In-situ measurement of the rate of235U fission induced by lunar neutrons

The depth profile of the neutron-induced fission rate of²³⁵U was directly measured to a depth of 350 g/cm² by the Apollo 17 Lunar Neutron Probe Experiment. The fission rate rises sharply from the surface to a broad maximum from 110 to 160 g/cm² and drops off at greater depths. The shape of theoretical depth profile of Lingenfelter et al. fits the measured capture rates well at all depths. The absolute magnitude of the experimental fission rates are (11±17)% lower than those calculated theoretically. The excellent agreement between theory and experiment implies that conclusions drawn previously by interpreting lunar sample data with the theoretical capture rates will not require revision. In particular lunar surface processes, rather than uncertainties in the capture rates, are required to explain the relatively low neutron fluences observed for surface soil samples compared to the fluences expected for a uniformly mixed regolith.     

Studies on the thermoluminescence depth profile produced by 600-MeV protons in artificial lunar soil

The thermoluminescence (TL) of various plagioclase feldspars embedded in a thick target of 150 kg of artificial lunar soil was measured after a 600-MeV proton irradiation. No correlation was observed between the parameters of the characteristic feldspar glow peak and the anorthite contents. The relative TL sensitivities of the individual plagioclase variants were measured and found to be practically the same for⁶⁰Co-γ- and 600-MeV proton-irradiated samples.The TL intensity distribution within the target arrangement, converted to a 2π isotropic p-influx, resulted in an approximate TL depth profile of a thermally undisturbed lunar soil bomarded by galactic cosmic protons. The undisturbed TL intensity at a depth of 28 g/cm² (? 17 cm) decreased to 39% at a depth of 106 g/cm² (? 60 cm). For the evaluation of the temperature gradients by TL in lunar samples the experimental data at the sites of Taurus-Littrow and of Hadley-Rille yielded minimum depth intervals for sampling of ～ 20 cm and ～ 40 cm respectively, presuming an error of ± 15% in the TL determination. Certain aspects are seen by using the relation TL intensity/²²Na-activity ratio versus depth (thus representing the total ionization profile) to establish²²Na depth profiles.     

A temperature-dependent multi-relaxation spectroscopic dielectric model for thawed and frozen organic soil at 0.05–15 GHz

A dielectric model for thawed and frozen Arctic organic-rich soil (50% organic matter) has been developed. The model is based on soil dielectric measurements that were collected over ranges of gravimetric moisture from 0.03 to 0.55 g/g, dry soil density from 0.72 to 0.87 g/cm³, and temperature from 25 to −30 °C (cooling run) in the frequency range of 0.05–15 GHz. The refractive mixing dielectric model was applied with the Debye multi-relaxation equations to fit the measurements of the soil’s complex dielectric constant as a function of soil moisture and wave frequency. The spectroscopic parameters of the dielectric relaxations for the bound, transient bound, and unbound soil water components were derived and were complimented by the thermodynamic parameters to obtain a complete set of parameters for the proposed temperature-dependent multi-relaxation spectroscopic dielectric model for moist soils. To calculate the complex dielectric constant of the soil, the following input variables must be assigned: (1) density of dry soil, (2) gravimetric moisture, (3) wave frequency, and (4) temperature. The error of the dielectric model was evaluated and yielded RMSE_ε′ values of 0.348 and 0.188 for the soil dielectric constant and the loss factor, respectively. These values are on the order of the dielectric measurement error itself. The proposed dielectric model can be applied in active and passive microwave remote sensing techniques to develop algorithms for retrieving the soil moisture and the freeze/thaw state of organic-rich topsoil in the Arctic regions.     

Isotopic and REE studies of lunar basalt 12038: implications for petrogenesis of aluminous mare basalts

We report Sr, Nd, and Sm isotopic studies of lunar basalt 12038, one of the so-called aluminous mare basalts. A precise internal Rb-Sr isochron yields a crystallization age of 3.35±0.09 AE and initial⁸⁷Sr/⁸⁶Sr=0.69922?2 (2σ error limits, 1AE=10⁹ years, λ(⁸⁷Rb)=0.0139AE^?1). An internal Sm-Nd isochron yields an age of 3.28±0.23AE and initial¹⁴³Nd/¹⁴⁴Nd=0.50764?28. Present-day¹⁴³Nd/¹⁴⁴Nd is less than the “chondritic” value, i.e. ?(Nd, 0)=?2.3±0.4 where ?(Nd) is the deviation of¹⁴³Nd/¹⁴⁴Nd from chondritic evolution, expressed as parts in 10⁴. At the time of crystallization ?(Nd, 3.2AE)=1.5±0.6.We have successfully modeled the evolution of the Sr and Nd isotopic compositions and the REE abundances within the framework of our earlier model for Apollo 12 olivine-pigeonite and ilmenite basalts. The isotopic and trace element features of 12038 can be modeled as produced by partial melting of a cumulate mantle source which crystallized from a lunar magma ocean with a chondrite-normalized REE pattern of constant negative slope. Chondrite-normalized La/Yb=2.2 for this hypothetical magma ocean pattern. A plot of I(Sr) versus ?(Nd) for the Apollo 12 basalts clearly shows the influence of varying proportions of olivine, clinopyroxene, orthopyroxene, and plagioclase in the basalt source regions. A small percentage of plagioclase (～5%) in the 12038 source apparently is responsible for low I(Sr) and ?(Nd) in this basalt. Aluminous mare basalts from Mare Crisium (Luna 24) and by inference Mare Fecunditatis (Luna 16) occupy locations on the I(Sr)-?(Nd) plot similar to that of 12038, implying that some basalts from three widely separated lunar regions came from plagioclase-bearing source regions. A summary of model calculations for mare basalts shows a record of lunar mantle solidification during the period when REE abundances in the lunar magma ocean increased from ～20× chondritic to >100× chondritic. Although there is a general trend from olivine to clinopyroxene-dominated source regions with progressive magma ocean evolution, significant mineralogical heterogeneities in mantle composition apparently formed at any given stage of evolution, as evidenced in particular by the three Apollo 12 magma types.     

Details of magnetic polarity transitions recorded in a high deposition rate deep-sea core

Concentrations of the (n, γ)-produced radionuclide⁶⁰Co were measured in lunar samples at various depths from the surface down to 360 g/cm². By comparing the data obtained to calculated production rates (based on the work of Lingenfelter et al. [8]) we determined the present day lunar neutron production rate, which was found to be (12 ± 3)neutrons/cm²sec (E < 10MeV).     

Water uptake by trees in a riparian hardwood forest (Rhine floodplain,France)

Water flow in the soil–root–stem system was studied in a flooded riparian hardwood forest in the upper Rhine floodplain. The study was undertaken to identify the vertical distribution of water uptake by trees in a system where the groundwater is at a depth of less than 1 m. The three dominant ligneous species (Quercus robur, Fraxinus excelsior and Populus alba) were investigated for root structure (vertical extension of root systems), leaf and soil water potential (Ψ_m), isotopic signal (¹⁸O) of soil water and xylem sap. The root density of oak and poplar was maximal at a depth of 20 to 60 cm, whereas the roots of the ash explored the surface horizon between 0 and 30 cm, which suggests a complementary tree root distribution in the hardwood forest. The flow density of oak and poplar was much lower than that of the ash. However, in the three cases the depth of soil explored by the roots reached 1·2 m, i.e. just above a bed of gravel. The oak roots had a large lateral distribution up to a distance of 15 m from the trunk. The water potential of the soil measured at 1 m from the trunk showed a zone of strong water potential between 20 and 60 cm deep. The vertical profile of soil water content varied from 0·40 to 0·50 cm³ cm^?3 close to the water table, and 0·20 to 0·30 cm³ cm^?3 in the rooting zone. The isotopic signal of stem water was constant over the whole 24‐h cycle, which suggested that the uptake of water by trees occurred at a relatively constant depth. By comparing the isotopic composition of water between soil and plant, it was concluded that the water uptake occurred at a depth of 20 to 60 cm, which was in good agreement with the root and soil water potential distributions. The riparian forest therefore did not take water directly from the water table but from the unsaturated zone through the effect of capillarity. Copyright © 2007 John Wiley & Sons, Ltd.     

Oxygen isotope constraints on the origin and differentiation of the Moon

We report new high-precision laser fluorination three-isotope oxygen data for lunar materials. Terrestrial silicates with a range of δ¹⁸O values (− 0.5 to 22.9‰) were analyzed to independently determine the slope of the terrestrial fractionation line (TFL; λ = 0.5259 ± 0.0008; 95% confidence level). This new TFL determination allows direct comparison of lunar oxygen isotope systematics with those of Earth. Values of Δ¹⁷O for Apollo 12, 15, and 17 basalts and Luna 24 soil samples average 0.01‰ and are indistinguishable from the TFL. The δ¹⁸O values of high- and low-Ti lunar basalts are distinct. Average whole-rock δ¹⁸O values for low-Ti lunar basalts from the Apollo 12 (5.72 ± 0.06‰) and Apollo 15 landing sites (5.65 ± 0.12‰) are identical within error and are markedly higher than Apollo 17 high-Ti basalts (5.46 ± 0.11‰). Evolved low-Ti LaPaz mare-basalt meteorite δ¹⁸O values (5.67 ± 0.05‰) are in close agreement with more primitive low-Ti Apollo 12 and 15 mare basalts. Modeling of lunar mare-basalt source composition indicates that the high- and low-Ti mare-basalt mantle reservoirs were in oxygen isotope equilibrium and that variations in δ¹⁸O do not result from fractional crystallization. Instead, these differences are consistent with mineralogically heterogeneous mantle sources for mare basalts, and with lunar magma ocean differentiation models that result in a thick feldspathic crust, an olivine–pyroxene-rich mantle, and late-stage ilmenite-rich zones that were convectively mixed into deeper portions of the lunar mantle. Higher average δ¹⁸O (WR) values of low-Ti basalts compared to terrestrial mid ocean ridge basalts (Δ=0.18‰) suggest a possible oxygen isotopic difference between the terrestrial and lunar mantles. However, calculations of the δ¹⁸O of lunar mantle olivine in this study are only 0.05‰ higher than terrestrial mantle olivine. These observations may have important implications for understanding the formation of the Earth–Moon system.     

The distribution of helium in oceanic basalt glasses

We have determined the concentrations and isotopic composition of helium in oceanic basaltic glass both by melting and by crushing in vacuo. A significant fraction of the helium is released by crushing, confirming that it resides within the vesicles. Comparison of volume percent vesicles to the fraction of helium contained in the vesicles gives qualitative agreement with experimental gas-melt partitioning studies. Measured concentrations are therefore, a function of original helium content, magmatic history, vesicle size and quantity, and grain size analyzed. Helium released by crushing is isotopically indistinguishable from that contained in the glass. Diffusion rates for helium in basaltic glass (in the temperature range 125–400°C) determined using the method of stepwise heating, yielded an activation energy of 19.9 ± 1 kcal/mole andlnD₀ = ?2.7 ± 0.6 (cgs units). Extrapolation of these results to ocean floor temperatures (0°C) gives a diffusivity of 1.0 ± 0.6 × 10^?17 cm²/s, indicating that diffusion is an insignificant mechanism for helium loss from fresh basaltic glasses. The³He/⁴He ratios are remarkably constant (at 1.10 ± 0.03 × 10^?5) for samples from the Mid-Atlantic Ridge (FAMOUS area and 23°N), the Juan de Fuca Ridge, the Galapagos spreading center, the Mid-Cayman Rise, and the Central Indian Ocean Ridge. This result is interpreted in terms of similar geochemical histories within the source regions for these samples.     

Neutron capture effects in lunar gadolinium and the irradiation histories of some lunar rocks

The Gd isotopic composition in 19 lunar rock and soil samples from three Apollo sites is reported. The analytical techniques and the high precision mass spectrometric measurements are discussed. Enrichments in¹⁵⁸GdO/¹⁵⁷GdO due to neutron capture range up to 0.75%. Integrated ‘thermal’ neutron fluxes derived from the isotopic anomalies of Gd are compared with spallation Kr data from aliquot samples to construct a model which gives both average cosmic-ray irradiation depths and effective neutron exposure ages (T_n) for some rocks. In the case of rock 12053, this yields an average sample location of ∼300 g/cm² below the lunar surface and an effective irradiation age of ∼230 my, compared to 99 my obtained by the⁸¹Kr-Kr method. Rock 14310 is the first lunar sample where Kr anomalies due to resonance neutron capture in Br are observed. A⁸¹Kr-Kr exposure age of 262 ± 7 my is calculated for this rock.     

Global electromagnetic induction in the Moon and planets

A summary of experiments and analyses concerning electromagnetic induction in the Moon and other extraterrestrial bodies is presented. Magnetic step-transient measurements made on the lunar dark side show the eddy current response to be the dominant induction mode of the Moon. Analysis of the poloidal field decay of the eddy currents has yielded a range of monotonic conductivity profiles for the lunar interior: the conductivity rises from 3·10^?4 mho/m at a depth of 170 km to 10^?2 mho/m at 1000 km depth. The static magnetization field induction has been measured and the whole-Moon relative magnetic permeability has been calculated to be $\text{μ}\text{μ}{}_0\text{= 1.01 ± 0.06}$. The remanent magnetic fields, measured at Apollo landing sites, range from 3 to 327 γ. Simultaneous magnetometer and solar wind spectrometer measurements show that the 38-γ remanent field at the Apollo 12 site is compressed to 54 γ by a solar wind pressure increase of 7·10^?8 dyn/cm². The solar wind confines the induced lunar poloidal field; the field is compressed to the surface on the lunar subsolar side and extends out into a cylindrical cavity on the lunar antisolar side. This solar wind confinement is modeled in the laboratory by a magnetic dipole enclosed in a superconducting lead cylinder; results show that the induced poloidal field geometry is modified in a manner similar to that measured on the Moon. Induction concepts developed for the Moon are extended to estimate the electromagnetic response of other bodies in the solar system.     

Oxygen isotope measurements of phosphate from fish teeth and bones

In situ measurements of lunar surface brightness temperatures made as a part of the Apollo Lunar Surface Experiments Package at the Apollo 15 Hadley Rille landing site are reported. Data derived from 5 thermocouples of the Heat Flow Experiment, which are lying on or just above the surface, are used to examine the thermal properties of the upper 15 cm of the lunar regolith using eclipse and nighttime cool-down temperatures. Application of finite-difference techniques in modeling the lunar soil shows the thermocouple data are best fit by a model consisting of a low-density and low-thermal conductivity surface layer approximately 2 cm thick overlying a region increasing in conductivity and density with depth. Conductivities on the order of 1 × 10^?5 W/cm-°K are postulated for the upper layer, with conductivity increasing to the order of 1 × 10^?4 W/cm-°K at depths exceeding 20 cm. An increase in mean temperature with depth indicates that the ratio of radiative to conductive transfer at 350°K is 2.7 for at least the upper few centimeters of lunar soil; this value is nearly twice that measured for returned lunar fines. The thermal properties model deduced from Apollo 15 surface temperatures is consistent with earth-based microwave observations if electrical properties measured on returned lunar fines are assumed.     

Donnees experimentales sur la diffusion des elements majeurs entre verres ou liquides de compositions basaltique,rhyolitique et phonolitique,entre 900°C et 1300°C,a pression ordinaire

Diffusion coefficients for Si, Ti, Al, Na, K, Ca, Mg and Fe between pairs of glasses of basaltic, rhyolitic or phonolitic compositions have been determinated experimentally. This method involves the heating of coaxial cylinders of paired glasses under atmospheric conditions, over a range of temperatures from 900 to 1300°C, followed by microprobe analysis determination of the concentration gradients across the interface.The measured diffusivities are similar for all cations and range from 10^?13 cm²/s at 900°C to 5 × 10^?9 cm²/s at 1300°C. Depending mainly on the composition contrast, the diffusion is characterized by asymmetrical concentration profiles. This peculiar feature increases with temperature and chemical gradients across the contact surface of the glasses and leads to higher diffusion coefficients (D) in the more “basic” glass of a given pair. In the case of the rhyolite-basalt couple, this variation increases by a factor of about 10 at 1300°C. Diffusion dependence on temperature follows an Arrhenius equation which gives activation energies ranging from 65 to 85 kcal/mole. Assuming a constant and overall D for the two glasses we have attempted to apply our results to some geological examples such as exchanges between molten enclaves and liquids of contrasting composition.     

The abundances of3H and 14C in the solar wind

Tritium is measured as a function of depth in a Surveyor 3 sample. The upper limit for solar-wind-implanted tritium gives a³H/¹H limit for the solar wind of 1 × 10^?11. The temperature release patterns of¹⁴C from lunar soils are measured. The¹⁴C release patterns from surface soils differ from a trench bottom soil and gives evidence for the presence of¹⁴C in the solar wind with a¹⁴C/¹H ratio of approximately 4 × 10^?11. The implications of these radio nuclide abundances in the solar wind are discussed.     

The earth's thermal profile: Is there a mid-mantle thermal boundary layer?

Shock observations on melting of iron by Brown and McQueen with the inner core boundary (ICB) density contrast estimated by Masters are used with the assumption that the light ingredient of the outer core is oxygen to calculate the boundary temperature T_ICB = (5000 ± 900) K. Adiabatic extrapolation to the core-mantle boundary (CMB) gives T_ICB = (3800 ± 800) K. The temperature increment across the D″ layer is not well constrained, but is estimated to be T_D″ = (800 ± 400) K and a slightly superadiabatic extrapolation to 670 km gives T_{670 +} = (2300 ± 950) K. This is only about 300 K higher than the extrapolation to the same level from the upper mantle, T_670? = (1970 ± 150) K. The difference is far too small to make a viable mid-mantle boundary layer. Remaining unceertainties are too large to discount such a boundary layer with certainty, but agreement of our new temperature profile with temperatures deduced from equation of state studies on the lower mantle and core encourages the view that we are converging to a well-determined temperature profile for the Earth.     

Trapped solar and cosmogenic noble gas abundances in Apollo 15 and 16 deep drill samples

Abundances and isotopic compositions of all the stable noble gases have been measured in 19 different depths of the Apollo 15 deep drill core, 7 different depths of the Apollo 16 deep drill core, and in several surface fines and breccias. All samples analyzed from both drill cores contain large concentrations of solar wind implanted gases, which demonstrates that even the deepest layers of both cores have experienced a lunar surface history. For the Apollo 15 core samples, trapped⁴He concentrations are constant to within a factor of two; elemental ratios show even greater similarities with mean values of⁴He/²²Ne= 683±44,²²Ne/³⁶Ar= 0.439±0.057,³⁶Ar/⁸⁴Kr= 1.60±0.11·10³, and⁸⁴Kr/¹³²Xe= 5.92±0.74. Apollo 16 core samples show distinctly lower⁴He contents,⁴He/²²Ne(567±74), and²²Ne/³⁶Ar(0.229±0.024), but their heavy-element ratios are essentially identical to Apollo 15 core samples. Apollo 16 surface fines also show lower values of⁴He/²²Ne and²²Ne/³⁶Ar. This phenomenon is attributed to greater fractionation during gas loss because of the higher plagioclase contents of Apollo 16 fines. Of these four elemental ratios as measured in both cores, only the²²Ne/³⁶Ar for the Apollo 15 core shows an apparent depth dependance. No unambiguous evidence was seen in these core materials of appreciable variations in the composition of the solar wind. Calculated concentrations of cosmic ray-produced²¹Ne,⁸⁰Kr, and¹²⁶Xe for the Apollo 15 core showed nearly flat (within a factor of two) depth profiles, but with smaller random concentration variations over depths of a few cm. These data are not consistent with a short-term core accretion model from non-irradiated regolith. The Apollo 15 core data are consistent with a combined accretion plus static time of a few hundred million years, and also indicate variable pre-accretion irradiation of core material. The lack of large variations in solar wind gas contents across core layers is also consistent with appreciable pre-accretion irradiation. Depth profiles of cosmogenic gases in the Apollo 16 core show considerably larger concentrations of cosmogenic gases below ～65 cm depth than above. This pattern may be interpreted either as an accretionary process, or by a more recent deposition of regolith to the upper ～70 cm of the core. Cosmogenic gas concentrations of several Apollo 16 fines and breccias are consistent with ages of North Ray Crater and South Ray Crater of ～50·10⁶ and ～2·10⁶ yr, respectively.     

Depth profile of53Mn in the lunar surface

Measurements of cosmic-ray produced⁵³Mn are reported for a series of lunar surface samples down to a depth of 416 g/cm². These results clearly illustrate the decrease in activity with depth as the incident galactic cosmic rays are absorbed. Below 60 g/cm² the production rate decreases exponentially with a mean length, λ, of about 220 g/cm². These results indicate that, at the Apollo 15 site, the lunar regolith has been unmixed, on a meter scale, for the last 5 my. The neutron activation technique for⁵³Mn, which allowed samples smaller than 200 mg to be used for these measurements, is described.     

X-ray study and mössbauer spectroscopy on lunar ilmenites (Apollo 11)

A comparison of lunar ilmenites (Apollo 11, 10047, 13) with terrestrial ilmenites by means of electron microprobe analysis, X-ray and Mössbauer spectrometry showed that the lunar samples contained no Fe³⁺ but excess Ti³⁺. This causes an increase of thec-axis as compared with stoichiometric ilmenite.     

The Dependence of Constitutive Properties on Temperature and Effective Normal Stress in Seismogenic Environments

— We have evaluated how the parameters prescribing the slip-dependent constitutive law are affected by temperature and effective normal stress, by conducting the triaxial fracture experiments on Tsukuba-granite samples in seismogenic environments, which correspond to a depth range to 15 km. The normalized critical slip displacement D _c almost remains constant below 300^oC (insensitive to both temperature and effective normal stress σ _n ^eff); D _c increases with increasing temperature above 300 °C, and the rate of D _c increase with temperature tends to be largest at higher σ _n ^eff. The breakdown stress drop Δτ _b for the granite at constant σ _n ^eff is roughly 80 MPa below 300 °C, and does not depend on σ _n ^eff. Above 300 °C, Δτ _b decreases gradually with increasing temperature, and the rate of Δτ _b reduction with temperature increases at higher σ _n ^eff. The peak shear strength τ _p increases nearly linearly with increasing σ _n ^eff below 300 °C. However, τ _p becomes lower above 300 °C, deviating from the linear relation extrapolated from below 300 °C. This is consistent with the onset of crystal plastic deformation mechanisms of Tsukuba granite.     

Heat flow studies: Constraints on the distribution of uranium,thorium and potassium in the continental crust

To study the amount of heat generated by radioactive decay in the continental crust, the usual practice in the literature is to fit to the heat flow and radioactivity data a relationship of the form: Q = Q_r + D · A where Q and A are the observed heat flow and radiogenic heat production. Q_r is the “reduced” heat flow and D is a depth scale. This procedure implicitly assumes that uranium, thorium and potassium have identical distributions in the crust. We suggest that significant information may be lost as the three radioelements may in fact be affected by processes operating over different depths.Data published for four heat flow provinces throughout the world are used to estimate the distributions of uranium, thorium and potassium in the continental crust. These distributions are characterized by a depth scales defined as follows: D_i =∫0h C_i(z)C_i(0)dz where h is the thickness of the layer containing the bulk of radioactivity and C_i(z) the concentration of element i at depth z. Three depth scales are computed from a least-squares fit to the following relationship: Q = Q_r + D_U · A_U + D_T · A_T + D_K · A_T where Q is the observed heat flow and Q_r some constant (a reduced heat flow). A_i is the heat generation rate due to the radioactive decay of element i, and D_i is the corresponding depth scale.The analysis suggests that the three distributions are different and that they have the same basic features in the four provinces considered. The depth scale for potassium is large in granitic areas, that for thorium is small and that for uranium lies between the other two.We propose a simple model according to which each radioelement essentially provides a record for one process. Potassium gives a depth scale for the primary differentiation of the crust. Thorium gives the depth scale of magmatic or metamorphic fluid circulation. Finally, the uranium distribution reflects the late effects of alteration due to meteoric water. We show that the heat flow and radioactivity data are compatible with this model.Our analysis and numerical results are supported by data from deep boreholes and by geochemical evidence, such as detailed investigations of plutonic series and studies of U-Th-Pb systematics.     

Sublethal and lethal effects of sediments applied to common Caribbean Reef corals in the field

Experiments to measure natural rates of sedimentation and to assess the tolerance of coral species to increased sedimentation were conducted at San Cristobal Reef, Puerto Rico. Sedimentation rates were measured over an 18 month period. Calcareous sediments were applied to colonies of Montastraea annularis, Diploria strigosa, D. clivosa, Acropora palmata and A. cervicornis in different frequencies and in different doses.Mean sedimentation rates from sediment traps were 9.6±2.4 (S.E.) mg cm^?2 · day^?1 at 10 cm above the bottom and 2.5±0.9 (S.E.) and 2.6±1.2 (S.E.) mg cm^?2 · day^?1 for two sets of traps at 50 cm above the bottom. Sediment application experiments indicated A. palmata was the least tolerant of the species tested. Although A. cervicornis and D. strigosa colonies were not significantly affected, single applications of 800 mg cm^?2 to M. annularis colonies and of 200 mg cm^?2 to A. palmata colonies caused death of underlying coral tissue. Algae colonized the smothered portions of these corals.