不同光环境对桤木幼苗生长和光合特性的影响

通过设置3个光照强度(100%、56.2% 和12.5%),模拟森林幼苗生长的旷地(采伐迹地)、林窗和林下光环境,研究不同光照强度对外来种台湾桤木和乡土种四川桤木幼苗的生长、光合特性以及生物量积累与分配的影响.结果表明： 低光环境限制了两种桤木幼苗形态指标的增长,适当遮荫的林窗环境比旷地更有利于幼苗的生长.台湾桤木幼苗具有较高的比叶面积和相对生长速率,较大的单叶面积、叶长、叶宽、株高和基径,较少的叶片数和较低的叶面积比、叶柄长.低光环境下,台湾桤木幼苗的最大净光合速率、光饱和点和表观光量子效率较高,光补偿点和暗呼吸速率较低.随着光照强度的降低,台湾桤木幼苗具有更高的根生物量比和更低的叶生物量比;四川桤木幼苗则相反,加剧了动物取食和机械损伤的风险.     

Cuffing‐based photoacoustic flowmetry in humans in the optical diffusive regime

Measuring blood flow speed in the optical diffusive regime in humans has been a long standing challenge for photoacoustic tomography. In this work, we proposed a cuffing‐based method to quantify blood flow speed in humans with a handheld photoacoustic probe. By cuffing and releasing the blood vessel, we can measure the blood flow speed downstream. In phantom experiments, we demonstrated that the minimum and maximum measurable flow speeds were 0.035 mm/s and 42 mm/s, respectively. In human experiments, flow speeds were measured in three different blood vessels: a radial artery in the right forearm, a radial artery in the index finger of the right hand, and a radial vein in the right forearm. Taking advantage of the handheld probe, our method can potentially be used to monitor blood flow speed in the clinic and at the bedside.

     

Rate of forcing and the forecastability of critical transitions

Critical transitions are qualitative changes of state that occur when a stochastic dynamical system is forced through a critical point. Many critical transitions are preceded by characteristic fluctuations that may serve as model‐independent early warning signals, implying that these events may be predictable in applications ranging from physics to biology. In nonbiological systems, the strength of such early warning signals has been shown partly to be determined by the speed at which the transition occurs. It is currently unknown whether biological systems, which are inherently high dimensional and typically display low signal‐to‐noise ratios, also exhibit this property, which would have important implications for how ecosystems are managed, particularly where the forces exerted on a system are anthropogenic. We examine whether the rate of forcing can alter the strength of early warning signals in (1) a model exhibiting a fold bifurcation where a state shift is driven by the harvesting of individuals, and (2) a model exhibiting a transcritical bifurcation where a state shift is driven by increased grazing pressure. These models predict that the rate of forcing can alter the detectability of early warning signals regardless of the underlying bifurcation the system exhibits, but that this result may be more pronounced in fold bifurcations. These findings have important implications for the management of biological populations, particularly harvested systems such as fisheries, and suggest that knowing the class of bifurcations a system will manifest may help discriminate between true‐positive and false‐positive signals.     

Experimental test of the ecosystem impacts of the keystone predator Triops cancriformis (Branchiopoda: Notostraca) in temporary ponds

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A hydrologically sensitive invertebrate community index for New Zealand rivers

Identifying ecological response variables sensitive to hydrological change is a key step in determining the impacts of river flow alterations on aquatic ecosystems and in setting environmental flows that sustain certain ecological values. Building on the successful use of flow regime sensitive aquatic invertebrate indices in other countries, particularly the UK based Lotic Index for Flow Evaluation (LIFE), we provide two variants of a similar index for use in New Zealand (LIFENZ and a weighted variant: LIFENZ_W). As in the original LIFE, the New Zealand indices were based on water velocity preference categories assigned to aquatic invertebrate taxa using professional judgement. To calculate the indices a lookup table is used to assign a score to each taxon based on their velocity category and abundance. For the LIFENZ_W variant an additional step down weighted the scores if the taxon has a general compared to a more specific velocity preference. The two index variants were correlated with each other and to similar environmental parameters. Across a total of 74 sites, both indices were correlated with depth-averaged water velocity. Changes in index values, both between sites and temporally within sites, were predominantly associated with changes in hydrological parameters, such as the magnitude and length of time since a recent high flow, and to a lesser degree with other physico-chemical parameters. Commonly used indices in New Zealand designed to respond to nutrient enrichment (MCI and variants) were not correlated with local water velocity, but were correlated with antecedent flow conditions and were likely influenced by effects of flow stability on algal growth. Further testing of LIFENZ and LIFENZ_W in combination with MCI is recommended, particularly in rivers subject to more extreme hydrological and water quality stresses and with regard to other physical parameters such as hydraulic habitat. However, the LIFENZ and its weighted variant (LIFENZ_W) appear to be useful tools for understanding and managing the effects of hydrological alteration on aquatic invertebrate communities in New Zealand. As LIFENZ and LIFENZ_W were strongly correlated and only showed a relatively small deviation from a slope of 1 we recommend the use of the more straightforward LIFENZ in almost all circumstances.     

Assessing hydrologic alteration: Evaluation of different alternatives according to data availability

The natural flow regime of rivers across the world has been largely modified. Understanding the extent to which the flow regime deviates from natural conditions is necessary for designing sound management and restoration measures. In this regard, ‘Indicators of Hydrologic Alteration’ is currently considered one of the most effective approaches for assessing hydrologic alteration (HA). However, several generalized drawbacks such as the climatic variability between the pre- and post-impacted series and the scarcity of hydrological data in many impaired rivers should be addressed. In this study, a protocol with the following five alternative designs based on data availability is presented: (1) Paired-Before–After Control–Impact (BACIP), (2) Before–After (BA), (3) Control–Impact (CI), (4) Hydrological Classification (HC) and (5) Predicted Hydrological indices (HP). BACIP compares the status of the impacted gauge before and after the perturbation is started, in addition to controlling for natural climatic changes. Hence, it has been considered as the reference benchmark for all other designs. When this protocol was applied to 11 reservoirs situated in the northern third of the Iberian Peninsula, the BA design was able to correctly identify most of the non-significant HA but failed in almost one quarter of the significant alterations. Similarly, BACIP and CI showed an agreement of >80%. This suggests that the method is suitable when proper data are unavailable for BACIP or BA. In addition, our results indicated that the critical thresholds for HA varied depending on the hydrological index being considered. Significant HAs ranged from <5% for the number of days with increasing and decreasing flows to >64% for the duration of low-flow pulses. To delineate adequate thresholds, further research combining hydrological analyses with the biological response to the HA is warranted. Finally, the application of HC and HP designs revealed a significant degree of uncertainty related to the intra-class variability and the predictive error of the models. Therefore, 25% of the analysis could not be evaluated. However, in the evaluable cases, the HC and HP designs correctly assessed >75% of the HA, which highlighted the potential of this method in cases of scarce streamflow data.     

Seasonal distribution of increased precipitation in maternal environments influences offspring performance of Potentilla tanacetifolia in a temperate steppe ecosystem

Aims Precipitation is predicted to increase in arid and semiarid regions under climate change, with greater changes in intra- and inter-annual distribution in the future. As a major limiting factor in these regions, changes in precipitation undoubtedly influence plant growth and productivity. However, how the temporal shifts in precipitation will impact plant populations are uncertain.     

Anthropogenic modifications to fire regimes in the wider Serengeti‐Mara ecosystem

Fire is a key driver in savannah systems and widely used as a land management tool. Intensifying human land uses are leading to rapid changes in the fire regimes, with consequences for ecosystem functioning and composition. We undertake a novel analysis describing spatial patterns in the fire regime of the Serengeti‐Mara ecosystem, document multidecadal temporal changes and investigate the factors underlying these patterns. We used MODIS active fire and burned area products from 2001 to 2014 to identify individual fires; summarizing four characteristics for each detected fire: size, ignition date, time since last fire and radiative power. Using satellite imagery, we estimated the rate of change in the density of livestock bomas as a proxy for livestock density. We used these metrics to model drivers of variation in the four fire characteristics, as well as total number of fires and total area burned. Fires in the Serengeti‐Mara show high spatial variability—with number of fires and ignition date mirroring mean annual precipitation. The short‐term effect of rainfall decreases fire size and intensity but cumulative rainfall over several years leads to increased standing grass biomass and fuel loads, and, therefore, in larger and hotter fires. Our study reveals dramatic changes over time, with a reduction in total number of fires and total area burned, to the point where some areas now experience virtually no fire. We suggest that increasing livestock numbers are driving this decline, presumably by inhibiting fire spread. These temporal patterns are part of a global decline in total area burned, especially in savannahs, and we caution that ecosystem functioning may have been compromised. Land managers and policy formulators need to factor in rapid fire regime modifications to achieve management objectives and maintain the ecological function of savannah ecosystems.