{"title":"放牧强度对年植被的影响。","authors":"M. Pitt, H. Heady","doi":"10.2307/3897553","DOIUrl":null,"url":null,"abstract":"Pastures grazed by sheep at moderate and 1%, 2-, and 2% times the moderate stocking rate from 1969-1973 were analyzed for relative changes in cover, herbage productivity, and botanical composition. All four pastures were less productive in 1973 than in 1969, but exhibited similar trends in cover and botanical composition regardless of grazing intensity. Only grazing at 2 ‘/z times the moderate stocking rate produced a residual decline in productivity following 1 year of rest from the grazing treatment. However, this decline in productivity was managerially negligible compared to other stocking rates, and would probably disappear within 2-3 years in response to the overriding influence of annual weather, especially precipitation, patterns. Hormay (1944) suggested that moderate stocking rates provided the best grazing technique in the annual type. Old vegetation left on the ground at the end of each grazing season would enhance soil fertility, provide progressively improved range condition, and ultimately promote high livestock weight gains. Grazing either greater or less than this moderate level would produce changes in both total herbage productivity and relative botanical composition. Heady ( 1958) postulated. that grazing occurred first on taller plant species, thereby increasing the relative proportion of shorter plant species. Alternatively, complete elimination of grazing animals encouraged taller annual plants relative to short plant species. Talbot et al. ( 1939), Talbot and Biswell ( 1942), and Jones and Evans (1960) all found that exclusion of grazing animals quickly led to grass dominance, particularly taller species, such as ripgut (Bromus rigidus). Biswell (1956) held the opinion that this increase in ripgut occurred at the expense of true clovers (Trifolium spp.) and bur-clover (Medicago hispida), with plant succession proceeding from forbs to soft chess (Bromus n&is), to wild oats (Avena spp.) to ripgut. Biswell (1956) hypothesized that the impact of grazing on botanical composition in the annual type operated primarily by altering the accumulation of mulch. Heady (1958, 1961) supported Biswell’s hypothesis by demonstrating that mulch exceeding 700 pounds per acre in Northern California encouraged taller grasses such as soft chess and ripgut. With no mulch accumulation small, unpalatable forbs such as goldfields (Bueriu chrysostomu), smooth cat’s ear (Hypochoeris glabra), and owl’s clover (Orthocurpus eriunthus) proliferated. With small amounts of mulch, diminutive, low-forage-value grasses such as little quaking grass (Briza minor) and silver hairgrass (Aira caryophylfea) abounded. Annual fescues (Festuca spp.) Authors are assistant professor of’ range ecology. University of British Columbia, Department of Piant Science, Vancouver, Canada V6T IW5; and professor of range management, University of California, Berkeley 94720. Manuscript received February 10, 1979. and nitgrass (Gastridium ventricosum) peaked in percent botanical composition with intermediate amounts of mulch, while filaree (Erodiurn spp.) was not significantly influenced by varying amounts of mulch. The amount of mulch present during germination exerts a major influence on total herbage productivity as well as botanican1 composition. Hooper and Heady (1970), at the Hopland Field Station in Northern California, discovered that removing all mulch prior to germination drastically reduced subsequent forage production compared to sites where mulch was not removed. Importantly, a single manipulation stimulated this response, and a moderate amount of mulch produced maximum herbage productivity. Although mulch influences botanical composition and herbage productivity of the annual type within a particular growing season, these differences are temporary and tend to persist only so long as the grazing and/or clipping treatments are maintained. At the San Joaquin Experimental Range, both Talbot and Biswell (1942) and Bentley and Talbot (1951) noted no pronounced, long-term effects in total yield as a result of grazing at both light and heavy stocking rates. However, these results cannot be readily applied to other areas in the annual type where forage production potentials are confounded by local seasonal variability and/or microsite differences (Biswell 1956; Heady 196 1; Smith 1970). Rossiter (1966) concluded that such microsite variabilities accounted for the lack of quantitative data describing the long-term impact of stocking rates on productivity and botanical composition throughout much of the annual type. This paper provides data describing the residual impact of gmzing on annual vegetation occurring in the coastal mountain ranges of Northern California. Location and Methods of Study The study was conducted at the Hopland Field Station located in Mendocino County in the central portion of the coast mountain ranges. The climate of the area is subhumid to humid mesothermal. The winters are mild with occasional frost in valley bottoms, and infrequent, light snow at higher elevations. The average annual rainfall is 89 cm with virtually no rain falling between June and September. Fog occurs frequently in valley bottoms during late fall, winter, and early spring, and occasionally during the summer. Average summer and fall temperatures range from 20-25°C (Pitt 1975). The pastures used in this study were initially fenced in 1953 to investigate the impact of continuous versus rotational grazing on both animal performance and vegetational response (Pitt 1975). Beginning in 196 1, these pastures enclosing approximately 11 ha each were calibrated to equalize grazing intensity. Equal grazing intensity among pastures Sl, S2, S3, and S7 occurred when: (1) lamb weights at 120 JOURNAL OF RANGE MANAGEMENT32(2), March 1979 days were similar in all pastures, and (2) equal ewe weight loss at the end of the dry period occurred in all pastures. The following grazing treatments existed in the summer of 1962: S 1, S3, and S7 contained 13 sheep, while S2 supported 20 sheep. These pastures operated on a yearlong basis throughout the calibration period during which time numbers of animals were adjusted in each pasture to obtain as near equal gains and losses as possible per individual among all pastures. This grazing intensity was on the heavy side of stocking so that animals were under stress and their weights reflected pasture effects rather than effects due to inherent properties of individual animals. The number of sheep in each pasture at the end of the calibration period in the summer of 1964 constituted a standard stocking intensity for all future experiments. The study investigating effects of different grazing intensities on annual vegetation began in the 1968-1969 grazing season. The calibrated stocking rate continued in pasture S3, while 1X-, 2-, and 2’/2-times the previous calibrated stocking rates were introduced into pastures S 1, S7, and S2, respectively. All pastures were grazed on a continuous yearlong basis with the same animals, insofar as possible. Vegetation was sampled twice each year: once at the beginning of the growing season in the fall of each year, and again at the end of the growing season in June. Each pasture contained 24 sampling locations consisting of a 1 -m diameter wire mesh exclosure and an outside stake. Each exclosure occurred in a homogeneous sampling unit approximately 8 m in diameter. Exclosure and associated outside stakes were moved prior to each fall sampling date to a different but vegetationally similar spot within this sampling unit. Changes noted in botanical composition or herbage productivity throughout the course of the study were therefore not the result of repeated sampling of the same location. Herbage productivity of each pasture was estimated by clipping a square plot 0.099 m” in size (1 ft’) to ground level at each sampling location, while botanical composition, cover, and height of annual vegetation were estimated with 30 points taken with a IO-point frame. All of these parameters, both inside and outside the exclosures, were estimated at the June sampling date, while only outside herbage productivity was measured at the fall sampling date. Vegetational Responses Tables 1,2,3, and 4 summarize data collected in pastures S3, Sl , S7, and S2, respectively. Only those values for ungrazed June vegetation are listed. Vegetational parameters measured in June, the end of the growing season, characterize the yearly response of annual vegetation to each associated animal stocking rate. Measurements in ungrazed vegetation characterize the carryover effect of stocking rate from one year to the next. Since the cages are moved each year, ungrazed vegetation reflects the residual impact of stocking rate 1 year following removal of gxazing. Alternatively, measurements in grazed vegetation primarily reflect vegetational variability within a single growing or grazmg season and may not indicate the impact of stocking rate over time. Ungrazed June vegetation in 1969 represents baseline values and not the result of any stocking rate treatments. Ungrazed June vegetation in 1973 represents values resulting from 4 years of stocking rate treatment followed by 1 year of rest. Table 5 summarizes results from a two-way analysis of variance analyzing the impacts of stocking rate and yearly variability on herbage productivity, cover, and botanical composition. Ungrazed June vegetation in 1969 was not subjected to any grazing treatment. Therefore, only 4 years of data, ungrazed June vegetation for the years 1970 through 1973 inclusive, were used in this analysis. Many researchers have described the dramatic impact of yearly weather patterns on annual vegetation (Talbot et al. 1939; Bentley and Talbot 195 1; Heady 1956; Heady 1958; Naveh 1967; McNaughton 1968; Hooper and Heady 1970; Murphy 1970; Duncan and Woodmansee 1975; Pitt 1975). These studies all indicate that observed trends in standing crop, cover, and botanical composition in","PeriodicalId":16918,"journal":{"name":"Journal of Range Management","volume":"12 1","pages":"109-114"},"PeriodicalIF":0.0000,"publicationDate":"1979-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"18","resultStr":"{\"title\":\"The effects of grazing intensity on annual vegetation.\",\"authors\":\"M. Pitt, H. Heady\",\"doi\":\"10.2307/3897553\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Pastures grazed by sheep at moderate and 1%, 2-, and 2% times the moderate stocking rate from 1969-1973 were analyzed for relative changes in cover, herbage productivity, and botanical composition. All four pastures were less productive in 1973 than in 1969, but exhibited similar trends in cover and botanical composition regardless of grazing intensity. Only grazing at 2 ‘/z times the moderate stocking rate produced a residual decline in productivity following 1 year of rest from the grazing treatment. However, this decline in productivity was managerially negligible compared to other stocking rates, and would probably disappear within 2-3 years in response to the overriding influence of annual weather, especially precipitation, patterns. Hormay (1944) suggested that moderate stocking rates provided the best grazing technique in the annual type. Old vegetation left on the ground at the end of each grazing season would enhance soil fertility, provide progressively improved range condition, and ultimately promote high livestock weight gains. Grazing either greater or less than this moderate level would produce changes in both total herbage productivity and relative botanical composition. Heady ( 1958) postulated. that grazing occurred first on taller plant species, thereby increasing the relative proportion of shorter plant species. Alternatively, complete elimination of grazing animals encouraged taller annual plants relative to short plant species. Talbot et al. ( 1939), Talbot and Biswell ( 1942), and Jones and Evans (1960) all found that exclusion of grazing animals quickly led to grass dominance, particularly taller species, such as ripgut (Bromus rigidus). Biswell (1956) held the opinion that this increase in ripgut occurred at the expense of true clovers (Trifolium spp.) and bur-clover (Medicago hispida), with plant succession proceeding from forbs to soft chess (Bromus n&is), to wild oats (Avena spp.) to ripgut. Biswell (1956) hypothesized that the impact of grazing on botanical composition in the annual type operated primarily by altering the accumulation of mulch. Heady (1958, 1961) supported Biswell’s hypothesis by demonstrating that mulch exceeding 700 pounds per acre in Northern California encouraged taller grasses such as soft chess and ripgut. With no mulch accumulation small, unpalatable forbs such as goldfields (Bueriu chrysostomu), smooth cat’s ear (Hypochoeris glabra), and owl’s clover (Orthocurpus eriunthus) proliferated. With small amounts of mulch, diminutive, low-forage-value grasses such as little quaking grass (Briza minor) and silver hairgrass (Aira caryophylfea) abounded. Annual fescues (Festuca spp.) Authors are assistant professor of’ range ecology. University of British Columbia, Department of Piant Science, Vancouver, Canada V6T IW5; and professor of range management, University of California, Berkeley 94720. Manuscript received February 10, 1979. and nitgrass (Gastridium ventricosum) peaked in percent botanical composition with intermediate amounts of mulch, while filaree (Erodiurn spp.) was not significantly influenced by varying amounts of mulch. The amount of mulch present during germination exerts a major influence on total herbage productivity as well as botanican1 composition. Hooper and Heady (1970), at the Hopland Field Station in Northern California, discovered that removing all mulch prior to germination drastically reduced subsequent forage production compared to sites where mulch was not removed. Importantly, a single manipulation stimulated this response, and a moderate amount of mulch produced maximum herbage productivity. Although mulch influences botanical composition and herbage productivity of the annual type within a particular growing season, these differences are temporary and tend to persist only so long as the grazing and/or clipping treatments are maintained. At the San Joaquin Experimental Range, both Talbot and Biswell (1942) and Bentley and Talbot (1951) noted no pronounced, long-term effects in total yield as a result of grazing at both light and heavy stocking rates. However, these results cannot be readily applied to other areas in the annual type where forage production potentials are confounded by local seasonal variability and/or microsite differences (Biswell 1956; Heady 196 1; Smith 1970). Rossiter (1966) concluded that such microsite variabilities accounted for the lack of quantitative data describing the long-term impact of stocking rates on productivity and botanical composition throughout much of the annual type. This paper provides data describing the residual impact of gmzing on annual vegetation occurring in the coastal mountain ranges of Northern California. Location and Methods of Study The study was conducted at the Hopland Field Station located in Mendocino County in the central portion of the coast mountain ranges. The climate of the area is subhumid to humid mesothermal. The winters are mild with occasional frost in valley bottoms, and infrequent, light snow at higher elevations. The average annual rainfall is 89 cm with virtually no rain falling between June and September. Fog occurs frequently in valley bottoms during late fall, winter, and early spring, and occasionally during the summer. Average summer and fall temperatures range from 20-25°C (Pitt 1975). The pastures used in this study were initially fenced in 1953 to investigate the impact of continuous versus rotational grazing on both animal performance and vegetational response (Pitt 1975). Beginning in 196 1, these pastures enclosing approximately 11 ha each were calibrated to equalize grazing intensity. Equal grazing intensity among pastures Sl, S2, S3, and S7 occurred when: (1) lamb weights at 120 JOURNAL OF RANGE MANAGEMENT32(2), March 1979 days were similar in all pastures, and (2) equal ewe weight loss at the end of the dry period occurred in all pastures. The following grazing treatments existed in the summer of 1962: S 1, S3, and S7 contained 13 sheep, while S2 supported 20 sheep. These pastures operated on a yearlong basis throughout the calibration period during which time numbers of animals were adjusted in each pasture to obtain as near equal gains and losses as possible per individual among all pastures. This grazing intensity was on the heavy side of stocking so that animals were under stress and their weights reflected pasture effects rather than effects due to inherent properties of individual animals. The number of sheep in each pasture at the end of the calibration period in the summer of 1964 constituted a standard stocking intensity for all future experiments. The study investigating effects of different grazing intensities on annual vegetation began in the 1968-1969 grazing season. The calibrated stocking rate continued in pasture S3, while 1X-, 2-, and 2’/2-times the previous calibrated stocking rates were introduced into pastures S 1, S7, and S2, respectively. All pastures were grazed on a continuous yearlong basis with the same animals, insofar as possible. Vegetation was sampled twice each year: once at the beginning of the growing season in the fall of each year, and again at the end of the growing season in June. Each pasture contained 24 sampling locations consisting of a 1 -m diameter wire mesh exclosure and an outside stake. Each exclosure occurred in a homogeneous sampling unit approximately 8 m in diameter. Exclosure and associated outside stakes were moved prior to each fall sampling date to a different but vegetationally similar spot within this sampling unit. Changes noted in botanical composition or herbage productivity throughout the course of the study were therefore not the result of repeated sampling of the same location. Herbage productivity of each pasture was estimated by clipping a square plot 0.099 m” in size (1 ft’) to ground level at each sampling location, while botanical composition, cover, and height of annual vegetation were estimated with 30 points taken with a IO-point frame. All of these parameters, both inside and outside the exclosures, were estimated at the June sampling date, while only outside herbage productivity was measured at the fall sampling date. Vegetational Responses Tables 1,2,3, and 4 summarize data collected in pastures S3, Sl , S7, and S2, respectively. Only those values for ungrazed June vegetation are listed. Vegetational parameters measured in June, the end of the growing season, characterize the yearly response of annual vegetation to each associated animal stocking rate. Measurements in ungrazed vegetation characterize the carryover effect of stocking rate from one year to the next. Since the cages are moved each year, ungrazed vegetation reflects the residual impact of stocking rate 1 year following removal of gxazing. Alternatively, measurements in grazed vegetation primarily reflect vegetational variability within a single growing or grazmg season and may not indicate the impact of stocking rate over time. Ungrazed June vegetation in 1969 represents baseline values and not the result of any stocking rate treatments. Ungrazed June vegetation in 1973 represents values resulting from 4 years of stocking rate treatment followed by 1 year of rest. Table 5 summarizes results from a two-way analysis of variance analyzing the impacts of stocking rate and yearly variability on herbage productivity, cover, and botanical composition. Ungrazed June vegetation in 1969 was not subjected to any grazing treatment. Therefore, only 4 years of data, ungrazed June vegetation for the years 1970 through 1973 inclusive, were used in this analysis. Many researchers have described the dramatic impact of yearly weather patterns on annual vegetation (Talbot et al. 1939; Bentley and Talbot 195 1; Heady 1956; Heady 1958; Naveh 1967; McNaughton 1968; Hooper and Heady 1970; Murphy 1970; Duncan and Woodmansee 1975; Pitt 1975). These studies all indicate that observed trends in standing crop, cover, and botanical composition in\",\"PeriodicalId\":16918,\"journal\":{\"name\":\"Journal of Range Management\",\"volume\":\"12 1\",\"pages\":\"109-114\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1979-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"18\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Range Management\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2307/3897553\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Range Management","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2307/3897553","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 18
摘要
分析了1969 ~ 1973年在中等、1%、2%和2%的中等载畜率下,绵羊放牧草场的覆盖度、牧草生产力和植物组成的相对变化。所有四个牧场在1973年的产量都低于1969年,但在覆盖和植物组成方面表现出相似的趋势,而与放牧强度无关。在休养1年后,只有以2’/z倍的适度载畜率放牧才会产生剩余的生产力下降。然而,与其他放养率相比,这种生产力的下降在管理上可以忽略不计,并且可能在2-3年内由于年度天气,特别是降水模式的主要影响而消失。Hormay(1944)认为,在一年生类型中,适度的载畜率提供了最佳的放牧技术。在每个放牧季节结束时留在地面上的旧植被可以提高土壤肥力,逐步改善牧场条件,最终促进牲畜增重。高于或低于这一中等水平的放牧都会引起牧草总产量和相对植物组成的变化。Heady(1958)假设。这种放牧首先发生在较高的植物物种上,从而增加了较矮植物物种的相对比例。另一种方法是,完全消除食草动物会鼓励较高的一年生植物相对于较矮的植物种类。Talbot et al.(1939)、Talbot and Biswell(1942)以及Jones and Evans(1960)都发现,排除放牧动物会迅速导致草类占优势,尤其是体型较高的物种,如rigut (Bromus rigidus)。Biswell(1956)认为,ripgut的增加是以牺牲真三叶草(Trifolium spp.)和刺三叶草(Medicago hispida .)为代价的,植物演替过程是从草本植物到软苜蓿(Bromus n&is),再到野生燕麦(Avena spp.)再到ripgut。Biswell(1956)假设放牧对一年生类型植物组成的影响主要是通过改变地膜的积累来实现的。Heady(1958, 1961)支持Biswell的假设,他证明,在北加州,每英亩超过700磅的地膜会促进草的生长,如软象棋和ripgut。在没有地膜积累的情况下,像金地(Bueriu chrysostomu)、光滑的猫耳(Hypochoeris glabra)和猫头鹰的三叶草(Orthocurpus eriunthus)这样的小而难吃的植物大量繁殖。在少量覆盖物的覆盖下,大量生长着小的、低饲料价值的草,如小摇草(Briza minor)和银毛草(Aira caryophylfea)。一年生羊茅(Festuca spp.)作者为“牧场生态学”助理教授。英属哥伦比亚大学植物科学系,加拿大温哥华V6T IW5;加州大学伯克利分校(94720)牧场管理教授。1979年2月10日收稿。在中等覆盖量下,氮草(Gastridium osum)的植物组成百分比最高,而丝草(Erodiurn spp)受不同覆盖量的影响不显著。发芽期间覆盖的数量对牧草总产量和植物成分构成有重要影响。Hooper和Heady(1970)在北加州的Hopland Field Station发现,与未去除地膜的地方相比,在发芽前去除所有地膜大大减少了随后的饲料产量。重要的是,一个单一的操作刺激了这种反应,适度的覆盖产生了最大的牧草生产力。虽然覆盖物在一个特定的生长季节影响一年生类型的植物组成和牧草生产力,但这些差异是暂时的,只有在放牧和/或修剪处理保持不变的情况下才会持续存在。在圣华金实验牧场,Talbot和Biswell(1942年)以及Bentley和Talbot(1951年)都注意到,无论是轻放养率还是重放养率,放牧对总产量都没有明显的长期影响。然而,这些结果不能轻易应用于其他地区的一年生类型,在这些地区,饲料生产潜力受到当地季节变化和/或微型场地差异的影响(Biswell 1956;海蒂196;史密斯1970年)。Rossiter(1966)的结论是,这种微站点的变化是缺乏描述载畜率对生产力和植物组成的长期影响的定量数据的原因。本文提供了描述在北加州沿海山脉发生的gmzing对年植被的残余影响的数据。研究地点和方法该研究在位于海岸山脉中部门多西诺县的霍普兰野外研究站进行。该地区气候属半湿润至湿润中温气候。 这些研究都表明,观察到的趋势,直立作物,覆盖和植物组成
The effects of grazing intensity on annual vegetation.
Pastures grazed by sheep at moderate and 1%, 2-, and 2% times the moderate stocking rate from 1969-1973 were analyzed for relative changes in cover, herbage productivity, and botanical composition. All four pastures were less productive in 1973 than in 1969, but exhibited similar trends in cover and botanical composition regardless of grazing intensity. Only grazing at 2 ‘/z times the moderate stocking rate produced a residual decline in productivity following 1 year of rest from the grazing treatment. However, this decline in productivity was managerially negligible compared to other stocking rates, and would probably disappear within 2-3 years in response to the overriding influence of annual weather, especially precipitation, patterns. Hormay (1944) suggested that moderate stocking rates provided the best grazing technique in the annual type. Old vegetation left on the ground at the end of each grazing season would enhance soil fertility, provide progressively improved range condition, and ultimately promote high livestock weight gains. Grazing either greater or less than this moderate level would produce changes in both total herbage productivity and relative botanical composition. Heady ( 1958) postulated. that grazing occurred first on taller plant species, thereby increasing the relative proportion of shorter plant species. Alternatively, complete elimination of grazing animals encouraged taller annual plants relative to short plant species. Talbot et al. ( 1939), Talbot and Biswell ( 1942), and Jones and Evans (1960) all found that exclusion of grazing animals quickly led to grass dominance, particularly taller species, such as ripgut (Bromus rigidus). Biswell (1956) held the opinion that this increase in ripgut occurred at the expense of true clovers (Trifolium spp.) and bur-clover (Medicago hispida), with plant succession proceeding from forbs to soft chess (Bromus n&is), to wild oats (Avena spp.) to ripgut. Biswell (1956) hypothesized that the impact of grazing on botanical composition in the annual type operated primarily by altering the accumulation of mulch. Heady (1958, 1961) supported Biswell’s hypothesis by demonstrating that mulch exceeding 700 pounds per acre in Northern California encouraged taller grasses such as soft chess and ripgut. With no mulch accumulation small, unpalatable forbs such as goldfields (Bueriu chrysostomu), smooth cat’s ear (Hypochoeris glabra), and owl’s clover (Orthocurpus eriunthus) proliferated. With small amounts of mulch, diminutive, low-forage-value grasses such as little quaking grass (Briza minor) and silver hairgrass (Aira caryophylfea) abounded. Annual fescues (Festuca spp.) Authors are assistant professor of’ range ecology. University of British Columbia, Department of Piant Science, Vancouver, Canada V6T IW5; and professor of range management, University of California, Berkeley 94720. Manuscript received February 10, 1979. and nitgrass (Gastridium ventricosum) peaked in percent botanical composition with intermediate amounts of mulch, while filaree (Erodiurn spp.) was not significantly influenced by varying amounts of mulch. The amount of mulch present during germination exerts a major influence on total herbage productivity as well as botanican1 composition. Hooper and Heady (1970), at the Hopland Field Station in Northern California, discovered that removing all mulch prior to germination drastically reduced subsequent forage production compared to sites where mulch was not removed. Importantly, a single manipulation stimulated this response, and a moderate amount of mulch produced maximum herbage productivity. Although mulch influences botanical composition and herbage productivity of the annual type within a particular growing season, these differences are temporary and tend to persist only so long as the grazing and/or clipping treatments are maintained. At the San Joaquin Experimental Range, both Talbot and Biswell (1942) and Bentley and Talbot (1951) noted no pronounced, long-term effects in total yield as a result of grazing at both light and heavy stocking rates. However, these results cannot be readily applied to other areas in the annual type where forage production potentials are confounded by local seasonal variability and/or microsite differences (Biswell 1956; Heady 196 1; Smith 1970). Rossiter (1966) concluded that such microsite variabilities accounted for the lack of quantitative data describing the long-term impact of stocking rates on productivity and botanical composition throughout much of the annual type. This paper provides data describing the residual impact of gmzing on annual vegetation occurring in the coastal mountain ranges of Northern California. Location and Methods of Study The study was conducted at the Hopland Field Station located in Mendocino County in the central portion of the coast mountain ranges. The climate of the area is subhumid to humid mesothermal. The winters are mild with occasional frost in valley bottoms, and infrequent, light snow at higher elevations. The average annual rainfall is 89 cm with virtually no rain falling between June and September. Fog occurs frequently in valley bottoms during late fall, winter, and early spring, and occasionally during the summer. Average summer and fall temperatures range from 20-25°C (Pitt 1975). The pastures used in this study were initially fenced in 1953 to investigate the impact of continuous versus rotational grazing on both animal performance and vegetational response (Pitt 1975). Beginning in 196 1, these pastures enclosing approximately 11 ha each were calibrated to equalize grazing intensity. Equal grazing intensity among pastures Sl, S2, S3, and S7 occurred when: (1) lamb weights at 120 JOURNAL OF RANGE MANAGEMENT32(2), March 1979 days were similar in all pastures, and (2) equal ewe weight loss at the end of the dry period occurred in all pastures. The following grazing treatments existed in the summer of 1962: S 1, S3, and S7 contained 13 sheep, while S2 supported 20 sheep. These pastures operated on a yearlong basis throughout the calibration period during which time numbers of animals were adjusted in each pasture to obtain as near equal gains and losses as possible per individual among all pastures. This grazing intensity was on the heavy side of stocking so that animals were under stress and their weights reflected pasture effects rather than effects due to inherent properties of individual animals. The number of sheep in each pasture at the end of the calibration period in the summer of 1964 constituted a standard stocking intensity for all future experiments. The study investigating effects of different grazing intensities on annual vegetation began in the 1968-1969 grazing season. The calibrated stocking rate continued in pasture S3, while 1X-, 2-, and 2’/2-times the previous calibrated stocking rates were introduced into pastures S 1, S7, and S2, respectively. All pastures were grazed on a continuous yearlong basis with the same animals, insofar as possible. Vegetation was sampled twice each year: once at the beginning of the growing season in the fall of each year, and again at the end of the growing season in June. Each pasture contained 24 sampling locations consisting of a 1 -m diameter wire mesh exclosure and an outside stake. Each exclosure occurred in a homogeneous sampling unit approximately 8 m in diameter. Exclosure and associated outside stakes were moved prior to each fall sampling date to a different but vegetationally similar spot within this sampling unit. Changes noted in botanical composition or herbage productivity throughout the course of the study were therefore not the result of repeated sampling of the same location. Herbage productivity of each pasture was estimated by clipping a square plot 0.099 m” in size (1 ft’) to ground level at each sampling location, while botanical composition, cover, and height of annual vegetation were estimated with 30 points taken with a IO-point frame. All of these parameters, both inside and outside the exclosures, were estimated at the June sampling date, while only outside herbage productivity was measured at the fall sampling date. Vegetational Responses Tables 1,2,3, and 4 summarize data collected in pastures S3, Sl , S7, and S2, respectively. Only those values for ungrazed June vegetation are listed. Vegetational parameters measured in June, the end of the growing season, characterize the yearly response of annual vegetation to each associated animal stocking rate. Measurements in ungrazed vegetation characterize the carryover effect of stocking rate from one year to the next. Since the cages are moved each year, ungrazed vegetation reflects the residual impact of stocking rate 1 year following removal of gxazing. Alternatively, measurements in grazed vegetation primarily reflect vegetational variability within a single growing or grazmg season and may not indicate the impact of stocking rate over time. Ungrazed June vegetation in 1969 represents baseline values and not the result of any stocking rate treatments. Ungrazed June vegetation in 1973 represents values resulting from 4 years of stocking rate treatment followed by 1 year of rest. Table 5 summarizes results from a two-way analysis of variance analyzing the impacts of stocking rate and yearly variability on herbage productivity, cover, and botanical composition. Ungrazed June vegetation in 1969 was not subjected to any grazing treatment. Therefore, only 4 years of data, ungrazed June vegetation for the years 1970 through 1973 inclusive, were used in this analysis. Many researchers have described the dramatic impact of yearly weather patterns on annual vegetation (Talbot et al. 1939; Bentley and Talbot 195 1; Heady 1956; Heady 1958; Naveh 1967; McNaughton 1968; Hooper and Heady 1970; Murphy 1970; Duncan and Woodmansee 1975; Pitt 1975). These studies all indicate that observed trends in standing crop, cover, and botanical composition in