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Martin B. Goldhaber

Publications and source records attributed to Martin B. Goldhaber.

At least 19 recordsLinked to original sources

The Modern Geological Survey; a model for research, innovation, synthjesis: A USGS perspective

Geological Surveys have long filled the role of providing Earth system science data and knowledge. These functions are increasingly complicated by accelerating environmental and societal change. Here we describe the USGS response to these evolving conditions. Underpinning the USGS approach is the recognition that many of the issues facing the U.S. and the world involve the interaction among geologic, hydrologic, and biologic processes, and how these interactions in turn affect society. Therefore, a goal of USGS planning is fostering interdisciplinary science. This focus is occurring in part through implementation of the recommendations of strategic planning teams. The USGS has also put in place groups building a broad information technology infrastructure as well as identifying and disseminating new Earth science research tools. In addition, the USGS has established an analysis and synthesis center that brings together groups of scientists who address interdisciplinary Earth system science issues. The goal is for these building blocks to evolve towards a comprehensive USGS data and knowledge platform; EarthMAP (Earth Monitoring, Assessment, and Projection). We also recognize that the modern geological survey must be a member of a community of geological surveys contributing data to a global database of 3-dimensional biogeophysical observations and interpretations.

Book chapter↗

Using halogens (Cl, Br, I) to understand the hydrogeochemical evolution of drought-derived saline porewater beneath a prairie wetland

Numerous closed-basin prairie wetlands throughout the Prairie Pothole Region (PPR) of North America maintain moderate surface pond salinities (total dissolved solids [TDS] from 1 to 10 g L − 1 ) under semiarid climate by accumulation of gypsum and saline lenses of sulfate-rich porewater (TDS > 10 g L − 1 ) in wetland sediments during droughts. In order to understand the hydrogeochemical origin and composition of these saline porewaters, we made a detailed geochemical survey of Cl − , SO 4 2 − , Br, and I in the porewater, pondwater, and upland groundwater of a typical closed-basin prairie wetland (P1 in the Cottonwood Lake study area, North Dakota). Concentrations of Cl − ranged up to 5.9 mM in the saline porewaters, and was strongly correlated with SO 4 2 − and Br (Pearson's r > 0.7, p < 0.05; concentrations ranging up to 131 mM and 39 μM, respectively) due to the conservative effects of surface water evaporation. In contrast, total dissolved I was not significantly correlated with Cl − (Pearson's r = 0.18, p = 0.273) and was concentrated in porewaters located above the saline lenses with a peak concentration of 4.1 μM beneath the center of the wetland— the highest value for dissolved I ever measured in a terrestrial aquatic system and an order of magnitude above that of seawater. We hypothesize that chromatographic separation between more mobile anions (Cl − , SO 4 2 − , Br − ) and I occurs during droughts when wetland ponds dry and sedimentary iodide (I − ) oxidizes to its less-mobile form, iodate (IO 3 − ). Understanding the origin and geochemical composition of porewater salinity that develops beneath prairie wetlands during drought can help to fingerprint sources of salinity to wetland ponds during wet climate and elucidate halogen systematics in saline and organic-rich subsurface environments associated with hydrocarbon generation.

North Dakota↗

Drought-induced recharge promotes long-term storage of porewater salinity beneath a prairie wetland

Subsurface storage of sulfate salts allows closed-basin wetlands in the semiarid Prairie Pothole Region (PPR) of North America to maintain moderate surface water salinity (total dissolved solids [TDS] from 1 to 10 g L −1 ), which provides critical habitat for communities of aquatic biota. However, it is unclear how the salinity of wetland ponds will respond to a recent shift in mid-continental climate to wetter conditions. To understand better the mechanisms that control surface-subsurface salinity exchanges during regional dry-wet climate cycles, we made a detailed geoelectrical study of a closed-basin prairie wetland (P1 in the Cottonwood Lake Study Area, North Dakota) that is currently experiencing record wet conditions. We found saline lenses of sulfate-rich porewater (TDS > 10 g L −1 ) contained in fine-grained wetland sediments 2–4 m beneath the bathymetric low of the wetland and within the currently ponded area along the shoreline of a prior pond stand ( c . 1983). During the most recent drought (1988–1993), the wetland switched from a groundwater discharge to recharge function, allowing salts dissolved in surface runoff to move into wetland sediments beneath the bathymetric low of the basin. However, groundwater levels during this time did not decline to the elevation of the saline lenses, suggesting these features formed during more extended paleo-droughts and are stable in the subsurface on at least centennial timescales. We hypothesize a “drought-induced recharge” mechanism that allows wetland ponds to maintain moderate salinity under semiarid climate. Discharge of drought-derived saline groundwater has the potential to increase the salinity of wetland ponds during wet climate.

North Dakota↗

Grand challenges for integrated USGS science — A workshop report

Executive Summary The U.S. Geological Survey (USGS) has a long history of advancing the traditional Earth science disciplines and identifying opportunities to integrate USGS science across disciplines to address complex societal problems. The USGS science strategy for 2007–2017 laid out key challenges in disciplinary and interdisciplinary arenas, culminating in a call for increased focus on a number of crosscutting science directions. Ten years on, to further the goal of integrated science and at the request of the Executive Leadership Team (ELT), a workshop with three dozen invited scientists spanning different disciplines and career stages in the Bureau convened on February 7–10, 2017, at the USGS John Wesley Powell Center for Analysis and Synthesis in Fort Collins, Colorado. The workshop focused on identifying “grand challenges” for integrated USGS science. Individual participants identified nearly 70 potential grand challenges before the workshop and through workshop discussions. After discussion, four overarching grand challenges emerged: Natural resource security, Societal risk from existing and emerging threats, Smart infrastructure development, and Anticipatory science for changing landscapes. Participants also identified a “comprehensive science challenge” that highlights the development of integrative science, data, models, and tools—all interacting in a modular framework—that can be used to address these and other future grand challenges: Earth Monitoring, Analyses, and Projections (EarthMAP) EarthMAP is our long-term vision for an integrated scientific framework that spans traditional scientific boundaries and disciplines, and integrates the full portfolio of USGS science: research, monitoring, assessment, analysis, and information delivery. The Department of Interior, and the Nation in general, have a vast array of information needs. The USGS meets these needs by having a broadly trained and agile scientific workforce. Encouraging and supporting cross-discipline engagement would position the USGS to tackle complex and multifaceted scientific and societal challenges in the 21st Century.

Open-File Report↗

The interacting roles of climate, soils, and plant production on soil microbial communities at a continental scale

Soil microbial communities control critical ecosystem processes such as decomposition, nutrient cycling, and soil organic matter formation. Continental scale patterns in the composition and functioning of microbial communities are related to climatic, biotic, and edaphic factors such as temperature and precipitation, plant community composition, and soil carbon, nitrogen, and pH. Although these relationships have been well explored individually, the examination of the factors that may act directly on microbial communities vs. those that may act indirectly through other ecosystem properties has not been well developed. To further such understanding, we utilized structural equation modeling (SEM) to evaluate a set of hypotheses about the direct and indirect effects of climatic, biotic, and edaphic variables on microbial communities across the continental United States. The primary goals of this work were to test our current understanding of the interactions among climate, soils, and plants in affecting microbial community composition, and to examine whether variation in the composition of the microbial community affects potential rates of soil enzymatic activities. A model of interacting factors created through SEM shows several expected patterns. Distal factors such as climate had indirect effects on microbial communities by influencing plant productivity, soil mineralogy, and soil pH, but factors related to soil organic matter chemistry had the most direct influence on community composition. We observed that both plant productivity and soil mineral composition were important indirect influences on community composition at the continental scale, both interacting to affect organic matter content and microbial biomass and ultimately community composition. Although soil hydrolytic enzymes were related to the moisture regime and soil carbon, oxidative enzymes were also affected by community composition, reflected in the abundance of soil fungi. These results highlight that soil microbial communities can be modeled within the context of multiple interacting ecosystem properties acting both directly and indirectly on their composition and function, and this provides a rich and informative context with which to examine communities. This work also highlights that variation in climate, microbial biomass, and microbial community composition can affect maximum rates of soil enzyme activities, potentially influencing rates of decomposition and nutrient mineralization in soils.

Ecology↗

Controls on the geochemical evolution of Prairie Pothole Region lakes and wetlands over decadal time scales

One hundred sixty-seven Prairie Pothole lakes, ponds and wetlands (largely lakes) previously analyzed chemically during the late 1960’s and early to mid-1970’s were resampled and reanalyzed in 2011–2012. The two sampling periods differed climatically. The earlier sampling took place during normal to slightly dry conditions, whereas the latter occurred during and immediately following exceptionally wet conditions. As reported previously in Mushet et al. ( 2015 ), the dominant effect was expansion of the area of these lakes and dilution of their major ions. However, within that context, there were significant differences in the evolutionary pathways of major ions. To establish these pathways, we employed the inverse modeling computer code NetpathXL. This code takes the initial and final lake composition and, using mass balance constrained by the composition of diluting waters, and input and output of phases, calculates plausible geochemical evolution pathways. Despite the fact that in most cases major ions decreased, a subset of the lakes had an increase in SO 4 2− . This distinction is significant because SO 4 2− is the dominant anion in a majority of Prairie Pothole Region wetlands and lakes. For lakes with decreasing SO 4 2− , the proportion of original lake water required for mass balance was subordinate to rainwater and/or overland flow. In contrast, lakes with increasing SO 4 2− between the two sampling episodes tended to be dominated by original lake water. This suite of lakes tended to be smaller and have lower initial SO 4 2− concentrations such that inputs of sulfur from dissolution of the minerals gypsum or pyrite had a significant impact on the final sulfur concentration given the lower dilution factors. Thus, our study provides context for how Prairie Pothole Region water bodies evolve geochemically as climate changes. Because wetland geochemistry in turn controls the ecology of these water bodies, this research contributes to the prediction of the impact of climate change on this important complex of ecosystems.

North Dakota↗

Changes in pond water levels and surface extent due to climate variability alter solute sources to closed-basin Prairie-Pothole wetland ponds, 1979 to 2012

Wetter conditions beginning in 1993 resulted in marked changes in water levels and surface extent of prairie-pothole region wetland ponds, including closed-basin wetlands in the Cottonwood Lake area of North Dakota, U.S.A. Pond water levels after 1993 were consistently 0.5 to 2 m higher than during 1979–1993 (≤ 1 m deep) in wetlands lacking surface or substantial groundwater outlets, and ponds of some wetlands merged. Pond surface areas after 1993 were as much as twice pre-1993 areas. Weathered glacial till in the inundated uplands provided a source of solutes from the subsurface beyond the extent of the weathered wetland periphery and wetland sediments that existed before 1993. Increased pond peripheries also provided for more movement of solutes from shallow groundwater into wetland ponds during the wetter period. Long periods of higher water levels during pronounced wetter conditions can be associated with increased specific conductance for some wetland ponds. In wetlands receiving no groundwater input, specific conductance values of ponded waters were indistinguishable between wetter and preceding conditions. Thus, changes in specific conductance in wetland ponds during wetter climate conditions cannot be assumed to be uniform, a result of changing watershed solute sources.

Wetlands↗

Chemical and biotic characteristics of prairie lakes and large wetlands in south-central North Dakota—Effects of a changing climate

The climate of the prairie pothole region of North America is known for variability that results in significant interannual changes in water depths and volumes of prairie lakes and wetlands; however, beginning in July 1993, the climate of the region shifted to an extended period of increased precipitation that has likely been unequaled in the preceding 500 years. Associated changing water volumes also affect water chemical characteristics, with potential effects on fish and wildlife populations. To explore the effect of changing climate patterns, in 2012 and 2013, the U.S. Geological Survey revisited 167 of 178 prairie lakes and large wetlands of south-central North Dakota that were originally sampled in the mid-1960s to mid-1970s. During the earlier sampling period, these lakes and wetlands displayed a great range of chemical characteristics (for example, specific conductance ranged from 365 microsiemens per centimeter at 25 degrees Celsius to 70,300 microsiemens per centimeter at 25 degrees Celsius); however, increased water volumes have resulted in greatly reduced variation among lakes and wetlands and a more homogeneous set of chemical conditions defined by pH, specific conductance, and concentrations of major cations and anions. High concentrations of dissolved solids previously limited fish occurrence in many of the lakes and wetlands sampled; however, freshening of these lakes and large wetlands has allowed fish to populate and flourish where they were previously absent. Conversely, the freshening of previously saline lakes and wetlands has resulted in concurrent shifts away from invertebrate species adapted to live in these highly saline environments. A shift in the regional climate has changed a highly diverse landscape of wetlands (fresh to highly saline) to a markedly more homogeneous landscape that has reshaped the fish and wildlife communities of this ecologically and economically important region.

North Dakota↗

Weathering and transport of chromium and nickel from serpentinite in the Coast Range ophiolite to the Sacramento Valley, California, USA

A soil geochemical study in northern California was done to investigate the role that weathering and transport play in the regional distribution and mobility of geogenic Cr and Ni, which are both potentially toxic and carcinogenic. These elements are enriched in ultramafic rocks (primarily serpentinite) and the soils derived from them (1700&ndash;10,000 mg Cr per kg soil and 1300&ndash;3900 mg Ni per kg soil) in the Coast Range ophiolite. Chromium and Ni have been transported eastward from the Coast Range into the western Sacramento Valley and as a result, valley soil is enriched in Cr (80&ndash;1420 mg kg &minus;1 ) and Ni (65&ndash;224 mg kg &minus;1 ) compared to median values of U.S. soils of 50 and 15 mg kg &minus;1 , respectively. Nickel in ultramafic source rocks and soils is present in serpentine minerals (lizardite, antigorite, and chrysotile) and is more easily weathered compared to Cr, which primarily resides in highly refractory chromite ([Mg,Fe 2+ ][Cr 3+ ,Al,Fe 3+ ] 2 O 4 ). Although the majority of Cr and Ni in soils are in refractory chromite and serpentine minerals, the etching and dissolution of these minerals, presence of Cr- and Ni-enriched clay minerals and development of nanocrystalline Fe (hydr)oxides is evidence that a significant fractions of these elements have been transferred to potentially more labile phases.

California↗

Soil formation: Chapter 6

Soil formation reflects the complex interaction of many factors, among the most important of which are (i) the nature of the soil parent material, (ii) regional climate, (iii) organisms, including humans, (iv) topography and (v) time. These processes operate in Earth's critical zone; the thin veneer of our planet where rock meets life. Understanding the operation of these soil-forming factors requires an interdisciplinary approach and is a necessary predicate to charactering soil processes and functions, mitigating soil degradation and adapting soil management to environmental change. In this chapter, we discuss how these soil-forming factors operate both singly and in concert in natural and human modified environments. We emphasize the role that soil organic matter plays in these processes to provide context for understanding the benefits that it bestows on humanity.

Book chapter↗

Hydrogeochemistry of prairie pothole region wetlands: Role of long-term critical zone processes

This study addresses the geologic and hydrogeochemical processes operating at a range of scales within the prairie pothole region (PPR). The PPR is a 750,000 km 2 portion of north central North America that hosts millions of small wetlands known to be critical habitat for waterfowl and other wildlife. At a local scale, we characterized the geochemical evolution of the 92-ha Cottonwood Lake study area (CWLSA), located in North Dakota, USA. Critical zone processes are the long-term determinant of wetland water and groundwater geochemistry via the interaction of oxygenated groundwater with pyrite in the underlying glacial till. Pyrite oxidation produced a brown, iron oxide-bearing surface layer locally over 13 m thick and an estimated minimum of 1.3 &times; 10 10 g sulfate (SO 4 2 &minus; ) at CWLSA. We show that the majority of this SO 4 2&minus; now resides in solid-phase gypsum (CaSO 4 &bull;2H 2 O) and gypsum-saturated groundwater. Results from the CWLSA were scaled up to a 9700 km 2 area surrounding CWLSA using ~ 1800 drill logs and literature data on wetland water chemistry for 178 wetlands within this larger area. The oxidized brown zone depth and wetland water compositional trends are very similar to the CWLSA. Additionally, surface water data from 176 southern Canadian pothole wetlands that conform to the same wetland water geochemical trends as those recorded in the CWLSA further corroborate that SO 4 2 &minus; accumulation driven by pyrite oxidation is a nearly ubiquitous process in the prairie pothole region and distinguishes PPR wetlands from other wetlands worldwide that have a similar overall hydrology.

Manitoba, North Dakota, Saskatchewan↗

Laboratory investigations of the effects of nitrification-induced acidification on Cr cycling in vadose zone material partially derived from ultramafic rocks

Sacramento Valley (California, USA) soils and sediments have high concentrations of Cr(III) because they are partially derived from ultramafic material. Some Cr(III) is oxidized to more toxic and mobile Cr(VI) by soil Mn oxides. Valley soils typically have neutral to alkaline pH at which Cr(III) is highly immobile. Much of the valley is under cultivation and is both fertilized and irrigated. A series of laboratory incubation experiments were conducted to assess how cultivation might impact Cr cycling in shallow vadose zone material from the valley. The first experiments employed low (7.1 mmol N per kg soil) and high (35 mmol N kg − 1 ) concentrations of applied (NH 4 ) 2 SO 4 . Initially, Cr(VI) concentrations were up to 45 and 60% greater than controls in low and high incubations, respectively. After microbially-mediated oxidation of all NH 4 + , Cr(VI) concentrations dropped below control values. Increased nitrifying bacterial populations (estimated by measurement of phospholipid fatty acids) may have increased the Cr(VI) reduction capacity of the vadose zone material resulting in the observed decreases in Cr(VI). Another series of incubations employed vadose zone material from a different location to which low (45 meq kg − 1 ) and high (128 meq kg − 1 ) amounts of NH 4 Cl, KCl, and CaCl 2 were applied. All treatments, except high concentration KCl, resulted in mean soil Cr(VI) concentrations that were greater than the control. High concentrations of water-leachable Ba 2 + (mean 38 μmol kg − 1 ) in this treatment may have limited Cr(VI) solubility. A final set of incubations were amended with low (7.1 mmol N kg − 1 ) and high (35 mmol N kg − 1 ) concentrations of commercial liquid ammonium polyphosphate (APP) fertilizer which contained high concentrations of Cr(III). Soil Cr(VI) in the low APP incubations increased to a concentration of 1.8 μmol kg − 1 (5 × control) over 109 days suggesting that Cr(III) added with the APP fertilizer was more reactive than naturally-occurring soil Cr(III).

Science of the Total Environment↗

The role of critical zone processes in the evolution of the Prairie Pothole Region wetlands

The Prairie Pothole Region, which occupies 900,000 km2 of the north central USA and south central Canada, is one of the most important ecosystems in North America. It is characterized by millions of small wetlands whose chemistry is highly variable over short distances. The study involved the geochemistry of surface sediments, wetland water, and groundwater in the Cottonwood Lakes area of North Dakota, USA, whose 92 ha includes the dominant wetland hydrologic settings. The data show that oxygenated groundwater interacting with pyrite resident in a component of surficial glacial till derived from the marine Pierre Shale Formation has, over long periods of time, focused SO 4 2 - -bearing fluids from upland areas to topographically low areas. In these low areas, SO 4 2 - -enriched groundwater and wetlands have evolved, as has the CaSO4 mineral gypsum. Sulfur isotope data support the conclusion that isotopically light pyrite from marine shale is the source of SO 4 2 - . Literature data on wetland water composition suggests that this process has taken place over a large area in North Dakota.

North Dakota↗

Carbon and nitrogen biogeochemistry of a Prairie Pothole Wetland, Stutsman County, North Dakota, USA

The concentration and form of dissolved organic C (DOC) and N species (NH 4 + and NO 3 - ) were investigated as part of a larger hydrogeochemical study of the Cottonwood Lake Study Area within the Prairie Potholes region. Groundwater, pore water and surface wetland water data were used to help characterize the relationships between surface and groundwater with respect to nutrient dynamics. Photosynthesis and subsequent decomposition of vegetation in these hydrologically dynamic wetlands generates a large amount of dissolved C and N, although the subsurface till, derived in part from organic matter rich Pierre Shale, is a likely secondary source of nutrients in deeper groundwater. While surface water DOC concentrations ranged from 2.2 to 4.6 mM, groundwater values were 0.15 mM to 3.7 mM. Greater specific UV absorbance (SUVA 254 ) in the wetland water column and in soil pore waters relative to groundwater indicate more reactive DOC in the surface to near-surface waters. Circumneutral wetlands had greater SUVA254, possibly because of variations in vegetation communities. The dominant inorganic nitrogen species was NH 4 + in both wetland water and most ground water samples. The exceptions were 3 wells with NO 3 - ranging from 38 to 115 μM. Shallow groundwater wells (Well 28 and Well 13S) with greater connection to wetland surface water had greater NH 4 + concentrations (1.1 mM and 120 μM) than other well samples (3–90 μM). Pore water nutrient chemistry was more similar to surface water than ground water. Nitrogen results suggest reducing conditions in both groundwater and surface water, possibly due to the microbial uptake of O 2 by decaying vegetation in the wetland water column, labile organic C available in shallow groundwater, or the oxidation of pyrite associated with the subsurface.

North Dakota↗

Using stable isotopes to understand hydrochemical processes in and around a Prairie Pothole wetland in the Northern Great Plains, USA

Millions of internally drained wetland systems in the Prairie Potholes region of the northern Great Plains (USA and Canada) provide indispensable habitat for waterfowl and a host of other ecosystem services. The hydrochemistry of these systems is complex and a crucial control on wetland function, flora and fauna. Wetland waters can have high concentrations of SO 2- 4 due to the oxidation of large amounts of pyrite in glacial till that is in part derived from the Pierre shale. Water chemistry including δ 18 O H2O , δ 2 H H2O , and δ 34 S SO4 values, was determined for groundwater, soil pore water, and wetland surface water in and around a discharge wetland in North Dakota. The isotopic data for the first time trace the interaction of processes that affect wetland chemistry, including open water evaporation, plant transpiration, and microbial SO 4 reduction.

Applied Geochemistry↗

Chromium(VI) generation in vadose zone soils and alluvial sediments of the southwestern Sacramento Valley, California: a potential source of geogenic Cr(VI) to groundwater

Concentrations of geogenic Cr(VI) in groundwater that exceed the World Health Organization’s maximum contaminant level for drinking water (50 μg L −1 ) occur in several locations globally. The major mechanism for mobilization of this Cr(VI) at these sites is the weathering of Cr(III) from ultramafic rocks and its subsequent oxidation on Mn oxides. This process may be occurring in the southern Sacramento Valley of California where Cr(VI) concentrations in groundwater can approach or exceed 50 μg L −1 . To characterize Cr geochemistry in the area, samples from several soil auger cores (approximately 4 m deep) and drill cores (approximately 25 m deep) were analyzed for total concentrations of 44 major, minor and trace elements, Cr associated with labile Mn and Fe oxides, and Cr(VI). Total concentrations of Cr in these samples ranged from 140 to 2220 mg per kg soil. Between 9 and 70 mg per kg soil was released by selective extractions that target Fe oxides, but essentially no Cr was associated with the abundant reactive Mn oxides (up to ~1000 mg hydroxylamine-reducible Mn per kg soil was present). Both borehole magnetic susceptibility surveys performed at some of the drill core sites and relative differences between Cr released in a 4-acid digestion versus total Cr (lithium metaborate fusion digestion) suggest that the majority of total Cr in the samples is present in refractory chromite minerals transported from ultramafic exposures in the Coast Range Mountains. Chromium(VI) in the samples studied ranged from 0 to 42 μg kg −1 , representing a minute fraction of total Cr. Chromium(VI) content was typically below detection in surface soils (top 10 cm) where soil organic matter was high, and increased with increasing depth in the soil auger cores as organic matter decreased. Maximum concentrations of Cr(VI) were up to 3 times greater in the deeper drill core samples than the shallow auger cores. Although Cr(VI) in these vadose zone soils and sediments was only a very small fraction of the total solid phase Cr, they are a potentially important source for Cr(VI) to groundwater. Enhanced groundwater recharge through the vadose zone due to irrigation could carry Cr(VI) from the vadose zone to the groundwater and may be the mechanism responsible for the correlation observed between elevated Cr(VI) and NO 3 - source concentrations in previously published data for valley groundwaters. Incubation of a valley subsoil showed a Cr(VI) production rate of 24 μg kg −1 a −1 suggesting that field Cr(VI) concentrations could be regenerated annually. Increased Cr(VI) production rates in H + -amended soil incubations indicate that soil acidification processes such as nitrification of ammonium in fertilizers could potentially increase the occurrence of geogenic Cr(VI) in groundwater. Thus, despite the natural origin of the Cr, Cr(VI) generation in the Sacramento Valley soils and sediments has the potential to be influenced by human activities.

California↗

It's not just about climate change - What about soils?

Vladimir Vernadsky was one of the giants of geochemistry. Considered the founder of the fi eld of biogeochemistry and a true pioneer in “whole Earth” studies, he realized by 1945 that “Man under our very eyes is becoming a mighty and ever-growing geological force.” In the intervening 65 years, his “ever-growing force” has become a tidal wave. The global population has been increasing exponentially since the beginning of the industrial revolution, and as a result has increased by nearly a factor of three between 1945, when his observation was published, and today (see fi gure). Current projections anticipate a population exceeding 9 billion by 2050. This explosive human population growth has been fueled by ancient hydrocarbons and has come with high costs. Most Earth scientists are concerned with the implications of the rapid accumulation of greenhouse gases in the atmosphere. The consequences include a climate state without polar ice, acidifying oceans, and increasingly variable water fl uxes. The rate and extent of these and many other negative climate-related impacts, and how to mitigate them, have caused a vigorous discussion on climate change that is in the news on a nearly daily basis.

Elements↗