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Monday, July 15, 2019

Biodiversity

From Wikipedia, the free encyclopedia
 
A sampling of fungi collected during summer 2008 in Northern Saskatchewan mixed woods, near LaRonge is an example regarding the species diversity of fungi. In this photo, there are also leaf lichens and mosses.
 
Biodiversity is the variety and variability of life on Earth. Biodiversity is typically a measure of variation at the genetic, species, and ecosystem level. Terrestrial biodiversity is usually greater near the equator, which is the result of the warm climate and high primary productivity. Biodiversity is not distributed evenly on Earth, and is richest in the tropics. These tropical forest ecosystems cover less than 10 percent of earth's surface, and contain about 90 percent of the world's species. Marine biodiversity is usually highest along coasts in the Western Pacific, where sea surface temperature is highest, and in the mid-latitudinal band in all oceans. There are latitudinal gradients in species diversity. Biodiversity generally tends to cluster in hotspots, and has been increasing through time, but will be likely to slow in the future.

Rapid environmental changes typically cause mass extinctions. More than 99.9 percent of all species that ever lived on Earth, amounting to over five billion species, are estimated to be extinct. Estimates on the number of Earth's current species range from 10 million to 14 million, of which about 1.2 million have been documented and over 86 percent have not yet been described. More recently, in May 2016, scientists reported that 1 trillion species are estimated to be on Earth currently with only one-thousandth of one percent described. The total amount of related DNA base pairs on Earth is estimated at 5.0 x 1037 and weighs 50 billion tonnes. In comparison, the total mass of the biosphere has been estimated to be as much as 4 TtC (trillion tons of carbon). In July 2016, scientists reported identifying a set of 355 genes from the Last Universal Common Ancestor (LUCA) of all organisms living on Earth.

The age of the Earth is about 4.54 billion years. The earliest undisputed evidence of life on Earth dates at least from 3.5 billion years ago, during the Eoarchean Era after a geological crust started to solidify following the earlier molten Hadean Eon. There are microbial mat fossils found in 3.48 billion-year-old sandstone discovered in Western Australia. Other early physical evidence of a biogenic substance is graphite in 3.7 billion-year-old meta-sedimentary rocks discovered in Western Greenland. More recently, in 2015, "remains of biotic life" were found in 4.1 billion-year-old rocks in Western Australia. According to one of the researchers, "If life arose relatively quickly on Earth .. then it could be common in the universe."

Since life began on Earth, five major mass extinctions and several minor events have led to large and sudden drops in biodiversity. The Phanerozoic eon (the last 540 million years) marked a rapid growth in biodiversity via the Cambrian explosion—a period during which the majority of multicellular phyla first appeared. The next 400 million years included repeated, massive biodiversity losses classified as mass extinction events. In the Carboniferous, rainforest collapse led to a great loss of plant and animal life. The Permian–Triassic extinction event, 251 million years ago, was the worst; vertebrate recovery took 30 million years. The most recent, the Cretaceous–Paleogene extinction event, occurred 65 million years ago and has often attracted more attention than others because it resulted in the extinction of the non-avian dinosaurs.

The period since the emergence of humans has displayed an ongoing biodiversity reduction and an accompanying loss of genetic diversity. Named the Holocene extinction, the reduction is caused primarily by human impacts, particularly habitat destruction. Conversely, biodiversity positively impacts human health in a number of ways, although a few negative effects are studied.

The United Nations designated 2011–2020 as the United Nations Decade on Biodiversity. and 2021-2030 as the United Nations Decade on Ecosystem Restoration  According to a 2019 Global Assessment Report on Biodiversity and Ecosystem Services by IPBES, 25% of plant and animal species are threatened with extinction as the result of human activity.

History of terminology

  • 1916 - The term biological diversity was used first by J. Arthur Harris in "The Variable Desert," Scientific American, JSTOR 6182: "The bare statement that the region contains a flora rich in genera and species and of diverse geographic origin or affinity is entirely inadequate as a description of its real biological diversity."
  • 1975 - The term natural diversity was introduced (by The Science Division of The Nature Conservancy in a 1975 study, "The Preservation of Natural Diversity.")
  • 1980 - Thomas Lovejoy introduced the term biological diversity to the scientific community in a book. It rapidly became commonly used.
  • 1985 - According to Edward O. Wilson, the contracted form biodiversity was coined by W. G. Rosen: "The National Forum on BioDiversity ... was conceived by Walter G.Rosen ... Dr. Rosen represented the NRC/NAS throughout the planning stages of the project. Furthermore, he introduced the term biodiversity".
  • 1985 - The term "biodiversity" appears in the article, "A New Plan to Conserve the Earth's Biota" by Laura Tangley.
  • 1988 - The term biodiversity first appeared in a publication.
  • The present - the term has achieved widespread use.

Definitions

Prior term

"Biodiversity" is most commonly used to replace the more clearly defined and long established terms, species diversity and species richness.

Alternate terms

Biologists most often define biodiversity as the "totality of genes, species and ecosystems of a region". An advantage of this definition is that it seems to describe most circumstances and presents a unified view of the traditional types of biological variety previously identified:
  • taxonomic diversity (usually measured at the species diversity level)
  • ecological diversity (often viewed from the perspective of ecosystem diversity)
  • morphological diversity (which stems from genetic diversity and molecular diversity)
  • functional diversity (which is a measure of the number of functionally disparate species within a population (e.g. different feeding mechanism, different motility, predator vs prey, etc.)) This multilevel construct is consistent with Datman and Lovejoy.

Wilcox 1982

An explicit definition consistent with this interpretation was first given in a paper by Bruce A. Wilcox commissioned by the International Union for the Conservation of Nature and Natural Resources (IUCN) for the 1982 World National Parks Conference. Wilcox's definition was "Biological diversity is the variety of life forms...at all levels of biological systems (i.e., molecular, organismic, population, species and ecosystem)..."

Genetic: Wilcox 1984

Biodiversity can be defined genetically as the diversity of alleles, genes and organisms. They study processes such as mutation and gene transfer that drive evolution.

United Nations 1992

The 1992 United Nations Earth Summit defined "biological diversity" as "the variability among living organisms from all sources, including, 'inter alia', terrestrial, marine and other aquatic ecosystems and the ecological complexes of which they are part: this includes diversity within species, between species and of ecosystems". This definition is used in the United Nations Convention on Biological Diversity.

Gaston and Spicer 2004

Gaston & Spicer's definition in their book "Biodiversity: an introduction" is "variation of life at all levels of biological organization".

Distribution

Biodiversity is not evenly distributed, rather it varies greatly across the globe as well as within regions. Among other factors, the diversity of all living things (biota) depends on temperature, precipitation, altitude, soils, geography and the presence of other species. The study of the spatial distribution of organisms, species and ecosystems, is the science of biogeography

Diversity consistently measures higher in the tropics and in other localized regions such as the Cape Floristic Region and lower in polar regions generally. Rain forests that have had wet climates for a long time, such as Yasuní National Park in Ecuador, have particularly high biodiversity.

Terrestrial biodiversity is thought to be up to 25 times greater than ocean biodiversity. A new method used in 2011, put the total number of species on Earth at 8.7 million, of which 2.1 million were estimated to live in the ocean. However, this estimate seems to under-represent the diversity of microorganisms.

Latitudinal gradients

Generally, there is an increase in biodiversity from the poles to the tropics. Thus localities at lower latitudes have more species than localities at higher latitudes. This is often referred to as the latitudinal gradient in species diversity. Several ecological factors may contribute to the gradient, but the ultimate factor behind many of them is the greater mean temperature at the equator compared to that of the poles.

Even though terrestrial biodiversity declines from the equator to the poles, some studies claim that this characteristic is unverified in aquatic ecosystems, especially in marine ecosystems. The latitudinal distribution of parasites does not appear to follow this rule.

In 2016, an alternative hypothesis ("the fractal biodiversity") was proposed to explain the biodiversity latitudinal gradient. In this study, the species pool size and the fractal nature of ecosystems were combined to clarify some general patterns of this gradient. This hypothesis considers temperature, moisture, and net primary production (NPP) as the main variables of an ecosystem niche and as the axis of the ecological hypervolume. In this way, it is possible to build fractal hypervolumes, whose fractal dimension rises up to three moving towards the equator.

Hotspots

A biodiversity hotspot is a region with a high level of endemic species that have experienced great habitat loss. The term hotspot was introduced in 1988 by Norman Myers. While hotspots are spread all over the world, the majority are forest areas and most are located in the tropics

Brazil's Atlantic Forest is considered one such hotspot, containing roughly 20,000 plant species, 1,350 vertebrates and millions of insects, about half of which occur nowhere else. The island of Madagascar and India are also particularly notable. Colombia is characterized by high biodiversity, with the highest rate of species by area unit worldwide and it has the largest number of endemics (species that are not found naturally anywhere else) of any country. About 10% of the species of the Earth can be found in Colombia, including over 1,900 species of bird, more than in Europe and North America combined, Colombia has 10% of the world's mammals species, 14% of the amphibian species and 18% of the bird species of the world. Madagascar dry deciduous forests and lowland rainforests possess a high ratio of endemism. Since the island separated from mainland Africa 66 million years ago, many species and ecosystems have evolved independently. Indonesia's 17,000 islands cover 735,355 square miles (1,904,560 km2) and contain 10% of the world's flowering plants, 12% of mammals and 17% of reptiles, amphibians and birds—along with nearly 240 million people. Many regions of high biodiversity and/or endemism arise from specialized habitats which require unusual adaptations, for example, alpine environments in high mountains, or Northern European peat bogs.

Accurately measuring differences in biodiversity can be difficult. Selection bias amongst researchers may contribute to biased empirical research for modern estimates of biodiversity. In 1768, Rev. Gilbert White succinctly observed of his Selborne, Hampshire "all nature is so full, that that district produces the most variety which is the most examined."

Evolution

Apparent marine fossil diversity during the Phanerozoic

Chronology

Biodiversity is the result of 3.5 billion years of evolution. The origin of life has not been definitely established by science, however some evidence suggests that life may already have been well-established only a few hundred million years after the formation of the Earth. Until approximately 600 million years ago, all life consisted of microorganismsarchaea, bacteria, and single-celled protozoans and protists

The history of biodiversity during the Phanerozoic (the last 540 million years), starts with rapid growth during the Cambrian explosion—a period during which nearly every phylum of multicellular organisms first appeared. Over the next 400 million years or so, invertebrate diversity showed little overall trend and vertebrate diversity shows an overall exponential trend. This dramatic rise in diversity was marked by periodic, massive losses of diversity classified as mass extinction events. A significant loss occurred when rainforests collapsed in the carboniferous. The worst was the Permian-Triassic extinction event, 251 million years ago. Vertebrates took 30 million years to recover from this event.

The fossil record suggests that the last few million years featured the greatest biodiversity in history. However, not all scientists support this view, since there is uncertainty as to how strongly the fossil record is biased by the greater availability and preservation of recent geologic sections. Some scientists believe that corrected for sampling artifacts, modern biodiversity may not be much different from biodiversity 300 million years ago, whereas others consider the fossil record reasonably reflective of the diversification of life. Estimates of the present global macroscopic species diversity vary from 2 million to 100 million, with a best estimate of somewhere near 9 million, the vast majority arthropods. Diversity appears to increase continually in the absence of natural selection.

Diversification

The existence of a global carrying capacity, limiting the amount of life that can live at once, is debated, as is the question of whether such a limit would also cap the number of species. While records of life in the sea shows a logistic pattern of growth, life on land (insects, plants and tetrapods) shows an exponential rise in diversity. As one author states, "Tetrapods have not yet invaded 64 per cent of potentially habitable modes and it could be that without human influence the ecological and taxonomic diversity of tetrapods would continue to increase in an exponential fashion until most or all of the available ecospace is filled."

It also appears that the diversity continue to increase over time, especially after mass extinctions.

On the other hand, changes through the Phanerozoic correlate much better with the hyperbolic model (widely used in population biology, demography and macrosociology, as well as fossil biodiversity) than with exponential and logistic models. The latter models imply that changes in diversity are guided by a first-order positive feedback (more ancestors, more descendants) and/or a negative feedback arising from resource limitation. Hyperbolic model implies a second-order positive feedback. The hyperbolic pattern of the world population growth arises from a second-order positive feedback between the population size and the rate of technological growth. The hyperbolic character of biodiversity growth can be similarly accounted for by a feedback between diversity and community structure complexity. The similarity between the curves of biodiversity and human population probably comes from the fact that both are derived from the interference of the hyperbolic trend with cyclical and stochastic dynamics.

Most biologists agree however that the period since human emergence is part of a new mass extinction, named the Holocene extinction event, caused primarily by the impact humans are having on the environment. It has been argued that the present rate of extinction is sufficient to eliminate most species on the planet Earth within 100 years.

In 2011, in his Biodiversity-related Niches Differentiation Theory, Roberto Cazzolla Gatti proposed that species themselves are the architects of biodiversity, by proportionally increasing the number of potentially available niches in a given ecosystem. This study led to the idea that biodiversity is autocatalytic. An ecosystem of interdependent species can be, therefore, considered as an emergent autocatalytic set (a self-sustaining network of mutually "catalytic" entities), where one (group of) species enables the existence of (i.e., creates niches for) other species. This view offers a possible answer to the fundamental question of why so many species can coexist in the same ecosystem.

New species are regularly discovered (on average between 5–10,000 new species each year, most of them insects) and many, though discovered, are not yet classified (estimates are that nearly 90% of all arthropods are not yet classified). Most of the terrestrial diversity is found in tropical forests and in general, land has more species than the ocean; some 8.7 million species may exists on Earth, of which some 2.1 million live in the ocean.

Ecosystem services

Summer field in Belgium (Hamois). The blue flowers are Centaurea cyanus and the red are Papaver rhoeas.

The balance of evidence

"Ecosystem services are the suite of benefits that ecosystems provide to humanity." The natural species, or biota, are the caretakers of all ecosystems. It is as if the natural world is an enormous bank account of capital assets capable of paying life sustaining dividends indefinitely, but only if the capital is maintained.

These services come in three flavors:
  1. Provisioning services which involve the production of renewable resources (e.g.: food, wood, fresh water)
  2. Regulating services which are those that lessen environmental change (e.g.: climate regulation, pest/disease control)
  3. Cultural services represent human value and enjoyment (e.g.: landscape aesthetics, cultural heritage, outdoor recreation and spiritual significance)
There have been many claims about biodiversity's effect on these ecosystem services, especially provisioning and regulating services. After an exhaustive survey through peer-reviewed literature to evaluate 36 different claims about biodiversity's effect on ecosystem services, 14 of those claims have been validated, 6 demonstrate mixed support or are unsupported, 3 are incorrect and 13 lack enough evidence to draw definitive conclusions.

Services enhanced

Provisioning services
Greater species diversity
  • of plants increases fodder yield (synthesis of 271 experimental studies).
  • of plants (i.e. diversity within a single species) increases overall crop yield (synthesis of 575 experimental studies). Although another review of 100 experimental studies reports mixed evidence.
  • of trees increases overall wood production (Synthesis of 53 experimental studies). However, there is not enough data to draw a conclusion about the effect of tree trait diversity on wood production.
Regulating services
Greater species diversity
  • of fish increases the stability of fisheries yield (Synthesis of 8 observational studies)
  • of natural pest enemies decreases herbivorous pest populations (Data from two separate reviews; Synthesis of 266 experimental and observational studies; Synthesis of 18 observational studies. Although another review of 38 experimental studies found mixed support for this claim, suggesting that in cases where mutual intraguild predation occurs, a single predatory species is often more effective
  • of plants decreases disease prevalence on plants (Synthesis of 107 experimental studies)
  • of plants increases resistance to plant invasion (Data from two separate reviews; Synthesis of 105 experimental studies; Synthesis of 15 experimental studies)
  • of plants increases carbon sequestration, but note that this finding only relates to actual uptake of carbon dioxide and not long term storage, see below; Synthesis of 479 experimental studies)
  • plants increases soil nutrient remineralization (Synthesis of 103 experimental studies)
  • of plants increases soil organic matter (Synthesis of 85 experimental studies)

Services with mixed evidence

Provisioning services
  • None to date
Regulating services
  • Greater species diversity of plants may or may not decrease herbivorous pest populations. Data from two separate reviews suggest that greater diversity decreases pest populations (Synthesis of 40 observational studies; Synthesis of 100 experimental studies). One review found mixed evidence (Synthesis of 287 experimental studies), while another found contrary evidence (Synthesis of 100 experimental studies)
  • Greater species diversity of animals may or may not decrease disease prevalence on those animals (Synthesis of 45 experimental and observational studies), although a 2013 study offers more support showing that biodiversity may in fact enhance disease resistance within animal communities, at least in amphibian frog ponds. Many more studies must be published in support of diversity to sway the balance of evidence will be such that we can draw a general rule on this service.
  • Greater species and trait diversity of plants may or may not increase long term carbon storage (Synthesis of 33 observational studies)
  • Greater pollinator diversity may or may not increase pollination (Synthesis of 7 observational studies), but a publication from March 2013 suggests that increased native pollinator diversity enhances pollen deposition (although not necessarily fruit set as the authors would have you believe, for details explore their lengthy supplementary material).

Services hindered

Provisioning services
  • Greater species diversity of plants reduces primary production (Synthesis of 7 experimental studies)
Regulating services
  • greater genetic and species diversity of a number of organisms reduces freshwater purification (Synthesis of 8 experimental studies, although an attempt by the authors to investigate the effect of detritivore diversity on freshwater purification was unsuccessful due to a lack of available evidence (only 1 observational study was found
Provisioning services
  • Effect of species diversity of plants on biofuel yield (In a survey of the literature, the investigators only found 3 studies)
  • Effect of species diversity of fish on fishery yield (In a survey of the literature, the investigators only found 4 experimental studies and 1 observational study)
Regulating services
  • Effect of species diversity on the stability of biofuel yield (In a survey of the literature, the investigators did not find any studies)
  • Effect of species diversity of plants on the stability of fodder yield (In a survey of the literature, the investigators only found 2 studies)
  • Effect of species diversity of plants on the stability of crop yield (In a survey of the literature, the investigators only found 1 study)
  • Effect of genetic diversity of plants on the stability of crop yield (In a survey of the literature, the investigators only found 2 studies)
  • Effect of diversity on the stability of wood production (In a survey of the literature, the investigators could not find any studies)
  • Effect of species diversity of multiple taxa on erosion control (In a survey of the literature, the investigators could not find any studies – they did however find studies on the effect of species diversity and root biomass)
  • Effect of diversity on flood regulation (In a survey of the literature, the investigators could not find any studies)
  • Effect of species and trait diversity of plants on soil moisture (In a survey of the literature, the investigators only found 2 studies)
Other sources have reported somewhat conflicting results and in 1997 Robert Costanza and his colleagues reported the estimated global value of ecosystem services (not captured in traditional markets) at an average of $33 trillion annually.

Since the stone age, species loss has accelerated above the average basal rate, driven by human activity. Estimates of species losses are at a rate 100-10,000 times as fast as is typical in the fossil record. Biodiversity also affords many non-material benefits including spiritual and aesthetic values, knowledge systems and education.

Agriculture

Agricultural diversity can be divided into two categories: intraspecific diversity, which includes the genetic variety within a single species, like the potato (Solanum tuberosum) that is composed of many different forms and types (e.g. in the U.S. they might compare russet potatoes with new potatoes or purple potatoes, all different, but all part of the same species, S. tuberosum).

The other category of agricultural diversity is called interspecific diversity and refers to the number and types of different species. Thinking about this diversity we might note that many small vegetable farmers grow many different crops like potatoes and also carrots, peppers, lettuce etc.

Agricultural diversity can also be divided by whether it is ‘planned’ diversity or ‘associated’ diversity. This is a functional classification that we impose and not an intrinsic feature of life or diversity. Planned diversity includes the crops which a farmer has encouraged, planted or raised (e.g. crops, covers, symbionts and livestock, among others), which can be contrasted with the associated diversity that arrives among the crops, uninvited (e.g. herbivores, weed species and pathogens, among others).

The control of associated biodiversity is one of the great agricultural challenges that farmers face. On monoculture farms, the approach is generally to eradicate associated diversity using a suite of biologically destructive pesticides, mechanized tools and transgenic engineering techniques, then to rotate crops. Although some polyculture farmers use the same techniques, they also employ integrated pest management strategies as well as strategies that are more labor-intensive, but generally less dependent on capital, biotechnology and energy.

Interspecific crop diversity is, in part, responsible for offering variety in what we eat. Intraspecific diversity, the variety of alleles within a single species, also offers us choice in our diets. If a crop fails in a monoculture, we rely on agricultural diversity to replant the land with something new. If a wheat crop is destroyed by a pest we may plant a hardier variety of wheat the next year, relying on intraspecific diversity. We may forgo wheat production in that area and plant a different species altogether, relying on interspecific diversity. Even an agricultural society which primarily grows monocultures, relies on biodiversity at some point.
  • The Irish potato blight of 1846 was a major factor in the deaths of one million people and the emigration of about two million. It was the result of planting only two potato varieties, both vulnerable to the blight, Phytophthora infestans, which arrived in 1845
  • When rice grassy stunt virus struck rice fields from Indonesia to India in the 1970s, 6,273 varieties were tested for resistance. Only one was resistant, an Indian variety and known to science only since 1966. This variety formed a hybrid with other varieties and is now widely grown.
  • Coffee rust attacked coffee plantations in Sri Lanka, Brazil and Central America in 1970. A resistant variety was found in Ethiopia. The diseases are themselves a form of biodiversity.
Monoculture was a contributing factor to several agricultural disasters, including the European wine industry collapse in the late 19th century and the US southern corn leaf blight epidemic of 1970.
Although about 80 percent of humans' food supply comes from just 20 kinds of plants, humans use at least 40,000 species. Many people depend on these species for food, shelter and clothing. Earth's surviving biodiversity provides resources for increasing the range of food and other products suitable for human use, although the present extinction rate shrinks that potential.

Human health

The diverse forest canopy on Barro Colorado Island, Panama, yielded this display of different fruit
 
Biodiversity's relevance to human health is becoming an international political issue, as scientific evidence builds on the global health implications of biodiversity loss. This issue is closely linked with the issue of climate change, as many of the anticipated health risks of climate change are associated with changes in biodiversity (e.g. changes in populations and distribution of disease vectors, scarcity of fresh water, impacts on agricultural biodiversity and food resources etc.). This is because the species most likely to disappear are those that buffer against infectious disease transmission, while surviving species tend to be the ones that increase disease transmission, such as that of West Nile Virus, Lyme disease and Hantavirus, according to a study done co-authored by Felicia Keesing, an ecologist at Bard College and Drew Harvell, associate director for Environment of the Atkinson Center for a Sustainable Future (ACSF) at Cornell University.

The growing demand and lack of drinkable water on the planet presents an additional challenge to the future of human health. Partly, the problem lies in the success of water suppliers to increase supplies and failure of groups promoting preservation of water resources. While the distribution of clean water increases, in some parts of the world it remains unequal. According to the World Health Organisation (2018) only 71% of the global population used a safely managed drinking-water service.

Some of the health issues influenced by biodiversity include dietary health and nutrition security, infectious disease, medical science and medicinal resources, social and psychological health. Biodiversity is also known to have an important role in reducing disaster risk and in post-disaster relief and recovery efforts.

Biodiversity provides critical support for drug discovery and the availability of medicinal resources. A significant proportion of drugs are derived, directly or indirectly, from biological sources: at least 50% of the pharmaceutical compounds on the US market are derived from plants, animals and micro-organisms, while about 80% of the world population depends on medicines from nature (used in either modern or traditional medical practice) for primary healthcare. Only a tiny fraction of wild species has been investigated for medical potential. Biodiversity has been critical to advances throughout the field of bionics. Evidence from market analysis and biodiversity science indicates that the decline in output from the pharmaceutical sector since the mid-1980s can be attributed to a move away from natural product exploration ("bioprospecting") in favor of genomics and synthetic chemistry, indeed claims about the value of undiscovered pharmaceuticals may not provide enough incentive for companies in free markets to search for them because of the high cost of development; meanwhile, natural products have a long history of supporting significant economic and health innovation. Marine ecosystems are particularly important, although inappropriate bioprospecting can increase biodiversity loss, as well as violating the laws of the communities and states from which the resources are taken.

Business and industry

Agriculture production, pictured is a tractor and a chaser bin
 
Many industrial materials derive directly from biological sources. These include building materials, fibers, dyes, rubber and oil. Biodiversity is also important to the security of resources such as water, timber, paper, fiber and food. As a result, biodiversity loss is a significant risk factor in business development and a threat to long term economic sustainability.

Leisure, cultural and aesthetic value

Biodiversity enriches leisure activities such as hiking, birdwatching or natural history study. Biodiversity inspires musicians, painters, sculptors, writers and other artists. Many cultures view themselves as an integral part of the natural world which requires them to respect other living organisms. 

Popular activities such as gardening, fishkeeping and specimen collecting strongly depend on biodiversity. The number of species involved in such pursuits is in the tens of thousands, though the majority do not enter commerce.

The relationships between the original natural areas of these often exotic animals and plants and commercial collectors, suppliers, breeders, propagators and those who promote their understanding and enjoyment are complex and poorly understood. The general public responds well to exposure to rare and unusual organisms, reflecting their inherent value. 

Philosophically it could be argued that biodiversity has intrinsic aesthetic and spiritual value to mankind in and of itself. This idea can be used as a counterweight to the notion that tropical forests and other ecological realms are only worthy of conservation because of the services they provide.

Ecological services

Eagle Creek, Oregon hiking
 
Biodiversity supports many ecosystem services:
"There is now unequivocal evidence that biodiversity loss reduces the efficiency by which ecological communities capture biologically essential resources, produce biomass, decompose and recycle biologically essential nutrients... There is mounting evidence that biodiversity increases the stability of ecosystem functions through time... Diverse communities are more productive because they contain key species that have a large influence on productivity and differences in functional traits among organisms increase total resource capture... The impacts of diversity loss on ecological processes might be sufficiently large to rival the impacts of many other global drivers of environmental change... Maintaining multiple ecosystem processes at multiple places and times requires higher levels of biodiversity than does a single process at a single place and time."
It plays a part in regulating the chemistry of our atmosphere and water supply. Biodiversity is directly involved in water purification, recycling nutrients and providing fertile soils. Experiments with controlled environments have shown that humans cannot easily build ecosystems to support human needs; for example insect pollination cannot be mimicked, though there have been attempts to create artificial pollinators using unmanned aerial vehicles. The economic activity of pollination alone represented between $2.1-14.6 billions in 2003.

Number of species

Discovered and predicted total number of species on land and in the oceans
 
According to Mora and colleagues, the total number of terrestrial species is estimated to be around 8.7 million while the number of oceanic species is much lower, estimated at 2.2 million. The authors note that these estimates are strongest for eukaryotic organisms and likely represent the lower bound of prokaryote diversity. Other estimates include:
  • 220,000 vascular plants, estimated using the species-area relation method
  • 0.7-1 million marine species
  • 10–30 million insects; (of some 0.9 million we know today)
  • 5–10 million bacteria;
  • 1.5-3 million fungi, estimates based on data from the tropics, long-term non-tropical sites and molecular studies that have revealed cryptic speciation. Some 0.075 million species of fungi had been documented by 2001)
  • 1 million mites
  • The number of microbial species is not reliably known, but the Global Ocean Sampling Expedition dramatically increased the estimates of genetic diversity by identifying an enormous number of new genes from near-surface plankton samples at various marine locations, initially over the 2004-2006 period. The findings may eventually cause a significant change in the way science defines species and other taxonomic categories.
Since the rate of extinction has increased, many extant species may become extinct before they are described. Not surprisingly, in the animalia the most studied groups are birds and mammals, whereas fishes and arthropods are the least studied animals groups.

Measuring biodiversity

Species loss rates

No longer do we have to justify the existence of humid tropical forests on the feeble grounds that they might carry plants with drugs that cure human disease. Gaia theory forces us to see that they offer much more than this. Through their capacity to evapotranspirate vast volumes of water vapor, they serve to keep the planet cool by wearing a sunshade of white reflecting cloud. Their replacement by cropland could precipitate a disaster that is global in scale.
During the last century, decreases in biodiversity have been increasingly observed. In 2007, German Federal Environment Minister Sigmar Gabriel cited estimates that up to 30% of all species will be extinct by 2050. Of these, about one eighth of known plant species are threatened with extinction. Estimates reach as high as 140,000 species per year (based on Species-area theory). This figure indicates unsustainable ecological practices, because few species emerge each year. Almost all scientists acknowledge that the rate of species loss is greater now than at any time in human history, with extinctions occurring at rates hundreds of times higher than background extinction rates. As of 2012, some studies suggest that 25% of all mammal species could be extinct in 20 years.

In absolute terms, the planet has lost 58% of its biodiversity since 1970 according to a 2016 study by the World Wildlife Fund. The Living Planet Report 2014 claims that "the number of mammals, birds, reptiles, amphibians and fish across the globe is, on average, about half the size it was 40 years ago". Of that number, 39% accounts for the terrestrial wildlife gone, 39% for the marine wildlife gone and 76% for the freshwater wildlife gone. Biodiversity took the biggest hit in Latin America, plummeting 83 percent. High-income countries showed a 10% increase in biodiversity, which was canceled out by a loss in low-income countries. This is despite the fact that high-income countries use five times the ecological resources of low-income countries, which was explained as a result of process whereby wealthy nations are outsourcing resource depletion to poorer nations, which are suffering the greatest ecosystem losses.

A 2017 study published in PLOS One found that the biomass of insect life in Germany had declined by three-quarters in the last 25 years. Dave Goulson of Sussex University stated that their study suggested that humans "appear to be making vast tracts of land inhospitable to most forms of life, and are currently on course for ecological Armageddon. If we lose the insects then everything is going to collapse."

Threats

In 2006, many species were formally classified as rare or endangered or threatened; moreover, scientists have estimated that millions more species are at risk which have not been formally recognized. About 40 percent of the 40,177 species assessed using the IUCN Red List criteria are now listed as threatened with extinction—a total of 16,119.

Jared Diamond describes an "Evil Quartet" of habitat destruction, overkill, introduced species and secondary extinctions. Edward O. Wilson prefers the acronym HIPPO, standing for Habitat destruction, Invasive species, Pollution, human over-Population and Over-harvesting. The most authoritative classification in use today is IUCN's Classification of Direct Threats (version 2.0 released in 2016) which has been adopted by major international conservation organizations such as the US Nature Conservancy, the World Wildlife Fund, Conservation International and BirdLife International.
The 11 main direct threats to conservation are: 

1. residential & commercial development
  • housing & urban areas (urban areas, suburbs, villages, vacation homes, shopping areas, offices, schools, hospitals)
  • commercial & industrial areas (manufacturing plants, shopping centers, office parks, military bases, power plants, train & ship yards, airports)
  • tourism & recreational areas (skiing, golf courses, sports fields, parks, campgrounds)
2. farming activities
  • agriculture (crop farms, orchards, vineyards, plantations, ranches)
  • aquaculture (shrimp or fin fish aquaculture, fish ponds on farms, hatchery salmon, seeded shellfish beds, artificial algal beds)
3. energy production & mining
  • renewable energy production (geothermal, solar, wind, & tidal farms)
  • non-renewable energy production (oil and gas drilling)
  • mining (fuel and minerals)
4. transportation & service corridors
  • service corridors (electrical & phone wires, aqueducts, oil & gas pipelines)
  • transport corridors (roads, railroads, shipping lanes, and flight paths)
  • collisions with the vehicles using the corridors
  • associated accidents and catastrophes (oil spills, electrocution, fire)
5. biological resource usages
  • hunting (bushmeat, trophy, fur)
  • persecution (predator control and pest control, superstitions)
  • plant destruction or removal (human consumption, free range livestock foraging, battling timber disease, orchid collection)
  • logging or wood harvesting (selective or clear cutting, firewood collection, charcoal production)
  • fishing (trawling, whaling, live coral or seaweed or egg collection)
6. human intrusions & activities that alter, destroy, simply disturb habitats and species from exhibiting natural behaviors
  • recreational activities (off-road vehicles, motorboats, jet-skis, snowmobiles, ultralight planes, dive boats, whale watching, mountain bikes, hikers, birdwatchers, skiers, pets in recreational areas, temporary campsites, caving, rock-climbing)
  • war, civil unrest, & military exercises (armed conflict, mine fields, tanks & other military vehicles, training exercises & ranges, defoliation, munitions testing)
  • illegal activities (smuggling, immigration, vandalism)
7. natural system modifications
  • fire suppression or creation (controlled burns, inappropriate fire management, escaped agricultural and campfires, arson)
  • water management (dam construction & operation, wetland filling, surface water diversion, groundwater pumping)
  • other modifications (reclamation projects, shoreline rip-rap, lawn cultivation, beach construction and maintenance, tree-thinning in parks)
  • removing/reducing human maintenance (mowing meadows, reduction in controlled burns, lack of indigenous management of key ecosystems, ceasing supplemental feeding of condors)
8. invasive & problematic species, pathogens & genes
  • invasive species (feral horses & household pets, zebra mussels, Miconia tree, kudzu, introduction for biocontrol)
  • problematic native species (overabundant native deer or kangaroo, overabundant algae due to loss of native grazing fish, locust-type plagues)
  • introduced genetic material (pesticide-resistant crops, genetically modified insects for biocontrol, genetically modified trees or salmon, escaped hatchery salmon, restoration projects using non-local seed stock)
  • pathogens & microbes (plague affecting rodents or rabbits, Dutch elm disease or chestnut blight, Chytrid fungus affecting amphibians outside of Africa)
9. pollution
  • household sewage & urban waste water (discharge from municipal waste treatment plants, leaking septic systems, untreated sewage, outhouses, oil or sediment from roads, fertilizers and pesticides from lawns and golf-courses, road salt)
  • industrial & military effluents (toxic chemicals from factories, illegal dumping of chemicals, mine tailings, arsenic from gold mining, leakage from fuel tanks, PCBs in river sediments)
  • agricultural & forestry effluents (nutrient loading from fertilizer run-off, herbicide run-off, manure from feedlots, nutrients from aquaculture, soil erosion)
  • garbage & solid waste (municipal waste, litter & dumped possessions, flotsam & jetsam from recreational boats, waste that entangles wildlife, construction debris)
  • air-borne pollutants (acid rain, smog from vehicle emissions, excess nitrogen deposition, radioactive fallout, wind dispersion of pollutants or sediments from farm fields, smoke from forest fires or wood stoves)
  • excess energy (noise from highways or airplanes, sonar from submarines that disturbs whales, heated water from power plants, lamps attracting insects, beach lights disorienting turtles, atmospheric radiation from ozone holes)
10. catastrophic geological events
  • earthquakes, tsunamis, avalanches, landslides, & volcanic eruptions and gas emissions
11. climate changes
  • ecosystem encroachment (inundation of shoreline ecosystems & drowning of coral reefs from sea level rise, sand dune encroachment from desertification)
  • changes in geochemical regimes (ocean acidification, changes in atmospheric CO2 affecting plant growth, loss of sediment leading to broad-scale subsidence)
  • changes in temperature regimes (heat waves, cold spells, oceanic temperature changes, melting of glaciers/sea ice)
  • changes in precipitation & hydrological regimes (droughts, rain timing, loss of snowcover, increased severity of floods)
  • severe weather events (thunderstorms, tropical storms, hurricanes, cyclones, tornadoes, hailstorms, ice storms or blizzards, dust storms, erosion of beaches during storms)

Habitat destruction

Deforestation and increased road-building in the Amazon Rainforest cause significant concern because of increased human encroachment upon wild areas, increased resource extraction and further threats to biodiversity.

Habitat destruction has played a key role in extinctions, especially in relation to tropical forest destruction. Factors contributing to habitat loss include: overconsumption, overpopulation, land use change, deforestation, pollution (air pollution, water pollution, soil contamination) and global warming or climate change.

Habitat size and numbers of species are systematically related. Physically larger species and those living at lower latitudes or in forests or oceans are more sensitive to reduction in habitat area. Conversion to "trivial" standardized ecosystems (e.g., monoculture following deforestation) effectively destroys habitat for the more diverse species that preceded the conversion. Even the simplest forms of agriculture affect diversity – through clearing/draining land, discouraging weeds and "pests", and encouraging just a limited set of domesticated plant and animal species. In some countries lack of property rights or lax law/regulatory enforcement necessarily leads to biodiversity loss (degradation costs having to be supported by the community).

A 2007 study conducted by the National Science Foundation found that biodiversity and genetic diversity are codependent—that diversity among species requires diversity within a species and vice versa. "If any one type is removed from the system, the cycle can break down and the community becomes dominated by a single species." At present, the most threatened ecosystems occur in fresh water, according to the Millennium Ecosystem Assessment 2005, which was confirmed by the "Freshwater Animal Diversity Assessment" organised by the biodiversity platform and the French Institut de recherche pour le développement (MNHNP).

Co-extinctions are a form of habitat destruction. Co-extinction occurs when the extinction or decline in one species accompanies similar processes in another, such as in plants and beetles.

A 2019 report has revealed that bees and other pollinating insects have been wiped out of almost a quarter of their habitats across the United Kingdom. The population crashes have been happening since 1980s and are affecting the biodiversity. The increase in industrial farming and pesticide use, combined with disease, invasive species and climate change is threatening the future of these insects and the agriculture they support.

Introduced and invasive species

Male Lophura nycthemera (silver pheasant), a native of East Asia that has been introduced into parts of Europe for ornamental reasons
 
Barriers such as large rivers, seas, oceans, mountains and deserts encourage diversity by enabling independent evolution on either side of the barrier, via the process of allopatric speciation. The term invasive species is applied to species that breach the natural barriers that would normally keep them constrained. Without barriers, such species occupy new territory, often supplanting native species by occupying their niches, or by using resources that would normally sustain native species. 

The number of species invasions has been on the rise at least since the beginning of the 1900s. Species are increasingly being moved by humans (on purpose and accidentally). In some cases the invaders are causing drastic changes and damage to their new habitats (e.g.: zebra mussels and the emerald ash borer in the Great Lakes region and the lion fish along the North American Atlantic coast). Some evidence suggests that invasive species are competitive in their new habitats because they are subject to less pathogen disturbance. Others report confounding evidence that occasionally suggest that species-rich communities harbor many native and exotic species simultaneously while some say that diverse ecosystems are more resilient and resist invasive plants and animals. An important question is, "do invasive species cause extinctions?" Many studies cite effects of invasive species on natives, but not extinctions. Invasive species seem to increase local (i.e.: alpha diversity) diversity, which decreases turnover of diversity (i.e.: beta diversity). Overall gamma diversity may be lowered because species are going extinct because of other causes, but even some of the most insidious invaders (e.g.: Dutch elm disease, emerald ash borer, chestnut blight in North America) have not caused their host species to become extinct. Extirpation, population decline and homogenization of regional biodiversity are much more common. Human activities have frequently been the cause of invasive species circumventing their barriers, by introducing them for food and other purposes. Human activities therefore allow species to migrate to new areas (and thus become invasive) occurred on time scales much shorter than historically have been required for a species to extend its range.

Not all introduced species are invasive, nor all invasive species deliberately introduced. In cases such as the zebra mussel, invasion of US waterways was unintentional. In other cases, such as mongooses in Hawaii, the introduction is deliberate but ineffective (nocturnal rats were not vulnerable to the diurnal mongoose). In other cases, such as oil palms in Indonesia and Malaysia, the introduction produces substantial economic benefits, but the benefits are accompanied by costly unintended consequences

Finally, an introduced species may unintentionally injure a species that depends on the species it replaces. In Belgium, Prunus spinosa from Eastern Europe leafs much sooner than its West European counterparts, disrupting the feeding habits of the Thecla betulae butterfly (which feeds on the leaves). Introducing new species often leaves endemic and other local species unable to compete with the exotic species and unable to survive. The exotic organisms may be predators, parasites, or may simply outcompete indigenous species for nutrients, water and light.

At present, several countries have already imported so many exotic species, particularly agricultural and ornamental plants, that their own indigenous fauna/flora may be outnumbered. For example, the introduction of kudzu from Southeast Asia to Canada and the United States has threatened biodiversity in certain areas.

Genetic pollution

Endemic species can be threatened with extinction through the process of genetic pollution, i.e. uncontrolled hybridization, introgression and genetic swamping. Genetic pollution leads to homogenization or replacement of local genomes as a result of either a numerical and/or fitness advantage of an introduced species. Hybridization and introgression are side-effects of introduction and invasion. These phenomena can be especially detrimental to rare species that come into contact with more abundant ones. The abundant species can interbreed with the rare species, swamping its gene pool. This problem is not always apparent from morphological (outward appearance) observations alone. Some degree of gene flow is normal adaptation and not all gene and genotype constellations can be preserved. However, hybridization with or without introgression may, nevertheless, threaten a rare species' existence.

Overexploitation

Overexploitation occurs when a resource is consumed at an unsustainable rate. This occurs on land in the form of overhunting, excessive logging, poor soil conservation in agriculture and the illegal wildlife trade

About 25% of world fisheries are now overfished to the point where their current biomass is less than the level that maximizes their sustainable yield.

The overkill hypothesis, a pattern of large animal extinctions connected with human migration patterns, can be used explain why megafaunal extinctions can occur within a relatively short time period.

Hybridization, genetic pollution/erosion and food security

The Yecoro wheat (right) cultivar is sensitive to salinity, plants resulting from a hybrid cross with cultivar W4910 (left) show greater tolerance to high salinity

In agriculture and animal husbandry, the Green Revolution popularized the use of conventional hybridization to increase yield. Often hybridized breeds originated in developed countries and were further hybridized with local varieties in the developing world to create high yield strains resistant to local climate and diseases. Local governments and industry have been pushing hybridization. Formerly huge gene pools of various wild and indigenous breeds have collapsed causing widespread genetic erosion and genetic pollution. This has resulted in loss of genetic diversity and biodiversity as a whole.

Genetically modified organisms contain genetic material that is altered through genetic engineering. Genetically modified crops have become a common source for genetic pollution in not only wild varieties, but also in domesticated varieties derived from classical hybridization.

Genetic erosion and genetic pollution have the potential to destroy unique genotypes, threatening future access to food security. A decrease in genetic diversity weakens the ability of crops and livestock to be hybridized to resist disease and survive changes in climate.

Climate change

Polar bears on the sea ice of the Arctic Ocean, near the North Pole. Climate change has started affecting bear populations.
 
Global warming is also considered to be a major potential threat to global biodiversity in the future. For example, coral reefs – which are biodiversity hotspots – will be lost within the century if global warming continues at the current trend.

Climate change has seen many claims about potential to affect biodiversity but evidence supporting the statement is tenuous. Increasing atmospheric carbon dioxide certainly affects plant morphology and is acidifying oceans, and temperature affects species ranges, phenology, and weather, but the major impacts that have been predicted are still just potential impacts. We have not documented major extinctions yet, even as climate change drastically alters the biology of many species. 

In 2004, an international collaborative study on four continents estimated that 10 percent of species would become extinct by 2050 because of global warming. "We need to limit climate change or we wind up with a lot of species in trouble, possibly extinct," said Dr. Lee Hannah, a co-author of the paper and chief climate change biologist at the Center for Applied Biodiversity Science at Conservation International.

A recent study predicts that up to 35% of the world terrestrial carnivores and ungulates will be at higher risk of extinction by 2050 because of the joint effects of predicted climate and land-use change under business-as-usual human development scenarios.

Human overpopulation

The world's population numbered nearly 7.6 billion as of mid-2017 (which is approximately one billion more inhabitants compared to 2005) and is forecast to reach 11.1 billion in 2100. Sir David King, former chief scientific adviser to the UK government, told a parliamentary inquiry: "It is self-evident that the massive growth in the human population through the 20th century has had more impact on biodiversity than any other single factor." At least until the middle of the 21st century, worldwide losses of pristine biodiverse land will probably depend much on the worldwide human birth rate. Biologists such as Paul R. Ehrlich and Stuart Pimm have noted that human population growth and overconsumption are the main drivers of species extinction.

According to a 2014 study by the World Wildlife Fund, the global human population already exceeds planet's biocapacity – it would take the equivalent of 1.5 Earths of biocapacity to meet our current demands. The report further points that if everyone on the planet had the Footprint of the average resident of Qatar, we would need 4.8 Earths and if we lived the lifestyle of a typical resident of the US, we would need 3.9 Earths.

The Holocene extinction

Rates of decline in biodiversity in this sixth mass extinction match or exceed rates of loss in the five previous mass extinction events in the fossil record. Loss of biodiversity results in the loss of natural capital that supplies ecosystem goods and services. From the perspective of the method known as Natural Economy the economic value of 17 ecosystem services for Earth's biosphere (calculated in 1997) has an estimated value of US$33 trillion (3.3x1013) per year.

Conservation

A schematic image illustrating the relationship between biodiversity, ecosystem services, human well-being and poverty. The illustration shows where conservation action, strategies and plans can influence the drivers of the current biodiversity crisis at local, regional, to global scales.
 
The retreat of Aletsch Glacier in the Swiss Alps (situation in 1979, 1991 and 2002), due to global warming.
 
Conservation biology matured in the mid-20th century as ecologists, naturalists and other scientists began to research and address issues pertaining to global biodiversity declines.

The conservation ethic advocates management of natural resources for the purpose of sustaining biodiversity in species, ecosystems, the evolutionary process and human culture and society.

Conservation biology is reforming around strategic plans to protect biodiversity. Preserving global biodiversity is a priority in strategic conservation plans that are designed to engage public policy and concerns affecting local, regional and global scales of communities, ecosystems and cultures. Action plans identify ways of sustaining human well-being, employing natural capital, market capital and ecosystem services.

In the EU Directive 1999/22/EC zoos are described as having a role in the preservation of the biodiversity of wildlife animals by conducting research or participation in breeding programs.

Protection and restoration techniques

Removal of exotic species will allow the species that they have negatively impacted to recover their ecological niches. Exotic species that have become pests can be identified taxonomically (e.g., with Digital Automated Identification SYstem (DAISY), using the barcode of life). Removal is practical only given large groups of individuals due to the economic cost. 

As sustainable populations of the remaining native species in an area become assured, "missing" species that are candidates for reintroduction can be identified using databases such as the Encyclopedia of Life and the Global Biodiversity Information Facility.
  • Biodiversity banking places a monetary value on biodiversity. One example is the Australian Native Vegetation Management Framework.
  • Gene banks are collections of specimens and genetic material. Some banks intend to reintroduce banked species to the ecosystem (e.g., via tree nurseries).
  • Reduction and better targeting of pesticides allows more species to survive in agricultural and urbanized areas.
  • Location-specific approaches may be less useful for protecting migratory species. One approach is to create wildlife corridors that correspond to the animals' movements. National and other boundaries can complicate corridor creation.

Protected areas

Protected areas are meant for affording protection to wild animals and their habitat which also includes forest reserves and biosphere reserves. Protected areas have been set up all over the world with the specific aim of protecting and conserving plants and animals. Some scientists have called on the global community to designate as protected areas 30 percent of the planet by 2030, and 50 percent by 2050, in order to mitigate biodiversity loss from anthropogenic causes.

National parks

National park and nature reserve is the area selected by governments or private organizations for special protection against damage or degradation with the objective of biodiversity and landscape conservation. National parks are usually owned and managed by national or state governments. A limit is placed on the number of visitors permitted to enter certain fragile areas. Designated trails or roads are created. The visitors are allowed to enter only for study, cultural and recreation purposes. Forestry operations, grazing of animals and hunting of animals are regulated. Exploitation of habitat or wildlife is banned.

Wildlife sanctuary

Wildlife sanctuaries aim only at conservation of species and have the following features:
  1. The boundaries of the sanctuaries are not limited by state legislation.
  2. The killing, hunting or capturing of any species is prohibited except by or under the control of the highest authority in the department which is responsible for the management of the sanctuary.
  3. Private ownership may be allowed.
  4. Forestry and other usages can also be permitted.

Forest reserves

The forests play a vital role in harbouring more than 45,000 floral and 81,000 faunal species of which 5150 floral and 1837 faunal species are endemic. Plant and animal species confined to a specific geographical area are called endemic species. In reserved forests, rights to activities like hunting and grazing are sometimes given to communities living on the fringes of the forest, who sustain their livelihood partially or wholly from forest resources or products. The unclassed forests covers 6.4 percent of the total forest area and they are marked by the following characteristics:
  1. They are large inaccessible forests.
  2. Many of these are unoccupied.
  3. They are ecologically and economically less important.

Steps to conserve the forest cover

  1. An extensive reforestation/afforestation programme should be followed.
  2. Alternative environment-friendly sources of fuel energy such as biogas other than wood should be used.
  3. Loss of biodiversity due to forest fire is a major problem, immediate steps to prevent forest fire need to be taken.
  4. Overgrazing by cattle can damage a forest seriously. Therefore, certain steps should be taken to prevent overgrazing by cattle.
  5. Hunting and poaching should be banned.

Zoological parks

In zoological parks or zoos, live animals are kept for public recreation, education and conservation purposes. Modern zoos offer veterinary facilities, provide opportunities for threatened species to breed in captivity and usually build environments that simulate the native habitats of the animals in their care. Zoos play a major role in creating awareness about the need to conserve nature.

Botanical gardens

In botanical gardens, plants are grown and displayed primarily for scientific and educational purposes. They consist of a collection of living plants, grown outdoors or under glass in greenhouses and conservatories. In addition, a botanical garden may include a collection of dried plants or herbarium and such facilities as lecture rooms, laboratories, libraries, museums and experimental or research plantings.

Resource allocation

Focusing on limited areas of higher potential biodiversity promises greater immediate return on investment than spreading resources evenly or focusing on areas of little diversity but greater interest in biodiversity.

A second strategy focuses on areas that retain most of their original diversity, which typically require little or no restoration. These are typically non-urbanized, non-agricultural areas. Tropical areas often fit both criteria, given their natively high diversity and relative lack of development.

Legal status

A great deal of work is occurring to preserve the natural characteristics of Hopetoun Falls, Australia while continuing to allow visitor access.

International

Global agreements such as the Convention on Biological Diversity, give "sovereign national rights over biological resources" (not property). The agreements commit countries to "conserve biodiversity", "develop resources for sustainability" and "share the benefits" resulting from their use. Biodiverse countries that allow bioprospecting or collection of natural products, expect a share of the benefits rather than allowing the individual or institution that discovers/exploits the resource to capture them privately. Bioprospecting can become a type of biopiracy when such principles are not respected.

Sovereignty principles can rely upon what is better known as Access and Benefit Sharing Agreements (ABAs). The Convention on Biodiversity implies informed consent between the source country and the collector, to establish which resource will be used and for what and to settle on a fair agreement on benefit sharing.

National level laws

Biodiversity is taken into account in some political and judicial decisions:
  • The relationship between law and ecosystems is very ancient and has consequences for biodiversity. It is related to private and public property rights. It can define protection for threatened ecosystems, but also some rights and duties (for example, fishing and hunting rights).
  • Law regarding species is more recent. It defines species that must be protected because they may be threatened by extinction. The U.S. Endangered Species Act is an example of an attempt to address the "law and species" issue.
  • Laws regarding gene pools are only about a century old. Domestication and plant breeding methods are not new, but advances in genetic engineering have led to tighter laws covering distribution of genetically modified organisms, gene patents and process patents. Governments struggle to decide whether to focus on for example, genes, genomes, or organisms and species.
Uniform approval for use of biodiversity as a legal standard has not been achieved, however. Bosselman argues that biodiversity should not be used as a legal standard, claiming that the remaining areas of scientific uncertainty cause unacceptable administrative waste and increase litigation without promoting preservation goals.

India passed the Biological Diversity Act in 2002 for the conservation of biological diversity in India. The Act also provides mechanisms for equitable sharing of benefits from the use of traditional biological resources and knowledge.

Analytical limits

Taxonomic and size relationships

Less than 1% of all species that have been described have been studied beyond simply noting their existence. The vast majority of Earth's species are microbial. Contemporary biodiversity physics is "firmly fixated on the visible [macroscopic] world". For example, microbial life is metabolically and environmentally more diverse than multicellular life (see e.g., extremophile). "On the tree of life, based on analyses of small-subunit ribosomal RNA, visible life consists of barely noticeable twigs. The inverse relationship of size and population recurs higher on the evolutionary ladder—to a first approximation, all multicellular species on Earth are insects". Insect extinction rates are high—supporting the Holocene extinction hypothesis.

Diversity study (botany)

The number of morphological attributes that can be scored for diversity study is generally limited and prone to environmental influences; thereby reducing the fine resolution required to ascertain the phylogenetic relationships. DNA based markers- microsatellites otherwise known as simple sequence repeats (SSR) were therefore used for the diversity studies of certain species and their wild relatives.

In the case of cowpea, a study conducted to assess the level of genetic diversity in cowpea germplasm and related wide species, where the relatedness among various taxa were compared, primers useful for classification of taxa identified, and the origin and phylogeny of cultivated cowpea classified show that SSR markers are useful in validating with species classification and revealing the center of diversity.

Sunday, July 14, 2019

Sexual selection

From Wikipedia, the free encyclopedia

Sexual selection creates colourful differences between sexes (sexual dimorphism) in Goldie's bird-of-paradise. Male above; female below. Painting by John Gerrard Keulemans (d.1912)
 
Sexual selection is a form of natural selection where one sex prefers a specific characteristic in an individual of the other sex. Peafowls exhibit sexual selection, in that, peahens look for peacocks with more "eyes" on their tail feathers. This results in the peacocks with more eyes reproducing more, leading to peacocks with more eyes becoming more common in subsequent generations.
 
Sexual selection is a mode of natural selection where members of one biological sex choose mates of the other sex to mate with (intersexual selection), and compete with members of the same sex for access to members of the opposite sex (intrasexual selection). These two forms of selection mean that some individuals have better reproductive success than others within a population, either from being more attractive or preferring more attractive partners to produce offspring. For instance, in the breeding season, sexual selection in frogs occurs with the males first gathering at the water's edge and making their mating calls: croaking. The females then arrive and choose the males with the deepest croaks and best territories. In general, males benefit from frequent mating and monopolizing access to a group of fertile females. Females can have a limited number of offspring and maximize the return on the energy they invest in reproduction. 

The concept was first articulated by Charles Darwin and Alfred Russel Wallace who described it as driving species adaptations and that many organisms had evolved features whose function was deleterious to their individual survival, and then developed by Ronald Fisher in the early 20th century. Sexual selection can, typically, lead males to extreme efforts to demonstrate their fitness to be chosen by females, producing sexual dimorphism in secondary sexual characteristics, such as the ornate plumage of birds such as birds of paradise and peafowl, or the antlers of deer, or the manes of lions, caused by a positive feedback mechanism known as a Fisherian runaway, where the passing-on of the desire for a trait in one sex is as important as having the trait in the other sex in producing the runaway effect. Although the sexy son hypothesis indicates that females would prefer male offspring, Fisher's principle explains why the sex ratio is 1:1 almost without exception. Sexual selection is also found in plants and fungi.

The maintenance of sexual reproduction in a highly competitive world is one of the major puzzles in biology given that asexual reproduction can reproduce much more quickly as 50% of offspring are not males, unable to produce offspring themselves. Many non-exclusive hypotheses have been proposed, including the positive impact of an additional form of selection, sexual selection, on the probability of persistence of a species.

History

Darwin

Sexual selection was first proposed by Charles Darwin in The Origin of Species (1859) and developed in The Descent of Man and Selection in Relation to Sex (1871), as he felt that natural selection alone was unable to account for certain types of non-survival adaptations. He once wrote to a colleague that "The sight of a feather in a peacock's tail, whenever I gaze at it, makes me sick!" His work divided sexual selection into male-male competition and female choice.
... depends, not on a struggle for existence, but on a struggle between the males for possession of the females; the result is not death to the unsuccessful competitor, but few or no offspring.
... when the males and females of any animal have the same general habits ... but differ in structure, colour, or ornament, such differences have been mainly caused by sexual selection.
These views were to some extent opposed by Alfred Russel Wallace, mostly after Darwin's death. He accepted that sexual selection could occur, but argued that it was a relatively weak form of selection. He argued that male-male competitions were forms of natural selection, but that the "drab" peahen's coloration is itself adaptive as camouflage. In his opinion, ascribing mate choice to females was attributing the ability to judge standards of beauty to animals (such as beetles) far too cognitively undeveloped to be capable of aesthetic feeling.

Ronald Fisher

Ronald Fisher, the English statistician and evolutionary biologist developed a number of ideas about sexual selection in his 1930 book The Genetical Theory of Natural Selection including the sexy son hypothesis and Fisher's principle. The Fisherian runaway describes how sexual selection accelerates the preference for a specific ornament, causing the preferred trait and female preference for it to increase together in a positive feedback runaway cycle. In a remark that was not widely understood for another 50 years he said:
... plumage development in the male, and sexual preference for such developments in the female, must thus advance together, and so long as the process is unchecked by severe counterselection, will advance with ever-increasing speed. In the total absence of such checks, it is easy to see that the speed of development will be proportional to the development already attained, which will therefore increase with time exponentially, or in geometric progression. —Ronald Fisher, 1930
This causes a dramatic increase in both the male's conspicuous feature and in female preference for it, resulting in marked sexual dimorphism, until practical physical constraints halt further exaggeration. A positive feedback loop is created, producing extravagant physical structures in the non-limiting sex. A classic example of female choice and potential runaway selection is the long-tailed widowbird. While males have long tails that are selected for by female choice, female tastes in tail length are still more extreme with females being attracted to tails longer than those that naturally occur. Fisher understood that female preference for long tails may be passed on genetically, in conjunction with genes for the long tail itself. Long-tailed widowbird offspring of both sexes inherit both sets of genes, with females expressing their genetic preference for long tails, and males showing off the coveted long tail itself.

Richard Dawkins presents a non-mathematical explanation of the runaway sexual selection process in his book The Blind Watchmaker. Females that prefer long tailed males tend to have mothers that chose long-tailed fathers. As a result, they carry both sets of genes in their bodies. That is, genes for long tails and for preferring long tails become linked. The taste for long tails and tail length itself may therefore become correlated, tending to increase together. The more tails lengthen, the more long tails are desired. Any slight initial imbalance between taste and tails may set off an explosion in tail lengths. Fisher wrote that:
The exponential element, which is the kernel of the thing, arises from the rate of change in hen taste being proportional to the absolute average degree of taste. —Ronald Fisher, 1932
The peacock tail in flight, the classic example of a Fisherian runaway
 
The female widow bird chooses to mate with the most attractive long-tailed male so that her progeny, if male, will themselves be attractive to females of the next generation - thereby fathering many offspring that carry the female's genes. Since the rate of change in preference is proportional to the average taste amongst females, and as females desire to secure the services of the most sexually attractive males, an additive effect is created that, if unchecked, can yield exponential increases in a given taste and in the corresponding desired sexual attribute.
It is important to notice that the conditions of relative stability brought about by these or other means, will be far longer duration than the process in which the ornaments are evolved. In most existing species the runaway process must have been already checked, and we should expect that the more extraordinary developments of sexual plumage are not due like most characters to a long and even course of evolutionary progress, but to sudden spurts of change. —Ronald Fisher, 1930
Since Fisher's initial conceptual model of the 'runaway' process, Russell Lande and Peter O'Donald have provided detailed mathematical proofs that define the circumstances under which runaway sexual selection can take place.

Theory

Reproductive success

Extinct Irish elk (Megaloceros giganteus). These antlers span 2.7 metres (8.9 ft) and have a mass of 40 kg (88 lb).
 
The reproductive success of an organism is measured by the number of offspring left behind, and their quality or probable fitness

Sexual preference creates a tendency towards assortative mating or homogamy. The general conditions of sexual discrimination appear to be (1) the acceptance of one mate precludes the effective acceptance of alternative mates, and (2) the rejection of an offer is followed by other offers, either certainly or at such high chance that the risk of non-occurrence is smaller than the chance advantage to be gained by selecting a mate.

The conditions determining which sex becomes the more limited resource in intersexual selection have been hypothesized with Bateman's principle, which states that the sex which invests the most in producing offspring becomes a limiting resource for which the other sex competes, illustrated by the greater nutritional investment of an egg in a zygote, and the limited capacity of females to reproduce; for example, in humans, a woman can only give birth every ten months, whereas a male can become a father numerous times in the same period.

Modern interpretation

Male mountain gorilla, a tournament species
 
The sciences of evolutionary psychology, human behavioural ecology, and sociobiology study the influence of sexual selection in humans. 

Darwin's ideas on sexual selection were met with scepticism by his contemporaries and not considered of great importance in the early 20th century, until in the 1930s biologists decided to include sexual selection as a mode of natural selection. Only in the 21st century have they become more important in biology. The theory however is generally applicable and analogous to natural selection.

Flour beetle
 
Tungara frog
 
Research in 2015 indicates that sexual selection, including mate choice, "improves population health and protects against extinction, even in the face of genetic stress from high levels of inbreeding" and "ultimately dictates who gets to reproduce their genes into the next generation - so it's a widespread and very powerful evolutionary force." The study involved the flour beetle over a ten-year period where the only changes were in the intensity of sexual selection.

Another theory, the handicap principle of Amotz Zahavi, Russell Lande and W. D. Hamilton, holds that the fact that the male is able to survive until and through the age of reproduction with such a seemingly maladaptive trait is taken by the female to be a testament to his overall fitness. Such handicaps might prove he is either free of or resistant to disease, or that he possesses more speed or a greater physical strength that is used to combat the troubles brought on by the exaggerated trait. Zahavi's work spurred a re-examination of the field, which has produced an ever-accelerating number of theories. In 1984, Hamilton and Marlene Zuk introduced the "Bright Male" hypothesis, suggesting that male elaborations might serve as a marker of health, by exaggerating the effects of disease and deficiency. In 1990, Michael Ryan and A.S. Rand, working with the tungara frog, proposed the hypothesis of "Sensory Exploitation", where exaggerated male traits may provide a sensory stimulation that females find hard to resist. Subsequently, the theories of the "Gravity Hypothesis" by Jordi Moya-Larano et al. (2002), invoking a simple biomechanical model to account for the adaptive value for smaller male spiders of speed in clmbing vertical surfaces, and "Chase Away" by Brett Holland and William R. Rice have been added. In the late 1970s, Janzen and Mary Willson, noting that male flowers are often larger than female flowers, expanded the field of sexual selection into plants.

In the past few years, the field has exploded to include other areas of study, not all of which fit Darwin's definition of sexual selection. These include cuckoldry, nuptial gifts, sperm competition, infanticide (especially in primates), physical beauty, mating by subterfuge, species isolation mechanisms, male parental care, ambiparental care, mate location, polygamy, and homosexual rape in certain male animals. 

Focusing on the effect of sexual conflict, as hypothesized by William Rice, Locke Rowe et Göran Arnvist, Thierry Lodé argues that divergence of interest constitutes a key for evolutionary process. Sexual conflict leads to an antagonistic co-evolution in which one sex tends to control the other, resulting in a tug of war. Besides, the sexual propaganda theory only argued that mates were opportunistically led, on the basis of various factors determining the choice such as phenotypic characteristics, apparent vigour of individuals, strength of mate signals, trophic resources, territoriality, etc., but and could explain the maintenance of genetic diversity within populations.

Several workers have brought attention to the fact that elaborated characters that ought to be costly in one way or another for their bearers (e.g., the tails of some species of Xiphophorus fish) do not always appear to have a cost in terms of energetics, performance or even survival. One possible explanation for the apparent lack of costs is that "compensatory traits" have evolved in concert with the sexually selected traits.

Toolkit of natural selection

Protarchaeopteryx - skull based on Incisivosaurus and wings on Caudipteryx
 
Sexual selection may explain how certain characteristics (such as feathers) had distinct survival value at an early stage in their evolution. Geoffrey Miller proposes that sexual selection might have contributed by creating evolutionary modules such as Archaeopteryx feathers as sexual ornaments, at first. The earliest proto-birds such as China's Protarchaeopteryx, discovered in the early 1990s, had well-developed feathers but no sign of the top/bottom asymmetry that gives wings lift. Some have suggested that the feathers served as insulation, helping females incubate their eggs. But perhaps the feathers served as the kinds of sexual ornaments still common in most bird species, and especially in birds such as peacocks and birds-of-paradise today. If proto-bird courtship displays combined displays of forelimb feathers with energetic jumps, then the transition from display to aerodynamic functions could have been relatively smooth.

Sexual selection sometimes generates features that may help cause a species' extinction, as has been suggested for the giant antlers of the Irish elk (Megaloceros giganteus) that became extinct in Pleistocene Europe. However, sexual selection can also do the opposite, driving species divergence - sometimes through elaborate changes in genitalia - such that new species emerge.

Sexual dimorphism

Sex differences directly related to reproduction and serving no direct purpose in courtship are called primary sexual characteristics. Traits amenable to sexual selection, which give an organism an advantage over its rivals (such as in courtship) without being directly involved in reproduction, are called secondary sex characteristics

The rhinoceros beetle is a classic case of sexual dimorphism. Plate from Darwin's Descent of Man, male at top, female at bottom
 
In most sexual species the males and females have different equilibrium strategies, due to a difference in relative investment in producing offspring. As formulated in Bateman's principle, females have a greater initial investment in producing offspring (pregnancy in mammals or the production of the egg in birds and reptiles), and this difference in initial investment creates differences in variance in expected reproductive success and bootstraps the sexual selection processes. Classic examples of reversed sex-role species include the pipefish, and Wilson's phalarope. Also, unlike a female, a male (except in monogamous species) has some uncertainty about whether or not he is the true parent of a child, and so is less interested in spending his energy helping to raise offspring that may or may not be related to him. As a result of these factors, males are typically more willing to mate than females, and so females are typically the ones doing the choosing (except in cases of forced copulations, which can occur in certain species of primates, ducks, and others). The effects of sexual selection are thus held to typically be more pronounced in males than in females.

Differences in secondary sexual characteristics between males and females of a species are referred to as sexual dimorphisms. These can be as subtle as a size difference (sexual size dimorphism, often abbreviated as SSD) or as extreme as horns and colour patterns. Sexual dimorphisms abound in nature. Examples include the possession of antlers by only male deer, the brighter coloration of many male birds in comparison with females of the same species, or even more distinct differences in basic morphology, such as the drastically increased eye-span of the male stalk-eyed fly. The peacock, with its elaborate and colourful tail feathers, which the peahen lacks, is often referred to as perhaps the most extraordinary example of a dimorphism. Male and female black-throated blue warblers and Guianan cock-of-the-rocks also differ radically in their plumage. Early naturalists even believed the females to be a separate species. The largest sexual size dimorphism in vertebrates is the shell dwelling cichlid fish Neolamprologus callipterus in which males are up to 30 times the size of females. Many other fish such as guppies also exhibit sexual dimorphism. Extreme sexual size dimorphism, with females larger than males, is quite common in spiders and birds of prey.

The Role of Male-Male Competition in Sexual Selection

Male-male competition occurs when two males of the same species compete for the opportunity to mate with a female. Sexually dimorphic traits, size, sex ratio  and the social situation  may all play a role in the effects male-male competition has on the reproductive success of a male and the mate choice of a female.

Conditions that Influence Competition

Sex Ratio

Japanese medaka, Orzyas latipes.
 
There are multiple types of male-male competition that may occur in a population at different times depending on the conditions. Competition variation occurs based on the frequency of various mating behaviours present in the population. One factor that can influence the type of competition observed is the population density of males. When there is a high density of males present in the population, competition tends to be less aggressive and therefore sneak tactics and disruptions techniques are more often employed. These techniques often indicate a type of competition referred to as scramble competition. In Japanese medaka, Oryzias latipes, sneaking behaviours refer to when a male interrupts a mating pair during copulation by grasping on to either the male or the female and releasing their own sperm in the hopes of being the one to fertilize the female. Disruption is a technique which involves one male bumping the male that is copulating with the female away just before his sperm is released and the eggs are fertilized.

However, all techniques are not equally successful when in competition for reproductive success. Disruption results in a shorter copulation period and can therefore disrupt the fertilization of the eggs by the sperm, which frequently results in lower rates of fertilization and smaller clutch size.

Resource Value and Social Ranking

Another factor that can influence male-male competition is the value of the resource to competitors. Male-male competition can pose many risks to a male's fitness, such as high energy expenditure, physical injury, lower sperm quality and lost paternity. The risk of competition must therefore be worth the value of the resource. A male is more likely to engage in competition for a resource that improves their reproductive success if the resource value is higher. While male-male competition can occur in the presence or absence of a female, competition occurs more frequently in the presence of a female. The presence of a female directly increases the resource value of a territory or shelter and so the males are more likely to accept the risk of competition when a female is present. The smaller males of a species are also more likely to engage in competition with larger males in the presence of a female. Due to the higher level of risk for subordinate males, they tend to engage in competition less frequently than larger, more dominant males and therefore breed less frequently than dominant males. This is seen in many species, such as the Omei treefrog, Rhacophorus omeimontis, where larger males obtained more mating opportunities and successfully mated with larger mates. 

Winner-Loser Effects

A third factor that can impact the success of a male in competition is winner-loser effects. Burrowing crickets, velarifictorous aspersus, compete for burrows to attract females using their large mandibles for fighting.  Female burrowing crickets, are more likely to choose winner of a competition in the 2 hours after the fight. The presence winning male suppresses mating behaviours of the losing males because the winning male tends to produce more frequent and enhanced mating calls in this period of time.

Effect of Male-Male Competition on Female Fitness

Male-male competition can both positively and negatively affect female fitness. When there is a high density of males in a population and a large number of males attempting to mate with the female, she is more likely to resist mating attempts, resulting in lower fertilization rates. High levels of male-male competition can also result in a reduction in female investment in mating. Many forms of competition can also cause significant distress for the female negatively impacting her ability to reproduce. An increase in male-male competition can affect a females ability to select the best mates, and therefore decrease the likelihood of successful reproduction.

However, group mating in Japanese medaka has been shown to positively affect the fitness of females due to an increase in genetic variation, a higher likelihood of paternal care and a higher likelihood of successful fertilization.

Examples

A leaf-footed cactus bug, Narnia femorata.
 
In Japanese medaka, females mate daily during mating season. Males compete for the opportunity to mate with the female by displaying themselves aggressively and chasing each other. To obtain the selection of the females, they court the females prior to copulation by performing a courting behaviour referred to as "quick circles".

In leaf-footed cactus bugs, Narnia femorata, males compete for territories where females can lay their eggs. Males compete more intensely for cacti territories with fruit to attract females. In this species, the males possess sexually dimorphic traits, such as their larger size and hind legs, which are used to gain the most advantage over competitors when females are present, but are not used in the absence of females. 

Anuran (such as frogs) select habitats (pools) free of conspecifics in order to minimize male-male competition for both themselves and their offspring. Displays are used in attempt to keep competitors out of their territory and deter sneaking behaviours, while fighting is only used when necessary due to the high costs and risks associated with fighting.

In different taxa

SEM image of lateral view of a love dart of the land snail Monachoides vicinus. The scale bar is 500 μm (0.5 mm).
Human spermatozoa can reach 250 million in a single ejaculation
Sexual selection has been observed to occur in plants, animals and fungi. In certain hermaphroditic snail and slug species of molluscs the throwing of love darts is a form of sexual selection. Certain male insects of the lepidoptera order of insects cement the vaginal pores of their females.

A male bed bug (Cimex lectularius) traumatically inseminates a female bed bug (top). The female's ventral carapace is visibly cracked around the point of insemination.
 
Today, biologists say that certain evolutionary traits can be explained by intraspecific competition - competition between members of the same species - distinguishing between competition before or after sexual intercourse

Illustration from The Descent of Man showing the tufted coquette Lophornis ornatus: female on left, ornamented male on right
 
Before copulation, intrasexual selection - usually between males - may take the form of male-to-male combat. Also, intersexual selection, or mate choice, occurs when females choose between male mates. Traits selected by male combat are called secondary sexual characteristics (including horns, antlers, etc.), which Darwin described as "weapons", while traits selected by mate (usually female) choice are called "ornaments". Due to their sometimes greatly exaggerated nature, secondary sexual characteristics can prove to be a hindrance to an animal, thereby lowering its chances of survival. For example, the large antlers of a moose are bulky and heavy and slow the creature's flight from predators; they also can become entangled in low-hanging tree branches and shrubs, and undoubtedly have led to the demise of many individuals. Bright colourations and showy ornamenations, such as those seen in many male birds, in addition to capturing the eyes of females, also attract the attention of predators. Some of these traits also represent energetically costly investments for the animals that bear them. Because traits held to be due to sexual selection often conflict with the survival fitness of the individual, the question then arises as to why, in nature, in which survival of the fittest is considered the rule of thumb, such apparent liabilities are allowed to persist. However, one must also consider that intersexual selection can occur with an emphasis on resources that one sex possesses rather than morphological and physiological differences. For example, males of Euglossa imperialis, a non-social bee species, form aggregations of territories considered to be leks, to defend fragrant-rich primary territories. The purpose of these aggregations is only facultative, since the more suitable fragrant-rich sites there are, the more habitable territories there are to inhabit, giving females of this species a large selection of males with whom to potentially mate.

After copulation, male–male competition distinct from conventional aggression may take the form of sperm competition, as described by Parker in 1970. More recently, interest has arisen in cryptic female choice, a phenomenon of internally fertilised animals such as mammals and birds, where a female can get rid of a male's sperm without his knowledge.

Victorian cartoonists quickly picked up on Darwin's ideas about display in sexual selection. Here he is fascinated by the apparent steatopygia in the latest fashion.
 
Finally, sexual conflict is said to occur between breeding partners, sometimes leading to an evolutionary arms race between males and females. Sexual selection can also occur as a product of pheromone release, such as with the stingless bee, Trigona corvina.

Female mating preferences are widely recognized as being responsible for the rapid and divergent evolution of male secondary sexual traits. Females of many animal species prefer to mate with males with external ornaments - exaggerated features of morphology such as elaborate sex organs. These preferences may arise when an arbitrary female preference for some aspect of male morphology — initially, perhaps, a result of genetic drift — creates, in due course, selection for males with the appropriate ornament. One interpretation of this is known as the sexy son hypothesis. Alternatively, genes that enable males to develop impressive ornaments or fighting ability may simply show off greater disease resistance or a more efficient metabolism, features that also benefit females. This idea is known as the good genes hypothesis

Bright colors that develop in animals during mating season function to attract partners. It has been suggested that there is a causal link between strength of display of ornaments involved in sexual selection and free radical biology. To test this idea, experiments were performed on male painted dragon lizards. Male lizards are brightly conspicuous in their breeding coloration, but their color declines with aging. Experiments involving administration of antioxidants to these males led to the conclusion that breeding coloration is a reflection of innate anti-oxidation capacity that protects against oxidative damage, including oxidative DNA damage. Thus color could act as a “health certificate” that allows females to visualize the underlying oxidative stress induced damage in potential mates. 

Darwin conjectured that heritable traits such as beards and hairlessness in different human populations are results of sexual selection in humans. Geoffrey Miller has hypothesized that many human behaviours not clearly tied to survival benefits, such as humour, music, visual art, verbal creativity, and some forms of altruism, are courtship adaptations that have been favoured through sexual selection. In that view, many human artefacts could be considered subject to sexual selection as part of the extended phenotype, for instance clothing that enhances sexually selected traits. Some argue that the evolution of human intelligence is a sexually selected trait, as it would not confer enough fitness in itself relative to its high maintenance costs.

Fisherian runaway

From Wikipedia, the free encyclopedia
 
The peacock tail in flight, the classic example of an ornament assumed to be a Fisherian runaway
 
Fisherian runaway or runaway selection is a sexual selection mechanism proposed by the mathematical biologist Ronald Fisher in the early 20th century, to account for the evolution of exaggerated male ornamentation by persistent, directional female choice. An example is the colourful and elaborate peacock plumage compared to the relatively subdued peahen plumage; the costly ornaments, notably the bird's extremely long tail, appear to be incompatible with natural selection. Fisherian runaway can be postulated to include sexually dimorphic phenotypic traits such as behaviour expressed by either sex. 

Extreme and apparently maladaptive sexual dimorphism represented a paradox for evolutionary biologists from Charles Darwin's time up to the modern synthesis. Darwin attempted to resolve the paradox by assuming genetic bases for both the preference and the ornament, and supposed an "aesthetic sense" in higher animals, leading to powerful selection of both characteristics in subsequent generations. Fisher developed the theory further by assuming genetic correlation between the preference and the ornament, that initially the ornament signalled greater potential fitness (the likelihood of leaving more descendants), so preference for the ornament had a selective advantage. Subsequently, if strong enough, female preference for exaggerated ornamentation in mate selection could be enough to undermine natural selection even when the ornament has become non-adaptive. Over subsequent generations this could lead to runaway selection by positive feedback, and the speed with which the trait and the preference increase could (until counter-selection interferes) increase exponentially ("geometrically").

Fisherian runaway has been difficult to demonstrate empirically, because it has been difficult to detect both an underlying genetic mechanism and a process by which it is initiated.

History

Female (left) and male (right) pheasant, a sexually dimorphic species
 
Charles Darwin published a book on sexual selection in 1871 called The Descent of Man, and Selection in Relation to Sex, which garnered interest upon its release but by the 1880s the ideas had been deemed too controversial and were largely neglected. Alfred Russel Wallace disagreed with Darwin, particularly after Darwin's death, that sexual selection was a real phenomenon. R.A. Fisher was one of the few other biologists to engage with the question. When Wallace stated that animals show no sexual preference in his 1915 paper, The evolution of sexual preference, Fisher publicly disagreed:
The objection raised by Wallace ... that animals do not show any preference for their mates on account of their beauty, and in particular that female birds do not choose the males with the finest plumage, always seemed to the writer a weak one; partly from our necessary ignorance of the motives from which wild animals choose between a number of suitors; partly because there remains no satisfactory explanation either of the remarkable secondary sexual characters themselves, or of their careful display in love-dances, or of the evident interest aroused by these antics in the female; and partly also because this objection is apparently associated with the doctrine put forward by Sir Alfred Wallace in the same book, that the artistic faculties in man belong to his "spiritual nature," and therefore have come to him independently of his "animal nature" produced by natural selection.
Fisher, in the foundational 1930 book, The Genetical Theory of Natural Selection, first outlined a model by which runaway inter-sexual selection could lead to sexually dimorphic male ornamentation based upon female choice and a preference for "attractive" but otherwise non-adaptive traits in male mates. He suggested that selection for traits that increase fitness may be quite common:
[O]ccasions may not be infrequent when a sexual preference of a particular kind may confer a selective advantage, and therefore become established in the species. Whenever appreciable differences exist in a species, which are in fact correlated with selective advantage, there will be a tendency to select also those individuals of the opposite sex which most clearly discriminate the difference to be observed, and which most decidedly prefer the more advantageous type. Sexual preference originated in this way may or may not confer any direct advantage upon the individuals selected, and so hasten the effect of the Natural Selection in progress. It may therefore be far more widespread than the occurrence of striking secondary sexual characters.
Fisher, R.A. (1930) The Genetical Theory of Natural Selection. ISBN 0-19-850440-3
A strong female choice for the expression alone, as opposed to the function, of a male ornament can oppose and undermine the forces of natural selection and result in the runaway sexual selection that leads to the further exaggeration of the ornament (as well as the preference) until the costs (incurred by natural selection) of the expression become greater than the benefit (bestowed by sexual selection).

Peacocks and sexual dimorphism

The peacock, on the right, is courting the peahen, on the left.
 
The plumage dimorphism of the peacock and peahen of the species within the genus Pavo is a prime example of the ornamentation paradox that has long puzzled evolutionary biologists; Darwin wrote in 1860:
The sight of a feather in a peacock’s tail, whenever I gaze at it, makes me sick!
The peacock's colorful and elaborate tail requires a great deal of energy to grow and maintain. It also reduces the bird's agility, and may increase the animal's visibility to predators. The tail appears to lower the overall fitness of the individuals who possess it. Yet, it has evolved, indicating that peacocks with longer and more colorfully elaborate tails have some advantage over peacocks who don’t. Fisherian runaway posits that the evolution of the peacock tail is made possible if peahens have a preference to mate with peacocks that possess a longer and more colourful tail. Peahens that select males with these tails in turn have male offspring that are more likely to have long and colourful tails and thus are more likely to be sexually successful themselves. Equally importantly, the female offspring of these peahens are more likely to have a preference for peacocks with longer and more colourful tails. However, though the relative fitness of males with large tails is higher than those without, the absolute fitness levels of all the members of the population (both male and female) is less than it would be if none of the peahens (or only a small number) had a preference for a longer or more colorful tail.

Initiation

Fisher outlined two fundamental conditions that must be fulfilled in order for the Fisherian runaway mechanism to lead to the evolution of extreme ornamentation:
  1. Sexual preference in at least one of the sexes
  2. A corresponding reproductive advantage to the preference.
Fisher argued in his 1915 paper, "The evolution of sexual preference" that the type of female preference necessary for Fisherian runaway could be initiated without any understanding or appreciation for beauty. Fisher suggested that any visible features that indicate fitness, that are not themselves adaptive, that draw attention, and that vary in their appearance amongst the population of males so that the females can easily compare them, would be enough to initiate Fisherian runaway. This suggestion is compatible with his theory, and indicates that the choice of feature is essentially arbitrary, and could be different in different populations. Such arbitrariness is borne out by mathematical modelling, and by observation of isolated populations of sandgrouse, where the males can differ markedly from those in other populations.

Genetic basis

Fisherian runaway assumes that sexual preference in females and ornamentation in males are both genetically variable (heritable).
If instead of regarding the existence of sexual preference as a basic fact to be established only by direct observation, we consider that the tastes of organisms … be regarded as the products of evolutionary change, governed by the relative advantage which such tastes may confer. Whenever appreciable differences exist in a species … there will be a tendency to select also those individuals of the opposite sex which most clearly discriminate the difference to be observed, and which most decidedly prefer the more advantageous type.
Fisher, R.A. (1930) The Genetical Theory of Natural Selection. ISBN 0-19-850440-3

Female choice

Fisher argued that the selection for exaggerated male ornamentation is driven by the coupled exaggeration of female sexual preference for the ornament.
Certain remarkable consequences do, however, follow ... in a species in which the preferences of … the female, have a great influence on the number of offspring left by individual males. ... development will proceed, so long as the disadvantage is more than counterbalanced by the advantage in sexual selection … there will also be a net advantage in favour of giving to it a more decided preference.
Fisher, R.A. (1930) The Genetical Theory of Natural Selection. ISBN 0-19-850440-3

Positive feedback

Over time a positive feedback mechanism will see more exaggerated sons and choosier daughters being produced with each successive generation; resulting in the runaway selection for the further exaggeration of both the ornament and the preference (until the costs for producing the ornament outweigh the reproductive benefit of possessing it).
The two characteristics affected by such a process, namely [ornamental] development in the male, and sexual preference for such development in the female, must thus advance together, and … will advance with ever increasing speed. [I]t is easy to see that the speed of development will be proportional to the development already attained, which will therefore increase with time exponentially, or in a geometric progression.
Fisher, R.A. (1930) The Genetical Theory of Natural Selection. ISBN 0-19-850440-3
Such a process must soon run against some check. Two such are obvious. If carried far enough … counterselection in favour of less ornamented males will be encountered to balance the advantage of sexual preference; … elaboration and … female preference will be brought to a standstill, and a condition of relative stability will be attained. It will be more effective still if the disadvantage to the males of their sexual ornaments so diminishes their numbers surviving, relative to the females, as to cut at the root of the process, by demising the reproductive advantage to be conferred by female preference.
Fisher, R.A. (1930) The Genetical Theory of Natural Selection. ISBN 0-19-850440-3

Alternative hypotheses

Several alternative hypotheses use the same genetic runaway (or positive feedback) mechanism but differ in the mechanisms of the initiation. The sexy son hypothesis (also proposed by Fisher) suggests that females that choose desirably ornamented males will have desirably ornamented (or sexy) sons, and that the effect of that behaviour on spreading the female's genes through subsequent generations may outweigh other factors such as the level of parental investment by the father.

Indicator hypotheses suggest that females choose desirably ornamented males because the cost of producing the desirable ornaments is indicative of good genes by way of the individual's vigour. 

Other hypotheses for the evolution of male ornamentation include the sensory bias hypothesis, the compatibility hypothesis and the handicap principle.

Inequality (mathematics)

From Wikipedia, the free encyclopedia https://en.wikipedia.org/wiki/Inequality...