Belowground biomass, production, and carbon cycling in mature Norway spruce, Maine, U.S.A.

2003 ◽  
Vol 33 (2) ◽  
pp. 339-350 ◽  
Author(s):  
Christopher S Cronan

Two 55-year-old stands of Norway spruce (Picea abies (L.) Karst.) were sampled to determine belowground biomass, production and decomposition of fine and small roots, litterfall and litter decay rates, soil respiration rates, and carbon cycling patterns. Mean biomass of live fine (<1 mm) Norway spruce roots to a soil depth of 40 cm was 359 ash-free dry g·m–2, whereas biomass of live fine + small roots ([Formula: see text]3 mm) amounted to 561 g·m–2. Mean root production averaged 297 g·m–2·year–1 for roots <1 mm and 418 g·m–2·year–1 for roots [Formula: see text]3 mm. By comparison, needle litter production was 205 g·m–2·year–1. Norway spruce roots [Formula: see text]3 mm decomposed at a rate of 9.5% of total root mass per month during the growing season, compared with a needle litter annual decay rate of 22.3%·year–1. A partial carbon budget for Norway spruce indicated that annual needle litterfall mass was 98 g C·m–2·year–1, and annual carbon release from fresh litter decay was approximately 22 g·C·m–2·year–1. During the growing season, monthly CO2 flux from soil respiration was 69 g C·m–2·month–1, belowground C allocation to net production of roots [Formula: see text]3 mm was 33.5 g C·m–2·month–1, and C release from decomposition of roots [Formula: see text]3 mm was 31 g C·m–2·month–1. These values were also extrapolated to annual estimates of C fluxes.

Forests ◽  
2020 ◽  
Vol 11 (9) ◽  
pp. 943
Author(s):  
Katri Nissinen ◽  
Virpi Virjamo ◽  
Antti Kilpeläinen ◽  
Veli-Pekka Ikonen ◽  
Laura Pikkarainen ◽  
...  

We studied the growth responses of boreal Scots pine (Pinus sylvestris L.), Norway spruce (Picea abies L. Karst.) and silver birch (Betula pendula Roth) seedlings to simulated climate warming of an average of 1.3 °C over the growing season in a controlled field experiment in central Finland. We had six replicate plots for elevated and ambient temperature for each tree species. The warming treatment lasted for the conifers for three growing seasons and for the birch two growing seasons. We measured the height and diameter growth of all the seedlings weekly during the growing season. The shoot and root biomass and their ratios were measured annually in one-third of seedlings harvested from each plot in autumn. After two growing seasons, the height, diameter and shoot biomass were 45%, 19% and 41% larger in silver birch seedlings under the warming treatment, but the root biomass was clearly less affected. After three growing seasons, the height, diameter, shoot and root biomass were under a warming treatment 39, 47, 189 and 113% greater in Scots pine, but the root:shoot ratio 29% lower, respectively. The corresponding responses of Norway spruce to warming were clearly smaller (e.g., shoot biomass 46% higher under a warming treatment). As a comparison, the relative response of height growth in silver birch was after two growing seasons equal to that measured in Scots pine after three growing seasons. Based on our findings, especially silver birch seedlings, but also Scots pine seedlings benefitted from warming, which should be taken into account in forest regeneration in the future.


Land ◽  
2021 ◽  
Vol 10 (8) ◽  
pp. 805
Author(s):  
Delanie M. Spangler ◽  
Anna Christina Tyler ◽  
Carmody K. McCalley

Wetland ecosystems play a significant role in the global carbon cycle, and yet are increasingly threatened by human development and climate change. The continued loss of intact freshwater wetlands heightens the need for effective wetland creation and restoration. However, wetland structure and function are controlled by interacting abiotic and biotic factors, complicating efforts to replace ecosystem services associated with natural wetlands and making ecologically-driven management imperative. Increasing waterfowl populations pose a threat to the development and persistence of created wetlands, largely through intensive grazing that can shift vegetation community structure or limit desired plant establishment. This study capitalized on a long-term herbivore exclusion experiment to evaluate how herbivore management impacts carbon cycling and storage in a created wetland in Western New York, USA. Vegetation, above- and belowground biomass, soil carbon, carbon gas fluxes and decomposition rates were evaluated in control plots with free access by large grazers and in plots where grazers had been excluded for four years. Waterfowl were the dominant herbivore at the site. Grazing reduced peak growing season aboveground biomass by over 55%, and during the summer, gross primary productivity doubled in grazer exclusion plots. The shift in plant productivity led to a 34% increase in soil carbon after exclusion of grazers for five growing seasons, but no change in belowground biomass. Our results suggest that grazers may inhibit the development of soil carbon pools during the first decade following wetland creation, reducing the carbon sequestration potential and precluding functional equivalence with natural wetlands.


2017 ◽  
Vol 114 (24) ◽  
pp. 6322-6327 ◽  
Author(s):  
Christine V. Hawkes ◽  
Bonnie G. Waring ◽  
Jennifer D. Rocca ◽  
Stephanie N. Kivlin

Ecosystem carbon losses from soil microbial respiration are a key component of global carbon cycling, resulting in the transfer of 40–70 Pg carbon from soil to the atmosphere each year. Because these microbial processes can feed back to climate change, understanding respiration responses to environmental factors is necessary for improved projections. We focus on respiration responses to soil moisture, which remain unresolved in ecosystem models. A common assumption of large-scale models is that soil microorganisms respond to moisture in the same way, regardless of location or climate. Here, we show that soil respiration is constrained by historical climate. We find that historical rainfall controls both the moisture dependence and sensitivity of respiration. Moisture sensitivity, defined as the slope of respiration vs. moisture, increased fourfold across a 480-mm rainfall gradient, resulting in twofold greater carbon loss on average in historically wetter soils compared with historically drier soils. The respiration–moisture relationship was resistant to environmental change in field common gardens and field rainfall manipulations, supporting a persistent effect of historical climate on microbial respiration. Based on these results, predicting future carbon cycling with climate change will require an understanding of the spatial variation and temporal lags in microbial responses created by historical rainfall.


2018 ◽  
Vol 40 (2) ◽  
pp. 153 ◽  
Author(s):  
Xuexia Wang ◽  
Yali Chen ◽  
Yulong Yan ◽  
Zhiqiang Wan ◽  
Ran Chao ◽  
...  

The response of soil respiration to simulated climatic warming and increased precipitation was evaluated on the arid–semi-arid Stipa steppe of Inner Mongolia. Soil respiration rate had a single peak during the growing season, reaching a maximum in July under all treatments. Soil temperature, soil moisture and their interaction influenced the soil respiration rate. Relative to the control, warming alone reduced the soil respiration rate by 15.6 ± 7.0%, whereas increased precipitation alone increased the soil respiration rate by 52.6 ± 42.1%. The combination of warming and increased precipitation increased the soil respiration rate by 22.4 ± 11.2%. When temperature was increased, soil respiration rate was more sensitive to soil moisture than to soil temperature, although the reverse applied when precipitation was increased. Under the experimental precipitation (20% above natural rainfall) applied in the experiment, soil moisture was the primary factor limiting soil respiration, but soil temperature may become limiting under higher soil moisture levels.


2006 ◽  
Vol 55 (1) ◽  
pp. 59-68 ◽  
Author(s):  
Ferenc Ács ◽  
H. Breuer

The climatology of soil respiration in Hungary is presented. Soil respiration is estimated by a Thornthwaite-based biogeochemical model using soil hydrophysical data and climatological fields of precipitation and air temperature. Soil respiration fields are analyzed for different soil textures (sand, sandy loam, loam, clay loam and clay) and time periods (year, growing season and months).  Strong linear relationships were found between soil respiration and the actual evapotranspiration for annual and growing season time periods. In winter months soil respiration is well correlated with air temperature, while in summer months there is a quite variable relationship with water balance components. The strength of linear relationship between soil respiration and climatic variables is much better for coarser than for finer soil texture.


Forests ◽  
2021 ◽  
Vol 12 (10) ◽  
pp. 1427
Author(s):  
Chunju Cai ◽  
Zhihan Yang ◽  
Liang Liu ◽  
Yunsen Lai ◽  
Junjie Lei ◽  
...  

Nitrogen (N) deposition has been well documented to cause substantial impacts on ecosystem carbon cycling. However, the majority studies of stimulating N deposition by direct N addition to forest floor have neglected some key ecological processes in forest canopy (e.g., N retention and absorption) and might not fully represent realistic atmospheric N deposition and its effects on ecosystem carbon cycling. In this study, we stimulated both canopy and understory N deposition (50 and 100 kg N ha−1 year−1) with a local atmospheric NHx:NOy ratio of 2.08:1, aiming to assess whether canopy and understory N deposition had similar effects on soil respiration (RS) and net ecosystem production (NEP) in Moso bamboo forests. Results showed that RS, soil autotrophic (RA), and heterotrophic respiration (RH) were 2971 ± 597, 1472 ± 579, and 1499 ± 56 g CO2 m−2 year−1 for sites without N deposition (CN0), respectively. Canopy and understory N deposition did not significantly affect RS, RA, and RH, and the effects of canopy and understory N deposition on these soil fluxes were similar. NEP was 1940 ± 826 g CO2 m−2 year−1 for CN0, which was a carbon sink, indicating that Moso bamboo forest the potential to play an important role alleviating global climate change. Meanwhile, the effects of canopy and understory N deposition on NEP were similar. These findings did not support the previous predictions postulating that understory N deposition would overestimate the effects of N deposition on carbon cycling. However, due to the limitation of short duration of N deposition, an increase in the duration of N deposition manipulation is urgent and essential to enhance our understanding of the role of canopy processes in ecosystem carbon fluxes in the future.


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