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Linking Climate Change and Tree Productivity in Ranomafana National Park, Madagascar by Patricia C. Wright, Benjamin Greene. Jessica Scirbona, Paul Rakotonirina, Armand Razafitsiafajato, Jean de dieu Ramarolahy, and Paul Rasabo, Stony Brook University, Stony Brook, New York, USA and Centre ValBio, Ranomafana, Madagascar DRAFT without FIGURES OR TABLES This paper is prepared for the Conservation International Workshop “Climate Change in Madagascar-January 28-31, 2008 1 SUMMARY Madagascar has the highest levels of endemism and endangerment for more species than any other country in the world (Myers et al., 2000, Mittermeier et al., 2006). In Madagascar there is evidence that even low-level disturbance can have a large impact on forest dynamics and wildlife populations (Dehgan, 2003, King et al., 2005, Wright, 2006, Irwin, 2006, Arrigo-Nelson, 2006). Madagascar wildlife is closely aligned with natural systems exemplified by a 6 month hibernation by small mammals and amphibians, and strict seasonal breeding in lemurs and most wildlife (Wright, 1999, Wright et al., 2005). Many lemur species are on the brink of extinction (Mittermeier et al., 2006) and these species will be further challenged by changes in climate (Dunham et al., 2008). In order to better understand the impact of climate on the fauna and flora of the eastern rainforests of Madagascar, our research team at Ranomafana National Park has been monitoring daily temperature, daily rainfall, and monthly phenology and fruit production of over 200 individual trees, as well as lemur demography and feeding behavior. Although our data shows that mean annual rainfall totals are not changing, our data do suggest an increase in number of dry season months. In response to these subtle climatic differences are changes in fruiting patterns in some species of trees. The impact of major worldwide weather phenomena such as El Nino on fruit productivity has been noted in the Americas and Borneo (Foster, 1982, Wright et al., 1999. Harrison, et al., 2000, Hughes et al., 2000). As reported in the tree monitoring study presented here, El Nino and drought years also effects tree productivity in Madagascar. It has been documented that El Nino events have been increasing in their frequency in the past decade (Federov and Philander, 2000, Timmermann et al., 1999) . We have 2 preliminary data that suggest a decrease in successful reproduction in lemurs during years with extended dry seasons (King et al., 2005, Wright et al., 2008). We have found that lemur survival decreases by 65% during El Nino years and our mathematical modeling of lemur populationa suggest a serious endangerment problem may be just ahead, even within protected areas (Dunham et al., 2008). The analysis of the daily temperature data over a 20 year period did not show high temperatures rising or annual temperatures increasing in the rainforest. However minimum temperatures during the cold season were higher during the past ten years, compared to the previous decade. Future analysis will establish if this higher minimum temperature has an effect on tree reproduction. Our long term research points out the importance of monitoring a wide range of ecosystem changes in conjunction with monitoring rainfall and temperature trends through time to understand the far-reaching consequences to biodiversity. INTRODUCTION Madagascar is home to more endemic families and genera than any other conservation 'hotspot' in the world, and high rates of habitat loss and other anthropogenic disturbances severely threaten native species (Myers et al., 2000). Over 80% of the forest cover has already been lost and the populations of many remaining species are small and fragmented (Whitmore, 2000). The government of Madagascar has recently committed to increasing its protected areas from 1.7 million hectares to 6 million hectares (Goodman & Benstead, 2005). While there have been much research discussing the effects of habitat loss and hunting pressures on the viability of wildlife populations (Irwin et al., 2005, Lehman, 2002, Lehman et al., 2005, Mittermeier et al., 2006), the confounding effects of recent climate change and global climate cycles such as El Niño Southern Oscillations (ENSO) have rarely been broached 3 (Dunham et al., 2008). Given the potential role of human-induced climate change in altering the frequency of ENSO events (Fedorov & Philander, 2000; Timmermann et al., 1999), there is a critical need to assess the impact of climate changes on fruiting patterns of the forest trees which in turn effect the viability of wildlife populations. The high frequency of ENSO in the last few decades has raised questions about how human-induced climate change is affecting or will affect the frequency of ENSO (Fedorov & Philander, 2000; Timmermann et al., 1999). In Madagascar and southern Africa, ENSO events have been documented to cause drought (Thomson et al., 2003) and vegetation changes (Ingram & Dawson, 2005) which may negatively affect wildlife (Gould et al., 1999; Wright, 1999). The prospect of increased ENSO events in Madagascar is daunting given the severity of other anthropogenic threats to its biodiversity. A recent study showed that the immediate effects of an ENSO year can decrease lemur populations by 65% (Dunham et al., 2008). A further indication that climate change is affecting wildlife is shown in two studies of lemur demography. A demographic study of the Milne Edward’s sifaka (Propithecus edwardsi Mayor et al., 2004) showed that group sizes are variable, but overall populations may be diminishing (Pochron and Wright, 2003, Pochron et al., 2004). When the effect of rainfall on infant survival was examined (King et al., 2005), it was found that climate may have a serious impact. The results of comparing years with more dry season months to those years with more equal rainfall showed that infant survival was negatively impacted by the increase in dry months (Wright, 2006; Wright et al., 2008). This same trend was found in a long term study of demographics of Eulemur fulvus rufus at Ranoamafana National Park (Overdorff et al., 2008). In order to isolate the impact of many possible variables that may be affecting these wildlife populations, such as historic selective logging, predation events or stochastic 4 demographic changes (Pochron and Wright, 2003, Karpanty and Wright, 2006, Arrigo-Nelson, 2006), we have examined the effect of daily temperature, monthly rainfall and ENSO years on the food of the wildlife. By monitoring fruit production of rainforest trees at Ranomafana over the past 20 years, we can target the impact that weather and climate has on fruiting production and patterning. METHODS At Ranomafana National Park, located at (21 degrees, 16’ 38’’ South, 47 degrees 23’ 50’’ East) we have monitored individual mature trees over a 20 year period. Reproductive status and new leaf flush have been evaluated monthly for 25 canopy and mid-storey tree species between 1987 and 2007. This first set of 25 species include 15 genera and 17 families. Four examples of each species were originally chosen in 1987 for a total of 100 trees. In 1997 four individuals from an additional 25 species were added to the phenology. This increases the monthly monitored sample to 50 species (200 trees) from more than 26 genera and 19 families. The families represented by three or more species include Clusiaceae, Myrtaceae, Moraceae, Sapindaceae, Lauraceae, and Anacardiaceae. Dead trees are replaced with new individuals from the same species. Originally all trees had a dbh larger than 10cm and mature individuals were chosen. For the first ten years growth measurements by dbh occurred every five years. For the past ten years dbh has been measured annually. Tree crowns have been evaluated from the ground using binoculars by local botanists trained by Missouri Botanical Garden. Reproductive status was scored on a five-point scale. Sterile trees were scored zero. Trees with from one reproductive structure to 25% of the crown bearing reproductive structures were scored one. Trees with 26–50%, 51–75% and 76–100% of the crown bearing reproductive structures were 5 scored two, three and four, respectively. These data are useful for comparing fruiting and flowering patterns to rainfall and temperature changes over this time period. These data have recently been entered into an excel spreadsheet for analysis. During the first sixteen years of this study (1987-2003), daily rainfall amounts were measured using a standard rainfall cylinder in metric units, placed in an open area near the research cabin inside the park. In 2003 a rainfall cylinder was placed in an open area next to the Centre ValBio, about a kilometer northeast of the original research cabin. A maximum-minimum thermometer with temperature measured in Centigrade units was placed under the canopy inside the forest near the research cabin from 1987-2003. One individual is responsible for collecting the rainfall and temperature data at 6am each morning. These data are entered into the computer each week. RESULTS Annual rainfall amounts over the twenty year period varied from a low of 1,794mm in 1997 to over 4000mm in 1996. On average 3,000mm of rain a year fell at Ranomafana National Park from 1987-2007, This rainfall mean is comparable to the national weather station mean of Ranomena and Ranomafanana rainfall from 1960-1980. However, there is a difference in pattern, when the variability of the rainfall each month is examined. Compared to the previous decades, the years 1987-2007 had more rain in the rainy season and more months that contained less than 100mm rain. Between 1960 and 1985 90% of the years had 11 or 12 “wet” months of more than 100mm of rain, while from 1986-2007 60% of the years had months with more than 100mm of rain. The monitoring of the fruit production of the trees showed that individual fruiting of trees was highly variable with less than a quarter of the trees monitored producing fruit each year. 6 Comparing the decade 1987-1996 to the decade 1997-2007 the fruit productivity drops from a mean of 25% to a mean of 9% of the trees giving fruit. Although fruits are available all year, the months from April to August show little fruiting and are limited to two or three fruiting species each month during this period. Some trees do not fruit the year after ENSO years,. These preliminary results show a huge decrease in fruit production over the past decade at Ranomafana and this decrease in food availability could result in a negative impact on wildlife populations. DISCUSSION Conservation of the wildlife of Madagascar has been a target of the government of Madagascar and conservationists for the past fifteen years (Myers et al., 1987, Myers et al., 2000, Mittermeier et al., 2005). The rampant deforestation of from 1.7-4.7% of the remaining forests of Madagascar, as well as hunting for food by humans, have been major factors threatening biodiversity (Irwin et al., 2000, 2005, Lehman, 2002, Achard, 2002). Although reports on the negative affects of drought on lemur populations in the dry south of Madagascar have been published (Jolly et al., 2002, Gould, 1999), there have been no countrywide examination of whether and how climate change is affecting the biodiversity. By examining twenty consecutive years of records of populations of lemurs, tropical trees, rainfall and temperatures at one site (Ranomafana National Park), we begin an attempt to understand the dynamics between climate change and biodiversity in the eastern rainforests of Madagascar. Although there are shorter (2-6 year) databases collecting flowering and fruiting activity on Malagasy trees from the western dry forests of Kirindy Forest (near Morandava) and Beza Mahafaly (south of Tulear), the Ranomafana Tree Phenology project is the only database that has monitored individual trees over a twenty year period in Madagascar. Simultaneously we have collected daily rainfall and maximum-minimum temperatures for this same twenty year period. 7 Our preliminary analyses of these long term databases from Ranomafana National Park show that climate and adult forest tree productivity may be closely linked. The accumulated data from Ranomafana suggests that changing global weather cycles may compound with deforestation and hunting to speed the threat to wildlife populations. We now know that the average fecundity of lemurs is over 65% lower during El Niño years (Dunham et al., 2008). In addition there is more lemur infant mortality during years with an extended dry season (King et al., 2005, Wright, 2006, Wright et al., 2008). The analysis presented in this paper shows that fruit productivity in this forest has diminished by half in the last decade. The fact that this lower fruit crop can be linked with years with more dry season months, may indicate that climate change is a partial cause for this decrease. In addition, temperature increases may also have a negative effect on fruit productivity and cryptic forest dynamics that may impact negatively on wildlife survival. Recent evidence from Costa Rica suggests that in years with higher minimum temperatures, increases in circumference of rainforest trees stops (Clark and Clark, in press). If an increase in minimum temperatures also arrests tree growth in Madagascar rainforest and this is coupled with lack of reproductive activity in these forest trees, this trend could have a major impact in the long term fitness of the endangered species that rely on these trees for food. Phenological databases of the span and completeness of this Ranomafana dataset are rare in the tropics. Joseph Wright on Barro Colorado Island, David and Deborah Clark in Costa Rica, Tim O’Brien in Indonesia and Colin Chapman in Kibale Forest in Uganda have comparable datasets over this time period (see Chapman et al., 2005a, b; Clark, 2007; Wright et al. 1999). It is important to take a comparative approach to understanding the effects of climate on tropical 8 trees worldwide. We then need to look at the impact on endangered populations of wildlife and develop effective management strategies. 9 ACKNOWLEDGEMENTS In Madagascar we would like to thank the National Association for the Management of Protected Areas (ANGAP), Department of Water and Forests, and the Ministry of the Environment, Water and Forests and the CAFF/CORE committee for authorization to do this research. Many thanks to B. Andriamihaja and A. Feistner and staffs of MICET, Centre ValBio, and ICTE for logistical help. Funding for the long-term monitoring was provided from the David and Lucile Packard Foundation, Douroucouli Foundation, the Wenner-Gren Foundation, the John D. and Catherine T. MacArthur Foundation, National Geographic Society, National Science Foundation, Earthwatch Institute, and Stony Brook University. The late Georges Rakotonirina and Michael Todd are acknowledged for setting up the phenology tree system in 1987. Both G. Rakotonirina and William Rakotonirina took data for the first decade. Tiana Razafindratsita and Aimee are gratefully acknowled for collecting much of the first ten years of climate data. Jukka Jernvall graciously assisted with data analysis. Our appreciation to Lee Hannah from Conservation International for inviting us to share our data for the Climate Change Workshop held in Madagascar January 28-31. 10 REFERENCES Achard, F., Eva H. D., Stibig H., Mayaux P., Gallego J., Richards T., Malingreau J., 2002. Determination of deforestation rates of the world's humid tropical forests. Science 297, 999-1002. ANGAP, 2003. Carte de localisation du Parc National de Ranomafana. Map by Association Nationale pour la Gestion des Aires Protégées/FTM, Ranomafana. Arrigo-Nelson, S. J. 2006. The impact of selective logging on feeding patterns in an endangered lemur, Propithecus edwardsi, in Ranomafana National Park, Madagascar. Unpubl. Ph. D dissertation, Stony Brook University, NY. 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T., Phillips O. L., Williams S. E., 2004. Extinction risk from climate change. Nature 427, 145-148. Thomson, M. D., Abayomi I., Barnston A. G., Levy M., Dilley M., 2003. El Niño and drought in southern Africa. Lancet 361, 437-438. 12 Timmermann, A., Oberhuber J., Bacher A., Esch M., M. L., E. R., 1999. Increased El Niño frequency in a climate model forced by future greenhouse warming. Nature 398, 694697. Whitmore, T. C., 2000. Madagascan deforestation rate during 1980. in: Lourenco, W., and Goodman, S. M., (Eds.), Diversité et endémisme à Madagascar. Mémoires de la Société de Biogéographie, Paris. pp. 125. Wright, P. C., 1997. The future of biodiversity in Madagascar; A view from Ranomafana National Park. in: Goodman, S. M., and Patterson, B. D., (Eds.), Natural change and human impact in Madagascar. Smithsonian Institution Press, Washington. pp. 381-405. Wright, P. C., 1999. 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The El Nino southern oscillation, variable fruit production and famine in a tropical forest. Ecology 80 (5): 1632-1647. 13