-fire vegetation recovery and is likely to be ongoing and long-lasting, with substantial implications for biodiversity conservation and ecosystem services.     

Assessing the extent and diversity of riparian ecosystems in Sonora, Mexico

Conservation of forested riparian ecosystems is of international concern. Relatively little is known of the structure, composition, diversity, and extent of riparian ecosystems in Mexico. We used high- and low-resolution satellite imagery from 2000 to 2006, and ground-based sampling in 2006, to assess the spatial pattern, extent, and woody plant composition of riparian forests across a range of spatial scales for the state of Sonora, Mexico. For all 3rd and higher order streams, river bottomlands with riparian forests occupied a total area of 2,301 km². Where forested bottomlands remained, on average, 34% of the area had been converted to agriculture while 39% remained forested. We estimated that the total area of riparian forest along the principal streams was 897 km². Including fencerow trees, the total forested riparian area was 944 km², or 0.5% of the total land area of Sonora. Ground-based sampling of woody riparian vegetation consisted of 92, 50 m radius circular plots. About 79 woody plant species were noted. The most important tree species, based on cover and frequency, were willow species Salix spp. (primarily S. goodingii and S. bonplandiana), mesquite species Prosopis spp. (primarily P. velutina), and Fremont cottonwood Populus fremontii. Woody riparian taxa at the reach scale showed a trend of increasing diversity from north to south within Sonora. Species richness was greatest in the willow-bald cypress Taxodium distichum var. mexicanum—Mexican cottonwood P. mexicana subsp. dimorphia ecosystem. The non-native tamarisk Tamarix spp. was rare, occurring at just three study reaches. Relatively natural stream flow patterns and fluvial disturbance regimes likely limit its establishment and spread.     

Diurnal changes in nitric oxide emissions from conventional tillage and pasture sites in the Amazon Basin: influence of soil temperature

We have investigated a subset of restoration practices applied to a degraded pasture at Fazenda Nova Vida, a 22000 ha cattle ranch in Rond^onia, Brazil. Nitric oxide (NO) and carbon dioxide (CO₂) emissions from soils were measured in conventional tillage and current pasture sites to assess N and C losses. Mean daily NO emissions from tilled plots were at least twice those from the pasture. Nitric oxide emissions from the tilled sites showed a strong diurnal pattern, while those from the pasture sites did not. Mean daytime NO emissions from the tilled sites were 9.7 g NO-N m^–2 h^–1, while mean nighttime emissions were 29.7 g NO-N m^–2 h^–1. In the pasture sites, NO emissions were 7.6 g NO-N m^–2 h^–1 during the day, and 7.7 g NO-N m^–2 h^–1 at night. Surface soil temperature was a good inverse predictor (r ²=0.75) of NO emissions from the tilled sites. Carbon dioxide emissions from the tilled sites were generally larger than CO₂ emissions from the pasture sites. The mean CO₂ emission rate from the tilled sites was 179 mg C m^–2 h^–1, while it was 123 mg C m^–2 h^–1 from the pasture sites. There was no distinct diurnal pattern for CO₂ emissions. We found that the very high temperatures measured at the soil surface in the tillage plots, in the range of 40–45°C, reduced the rate of NO emission. The reduction in NO emissions may be because of the sensitivity of autotrophic nitrifiers to high temperatures. This study provides insights on how land-use change may alter regional NO fluxes by exposing certain microbial communities to extreme environmental conditions. Future studies of NO emissions in tropical agricultural systems where soils are bare for extend periods need to make diurnal measurements or the daily fluxes will be substantially underestimated.     

Encroachment of woody plants and its impact on pastoral livestock production in the Borana lowlands, southern Oromia, Ethiopia

Encroachment of woody plants has been among the major threats to the livelihoods of Borana pastoralists and their ecosystem. An approach that integrated vegetation survey and pastoralists’ perception was followed to study the impacts of encroachment of woody plants in the Borana lowlands, Ethiopia. Density of woody species was determined in 192 plots of 500 m². Canopy cover of woody plants was estimated in 123 quadrates of 400 m². Pastoralists’ perception was assessed through group discussions and a semi‐structured questionnaire. Results showed that plant density was 3014 woody plants ha^?1. Cover of woody plants was 52%, indicating an increasing trend from ≤40% cover reported in the early 1990s. It was concluded that the increase of woody plants density and cover has crossed the critical threshold and has entered into the encroached condition. Principal components analysis (PCA) and redundancy analysis (RDA) also showed that woody plants were negatively correlated with herbaceous biomass. Commiphora africana, Acacia melliphera, A. drepanolobium, A. brevispica and Lannea rivae were among the dominant encroachers. RDA revealed that soil nutrients were positively correlated with woody plants density and cover. The pastoralists perceived that encroachment of woody plants had decreased the production of their grazingland. A ban on fire was perceived as the major factor that caused encroachment of woody plants. Re‐utilization of fire and strengthening of traditional rangeland management strategies are recommended.     

Woodland expansion in South African grassy biomes based on satellite observations (1990–2013): general patterns and potential drivers

Increases in woody plant cover in savanna grassland environments have been reported on globally for over 50 years and are generally perceived as a threat to rangeland productivity and biodiversity. Despite this, few attempts have been made to estimate the extent of woodland increase at a national scale, principally due to technical constraints such as availability of appropriate remote sensing products. In this study, we aimed to measure the extent to which woodlands have replaced grasslands in South Africa's grassy biomes. We use multiseason Landsat data in conjunction with satellite L‐band radar backscatter data to estimate the extent of woodlands and grasslands in 1990 and 2013. The method employed allows for a unique, nationwide measurement of transitions between grassland and woodland classes in recent decades. We estimate that during the 23‐year study period, woodlands have replaced grasslands over ~57 000 km² and conversely that grasslands have replaced woodlands over ~30 000 km², a net increase in the extent of woodland of ~27 000 km² and an annual increase of 0.22%. The changes varied markedly across the country; areas receiving over 500 mm mean annual precipitation showed higher rates of woodland expansion than regions receiving <500 mm (0.31% yr^?1 and 0.11% yr^?1, respectively). Protected areas with elephants showed clear loss of woodlands (?0.43% yr^?1), while commercial rangelands and traditional rangelands showed increases in woodland extent (>0.19% yr^?1). The woodland change map presented here provides a unique opportunity to test the numerous models of woody plant encroachment at a national/regional scale.     

Resource limitations to nitric oxide emissions from a sagebrush-steppe ecosystem

We monitored soil emissions of NO, NO₂, N₂O, and CO₂ throughout the summer dry season at a remote North American sagebrush-steppe ecosystem following application of several resources, including water, NH ₄ ⁺ , NO ₃ ^– and sucrose. Despite low levels of soil NH ₄ ^– (5.60±0.95 mg NH ₄ ^– -N per kg soil, mean ± S.E.), and NO ₃ ^– -N (1.34±0.20 mg NO ₃ ^– -N per kg soil), NO emissions ranged from about 0.2 to 2.8 ng NO-N m^–2 s^–1, comparable to rates measured from many agricultural, tropical, and other undisturbed ecosystems. Soil wetting increased NO emissions as much as 400-fold when initial gravimetric soil moisture contents were less than about 50 mg kg _soil ^–1 and soil temperature was greater than or equal to 20 °C. Wetting treatments with 20 mg NH ₄ ⁺ -N kg _soil ^–1 raised NO emission rates to a level that was nearly an order of magnitude higher than that observed after water addition alone. Wetting treatments with 20 mg NO ₃ ^– -N kg _soil ^–1 , 240 mg sucrose-C kg _soil ^–1 , or NO ₃ ^– plus sucrose had no statistically significant effect upon NO emissions. Soil denitrifying enzyme activity was low at this site, and N₂O emissions in the field were below detection limits. Soil nitrifying enzyme activity was extremely high at this site, indicating that the NH ₄ ⁺ released by ammonification would be consumed at least once every 1.7 days. These observations indicate that NO emissions from this undisturbed ecosystem were likely a consequence of high nitrification activity, and that sagebrush-steppe ecosystems may be a more important NO source than has been previously assumed.     

Woody plant invasion of grasslands: establishment of honey mesquite (Prosopis glandulosa var.glandulosa) on sites differing in herbaceous biomass and grazing history

Summary Emergence and survival of honey mesquite (Prosopis glandulosa var.glandulosa Torr.) seedlings was quantified on sites with contrasting grazing histories: long-term continuous grazing (LTG) and long-term protection (LTP) from grazing by cattle. On each site, different levels of heroaceous defoliation were imposed at monthly intervals (no defoliation=ND, moderate=MD and heavy=HD). The two weeks following seed dissemination appeared to be the most critical toProsopis establishment on LTP-ND plots. Openings in the herbaceous layer created by moderate defoliation of grasses on the LTP site increased germination and/or survival 7-to 8-fold during this period. However, increasing the degree of defoliation from moderate to heavy did not stimulate additional emergence on either the LTP or LTG site. Emergence from scarified seed placed in cattle dung (17 to 30%) was lower than that of bare seed placements in various microhabitats (43–60%). However, deposition of scarifiedProsopis seed in dung in conjunction with graminoid defoliation may be the most likely combination of events when livestock are present. Emergence from seeds transported into grasslands by other fauna likely would be low, unless seeds were deposited in areas where grasses had been defoliated.Prosopis survival was comparably high in dung and bare seed placements after one growing season. survival of seedlings present two weeks after seed dissemination ranged from 74 to 97% at the end of the second growing season. Seedling survival and shoot development (biomass, leaf area and height) were similar on LTP and LTG sites, regardless of the level of herbaceous defoliation or seed placement. In addition, the magnitude and patterns of net photosynthesis, stomatal conductance and xylem water potential were comparable among one-year-old seedtings on ND, MD and HD plots, even though differences in herbaceous species composition and above- and below-ground biomass between these treatments were substantial. Such data suggest competition for soil resources between grasses andProsopis may be minimal early in the life cycle ofProsopis. High rates ofProsopis emergence and establishment on LTP-MD plots are counter to the widespread assumption that long-term and/or heavy grazing is requisite forProsopis encroachment into grasslands. Results are discussed with regard to factors contributing to the recent, widespread invasion of this woody legume into grasslands of southwestern North America.Abbreviations LTG long-term grazed - LTP long-term protected from grazing - ND non-defoliated - MD moderate defoliation - HD heavy defoliation     

Net changes in regional woody vegetation cover and carbon storage in Texas Drylands, 1937–1999

Although local increases in woody plant cover have been documented in arid and semiarid ecosystems worldwide, there have been few long‐term, large‐scale analyses of changes in woody plant cover and aboveground carbon (C) stocks. We used historical aerial photography, contemporary Landsat satellite data, field observations, and image analysis techniques to assess spatially specific changes in woody vegetation cover and aboveground C stocks between 1937 and 1999 in a 400‐km² region of northern Texas, USA. Changes in land cover were then related to topo‐edaphic setting and historical land‐use practices. Mechanical or chemical brush management occurred over much of the region in the 1940–1950s. Rangelands not targeted for brush management experienced woody cover increases of up to 500% in 63 years. Areas managed with herbicides, mechanical treatments or fire exhibited a wide range of woody cover changes relative to 1937 (?75% to + 280%), depending on soil type and time since last management action. At the integrated regional scale, there was a net 30% increase in woody plant cover over the 63‐year period. Regional increases were greatest in riparian corridors (33%) and shallow clay uplands (26%) and least on upland clay loams (15%). Allometric relationships between canopy cover and aboveground biomass were used to estimate net aboveground C storage changes in upland (nonriparian) portions of regional landscapes. Carbon stocks increased from 380 g C m^?2 in 1937 to 500 g C m^?2 in 1999, a 32% net increase across the 400 km² region over the 63‐year period. These plant C storage change estimates are highly conservative in that they did not include the substantial increases in woody plant cover observed within riparian landscape elements. Results are discussed in terms of implications for ‘carbon accounting’ and the global C cycle.     

Rates of woody encroachment in African savannas reflect water constraints and fire disturbance

Aim

The aims of this study were to (1) estimate current rates of woody encroachment across African savannas; (2) identify relationships between change in woody cover and potential drivers, including water constraints, fire frequency and livestock density. The found relationships led us to pursue a third goal: (3) use temporal dynamics in woody cover to estimate potential woody cover.

Location

Sub‐Saharan African savannas.

Methods

The study used very high spatial resolution satellite imagery at sites with overlapping older (2002–2006) and newer (2011–2016) imagery to estimate change in woody cover. We sampled 596 sites in 38 separate areas across African savannas. Areas with high anthropogenic impact were avoided in order to more clearly identify the influence of environmental factors. Relationships between woody cover change and potential drivers were identified using linear regression and simultaneous autoregression, where the latter accounts for spatial autocorrelation.

Results

The mean annual change in woody cover across our study areas was 0.25% per year. Although we cannot explain the general trend of encroachment based on our data, we found that change rates were positively correlated with the difference between potential woody cover and actual woody cover (a proxy for water availability; p < .001), and negatively correlated with fire frequency (p < .01). Using the relationship between rates of encroachment and initial cover, we estimated potential woody cover at different rainfall levels.

Main conclusions

The results indicate that woody encroachment is ongoing and widespread across African savannas. The fact that the difference between potential and actual cover was the most significant predictor highlights the central role of water availability and tree–tree competition in controlling change in woody populations, both in water‐limited and mesic savannas. Our approach to derive potential woody cover from the woody cover change trajectories demonstrates that temporal dynamics in woody populations can be used to infer resource limitations.     

Vegetation dynamics in a Quercus‐Juniperus savanna: An isotopic assessment

Abstract. Woody plants are increasing in many grassland and savanna ecosystems around the world. As a case in point, the Edwards Plateau of Texas, USA, is a vast region (93 000 km²) in which rapid woody encroachment appears to be occurring. The native vegetation (prior to the Anglo‐European settlement 150–200 yr ago) and the biogeochemical consequences of woody encroachment in this region, however, are poorly understood. To assess these matters we measured plant and soil δ¹³C, soil organic C and soil N content from grasslands and two important woody patch types (mature Quercus virginiana clusters and Juniperus ashei woodlands) in this region. Soil δ¹³C values showed that relative productivity of C₃ species has increased in grassland and both woody habitats in recent times. δ¹³C of SOC in grasslands and Q. virginiana clusters increased with depth from the litter layer to 30 cm (grasslands =?21 to ?13‰Q. virginiana clusters =?27 to ?17‰) and were significantly different between habitats at all depths, indicating that Q. virginiana has been a long‐term component of the landscape. In J. ashei woodlands, soil δ¹³C values (at 20–30 cm depth) near the woodland edge (‐13‰) converged with those of an adjacent grassland (‐13‰) while those from the woodland interior (‐15‰) remained distinct, indicating that the woodland has been present for many years but has recently expanded. Concentrations and densities of SOC and total N were generally greater in woody patches than in grasslands. However, differences in the amount of SOC and N stored beneath the two woody patch types indicates that C and N sequestration potentials are species dependent.     

Distribution and size of capercaillie leks in relation to old forest fragmentation

Summary Distribution and size of 38 capercaillie Tetrao urogallus leks were related to amount and configuration of old forest patches in two south-east Norwegian coniferous forests. The smallest occupied patch was 48 ha containing a solitary displaying cock. All patches larger than 1 km² contained leks. Number of cocks per lek increased with increasing patch size. Number of leks per patch increased in a step-wise manner with one lek added for each 2.5–3 km² increase in patch size. In large patches there was one lek per 3–5 km² old forest, and density of lekking cocks was 2–2.5 per km². In small patches density of cocks varied considerably. Density of cocks was not related to patch isolation or patch shape. However, among leks surrounded by 50–60% old forest within a 1 km radius, number of cocks increased with increasing old forest fine-graininess. We argue that when old forests cover more than 50%, a fine-grained mosaic may support higher densities of lekking cocks than a coarse-grained mosaic. Conversely, when old forests cover less than 50%, a fine-grained mosaic is unfavourable, because each old forest patch becomes too small and isolated. Finally, we present a predictive model of how old forest fragmentation influences density of leks, number of cocks per lek, and total density of cocks.     

Changes in aboveground primary production and carbon and nitrogen pools accompanying woody plant encroachment in a temperate savanna

When woody plant abundance increases in grasslands and savannas, a phenomenon widely observed worldwide, there is considerable uncertainty as to whether aboveground net primary productivity (ANPP) and ecosystem carbon (C) and nitrogen (N) pools increase, decrease, or remain the same. We estimated ANPP and C and N pools in aboveground vegetation and surface soils on shallow clay and clay loam soils undergoing encroachment by Prosopis glandulosa in the Southern Great Plains of the United States. Aboveground Prosopis C and N mass increased linearly, and ANPP increased logarithmically, with stand age on clay loam soils; on shallow clays, Prosopis C and N mass and ANPP all increased linearly with stand age. We found no evidence of an asymptote in trajectories of C and N accumulation or ANPP on either soil type even following 68 years of stand development. Production and accumulation rates were lower on shallow clay sites relative to clay loam sites, suggesting strong edaphic control of C and N accumulation associated with woody plant encroachment. Response of herbaceous C mass to Prosopis stand development also differed between soil types. Herbaceous C declined with increasing aboveground Prosopis C on clay loams, but increased with increasing Prosopis C on shallow clays. Total ANPP (Prosopis+herbaceous) of sites with the highest Prosopis basal area were 1.2 × and 4.0 × greater than those with the lowest Prosopis basal area on clay loam and shallow clay soils, respectively. Prosopis ANPP more than offset declines in herbaceous ANPP on clay loams and added to increased herbaceous ANPP on shallow clays. Although aboveground C and N pools increased substantially with Prosopis stand development, we found no corresponding change in surface soil C and N pools (0–10 cm). Overall, our findings indicate that Prosopis stand development significantly increases ecosystem C and N storage/cycling, and the magnitude of these impacts varied with stand age, soil type and functional plant traits     

Prosopis glandulosa and the nitrogen balance of rangelands: extent and occurrence of nodulation

Summary We report the recovery of root nodules from P. glandulosa var. glandulosa in the eastern portion of its range, where the species reaches its greatest vegetational development. Single cores 4.7 cm in diameter and up to 250 cm deep yielded from 0 to over 250 nodules. Nodules were found at all depths below 10 cm, with the highest concentration often around 100 cm. Detailed studies of three trees revealed relatively small volume densities of about 0.02 nodules cm^–3, high surface area densities of 2–4 nodules cm^–2, and high nodule biomass of 8–23 g m^–2, when compared to cultivated legumes. Nodules are small, weakly attached to roots that are seldom over 0.5 mm in diameter, and not easily observed under field conditions. No nodules were recovered from cores from the more arid western portion of P.glandulosa's range, although seedlings nodulated readily in these soils in the glasshouse as well as in most unamended soils from throughout mesquite's geographical range. Local differences in nodulating potential of soils included a negative association with mesquite canopies and a positive association with depth. These results suggest a significant role for biological fixation in the nitrogen regime and vegetation dynamics of Prosopis-dominated ecosystems.     

Data-driven estimation of nitric oxide emissions from global soils based on dominant vegetation covers

Soils are a major source of global nitric oxide (NO) emissions. However, estimates of soil NO emissions have large uncertainties due to limited observations and multifactorial impacts. Here, we mapped global soil NO emissions, integrating 1356 in-situ NO observations from globally distributed sites with high-resolution climate, soil, and management practice data. We then calculated global and national total NO budgets and revealed the contributions of cropland, grassland, and forest to global soil NO emissions at the national level. The results showed that soil NO emissions were explained mainly by N input, water input and soil pH. Total above-soil NO emissions of the three vegetation cover types were 9.4 Tg N year⁻¹ in 2014, including 5.9 Tg N year⁻¹ (1.04, 95% confidence interval [95% CI]: 0.09–1.99 kg N ha⁻¹ year⁻¹) emitted from forest, 1.7 Tg N year⁻¹ (0.68, 95% CI: 0.10–1.26 kg N ha⁻¹ year⁻¹) from grassland, and 1.8 Tg N year⁻¹ (0.98, 95% CI: 0.42–1.53 kg N ha⁻¹ year⁻¹) from cropland. Soil NO emissions in approximately 57% of 213 countries surveyed were dominated by forests. Our results provide updated inventories of global and national soil NO emissions based on robust data-driven models. These estimates are critical to guiding the mitigation of soil NO emissions and can be used in combination with biogeochemical models.     

Savanna woody encroachment is widespread across three continents

Tropical savannas are a globally extensive biome prone to rapid vegetation change in response to changing environmental conditions. Via a meta‐analysis, we quantified savanna woody vegetation change spanning the last century. We found a global trend of woody encroachment that was established prior the 1980s. However, there is critical regional variation in the magnitude of encroachment. Woody cover is increasing most rapidly in the remaining uncleared savannas of South America, most likely due to fire suppression and land fragmentation. In contrast, Australia has experienced low rates of encroachment. When accounting for land use, African savannas have a mean rate annual woody cover increase two and a half times that of Australian savannas. In Africa, encroachment occurs across multiple land uses and is accelerating over time. In Africa and Australia, rising atmospheric CO₂, changing land management and rainfall are likely causes. We argue that the functional traits of each woody flora, specifically the N‐fixing ability and architecture of woody plants, are critical to predicting encroachment over the next century and that African savannas are at high risk of widespread vegetation change.     

Evidence of Physiological Decoupling from Grassland Ecosystem Drivers by an Encroaching Woody Shrub

Shrub encroachment of grasslands is a transformative ecological process by which native woody species increase in cover and frequency and replace the herbaceous community. Mechanisms of encroachment are typically assessed using temporal data or experimental manipulations, with few large spatial assessments of shrub physiology. In a mesic grassland in North America, we measured inter- and intra-annual variability in leaf δ¹³C in Cornus drummondii across a grassland landscape with varying fire frequency, presence of large grazers and topographic variability. This assessment of changes in individual shrub physiology is the largest spatial and temporal assessment recorded to date. Despite a doubling of annual rainfall (in 2008 versus 2011), leaf δ¹³C was statistically similar among and within years from 2008-11 (range of −28 to −27‰). A topography*grazing interaction was present, with higher leaf δ¹³C in locations that typically have more bare soil and higher sensible heat in the growing season (upland topographic positions and grazed grasslands). Leaf δ¹³C from slopes varied among grazing contrasts, with upland and slope leaf δ¹³C more similar in ungrazed locations, while slopes and lowlands were more similar in grazed locations. In 2011, canopy greenness (normalized difference vegetation index – NDVI) was assessed at the centroid of individual shrubs using high-resolution hyperspectral imagery. Canopy greenness was highest mid-summer, likely reflecting temporal periods when C assimilation rates were highest. Similar to patterns seen in leaf δ¹³C, NDVI was highest in locations that typically experience lowest sensible heat (lowlands and ungrazed). The ability of Cornus drummondii to decouple leaf physiological responses from climate variability and fire frequency is a likely contributor to the increase in cover and frequency of this shrub species in mesic grassland and may be generalizable to other grasslands undergoing woody encroachment.     

Soil C and N responses to woody plant expansion in a mesic grassland

Changes in land management and reductions in fire frequency have contributed to increased cover of woody species in grasslands worldwide. These shifts in plant community composition have the potential to alter ecosystem function, particularly through changes in soil processes and properties. In semi-arid grasslands, the invasion of shrubs and trees is often accompanied by increases in soil resources and more rapid N and C cycling. We assessed the effects of shrub encroachment in a mesic grassland in Kansas (USA) on soil CO₂ flux, extractable inorganic N, and N mineralization beneath shrub communities (Cornus drummondii) and surrounding undisturbed grassland sites. In this study, a shift in plant community composition from grassland to shrubland resulted in a 16% decrease in annual soil CO₂ flux(4.78 kg CO₂ m^–2 year^–1 for shrub dominated sites versus 5.84 kg CO₂ m^–2 year^–1 for grassland sites) with no differences in total soil C or N or inorganic N. There was considerable variability in N mineralization rates within sites, which resulted in no overall difference in cumulative N mineralized during this study (4.09 g N m^–2 for grassland sites and 3.03 g N m^–2 for shrub islands). These results indicate that shrub encroachment into mesic grasslands does not significantly alter N availability (at least initially), but does alter C cycling by decreasing soil CO₂ flux.     

Managing Semi-Arid Rangelands for Carbon Storage: Grazing and Woody Encroachment Effects on Soil Carbon and Nitrogen

High grazing intensity and wide-spread woody encroachment may strongly alter soil carbon (C) and nitrogen (N) pools. However, the direction and quantity of these changes have rarely been quantified in East African savanna ecosystem. As shifts in soil C and N pools might further potentially influence climate change mitigation, we quantified and compared soil organic carbon (SOC) and total soil nitrogen (TSN) content in enclosures and communal grazing lands across varying woody cover i.e. woody encroachment levels. Estimated mean SOC and TSN stocks at 0–40 cm depth varied across grazing regimes and among woody encroachment levels. The open grazing land at the heavily encroached site on sandy loam soil contained the least SOC (30 ± 2.1 Mg ha^-1) and TSN (5 ± 0.57 Mg ha^-1) while the enclosure at the least encroached site on sandy clay soil had the greatest mean SOC (81.0 ± 10.6 Mg ha^-1) and TSN (9.2 ± 1.48 Mg ha^-1). Soil OC and TSN did not differ with grazing exclusion at heavily encroached sites, but were twice as high inside enclosure compared to open grazing soils at low encroached sites. Mean SOC and TSN in soils of 0–20 cm depth were up to 120% higher than that of the 21–40 cm soil layer. Soil OC was positively related to TSN, cation exchange capacity (CEC), but negatively related to sand content. Our results show that soil OC and TSN stocks are affected by grazing, but the magnitude is largely influenced by woody encroachment and soil texture. We suggest that improving the herbaceous layer cover through a reduction in grazing and woody encroachment restriction are the key strategies for reducing SOC and TSN losses and, hence, for climate change mitigation in semi-arid rangelands.