1. Introduction
As world population rises (2.5, 4.1, and 6.5 billion individuals in 1950, 1975, and 2005, respectively; United Nations 2005), human-induced environmental pressures mount. By some measures, one of the most pressing environmental issues is global climate change related to rising atmospheric concentrations of greenhouse gases (GHGs). The link between observed rising atmospheric concentrations of CO2 and other GHGs, and observed rising global mean temperature and other climatic changes, is not unequivocally established. Nevertheless, the accumulating evidence makes the putative link harder to dismiss. As early as 2000, the United Nations–sponsored Intergovernmental Panel on Climate Change (Houghton et al. 2001) found the evidence sufficiently strong to state that “there is new and stronger evidence that most of the warming observed over the last 50 years is attributable to human activities” and that “[t]he balance of evidence suggests a discernible human influence on global climate.”
If one views anthropogenic climate change as an undesirable eventuality, it follows that modifying the ways we conduct various aspects of our lives is required in order to reduce GHG emissions. Many changes can realistically only occur following policy changes (e.g., switching some transportation volume to less CO2-intensive modes). However, in addition to policy-level issues, energy consumption is strongly affected by individual personal, daily-life choices. Perhaps the most frequently discussed such choice is the vehicle one drives, indeed a very important element of one's planetary footprint. As we show below, an important albeit often overlooked personal choice of substantial GHG emission consequences is one's diet. Evaluating the implications of dietary choices to one's planetary footprint (narrowly defined here as total personal GHG emissions) and comparing those implications to the ones associated with personal transportation choices are the purposes of the current paper.
2. Comparative energy consumption by food production
In 1999, Heller and Keoleian (2000) estimated the total energy used in food production (defined here as agricultural production combined with processing and distribution) to be 10.2 × 1015 BTU yr−1. Given a total 1999 U.S. energy consumption of 96.8 × 1015 BTU yr−1 (Table 1.1 in U.S. Department of Energy 2004a), energy used for food production accounted for 10.5% of the total energy used. In 2002, the food production system accounted for 17% of all fossil fuel use in the United States (Horrigan et al. 2002). For example, Unruh (2002) states that delivered energy consumption by the food industry, 1.09 × 1018 J in 1998, rose to 1.16 × 1018 J in 2000 and is projected to rise by 0.9% yr−1, reaching 1.39 × 1018 J in 2020. Unruh (2002) also reports that delivered energy consumption in the crops and other agricultural industries (the latter consisting of, e.g., animal and fishing) increases, on average, by 1% and 0.9% yr−1, respectively. Thus, food production, a function of our dietary choices, represents a significant and growing energy user.
To place energy consumption for food production in a broader context, we compare it to the more often cited energy sink, personal transportation. The annual U.S. per capita vehicle miles of travel was 9848 in 2003 (Table PS-1 in U.S. Department of Transportation 2004). Using the same source, and focusing on cars (i.e., excluding buses and heavy commercial trucks), per capita vehicle miles traveled becomes 8332, of which an estimated 63% are traveled on highways (Table VM-1 U.S. Department of Transportation 2004). According to the U.S. Department of Energy's (2005) table of most and least efficient vehicles (http://www.fueleconomy.gov/feg/best/bestworstNF.shtml) and considering only highly popular models, the 2005 vehicle miles per gallon (mpg) range is bracketed by the Toyota Prius' 60:51 (highway:city) on the low end and by Chevrolet Suburban's 11:15. At near average is the Toyota Camry Solara's 24:33 mpg. The salient transportation calculation (Table 1) demonstrates that, depending on the vehicle model, an American is likely to consume between 1.7 × 107 and 6.8 × 107 BTU yr−1 for personal transportation. This amounts to emissions of 1.19–4.76 ton CO2 based on the estimated conversion factor of 7 × 10−8 ton CO2 BTU−1 derived from the 2003 U.S. total energy consumption, 98.6 × 1015 BTU (U.S. Department of Energy 2004a), and total CO2 emissions of 6935.9 × 106 ton (U.S. Department of Energy 2004b).
The next logical step is quantifying the range of GHG emissions associated with various reasonable dietary choices. In exploring this question, we note that food production also releases non-CO2 GHGs unrelated to fossil fuel combustion (e.g., methane emissions due to animal manure treatment). In comparing below the GHG burden exerted by various reasonable dietary choices we take note of both contributions.
3. Plant-based versus animal-based diets
To address the variability in energy consumption and GHG emissions for food, we focus on a principal source of such variability, plant- versus animal-based diets. To facilitate a quantitative analysis, we define and consider several semirealistic mixed diets: mean American, red meat, fish, poultry, and lacto-ovo vegetarian. These diets are shown schematically in Figure 1. To obtain the mean American diet, we use actual per capita food supply data summarized in the Food Balance Sheets for 2002 (FAOSTAT 2005). Those balance sheets report a total gross caloric consumption of 3774 kcal per person per day, of which 1047 kcal, or 27.7%, is animal based. Of those 1047 kcal day−1, 41% are derived from dairy products, 5% from eggs, and the remaining 54% from various meats. For comparison, we let all diets, including the exclusively plant-based one (“vegan”), comprise the same total number of gross calories, 3774 kcal day−1.
The red meat, fish, and poultry diets we consider share similar dairy and egg portions, 41% and 5% of the animal-based caloric fraction of the diet (Figure 1). The remaining 54% of the animal-based portion of the diet is attributed to the sole source given by the diet name. For example, the animal-based part of the red meat diet comprises 41%, 5%, and 54% of the animal-based calories from dairy, eggs, and red meat, respectively. For the purposes of this paper, we define red meat as comprising 35.6% beef, 62.6% pork, and 1.8% lamb, reflecting the proportions of these meats in the FAOSTAT data. In the lacto-ovo diet, we set the total animal-based energy derived from eggs and dairy to 15% and 85% based on values from Table 1 of Pimentel and Pimentel (2003).
Specific diets vary widely in the fraction of caloric input from animal sources (hereafter α). For example, Haddad and Tanzman (2003) suggest that lacto-ovo vegetarian diets in the United States contain less than 15% of their calories from animal sources, well below the 27.7% derived from animal sources in the mean American diet. We therefore calculate the energy and GHG impact of each diet over a range of this fraction, 0% ≤ a ≤ 50%, where α = 0 corresponds to a vegan diet.
3.1. Greenhouse effects of direct energy consumption
This section addresses the greenhouse burden by agriculture that is directly exerted through (mostly fossil fuel) energy consumption and the subsequent CO2 release. The fossil fuel inputs treated here are related to direct energy needs such as irrigation energy costs, fuel requirements of farm machinery, and labor. We are interested in the range of this burden affected by dietary choices, especially plant- versus animal-based diets.
We define energy efficiency as the percentage of fossil fuel input energy that is retrieved as edible energy [e = 100 × (output edible energy)/(fossil energy input); see Table 2]. We derive energy efficiency e of various animal-based food items by combining available estimates of (edible energy in protein output)/(fossil energy input) (Pimentel and Pimentel 1996a) and the total energy content relative to the energy from protein. The estimated energy efficiency of protein in animal products (Pimentel and Pimentel 1996a) varies from 0.5% for lamb to ∼5% for chicken and milk to 3% for beef (second column of Table 2). This wide range reflects the different reproductive life histories of various animals, their feed, their genetic ability to convert nutrients and feed energy into body protein, fat, and offspring, the intensity of their rearing, and environmental factors (heat, humidity, severe cold) to which they are subjected, among other factors. Accounting for the total energy content relative to the energy from protein (Table 2; U.S. Department of Agriculture 2005), these numbers translate to roughly 1%, 20%, and 6% (e = 0.1, 0.2, and 0.06). The weighted mean efficiency of meat [red meat (consisting of beef, pork, and lamb, as previously defined), fish, and poultry] in the American diet is 9.32% (U.S. Department of Agriculture 2002; see Table 3). These efficiencies are readily comparable with the energy efficiency f of plant-based foods estimated by Pimentel and Pimentel (1996b, c): 60% for tomatoes, ∼170% for oranges and potatoes, and 500% for oats. The wide range of f reflects differences in farming intensity, including labor, machinery operation, and synthetic chemical requirements.
The efficiencies are e = 0.1152 (fish), 0.1152 (red meat), 0.1405 (average American diet), 0.1876 (poultry), and 0.1919 (lacto-ovo). Recall that the red meat, mean American, fish, and poultry diets derive 41% and 5% of their animal-based calories from dairy and eggs; thus, the weighted-mean efficiency e of the diets reflects the higher efficiency of dairy and egg relative to fish or red meats. The specific (not weighted mean) efficiency of poultry production is between those of dairy and eggs (Table 2). The notable equality of fish and red meat efficiencies reflects 1) the large energy demands of the long-distance voyages required for fishing large predatory fishes such as swordfish and tuna toward which western diets are skewed, and 2) the relatively low energetic efficiency of salmon farming. Note that similar e values for two or more diets (such as the poultry and lacto-ovo above) reflect similar overall energetic efficiency of the total diets only if those diets also share α, the animal-based caloric fraction of the diet. However, recall the aforementioned Haddad and Tanzman (2003) suggestion that American lacto-ovo vegetarians eat less than 15% of their calories from animal sources, indicating that the overall energetic efficiency of lacto-ovo diets is higher than that of the average poultry diet assumed here, with α = 0.277, the same fraction as that of the mean American diet.
Note that the difference among the three diet groups is larger than the range in efficiencies arising from different values of f for a given mean e. Figure 2 shows that a person consuming the average American diet, with average caloric efficiencies of the animal- and plant-based portions of the diet, releases 701 kg of CO2 yr−1 beyond the emissions of a person consuming only plants. Compared with driving a Toyota Camry under the conditions of Table 1, this amounts to 100 × 0.701/2.24 ≈ 31.3%, that is, roughly a third of the greenhouse costs of personal transportation.
3.2. Greenhouse effects in addition to energy inputs
Of agriculture's various non-energy-related GHG emissions, we focus below on the two main non-CO2 GHGs emitted by agriculture, methane, CH4, and nitrous oxide, N2O. In 2003, U.S. methane emissions from agriculture totaled 182.8 × 106 ton CO2-eq, of which 172.2 × 106 ton CO2-eq are directly due to livestock (U.S. Department of Energy 2004b). The same report also estimates the 2003 agriculture-related nitrous oxide emissions, 233.3 × 106 ton CO2-eq, of which 60.7 × 106 ton CO2-eq are due to animal waste. Thus, the production of livestock in the U.S. emitted methane and nitrous oxide is equivalent to at least 172.2 × 106 + 60.7 × 106 = 232.9 × 106 ton CO2 in 2003. With 291 million Americans in 2003, this amounts to 800 kg CO2-eq per capita annually in excess of the emissions associated with a vegan diet.
One may reasonably argue that the ∼0.8 ton CO2-eq per person per year due to non-CO2 GHGs does not accurately represent the difference between animal- and plant-based diets, which is our object of inquiry; if there were no animal-based food production at all, plant-based food production would have to increase. However, such a hypothetical transition will produce zero methane and nitrous oxide emissions in the categories considered above, animal waste management, and enteric fermentation by ruminants. Ignored categories, principally soil management, will indeed have to increase, but over an area far smaller than that vacated by eliminating feed production for animals. For example, Reijnders and Soret (2003) report that, per unit protein produced, meat production requires 6 to 17 times as much land as soy. Therefore, the net reduction in methane and nitrous oxide emissions will have to be larger than our estimate presented here.
Approximately 74% of the total nitrous oxide emissions from agriculture, ∼173 × 106 ton CO2-eq, are due to nitrogen fertilization of cropland, which supports production of both animal- and plant-based foods. The exact partitioning of nitrogen fertilization into animal feed and human food is a complex bookkeeping exercise beyond the scope of this paper. Consequently, we ignore this large contribution below. Nevertheless, simple analysis of the Food Balance Sheets (FAOSTAT 2005) and Agriculture Production Database (FAOSTAT 2005) data shows that the portion of those 173 × 106 ton CO2-eq attributable to animal production is at least equal to, and probably larger than that attributable to plants, thereby rendering our estimate of the GHG burden exerted by animal-based food production a lower bound.
The value of 800 kg CO2-eq yr−1 due to non-CO2 emissions computed above represents the composition of the actual mean American diet. To calculate the added non-CO2 burden of specific diets, we must first compute, from the mean American diet, the burden for individual food items.
This calculation requires intermediate steps, as available data are for specific farm animals, not individual food items. Using annual emissions reported by the U.S. Department of Energy (2004b), in Table 4 we sum the contributions of methane from enteric fermentation and manure management and the nitrous oxide from manure management for cattle, pigs, poultry, sheep, and goats. To partition cattle methane emissions from enteric fermentation [108.72 million ton CO2-eq; Table 21 in U.S. Department of Energy (2004b)] among beef (75.46%) and dairy (24.54%) cattle, we use emission ratios derived from Table 5-3 of U.S. Environmental Protection Agency (2005) (we apply these ratios to the 2003 data, but we do not use the absolute values, because the table's latest entry is 2001). We similarly use Table 5-5 of U.S. Environmental Protection Agency (2005) to partition nitrous oxide emissions from cattle manure management, 56.3 million ton CO2-eq [Table 28 in U.S. Department of Energy (2004b)], among dairy (39%) and beef (61%) cattle.
Table 28 in U.S. Department of Energy (2004b) reports emissions of 1.3 million ton CO2-eq from N2O due to poultry manure management. Because we do not have direct information on the partitioning of these emissions among eggs and poultry meat, we assume this partition in N2O is proportional to total manure mass and thus is roughly similar to the partitioning of methane from poultry manure management, 47.38% and 52.62% for eggs and meat, respectively (Table 22 in U.S. Department of Energy 2004b). We thus partition the 1.3 million ton CO2-eq from N2O due to poultry manure management as 0.62 and 0.68 million ton CO2-eq due to eggs and poultry meat, respectively.
To obtain the per capita daily emissions associated with food items, we divide the individual non-CO2 GHG annual sums (Table 4, fourth numeric column) by the U.S. 2003 population, 291 million, and 365 days. The results, in grams of CO2-eq per day, are shown in the first numeric column in Table 5. To calculate emissions per kcal associated with the consumption of individual food items, we divide the per capita daily emissions (Table 5, first numeric column) by the respective per capita consumptions (FAOSTAT 2005; Table 5, second numeric column). These divisions yield the non-CO2 GHG emissions per kcal reported in the rightmost column in Table 5. Importantly, the non-CO2 GHG emissions per kcal vary by as much as a factor of 70 for the animal-based food items considered, rendering some animal-based options (e.g., poultry meat) far more benign than other ones (most notably beef).
In addition to amplifying the GHG burden of all mixed diets, the added inclusion of non-CO2 GHGs reveals several consequences of dietary choices. First, red meat and fish diets, which previously coincided because the only consideration was caloric efficiency e, which is roughly 0.11 for both, are now clearly distinct. Second, with the effect of non-CO2 GHGs included, the fish diet results in lower GHG emissions than both the red meat and mean American diets. This is partly attributable to our choice to ignore small non-CO2 GHG emissions associated with fish consumption. Third, the lacto-ovo vegetarian diet appears to result in higher GHG emissions than the poultry diet. According to our calculations this is true for any α; however, if lacto-ovo vegetarians eat less than average animal products, as suggested by Haddad and Tanzman (2003), the relevant comparison is not for a given α (a vertical line in Figure 3), but rather between one α for lacto-ovo diet, for example, α ≈ 0.15, and a higher one for poultry, for example, α ≈ 0.27.
To place the planetary consequences of dietary choices in a broader context, note that at mean U.S. caloric efficiency (blue line in Figure 3), it only requires a dietary intake from animal products of ∼20%, well below the national average, 27.7%, to increase one's GHG footprint by an amount similar to the difference between an ultraefficient hybrid (Prius) and an average sedan (Camry). For a person consuming a red meat diet at ∼35% of calories from animal sources, the added GHG burden above that of a plant eater equals the difference between driving a Camry and an SUV. These results clearly demonstrate the primary effect of one's dietary choices on one's planetary footprint, an effect comparable in magnitude to the car one chooses to drive.
4. Are plant-based diets safe?
The thrust of this paper has been that the United States bears a GHG burden for the animal-based portion of its collective diet. From Figure 3 we can estimate this burden as roughly 1.485 ton CO2-eq per person per year × 291 million Americans ≈ 432 million ton CO2-eq yr−1 nationwide, or ∼6.2% of the total [69 335.7 million ton CO2-eq in 2003 (Table ES2 of U.S. Department of Energy 2004b)]. To the extent one subscribes to the notion that reducing GHG emissions is desirable, a corollary of this estimate is that it is advantageous to minimize the animal-based portion of the mean American diet. This raises the question of whether a plant-based diet is nutritionally adequate for public health. The following section addresses this question. The available evidence suggests that plant-based diets are safe, and are probably nutritionally superior to mixed diets deriving a large fraction of their calories from animals.
The adverse effects of dietary animal fat intake on cardiovascular diseases is by now well established (see Willett 2001 for a comprehensive review). Similar effects are also seen when meat, rather than fat, intake is considered (e.g., Key et al. 1999; Erlinger and Appel 2003). Less widely appreciated—despite being just as persuasively demonstrated, exhaustively researched, and robustly reproducible—are the links between animal protein consumption and cancer (for a thorough review, see Campbell and Campbell 2004).
The first studies linking dietary animal protein and cancer (e.g., Mgbodile and Campbell 1972; Preston et al. 1976) focused on cancer initiation, the brief process during which cancer-causing mutations first occur. Collectively, they documented numerous cellular mechanisms by which cancer initiation increases under high animal protein diets. Follow-up studies (e.g., Appleton and Campbell 1982; Dunaif and Campbell 1987) addressed cancer promotion after initiation, showing dramatically increased precancerous deformities in response to a given carcinogen dose under high animal protein diets. To unambiguously implicate animal protein in the observed enhanced cancer promotion, Schulsinger et al. (1989) compared induced carcinogenesis under high protein diets of animal and plant origins. Cancer promotion was significantly enhanced under animal-protein-rich diet. Youngman (1990) and Youngman and Campbell (1992) extended these results to clinical cancer (as opposed to cancer precursors), showing roughly an order of magnitude higher tumor incidence in rats on high animal-protein diets who lived their full natural life span. Similar results were also obtained with different species and carcinogens (e.g., Cheng et al. 1997; Hu et al. 1997). Note that the above laboratory results were all obtained at protein intakes per unit body mass routinely consumed by Westerners, suggesting the applicability of the results to humans (Campbell and Campbell 2004).
Human epidemiological evidence indeed corroborates the link between animal-based diet and cancer. For example, Larsson et al. (2004) show enhancement of ovarian cancer with dairy consumption in Swedish women; Sieri et al. (2002) show a strong association between animal protein intake and breast cancer in Italian women; Chao et al. (2005) show a tight positive relationship between meat consumption and colorectal cancer; and Fraser (1999) demonstrates an approximate halving of colon and prostate cancer risk among vegetarians. Barnard et al. (1995) documented the disease burden exerted by seven major diseases on the health care system directly related to meat consumption. Some of the above cited results may well be challenged in the future. Nevertheless, it is hard to avoid the conclusion, reached by, for example, Sabate (2003), that animal-based diets discernibly increase the likelihood of both cardiovascular diseases and certain types of cancer. To our knowledge, there is currently no credible evidence that plant-based diets actually undermine health; the balance of available evidence suggests that plant-based diets are at the very least just as safe as mixed ones, and are most likely safer.
5. Conclusions
We examine the greenhouse gas emissions associated with plant- and animal-based diets, considering both direct and indirect emissions (i.e., CO2 emissions due to fossil fuel combustion, and methane and nitrous oxide CO2-equivalent emissions due to animal-based food production). We conclude that a person consuming a mixed diet with the mean American caloric content and composition causes the emissions of 1485 kg CO2-equivalent above the emissions associated with consuming the same number of calories, but from plant sources. Far from trivial, nationally this difference amounts to over 6% of the total U.S. greenhouse gas emissions. We conclude by briefly addressing the public health safety of plant-based diets, and find no evidence for adverse effects.
Acknowledgments
We thank two anonymous reviewers for their thoughtful, pertinent comments, and Editor Foley for handling the manuscript and suggesting numerous useful improvements.
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Energy consumption for personal travel.
Energetic efficiencies for a few representative food items derived from land animals, aquatic animals, and plants.
Weighted-mean energetic efficiency of the animal-based portion of the hypothetical mixed diets considered in this paper.
Non-CO2 GHG emissions associated with the production of various food items. Units are 106 CO2-eq yr−1, except column 6.
Non-CO2 GHG emissions per unit food consumed, derived from the actual mean American diet in the Food Balance Sheets (FAOSTAT 2005).
Non-CO2 GHG emissions of the hypothetical diets considered in this paper.