Megafauna —

First Victims of the Human-Caused Extinction
Baz Edmeades
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Chapter 14

Fire

Swartkrans cave, situated in the Sterkfontein valley about thirty miles north-west of Johannesburg, is the single richest hominid site in Africa. As we’ll see presently, its oldest deposits – Members 1 to 3 – have yielded, between them, the skeletal remains of two hominid species that were living in the early Pleistocene, as well as tools made of both bone and stone, and animal bones butchered by hominid meat-eaters.

Excavating grid square W3/S2 in Member 3 of this treasure-house of early-Pleistocene hominid life on March 21, 1984, George Moenda, working with Bob Brain, found an apparently charred piece of bone. Had this specimen come from a later archeological excavation, Brian tells us,

…I would have had no hesitation in assuming that it had been partly charred in a fire, but at an estimated age in excess of a million years, the presence of burnt bone in a hominid living area required further verification.

He accordingly took a sample of it to the National Physical Laboratory of South Africa’s Council for Scientific and Industrial Research, where analysis confirmed that the blackening of the bone was, in fact, caused by fire rather than chemical staining.

By the time the excavation of Member 3 was completed, 270 pieces of burned bone had come to light. Although a few of them had been found grouped in clusters, it’s clear that those burned bones were, for the most part, the products of a great many separate fires:

In one grid square, W3/S3, burnt bones occur in 23 excavation spits, each 10 cm deep, indicating that the bones were heated in frequently recurring fires during the deposition period of this stratigraphic unit, which may have spanned several thousand years.

The distribution of these burned bones throughout such a large portion of the six-meter-deep gully of calcified debris which constitutes Member 3, doesn’t only suggest a long history of fire-use in or near the entrance to the Member 3 gully; it also excludes the possibility that the burned bones could have “contaminated” that Member, i.e. found their way into it at some relatively recent time.

In order to find out whether the bones were burned in natural fires, or in fires made and/or tended by the hominids who lived in that area, it was necessary to establish the temperatures to which they had been subjected. Grass or brush fires typically burn cooler than 250 degrees Celsius, while hearths or campfires can reach or exceed the 600 degree mark. In a test "hearth" fire made with wood from Celtis africana, an African relative of the elm which commonly grows in the entrances of karst caves like Swartkrans, Brain measured temperatures of up to 860 degrees Celsius. A test fire made with the wood of Acacia karoo, another tree which is presently common in the vicinity of Swartkrans, peaked at 688 degrees.

There is, of course, no absolute rule that brush or veld fires will not exceed 250 degrees Celsius. Grass fires can ignite dead trees, or parts of trees, to produce, in localized patches, the high temperatures characteristic of hearths. It’s unlikely, however, that anything beyond a small percentage of a collection of naturally-burned bones (which would be more-or-less evenly distributed on the veld and not concentrated in the vicinity of logs) will be heated to those temperatures.

To begin the task of determining the temperatures at which the Swartkrans bones were burned, Brain experimentally heated a large selection of fresh and weathered bones in a kiln at selected temperatures. He found that the color of these bones changed to dark brown or black in the vicinity of 300 degrees Celsius. At higher temperatures this discoloration faded and the bones started becoming “calcined.” At about 600 degrees they would become grayish-white in color, and tend to be lighter in weight.

In order to create a histological or microscopic record of these changes, Brain cut the fresh, defleshed radius of a hartebeest into seven transverse segments, and heated those segments, respectively, to 200, 300, 400, 500, 600, 700 and 800 degrees Celsius for thirty minutes, cooling them slowly thereafter. Thin sections prepared from each of these segments displayed more-or-less unique microscopic features, characteristic of the particular temperature to which it had been subjected. Another portion of each of those bone-segments was sent to Andrew Sillen, then of the Archeometry Laboratory of the Department of Archeology at the University of Cape Town, for chemical analysis.

With the knowledge they had gained from this controlled heating, Brain and Sillen then subjected the burned bones found at Swartkrans’ Member 3 to histological and chemical analyses, establishing that well over half of them had been subjected to temperatures of 300 degrees or more. Forty-seven percent had become calcined and grayish-white in color, and were found to have been heated to temperatures approaching or exceeding the 600-degree mark. Dr. Anne Skinner and her colleagues at Williams College in Williamstown, Massachusetts, have recently confirmed these findings by using ESR to test samples of the bones in question for the presence of the different kinds of free radicals which are created by burning at different temperatures.

The picture that has emerged from these analyses makes it highly unlikely that anything but a small minority of those bones could have been burned in natural fires. We know, in addition, that hominids ate meat off at least some of the burned bones found in Member 3, because four of them display cut- and/or chop marks made by stone tools. (No cutmarked bones have been found outside Member 3.) Of the 59,218 unburned bone fragments found that Member, a total of twelve (0.02%) are cut- or chop-marked; of the 270 burned bones found there, four (1.48%) are marked in that way. The fact that only one in 4,934.8 of the unburned bones are cutmarked, while one in 67.5 of the burned bones are marked in that way, would be a puzzling one if we assumed a “natural” or non-hominid cause for the bone-burning, but it makes complete sense if we accept that the burning of those bones was, like their cut-marking, carried out by hominids.

With the exception of the lower bank of Member 1, in which three specimens were found, no other burned bones were found in any of the other Swartkrans members although each of those other Members yielded, as we’ve seen, plenty of other evidence of hominid remains and tools. Could this mean that the entrance to Member 3 had, at the relevant time, some feature like, say, a dolomite overhang which made it convenient to build fires in its immediate vicinity, a feature which the other Members lacked while they were accumulating? Or could it indicate that the hominids only learned to use fire around the time that Member 3 started accumulating? Or that the hominids in question had only been capable of harvesting naturally-ignited fire before the accumulation of Member 3, (which could explain why three burned-bone specimens were found in the Member 1) and that they had learned, by the time Member 3 was accumulating, to make fire rather than relying on the relatively infrequent occurrence of naturally-ignited fires in that area? The latter two possibilities are both reconcilable with East African evidence which suggests, as we’ll see presently, that fire-use by hominids started between 1.7 and 1.6 million years ago, while faunal and ESR dating suggest that Swartkrans’ three older Members accumulated in the vicinity of 1.6 million years ago.

Eight hundred seventy-seven stone specimens adjudged to be hominid artifacts were found in Members 1, 2 and 3. These hominid-fractured stones, which consist mostly of cores and unmodified waste, aren’t easy to classify. Clark Howell, of U.C. Berkeley’s Laboratory for Human Evolutionary Studies, thinks they “approximate the Developed Oldowan of eastern Africa…” Howell points out, however, that a number of bifaces, a pick-like piece, and a cleaver-ended specimen, obtained from dump breccia residues presumably originating from Member 3, raise the possibility of this Member contained an Acheulian element.

Member 3 also yielded forty-one bone specimens – mainly fragments of long bones and horn-cores – whose points are scratched and rounded in ways that show that they were used to for digging. A total of 84 such implements were found in Members 1, 2 and 3, and a few more have been unearthed at nearby Sterkfontein and Driemolen. Brain concluded from experimental work done with modern replicas of those tools, that the originals were used to unearth plant storage organs like the bulbs of Ledebouria, and corms of the genus Hypoxis, both of which are still found in the vicinity of Swartkrans. Experimental work by Lucinda Backwell and Francesco d’Errico, has persuaded those researchers that the width and orientation of the striations on those tools, may approximate more closely the wear-pattern created by digging in termite mounds.

A delicate, awl-like artifact from Member 3, SKX 37052, has a point which is marked by both circumferential and longitudinal scratches, together with polish. “This tool may well have been used,” Bob Brain and Pat Shipman wrote,

…for piercing holes in skins and other soft materials, as similar microscopic wear has been documented on experimentally made and used awls.

The evidence discussed here suggests that the Swartkrans hominids of Member 1-3 times may well have made simple carrying bags from animal skins, in which they transported their tools, as well as possibly their gathered food. This could explain the evidence for the apparent use of the same tools over successive days or weeks.

 

* * *

Hominid remains – mostly fragmented like the majority of the bone specimens found in that cave – are extremely abundant at Swartkrans. Skeletal parts representing an estimated 116 individuals of the species Paranthropus robustus have been found in the cave’s three “old” Members. Homo – presumably Homo erectus – is present in Swartkrans, too, but in much smaller numbers: fragments (including one lower jaw) represent perhaps three individuals in Member 1, and two in Member 2. The fact that no remains clearly identified with Homo were found in Member 3 does not mean that this genus was absent from Swartkrans area during the time that Member was accumulating: lions and sabertooth cats appear even less frequently in the Swartkrans deposits than Homo does, but it would be unrealistic to conclude from that fact, that big cats must necessarily have been absent, or even rare, in that area during the times in which their remains don’t show up.

Which of the two human-like beings whose remains have been found at Swartkrans made the tools, and tended the fires in which the Member 3 bones were burned?

When Louis Leakey’s family unearthed a specimen of both Paranthropus and the gracile hominid OH7 in 1.8 million-year-old deposits at Olduvai in which stone tools had been found, they were confronted – at least in regard to the tools – with a similar question. Leakey conceded that it was possible that both hominid species had made and used those tools, but inclined to the view that the species which he called Homo habilis “was the more advanced tool-maker, and that the Zinjanthropus [i.e. Paranthropus] skull represents an intruder (or a victim) on the Homo habilis living site.”

It’s by no means impossible that Paranthropus could, on occasion, have become a victim of Homo. Homo erectus had, as we’ve seen, become an expert hunter of large animals in the early Pleistocene, and there’s no reason to think that large primates would have been excluded from their list of prey species. Erectus is thought to have butchered giant gelada baboons later in the Pleistocene, on the basis of 700,000-old-year-old evidence found at the DE/89 B site at Olorgesailie in Kenya, and we know that contemporary humans kill and eat chimpanzees. It’s interesting, too, to note in this regard, that the burned bones found in Swartkrans’ Member 3 include a Paranthropus finger-bone. (Those bones also include one each of a baboon, a zebra, a guinea fowl, a dassie and a meerkat, while the rest are those of a group of antelopes and other split-hoof animals which zoologists refer to as bovids.)

The relationship between Homo erectus and Paranthropus would have been a strange one from the point of view of present-day humans. Erectus – less intelligent, we can assume, than sapiens was to become – would have been sharing a habitat with a fellow-primate which was probably quite a bit more intelligent than present-day chimps or gorillas. Randall Susman’s anatomical investigations have led him to the conclusion that Paranthropus’ hands were well-adapted to precision grasping and the use of tools. It’s clear that Paranthropus and Homo were genetically isolated from each other, but there’s no reason why simple technological memes could not have flowed between them. It would not be surprising, at any rate, if digging-tools like those found at Swartkrans, as well as wooden implements of various kinds, were used by both hominids. One could speculate that Paranthropus might have used crude stone tools – and perhaps even the discarded Acheulian tools they would occasionally have come across. Acheulian tools are, however, so frequently and reliably associated with Homo erectus, and associated with it, moreover, for so long after Paranthropus becomes extinct around .9 million years ago, that there can be little doubt that erectus was the developer and practitioner of the of the Acheulian industry (and, indeed, its immediate predecessor, the Developed Oldowan).

In the absence of evidence suggesting otherwise, I’ll continue to presume, therefore, that advanced technologies like the making of Acheulian tools and the use of fire were the exclusive preserves of the big new hominid whose brain-capacity was about 50% larger than that of both its Pliocene ancestors and its robust contemporaries.

 

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When did the fire-use evidenced in Swartkrans take place? Unlike many of the bones and hominid-associated objects from East Africa, which are often conveniently sandwiched between easy-to-date layers of volcanic ash, those found in South Africa’s limestone caves are notoriously difficult to date. The fossil- and artifact-bearing deposits of Swartkrans entered that cave at different times, falling into it or sliding down “talus” slopes through different entrances or holes in its roof. At times when the cave was accessible, some objects are thought to have been carried into it by four-footed carnivores or hominids. The body of debris presently found in that cave constitutes, therefore, what Brain understatedly calls “a depositional mosaic of considerable complexity.”

In a professional involvement with the cave that has lasted more than half a century, Brain has resolved that mosaic into five more-or-less distinct “Members.” Those Members represent, in Brain’s view, depositional episodes which alternated with erosional phases, in cycles which were probably driven by precipitation changes triggered, in their turn, by the 40,000-year glacial cycles which the planet was experiencing up to a million years ago. The deposits are numbered in the order in which they appear to have accumulated in the cave, with Member 1 being the oldest, Member 2 being the second-oldest and so on.

In the 1960s and 70s Elizabeth Vrba – then of the Transvaal Museum, now of Yale – made a detailed and comprehensive study of the fossil bovids from Swartkrans and other hominid-bearing cave deposits. On the basis of when those bovid species had made first and last appearances in deposits elsewhere in Africa – deposits which could be securely dated by stratigraphic and other means – she concluded in 1982 that a portion of Member 1, the so-called “Hanging Remnant,” was between 1.8 and 1.5 million years old. With the exception of the burned and/or cutmarked bones we’ve been discussing, the hominid-associated objects found in Members 2 and 3 don’t differ significantly from those of Member 1. Apart from the fact that Homo doesn’t appear in Member 3, the hominid remains recovered from the three “old” Members don’t differ from each other either. The animal ensembles found in those three Members are also substantially similar. Members 1, 2 and 3 are presumed, for these reasons, to have accumulated in relatively rapid succession to each other.

A 2004 review of the fauna of Swartkrans’ Members 1-3 by Darryl de Ruiter, now of Texas A&M, yielded an estimate for the age of those Members which was very close to the result produced by Elizabeth Vrba’s study of Member 1’s “Hanging Remnant.” De Ruiter concluded that, although Members 2 and 3 were contaminated by some recent material, all three of the older Members were deposited in the neighborhood of 1.6 million years ago.

Direct ESR testing of two hominid teeth and two bovid teeth by Rainer Grün, Darryl Curnoe and others have produced findings which are in agreement with those of Vrba and de Ruiter, yielding an age of between 1,470,000 and 1,790,000 with a median of 1.63 million years for the “Hanging Remnant” of Member 1 in which those teeth were found.

As one might expect from deposits which accumulated before the 1.4 million-year-ago “hemorrhage” of megafaunal diversity we talked about in Chapter 12, Swartkrans’ Members 1, 2 and 3 contain several species which disappeared in that hemorrhage – the cheetah-like Chasmaporthetes hyena makes two appearances, along with the machairodonts Dinofelis (one appearance in Member 1) and Megantereon (one appearance in Member 3).

In the sense that God is (as Ludwig Mies van der Rohe famously remarked) “in the details,” the truth about hominid fire-use in the early Pleistocene is, I believe, discernable in the details of Bob Brain’s meticulously-documented excavation and analysis of the burned bones in Swartkrans’ Member 3. Those details do not, in my view, merely suggest that hominids may have been using fire by 1.5 million years ago. They raise, instead, an overwhelming likelihood – a practical certainty – that they were doing so.

 

* * *

Because signs of fire-use are not, until the later Pleistocene, found as frequently as, say, stone tools are, Ian Tattersall suspects that fire-use may have been a “rather intermittent” part of human life in the earlier parts of that Epoch. I’m prepared to accept that small and isolated hominid populations, like the approximately 10,000 members of sapiens confined to Tasmania by a rise in the sea-level at the end of the last glaciation, may have lost the art of fire-making, but it doesn’t seem likely to me that a such a powerful and useful technology could, at any time after it was developed, have been abandoned or lost throughout the entire African and South Asian range which our family occupied in the Early Pleistocene. The fact that fires feed on organic material – mainly wood – which is preserved far less frequently than stone artifacts, is, in my view, a more likely explanation for the fact that we don’t find the signs of fire-use as consistently as, say, stone tools.

But stone artifacts are themselves able to provide information about early hominid fire-use. When “siliceous” stone such as basalt or quartz (as distinct, say, from “calcereous” material such as limestone) undergoes prolonged exposure to temperatures exceeding 250 degrees Celsius, (which marks, as we’ve seen, the borderline between the “campfire” and “brush fire” temperature-ranges) its surface undergoes characteristic color and texture changes, developing, in particular, dimple-like scars called “potlid fractures.” A survey by Brian Ludwig of Rutgers University of stone artifacts – and of the waste pieces or “debitage” produced in the making of such artifacts – revealed a telling pattern of thermal alteration. Ludwig personally examined almost 40,000 pieces of hominid-modified stone from nearly fifty sites in the Olduvai and Turkana basins, covering a period of 2.5 million to less than one million years ago. In doing so, he found no potlid fractures on any specimens dating from before about 1.6 million years ago. After that time, however, a small but consistent proportion of the stone does display potlid fractures, over a wide variety of sites including Olduvai where, despite the preservation of a rich store of hominid-modified material, no signs of fire-use had previously been found.

The other area surveyed by Ludwig, the Turkana basin, had, however, yielded signs of hominid fire-use prior to his survey. These were first identified in the 1970s , when Jack Harris, who had been Ludwig’s teacher at Rutgers, examined several patches of apparently baked reddish earth at a cluster of sites known as FxJi-20, situated in the 1.6 million-year-old Okote tuff at Koobi Fora. Harris and some of his colleagues became interested in those patches when they realized that they resembled the present-day spots on which local tribespeople had made overnight campfires. These apparently-baked patches were situated in an area which had yielded a number of hominid artifacts, some of which were apparently discolored and/or fractured by heat. It also contained a scattering of faunal remains which included the lower jaw of a Paranthropus – KNM-ER 3230.

A 1978 suggestion by Harris that the reddish patches were remnants of fire-places or hearths, provoked a skeptical response. They could, his critics asserted, have been created by bush fires. Alternately, their discoloration could have been caused by either fungal invasion or the precipitation of iron particles.

Ralph Rowlett, an anthropologist from the University of Missouri, then established, by thermoluminescence tests of four of the discolored patches conducted in association with Charles Peters, that those patches had been heated more recently than the volcanic soil in which they were situated. That considerably diminished the possibility that they could have resulted from non-thermal processes. Rowlett also eliminated the possibility that they had been directly caused by lightning strikes by examining known strike sites in Africa and the United States. He concluded that the discolored Koobi Fora patches – which were between 12 to 20 inches in diameter – would have been much smaller if they had represented lightning strikes. Those patches were not, moreover, associated with fulgurites, the glassy bits of fused sand that are produced by such strikes.

Rowlett, Randy Bellomo (then with the University of South Florida, now of the University of Wisconsin-Milwaukee) and others found melted crystals in the patches which indicated that the fires causing them had produced temperatures close to 400 degrees Celsius. (Grass- and brush fires do not, as we’ve seen, usually exceed 300 degrees Celsius.) We’ve seen, though, that grass- or brush fires on Africa’s savannas can and do ignite logs and/or dead tree-stumps, which can burn hotter than the fire which ignited them. The likelihood that discolored patches had been produced in this way was tested by two different methods.

Firstly, an archeomagnetic analysis of several possible fire-places at Koobi Fora’s FxJi-20 Main site by Randy Bellomo yielded evidence that they had been re-heated several times over a period of several years. It’s not unlikely that camp-fires would be re-lighted repeatedly on particular spots which tradition and convenience might have established as hearths, but highly unlikely that “natural” ignition of logs and stumps would have occurred repeatedly on the same places.

Secondly, Ralph Rowlett (together with Robert Graber and Michael Davis) examined the phytoliths left by various kind of fires, including the those which had discolored the suspected Koobi Fora fireplaces. Phytoliths are microscopic bodies of opaline silica formed in epidermal and other cells of the growing plant, from silica dissolved in ground water originally absorbed by the plant’s roots. They typically survive both the decay and incineration of the plant which produced them, and can often be used to identify the species or, at least, the general botanical category of that plant. Rowlett and his colleagues reasoned that a fire consisting of a naturally-ignited log or stump would only leave one kind, or, at any rate, relatively few kinds, of phytolith. Fires which were, on the other hand, started by hominids, would have left many kinds, because they would have been kindled and fed with grass, leaves, twigs, sticks and logs from a variety of plant species.

A comparison of phytolith residues of test camp-fires made by students (who were not told what the nature of the study was) in savanna-like surroundings, and of stumps that had been experimentally set alight, confirmed that the former produced a heterogeneous collection of phytoliths, while the latter left a residue which tended to be homogenous.

Rowlett and his associates noted another difference between the test fires in which logs and stumps were ignited, and those in which camp fires had been made: the former left residues with irregular shapes, while the latter left basin- or lens-shaped residues.

Three of the four discolored patches at Koobi Fora’s FxJi 20 E site, were basin-shaped, while a fourth, situated some distance from the others, was irregular. The basin-shaped patches were found to contains even more kinds of phytoliths than the test camp-fires had, while the remaining, irregular one contained only one kind, and was presumed, accordingly, to have been made by naturally-ignited tree.

Swartkrans and Koobi Fora are not the only sites at which researchers have found possible evidence of early-Pleistocene fire-use by hominids. Hominid-used fire may also have discolored the clumps of earth discovered in Chesowanja in Kenya, which were also dated to about 1.6 million years b.p.

Israel has provided a link between these early African sites, and later European evidence of hominid fire-use. Burned seeds, wood, and flint found at Gesher Benot Ya’aqov in the Northern part of that country, suggest that humans were, nearly 790,000 years ago, controlling fire at this site. The diverse collection of plant material burned there, includes three species which had edible fruits or seeds: olive, wild barley, and wild grape. The distribution of burned fragments of flint at the site, was, moreover, suggestive to investigators from the Hebrew University in Jerusalem and Bar-Illan University in Ramat-Gan, that burning had occurred on specific spots, possibly suggesting the locations of hearths.

 

* * *

Bob Brain was careful to point out that the hominids who burned the Swartkrans bones had not necessarily learned how to make fire. He thought it was, instead, likely that they had harvested their fire from naturally-ignited flames.

How might that “harvesting” have begun? Birds and mammals often converge on African veld fires to prey on small mammals and insects flushed out by the flames. Hominids could initially have been drawn to such fires for the same reason. Eventually, the inventive, curious natures of those beings might have prompted them to literally “play with fire” at upwind or non-threatening edges of those burns. That could have taught them enough about the dynamics of fire to enable them to “harvest” flames or embers, and use them to build and maintain fires at places of their own choosing.

How frequently would natural fires have occurred? In Southern Africa, the overwhelming majority of such fires burn in September and October when dry electric storms ignite grass or brush before the summer rains begin. In an article entitled “Fire behaviour in the Kruger National Park,” published in the Journal of the Grassland Society of Southern Africa in 1985, W. Trollope and A. Potgieter report that lightning-caused fires can be expected to burn any given area in the Kruger National Park at intervals ranging between five and ten years. Several subsequent studies have confirmed that a large proportion of Kruger’s savanna remains unaffected by natural fire for years at a time. Daniel Koen, who has studied the issue of naturally-caused highveld fires intensively to formulate a fire-policy for Suikerbosrand nature reserve just south of Johannesburg, tells me that, even though Suikerbosrand is one of the most lightning-prone areas in South Africa, many parts of the reserve can go for years without being burned by lightning-caused fires. The incidence of lighting-strikes varies widely from year to year, and periods in which lightning-caused fires don’t occur in the Reserve, or affect only a small part of it, can be interrupted by a summer in which lightning strikes are widespread and frequent. Under such circumstances, successive lightning-ignited fires can start in close proximity to each other in a single season, if each is extinguished by rain before it burns all the available fuel in that area.

As we’ve just seen, though, lightning-caused fires normally take place much less frequently than this. By August of 2005 I had, for instance, been waiting more than two years for the veld around my favorite walking trail in Suikerbosrand reserve, Bokmakierie, to burn. (My impatience had to do with the fact that fire, followed by rain, transforms Bokmakierie into a verdant Alpine meadow, in which a well-beyond-Alpine diversity of plants begins to flower.) Most of the Bokmakierie area was finally burned in late 2005, whose rainy season was characterized by an exceptional number of electric storms, by one or more lightning-ignited fires, and by another started by a visitor or staff member next to a public road.

I’m impressed – especially in view of the fact that natural, harvestable fires would probably have occurred relatively infrequently – by the abundance and the ubiquity of burned bone found in Swartkranz’s Member 3. I suspect, moreover, that a great many “archeologically invisible” fires – i.e. fires which didn’t contain bone – must, in addition, have been made in that Member’s catchment area: bones would not always have been available to the fire-users, and bone produces, beside that, an acrid, unpleasant-smelling smoke when it’s thrown into a fire. Taken together with the fact that fire-use seems, from the investigations of Rowlett, Bellomo, Ludwig and others, to have become a widespread phenomenon in Africa around 1.6 million years b.p., the high frequency of hominid-tended fires evidenced at Swartkrans prompts me to speculate that the beings who tended those fires could, by the time Member 3 was accumulating, have overcome their dependence on harvested fire, and learned to kindle flames at will.

Hominids who were still dependant on harvesting fire, would probably have learned, after a while, to keep their fires going for relatively long periods of time, and to transport embers over relatively long distances. Days or weeks after such harvestings, however, inattention, sleep, local fuel exhaustion, or rain would inevitably have deprived them of fire for months or even years at a time. Each of those losses would have been a bitter disappointment, because the harvesters would, by that time, have experienced the comfort – and the enormous increase in personal safety – that fire could bring to their nights. Finding a way of kindling a flame would, therefore, have become a very pressing issue indeed.

Would the average erectus have been able to find such a way? No more, I imagine, than the average sapiens would have been able to invent the polymerase chain reaction in the late twentieth century. (The PCR, a cornerstone of the biotech industry, makes it possible to multiply strands of DNA to large quantities for a great many scientific, medical, forensic and industrial purposes. It earned Kary Mullis, who invented it in 1981, a Nobel Prize, the prestigious Japan Prize, and a place in the National Inventors Hall of Fame. In 1991 Hoffman-La Roche bought the patent for this process from Mullis’ former employer for $300 million – possibly the highest price ever paid for a piece of intellectual property.)

Acheulian tools, which were used for purposes as disparate as digging in the earth, butchery, leatherwork, woodwork and scything soft plant material, attest to relatively high levels of ingenuity. So does the harvesting, transportation, and maintenance of fire. It doesn’t seem unlikely to me, therefore, that one or more erectus counterpart of Kary Mullis could have noticed, somewhere between 1.7 and 1.5 million years ago, that sparks struck while knapping certain kinds of stone, could fall, still glowing, onto dry organic material and set it smoldering, and that he (or she or they) could have exploited that state of affairs to make the discovery that Charles Darwin regarded as “the greatest ever made by man, excepting language.”

 

* * *

One of the characters in Ernest Hemingway’s The Sun Also Rises asks another how he went bankrupt. “At first slowly,” the other replies, “and then quickly.” That’s the schedule on which exponential growth takes place – invest money at compound interest, and the return mounts up slowly at first, and then quickly. One dollar invested at an annually compounding rate of 14.8153622%, will yield a million dollars at the end of a century, but it will take just under 90 years to earn a quarter of a million dollars, almost 95 years to reach the half-million dollar mark, and nearly 98 to produce three-quarters of a million.

Technological evolution is as complex as hominid life itself. The growth of its power could not, therefore, be expected to trace out the smooth upward curve which a simple mathematical exponent produces. We would expect, instead, to see a generally exponential increase, punctuated by relatively abrupt rises, plateaus and even local reversals. Like our one-dollar investment, that “generally exponential” increase would have seemed to dawdle along for the first eighty or ninety percent of its history, before accelerating dramatically toward the end of the Pleistocene. This initial dawdle has given rise to the conventional view that the first two million years of hominid tool-making were characterized by what Carl Swisher and his co-authors refer to in their Java Man as a “mind-numbing lack of innovation.” It has also led many paleontologists to conclude that what they regard as “advanced” abilities of our species, such as the use of language, the creation of art, and the hunting of big game, were all acquired very recently in a “Great Leap Forward” or “Human Revolution” which took place less than 50,000 years ago.

If you imagine, though, that our one-dollar investment produced nothing of value in the first seventy or eighty years of its existence – that it was characterized by a “mind-numbing” lack of growth during that time – then you haven’t grasped the nature of exponential increase. After fifty years, that one-dollar investment will have earned one thousand dollars. That’s only a one-thousandth of the million dollars it would earn after a century, but it’s also a thousand times more than the starting amount. The inventive capacity of Homo erectus had reached a comparable point around 1.5 million years ago: its products were still very crude compared to the devices and processes which would make H. sapiens a world-conqueror toward the end of the Pleistocene, but they had already conferred on their inventors a degree of power which was overwhelming in the naïve world of the early Pleistocene. Another million and a half years would have to go by before members of our family would become able to make the warm clothes and footwear that would allow them to penetrate Northern Eurasia and go from there to the New World, but cultural evolution had, by the time the Acheulian revolution was taking place, already begun to outpace its genetic progenitor, “surprising” an ecosystem whose other members were still exclusively reliant on genetic evolution, and overwelming many of them in the “ontogenetic ambushes” that we talked about in Chapter 11.

Fire-use alone must have added enormously to the ecological power of its discoverers. Fire could repel predators, and/or reveal their presence at night. It must also have been used to drive prey animals, and, in some circumstances, to kill them. Through its ability to neutralize bacteria and toxins, and to release nutrients, hominid-controlled fire would, in addition, have caused what Jonathan Kingdon calls “a vast extension in the food base.” This would probably have caused an increase in the population of erectus, which would, in turn, have increased the impact of its other ontogenetic innovations.

Despite its immense importance, fire-use was, however, only one manifestation of the mental illumination which was allowing erectus to increase its ecological power so dramatically in the early Pleistocene. It seems probable, for instance, that this species was, by that time, also exchanging and refining ideas through the use of language.

Evidence for the latter proposition – which I reviewed briefly in Chapters 9 and 11 – includes the possibility that a brain structure comparable in achitecture and function to Broca’s area was present in Leakey’s KNMR 1470 find; the anatomical evidence that hominid brains might have become more-or-less strongly lateralized by the early Pleistocene; the archeological evidence of right-handedness which lends support to the latter proposition; and the apparent descent of the larynx evidenced in several Homo erectus skulls. In Chapter 7 of his 1994 Origin of Humankind, Richard Leakey concludes from these indications that the earliest members of the genus Homo were already language-users. But language-use didn’t arise abruptly – either 30,000 years ago, or with the advent, in the early Pleistocene, of what we’ve arbitrarily defined as the genus Homo. Both Steven Pinker’s 1994 Language Instinct and Terrence Deacon’s 1998 The Symbolic Species – The co-evolution of language and the brain, provide support for Raymond Dart’s 1925 thesis that Australopithecus had, back in the Pliocene, already “laid down the foundations of that discriminate knowledge of the appearance, feeling and sound of things that was a necessary milestone in the acquisition of articulate speech.”

 

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We can imagine, therefore, that instructions, warnings, and encouragement would have been shouted back and forth as a group of early-Pleistocene erectus closed in on a Deinotherium (or, indeed, a Loxodonta) with their tool-sharpened wooden spears, driving it, perhaps, toward a concealed ditch which they had dug with their big Acheulian picks. If we could somehow transport a herd of present-day Loxodonta or Elephas back into the early Pleistocene, its members would probably turn on those erectus attackers, kill one to two of them, and scatter the survivors like chaff. As we’ve seen, however, the high levels of comprehension, social cohesion, and instinctive aggression toward hominids which would enable them to do so, would not have existed in the early Pleistocene.

Early-Pleistocene elephant species would obviously have had a more varied and effective set of behavioral defenses against predators than the giant tortoises we talked about in Chapter 11, but they must, in comparison with their modern-day counterparts, have relied more heavily on their size, and on the thickness of their outer “walls,” than on behavioral flexibility, to repel predators. The machairodont or sabertooth cats had evolved “siege engines” – powerful forequarters and necks, and elongated upper canines – to breach the castle-like fortifications of these and other megaherbivores. Regardless of the danger that this equipment would have posed to individual megaherbivores – especially immature and older ones – it did not threaten any of the species against which it was directed with extermination. The relatively sudden acceleration in human ingenuity which took place in the early Pleistocene did, however, pose a threat of that kind. Just as gunpowder rendered castles obsolete in the early middle ages, our family’s rapidly growing ability to invent and improvise had a fatal impact on species whose defense strategies were focused too exclusively on large size and a fortified exterior. Most of Africa’s megaherbivores disappeared, as we’ve seen, around 1.4 million years ago, together with the machairodont cats and giant hyenas which were dependant on them.

 

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We discussed, in Chapter 1, the counterintuitive truth that vulnerability to human-caused extinction increases with size. The fact that the great majority of the twenty-odd proboscidean or elephant-like species that were in existence at the beginning of the Pleistocene have become extinct should not, therefore, be a surprising one. It’s surprising, on the contrary, that two of those species, Loxodonta africana and Elephas maximus, have survived into the present. Their survival tells us that the Acheulian “avalanche” which overwhelmed Africa’s other proboscideans was moving slowly enough that phylogenetic evolution managed, in the cases of those two species, to stay ahead of it.

By the time Loxodonta and Elephas were subjected to the relatively fast surge in our species’ power which took place in the late Pleistocene – the surge which killed off all the proboscidean species that inhabited Northern Eurasia and the New World – those two survivors were behaviorally equipped by their early-Pleistocene trials with our family, and by more than a million years of subsequent conflict and co-evolution with that family, to withstand it.

 

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