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Jeffrey Kelleway

Publications and source records attributed to Jeffrey Kelleway.

5 recordsLinked to original sources

Tidal forested wetlands can be incorporated into blue carbon conservation and restoration strategies

Purpose of Review Blue carbon is an important concept for environmental policy. Blue carbon strategies (conservation and restoration for carbon gain) have been primarily implemented with mangroves, though are likely to be suitable for other tidal forested wetlands. Here, we discuss the expanding definition of blue carbon encompassing all tidal forested wetlands, synthesize ecological and carbon sink knowledge of tidal forested wetlands, and reflect on key actions in mangrove blue carbon research and implementation that could be applied to other tidal forested wetlands. Recent Findings Conceptually, the blue carbon concept has now expanded beyond traditional coastal vegetated ecosystems to include all tidal wetlands, including tidal forested wetlands. Emerging data on carbon sequestration, emissions, and budgets from around the world now show that many tidal forested wetland ecosystems are carbon sinks at a magnitude similar to mangroves. At the global scale, mangroves have become incorporated into blue carbon strategies rapidly compared to other tidal forested wetlands, facilitated by agenda-setting papers, adequate data addressing concerns on emissions and permanence, the availability of global maps, a clear ecosystem definition, clear accounting and policy frameworks, and international stakeholders who acted as high profile ecosystem advocates, alongside long-term capacity building efforts. This provides a roadmap for implementation in other tidal forested wetlands. Summary Tidal forested wetlands other than mangroves have high potential for blue carbon management. Many tidal forested wetlands share biophysical similarities with mangroves, carbon stocks can be similar, and methane emissions are often no higher. An increasing evidence base, challenging assumptions around greenhouse gas fluxes, and robust engagement with policy actors and frameworks, could increase the use of blue carbon for tidal forested wetland conservation and restoration.

Current Forestry Reports

All tidal wetlands are blue carbon ecosystems

Managing coastal wetlands is one of the most promising activities to reduce atmospheric greenhouse gases, and it also contributes to meeting the United Nations Sustainable Development Goals. One of the options is through blue carbon projects, in which mangroves, saltmarshes, and seagrass are managed to increase carbon sequestration and reduce greenhouse gas emissions. However, other tidal wetlands align with the characteristics of blue carbon. These wetlands are called tidal freshwater wetlands in the United States, supratidal wetlands in Australia, transitional forests in Southeast Asia, and estuarine forests in South Africa. They have similar or larger potential for atmospheric carbon sequestration and emission reductions than the currently considered blue carbon ecosystems and have been highly exploited. In the present article, we suggest that all wetlands directly or indirectly influenced by tides should be considered blue carbon. Their protection and restoration through carbon offsets could reduce emissions while providing multiple cobenefits, including biodiversity.

BioScience

Practical guide to measuring wetland carbon pools and fluxes

Wetlands cover a small portion of the world, but have disproportionate influence on global carbon (C) sequestration, carbon dioxide and methane emissions, and aquatic C fluxes. However, the underlying biogeochemical processes that affect wetland C pools and fluxes are complex and dynamic, making measurements of wetland C challenging. Over decades of research, many observational, experimental, and analytical approaches have been developed to understand and quantify pools and fluxes of wetland C. Sampling approaches range in their representation of wetland C from short to long timeframes and local to landscape spatial scales. This review summarizes common and cutting-edge methodological approaches for quantifying wetland C pools and fluxes. We first define each of the major C pools and fluxes and provide rationale for their importance to wetland C dynamics. For each approach, we clarify what component of wetland C is measured and its spatial and temporal representativeness and constraints. We describe practical considerations for each approach, such as where and when an approach is typically used, who can conduct the measurements (expertise, training requirements), and how approaches are conducted, including considerations on equipment complexity and costs. Finally, we review key covariates and ancillary measurements that enhance the interpretation of findings and facilitate model development. The protocols that we describe to measure soil, water, vegetation, and gases are also relevant for related disciplines such as ecology. Improved quality and consistency of data collection and reporting across studies will help reduce global uncertainties and develop management strategies to use wetlands as nature-based climate solutions.

Wetlands

Widespread retreat of coastal habitat is likely at warming levels above 1.5 °C

Several coastal ecosystems—most notably mangroves and tidal marshes—exhibit biogenic feedbacks that are facilitating adjustment to relative sea-level rise (RSLR), including the sequestration of carbon and the trapping of mineral sediment 1 . The stability of reef-top habitats under RSLR is similarly linked to reef-derived sediment accumulation and the vertical accretion of protective coral reefs 2 . The persistence of these ecosystems under high rates of RSLR is contested 3 . Here we show that the probability of vertical adjustment to RSLR inferred from palaeo-stratigraphic observations aligns with contemporary in situ survey measurements. A deficit between tidal marsh and mangrove adjustment and RSLR is likely at 4 mm yr −1 and highly likely at 7 mm yr −1 of RSLR. As rates of RSLR exceed 7 mm yr −1 , the probability that reef islands destabilize through increased shoreline erosion and wave over-topping increases. Increased global warming from 1.5 °C to 2.0 °C would double the area of mapped tidal marsh exposed to 4 mm yr −1 of RSLR by between 2080 and 2100. With 3 °C of warming, nearly all the world’s mangrove forests and coral reef islands and almost 40% of mapped tidal marshes are estimated to be exposed to RSLR of at least 7 mm yr −1 . Meeting the Paris agreement targets would minimize disruption to coastal ecosystems.

Nature

Life stage influences the resistance and resilience of black mangrove forests to winter climate extremes

In subtropical coastal wetlands on multiple continents, climate change-induced reductions in the frequency and intensity of freezing temperatures are expected to lead to the expansion of woody plants (i.e., mangrove forests) at the expense of tidal grasslands (i.e., salt marshes). Since some ecosystem goods and services would be affected by mangrove range expansion, there is a need to better understand mangrove sensitivity to freezing temperatures as well as the implications of changing winter climate extremes for mangrove-salt marsh interactions. In this study, we investigated the following questions: (1) how does plant life stage (i.e., ontogeny) influence the resistance and resilience of black mangrove (Avicennia germinans) forests to freezing temperatures; and (2) how might differential life stage responses to freeze events affect the rate of mangrove expansion and salt marsh displacement due to climate change? To address these questions, we quantified freeze damage and recovery for different life stages (seedling, short tree, and tall tree) following extreme winter air temperature events that occurred near the northern range limit of A. germinans in North America. We found that life stage affects black mangrove forest resistance and resilience to winter climate extremes in a nonlinear fashion. Resistance to winter climate extremes was high for tall A. germinans trees and seedlings, but lowest for short trees. Resilience was highest for tall A. germinans trees. These results suggest the presence of positive feedbacks and indicate that climate-change induced decreases in the frequency and intensity of extreme minimum air temperatures could lead to a nonlinear increase in mangrove forest resistance and resilience. This feedback could accelerate future mangrove expansion and salt marsh loss at rates beyond what would be predicted from climate change alone. In general terms, our study highlights the importance of accounting for differential life stage responses and positive feedbacks when evaluating the ecological effects of changes in the frequency and magnitude of climate extremes.

Louisiana