民族与时尚:清代的鹿肉消费及其特征

鹿在满人生活中占有重要地位,鹿肉是满人消费的重要对象。清代官方记载食用鹿肉的来源主要有三:东三省进贡、木兰围场和新疆进贡。通过鹿肉赏赐,汉人品尝到具有满族特色的食品,并对鹿肉的美味津津乐道。京城旗人消费鹿肉,皇帝赏赐官员鹿肉,显示了清代鹿肉消费的民族特色。鹿肉产量较少,故鹿肉的赏赐形成了制度。鹿肉价格较贵,对鹿肉的消费始终被限制在一定的阶层范围内。     

经济行为与环境变化:清前期台湾野生鹿消失探析

鹿曾经是台湾数量最庞大的野生动物群之一。明末以来,随着台湾贸易交流的活跃,鹿成为大宗出口商品,土著居民由原先捕鹿作为民生用品逐渐发展至为市场服务;清前期大陆移民入台的农业垦殖又破坏了鹿原有的生态环境。人类经济行为引发的环境变化,最终导致了野生鹿在台湾渐趋消失。     

Changes in the size and shape of fallow deer—evidence for the movement and management of a species

The European fallow deer (Dama dama dama) is native to the eastern Mediterranean and whilst it is clear that its dispersion from this region was the result of human transportation, the timing and circumstances of its post‐glacial diffusion are still uncertain. Archaeological fallow deer remains offer perhaps the best opportunity to understand the deep history of the species, with measurements of ancient bones providing important information about an individual's sex and size. Unfortunately, the fragmentary nature of archaeological remains means that metrical samples are usually too small to draw any meaningful conclusions. Biometrical scaling techniques can increase the size of the sample available for comparison and in this paper log ratios are used in combination with traditional metrical analysis to provide new information about archaeological fallow deer populations, in particular highlighting the size variations across time and space and shifts in hunting and management practices. Copyright © 2011 John Wiley & Sons, Ltd.     

Prehistoric hunting pressure estimated by the age composition of excavated sika deer (Cervus Nippon) using the annual layer of tooth cement

Age of excavated sika deer was determined not only by the cement-annuli method but also by the observation method to avoid unnecessary destruction of archaeological materials. The observation method is based on tooth replacement, wear index and the appearance of cervical lines on the molar teeth. Stepwise discriminant analysis was used to establish a criterion for the age determination of excavated mandibles. Then the annulation method was carried out for well-preserved specimens older than 3–5 years. The age composition of excavated deer mandibles seems to have changed through the Jomon Period. Age composition at the Torihama sites (the Early Jomon Period) was characterized by an abundance of aged individuals, showing a close similarity with that of the recent deer population under protected conditions. Deer from the Kidosaku and Yahagi sites (the Late Jomon Period) and the SambuUbayama site (the Latest Jomon Period) were composed mainly of deer younger than 5 years, which seems to correspond to that of the recent hunted population living under natural conditions in Hokkaido. These data suggest that the hunting pressure increased during the Late and Latest Jomon Periods and compares with the pressures on recent hunted populations of sika deer.     

Analysis of faunal remains from the Kretuonas lake settlement

The Middle (Kretuonas 1B), Late Neolithic (Zemaitiške 1 and Zemaitiške 2) and Old Bronze Age (Kretuonas 1C) settlements near Kretuonas Lake (Svencioneliai district, Reskutenai village) yielded many artefacts of bone, antler, horn and teeth (750 in total). In the Kretuonas 1B assemblage, deer bones accounted for 50.5 per cent, elk bones 19.7 per cent and boar bones for 27.7 per cent of the total. In the Zemaitiške 1 and 2 settlements the respective portions were 27.7 and 62.0 per cent deer, 6.8 and 20.0 per cent elk and 10.1 per cent boar. In Kretuonas 1C the proportions were 10.9, 36.0 and 7.5 per cent respectively. In the Kretuonas 1B settlement 32 artefacts were identified, 16 from deer bone, four from elk and four from boar. In the Zemaitiške 2 settlement there were 114 artefacts of which 57 were identified to species. Of these, 39 were from deer, eight from elk and four from boar. Finally, in the Kretuonas 1C settlement, of the 531 artefacts found, 120 were identified to species and of these 49 were from deer, 44 from elk, nine from boar and nine from bear.     

Estimation of age at death of sika deer (Cervus nippon) from an archaeological site based on radiographs of mandibular molariform tooth development

The development of permanent premolar and molar teeth was examined in mandibular radiographs from wild sika deer (Cervus nippon) of known ages (74 males, 66 females, 4 unknown; age range 1–54 months) from Hyogo Prefecture. Tooth development was scored according to the method described by Brown & Chapman (1991a, b). Stage‐specific scores for all molar and premolar teeth were summed, and simple cubic regression analysis was used to analyse the relationship between the total score and age in months. Our analysis showed a strong cubic correlation between the total score and chronological age in months. The equation obtained from this analysis was used to estimate age within a 95% prediction interval in seven archaeological specimens from the Asahi archaeological site in central Japan. Copyright © 2010 John Wiley & Sons, Ltd.     

First Introduction and Early Exploitation of the Persian Fallow Deer on Cyprus (8000–6000 cal. bc)

The Persian fallow deer (Dama dama mesopotamica) is currently a threatened species. However, it played an important role in many Late Glacial and Early Holocene human societies in the Near and Middle East. This is especially true of the island of Cyprus, where it was introduced at the beginning of the Neolithic and held a predominant place in human subsistence throughout Cypriot prehistory until the Bronze Age. The earliest levels of the extensive Cypriot Pre‐Pottery Neolithic B site of Shillourokambos, occupied between 8400 and 7000 cal. bc , provided 3036 identified remains of this deer. It was possible to measure or determine the age‐at‐death for 1361 and 1444 remains, respectively. Analyses allow for discussions on when the fallow deer was introduced to the island of Cyprus, its origin and how populations were managed. These studies also lead to the reconstruction of acquisition and butchery techniques, as well as culinary practices, and the morphological evolution of males and females throughout time. The Persian fallow deer was introduced to Cyprus later than suids, dogs, cats, goats and cattle, and at nearly the same time as sheep, towards ca 8000 cal. bc . Despite the absence of any skeletal changes, this introduction may reflect an attempt to domesticate the fallow deer on the nearby continental mainland. However, after being introduced to the island, deer appear to have been released into the wild and hunted. Copyright © 2015 John Wiley & Sons, Ltd.     

The morphological distinction between bones and teeth of fallow deer (Dama dama) and red deer (Cervus elaphus)

Morphological characters for the separation of red and fallow deer remains are described. These encompass antlers, permanent dentition, and postcranial bones. The characters were tested on samples of known red and fallow deer from an array of contexts, thus helping to ensure their validity across different populations. An attempt is made to quantify the reliability of each character, using a simple arithmetic method of scoring and analysing the test data. This forms the basis for a more objective assessment of the identity of an unknown specimen.     

Fork formation and other signs of osteophagia on a long bone swallowed by a red deer stag (Cervus elaphus)

A right anterior cannon bone (os metacarpale 3 + 4) of a red deer that was found in the reticulum of a 7-year-old red deer stag is described. The bone, which had accidentally been swallowed by the stag, showed clear signs of bone chewing (osteophagia), the most prominent being the formation of a fork at its distal end. Knowledge of the possible bone changes brought about by ruminant osteophagia may prevent the erroneous interpretation of skeletal remains as being worked by hominids.     

Refining the Quadratic Crown Height Method of age estimation: do elk teeth wear quadratically with age?

Teeth are the basis for the best methods for estimating the age-at-death of archaeological and paleontological faunal remains, because they change by eruption and wear throughout an individual's life and because they preserve well. However, age-at-death can be difficult to estimate when teeth are isolated or when no known-age reference sample is available. For these reasons, researchers developed the Quadratic Crown Height Method (QCHM), a set of quadratic formulae that can be used to predict age-at-death from tooth crown height, when unworn crown height and the ages when the tooth erupts and when its crown height should reach zero can be estimated. Previous tests of the QCHM suggest that modified equations could improve the method. Here, we use crown height measurements on a sample of 226 known-age Rocky Mountain elk (Cervus elaphus) to perform such modifications. We adjust the age at which each tooth type's crown height reaches zero from the species' potential ecological longevity or average maximum life span to an age that we empirically estimate for each tooth type. We also empirically assess whether for different elk teeth the exponent in the QCHM formula is actually equal to 2; it is for M1, but for P4 it is about 1, indicating a roughly linear relationship. The exponents for M2 and M3 are intermediate, being closer to 1.5. Because different teeth wear at different rates and wear completely away at different ages, we recommend that researchers use the modified equations provided here to estimate age-at-death for samples of Cervus elaphus.