Dergiler / Turkish Journal of Agriculture and Forestry / 2020 / Cilt: 44 - Sayı: 4

Elevated in-soil CO2affects physiology and growth of Pinus densiflora and Quercus variabilis seedlings under an artificial CO2release experiment

Sayfa
339–349
Yayın Tarihi
2022-10-19
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Q. variabilis showed an increase in mortality, with a low percentage of fine root (

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:It is important to understand how woody species are affected by elevated in-soil CO2 for carbon capture and storage (CCS).
📊
Temel Bulgular & Veri:Astudy was conducted to analyze the effects of artificially released in-soil CO2 on the physiology and growth of 4-year-old Pinus densifloraand 3-year-old Quercus variabilis seedlings.
💡
Sonuç & Katkı:Q. variabilis showed an increase in mortality, with a low percentage of fine root (
🔬Tür:Araştırma Makalesi
📍Kapsam:2017 Verileri
⚙️Değişkenler:Alan Parametreleri

Abstract

It is important to understand how woody species are affected by elevated in-soil CO2 for carbon capture and storage (CCS). Astudy was conducted to analyze the effects of artificially released in-soil CO2 on the physiology and growth of 4-year-old Pinus densifloraand 3-year-old Quercus variabilis seedlings. Approximately 7.9 kg CO2 plot–1 d–1 was released at a depth of 0.5 m over the period from20 June to 20 July 2017. For both species, chlorophyll fluorescence and content, photosynthetic rate, and leaf size significantly decreasedafter the CO2 release. However, stomatal behavior varied between these species under the elevated in-soil CO2 conditions. Elevatedin-soil CO2 inhibited plant physiological functions by limiting available in-soil O2. The leaf size of treatment plots showed significantlylower values of 0.60 ± 0.05 cm2 for P. densiflora and 12.05 ± 1.47 cm2 for Q. variabilis compared to those of control plots of 0.90 ± 0.09cm2 for P. densiflora and 21.84 ± 3.62 cm2 for Q. variabilis, whereas the number of leaves increased from 2697 ± 153 leaves to 3121 ±255 leaves for P. densiflora and from 95 ± 4 leaves to 288 ± 52 leaves for Q. variabilis. It was found that the decrease in leaf size resultedin a second flush, which increased the total leaf area per seedling. The biomass of P. densiflora significantly decreased in the treatmentplots (P < 0.05). Q. variabilis showed an increase in mortality, with a low percentage of fine root (

🔖

Bu Makaleye Atıf Yap

CHANG, H., HAN, S. H., KIM, S., SON, Y., KIM, H. J. (2022). Elevated in-soil CO2affects physiology and growth of Pinus densiflora and Quercus variabilis seedlings under an artificial CO2release experiment. Turkish Journal of Agriculture and Forestry, Cilt: 44 - Sayı: 4, 339–349. https://ajindex.com/articles/599154

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (9)

  1. Attia Z, Domec J-C, Oren R, Way DA, Moshelion M (2015). Growth and physiological responses of isohydric and anisohydric poplars to drought. Journal of Experimental Botany 66: 4373- 4381. Austin MP, Groves RH, Fresco LMF, Laye PE (1986). Relative growth of six thistle species along a nutrient gradient with multispecies competition. Journal of Ecology 73: 667-684.
  2. Bachu S (2000). Sequestration of CO2 in geologic media: criteria and approaches for site selection in response to climate change. Energy Conversion and Management 41: 953-970.
  3. Barnes JD, Balaguer L, Manrique E, Elvira S, Davison AW (1992). A reappraisal of the use of DMSO for the extraction and determination of chlorophylls a and b in lichens and higher plants. Environmental and Experimental Botany 32: 85-100.
  4. Bellante GJ, Powell SL, Lawrence RL, Repasky KS, Dougher T (2014). Hyperspectral detection of a subsurface CO2 leak in the presence of water stressed vegetation. PLoS ONE 9: e108299. Benson SM, Gasperikova E, Hoversten GM (2005). Monitoring protocols and life-cycle costs for geologic storage of carbon dioxide. In: Proceedings of the 7th International Conference on Greenhouse Gas Control Technologies (GHGT-7): 1259-1266.
  5. Borchert R (1975). Endogenous shoot growth rhythms and indeterminate shoot growth in Oak. Physiologia Plantarum 35: 152-157.
  6. Brooks TJ, Wall GW, Pinter Jr PJ, Kimball BA, LaMorte RL et al. (2000). Acclimation response of spring wheat in a freeair CO2 enrichment (FACE) atmosphere with variable soil nitrogen regimes. 3. Canopy architecture and gas exchange. Photosynthesis Research 66: 97-108.
  7. Buckley TN (2005). The control of stomata by water balance. New Phytologist 168: 275-292.
  8. Byun J, Lee W, Nor D, Kim S, Choi J et al. (2010). The relationship between tree radial growth and topographic and climate factors in red pine and oak in central regions of Korea. Journal of Korean Forestry Society 99: 908-913 (in Korean with English abstract). Casper BB, Forseth IN, Kempenich H, Seltzer S, Xavier K (2001). Drought prolongs leaf life span in the herbaceous desert perennial Crytantha flave. Functional Ecology 15: 740-747.
  9. Chapman SP, Paget CM, Johnson GN, Schwartz JM (2015). Flux balance analysis reveals acetate metabolism modulates cyclic electron flow and alternative glycolytic pathways in Chlamydomonas reinhardtii. Frontiers in Plant Science 6: 474. Comstock JP (2002). Hydraulic and chemical signaling in the control of stomatal conductance and transpiration. Journal of Experimental B