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Interspecies specific interactions are generally regarded as drivers of plant productivity in multispecies agroecosystems. Complementary use of resource in diverse communities can enhance community productivity through optimal use of plant-available resources and positive interactions such as facilitation can ameliorate high abiotic stress conditions. We studied the effects on physiological response, leaf traits and water use efficiency of a multifunctional species intercropping system consisting of peanut (Arachis hypogaea L.), watermelon [Citrullus lanatus (Thunb.) Matsum. & Nakai], okra [Abelmoschus esculentus (L.) Moench], cowpea [Vigna unguiculata (L.) Walp.], and pepper (Capsicum annuum L.) planted alone or in various intercropping combinations in a low fertilizer input system in the peak of summer heat in Texas. Differences in gas exchange measurements were detected only in watermelon in year 2 of the study when okra was the dominant crop. This same year watermelon specific leaf area (SLA) was significantly higher when okra was present in a treatment and particularly in the three and four species combinations, Wpwo and Wpwoc, 27.5 and 31.0 m2 kg−1, respectively, as compared to watermelon grown in monoculture, strip intercropped with peanut (Spw) and within row intercropped with peanut (Wpw), 20.4, 20.1, and 19.8 m2 kg−1, respectively. This corresponds with an increase watermelon leaf N concentration and a decrease in leaf C:N ratio in Wpwo and Wpwoc treatments. No differences in d13C composition, a measure of water use efficiency over the leaf lifespan, were detected across cropping system for each species. Water use efficiency based on per plant production (WUEyield) indicated an increase in water use efficiency in dominant crops such as watermelon in 2011 and okra in 2012, but a reduction in WUEyield subordinate crops such as cowpea and pepper both years of the study. Peanut grown in monoculture and strip intercropped with watermelon had significantly lower leaf water potential values in 2012, −2.2 and −2.1 MPa, respectively, as compared to intercropping systems increasing in level of integration (Wpw = − 1.1, Wpwo = − 0.6, Wpwoc = − 1.3, Wall = −1.1 MPa), indicating peanut benefited from alterations to microclimate and facilitative interactions with companion crops in some intercropping systems through a reduction in plant water stress. The results from this study suggest there may be a benefit to a multifunctional intercropping system in the form of increased food production per unit of water input in dominant crops and reduced water stress for some component species. This is important to producers; showing a method to increase overall crop production without increasing water inputs.

Premise While root-order approaches to fine-root classification have shown wide utility among wild plants, they have seen limited use for perennial crop plants. Moreover, inadequate characterization of fine roots across species of domesticated perennial crops has led to a knowledge gap in the understanding of evolutionary and functional patterns associated with different fine-root orders. Methods We examined fine-root traits of common horticultural fruit and nut crops: Malus ×domestica, Prunus persica, Vitus vinifera, Prunus dulcis, and Citrus ×clementina. Additional roots were sampled from 33 common perennial horticultural crops, native to tropical, subtropical, and temperate regions, to examine variation in 1st- and 2nd-order absorptive roots. Results First-order roots of grape and 1st- and 2nd-order roots of apple and peach were consistently thin, nonwoody, mycorrhizal, and had high N:C ratios. In contrast, 4th- and 5th-order roots of grape and 5th-order roots of apple and peach were woody, nonmycorrhizal, had low N:C ratios, and were thicker than lower-order roots. Among the 33 horticultural species, diameter of 1st- and 2nd-order roots varied about 15-fold, ranging from 0.04 to 0.60 mm and 0.05 to 0.89 mm respectively. This variation generally was phylogenetically conserved across plant lineages. Conclusions Collectively, our research shows that root-order characterization has considerably more utility than an arbitrary diameter cutoff for identifying roots of different functions in perennial horticultural crops. In addition, much of the variation in root diameter among species can be predicted by evolutionary relationships.

A greenhouse study was conducted to evaluate the growth and development of poinsettia ‘Prestige Red’ (Euphorbia pulcherrima) grown in a commercial peat-based potting mix (Sunshine Mix #1) amended with biochar at 0%, 20%, 40%, 60%, 80%, or 100% (by volume) at four different fertigation regimes: F1: 100 to 200 mg·L−1 nitrogen (N), F2: 200 to 300 mg·L−1 N (control), F3: 300 to 400 mg·L−1 N, or F4: 400 to 500 mg·L−1 N. The experiment was a two-factor factorial design with 10 replications for each combination of biochar by fertigation. As the percentage of biochar increased, root substrate pore space and bulk density increased, while container capacity decreased. Root rot and red bract necrosis only occurred in F4 combined with 100% biochar. Plants grown in 40% biochar had a similar growth and development to those in 0% biochar. Up to 80% biochar, plants exhibited no significant change, except in terms of dry weight, which decreased at higher biochar percentages (60% and 80%). In summary, at a fertigation rate of 100 mg·L−1 N to 400 mg·L−1 N, up to 80% biochar could be used as an amendment to peat-based root substrate with acceptable growth reduction and no changes in quality.

This research shows that elevated CO2, climate warming, and management impact shoot and root nitrogen concentrations in different ways in managed pastures. Management (clipping frequency) had the strongest impact on aboveground tissue N concentrations, while the impact of the climate change drivers on shoot N concentration was interactive and varied seasonally. Green leaf N concentrations were decreased by elevated CO2 and increased by more frequent clipping. Both warming treatments increased leaf N concentrations under ambient CO2 concentrations, but did not significantly alter leaf N concentrations under elevated CO2 concentrations. Fine root N concentrations were mostly unaffected by the treatments, although elevated CO2 decreased root N concentration in deeper soil layers. The interactive nature of the climate change drivers through time, as well as the fact that root N concentration response to the treatments was entirely different from aboveground responses, highlights the complexity in predicting plant N nutrition responses to projected climate change., Forecasting the effects of climate change on nitrogen (N) cycling in pastures requires an understanding of changes in tissue N. We examined the effects of elevated atmospheric CO2 concentration, atmospheric warming and simulated grazing (clipping frequency) on aboveground and belowground tissue N concentrations and C : N ratios of a C3 pasture grass. Phalaris aquatica L. cv. ‘Holdfast’ was grown in the field in six transparent temperature gradient tunnels (18 × 1.5 × 1.5 m each), three at ambient atmospheric CO2 and three at 759 p.p.m. CO2. Within each tunnel, there were three air temperature treatments: ambient control, +2.2/+4.0 °C above ambient day/night warming and +3.0 °C continuous warming. A frequent and an infrequent clipping treatment were applied to each warming × CO2 combination. Green leaf N concentrations were decreased by elevated CO2 and increased by more frequent clipping. Both warming treatments increased leaf N concentrations under ambient CO2 concentrations, but did not significantly alter leaf N concentrations under elevated CO2 concentrations. Nitrogen resorption from leaves was decreased under elevated CO2 conditions as well as by more frequent clipping. Fine root N concentrations decreased strongly with increasing soil depth and were further decreased at the 10–60 cm soil depths by elevated CO2 concentrations. The interaction between the CO2 and warming treatments showed that leaf N concentration was affected in a non-additive manner. Changes in leaf C : N ratios were driven by changes in N concentration. Overall, the effects of CO2, warming and clipping treatments on aboveground tissue N concentrations were much greater than on belowground tissue.

Summary • This study examined the effects of warming, elevated atmospheric CO 2 and cutting regimen on the growth of Phalaris aquatica cv. Holdfast swards. • Six temperature gradient tunnels (TGT) were used to manipulate both air temperature and atmospheric CO 2 concentrations (ambient and 750 ppm). Within each tunnel, there were three temperature treatments: no warming, constant warming of +3.0 ° C and a daytime warming of 2.2 ° C combined with a night-time warming of 4.0 ° C and two defoliation frequencies. •A veraged across 20 months of growth, there was a positive effect of elevated atmospheric CO 2 (+11%), no effect of either warming treatment and a negative effect of frequent cutting ( − 19%) on total above ground biomass production. The responses to all treatments, however, were strongly seasonal. • Positive responses to CO 2 were statistically significant only in the spring, when plant growth was strongest. No evidence was found that high night-time warming had different effects on plant growth and plant responses to elevated atmospheric CO 2 , than constant warming.

Polar-desert plants experience low average air temperatures during their short growing season (4–8 °C mean July temperature). In addition, low availability of inorganic nitrogen in the soil may also limit plant growth. Our goals were to elucidate which N sources can be acquired by polar-desert plants, and how growth and N-uptake are affected by low growth temperatures. We compared rates of N-uptake and increases in mass and leaf area of two polar-desert species (Cerastium alpinum L. and Saxifraga caespitosa L.) over a period of 3 weeks when grown at two temperatures (6 °C vs. 15 °C) and supplied with either glycine, NH4 + or NO3 −. At 15 °C, plants at least doubled their leaf area, whereas there was no change in leaf area at 6 °C. Measured mean N-uptake rates varied between 0.5 nmol g−1 root DM s−1 on glycine at 15 °C and 7.5 nmol g−1 root DM s−1 on NH4 + at 15 °C. Uptake rates based upon increases in mass and tissue N concentrations showed that plants had a lower N-uptake rate at 6 °C, regardless of N source or species. We conclude that these polar-desert plants can use all three N sources to increase their leaf area and support flowering when grown at 15 °C. Based upon short-term (8 h) uptake experiments, we also conclude that the short-term capacity to take up inorganic or organic N is not reduced by low temperature (6 °C). However, net N-uptake integrated over a three-week period is severely reduced at 6 °C.

ently maintain or very quickly recover P and water uptake capacity. This behaviour is consistent with an The effects of prolonged exposure to dry surface soil overall rooting strategy where essentially no surface on the capacity of roots to take up water and phos- roots are shed following prolonged exposure to dry phorus were examined in mycorrhizal sour orange soil. (Citrus aurantium L.) seedlings grown in pots with upper and lower portions separated hydraulically. In Key words: Drought, split-root, 32P, citrus, uptake kinetics, the first experiment, upper portions of the pots were phosphorus uptake, water uptake, sour orange, Citrus either irrigated every 2‐3 d, droughted for 14 d, aurantium. droughted for 43 d, or droughted for 42 d followed by 8 d re-irrigation. Lower portions of the pots were irrig- Introduction ated and fertilized every 2‐3 d. Phosphorus uptake capacity was estimated in excised roots using 32 Pi n The soil surface layers, with their accumulation of roots, aerated 50, 750, and 1500 mM P solutions. Exposure organic matter and nutrients, commonly undergo large to dry soil had no appreciable effect on P uptake fluctuations in temperature, water content, and nutrient capacity. In the second experiment, the ability of intact availability. These fluctuations promote pulses of nutrient roots to acquire water and P in the 8 d following release by increasing microbial biomass turnover (Reid, rewatering after roots were exposed to localized 1974; Stark, 1994; Cui and Caldwell, 1997). Moisture drought for 14 and 43 d was examined. Roots were and temperature fluctuations may cause opportunities for observed non-destructively using small transparent nutrient uptake by roots in the litter, organic and surface tubes (2 cm diameter) and a rigid borescope. Soil water mineral layers to be brief and unpredictable (Grime, depletion was monitored using time-domain reflectro- 1994). There are at least two basic strategies for exploiting metry. Phosphorus (32P) was added at various depths resources in soil surface layers that periodically dry and in the soil in the upper compartment and uptake was which may develop high temperatures. One strategy is to assessed by non-destructively counting beta particle grow rapidly relatively thin inexpensive roots that have emissions from leaves using a scintillation probe. high absorptive capacity when the soil is wet, and then Similar to the first experiment, localized drought had rapidly shed these roots when the soil becomes dry or no effect on P uptake and soil water depletion in citrus otherwise unfavourable. This kind of root strategy is roots compared to continuously irrigated plants. Water commonly found in hot desert climates with desert succuand P uptake in the first few days apparently occurred lents (Huang and Nobel, 1992) and in certain desert from existing roots because of delayed production of half-shrubs like Cryptantha (personal observation). In new roots in the droughted treatment. Thus, citrus addition, many annual crops seem to exhibit this strategy ( Eissenstat and Yanai, 1997). roots exposed to extended periods of dry soil appar

Aquatic seedlings of Ranunculus peltatus Schrank were subjected to three levels of droughl (dry, saturated and flooded) at two different phenological stages, vegetative stage and at onset of flowering. Changes in growth form, timing of flowering, number of flowers and fiuits and the number of seeds per fruit were monitored to test the effect of drought on reproduction. Plants that were transferred to a terrestrial, but water-saturated, environment at a vegetative stage rapidly changed from an aquatic, spreading, elongated growth form to a prostrate growth form and produced only slightly fewer seeds per pot (86) than the flooded control plants (93). Total seed production was decreased by 1000 seeds per pot in both saturated treatments compared to the control treatment. There was no significant difference in total seed production between plants encountering drought at a vegetative or a flowering stage (2471 vs. 2348 seeds per pot). Plants subjected to air drying of the soil (no water added) at both phenological stages changed growth form, but flower, fruit and seed production was negligible. The fact that total seed production was still relatively high under water-saturated conditions at both phenological stages may explains partially why this species is successful in temporary marshes where drought often occurs during its lifecycle. ~_3 1997 Elsevier Science B.V.

Changes in function as an individual root ages has important implications for understanding resource acquisition, competitive ability and optimal lifespan. Both nitrate uptake and respiration rates of differently aged fine roots of grape (Vitis rupestris x V. riparia cv. 3309 C) were measured. The resulting data were then used to simulate nitrate uptake efficiency and nutrient depletion as a function of root age. Both nitrate uptake and root respiration declined remarkably quickly with increasing root age. The decline in both N uptake and root respiration corresponded with a strong decline in root N concentration, suggesting translocation of nitrogen out of the roots. For simulations where no nutrient depletion occurs at the root surface, daily uptake efficiency was maximal at root birth and lifetime nitrate uptake efficiency slowly increased as the roots aged. Simulations of growth of roots into unoccupied soil using a solute transport model indicated the advantage of high uptake capacity in new roots under competitive conditions where nitrate availability is very transitory.

Shallow-rooted plants were studied on unirrigated modular green roof trays. Four species had 100% survival, six had varied survival rates and five had no survivors. These outcomes suggest that water conservation practices can be an effective approach for green roofs., Background and aims The application of green roof technology has become more common in the central, northwestern and eastern USA, and is now being employed across the southern USA as well. However, there is little research in the literature that evaluated plant survival on unirrigated green roofs in subtropical climates that experience frequent drought and heat stress. Here, we summarize the results of a study of plant establishment on a modular green roof in south-central Texas. Methodology Fifteen plant species were field tested in 11.4-cm-deep green roof modules on a four-storey building in College Station, Texas, with irrigation limited to the first several weeks of establishment. Climate data, plant growth and species survival were measured over three growing seasons. Principal results Four species survived growing seasons without any losses: Graptopetalum paraguayense, Malephora lutea, Manfreda maculosa and Phemeranthus calycinus. Six species experienced varying levels of mortality: Bulbine frutescens, Delosperma cooperi, Lampranthus spectabilis, Sedum kamtschaticum, Sedum mexicanum and Nassella tenuissima. Five species had no survivors: Dichondra argentea, Stemodia lanata, Myoporum parvifolium, Sedum moranense and Sedum tetractinum. Conclusions The establishment and survival of several plant species without any mortality suggests that irrigation limited to the first few weeks after planting may be an effective approach on green roofs in spite of the more challenging climatic conditions in the southern USA. Since the climate in south-central Texas had been consistently drier and warmer than normal during the study period, longer-term research on these species is recommended to expand knowledge of establishment requirements for these species under a wider range of conditions, including wetter than normal years.

We only have a limited understanding of the nutrient uptake physiology of individual roots as they age. Despite this shortcoming, the importance of nutrient uptake processes to our understanding of plant nutrition and nutrient cycling cannot be underestimated. In this study, we used a 15N depletion method that allowed for the measurement of nitrate-N uptake rates on intact, individual, fine roots of known age. We expected that N uptake would decline rapidly as fine roots aged, regardless of the environmental conditions and species used. We compared age dependent uptake patterns of young grape cuttings with those of mature vines and with those of tomato. Although patterns of declining uptake with increasing root age were similar for all species and conditions tested, large differences in maximum N uptake rates existed between young cuttings and mature vines, and between woody and herbaceous species. Maximum rates were 10-fold higher for tomato and 3-fold higher for the grape cuttings, when compared with uptake rates of fine roots of mature vines. Coefficients of variation ranged from 43 to 122% within root age groups. The large variability in physiological characteristics of fine roots of the same age, diameter and order suggests that there is a functional diversity within fine roots that is still poorly understood.