Rose Atoll: an annotated bibliography

K. Rodgers, I. Mcallan, C. Cantrell, Bonnie J. Ponwith
{"title":"Rose Atoll: an annotated bibliography","authors":"K. Rodgers, I. Mcallan, C. Cantrell, Bonnie J. Ponwith","doi":"10.3853/J.1031-8062.9.1993.70","DOIUrl":null,"url":null,"abstract":"Over 290 citations of published monographs, articles from learned journals, periodical features, official reports, letters, notes, some limited circulation andlor unpublished documents, and unofficial reports, concerned with the geology, geography, pedology, biology, meteorology, oceanography and history of Rose Atoll, American Samoa, are indexed and annotated. RODGERS, K.A., I.A.W. MCALLAN, C. CANTRELL & B.J. PONWITH. 1992. Rose Atoll: an annotated bibliography. Technical Reports of the Australian Museum 9: 1-37. Rose Atoll lies at the extreme eastern end of the Samoan island volcanic chain (14'32's 168\"08'W), 240 km east-south-east of Pago Pago Harbor (Fig.1). It is of a roughly square shape. The fringing reef and lagoon together cover just 640 ha making it one of the smallest atolls in the world. The fetch of the lagoon is about 2 km and the maximum depth about 20 m. The coralline algal reef has a uniform, 500 m width and is largely submerged at low tide. A single channel in the north-east, 1.8-15 m deep, links the lagoon to the sea. The atoll is one of the least disturbed areas of the world. Its benthic community is unique in Samoa, being dominated by encrusting coralline algae, and having a relative abundance of soft corals with a comparable impoverishment in hard species (Itano, 1987, cited in United Nations Environment Programme, 1988). The atoll has been established as a National Wildlife Refuge since 5 July 1973, and annual resource surveys are carried out by US Fish and Wildlife Service and American Samoan Government personnel. These include both the lagoon and outer reef as well as the islets, thus affording an invaluable scientific baseline for biological and geological studies of low Pacific islands. Excellent summary reviews of the history and natural history of the atoll are given by Setchell (1924) and Sachet (1954). A highly detailed, up-to-date account of the terrestrial biology is contained in Amerson et al. (1982a,b). 2 Technical Reports of the Australian Museum (1993) Geological and Biological Notes The Samoan Islands are part of a chain of searnounts, shallow banks and drowned atolls which extend 1700 km to the north-west. All are volcanic in origin and lie in a line with the correct orientation to have been generated by the present motion of the Pacific plate over a fixed hot spot (Natland, 1980; Menard, 1986). Both the size of the islands, and the proportion of them covered by Quaternary lava flows, increases to the west, in contrast to the Hawaiian, Society, and Marquesas chains. In these lineaments, submerged volcanic mounds, both drowned and capped by atoll reefs, occur at the western end, but in the Samoan chain Rose Atoll lies to the east. The age of Rose's volcanic substrate is not known, but it could be very young (Natland, 1980 but cf. Menard, 1986). Unlike the seemingly more mature, drowned atolls and flat banks to the west, Rose lacks wide offshore banks. In his studies of the petrology of the Samoan chain, Natland seems to have been unaware that basalt rocks had been reported and recovered from Rose (e.g., Natland, 1980; Natland & Turner, 1985). The nature of these particular rocks, and even their very existence, has been a subject of some confusion in the literature. They were first reported by members of the United States Exploring Expedition (e.g., Couthouy, 1844; Wilkes, 1844; Dana, 1851; Pickering, 1876). Mayor (1921b, 1924b) specifically looked for but failed to find any trace of them and he and Setchell (1924) dismissed the earlier reports as incorrect identifications of weathered limestone. However, Schultz (1940, 1943), located and collected from a dozen basalt boulders lying loose on the reef flat. Sachet (1954) reported that Gilbert Corwin of the US National Museum had identified the samples as olivine basalt. There are only two islets upon the reef (Fig.l,2): Rose Island in the east and Sand Island to the north. Total land area is 7.77 ha. Aggradation and degradation are active around the islets' margins and published descriptions of the atoll indicate that variation has occurred in area, shape and even position of the islets within historic times (e.g., Mayor, 1921b; Setchell, 1924; Bryan, 1938; Schultz, 1943; Amerson et al., 1982a; Ludwig, 1982a; cf. Sachet, 1954: 1-2; and see Figs 1,3acpa-d). Rose displays the dynamic character so typical of low islands in general, and atolls in particular. Perhaps, the small size of the atoll has helped heighten different observers's awareness of its active physical environment. The following descriptions are taken in large part from United Nations Environment Programme (1988) report of Susan Wells. Rose Island is located on the lagoon half of the reef in the windward corner of the atoll square (Fig.1). It is a roughly oval islet about 180 X 200 m, covering 5.18 ha, having a 1.0 km shoreline, and a maximum altitude of 3.0 m (Fig.2). It consists of raised reef rock and a coquina of worn fragments of lithothamnium, Favites, Porites, Symphallia, Pocillopora, Acropora, Tridacna, Fig.1. Sketch map of Rose Atoll, after Amerson et al. (1982a). Insert indicates location of Rose within the Samoan island chain. Rodgers et al.: Rose Atoll, bibliography 3 gastropod shells and echinoderms. A phosphatic soil, rich in humus has developed on the coquina beneath a large grove of Pisonia grandis. Sand Island is a bank of coralgal sand with an 0.5 km shoreline and reaching about 5.2 m above sea level. It covers 2.59 ha and presently lies on the lagoon side of the reef, due east of the lagoon entrance channel, with a broad reef flat extending seawards. It is intermittently vegetated and following Humcane Ofa in February 1990, it was swept clear save for one Messerschmidia tree. It now hosts seedling growth of Boerhavia and Messerschmidia. The lagoon floor has an undulating sandy bottom much of which is covered with algae and small scattered colonies of Acropora. Flat-topped, steep-sided pinnacles jut up from the floor and are encrusted by coralline algae, with both hard and soft corals on the vertical and undercut sides. Descriptions of the reef and the reef flat are given by Mayor (1921b) and Wass (n.d. a,b) which are summarised in United Nations Environment Programme (1988). The upper surface of the reef is a hard, smoothfloored flat, awash at low tide, and covered with vigorous growths of Porolithon that form connected pink patches and ridges up to 15 cm high and 15 cm to a metre or more wide. The inner lagoon edge is covered by coral blocks, the larger of which have flattened tops, also encrusted by coralline algae, and with both algae and soft corals coating their sides. Most of these blocks lie loose on the flat but some are attached by slender pedicels. Mayor (1921b) noted one loose boulder which he estimated weighed 46 tons. He argued (1921b, 1921c, 1924b) that the appearance of these boulders lent support to the rim of the atoll having once been 6 to 8 feet (1.8-2.4 m) higher than at present (cf. Stoddart, 1969). The remainder of the reef flat is rubble-strewn and also heavily encrusted by coralline algae and scattered colonies of Acropora. The basalt boulders, noted earlier, are part of the rubble of the flat. Their apparent comings and goings give further indication of the dynamic nature of the atoll environment. The reef front extends from a depth of 4 m in a series of irregular steep steps to about 50 m depth. The upper portion is dissected by ridges and surge channels. The irregular, high magnesium calcite substrate is encrusted thickly with coralline algae. Corals, including Acropora and Pocillopora, are abundant and diverse but table and staghorn varieties are lacking. No reports of the outer reef have been published at the time of writing. Several authors (e.g., Setchell, 1924; Sachet, 1954) have drawn attention to the number of native vascular plant species found on Rose being restricted to three: Pisonia grandis, Boerhavia tetrandra, and Portulaca lutea which form a small evergreen orthophyll softwood forest. At the time of their intensive survey of the atoll, Amerson et al. (1982a,b) found the number of species had increased to include Messerschmidia argentea, Ipomoea macrantha, and Suriana rnaritima, the latter having anived only very recently. Several attempts have been made to introduce coconut palms Cocos nucifera. The number surviving varies (20 in 1938, 12 in 1953), as do reports of their health (cf. Sachet, 1954:5,16). Fig.2. Aerial photograph of Rose Island about 1988. Department of Marine and Wildlife Resources, Pago Pago. 4 Technical Reports of the Australian Museum (1993) To Pacific ornithologists Rose means seabirds. All observers have commented on the very large seabird population which dominates the life of the atoll. About 97% of the total seabird population of American Samoa is resident on Rose, consisting of about 312,000 birds of 20 species. There are large nesting colonies of both the Greater and Lesser Frigatebirds (Fregata minor and F . ariel), of the Red-footed, Brown and Masked Boobies (Sula sula, S. leucogaster and S . dactylatra), of Redtailed Tropicbirds (Phaethon rubricauda), of White and Sooty Terns (Gygis alba and Sterna fuscata), of Brown and Black Noddies (Anous stolidus, A. tenuirostiris), and of Reef Herons (Egretta sacra). In addition about a dozen migrants and visitors have been recorded from the atoll including the White-tailed Tropicbird (P. lepturus), Pacific Golden Plover (Pluvialisfulva), Ruddy Turnstone (Arenaria interpres), Bristle-thighed Curlew (Nurnenius tahitiensis), Bar-tailed Godwit (Limosa lapponica), Wandering Tattler (Heteroscelus incanus), Sanderling (Calidris alba), Long-tailed Cuckoo (Urodynamis taitensis). A small white egret has been reported by Scott et al. (1983). Hawksbills, Eretmochelys imbricata, and Green Turtles, Chelonia mydas, nest on the atoll. Other herpetofauna records include Gehyra oceanica, the Polynesian Gecko and Lepidodactylus lugubris, the Mourning Gec","PeriodicalId":279740,"journal":{"name":"Technical Reports of The Australian Museum","volume":"6 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1993-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"8","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Technical Reports of The Australian Museum","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3853/J.1031-8062.9.1993.70","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 8

Abstract

Over 290 citations of published monographs, articles from learned journals, periodical features, official reports, letters, notes, some limited circulation andlor unpublished documents, and unofficial reports, concerned with the geology, geography, pedology, biology, meteorology, oceanography and history of Rose Atoll, American Samoa, are indexed and annotated. RODGERS, K.A., I.A.W. MCALLAN, C. CANTRELL & B.J. PONWITH. 1992. Rose Atoll: an annotated bibliography. Technical Reports of the Australian Museum 9: 1-37. Rose Atoll lies at the extreme eastern end of the Samoan island volcanic chain (14'32's 168"08'W), 240 km east-south-east of Pago Pago Harbor (Fig.1). It is of a roughly square shape. The fringing reef and lagoon together cover just 640 ha making it one of the smallest atolls in the world. The fetch of the lagoon is about 2 km and the maximum depth about 20 m. The coralline algal reef has a uniform, 500 m width and is largely submerged at low tide. A single channel in the north-east, 1.8-15 m deep, links the lagoon to the sea. The atoll is one of the least disturbed areas of the world. Its benthic community is unique in Samoa, being dominated by encrusting coralline algae, and having a relative abundance of soft corals with a comparable impoverishment in hard species (Itano, 1987, cited in United Nations Environment Programme, 1988). The atoll has been established as a National Wildlife Refuge since 5 July 1973, and annual resource surveys are carried out by US Fish and Wildlife Service and American Samoan Government personnel. These include both the lagoon and outer reef as well as the islets, thus affording an invaluable scientific baseline for biological and geological studies of low Pacific islands. Excellent summary reviews of the history and natural history of the atoll are given by Setchell (1924) and Sachet (1954). A highly detailed, up-to-date account of the terrestrial biology is contained in Amerson et al. (1982a,b). 2 Technical Reports of the Australian Museum (1993) Geological and Biological Notes The Samoan Islands are part of a chain of searnounts, shallow banks and drowned atolls which extend 1700 km to the north-west. All are volcanic in origin and lie in a line with the correct orientation to have been generated by the present motion of the Pacific plate over a fixed hot spot (Natland, 1980; Menard, 1986). Both the size of the islands, and the proportion of them covered by Quaternary lava flows, increases to the west, in contrast to the Hawaiian, Society, and Marquesas chains. In these lineaments, submerged volcanic mounds, both drowned and capped by atoll reefs, occur at the western end, but in the Samoan chain Rose Atoll lies to the east. The age of Rose's volcanic substrate is not known, but it could be very young (Natland, 1980 but cf. Menard, 1986). Unlike the seemingly more mature, drowned atolls and flat banks to the west, Rose lacks wide offshore banks. In his studies of the petrology of the Samoan chain, Natland seems to have been unaware that basalt rocks had been reported and recovered from Rose (e.g., Natland, 1980; Natland & Turner, 1985). The nature of these particular rocks, and even their very existence, has been a subject of some confusion in the literature. They were first reported by members of the United States Exploring Expedition (e.g., Couthouy, 1844; Wilkes, 1844; Dana, 1851; Pickering, 1876). Mayor (1921b, 1924b) specifically looked for but failed to find any trace of them and he and Setchell (1924) dismissed the earlier reports as incorrect identifications of weathered limestone. However, Schultz (1940, 1943), located and collected from a dozen basalt boulders lying loose on the reef flat. Sachet (1954) reported that Gilbert Corwin of the US National Museum had identified the samples as olivine basalt. There are only two islets upon the reef (Fig.l,2): Rose Island in the east and Sand Island to the north. Total land area is 7.77 ha. Aggradation and degradation are active around the islets' margins and published descriptions of the atoll indicate that variation has occurred in area, shape and even position of the islets within historic times (e.g., Mayor, 1921b; Setchell, 1924; Bryan, 1938; Schultz, 1943; Amerson et al., 1982a; Ludwig, 1982a; cf. Sachet, 1954: 1-2; and see Figs 1,3acpa-d). Rose displays the dynamic character so typical of low islands in general, and atolls in particular. Perhaps, the small size of the atoll has helped heighten different observers's awareness of its active physical environment. The following descriptions are taken in large part from United Nations Environment Programme (1988) report of Susan Wells. Rose Island is located on the lagoon half of the reef in the windward corner of the atoll square (Fig.1). It is a roughly oval islet about 180 X 200 m, covering 5.18 ha, having a 1.0 km shoreline, and a maximum altitude of 3.0 m (Fig.2). It consists of raised reef rock and a coquina of worn fragments of lithothamnium, Favites, Porites, Symphallia, Pocillopora, Acropora, Tridacna, Fig.1. Sketch map of Rose Atoll, after Amerson et al. (1982a). Insert indicates location of Rose within the Samoan island chain. Rodgers et al.: Rose Atoll, bibliography 3 gastropod shells and echinoderms. A phosphatic soil, rich in humus has developed on the coquina beneath a large grove of Pisonia grandis. Sand Island is a bank of coralgal sand with an 0.5 km shoreline and reaching about 5.2 m above sea level. It covers 2.59 ha and presently lies on the lagoon side of the reef, due east of the lagoon entrance channel, with a broad reef flat extending seawards. It is intermittently vegetated and following Humcane Ofa in February 1990, it was swept clear save for one Messerschmidia tree. It now hosts seedling growth of Boerhavia and Messerschmidia. The lagoon floor has an undulating sandy bottom much of which is covered with algae and small scattered colonies of Acropora. Flat-topped, steep-sided pinnacles jut up from the floor and are encrusted by coralline algae, with both hard and soft corals on the vertical and undercut sides. Descriptions of the reef and the reef flat are given by Mayor (1921b) and Wass (n.d. a,b) which are summarised in United Nations Environment Programme (1988). The upper surface of the reef is a hard, smoothfloored flat, awash at low tide, and covered with vigorous growths of Porolithon that form connected pink patches and ridges up to 15 cm high and 15 cm to a metre or more wide. The inner lagoon edge is covered by coral blocks, the larger of which have flattened tops, also encrusted by coralline algae, and with both algae and soft corals coating their sides. Most of these blocks lie loose on the flat but some are attached by slender pedicels. Mayor (1921b) noted one loose boulder which he estimated weighed 46 tons. He argued (1921b, 1921c, 1924b) that the appearance of these boulders lent support to the rim of the atoll having once been 6 to 8 feet (1.8-2.4 m) higher than at present (cf. Stoddart, 1969). The remainder of the reef flat is rubble-strewn and also heavily encrusted by coralline algae and scattered colonies of Acropora. The basalt boulders, noted earlier, are part of the rubble of the flat. Their apparent comings and goings give further indication of the dynamic nature of the atoll environment. The reef front extends from a depth of 4 m in a series of irregular steep steps to about 50 m depth. The upper portion is dissected by ridges and surge channels. The irregular, high magnesium calcite substrate is encrusted thickly with coralline algae. Corals, including Acropora and Pocillopora, are abundant and diverse but table and staghorn varieties are lacking. No reports of the outer reef have been published at the time of writing. Several authors (e.g., Setchell, 1924; Sachet, 1954) have drawn attention to the number of native vascular plant species found on Rose being restricted to three: Pisonia grandis, Boerhavia tetrandra, and Portulaca lutea which form a small evergreen orthophyll softwood forest. At the time of their intensive survey of the atoll, Amerson et al. (1982a,b) found the number of species had increased to include Messerschmidia argentea, Ipomoea macrantha, and Suriana rnaritima, the latter having anived only very recently. Several attempts have been made to introduce coconut palms Cocos nucifera. The number surviving varies (20 in 1938, 12 in 1953), as do reports of their health (cf. Sachet, 1954:5,16). Fig.2. Aerial photograph of Rose Island about 1988. Department of Marine and Wildlife Resources, Pago Pago. 4 Technical Reports of the Australian Museum (1993) To Pacific ornithologists Rose means seabirds. All observers have commented on the very large seabird population which dominates the life of the atoll. About 97% of the total seabird population of American Samoa is resident on Rose, consisting of about 312,000 birds of 20 species. There are large nesting colonies of both the Greater and Lesser Frigatebirds (Fregata minor and F . ariel), of the Red-footed, Brown and Masked Boobies (Sula sula, S. leucogaster and S . dactylatra), of Redtailed Tropicbirds (Phaethon rubricauda), of White and Sooty Terns (Gygis alba and Sterna fuscata), of Brown and Black Noddies (Anous stolidus, A. tenuirostiris), and of Reef Herons (Egretta sacra). In addition about a dozen migrants and visitors have been recorded from the atoll including the White-tailed Tropicbird (P. lepturus), Pacific Golden Plover (Pluvialisfulva), Ruddy Turnstone (Arenaria interpres), Bristle-thighed Curlew (Nurnenius tahitiensis), Bar-tailed Godwit (Limosa lapponica), Wandering Tattler (Heteroscelus incanus), Sanderling (Calidris alba), Long-tailed Cuckoo (Urodynamis taitensis). A small white egret has been reported by Scott et al. (1983). Hawksbills, Eretmochelys imbricata, and Green Turtles, Chelonia mydas, nest on the atoll. Other herpetofauna records include Gehyra oceanica, the Polynesian Gecko and Lepidodactylus lugubris, the Mourning Gec
玫瑰环礁:注释书目
已发表的专著、学术期刊的文章、期刊特稿、官方报告、信件、笔记、一些有限流通和未发表的文件以及非正式报告等290多个引文被编入索引和注释,涉及美属萨摩亚罗斯环礁的地质、地理、土壤学、生物学、气象学、海洋学和历史。罗杰斯,k.a., I.A.W.麦卡伦,c.坎特雷尔和b.j.庞威斯。1992. 玫瑰环礁:注释书目。澳大利亚博物馆技术报告9:1-37。罗斯环礁位于萨摩亚岛火山链的最东端(14′32′168′08′w),在帕果帕果港东南偏东240公里处(图1)。它大致是方形的。边缘的珊瑚礁和泻湖加起来只有640公顷,使它成为世界上最小的环礁之一。泻湖水深约2公里,最大水深约20米。珊瑚藻礁有一个均匀的500米宽,在退潮时大部分被淹没。东北部有一条1.8-15米深的通道,将泻湖与大海连接起来。这个环礁是世界上受干扰最少的地区之一。它的底栖生物群落在萨摩亚是独一无二的,主要是覆盖珊瑚藻类,软珊瑚相对丰富,而硬珊瑚相对贫乏(Itano, 1987,引自联合国环境规划署,1988)。自1973年7月5日以来,该环礁已被确定为国家野生动物保护区,美国鱼类和野生动物管理局和美属萨摩亚政府人员每年进行资源调查。其中包括泻湖和外礁以及小岛,从而为太平洋低地岛屿的生物和地质研究提供了宝贵的科学基线。Setchell(1924年)和Sachet(1954年)对环礁的历史和自然历史进行了极好的总结。Amerson等人(1982a,b)对陆地生物进行了非常详细的最新描述。2澳大利亚博物馆技术报告(1993年)地质和生物学注释萨摩亚群岛是向西北延伸1700公里的海山、浅滩和淹没的环礁链的一部分。所有这些都是火山形成的,并且都位于一条正确的方向线上,这些方向是由太平洋板块在一个固定热点上的当前运动产生的(Natland, 1980;梅纳德,1986)。与夏威夷群岛、社会群岛和马克萨斯群岛相比,岛屿的面积和被第四纪熔岩流覆盖的比例都向西增加。在这些地貌的西端,有被淹没或被环礁覆盖的火山丘,但在萨摩亚群岛的东部,有玫瑰环礁。罗斯火山底物的年龄尚不清楚,但它可能非常年轻(Natland, 1980,但参见Menard, 1986)。与西部那些看起来更成熟、被淹没的环礁和平坦的海岸不同,罗斯岛缺乏宽阔的近海海岸。在他对萨摩亚岛链的岩石学研究中,Natland似乎没有意识到在Rose已经发现了玄武岩(例如,Natland, 1980;Natland & Turner, 1985)。这些特殊岩石的性质,甚至它们的存在,一直是文献中一些困惑的主题。它们最早是由美国探险探险队的成员(例如,Couthouy, 1844;威尔克斯,1844;丹娜,1851;皮克林,1876)。Mayor (1921b, 1924b)专门寻找了它们,但没有找到任何痕迹,他和Setchell(1924)认为早期的报告是对风化石灰岩的错误鉴定。然而,Schultz(1940, 1943)在礁滩上找到并收集了十几块松散的玄武岩巨石。Sachet(1954)报道说,美国国家博物馆的Gilbert Corwin已经将这些样品鉴定为橄榄岩玄武岩。礁上只有两个小岛(图1、2):东边的玫瑰岛和北边的沙岛。总土地面积为7.77公顷。岛礁边缘的侵蚀和退化十分活跃,已发表的关于环礁的描述表明,在历史时期内,岛礁的面积、形状甚至位置都发生了变化(例如,Mayor, 1921b;Setchell, 1924;布莱恩,1938;舒尔茨,1943;Amerson et al., 1982;路德维希,1982;cf. Sachet, 1954: 1-2;见图1、图3 (pa-d)。罗斯岛表现出一般低地岛屿,特别是环礁的典型动态特征。也许,环礁的小尺寸有助于提高不同的观察者对其活跃的物理环境的认识。以下描述大部分摘自联合国环境规划署(1988年)苏珊·威尔斯的报告。玫瑰岛位于环礁广场迎风角的礁湖半上(图1)。它是一个约180 × 200米的椭圆形小岛,占地5.18公顷,海岸线长1.0公里,最高海拔3.0米(图2)。 它由凸起的礁岩和岩石界、Favites、Porites、Symphallia、Pocillopora、Acropora、Tridacna的磨损碎片组成,图1。罗斯环礁的草图,根据Amerson等人(1982a)。插入显示罗丝在萨摩亚岛链内的位置。罗杰斯等人:《玫瑰环礁》,参考书目3腹足类贝壳和棘皮动物。一大片大皮索尼亚小树林下的coquina上形成了富含腐殖质的磷质土壤。沙岛是一滩珊瑚沙,海岸线长0.5公里,海拔约5.2米。它占地2.59公顷,目前位于礁湖的泻湖一侧,在泻湖入口通道的正东,有一个广阔的礁滩向海延伸。它断断续续地被植被覆盖,在1990年2月的人道主义Ofa之后,除了一棵Messerschmidia树外,它被扫平了。它现在承载着布尔哈维亚和梅塞施米迪亚的幼苗生长。泻湖的底部是起伏的沙质底部,其中大部分覆盖着藻类和小而分散的鹿角藻群落。平顶、陡峭的尖顶从地面上伸出来,被珊瑚藻包裹着,垂直和凹边都有硬珊瑚和软珊瑚。对珊瑚礁和礁滩的描述由Mayor (1921b)和Wass (n.d.a,b)给出,并在联合国环境规划署(1988)中进行了总结。珊瑚礁的上表面是一块坚硬、光滑的平地,在退潮时被海水淹没,上面覆盖着生长旺盛的波洛石,形成了连接在一起的粉红色斑块和高达15厘米、15厘米到1米或更宽的脊。内环礁湖边缘被珊瑚块覆盖,较大的珊瑚块顶部扁平,也被珊瑚藻覆盖,藻类和软珊瑚都覆盖在它们的两侧。这些木块大多松散地躺在平地上,但也有一些由细长的花梗附着。马约尔(1921b)注意到一块松动的巨石,他估计有46吨重。他认为(1921b, 1921c, 1924b)这些巨石的出现支撑了环礁的边缘,它们曾经比现在高6至8英尺(1.8-2.4米)(cf. Stoddart, 1969)。礁滩的其余部分布满了碎石,还被珊瑚藻和分散的鹿角藻覆盖着。前面提到的玄武岩巨石是平地碎石的一部分。它们明显的来来去去进一步表明了环礁环境的动态性质。礁面以一系列不规则的陡峭台阶从4米的深度延伸到约50米的深度。上部由山脊和涌浪通道分割。不规则的高镁方解石基底上覆有厚厚的珊瑚藻。珊瑚,包括鹿角珊瑚和麻角珊瑚,数量丰富,种类繁多,但缺乏桌角珊瑚和鹿角珊瑚。在撰写本文时,尚未发表有关外礁的报告。几位作者(例如,塞切尔,1924;Sachet, 1954)引起了人们的注意,在玫瑰上发现的本土维管植物种类仅限于三种:Pisonia grandis, Boerhavia tetrandra和Portulaca lutea,它们形成了一个小型的常绿正叶木针叶林。Amerson等人(1982a,b)在对该环礁进行深入调查时发现,物种数量有所增加,包括阿根廷的Messerschmidia, macrantha和Suriana rnaritima,后者是最近才出现的。人们曾多次尝试引进椰子树Cocos nucifera。幸存的人数各不相同(1938年20人,1953年12人),关于他们健康状况的报告也各不相同(参见Sachet, 1954:5,16)。图2。1988年玫瑰岛的航拍照片。海洋和野生动物资源部,帕果帕果。4澳大利亚博物馆技术报告(1993)对太平洋鸟类学家来说,玫瑰是海鸟的意思。所有的观察者都评论说,在这个环礁上占据主导地位的海鸟数量非常多。美属萨摩亚约97%的海鸟栖息在罗斯岛上,包括20个物种的312,000只鸟。大军舰鸟和小军舰鸟(小军舰鸟和小军舰鸟)都有大型筑巢群。阿里尔),红脚鲣鸟,棕色鲣鸟和蒙面鲣鸟(苏拉苏拉,S. leucogaster和S。热带红尾鸟(Phaethon rubricauda)、白燕鸥和黑燕鸥(Gygis alba和Sterna fuscata)、褐燕鸥和黑燕鸥(Anous stolidus, A. tenuirostiris)以及礁鹭(Egretta sacra)。此外,在环礁上还发现了十几种候鸟和游客,包括白尾热带鸟(P. lepturus)、太平洋金鸻(Pluvialisfulva)、红背鸻(Arenaria interpres)、鬃腿鹬(Nurnenius tahitiensis)、斑尾鹬(Limosa lapponica)、流浪鹬(Heteroscelus incanus)、沙尾鹬(Calidris alba)、长尾杜鹃(Urodynamis taitensis)。Scott et al.(1983)曾报道过一种小白鹭。玳瑁和绿海龟在环礁上筑巢。 其他有记录的爬行动物群包括大洋壁虎、波利尼西亚壁虎和哀恸壁虎
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信