دورهٔ کامبرین حدود ۵۴۲ میلیون سال پیش آغاز شده و تا حدوداً ۴۸۸/۳ میلیون سال پیش ادامه داشتهاست.
نام کامبرین از نام کامبریا یعنی نام باستانی منطقهٔ ویلز بریتانیا گرفته شده زیرا در آنجا بود که صخرههایی از دورهٔ کامبرین برای نخستین بار بررسی شد. بر این پایه، در فارسی برای این دوره نام «کامبریایی» درستتر میبود ولی امروزه کامبرین در این معنی جا افتادهاست.
دوره کامبرین ۵۷۰ – ۵۰۵ میلیون سال گذشته دوره کامبرین به سه اشکوب زیرین، میانی و بالایی تقسیم میشود. سن کامبرین از ۷۵۰ تا ۵۱۰ میلیون سال قبل است. پیدایش آثار یخچالی در سنگهای رسوبی کامبرین چین و نقاط دیگر نشان میدهد که آب و هوای سردی در این نواحی حکم فرما بوده است. مطالعه رسوبات چین خورده کامبرین نشان دهنده آن است که در این دوره بزرگ ناودیسهایی در نقاط مختلفی از اروپا، آسیا و آمریکا وجود داشته است. بعضی از جانورانی که در تشکیلات کامبرین مشاهده شدهاند از نظر چینهشناسی اهمیت زیادی ندارند.
دوره کامبرین نقش اساسی و مهمی در تاریخ حیات بر روی زمین ایفا میکند. زمانی که اغلب گروههای بزرگ جانوران اولیه در قالب فسیل ظاهر شدند. این حادثه گاهی (انفجار کامبرین) نامیده میشود به دلیل اینکه زمان کمی برای ایجاد آن طی شدهاست. در ابتدا تصور میشد که سنگهای این دوره حاوی اولین و قدیمیترین فسیلهای جانوری است.
در اوایل دوره کامبرین، جانوران برای حفاظت و نگهداری اعضاء نرم خود، بخشهای سخت خود را توسعه دادند، برای مثال صدف خارجی بدن یک بازوپا به حجرههای غذایی تغییر شکل داد. در حالی که بافت خارجی تریلوبیتها پاها و ماهیچههای ثابت پیدا کردند. جانوران با داشتن اسکلت توان رشد بیشتری داشته و نواحی کلنی را در کف مختلف دریاها تشکیل دادند. بندپایان قادر به شنا کردن، حرکت سریع و توسعه اسکلت خود بودند. چون فسیل این جانوران یا به ندرت یافت شده و یا اینکه به خوبی حفظ نشدهاند. از این جانوران مرجانها را میتوان نام برد که تنوع زیادی نداشته و یا آنکه دارای اسکلت سخت نبودهاند. خارپوستان نیز در این دوره ظهور نمودهاند، ولی گوناگونی زیادی نداشتهاند. از نرمتنان وجود دوکفهایها مشکوک است و از شکم پایان هم جز چند نمونه ساده آثار بیشتری باقی نمانده است.
اولین جانوران در این دوره کوچک بوده و از فسفات برای تغذیه استفاده میکردند و همچنین اسفنجها نیز از سیلیس و در طی ۱۰ میلیون سال بعد جانوران بزرگتر از کربنات کلسیم برای تغذیه استفاده میکردند. در اواخر دوره کامبرین، اجداد بیشتر گروههای جانوران اصلی در دریا گسترش یافتند.
تقسیمات دوره کامبرین[ویرایش]
تقسیمات سیستم کامبرین از سال ۱۸۹۱ توسط والکت (Walcott) به صورت سه قسمتی پیشنهاد گردید که شامل کامبرین زیرین، میانی و بالایی است. اشکوبهای کامبرین عبارتند از:
اشکوب جورجین (Georgian): که وجه تسمیه آن از کلمه جورجیا شهری در آمریکاست و توسط والکت در سال ۱۸۹۱ به کار برده شده است. این اشکوب معادل اشکوب توماشین است. زون تریلوبیت اله نلوس کامبرین زیرین را مشخص مینماید.
اشکوب آکادین (Acadian): که نامش از محل آکادی (Acadie) در کانادا گرفته شده است و در سال ۱۸۶۷ توسط داوسون (Dawson) ابداع گردیده است. این اشکوب قسمتی از کامبرین میاین با تریلوبیتهای پرادوکسیدها را شامل میشود.
اشکوب پوتسدامین (Potsdamian): که شامل ماسه سنگهای پوتسدام نواحی نیویورک است. این اشکوب دارای نبودهای چینهشناسی بوده و نمیتواند بطور کامل معرف کامبرین بالایی باشد.
For other uses, see Cambrian (disambiguation).
The Cambrian Period (pronunciation: // or //) was the first geological period of the Paleozoic Era, of the Phanerozoic Eon lasting from 541 to 485.4 million years ago (mya), an interval of 55.6 million years. It was followed by the Ordovician Period. Its subdivisions, and its base, are somewhat in flux. The period was established (as “Cambrian series”) by Adam Sedgwick, who named it after Cambria, the Latinised form of Cymru, the Welsh name for Wales, where Britain's Cambrian rocks are best exposed. The Cambrian is unique in its unusually high proportion of lagerstätte sedimentary deposits. These are sites of exceptional preservation, where "soft" parts of organisms are preserved as well as their more resistant shells. This means that our understanding of the Cambrian biology surpasses that of some later periods.
The Cambrian marked a profound change in life on Earth; prior to the Cambrian, the majority of living organisms on the whole were small, unicellular and simple; the Precambrian Charnia being exceptional. Complex, multicellular organisms gradually became more common in the millions of years immediately preceding the Cambrian, but it was not until this period that mineralized—hence readily fossilized—organisms became common. The rapid diversification of lifeforms in the Cambrian, known as the Cambrian explosion, produced the first representatives of all modern animal phyla. Phylogenetic analysis has supported the view that during the Cambrian radiation, metazoa (animals) evolved monophyletically from a single common ancestor: flagellated colonial protists similar to modern choanoflagellates.
Although diverse life forms prospered in the oceans, the land was comparatively barren—with nothing more complex than a microbial soil crust and a few molluscs that emerged to browse on the microbial biofilm. Most of the continents were probably dry and rocky due to a lack of vegetation. Shallow seas flanked the margins of several continents created during the breakup of the supercontinent Pannotia. The seas were relatively warm, and polar ice was absent for much of the period.
The United States Federal Geographic Data Committee uses a "barred capital C" ⟨Є⟩ character similar to the capital letter Ukrainian Ye ⟨Є⟩ to represent the Cambrian Period. The proper Unicode character is U+A792 Ꞓ LATIN CAPITAL LETTER C WITH BAR.
Further information: Stratigraphy of the Cambrian
Despite the long recognition of its distinction from younger Ordovician Period rocks and older Supereon Precambrian rocks, it was not until 1994 that this time period was internationally ratified. The base of the Cambrian lies atop a complex assemblage of trace fossils known as the Treptichnus pedum assemblage. The use of Treptichnus pedum, a reference ichnofossil to mark the lower boundary of the Cambrian, is difficult as the occurrence of very similar trace fossils belonging to the Treptichnids group are found well below the T. pedum in Namibia, Spain and Newfoundland, and possibly, in the western USA. The stratigraphic range of T. pedum overlaps the range of the Ediacaran fossils in Namibia, and probably in Spain.
The Cambrian Period followed the Ediacaran Period and was followed by the Ordovician Period. The Cambrian is divided into four epochs (series) and ten ages (stages). Currently only two series and five stages are named and have a GSSP.
Because the international stratigraphic subdivision is not yet complete, many local subdivisions are still widely used. In some of these subdivisions the Cambrian is divided into three epochs with locally differing names – the Early Cambrian (Caerfai or Waucoban, Middle Cambrian (St Davids or Albertan, to mya) and Furongian ( to mya; also known as Late Cambrian, Merioneth or Croixan). Rocks of these epochs are referred to as belonging to the Lower, Middle, or Upper Cambrian.to mya),
Trilobite zones allow biostratigraphic correlation in the Cambrian.
Each of the local epochs is divided into several stages. The Cambrian is divided into several regional faunal stages of which the Russian-Kazakhian system is most used in international parlance:
*In Russian scientific thought the lower boundary of the Cambrian is suggested to be defined at the base of the Tommotian Stage which is characterized by diversification and global distribution of organisms with mineral skeletons and the appearance of the first Archaeocyath bioherms.
The time range for the Cambrian has classically been thought to have been from about 541 million years ago (mya) to about 485 mya. The lower boundary of the Cambrian was traditionally set at the earliest appearance of trilobites and also archeocyathids (literally "ancient cup") that are thought to be the earliest sponges and also the first non-microbial reef builders.
The end of the period was eventually set at a fairly definite faunal change now identified as an extinction event. Fossil discoveries and radiometric dating in the last quarter of the 20th century have called these dates into question. Date inconsistencies as large as 20 million years are common between authors. Framing dates of ca. 545 to 490 mya were proposed by the International Subcommission on Global Stratigraphy as recently as 2002.
A more precise date of 541 ± 0.3 mya for the extinction event at the beginning of the Cambrian has recently been submitted. The rationale for this precise dating is interesting in itself as an example of paleological deductive reasoning. Exactly at the Cambrian boundary there is a marked fall in the abundance of carbon-13, a "reverse spike" that paleontologists call an excursion. It is so widespread that it is the best indicator of the position of the Precambrian-Cambrian boundary in stratigraphic sequences of roughly this age. One of the places that this well-established carbon-13 excursion occurs is in Oman. Evidence from Oman of the carbon-isotope excursion relates to a mass extinction: the disappearance of distinctive fossils from the Precambrian coincides exactly with the carbon-13 anomaly. Fortunately, in the Oman sequence, so too does a volcanic ash horizon from which zircons provide a very precise age of 541 ± 0.3 mya (calculated on the decay rate of uranium to lead). This new and precise date tallies with the less precise dates for the carbon-13 anomaly, derived from sequences in Siberia and Namibia.
Plate reconstructions suggest a global supercontinent, Pannotia, was in the process of breaking up early in the period, with Laurentia (North America), Baltica, and Siberia having separated from the main supercontinent of Gondwana to form isolated land masses. Most continental land was clustered in the Southern Hemisphere at this time, but was drifting north. Large, high-velocity rotational movement of Gondwana appears to have occurred in the Early Cambrian.
With a lack of sea ice – the great glaciers of the Marinoan Snowball Earth were long melted – the sea level was high, which led to large areas of the continents being flooded in warm, shallow seas ideal for sea life. The sea levels fluctuated somewhat, suggesting there were 'ice ages', associated with pulses of expansion and contraction of a south polar ice cap.
The Earth was generally cold during the early Cambrian, probably due to the ancient continent of Gondwana covering the South Pole and cutting off polar ocean currents. However, average temperatures were 7 degrees Celsius higher than today. There were likely polar ice caps and a series of glaciations, as the planet was still recovering from an earlier Snowball Earth. It became warmer towards the end of the period; the glaciers receded and eventually disappeared, and sea levels rose dramatically. This trend would continue into the Ordovician period.
Although there were a variety of macroscopic marine plants[which?] no land plant (embryophyte) fossils are known from the Cambrian. However, biofilms and microbial mats were well developed on Cambrian tidal flats and beaches 500 mya., and microbes forming microbial Earth ecosystems, comparable with modern soil crust of desert regions, contributing to soil formation.
Main article: Cambrian explosion
Most animal life during the Cambrian was aquatic.
Trilobites were once assumed to be the dominant life form, but this has proven to be incorrect. Arthropods in general were by far the most dominant animals in the ocean, but trilobites were only a minor part of the total arthropod diversity. What made them so apparently abundant was their heavy armor that was reinforced by calcium carbonate (CaCO3), which fossilized far more easily than the fragile more purely chitin exoskeletons of other arthropods, leaving behind numerous preserved remains which give the false impression that they were the most abundant part of the fauna.
The period marked a steep change in the diversity and composition of Earth's biosphere. The Ediacaran biota suffered a mass extinction at the start of the Cambrian Period, which corresponded to an increase in the abundance and complexity of burrowing behaviour. This behaviour had a profound and irreversible effect on the substrate which transformed the seabed ecosystems. Before the Cambrian, the sea floor was covered by microbial mats. By the end of the Cambrian, burrowing animals had destroyed the mats in many areas through bioturbation, and gradually turned the seabeds into what they are today.[clarification needed] As a consequence, many of those organisms that were dependent on the mats became extinct, while the other species adapted to the changed environment that now offered new ecological niches. Around the same time there was a seemingly rapid appearance of representatives of all the mineralized phyla except the Bryozoa, which appeared in the Lower Ordovician. However, many of those phyla were represented only by stem-group forms; and since mineralized phyla generally have a benthic origin, they may not be a good proxy for (more abundant) non-mineralized phyla.
While the early Cambrian showed such diversification that it has been named the Cambrian Explosion, this changed later in the period, when there occurred a sharp drop in biodiversity. About 515 million years ago, the number of species going extinct exceeded the number of new species appearing. Five million years later, the number of genera had dropped from an earlier peak of about 600 to just 450. Also, the speciation rate in many groups was reduced to between a fifth and a third of previous levels. 500 million years ago, oxygen levels fell dramatically in the oceans, leading to hypoxia, while the level of poisonous hydrogen sulfide simultaneously increased, causing another extinction. The later half of Cambrian was surprisingly barren and show evidence of several rapid extinction events; the stromatolites which had been replaced by reef building sponges known as Archaeocyatha, returned once more as the archaeocyathids became extinct. This declining trend did not change until the Great Ordovician Biodiversification Event.
Some Cambrian organisms ventured onto land, producing the trace fossils Protichnites and Climactichnites. Fossil evidence suggests that euthycarcinoids, an extinct group of arthropods, produced at least some of the Protichnites. Fossils of the track-maker of Climactichnites have not been found; however, fossil trackways and resting traces suggest a large, slug-like mollusk.
In contrast to later periods, the Cambrian fauna was somewhat restricted; free-floating organisms were rare, with the majority living on or close to the sea floor; and mineralizing animals were rarer than in future periods, in part due to the unfavourable ocean chemistry.
Many modes of preservation are unique to the Cambrian, and some preserve soft body parts, resulting in an abundance of Lagerstätten.