The invasive annual cheatgrass releases more nitrogen than crested wheatgrass through root exudation and senescence

Plant-soil feedbacks are an important aspect of invasive species success. One type of feedback is alteration of soil nutrient cycling. Cheatgrass invasion in the western USA is associated with increases in plant-available nitrogen (N), but the mechanism for this has not been elucidated. We labeled cheatgrass and crested wheatgrass, a common perennial grass in western rangelands, with ¹⁵N-urea to determine if differences in root exudates and turnover could be a mechanism for increases in soil N. Mesocosms containing plants were either kept moist, or dried out during the final 10 days to determine the role of senescence in root N release. Soil N transformation rates were determined using ¹⁵N pool dilution. After 75 days of growth, cheatgrass accumulated 30 % more total soil N and organic carbon than crested wheatgrass. Cheatgrass roots released twice as much N as crested wheatgrass roots (0.11 vs. 0.05 mg N kg^?1 soil day^?1) in both soil moisture treatments. This occurred despite lower root abundance (7.0 vs. 17.3 g dry root kg^?1 soil) and N concentration (6.0 vs. 7.6 g N kg^?1 root) in cheatgrass vs. crested wheatgrass. We propose that increases in soil N pool sizes and transformation rates under cheatgrass are caused by higher rates of root exudation or release of organic matter containing relatively large amounts of labile N. Our results provide the first evidence for the underlying mechanism by which the invasive annual cheatgrass increases N availability and establishes positive plant-soil feedbacks that promote its success in western rangelands.     

Distribution of ecosystem C and N within contrasting vegetation types in a semiarid rangeland in the Great Basin,USA

Semiarid sagebrush ecosystems are being transformed by wildfire, rangeland improvement techniques, and exotic plant invasions, but the effects on ecosystem C and N dynamics are poorly understood. We compared ecosystem C and N pools to 1 m depth among historically grazed Wyoming big sagebrush, introduced perennial crested wheatgrass, and invasive annual cheatgrass communities, to examine whether the quantity and quality of plant inputs to soil differs among vegetation types. Natural abundance δ¹⁵N isotope ratios were used to examine differences in ecosystem N balance. Sagebrush-dominated sites had greater C and N storage in plant biomass compared to perennial or annual grass systems, but this was predominantly due to woody biomass accumulation. Plant C and N inputs to soil were greatest for cheatgrass compared to sagebrush and crested wheatgrass systems, largely because of slower root turnover in perennial plants. The organic matter quality of roots and leaf litter (as C:N ratios) was similar among vegetation types, but lignin:N ratios were greater for sagebrush than grasses. While cheatgrass invasion has been predicted to result in net C loss and ecosystem degradation, we observed that surface soil organic C and N pools were greater in cheatgrass and crested wheatgrass than sagebrush-dominated sites. Greater biomass turnover in cheatgrass and crested wheatgrass versus sagebrush stands may result in faster rates of soil C and N cycling, with redistribution of actively cycled N towards the soil surface. Plant biomass and surface soil δ¹⁵N ratios were enriched in cheatgrass and crested wheatgrass relative to sagebrush-dominated sites. Source pools of plant available N could become ¹⁵N enriched if faster soil N cycling rates lead to greater N trace gas losses. In the absence of wildfire, if cheatgrass invasion does lead to degradation of ecosystem function, this may be due to faster nutrient cycling and greater nutrient losses, rather than reduced organic matter inputs.     

Lateral root development, including responses to soil drying, of maize (Zea mays) and wheat (Triticum aestivum) seminal roots

The spatial distribution of lateral roots in the soil is an important factor influencing water and nutrient absorption. However, lateral root development has rarely been studied in detail, especially concerning morphological variations, mainly because such examinations are both time-consuming and laborious. We measured the number and length of all first-order lateral roots on the seminal roots of maize ( Zea mays L.) and wheat ( Triticum aestivum L.) to investigate variations in linear frequency and length. This was conducted with reference to species, root types, and positions on their parental roots. Although the linear frequency of first-order lateral roots varied along the root axis in maize, the variation was not as great as in wheat. Variations were found in the length of lateral roots among plant species, root types, and positions on their parental root axes. Such variations in the length of lateral roots along the root axes were caused by differences in the elongation period of lateral roots rather than those in the elongation rate. Additionally, we examined the effects of soil drying on lateral root development. As a response to soil drying, the length of lateral roots varied depending on the period they were placed under the stressed condition. Moderate soil drying could also accelerate the elongation of some lateral roots. Variations in the length of first-order lateral roots and their responses to soil drying could help distribute their tips thoroughly throughout the soil. This might be adaptive for water absorption for root system development when resources are limited.     

Tillering in Tussock Grasses in Relation to Defoliation and Apical Bud Removal

Experiments with five caespitose grass species from temperateand tropical environments showed that the number of lateralshoots (tillers) which emerged following defoliation was notincreased by leaving a greater residual leaf area. Increasedavailability of photosynthate (and perhaps other resources)was effective, however, in increasing the rate of growth anddegree of flowering of new lateral shoots in one tropical species,Panicum maximum. In two temperate Agropyron tussock grasses, decapitation (apicalbud removal) did not stimulate lateral shoot growth. This indicatedthat apical dominance was not a factor preventing growth oflateral buds just prior to inflorescence emergence on the parenttillers. However, defoliation, where both terminal buds andfoliage were removed from the parent tillers stimulated lateralbud growth. Hormones other than those produced by the apicalbud or light quality or intensity may control lateral bud growthin these species. In contrast to the temperate species, lateralbud growth was stimulated by both decapitation and defoliationin the three tropical species. This response is consistent withthe model of correlative inhibition by apical dominance. Agropyron desertorum, Agropyron spicatum, Heteropogon contortus, Panicum maximum, Themeda triandra, crested wheatgrass, bluebunch wheatgrass, black speargrass, green panic grass kangaroo grass, apical dominance, tillering, regrowth, grazing, tussock grasses     

Simple stereological procedure to estimate the number and dimensions of root hairs

We demonstrate a simple procedure for systematic, uniformly random sampling of a root system of known length to obtain practically unbiased estimates of the total number and dimensions of root hairs. Irrespective of the length of the root system, only 100 root hairs need to be counted to estimate the total number with sufficient precision. Numbers and dimensions of root hairs were estimated for five crested wheatgrass (Agropyron cristatum L.) root systems that had been grown for one month in a gel. Less than one hour was required to obtain estimates of root hair parameters for a single plant. There was low variability of spatial density of root hairs within a given branching order (CV < 15%); however, because of large variation in the total length of laterals, the total number of root hairs varied greatly (CV ∼70%). On average, root hairs provided half of the total surface area of a root system and a total length 20 times that of the roots. This revised version was published online in June 2006 with corrections to the Cover Date.     

Do invasive plants structure microbial communities to accelerate decomposition in intermountain grasslands?

Invasive plants are often associated with greater productivity and soil nutrient availabilities, but whether invasive plants with dissimilar traits change decomposer communities and decomposition rates in consistent ways is little known. We compared decomposition rates and the fungal and bacterial communities associated with the litter of three problematic invaders in intermountain grasslands; cheatgrass (Bromus tectorum), spotted knapweed (Centaurea stoebe) and leafy spurge (Euphorbia esula), as well as the native bluebunch wheatgrass (Pseudoroegneria spicata). Shoot and root litter from each plant was placed in cheatgrass, spotted knapweed, and leafy spurge invasions as well as remnant native communities in a fully reciprocal design for 6 months to see whether decomposer communities were species‐specific, and whether litter decomposed fastest when placed in a community composed of its own species (referred to hereafter as home‐field advantage–HFA). Overall, litter from the two invasive forbs, spotted knapweed and leafy spurge, decomposed faster than the native and invasive grasses, regardless of the plant community of incubation. Thus, we found no evidence of HFA. T‐RFLP profiles indicated that both fungal and bacterial communities differed between roots and shoots and among plant species, and that fungal communities also differed among plant community types. Synthesis. These results show that litter from three common invaders to intermountain grasslands decomposes at different rates and cultures microbial communities that are species‐specific, widespread, and persistent through the dramatic shifts in plant communities associated with invasions.     

Soil water dynamics,transpiration, and water losses in a crested wheatgrass and native shortgrass ecosystem

The status of water in soil and vegetation was monitored in a stand of crested wheatgrass (Agropyron cristatum) and a nearby shortgrass steppe during a growing season. This was done to determine if water use and losses were similar among two very different communities in a similar climate. Precipitation was similar throughout the study period for both the crested wheatgrass and native shortgrass communities. However, the native shortgrass community with greater root biomass had consistently greater soil water depletion in the deeper soil horizons than was found in the crested wheatgrass community. Greater depletion of soil water by native shortgrass species suggests that they might be more competitive than crested wheatgrass in a water-limited environment.Crested wheatgrass maintained high leaf water potential early in the season, but lower water potential during the latter part of the growing season as compared with the major species of the shortgrass steppe, blue grama (Bouteloua gracilis) and western wheatgrass (Agropyron smithii). Leaf conductance was lower for crested wheatgrass than for the native grasses during the later part of the growing season. Consequently, seasonal transpiration for crested wheatgrass was lower when compared with blue grama or western wheatgrass. Lower conductance allowed crested wheatgrass to maintain relatively high internal water potential and may have accounted for less soil water use at deeper soil depths during the latter part of the growing season.Water loss through transpiration was less for western wheatgrass than for either blue grama or crested wheatgrass because western wheatgrass had less leaf area. However, western wheatgrass was as efficient as the other species in its use of water. Crested wheatgrass transpired more water than blue grama early in the growing season, but less than either native species for the remainder of the growing season. Estimated seasonal transpiration loss was greater in the shortgrass ecosystem than in the established crested wheatgrass stand.     

Root proliferation characteristics of seven perennial arid-land grasses in nutrient-enriched microsites

We compared root proliferation in fertilized microsites among seven cultivars of five commonly planted cool-desert perennial grass species that differ in productivity and competitive ability. In a greenhouse experiment on nutrient-limited plants, one soil microsite in each pot received distilled water (control) and a second microsite received a rich, complete nutrient solution (fertilized). Roots in and adjacent to the microsites were mapped on Mylar windows for 22 days after the injections to determine the magnitude and timing of response in root length relative growth rates (RGRs). Because we provided adequate water, used a high level of fertilization in the treatment microsites, and conducted the experiments during rapid vegetative growth, the results provide a measure of the relative capacities and maximal rates of the grasses responses to enriched microsites. Root samples were harvested from control and fertilized microsites at the end of the experiment to determine the morphological basis of the proliferation response. In all seven grasses fine roots proliferated in the fertilized microsites faster than in the control microsites. The grasses did not differ in the timing of their response which showed a peak 7–8 days after injection. Although one species, Pseudoroegneria spicata cv. Goldar, had higher maximum root length RGR and higher RGR ratio (RGR in fertilized to RGR in control microsites) 7–8 days after injection, the seven grasses did not differ significantly in the magnitude of root length RGR response to fertilizer integrated over the 22 day experiment. The grasses also did not differ significantly in root morphological changes in fertilized mocrosites. Compared to roots in control microsites, roots in fertilized microsites had greater specific root length, length of secondary roots per length of main axis, number of lateral and sublateral roots per length of main axis, and mean lateral root length. Root proliferation was mainly the result of increased lateral branching and lateral root growth in all seven grasses. The consistency of root proliferation responses among these seven cultivars suggests that differences in the capacity for, maximum rate, or morphological basis of root proliferation are not directly related to ecological characteristics such as productivity and competitive ability. Other aspects of root response to nutrient enrichment, such as differential responses as a function of microsite nutrient concentration, plant phenology, plant nutrient status, or specific nutrient element(s), may still be important, but further experiments are required to determine whether different responses to enriched soil microsites among species correspond with know species differences in ecological characteristics.     

Lithium toxicity in seedlings of three cool season grasses

Summary Lithium toxicity in seedling of crested wheatgrass (Agropyron desertorum), Sherman bluegrass (Poa ampla), and Whitmar wheatgrass (Agropyron inerme) was investigated in 2 potted soil studies. Yields of roots and shoots were unaffected at 2.5 and 5 ppm but were significantly (P<0.05) depressed at 15 and 60 ppm. Li was much higher in the herbage than in the roots of grasses grown in Li treated soils. Species tolerancy to Li appeared to be: crested wheatgrass > Sherman bluegrass > Whitmar wheatgrass.The research is a cooperative investigation of the USDA, Science and Education Administration, Agricultural Research, and the Oregon State Agric. Exp. Sta., Squaw Butte Experiment Station, Burns, Technical Paper No. 4974 of the Oregon State Agric. Exp. Sta.     

Non-destructive,stereological estimation of plant root lengths,branching pattern and diameter distribution

The total length of a linear structure contained in an unbounded, transparent reference space can be estimated from ‘total vertical projections’ obtained by rotating the linear structure about an arbitrary ‘vertical’ axis, and projecting the linear structure onto a plane parallel to the axis of rotation. The total number of intersections between cycloid arcs with their minor axis perpendicular to the axis of rotation and the projected linear structure then provides an unbiased estimator of the total length of the structure. In this study, a stereological procedure based on the method of ‘total vertical projections’ was used to non-destructively estimate total root length, number of branches, diameter distribution and mean root diameter of crested wheatgrass plants (Agropyron cristatum L.) growing in a transparent medium. Root lengths, diameters, and number of branching points of various orders were determined at 3-day intervals over a 4-week growing period. The length estimator was very robust and efficient with sampling coefficients of error usually less than 5% for a total of 50–150 grid intersection counts over two projection directions per plant. Biological coefficients of variance for total length were between 30–70%, and were largely related to variation in the extent of branching. This revised version was published online in June 2006 with corrections to the Cover Date.     

Morphological plasticity following species-specific recognition and competition in two perennial grasses

Morphological characteristics and biomass allocation of two perennial grasses, Pseudoroegneria spicata (Pursh) A. Löve ssp. spicata (bluebunch wheatgrass) and Agropyron desertorum (Fisch. ex Link) Schult. (crested wheatgrass), were compared under different competition and nutrient treatments. The competitive responses of two plants grown in containers under field conditions were assessed in monocultures and mixtures in two experiments using different scales of nutrient application. In the Small-Scale Experiment, a localized fertilization was applied in the rooting zone between two plants; in the Large-Scale Experiment the entire container was supplied with nutrients. Agropyron responded more vigorously to fertilization than did Pseudoroegneria, but based on the relative performance of Agropyron in monoculture and mixture, it was not superior to Pseudoroegneria in resource competition. Pseudoroegneria was apparently able to recognize neighboring plants as either conspecifics or individuals of the other species. The responses included changes in shoot architecture, root morphology, and allocation between roots and shoots. Agropyron generally did not exhibit such morphological flexibility. In field plot plantings of 4-yr-old tussocks similar shoot differences were seen in Pseudoroegneria. There was, however, no indication of superior resource competition for Agropyron. Thus, any early advantage of Agropyron in vigorous growth of young plants in response to nutrients was apparently lost by the time the plants had reached this stage of development. Morphological and allocation flexibility of Pseudoroegneria may have compensated for slower, less vigorous growth. If species-specific recognition and morphological plasticity are common in nature, this complicates our attempts to understand mechanisms of competition.     

Plant architecture and the foraging success of ladybird beetles attacking the Russian wheat aphid

We examined the interaction between the fourteen-spotted ladybird beetle, Propylea quatuordecimpunctata (L.), and the Russian wheat aphid, Diuraphis noxia (Mordvilko), on two grasses with divergent leaf architectures. Like wheat, crested wheatgrass bears flat, broad leaves, whereas Indian ricegrass produces slender, tightly rolled leaves. In the absence of aphid prey, residence times and time budgets of larvae and adults of P. quatuordecimpunctata were similar on the two hosts, although larvae tended to remain longer on crested wheatgrass. When aphids were present, both predator stages dislodged, contacted, and captured aphids at higher rates on Indian ricegrass than on crested wheatgrass. Predator time budgets and behavior sequences also reflected a greater predation risk for D. noxia on Indian ricegrass, and were consistent with earlier, population-level experiments in the field. Comparisons between aphid-free and aphid-infested plants suggest that the effect of host plant in this tri-trophic system largely depended on differences in the availability of prey refuges rather than on differences in predator searching behavior; proportionally more aphids fed in exposed locations on Indian ricegrass than on crested wheatgrass. Plant architecture is likely to be an important component of the predation risk of D. noxia because of the aphid's tendency to feed in relatively concealed locations.     

Pathological Effects of Pratylenchus neglectus on Wheatgrasses

In controlled greenhouse and growth chamber studies, Pratylenchus neglectus reduced dry shoot and dry root weight of rangeland grasses. Greenar intermediate wheatgrass and Secar Snake River wheatgrass were more susceptible to P. neglectus than Hycrest crested wheatgrass, Fairway crested wheatgrass, and Nordan crested wheatgrass at a greenhouse bench temperature of 26 ± 3 C. Hycrest was the most tolerant to parasitism by P. neglectus. An initial nematode inoculum density of four nematodes/cm³ soil reduced dry shoot weights of Hycrest, Fairway, Nordan, Greenar, and Secar by 22%, 33%, 36%, 47%, and 49%, and reduced dry root weights by 26%, 31%, 32%, 38%, and 42%. There was a positive relationship between dry root weight, the nematode inoculum density, and the nematode reproduction index (final nematode population/initial nematode inoculum). However, there were more nematodes/g root tissue on Secar than on the crested wheatgrasses, and significantly more nematodes/g root tissue on Greenar, Fairway, and Nordan than on Hycrest. Pratylenchus neglectus was most pathogenic at four nematodes/cm³ soil at 30 C and least pathogenic at one nematode/cm³ soil at 15 C. Greenar and Secar were more susceptible to the nematode than Hycrest, Fairway, and Nordan at two and four nematodes/cm³ soil at 20 to 30 C. The nematode reproductive indices were greatest at 30 C and were positively correlated with dry root weight. Secar supported the most and Hycrest had the fewest nematodes/g root.     

武夷山不同海拔毛竹细根功能性状

细根作为植物最重要的资源获取功能器官,是影响陆地生态系统的重要组成部分。定量化毛竹的细根功能性状对于理解其生理生态特征响应及生活史策略至关重要。为揭示毛竹细根功能性状随海拔梯度的变化规律以及细根的适应策略,对武夷山不同海拔(840 m、1040 m、1240 m)毛竹细根的碳(C)、氮(N)、磷(P)含量和比根长(SRL)、比根面积(SRA)等性状进行测定,分析细根性状在海拔上的差异及其异速生长关系。结果表明：(1)不同海拔毛竹细根养分性状存在显著差异。毛竹细根C含量在海拔1040 m最大。随海拔升高,细根N、P含量均呈下降趋势,细根C∶N、C∶P随着海拔的升高而增加。(2)细根的结构性状在海拔梯度上差异显著。随海拔升高,细根平均根直径(AvgDiam)、SRL及SRA均呈下降趋势,而根组织密度(RTD)呈升高趋势。(3)细根性状间存在显著的异速生长关系。细根N与P含量存在显著的等速生长关系,二者与C含量存在显著异速生长关系;SRL与SRA存在显著的等速生长关系,二者与RTD存在显著的负等速生长关系,与N含量存在显著的异速生长关系;细根AvgDiam与RTD存在显著的负异速生长关系。毛...     

Estimates of root system topology of five plant species grown at steady-state nutrition

Results from a controlled growth-analysis experiment were used to illustrate some methods for measuring and describing root system topology. The experiment was performed in a nutrient solution system with an exponential nutrient supply and steady-state growth, to achieve well-defined levels of whole-plant nutrient status. Five naturally coexisting grassland species were included: The slow-growing forbs Polygala vulgaris L. and Crepis praemorsa (L.) F. L. Walth., and the grass Danthonia decumbens (L.) DC. were compared with the more common, fast-growing grasses Agrostis capillaris L. and Dactylis glomerata L. The most marked difference in morphological indices was a much higher specific root length in the grasses than in the forbs, which implies thinner roots. In contrast to the conclusions of previous studies, an index of the topology for the grasses was very similar to that for the forbs. The specific root lenght and link length apparently vary more between species and nutrient levels than topology does, and may therefore be more ecologically important. The only clear plastic response to growth-limiting nitrogen supply was a markedly increased link length in P. vulgaris. There were also indications that nitrogen limitation led to more herringbone-like root systems in P. vulgaris and C. praemorsa. In general, there was a clear tendency for the estimates of topology to change with plant size, which may make many topological indices, especially those based on regression slopes, very difficult to interpret. Until interactions with plant size, other morphological parameters and among-plant competition can be properly understood, the relevance of root topology for plant performance remains unclear. This revised version was published online in June 2006 with corrections to the Cover Date.     

Sagittal cresting in the South African australopithecines

The evidence for sagittal cresting, and more generally the position of the temporal lines is reviewed in the South African australopithecine sample. The position of the lines is dependent on both the allometric relation of the masticatory apparatus to cranial size and on individual variation. In the Swartkrans specimens, with generally bigger body size, the influence of allometry predominates, actually overshadowing the influence of individual variation. At Sterkfontein and Makapansgat with generally smaller body size and a resulting smaller allometric ratio, individual variation has a greater influence. Of the eleven adult South African specimens, the four largest are crested. The one smaller crested specimen comes from Sterkfontein. The crested Makapan specimen is intermediate in size. The pattern of australopithecine cresting is somewhat different from other hominoids, and is part of a total morphological pattern suggesting adaptation to a diet requiring powerful crushing during mastication.     

Fine‐root exploitation strategies differ in tropical old growth and logged‐over forests in Ghana

Understanding the changes in root exploitation strategies during post‐logging recovery is important for predicting forest productivity and carbon dynamics in tropical forests. We sampled fine (diameter < 2 mm) roots using the soil core method to quantify fine‐root biomass and architectural and morphological traits to determine root exploitation strategies in an old growth forest and in a 54‐yr‐old logged‐over forest influenced by similar parent material and climate. Seven root traits were considered: four associated with resource exploitation potential or an ‘extensive’ strategy (fine‐root biomass, length, surface area, and volume), and three traits which reflect exploitation efficiency or an ‘intensive’ strategy (specific root area, specific root length, and root tissue density). We found that total fine‐root biomass, length, surface area, volume, and fine‐root tissue density were higher in the logged‐over forest, whereas the old growth forest had higher total specific root length and specific root surface area than the logged‐over forest. The results suggest different root exploitation strategies between the forests. Plants in the old growth forest invest root biomass more efficiently to maximize soil volume explored, whereas plants in the logged‐over forest increase the spatial distribution of roots resulting in the expansion of the rhizosphere.     

Establishment of a plant regeneration system for wheatgrasses (Thinopyrum,Agropyron and Pascopyrum)

Wheatgrasses (Thinopyrum, Agropyron and Pascopyrum spp.) are a ubiquitous group of cool-season grasses used throughout much of the semiarid temperate world. In order to explore the potential of biotechnology to accelerate conventional breeding efforts, we developed an efficient plant regeneration system for different wheatgrass species: tall wheatgrass [Thinopyrum ponticum (Podp.) Liu and Wang], intermediate and pubescent wheatgrass [Thinopyrum intermedium (Host) Barkw. and D.R. Dewey], crested wheatgrass [Agropyron cristatum (L.) Gaertner], and western wheatgrass [Pascopyrum smithii (Rydb.) Löve]. Embryogenic callus was induced from mature and immature embryos and immature inflorescence with an induction frequency in the range of 0.5–8.3% for the different wheatgrass species tested. Individual embryogenic calluses were then used to establish single genotype-derived suspension cultures. Efficient plant regeneration was achieved from the established em-bryogenic suspensions with regeneration frequencies in the range of 20–65% for tall wheatgrass, 21–40% for intermediate and pubescent wheatgrasses, 32–51% for crested wheatgrass, and 25–48% for western wheatgrass. The cell suspension-derived wheatgrass plants were fertile and phenotypically normal in the field. The efficient plant regeneration system provides a solid basis for genetic transformation of wheatgrasses.     

Root vascular anatomy predicts maximum growth rates in savanna trees and grasses

Root-based functional traits are relatively overlooked as drivers of savanna plant community dynamics, an important gap in water-limited ecosystems. Recent work has shed light on patterns of trait coordination in roots, but less is known about the relationship between root functional traits, water acquisition, and plant demographic rates. Here, we investigated how fine-root vascular and morphological traits are related in two dominant PFTs (C₃ trees and C₄ grasses from the savanna biome), whether root traits can predict plant relative growth rate (RGR), and whether root trait multivariate relationships differ in trees and grasses. We used root data from 21 tree and 18 grass species grown under greenhouse conditions, and quantified a suite of vascular and morphological root traits. We used a principal components analysis (PCA) to identify common axes of trait variation, compared trait correlation matrices between the two PFTs, and investigated the relationship between PCA axes and individual traits and RGR. We found that there was no clear single axis integrating vascular and morphological traits, but found that vascular anatomy predicted RGR in both trees and grasses. Trait correlation matrices differed in trees and grasses, suggesting potentially divergent patterns of trait coordination between the two functional types. Our results suggested that, despite differences in trait relationships between trees and grasses, root conductivity may constrain maximum growth rate in both PFTs, highlighting the critical role that water relations play in savanna vegetation dynamics and suggesting that root water transport capacity is an important predictor of plant performance in the savanna biome.     

Modes of ontogenetic allometric shifts in crocodylian vertebrae

During postnatal ontogeny of vertebrates, allometric trends in certain morphological units or dimensions can shift drastically among isometry, positive allometry, and negative allometry. However, detailed patterns of allometric transitions in certain timings have not been explored well. Identifying the presence and nature of allometric shifts is essential for understanding the patterns of changes in relative size and shape and the proximal factors that are controlling these changes mechanistically. Allometric trends in 10 selected vertebrae (cervical 2–caudal 2) from hatchlings to very mature individuals of Alligator mississippiensis (Archosauria, Crocodylia) are reported in the present study. Allometric coefficients in 12 vertebral dimensions are calculated and compared relative to total body length, including centrum, neural spine, transverse process, zygapophysis, and neural pedicle. During the postnatal growth, positive allometry is the most common type of relative change (10 of the 12 dimensions), although the diameter of the neural canal shows a negative allometric trend. However, when using spurious breaks (i.e. allometric trends subdivided into growth stages using certain growth events, and key body sizes and/or ages), vertebral parts exhibit various pathways of allometric shifts. Based on allometric trends in three spurious breaks, separated by the end of endochondral ossification (body length: approximnately 0.9 m), sexual maturity (1.8 m), and the stoppage of body size increase (2.8 m), six types of ontogenetic allometric shifts are established. Allometric shifts exhibit a wide range from positive allometry restricted only in the early postnatal stage (Type I) to life‐long positive allometry (Type VI). This model of ontogenetic allometric shifts is then applied to interpret potential mechanisms (causes) of allometric changes, such as (1) growth itself (when allometric trend gradually decreases to isometric or negative allometric change: Type II–IV allometric shift); (2) developmental constraint (when positive allometry is limited only in the early growth stage: Type I allometric shift); and (3) functional or biomechanical drive (when positive allometry continues throughout ontogeny: Type VI allometric shift).