• Buillon (2011) Carbon cycle: Storage beneath mangroves. Nature Geoscience. 4: 282–283. • Donato et al (2011) Mangroves among the most carbon-rich forests in the tropics. Nature Geoscience. 4: 293–297. • Ellison (2008) Long-term retrospection on mangrove development using sediment cores and pollen analysis: A review. Aquatic Botany. 89, 2: 93-104. • McKee et al (2007) Caribbean mangroves adjust to rising sea level through biotic controls on change in soil elevation. Global Ecology and Biogeography. 16, 5: 545-556. • Wooller et al (2007) A multiproxy peat record of Holocene mangrove palaeoecology from Twin Cays, Belize. The Holocene. 17, 8: 1129-1139 • Wooller et al (2009) Late Holocene hydrologic and vegetation changes at Turneffe Atoll, Belize, compared with records from mainland Central America and Mexico. Palaios. 24, 10: 650-656. Review Long-term retrospection on mangrove development using sediment cores and pollen analysis: A review Joanna C. Ellison Aquatic Botany Volume 89, Issue 2, Pages 93-104 Abstract Mangroves are biogenic systems that accumulate sedimentary sequences, where cores can provide records of mangrove species variation in distribution with past climate change and sea-level change. Fossil evidence used for palaeoecological reconstruction is based on organic remains that preserve identifying features so that they can be identified to generic levels at least. This includes macrofossils such as fruit, flowers, wood or leaves, or microfossils particularly pollen. Anaerobic conditions in mangrove sediment allow the long-term preservation of these fossil records. Fossil pollen from core samples is concentrated for microscopic examination by use of standard chemical treatments, but refinements of these are necessary for the peculiarities of mangrove peat. Pollen diagrams are expressed in concentrations, or more usefully in mangrove environments as proportions relative to others, as this has been shown to demonstrate the depositional environment actually underneath the mangrove forest. Radiocarbon dating of sedimentary sequences is used to date palaeoecological successions shown by fossil sequences, or long-term sedimentation rates. Sediment accretion in the last 50–200 years can been analysed better using Cs137 and Pb210 analyses. From pollen and macrofossils mostly recovered from stratigraphic cores of sedimentary rock and more recent sediment, the evolution and dispersal of mangroves through geological time has been reconstructed. While reconstruction of actual temperatures in these earlier records is associative to the fossil types present, it is apparent that mangroves have always been tropical species, extending to higher latitudes only during global warm periods. Many sedimentary records show mangroves deeper than the present lower limit of mangrove growth at mean sealevel. These indicate sea-level rising over time, and mangroves keeping pace with rising sea-level. Stratigraphic dating shows accretion rates of 1 mm a−1 for low island locations, and up to 1.5 mm a−1 in high islands/continental margins. Sedimentary records can also show die-off of mangroves with more rapid sea-level rise and replacement by open water during rising sea-level, landward retreat of mangrove zones, or replacement of mangroves by freshwater forest with sedimentary infill. The causes of mangrove community changes identified in the palaeoecological record can only be inferred by comparison with ecological studies in the modern environment, the link between the two that may be possible through long-term mangrove monitoring being poorly established. Keywords: Stratigraphy; Pollen analysis; Palaeoecology; Macrofossil; Sedimentation; Palynolog PALAIOS; October 2009; v. 24; no. 10; p. 650-656; DOI: 10.2110/palo.2009.p09036r Late Holocene hydrologic and vegetation changes at Turneffe Atoll, Belize, compared with records from mainland Central America and Mexico Matthew J. Wooller*,1,2,5, Hermann Behling3, Juan Leon Guerrero4, Nele Jantz3 and Martin E. Zweigert3 Alaska Stable Isotope Facility, Water Environmental Research Center, University of Alaska Fairbanks, Fairbanks, Alaska 99775, USA 2 School of Fisheries and Ocean Sciences, University of Alaska Fairbanks, Fairbanks, Alaska 99775, USA 3 Department of Palynology and Climate Dynamics, Albrecht-von-Haller-Institute for Plant Sciences, University of Göttingen, Untere Karspüle 2, 37073 Göttingen, Germany 4 Biology and Wildlife, University of Alaska Fairbanks, Fairbanks, Alaska 99775, USA 5 ffmjw@uaf.edu 1 We present pollen and stable isotope ( 13C, 18O, 15N) data from a 4 m core (TNF-1) of primarily mangrove peat taken from Turneffe Atoll, Belize. Radiocarbon (accelerator mass spectrometry) dates show that the record represents ca. 5000 years of sediment accumulation. Vegetation composition varied between dominant mangroves (primarily Rhizophora mangle) and Chenopodiaceae-Amaranthaceae, most likely Salicornia bigelovii. The pollen data, along with inferences from stable isotope analyses of bulk peat and fossil leaf fragments, indicate that marked environmental changes occurred at this location over the past ca. 5000 years. There was a transition between ca. 4100 and 2900 cal yr BP, from vegetation dominated by relatively tall mangroves (R. mangle) to one dominated by Chenopodiaceae-Amaranthaceae and then Myrica, most likely wax myrtle (M. cerifera). These changes bracket a period centered at ca. 3500 calibrated years before present, where there is a peak in the 18O of mangrove leaf fragments. This timing corresponds with other paleoenvironmental records of climate drying in Central America and increases the geographic and habitat scope (i.e., mangrove habitat) of records documenting these changes. Interpretations of shifts in mangrove habitat, however, require consideration of additional environmental influences, including changes in groundwater hydrology and relative inputs of seawater and freshwater (i.e., precipitation) during the Holocene.