The value of linking paleoecological and neoecological perspectives to understand spatially-explicit ecosystem resilience

Context

Predicting ecosystem resilience is a challenge, especially as climate change alters disturbance regimes and conditions for recovery. Recent research has highlighted the importance of spatially-explicit disturbance and resilience processes to long-term ecosystem dynamics. “Neoecological” approaches characterize resilience mechanisms at relatively fine spatio-temporal resolutions, but results are difficult to extrapolate across broad temporal scales or climatic ranges. Paleoecological methodologies can consider the effects of climates that differ from today. However, they are often limited to coarse-grained spatio-temporal resolutions.

Methods

In this synthesis, we describe implicit and explicit examples of studies that incorporate both neo- and paleoecological approaches. We propose ways to build on the strengths of both approaches in an explicit and proactive fashion.

Results

Linking the two approaches is a powerful way to surpass their respective limitations. Aligning spatial scales is critical: Paleoecological sampling design should incorporate knowledge of the spatial characteristics of the disturbance process, and neoecological studies benefit from a longer-term context to their conclusions. In some cases, modeling can incorporate non-spatial data from paleoecological records or emerging spatial paleo-data networks with mechanistic disturbance/recovery processes that operate at fine spatiotemporal scales.

Conclusions

Linking these two complementary approaches is a powerful way to build a complete understanding of ecosystem disturbance and resilience.

     

Characterization of a novel potyvirus isolated from maize in Israel

A potyvirus (proposed name of Zea mosaic virus [ZeMV]) isolated from maize in Israel was analyzed by serology, sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) of capsid proteins, symptomatology, and sequencing. Parts of the nuclear inclusion b, coat protein, and 3' regions were sequenced; the amino acid sequence of ZeMV capsid was determined by time-of-flight mass spectrometry (TOFMS). The results of these analyses were compared with those of similar analyses of the following potyviruses: Maize dwarf mosaic virus (MDMV), Sugarcane mosaic virus strain MDB (SCMV-MDB), Johnsongrass mosaic virus(JGMV), Sorghum mosaic virus (SrMV), and an isolate of MDMV from Israel. Indirect enzyme-linked immunosorbent assay using ZeMV antiserum detected only ZeMV, and reciprocal tests using MDMV, JGMV, or SrMV antisera failed to detect ZeMV. ZeMV cross-reacted weakly when SCMV-MDB antiserum was used. The mass of ZeMV capsid was determined to be 36,810 Da by SDS-PAGE and 34,216 Da by TOFMS. The ZeMV systemically infected johnsongrass (Sorghum halepense), but did not infect oat (Avena sativa), pearl millet (Pennisetum glaucum), barley (Hordeum vulgare), or rye (Secale cereale). Necrosis was caused in 19 sorghum lines by SrMV, in 15 by ZeMV, in 14 by MDMV, and in 5 by JGMV and SCMV-MDB. The nucleic acid and amino acid sequences of ZeMV clearly showed that it is not a strain of JGMV, MDMV, SCMV, or SrMV.     

GAS EXCHANGE AND GROWTH OF TRITICALE SEEDLINGS UNDER DIFFERENT NITROGEN SUPPLY AND WATER STRESS

The effect of nitrogen (30 and 120 mg N per cuvette) on photosynthetic rate of four cultivars of triticale (‘Bolero’, ‘Grado’, ‘Largo’, and ‘Lasko’) grown 14 days in phytotron was strongly modified by water content (75, 45 and 35% of full water capacity). For plants grown under 35% of full water capacity, it was higher when they were grown under 30 than under 120 mg N/cuvette (9.88 and 8.76 μmol CO₂ m^?2 s^?1, respectively) but for plants grown under 45 and 75% of full water capacity there were not significant differences. Transpiration, stomatal conductance, photosynthetic water use efficiency, and internal water use efficiency were not influenced by nitrogen doses independently of water content. Photosynthetic rate, transpiration, stomatal conductance, photosynthetic water use efficiency, and dry matter of studied cultivars of triticale grown under 45 and 35% of full water capacity and both nitrogen doses were lower than for plants grown under 75% of full water capacity. With lowering of water content stomatal conductance was decreasing similarly as photosynthetic rate e.g. for plants grown under 35% of full water capacity as compared with those grown under 75% of full water capacity average stomatal conductance decreased from 0.209 to 0.138 mol H₂O m^?2 s^?1 and photosynthetic rate from 13.69 to 9.32 μmol CO₂ m^?2 s^?1 and as a result there were not significant differences in internal water use efficiency for all studied combinations (67.09 μmol CO₂ mol^?1 H₂O) which shows that stomatal factors were mainly responsible for changes of photosynthetic rate. With lowering of water content from 75 to 35% of full water capacity the decrease of photosynthetic rate and stomatal conductance was much higher than the decreases of transpiration (from 3.57 to 3.02 mmol H₂O m^?2 s^?1) what shows not direct dependence of transpiration on stomatal conductance (water use efficiency decreased from 3.87 to 3.10 μmol CO₂ mmol^?1 H₂O). The effect of nitrogen on dry matter production was strongly modified by water availability e.g. for plants grown under 35% of full water capacity, dry matter was similarly independent of nitrogen dose but for plants grown under 45 and 75% of full water capacity dry matter was significantly higher than when they were grown under 120 (79.05 and 86.75 mg, respectively) or with 30 mg N/cuvette (74.03 and 80.30 mg, respectively).