Tree rings are thought to be a powerful tool to reconstruct historical growth changes and have been widely used to assess tree responses to global warming. Demographic inferences suggest, however, that typical sampling procedures induce spurious trends in growth reconstructions. Here we use the world’s largest single tree-ring dataset (283,536 trees from 136,621 sites) from Quebec, Canada, to assess to what extent growth reconstructions based on these - and thus any similar - data might be affected by this problem. Indeed, straightforward growth rate reconstructions based on these data suggest a six-fold increase in radial growth of black spruce (Picea mariana) from ~0.5 mm yr⁻¹ in 1800 to ~2.5 mm yr⁻¹ in 1990. While the strong correlation (R² = 0.98) between this increase and that of atmospheric CO₂ could suggest a causal relationship, we here unambiguously demonstrate that this growth trend is an artefact of sampling biases caused by the absence of old, fast-growing trees (cf. “slow-grower survivorship bias”) and of young, slow-growing trees (cf. “big-tree selection bias”) in the dataset. At the moment, we cannot envision how to remedy the issue of incomplete representation of cohorts in existing large-scale tree-ring datasets. Thus, innovation will be needed before such datasets can be used for growth rate reconstructions.

The cycling of base cations (K, Ca, Mg, and Na) was investigated in a boreal balsam fir forest (the Lake Laflamme Watershed) between 1999 and 2005. Base cation budgets were calculated for the soil rooting zone that included atmospheric deposition and soil leaching losses, two scenarios of tree uptake (whole‐tree and stem‐only harvesting), and three scenarios of mineral weathering, leading to six different scenarios. In every scenario there was a net accumulation of Mg within the soil exchangeable reservoir, while Ca accumulated in four scenarios. Potassium was lost in five of the six scenarios. Contrary to Ca and Mg, immobilization of K within tree biomass (69 mol·ha⁻¹·yr⁻¹) was the main pathway of K losses from the soil exchangeable reservoir, being five times higher than losses via soil leaching (14 mol·ha⁻¹·yr⁻¹). The amounts of K contained within the aboveground biomass and the exchangeable soil reservoir were 3.3 kmol/ha and 4.2 kmol/ha, respectively. Whole‐tree harvesting may thus remove 44% of the K that is readily available for cycling in the short term, making this forest sensitive to commercial forestry operations. Similar values of annual K uptake as well as a similar distribution of K between tree biomass and soil exchangeable reservoirs at 14 other coniferous sites, distributed throughout the boreal forest of Québec, suggest that the Lake Laflamme Watershed results can be extrapolated to a much larger area. Stem‐only harvesting, which would reduce K exports due to biomass removal by 60%, should be used for these types of forest.

Tree growth and longevity trade-offs fundamentally shape the terrestrial carbon balance. Yet, we lack a unified understanding of how such trade-offs vary across the world’s forests. By mapping life history traits for a wide range of species across the Americas, we reveal considerable variation in life expectancies from 10 centimeters in diameter (ranging from 1.3 to 3195 years) and show that the pace of life for trees can be accurately classified into four demographic functional types. We found emergent patterns in the strength of trade-offs between growth and longevity across a temperature gradient. Furthermore, we show that the diversity of life history traits varies predictably across forest biomes, giving rise to a positive relationship between trait diversity and productivity. Our pan-latitudinal assessment provides new insights into the demographic mechanisms that govern the carbon turnover rate across forest biomes.