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1. Foliar nutrient concentrations of six northern hardwood species responded to nitrogen and phosphorus fertilization but did not predict tree growth

   https://doi.org/10.7717/peerj.13193  

   Hong, Daniel S. ; Gonzales, Kara E. ; Fahey, Timothy J. ; Yanai, Ruth D. ( January 2022 , PeerJ)

   Foliar chemistry can be useful for diagnosing soil nutrient availability and plant nutrient limitation. In northern hardwood forests, foliar responses to nitrogen (N) addition have been more often studied than phosphorus (P) addition, and the interactive effects of N and P addition have rarely been described. In the White Mountains of central New Hampshire, plots in ten forest stands of three age classes across three sites were treated annually beginning in 2011 with 30 kg N ha −1 y −1 or 10 kg P ha −1 y −1 or both or neither–a full factorial design. Green leaves of American beech ( Fagus grandifolia Ehrh.), pin cherry ( Prunus pensylvanica L.f.), red maple ( Acer rubrum L.), sugar maple ( A. saccharum Marsh.), white birch ( Betula papyrifera Marsh.), and yellow birch ( B. alleghaniensis Britton) were sampled pre-treatment and 4–6 years post-treatment in two young stands (last cut between 1988–1990), four mid-aged stands (last cut between 1971–1985) and four mature stands (last cut between 1883–1910). In a factorial analysis of species, stand age class, and nutrient addition, foliar N was 12% higher with N addition ( p < 0.001) and foliar P was 45% higher with P addition ( p <more »0.001). Notably, P addition reduced foliar N concentration by 3% ( p = 0.05), and N addition reduced foliar P concentration by 7% ( p = 0.002). When both nutrients were added together, foliar P was lower than predicted by the main effects of N and P additions ( p = 0.08 for N × P interaction), presumably because addition of N allowed greater use of P for growth. Foliar nutrients did not differ consistently with stand age class ( p  ≥ 0.11), but tree species differed ( p  ≤ 0.01), with the pioneer species pin cherry having the highest foliar nutrient concentrations and the greatest responses to nutrient addition. Foliar calcium (Ca) and magnesium (Mg) concentrations, on average, were 10% ( p < 0.001) and 5% lower ( p = 0.01), respectively, with N addition, but were not affected by P addition ( p = 0.35 for Ca and p = 0.93 for Mg). Additions of N and P did not affect foliar potassium (K) concentrations ( p = 0.58 for N addition and p = 0.88 for P addition). Pre-treatment foliar N:P ratios were high enough to suggest P limitation, but trees receiving N ( p = 0.01), not P ( p = 0.64), had higher radial growth rates from 2011 to 2015. The growth response of trees to N or P addition was not explained by pre-treatment foliar N, P, N:P, Ca, Mg, or K.« less
2. Measurement report: Leaf-scale gas exchange of atmospheric reactive trace species (NO₂, NO, O₃) at a northern hardwood forest in Michigan

   https://doi.org/10.5194/acp-20-11287-2020  

   Wang, Wei ; Ganzeveld, Laurens ; Rossabi, Samuel ; Hueber, Jacques ; Helmig, Detlev ( January 2020 , Atmospheric Chemistry and Physics)

   Abstract. During the Program for Research on Oxidants: PHotochemistry, Emissions, and Transport (PROPHET) campaign from 21 July to 3 August 2016,field experiments on leaf-level trace gas exchange of nitric oxide (NO), nitrogen dioxide (NO2), and ozone (O3) were conducted for thefirst time on the native American tree species Pinus strobus (eastern white pine), Acer rubrum (redmaple), Populus grandidentata (bigtooth aspen), and Quercus rubra (red oak) in a temperate hardwood forest inMichigan, USA. We measured the leaf-level trace gas exchange rates andinvestigated the existence of an NO2 compensation point, hypothesizedbased on a comparison of a previously observed average diurnal cycle ofNOx (NO2+NO) concentrations with that simulated using amulti-layer canopy exchange model. Known amounts of trace gases wereintroduced into a tree branch enclosure and a paired blank referenceenclosure. The trace gas concentrations before and after the enclosures weremeasured, as well as the enclosed leaf area (single-sided) and gas flow rate to obtain the trace gas fluxes with respect to leaf surface. There was nodetectable NO uptake for all tree types. The foliar NO2 and O3uptake largely followed a diurnal cycle, correlating with that of the leafstomatal conductance. NO2 and O3 fluxes were driven by theirconcentration gradient from ambient to leaf internal space. The NO2 lossmore »rate at the leaf surface, equivalently the foliar NO2 deposition velocity toward the leaf surface, ranged from 0 to 3.6 mm s−1 for bigtooth aspen and from 0 to 0.76 mm s−1 for red oak, both of which are∼90 % of the expected values based on the stomatalconductance of water. The deposition velocities for red maple and white pineranged from 0.3 to 1.6 and from 0.01 to 1.1 mm s−1, respectively, and were lower than predicted from the stomatal conductance, implying amesophyll resistance to the uptake. Additionally, for white pine, theextrapolated velocity at zero stomatal conductance was 0.4±0.08 mm s−1, indicating a non-stomatal uptake pathway. The NO2compensation point was ≤60 ppt for all four tree species andindistinguishable from zero at the 95 % confidence level. This agrees withrecent reports for several European and California tree species butcontradicts some earlier experimental results where the compensation pointswere found to be on the order of 1 ppb or higher. Given that the sampledtree types represent 80 %–90 % of the total leaf area at this site, theseresults negate the previously hypothesized important role of a leaf-scaleNO2 compensation point. Consequently, to reconcile these findings,further detailed comparisons between the observed and simulated in- and above-canopy NOx concentrations and the leaf- and canopy-scaleNOx fluxes, using the multi-layer canopy exchange model withconsideration of the leaf-scale NOx deposition velocities as well asstomatal conductances reported here, are recommended.« less
3. Tree variability limits the detection of nutrient treatment effects on sap flux density in a northern hardwood forest

   https://doi.org/10.7717/peerj.14410  

   Rice, Alexandrea M. ; Garrison-Johnston, Mariann T. ; Libenson, Arianna J. ; Yanai, Ruth D. ( January 2022 , PeerJ)

   The influence of nutrient availability on transpiration is not well understood, in spite of the importance of transpiration to forest water budgets. Soil nutrients have the potential to affect tree water use through indirect effects on leaf area or stomatal conductance. For example, following addition of calcium silicate to a watershed at Hubbard Brook, in New Hampshire, streamflow was reduced for 3 years, which was attributed to a 25% increase in evapotranspiration associated with increased foliar production. The first objective of this study was to quantify the effect of nutrient availability on sap flux density in a nitrogen, phosphorus, and calcium addition experiment in New Hampshire in which tree diameter growth, foliar chemistry, and soil nutrient availability had responded to treatments. We measured sap flux density in American beech ( Fagus grandifolia, Ehr.), red maple ( Acer rubrum L.), sugar maple ( Acer saccharum Marsh.), white birch ( Betula papyrifera Marsh.), or yellow birch (Betula alleghaniensis Britton.) trees, over five years of experiments in five stands distributed across three sites. In 2018, 3 years after a calcium silicate addition, sap flux density averaged 36% higher in trees in the treatment than the control plot, but this effect was not verymore »significant ( p = 0.07). Our second objective was to determine whether this failure to detect effects with greater statistical confidence was due to small effect sizes or high variability among trees. We found that tree-to-tree variability was high, with coefficients of variation averaging 39% within treatment plots. Depending on the species and year of the study, the minimum difference in sap flux density detectable with our observed variability ranged from 46% to 352%, for a simple ANOVA. We analyzed other studies reported in the literature that compared tree water use among species or treatments and found detectable differences ranging from 16% to 78%. Future sap flux density studies could benefit from power analyses to guide sampling intensity. Including pretreatment data, in the case of manipulative studies, would also increase statistical power.« less
4. Diet-Induced Plasticity of Linear Static Allometry Is Not So Simple for Grasshoppers: Genotype–Environment Interaction in Ontogeny Is Masked by Convergent Growth

   https://doi.org/10.1093/icb/icz137  

   Thompson, Daniel B. ( August 2019 , Integrative and Comparative Biology)

   Grasshoppers, Melanoplus sanguinipes (Orthoptera: Acrididae), develop larger head width (HW) and shorter leg length, relative to body size, when fed low nutrient, lignin-rich grasses compared to sibs fed a diet of high nutrient grasses. To elucidate how underlying genetic variation and plasticity of growth generate plasticity of this linear static allometry within coarse-grained environments, I measured head and leg size of three nymphal instars and adult grasshoppers raised on either a low or high nutrient diet within a half-sib quantitative genetic experiment. Doubly-multivariate repeated measures multiple analysis of variance (MANOVA) of head, mandible, and hind leg size and their rate of growth (mm/period) and growth period (days) through ontogeny were used to analyze how the ontogeny of diet-induced plasticity for these variables and additive genetic variation for plasticity (genotype × environment interaction [G×E]) contribute to plasticity in functional linear static allometry. Genetic variation for diet-induced plasticity (G×E) of head and leg size varied through ontogeny, as did genetic variation for plasticity of growth in third and fourth instar nymphs. Despite extensive genetic variation in plasticity of HW and leg length in fourth instar nymphs, the static allometry between head and leg was stable within each diet because the patternsmore »of G×E were similar for HW, leg length and their coordinated growth. Nutrient sensitive plasticity in growth shifted the intercept but not the slope of static allometry, a result consistent with one outcome of a graphical model of the relationships between G× E and plasticity of within environment static allometry. In addition, G×E of fourth instar head and leg size was reduced in adults by negatively size-dependent, convergent growth in the last period of ontogeny. Consequently, the bivariate reaction norms of head and leg size for adults exhibited no G×E and, again, plasticity in the intercept but not in the slope of static allometry. The ontogeny of seemingly simple diet-induced linear static allometry between functional body parts in grasshoppers arises from a complex combination of differing patterns of nutrient-sensitive growth, duration of growth, convergent growth, and G×E, all relevant to understanding the development and evolution of functional allometry in hemimetabolous insects.

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5. The hydraulic efficiency–safety trade‐off differs between lianas and trees

   https://doi.org/10.1002/ecy.2666  

   van der Sande, Masha T. ; Poorter, Lourens ; Schnitzer, Stefan A. ; Engelbrecht, Bettina M. J. ; Markesteijn, Lars ( April 2019 , Ecology)

   Hydraulic traits are important for woody plant functioning and distribution. Associations among hydraulic traits, other leaf and stem traits, and species’ performance are relatively well understood for trees, but remain poorly studied for lianas. We evaluated the coordination among hydraulic efficiency (i.e., maximum hydraulic conductivity), hydraulic safety (i.e., cavitation resistance), a suite of eight morphological and physiological traits, and species’ abundances for saplings of 24 liana species and 27 tree species in wet tropical forests in Panama. Trees showed a strong trade‐off between hydraulic efficiency and hydraulic safety, whereas efficiency and safety were decoupled in lianas. Hydraulic efficiency was strongly and similarly correlated with acquisitive traits for lianas and trees (e.g., positively with gas exchange rates and negatively with wood density). Hydraulic safety, however, showed no correlations with other traits in lianas, but with several in trees (e.g., positively with leaf dry matter content and wood density and negatively with gas exchange rates), indicating that in lianas hydraulic efficiency is an anchor trait because it is correlated with many other traits, while in trees both efficiency and safety are anchor traits. Traits related to shade tolerance (e.g., low specific leaf area and high wood density) were associated with highmore »local tree sapling abundance, but not with liana abundance. Our results suggest that different, yet unknown mechanisms determine hydraulic safety and local‐scale abundance for lianas compared to trees. For trees, the trade‐off between efficiency and safety will provide less possibilities for ecological strategies. For lianas, however, the uncoupling of efficiency and safety could allow them to have high hydraulic efficiency, and hence high growth rates, without compromising resistance to cavitation under drought, thus allowing them to thrive and outperform trees under drier conditions.

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