Helping a Species Go Extinct: The Sumatran Rhino in Borneo

The Sumatran rhinoceros has been declining in numbers for more than a century, primarily due to bunting and to loss of its habitat as land is converted to other uses. Only in the last quarter century has the international community made concerted efforts to reverse this decline. However, government officials, international funding agencies, and conservation organizations, while paying lip service to the need for strong action, have often taken the path of least resistance in helping this species. Much of the money and effort put toward Sumatran rhino conservation has focused on new technologies or politically expedient strategies that have little to do with the real reasons behind the rhino's decline. The primary means of Sumatran rhino conservation in Indonesia and Malaysia, where viable populations might still exist, is still the capture and attempted breeding of this species-which, until now, has failed. I examined the history of the Sumatran rhino in Borneo and the recent situation in Sabah, where at least two important populations of this species might still survive. Sabah is presented as a case study that is indicative of the plight of the Sumatran rhino throughout its present range.     

Fishing and echolocation behavior of the greater bulldog bat,Noctilio leporinus,in the field

When hunting for fish Noctilio leporinus uses several strategies. In high search flight it flies within 20–50 cm of the water surface and emits groups of two to four echolocation signals, always containing at least one pure constant frequency (CF) pulse and one mixed CF-FM pulse consisting of a CF component which is followed by a frequency-modulated (FM) component. The pure CF signals are the longest, with an average duration of 13.3 ms and a maximum of 17 ms. The CF component of the CF-FM signals averages 8.9 ms, the FM sweeps 3.9 ms. The CF components have frequencies of 52.8–56.2 kHz and the FM components have an average bandwidth of 25.9 kHz. A bat in high search flight reacts to jumping fish with pointed dips at the spot where a fish has broken the surface. As it descends to the water surface the bat shows the typical approach pattern of all bats with decreasing pulse duration and pulse interval. A jumping fish reveals itself by a typical pattern of temporary echo glints, reflected back to the bat from its body and from the water disturbance. In low search flight N. leporinus drops to a height of only 4–10 cm, with body parallel to the water, legs extended straight back and turned slightly downward, and feet cocked somewhat above the line of the legs and poised within 2–4 cm of the water surface. In this situation N. leporinus emits long series of short CF-FM pulses with an average duration of 5.6 ms (CF 3.1 and FM 2.6) and an average pulse interval of 20 ms, indicating that it is looking for targets within a short range. N. leporinus also makes pointed dips during low search flight by rapidly snapping the feet into the water at the spot where it has localized a jumping fish or disturbance. In the random rake mode, N. leporinus drops to the water surface, lowers its feet and drags its claws through the water in relatively straight lines for up to 10m. The echolocation behavior is similar to that of high search flight. This indicates that in this hunting mode N. leporinus is not pursuing specific targets, and that raking is a random or statistical search for surface fishes. When raking, the bat uses two strategies. In directed random rake it rakes through patches of water where fish jumping activity is high. Our interpretation is that the bat detects this activity by echolocation but prefers not to concentrate on a single jumping fish. In the absence of jumping fish, after flying for several minutes without any dips, N. leporinus starts to make very long rakes in areas where it has hunted successfully before (memory-directed random rake). Hunting bats caught a fish approximately once in every 50–200 passes through the hunting area.     

Spatial modeling and prediction under stationary non-geometric range anisotropy

For modeling spatial processes, we propose a rich parametric class of stationary range anisotropic covariance structures that, when applied in R², greatly increases the scope of variogram contors. Geometric anisotropy, which provides the most common generalization of isotropy within stationarity, is a special case. Our class is built from monotonic isotropic correlation functions and special cases include the Matérn and the general exponential functions. As a result, our range anisotropic correlation specification can be attached to a second order stationary spatial process model, unlike ad hoc approaches to range anisotropy in the literature. We adopt a Bayesian perspective to obtain full inference and demonstrate how to fit the resulting model using sampling-based methods. In the presence of measurement error/microscale effect, we can obtain both the usual predictive as well as the noiseless predictive distribution. We analyze a data set of scallop catches under the general exponential range anisotropic model, withholding ten sites to compare the accuracy and precision of the standard and noiseless predictive distributions.     

Population structure and genetic diversity in green turtles nesting at Tortuguero,Costa Rica,based on mitochondrial DNA control region sequences

The green turtle (Chelonia mydas) nesting population at Tortuguero, Costa Rica, is the largest nesting aggregation in the Atlantic, by at least an order of magnitude. Previous mitochondrial DNA (mtDNA) surveys based on limited sampling (n = 41) indicated low genetic diversity and low gene flow with other Caribbean nesting colonies. Furthermore, a survey of nuclear DNA diversity invoked the possibility of substructure within the Tortuguero rookery. To evaluate these characteristics, mtDNA control region sequences were determined for green turtles nesting at Tortuguero in 2001 (n = 157) and 2002 (n = 235). The increased sample revealed three additional haplotypes; five haplotypes are now known for Tortuguero female green turtles. Analyses of molecular variance indicated that there was no significant spatial population structure along the 30-km nesting beach. In addition, no temporal population structure was detected either between the two nesting seasons or within the nesting season. As a result of the larger sample size and additional haplotypes, estimates of genetic separation among Caribbean nesting colonies have changed and the concordance of phylogenetic and phylogeographic patterns reported in the past for green turtles in the Greater Caribbean has weakened. The five haplotypes from Tortuguero represent 36% of the haplotypes identified in green turtle nesting aggregations in the Greater Caribbean and 17% of the haplotypes known to occur in nesting or foraging aggregations in the Greater Caribbean. Haplotype diversity (0.16) and nucleotide diversity (0.0034) for the Tortuguero population are substantially lower than those for the combined rookeries in the Greater Caribbean (0.44 and 0.0078, respectively). Although comprehensive evaluation of regional genetic diversity requires nuclear DNA data, our study indicates that conserving genetic diversity in Caribbean green turtles will require careful management of the smaller rookeries in addition to the Tortuguero rookery.     

Sex ratios and life-history patterns of a solitary wasp,Trypoxylon (Trypargilum) politum (Hymenoptera : Sphecidae)

Summary Werren and Charnov (1978) and Seger (1983) proposed a model to explain a fairly common pattern of alternating sex ratio biases between generations in partially bivoltine insects. When first-generation males overlap and mate with females of the second generation, then females should bias sex ratios in favor of sons for the first generation and daughters for the second generation. In an intensive, 7-year study at four sites in northern Florida, pipe-organ mud-daubing wasps (Trypoxylon (Trypargilum) politum; Hymenoptera: Sphecidae) were found to have strongly male-biased sex ratios in the first or overwintering generation and 1:1 or female-biased sex ratios in the second or summer generation. These differences were not due to differences in mortality of the two sexes but rather resulted from changing female sex-allocation decisions. In some respects the mud dauber results fit Seger's model well: alternating sex ratios in partially bivoltine populations, first-generation males overlapping second-generation females and perhaps most convincingly, northern, univoltine populations do not have a male bias. Despite this qualitative fit, however, our data do not meet the quantitative predictions of the model. This could result from the fact that some assumptions of the model are not met by the life history of T. politum. Alternative explanations for alternating sex ratios include split sex ratios, seasonal differences in cost ratios, facultative maternal investment rules and facultative overwintering decisions by offspring. Despite the position that sex ratios have achieved in the modern study of evolution, it is clear that accurate, quantitative predictions on sex-allocation patterns demand the same detailed understanding of the biology of the organism that is required for the study of other adaptations.     

A comparative analysis of the photobiology of zooxanthellae and zoochlorellae symbiotic with the temperate clonal anemone <Emphasis Type="Italic">Anthopleura elegantissima</Emphasis> (Brandt). III. Seasonal effects of natural light and temperature on photosynthesis and respiration

The sea anemone Anthopleura elegantissima hosts two phylogenetically different symbiotic microalgae, a dinoflagellate Symbiodinium (zooxanthellae, ZX) and a chlorophyte (zoochlorellae, ZC). The photosynthetic productivity (P), respiration (R), and contribution of algal carbon translocated to the host (CZAR) in response to a year’s seasonal ambient changes of natural light and temperature are documented for both ZX- and ZC-bearing anemones. Light and temperature both affect photosynthesis, respiration, and CZAR, as well as various algal parameters; while there are evident seasonal differences, for the most part the relative effects on P, R, and CZAR by the two environmental variables cannot be determined. Net photosynthesis (P_n) of both ZX and ZC was significantly higher during spring and summer. During these seasons, the P_n of ZX was always greater than that of ZC. Regardless of algal symbiont, anemone respiration (R) was significantly higher during the spring and summer. The annual net carbon fixation rate of anemones with ZX and ZC was 325 and 276 mg C anemone⁻¹ year⁻¹, respectively, which translates to annual net community productivity rates of 92 and 60 g C m⁻¹ year⁻¹ for anemones with ZX or ZC, respectively. CZAR did not show a clear relationship with season; however the CZAR for ZX was always significantly greater than for ZC. Lower ZX growth rates, coupled with higher photosynthetic rates and higher CZAR estimates, compared to ZC, suggest that if A. elegantissima is simply carbon limited, ZX-bearing anemones should be the dominant symbiont in the field. However ZC-bearing anemones persist in low light and reduced temperature microhabitats, therefore more than the translocation of carbon from ZC must be involved. Given that global climate change will increase water temperatures, the potential for latitudinal range shifts of both ZC and ZX (S. californium and muscatinei) might be used as biological indicators of thermal shifts in the littoral zone of the Pacific Northwest.