Impacts of cyclone Larry on the vegetation structure of timber plantations,restoration plantings and rainforest on the Atherton Tableland,Australia

Abstract We examined the impact of severe cyclone ‘Larry’ on the vegetation structure of monoculture and mixed species timber plantations, restoration plantings and reference sites in upland rainforests on the Atherton Tableland, north Queensland, Australia. Sites were initially assessed in 2000 and resurveyed in 2006, 6–8 months after the cyclone traversed the region. In both surveys, timber plantations had a relatively open canopy, grassy understorey and few shrubs or small‐sized trees; whereas restoration plantings had a relatively closed canopy, an understorey of bare ground, leaf litter and rainforest seedlings, a high density of small‐diameter trees and a moderate representation of special life forms characteristic of rainforest. Cyclone damage varied with tree size, site type, proximity to the cyclone and stem density. First, the proportion of trees that were severely damaged by the cyclone (major branches broken, stem snapped or pushed over) increased with the diameter of trees across all site types. Second, damage to larger‐sized trees (>10 cm d.b.h., >20 cm d.b.h.) was proportionally highest in monoculture plantations, intermediate in mixed species plantations and rainforest, and lowest in restoration plantings. Third, within site types, damage levels decreased with distance from the cyclone track and with stem density. There was no evidence that topographical position influenced damage levels, at least for timber plantations. We tentatively attribute the high levels of damage experienced by timber plantations to their relatively open structure and the large size of stems in plantations. Restoration plantings generally escaped severe damage by the cyclone, but their continued development towards rainforest conditions may require a coordinated monitoring and maintenance programme to address the potential threat of weed invasion.     

Variation in above‐ground forest biomass across broad climatic gradients

Aim An understanding of the relationship between forest biomass and climate is needed to predict the impacts of climate change on carbon stores. Biomass patterns have been characterized at geographically or climatically restricted scales, making it unclear if biomass is limited by climate in any general way at continental to global scales. Using a dataset spanning multiple climatic regions we evaluate the generality of published biomass–climate correlations. We also combine metabolic theory and hydraulic limits to plant growth to first derive and then test predictions for how forest biomass should vary with maximum individual tree biomass and the ecosystem water deficit. Location Temperate forests and dry, moist and wet tropical forests across North, Central and South America. Methods A forest biomass model was derived from allometric functions and power‐law size distributions. Biomass and climate were correlated using extensive forest plot (276 0.1‐ha plots), wood density and climate datasets. Climate variables included mean annual temperature, annual precipitation, their ratio, precipitation of the driest quarter, potential and actual evapotranspiration, and the ecosystem water deficit. The water deficit uniquely summarizes water balance by integrating water inputs from precipitation with water losses due to solar energy. Results Climate generally explained little variation in forest biomass, and mixed support was found for published biomass–climate relationships. Our theory indicated that maximum individual biomass governs forest biomass and is constrained by water deficit. Indeed, forest biomass was tightly coupled to maximum individual biomass and the upper bound of maximum individual biomass declined steeply with water deficit. Water deficit similarly constrained the upper bound of forest biomass, with most forests below the constraint. Main conclusions The results suggest that: (1) biomass–climate models developed at restricted geographic/climatic scales may not hold at broader scales; (2) maximum individual biomass is strongly related to forest biomass, suggesting that process‐based models should focus on maximum individual biomass; (3) the ecosystem water deficit constrains biomass, but realized biomass often falls below the constraint; such that (4) biomass is not strongly limited by climate in most forests so that forest biomass may not predictably respond to changes in mean climate.     

Establishment of tree seedlings in the understory of restoration plantations: natural regeneration and enrichment plantings

Little is known about the potential of restoration plantations to provide appropriate understory conditions to support the establishment of seeds arriving from neighboring native forests. In this article, we investigated how seedling establishment is affected in the understory of restoration sites of different ages and assessed some of the potential environmental factors controlling this ecological process. We first compared the density and richness of native tree seedlings among 10‐, 22‐, and 55‐year‐old restoration plantations within the Atlantic Forest region of southeastern Brazil. Then, we undertook a seed addition experiment in each study site, during the wet season, and compared seedling emergence, survival, and biomass on local versus old‐growth forest soil (transferred from a reference ecosystem), in order to test whether local substrate could hamper seedling establishment. As expected, the oldest restoration site had higher density and richness of spontaneously regenerating seedlings. However, seedling establishment was less successful both in the oldest restoration planting and using substrate transferred from a reference ecosystem, where emergence and survival were lower, but surviving seedlings grew better. We attribute these results to lower light availability for seedlings in the understory of the oldest site and speculate that higher incidence of pathogens on old‐growth forest soil may have increased seedling mortality. We conclude that the understory of young restoration plantations provides suitable microsite conditions at the early establishment phases for the spontaneous regeneration or enrichment planting of native trees.     

A pre‐adaptive approach for tropical forest restoration during climate change using naturally occurring genetic variation in response to water limitation

Effective reforestation of degraded tropical forests depends on selecting planting material suited to the stressful environments typical at restoration sites that can be exacerbated by increased duration and intensity of dry spells expected with climate change. While reforestation efforts in nontropical systems are incorporating drought‐adapted genotypes into restoration programs to cope with drier conditions, such approaches have not been tested or implemented in tropical forests. As the first effort to examine genetic variation in plant response to drought in a tropical wet forest, we established a watering experiment using five replicated maternal lines (i.e. seedlings from different maternal trees) of five dipterocarp species native to Borneo. Apart from the expected species level variation in growth and herbivory (3‐fold variation in both cases), we also found intraspecific variation so that growth in some cases varied 2‐fold, and herbivory 3‐fold, among genetically different maternal lines. In two species we found that among‐maternal line variation in growth rate was negatively correlated with tolerance to water limitation, that is, the maternal lines that performed the best in the high water treatment lost proportionally more of their growth during water limitation. We argue that selection for tolerance to future drier conditions is not only likely to impact population genetics of entire forests, but likely extends from forest trees to the communities of canopy arthropods associated with these trees. In tropical reforestation efforts where increased drought is predicted from climate change, including plant material resilient to drier conditions may improve restoration effectiveness.     

Assessing the above‐ground biomass of a complex tropical rainforest using a canopy crane

Abstract Current estimates of the total biomass in tropical rainforests vary considerably; this is due in large part to the different approaches that are used to calculate biomass. In this study we have used a canopy crane to measure the tree architectures in a 1 ha plot of complex mesophyll vine forest at Cape Tribulation, Australia. Methods were developed to measure and calculate the crown and stem biomass of six major species of tree and palm (Alstonia scholaris (Apocynaceae), Cleistanthus myrianthus (Euphorbiaceae), Endiandra microneura (Lauraceae), Myristica insipida (Myristicaceae), Acmena graveolens (Myrtaceae), Normanbya normanbyi (Arecaceae)) using the unique access provided by the crane. This has allowed the first non‐destructive biomass estimate to be carried out for a forest of this type. Allometric equations which relate tree biomass to the measured variable ‘diameter at breast height’ were developed for the six species, and a general equation was also developed for trees on the plot. The general equation was similar in form to equations developed for tropical rainforests in Brazil and New Guinea. The species equations were applied at the level of families, the generalized equation was applied to the remaining species which allowed the biomass of a total of 680 trees to be calculated. This has provided a current estimate of 270 t ha⁻¹ above‐ground biomass at the Australian Canopy Crane site; a value comparable to lowland rainforests in Panama and French Guiana. Using the same tree database seven alternative allometric equations (literature equations for tropical rainforests) were used to calculate the site biomass, the range was large (252–446 t ha⁻¹) with only three equations providing estimates within 34 t ha⁻¹ (12.5%) of the site value. Our use of multiple species‐specific allometric equations has provided a site estimate only slightly larger (1%) than that obtained using allometric equations developed specifically for tropical wet rainforests. We have demonstrated that it is possible to non‐destructively measure the biomass in a complex forest using an on‐site canopy crane. In conjunction the development of crown maps and a detailed tree architecture database allows changes in forest structure to be followed quantitatively.     

Drivers of native species regeneration in the process of restoring natural forests from mono‐specific,even‐aged tree plantations: a quantitative review

A substantial proportion of the existing tree plantations has been established following clearing of native forests. This form of conversion has become widely unaccepted, and there are increasing demands to reverse it through ecological restoration. Yet, there is a lack of integrated knowledge on how best to restore. Here, we reviewed 68 studies to identify the main factors determining establishment success of regeneration of native woody species when restoring natural forests from plantation forests using active and passive approaches, beneath existing canopies, and following their removal. According to the evidence collected, herbivory, within‐gap position, soil properties, and ground cover type and structure had limited influence on regeneration, showing significant effects in less than 26% of cases in which their influence was tested. In contrast, spatial landscape configuration, overstorey structure, ground vegetation structure, overstorey composition, and climate and geomorphology had significant effects in 67, 47, 47, 52, and 63% of cases, respectively. Regeneration diversity and abundance increased with proximity to natural vegetation remnants and seed sources. Lower canopy and understorey stocking levels positively influenced regeneration, as did interventions to reduce them. Canopy cover reduction proved especially effective in warmer regions, in stands of broadleaved species, younger ages (<30 years), higher densities (>1,000 trees/ha), and taller canopies (>20 m). Restoration of native forests can be optimized by adopting interventions that prove most effective, and prioritizing more responsive stand types. However, the specific stand attributes and environmental factors described should be further studied to understand the mechanisms underlying their influence on regeneration.     

Influence of climate on individual tree growth and carbon sequestration in native‐tree plantings

Native ecosystems face challenges of past and ongoing human actions, including vegetation clearance and climate change arising from greenhouse gas emissions. Reforestation is an important tool for sequestering carbon, so we sought to determine how replanted native trees responded to weather, soil conditions and planting characteristics. We measured girth growth of 13 tree species in 19 native mixed‐species plantings and one remnant in south‐eastern Australia, bimonthly from 2011 to 2016; replantings ranged between 6 and 46 years at the commencement of measurements. Band dendrometers (flexible bands that record changes in girth) were used to measure growth, with 34 measurements per tree taken over 5 years. We used outcomes from models with several plausible weather future scenarios (Dry, Wet, Wet‐to‐Dry and Average) for 25 and 50 years for tree girth, and 25 years for carbon accumulation, into the future. Woody species richness enhanced girth growth of all tree species. Higher maximum temperatures and reduced rainfall, which generally are predicted for the region over coming decades, retarded growth of nine tree species. Planting tree density had no discernible association with growth for the range of planting densities used. The most and least carbon were sequestered in Wet and Dry projections, respectively. Three Acacia spp. (N‐fixers) grew slowest and would sequester least carbon, while four species of Eucalyptus grew fastest. These measurements of growth provide critical information for land managers to guide choice in replanting strategies for carbon storage.     

Dominance of legume trees alters nutrient relations in mixed species forest restoration plantings within seven years

Failures in reforestation are often attributed to nutrient limitation for tree growth. We compared tree performance and nitrogen and phosphorus relations in adjacent mixed-species plantings of contrasting composition, established for forest restoration on Ultisol soil, originally covered by tropical semi-deciduous Atlantic Forest in Southeast Brazil. Nutrient relations of four tree species occurring in both planting mixtures were compared between a legume-dominated, species-poor direct seeding mixture of early-successional species (“legume mixture”), and a species-diverse, legume-poor mixture of all successional groups (“diverse mixture”). After 7 years, the legume mixture had 6-fold higher abundance of N₂-fixing trees, 177% higher total tree basal area, 22% lower litter C/N, six-fold higher in situ soil resin-nitrate, and 40% lower in situ soil resin-P, compared to the diverse mixture. In the legume mixture, non-N₂-fixing legume Schizolobium parahyba (Fabaceae-Caesalpinioideae) had significantly lower proportional N resorption, and both naturally regenerating non-legume trees had significantly higher leaf N concentrations, and higher proportional P resorption, than in the diverse mixture. This demonstrate forms of plastic adjustment in all three non-N₂-fixing species to diverged nutrient relations between mixtures. By contrast, leaf nutrient relations in N₂-fixing Enterolobium contortisiliquum (Fabaceae-Mimosoideae) did not respond to planting mixtures. Rapid N accumulation in the legume mixture caused excess soil nitrification over nitrate immobilization and tighter P recycling compared with the diverse mixture. The legume mixture succeeded in accelerating tree growth and canopy closure, but may imply periods of N losses and possibly P limitation. Incorporation of species with efficient nitrate uptake and P mobilization from resistant soil pools offers potential to optimize these tradeoffs.     

格氏栲天然林与人工林枯枝落叶层碳库及养分库

通过对福建三明格氏栲天然林及在其采伐迹地上营造的 33年生格氏栲人工林和杉木人工林枯枝落叶层现存量与季节动态、C库及养分库的研究表明 ,格氏栲天然林、格氏栲人工林和杉木人工林枯枝落叶层现存量分别为 8.99t· hm- 2 、7.5 6t· hm- 2 和 4 .81t· hm- 2 ;枯枝落叶层中叶占现存量的比例分别为 6 4 .96 %、6 1.38%和 38.0 5 % ,枝占比例分别为 31.5 9%、37.83%和 4 2 .6 2 %。格氏栲天然林与人工林枯枝落叶层现存量最大值均出现在春季 ,而杉木人工林枯枝落叶层现存量最大值出现在夏季。格氏栲天然林枯枝落叶层 C贮量为 4 .0 2 t· hm- 2 ,分别是格氏栲人工林和杉木人工林的 1.2 2倍和 1.77倍 ;格氏栲天然林和人工林枯枝落叶层 C库与杉木人工林的差异均达到显著水平 (P<0 .0 5 )。格氏栲天然林、格氏栲人工林和杉木人工林枯枝落叶层养分贮量分别为 138.4 2 kg· hm- 2 、113.5 6 kg· hm- 2 和 72 .39kg· hm- 2 ;除 Mg外 ,格氏栲天然林枯枝落叶层中各种养分贮量均最高。与人工林相比 ,天然林枯枝落叶层现存量、C和养分贮量均最大。枯枝落叶层对林地长期生产力维持具有重要作用。     

人工油松林（Pinus tabulaeformis）恢复过程中土壤微生物生物量C、N的变化特征

采用时空替代法,选取15a（PF15）、25a（PF25）、30a（PF30）的人工油松林作为样地,并选取灌丛作为参考植被,研究了植被恢复过程中土壤微生物生物量C、N以及土壤养分的变化特征,同时探讨了它们之间的相互关系。研究结果表明随着恢复的进行,土壤质量得到了改善,主要表现为有机碳、全氮、粘粒含量、土壤含水量的上升和pH值、容重的下降。土壤微生物生物量C、N分别在155.00~885.64mg/kg和33.73~237.40mg/kg的范围内变化。土壤微生物生物量C、N在植被恢复的初期显著低于灌丛,而后随着恢复的进行逐步增长。土壤微生物生物量C、N与植被恢复时间的相关性没有达到统计学上的显著水平,但是土壤微生物生物量C与土壤有机碳、全氮、全磷呈显著正相关,这表明植被恢复过程中土壤微生物生物量与土壤养分状况关系密切,植被恢复通过改善土壤养分状况间接地影响土壤微生物生物量的变化。Cmic/TOC在1.38%~4.75%的范围内变化。Cmic/TOC随着植被恢复不断下降,Cmic/TOC与植被恢复时间和土壤有机碳呈显著负相关,这表明植被恢复过程中,惰性有机质积累导致供应土壤微生物的活性有机质减少,Cmic/TOC同时受土壤有机质的数量和质量影响。     

Beyond hectares: four principles to guide reforestation in the context of tropical forest and landscape restoration

New climate change agreements emerging from the 21st Conference of the Parties and ambitious international commitments to implement forest and landscape restoration (FLR) are generating unprecedented political awareness and financial mobilization to restore forests at large scales on deforested or degraded land. Restoration interventions aim to increase functionality and resilience of landscapes, conserve biodiversity, store carbon, and mitigate effects of global climate change. We propose four principles to guide tree planting schemes focused on carbon storage and commercial forestry in the tropics in the context of FLR. These principles support activities and land uses that increase tree cover in human‐modified landscapes, while also achieving positive socioecological outcomes at local scales, in an appropriate contextualization: (1) restoration interventions should enhance and diversify local livelihoods; (2) afforestation should not replace native tropical grasslands or savanna ecosystems; (3) reforestation approaches should promote landscape heterogeneity and biological diversity; and (4) residual carbon stocks should be quantitatively and qualitatively distinguished from newly established carbon stocks. The emerging global restoration movement and its growing international support provide strong momentum for increasing tree and forest cover in mosaic landscapes. The proposed principles help to establish a platform for FLR implementation and monitoring based on a broad set of socioenvironmental benefits including, but not solely restricted, to carbon mitigation and wood production.     

Non‐continuous reproductive phenology of animal‐dispersed species in young forest restoration plantings

Tree species that produce resources for fauna are recommended for forest restoration plantings to attract pollinators and seed dispersers; however, information regarding the flowering and fruiting of these species during early growth stages is scarce. We evaluated the reproductive phenology of animal‐dispersed tree species widely used in Atlantic Forest restoration. We marked 16 animal‐dispersed tree species in 3‐ to 8‐year‐old forest restoration plantings in Itu‐São Paulo, southeast Brazil. We noted the age of the first reproductive event, flowering and fruiting seasonality, percentage of trees that reached reproductive stages, and intensity of bud, flower, and fruit production for each species. Flowering and fruiting are seasonal for most species; only two, Cecropia pachystachya and Ficus guaranitica, exhibited continuous flowering and fruiting throughout the year; we also identified Schinus terebinthifolia and Dendropanax cuneatus fruiting in the dry season during resource scarcity. Therefore, we recommend all as framework species, that is, species that are animal‐dispersed with early flowering and fruiting potential, for forest restoration. Further, we recommend identifying and planting similar animal‐dispersed tree species that produce fruits constantly or in the dry season to maximize fauna resource availability throughout the year in tropical forest restoration plantings. Abstract in Portuguese is available with online material     

Quantifying above‐ and belowground biomass carbon loss with forest conversion in tropical lowlands of Sumatra (Indonesia)

Natural forests in South‐East Asia have been extensively converted into other land‐use systems in the past decades and still show high deforestation rates. Historically, lowland forests have been converted into rubber forests, but more recently, the dominant conversion is into oil palm plantations. While it is expected that the large‐scale conversion has strong effects on the carbon cycle, detailed studies quantifying carbon pools and total net primary production (NPP_total) in above‐ and belowground tree biomass in land‐use systems replacing rainforest (incl. oil palm plantations) are rare so far. We measured above‐ and belowground carbon pools in tree biomass together with NPP_total in natural old‐growth forests, ‘jungle rubber’ agroforests under natural tree cover, and rubber and oil palm monocultures in Sumatra. In total, 32 stands (eight plot replicates per land‐use system) were studied in two different regions. Total tree biomass in the natural forest (mean: 384 Mg ha^?1) was more than two times higher than in jungle rubber stands (147 Mg ha^?1) and >four times higher than in monoculture rubber and oil palm plantations (78 and 50 Mg ha^?1). NPP_total was higher in the natural forest (24 Mg ha^?1 yr^?1) than in the rubber systems (20 and 15 Mg ha^?1 yr^?1), but was highest in the oil palm system (33 Mg ha^?1 yr^?1) due to very high fruit production (15–20 Mg ha^?1 yr^?1). NPP_total was dominated in all systems by aboveground production, but belowground productivity was significantly higher in the natural forest and jungle rubber than in plantations. We conclude that conversion of natural lowland forest into different agricultural systems leads to a strong reduction not only in the biomass carbon pool (up to 166 Mg C ha^?1) but also in carbon sequestration as carbon residence time (i.e. biomass‐C:NPP‐C) was 3–10 times higher in the natural forest than in rubber and oil palm plantations.     

Biodiversity in species,traits, and structure determines carbon stocks and uptake in tropical forests

Impacts of climate change require that society urgently develops ways to reduce amounts of carbon in the atmosphere. Tropical forests present an important opportunity, as they take up and store large amounts of carbon. It is often suggested that forests with high biodiversity have large stocks and high rates of carbon uptake. Evidence is, however, scattered across geographic areas and scales, and it remains unclear whether biodiversity is just a co‐benefit or also a requirement for the maintenance of carbon stocks and uptake. Here, we perform a quantitative review of empirical studies that analyzed the relationships between plant biodiversity attributes and carbon stocks and carbon uptake in tropical forests. Our results show that biodiversity attributes related to species, traits or structure significantly affect carbon stocks or uptake in 64% of the evaluated relationships. Average vegetation attributes (community‐mean traits and structural attributes) are more important for carbon stocks, whereas variability in vegetation attributes (i.e., taxonomic diversity) is important for both carbon stocks and uptake. Thus, different attributes of biodiversity have complementary effects on carbon stocks and uptake. These biodiversity effects tend to be more often significant in mature forests at broad spatial scales than in disturbed forests at local spatial scales. Biodiversity effects are also more often significant when confounding variables are not included in the analyses, highlighting the importance of performing a comprehensive analysis that adequately accounts for environmental drivers. In summary, biodiversity is not only a co‐benefit, but also a requirement for short‐ and long‐term maintenance of carbon stocks and enhancement of uptake. Climate change policies should therefore include the maintenance of multiple attributes of biodiversity as an essential requirement to achieve long‐term climate change mitigation goals.     

Trade‐offs between carbon stocks and timber recovery in tropical forests are mediated by logging intensity

Forest degradation accounts for ~70% of total carbon losses from tropical forests. Substantial emissions are from selective logging, a land‐use activity that decreases forest carbon density. To maintain carbon values in selectively logged forests, climate change mitigation policies and government agencies promote the adoption of reduced‐impact logging (RIL) practices. However, whether RIL will maintain both carbon and timber values in managed tropical forests over time remains uncertain. In this study, we quantify the recovery of timber stocks and aboveground carbon at an experimental site where forests were subjected to different intensities of RIL (4, 8, and 16 trees/ha). Our census data span 20 years postlogging and 17 years after the liberation of future crop trees from competition in a tropical forest on the Guiana Shield, a globally important forest carbon reservoir. We model recovery of timber and carbon with a breakpoint regression that allowed us to capture elevated tree mortality immediately after logging. Recovery rates of timber and carbon were governed by the presence of residual trees (i.e., trees that persisted through the first harvest). The liberation treatment stimulated faster recovery of timber albeit at a carbon cost. Model results suggest a threshold logging intensity beyond which forests managed for timber and carbon derive few benefits from RIL, with recruitment and residual growth not sufficient to offset losses. Inclusion of the breakpoint at which carbon and timber gains outpaced postlogging mortality led to high predictive accuracy, including out‐of‐sample R² values >90%, and enabled inference on demographic changes postlogging. Our modeling framework is broadly applicable to studies that aim to quantify impacts of logging on forest recovery. Overall, we demonstrate that initial mortality drives variation in recovery rates, that the second harvest depends on old growth wood, and that timber intensification lowers carbon stocks.     

Carbon stocks,sequestration, and emissions of wetlands in south eastern Australia

Nontidal wetlands are estimated to contribute significantly to the soil carbon pool across the globe. However, our understanding of the occurrence and variability of carbon storage between wetland types and across regions represents a major impediment to the ability of nations to include wetlands in greenhouse gas inventories and carbon offset initiatives. We performed a large‐scale survey of nontidal wetland soil carbon stocks and accretion rates from the state of Victoria in south‐eastern Australia—a region spanning 237,000 km² and containing >35,000 temperate, alpine, and semi‐arid wetlands. From an analysis of >1,600 samples across 103 wetlands, we found that alpine wetlands had the highest carbon stocks (290 ± 180 Mg C_org ha^?1), while permanent open freshwater wetlands and saline wetlands had the lowest carbon stocks (110 ± 120 and 60 ± 50 Mg C_org ha^?1, respectively). Permanent open freshwater sites sequestered on average three times more carbon per year over the last century than shallow freshwater marshes (2.50 ± 0.44 and 0.79 ± 0.45 Mg C_org ha^?1 year^?1, respectively). Using this data, we estimate that wetlands in Victoria have a soil carbon stock in the upper 1 m of 68 million tons of C_org, with an annual soil carbon sequestration rate of 3 million tons of CO₂ eq. year^?1—equivalent to the annual emissions of about 3% of the state's population. Since European settlement (~1834), drainage and loss of 260,530 ha of wetlands may have released between 20 and 75 million tons CO₂ equivalents (based on 27%–90% of soil carbon converted to CO₂). Overall, we show that despite substantial spatial variability within wetland types, some wetland types differ in their carbon stocks and sequestration rates. The duration of water inundation, plant community composition, and allochthonous carbon inputs likely play an important role in influencing variation in carbon storage.