MANATEES IN FLORIDA: 2001Continuedby THOMAS H. FRASER, Ph.D Part of this emphasis on aerial surveys may be because of an early rejection of the capture, then marking (tagging) and subsequent recapture to use in a population model for estimating population size along with other data (Packard and Nichols, 1983). This method is one of the better ways to determine population estimates. Many carcasses are collected each year and given a cause of death. By knowing various manatee characteristics modeled population estimates can be made and sensitivity analyses completed. These characteristics include: general proportions of tagged animals to good minimum winter counts, proportion of tagged animals at specific warm water sites from recapture of live animals, growth, maturation, reproduction and mortality characteristics such as ages and sex of the dead animals with and without tags. MORTALITY ISSUES No statistical models are needed to show the positive changes with time for minimum manatee population and boater registration (Figure 4), boating related manatee deaths per 1000 registered boats and minimum manatee population per 1000 registered boats (Figure 5). Collinearity between population and boats is clear from Figure 4, even though these two variables are independent of one another. Figure 5 suggests that the rate of boating deaths is not changing faster than the number of registrations with respect to the population. Two other graphs with time are helpful in placing the boating related manatee deaths in perspective: minimum population counts and boating related deaths (Figure 6) and total deaths (adjusted for boating deaths) and boating related deaths (Figure 7). Figure 6 suggests that the population is growing much faster than the number of boating deaths. Figure 7 suggests that total mortality adjusted for boat-related mortality is growing faster. This change is consistent with the population growth in Figure 6. If boat-related mortality is adjusted per capita, then there is no apparent change with time (Figure 8). Mortality information is consistent with an increasing population of manatees. If the natural mortality rate has remained relatively unchanged over the past several decades, then relative changes should reflect trends in the general population. If the perinatal death rate has remained relatively unchanged over the past several decades, then relative changes should reflect trends in the female population. An examination of per capita manatee deaths more accurately determines relative mortality trend issues than just the use of annual numerical totals. Figure 9 shows that while the annual deaths are increasing, the annual deaths per 100 manatees are obviously not trending up. In Figure 10, annual perinatal deaths are increasing over time, but the annual deaths per 100 manatees are not trending up since about 1983. Figure 11 compares (per 100 manatees) an adjusted annual deaths (total-perinatal) with perinatal deaths. The perinatal line shows some pattern similarity and differences to the adjusted line suggesting that, perinatal deaths may be closely tied with adult mortality in some years (cold winters?, red tides?). Figure 12 shows the relationship between minimum population counts and perinatal deaths which suggest that the increase in perinatal deaths is much less than the increase in counts. The general State-wide relationships between boater registration and boat-related manatee deaths described above appear to break down in regional areas (Wright et al., 1995). They ascribed these differences to location of the artificial warm-water sources with respect to Intracoastal Waterways, to apparent size of the local manatee populations and to number of boats in the region. Figures 13-16 show the boater registrations in the Tampa Bay area, Indian River Lagoon north of Indian River County, the Charlotte Harbor Complex and Collier County. In each of these areas, there is no clear relationship for registration and boat related deaths. Comparing between regions, the contrasts between the graphs for registrations and boating deaths appear different (all boating deaths are on the same scale). The age distribution of carcasses (Table 3) show relatively few animals in the older age class. This distribution may be, in part, the result of an increasing population where younger animals are beginning to influence the relative abundance of older (25+) age classes. Only more data with comparisons among age frequencies may resolve such a hypothesis. Females deaths are considered more important than male deaths for population increase because of the relatively long pregnancy and calf association. Therefore, the ages at which females are dying are important to maintaining or increasing the population. Boating related deaths appear proportionally the same, by sex, for the totals. If the synoptic counts were getting better at counting and the increases in the counts just meant, not new young manatees in the population, but rather existing manatees not counted before, then the age frequency distribution should be skewed to older animals. Manatees in the Charlotte Harbor Complex suffered a natural mortality event (but aggravated by the location of the artificial warm-water site in the Caloosahatchee River) in 1996 that was attributed to the toxic effects of a sustained red-tide bloom during the late winter. About 149 deaths during a 2-3 month period were attributed to this cause. Just prior to this event as part of the synoptic aerial survey some 469 manatees were counted in Lee County on January 10, 1996. The day before, 434 were in the vicinity of the Florida Power and Light's artificial warm water discharge into the Orange River and then to the Caloosahatchee River. During the synoptic aerial survey of 5-6 January 2001, some 498 manatees were counted in Lee County, with 434 manatees located at the warm water discharge. These data suggest that manatees recouped their losses from the 1996 red tide and all other sources of mortality in just four years. Variables used in a general linear model were examined (Appendix 3) for relationships with boat-related deaths. This analysis demonstrate that the size of the manatee population will have a significant influence on boat-related deaths as suggested by Wright et al., (1995). However, because of collinearity or multicollinearity among boat registration, boating-related deaths, and minimum population counts the parameter estimates are unstable and have high standard errors. This collinearity or multicollinearity problems are not removed easily with satisfactory results.
Discussion A population model and estimates from such a model are needed for Florida to adopt quantitative biological goals which provides measures for healthy and sustainable population of manatees. The minimum population counts have not been considered by scientists to be useable for estimating the size of Florida's existing population. Performance criteria for existing and new regulatory zones should be established to: 1), determine types of zones needed, 2) determine effectiveness of existing zones, and 3) determine need for new zones. Additional regulatory zones should be adopted only after determining the status of the existing State manatee population. Numerical increases in boat-related manatee mortality should not be used to justify ever more restrictive State rules or County ordinances. Such ordinances should be justified by a manatee per capita rate. Knowledge of the status of population changes becomes very important in order to assess whether there is a departure from a boating mortality curve that is above a flat, stable rate as exists at present. By definition, the present and past manatee per capita mortality rates occurred during a period when there has clearly been net additions to the population and therefore are not likely to jeopardize the existence of the species. Boat-related mortality may be considered to have a negligible effect on status of the species in Florida. Florida lists the manatee as an endangered species. Florida has a process (Florida Administrative Code, 68A-27) which lays out the requirements of listing or reclassifying a species. FAC 68A-27.0012 is a recently approved format for submitting a petition (Appendix 4). Biological characteristics or guidelines are given for each category: endangered, threatened, and species of special concern (Appendix 4). Manatees appear to exceed the conditions necessary for reclassifying to a species of special concern, or perhaps, to be classified as recovered, based on examination of State criteria. Reasons for such consideration include an increasing population for at least 25 years, full occupation of its habitat without significant restriction on forage, water, or reproductive areas, and virtually no real probability of going extinct in the next 100 years due to boat interactions. One serious threat to Florida's manatees that has not been addressed, and should be, is a risk assessment for a highly infectious disease being acquired (such as a species-jumping distemper virus) as the result of overcrowding at artificial warm water discharges. The U. S. Fish & Wildlife Service (FWS) has population recovery criteria in its 1995 recovery plan. However, the FWS is in the process of revising that plan and assessing recovery criteria. Some numerical criteria are being considered for application to four regions of Florida. Any discussion of the Federal process must await FWS's actions over the next few months. However, there is a heavy reliance on artificial warm water discharges by manatees, north of the generally accepted natural winter range for manatees. How can this species be reclassified to recovered in Florida if manatees must rely on maintenance of a specific human altered habitat that may fail or have the source decommissioned even if all other criteria are met? CONCLUSIONS
LITERATURE CITED Ackerman, B. B., S. D. Wright, R. K. Bonde, D. K. Odell, and D. J. Banowetz. 1995. Trends and patterns in mortality of manatees in Florida, 1974-1992. PP.223-258. In: T. J. O'Shea, B. B. Ackerman & H. F. Percival, Editors. Population biology of the Florida Manatee. Information and Technology Report 1. 289 pp. Eberhardt, L. L. 1995. Integration of manatee life-history data and population modeling. PP 269- 279. In: T. J. O'Shea, B. B. Ackerman & H. F. Percival, Editors. Population biology of the Florida Manatee. Information and Technology Report 1. 289 pp. Flamm, R. O., L. I. Ward, & M. White, eds. 2000. Atlas of Marine Resources, Version 1.3. Florida Fish and Wildlife Conservation Commission, Florida |Marine Research Institute. Irvine, A. B. and H. W. Campbell. 1978. Aerial census of the West Indian manatee, Trichechus manatus, in the southeastern United States. Journal of Mammalogy, 59:613-630. Lefebvre, L. W., B. B. Ackerman, K. M. Portier & K. H. Pollock. 1995. Aerial survey as a technique for estimating trends in manatee population size—problems and perspectives. PP. 63-74. In: T. J. O'Shea, B. B. Ackerman & H. F. Percival, Editors. Population biology of the Florida Manatee. Information and Technology Report 1. 289 pp. Lewis, R. R., III. 1986. Marine wetland loss in Tampa Bay and management/restoration recommendations. PP. 159-174. In: E. D. Estevez, et al., Editors. Proceedings of the conference: managing cumulative effects in Florida wetlands. New College Environmental Studies Program Publication 37, Omnipress, Madison, Wisconsin.
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