Fine root biomass under light gap openings in an Amazon rain forest

Oecologia ◽  
1990 ◽  
Vol 83 (4) ◽  
pp. 541-545 ◽  
Author(s):  
Robert L. Sanford
2010 ◽  
Vol 27 (1) ◽  
pp. 73-81 ◽  
Author(s):  
Markus Adamek ◽  
Marife D. Corre ◽  
Dirk Hölscher

Abstract:Nitrogen (N) availability is a major control on fine-root growth and distribution with depth in forest soils. We investigated fine-root dynamics in response to N addition in a montane rain forest with N-limited above-ground production. Control and N-fertilized (125 kg urea-N ha−1 y−1) treatments were laid out in a paired-plot design with four replicates (each 40 × 40 m). During 1.5 y of treatment, fine root-biomass, necromass and production were assessed by sequential coring at three soil depths (organic layer, 0–10 cm and 10–20 cm mineral soil), whereas fine-root redistribution with depth was assessed by ingrowth cores. Total fine-root biomass, necromass and production in the controls were 458 ± 21 g m−2, 101 ± 9 g m−2 and 324 ± 33 g m−2 y−1, respectively. No significant difference at any depth was detected under N fertilization. Fine-root biomass in the organic layer decreased over time under N addition. At 10–20 cm in the mineral soil, fine-root biomass in ingrowth cores increased significantly after 1.5 y of N fertilization compared with the control. The increased available N may have induced the change in fine-root distribution to explore the deeper mineral soil for other nutrients which may cause additional limitation to above-ground production once N limitation is alleviated.


2013 ◽  
Vol 36 (7) ◽  
pp. 645-654 ◽  
Author(s):  
Yun-Ke LIU ◽  
Chuan FAN ◽  
Xian-Wei LI ◽  
Yin-Hua LING ◽  
Yi-Gui ZHOU ◽  
...  

2021 ◽  
Vol 130 ◽  
pp. 108031
Author(s):  
Wen Li ◽  
Yifei Shi ◽  
Dandan Zhu ◽  
Wenqian Wang ◽  
Haowei Liu ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Tina Unuk Nahberger ◽  
Gian Maria Niccolò Benucci ◽  
Hojka Kraigher ◽  
Tine Grebenc

AbstractSpecies of the genus Tuber have gained a lot of attention in recent decades due to their aromatic hypogenous fruitbodies, which can bring high prices on the market. The tendency in truffle production is to infect oak, hazel, beech, etc. in greenhouse conditions. We aimed to show whether silver fir (Abies alba Mill.) can be an appropriate host partner for commercial mycorrhization with truffles, and how earthworms in the inoculation substrate would affect the mycorrhization dynamics. Silver fir seedlings inoculated with Tuber. aestivum were analyzed for root system parameters and mycorrhization, how earthworms affect the bare root system, and if mycorrhization parameters change when earthworms are added to the inoculation substrate. Seedlings were analyzed 6 and 12 months after spore inoculation. Mycorrhization with or without earthworms revealed contrasting effects on fine root biomass and morphology of silver fir seedlings. Only a few of the assessed fine root parameters showed statistically significant response, namely higher fine root biomass and fine root tip density in inoculated seedlings without earthworms 6 months after inoculation, lower fine root tip density when earthworms were added, the specific root tip density increased in inoculated seedlings without earthworms 12 months after inoculation, and general negative effect of earthworm on branching density. Silver fir was confirmed as a suitable host partner for commercial mycorrhization with truffles, with 6% and 35% mycorrhization 6 months after inoculation and between 36% and 55% mycorrhization 12 months after inoculation. The effect of earthworms on mycorrhization of silver fir with Tuber aestivum was positive only after 6 months of mycorrhization, while this effect disappeared and turned insignificantly negative after 12 months due to the secondary effect of grazing on ectomycorrhizal root tips.


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