audubonguides

Shaping Our Understanding: Part III

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Wednesday, September 7th, 2011

One interesting implication of the whales being related to the hippopotamus is that intelligence must have evolved several times. Most researchers would define the whales and dolphins as among the most intelligent of mammals, and very few would put the hippo high on that scale. Intelligence is extremely complex and is certainly not a single-gene trait (nobody knows how many genes are involved, and it is very likely that different genes are involved in different intelligent species). However, the intelligent mammals are not especially closely related to each other, and no matter how you define intelligence, you can’t group all the intelligent mammals together under a single ancestor. Very few people would argue that “intelligent mammals” doesn’t include at least include some carnivores (wolves are perhaps the best example, but many carnivores are intelligent), many cetaceans and many or most primates. Many people would also include the elephant and some other species among the intelligent mammals. Those species are scattered all over the mammals, and are more closely related to animals nobody would consider intelligent than they are to each other, strongly suggesting that their intelligence is separately evolved. We are actually probably less closely related to dolphin and dog than we are to mice and rats (and dolphins and dogs aren’t close to each other, either).

Other animals, entirely apart from mammals, are also often considered intelligent. The farther one gets from the type of intelligence we are most familiar with, the tool using, collaborative, highly communicative intelligence of the primates, the harder it becomes for humans to define intelligence. It is easy for a human to see that an ape or a monkey is smart, because they are smart in fundamentally the same ways that we are. A dog or a dolphin is a little harder to see as “like us”, but there is still enough commonality between the ways humans, dogs and dolphins think about things that we can devise intelligence tests that work across that barrier, and, perhaps more importantly, we can see them (and they us) as kindred, intelligent spirits.

As we get farther away from ourselves on the evolutionary tree, this becomes harder. Some birds are highly intelligent, yet the mind of the raven is much harder for humans to penetrate than that of the chimpanzee, the dog, or even the entirely aquatic dolphin. Parrots, with their capacity for vocal mimicry, make it easier for us to see them as similar to us – they can speak our languages, and, it sometimes appears, know what they’re saying. It appears to many researchers that the mimic capability of the parrots goes beyond being a biological “tape recorder” to beginning to understand a few phrases of human language. Even so, the way birds think and emote is exotic to us in a way that similar features of mammals are not.

Yet another step away from us is the intelligence of the molluscs. By many definitions, octopus and squid are highly intelligent organisms, yet their form of intelligence is so alien to us that we share far less with them than we do even with the birds. While some scientists have said that an octopus is roughly as intelligent as a house cat, how can we ever know? A cat shares many experiences with us, even if it is a wild animal like a bobcat that has never lived with people. A bobcat lives fundamentally in our world, and, like most intelligent mammals and birds, takes care of its young and teaches them much of what they need to know. This touchstone, behavior that is learned from parents, older relatives and even non-relatives, is one thread that connects the intelligent mammals and birds – all of them (unlike many less intelligent mammals and birds) have long periods of parental care, and all seem to have some form of teaching and learning. A mouse is born knowing how to be a mouse, but a wolf isn’t born knowing how to be a wolf, or a raven how to be a raven.

The octopus is so alien to this world that it breeds once in its lifetime, lays eggs and then dies before the eggs ever hatch. Octopi DO seem to learn, but they learn strictly through experiment, because there is no older generation around to teach them. They are also almost entirely solitary, and communicate none of the knowledge each individual gains back to the group in any way. Humans, of course, are the exact opposite, with an intelligence based almost entirely on building on knowledge of past generations. Since the invention of writing, the human capacity to build and store knowledge has far outstripped that of any other species, but there are other examples of similar phenomena. Orca (so-called killer) whales have perhaps the most sophisticated nonhuman culture, with food preferences, vocal dialects and behaviors that are entirely learned, and that go back many generations in what appears to be a rich trove of lore that is completely different between populations. In some places, two populations of orcas can live alongside each other and barely interact – they’re biologically the same species, but have grown far enough apart culturally that they don’t interbreed, compete for prey, or even really interact (despite interactions within each population that are among the most complex of all creatures’). Compare this to the octopus, whose breeding system means that, by definition, no culture can exist. Each generation is starting over from scratch.

Maybe even more alien to us than the intelligence of the octopus is the intelligence of social insects. Is an ant “smart”? Not by any conventional definition – it is a fairly simple creature with a small number of entirely instinctual behaviors. An individual ant is no more or less intelligent than an individual mosquito by most definitions, yet an ant colony is capable of numerous behaviors we would characterize as intelligent. Some ant colonies can farm, others are capable of organized warfare, and simulated ant colonies are even used to determine efficient ways to route information. No individual member of the group has any intelligence to speak of, but the group as a whole behaves intelligently.

Intelligence is just one example of the power of evolution. Since evolutionary processes are essentially random, yet selective pressures produce highly successful organisms (if a given combination of traits is detrimental to survival, there are enough mutations around that something else will replace it). On the other hand, because the process has a lot of randomness, many different “solutions” to the same problem are likely to appear. It would be very difficult to fit a brain that was conventionally intelligent in an organism the size of an ant, but a colonial intelligence gives ants an advantage over solitary insects in many circumstances. There is almost certainly no relationship between the “intelligence” of social insects and that of birds or mammals, yet they convey many of the same advantages.

If you have enjoyed my series on taxonomy and evolution, some longer works worth reading are:

Anything by the great biologist and natural history essayist Stephen Jay Gould – numerous collections of essays, many on topics I’ve touched on.

On the Origin of Species by Charles Darwin – yes, it was written in 1859, and the language is not that of modern science, but it is amazing to see how well the Origin has stood up as a work of science, not just for its historical importance.

Shaping Our Understanding Part II

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Thursday, August 25th, 2011

In modern biological thinking, a valid clade (any grouping larger than a species, be it a genus, family, order, class, phylum, kingdom or some variation) is any group of an ancestor and all of its descendants. The ancestor can be chosen arbitrarily, but there are two rules. First, a clade cannot consist of some of the descendants of a given ancestor, with others excluded. Second, a clade cannot consist of descendants of two or more ancestors, unless they are the descendants of another ancestor further back (and the clade includes all descendants of that ancestor).

As an example, the dog family seems to be a valid clade according to current research. It contains dogs, coyotes, wolves, foxes and several other animals that are less familiar to us. There was a “proto-dog” that was the most recent common ancestor of all of these animals, that was not also the ancestor of any other animal. Within this clade, there is a smaller clade (equally valid) that consists of the genus Canis (domestic dogs, wolves and the coyote). The common ancestor of this clade is more recent than the ancestor of the larger family clade, and is an ancestor of dogs, wolves and the coyote, but NOT foxes or jackals. Since a clade can be defined from any ancestor, both are equally valid, and the smaller clade, corresponding to the Linnaean genus Canis, nests completely within the larger one, which corresponds to the Linnaean family Canidae.

Until the recent arrival of molecular techniques, scientists going back to Linnaeus had classified species based on appearance, although often basing classifications on highly technical details that required a microscope to see. To a lessor extent, behavior, especially among animals with complex behaviors, has influenced classification. Molecular techniques permit us to read the underlying genetic code directly, instead of making our best guess based on physical appearance and similar factors.

The dogs are a good example of a place where the molecular classification agrees with the means of classification used before the development of molecular techniques. Linnaeus was the first to describe both the family Canidae, and the genus Canis in their modern sense, both of which, as we’ve seen, are valid molecular clades.
In other cases, though, the genetic code gives us some surprising results – organisms that appear related turn out not to be, or those that appear very different are actually relatives. Examples of surprising clades are appearing throughout life as molecular data become more available for a wide range of species.
To demonstrate the effects of molecular taxonomy, I’ll choose a couple of favorite examples – a class, and an order within it, that make a great deal of sense from their appearance, but turn out to be partial clades (and the additional members to complete the clade are very surprising), and an order that fits in a surprising spot on the tree of life.

The clades with surprising members are the reptiles, and the lizards within them. There’s no such thing, biologically, as a reptile, and this is a recent discovery. If you think about “reptile”, most of us can come up with a large number of animals that fit the bill. Lizards, snakes and turtles all come to mind quickly, and with only a little more thought, we can add crocodilians and dinosaurs. No valid clade joins all of these animals without a significant number of surprising “extra members”. The lizards and snakes share a common ancestor and form a valid clade, there is another clade composed of turtles, and another with alligators and crocodiles. Another clade holds all the dinosaurs, but also contains all birds. The dinosaur/bird clade joins with the crocodile clade, then reaching for a more ancient ancestor, this clade joins with the lizard/snake clade. The turtles are less closely related to any of these animals than any of them are to each other. When we think about core reptiles, without having to include birds (which the average person doesn’t consider to be reptiles), all we get are lizards and snakes. Any attempt to add the crocodiles pulls both dinosaurs and birds along with them, and the turtles are so distantly related to anything else that any clade containing both turtles and lizards also contains crocodiles, snakes, dinosaurs and birds.

Within this broad group of reptiles, there are two surprises. One is that the birds are quite deeply nested within the dinosaurs. Birds and the classic carnivorous dinosaurs like Velociraptor and Tyrannosaurus rex are more closely related to each other than either one is to plant-eating dinosaurs such as Triceratops. The next time you see a Robin, realize that, in a real sense, you’re looking Velociraptor in the eye (OK – maybe it’s easier to see with a Bald Eagle).

The other surprise in the reptiles is that you can’t get a clean lizard clade. There are several clades composed entirely of what would commonly be called lizards, but any attempt to find a common ancestor that unifies them also includes the snake clade. All snakes do form a clade (all snakes are more closely related to all other snakes than any snake is to any lizard), but some “lizards” are more closely related to snakes than they are to other “lizards”, making a lizard clade that doesn’t also include the snakes impossible to define.

Moving over to the mammals (which are a valid clade with no surprising members), the whales have long been a bit of a mystery. Where do they fit within the mammals? Are they even a single clade, or are the baleen whales not all that closely related to the toothed whales? Prior to the arrival of molecular evolutionary biology, the whales had been placed all over the mammals, generally together but occasionally separated. The molecular evidence shows that the closest living relative of the whales (which are a single clade) is the hippopotamus.

Shaping Our Understanding

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Wednesday, August 17th, 2011


Last week’s entry covered how scientific names work and describe a given organism’s place in the evolutionary framework. This week, I’ll build both back and forward on that, going from the origins of the system to what modern molecular genetic research has told us about how life fits together (there are a few surprises)! We’ll look briefly at the careers of several biologists, from the 18th century to the present day, who have shaped our understanding of life.
We actually need to start more than a century before Darwin published On the Origin of Species, with Swedish physician and botanist Carolus Linnaeus (sometimes written as Carl Linnaeus or Carl von Linne). Linnaeus’ great contribution to biology was his two books Systema Naturae (1st edition 1735, but the influential edition is the 10th, of 1758), and Species Plantarum (1753), which introduced the binomial (genus and species) method for naming animals and plants, respectively. Linnaeus is also responsible for a significant portion of the system of names above the genus level, although some of those levels are later additions.
In addition to having invented the system of nomenclature we use today, Linnaeus named approximately 7,700 species of plants and 4,400 species of animals. Many of his names are still in use today, including such familiar organisms as the Harbor Seal (Phoca vitulina), the Red Maple (Acer rubrum) and even ourselves (Homo sapiens) – in 1959, his successors honored Linnaeus by designating him as the lectotype for humans – the formal description of human beings is “the animal species that includes Linnaeus”.
While Linnaeus was a great field biologist, leading expeditions throughout Sweden for most of his life, he rarely left Sweden, and never during the period when he classified thousands of species. Most of his classifications were based on material his students sent him from around the world. Students of Linnaeus traveled to an amazing variety of places (several sailed with Captain Cook, for example) and sent back specimens for Linnaeus to classify and name. He also came amazingly close to evolution without ever understanding it, and, in fact steadfastly denied the possibility that any sort of evolution could exist. Looked at through an evolutionary lens, it seems amazing that anyone could have completed this brilliant work of classification without becoming aware that organisms were related to each other. Linnaeus placed humans, monkeys and apes together in the Primates, while always maintaining that each species was separately created in an unrelated event, and that his system was merely a method of organization – he was famous for saying “God created, Linnaeus organized”. Linnaeus came amazingly close to evolution several times without actually seeing it – in addition to correctly grouping humans with other primates for the first time, he was also the first to recognize that both bats and whales are mammals. He seems in all those cases to have been acutely aware of biological relationships, yet unable to make the mental leap from separate creation to an evolutionary paradigm that would permit these species to actually BE related.
After Linnaeus designed the modern system of biological classification and hugely expanded the number of known species, many scientists began to wonder whether each species was, in fact, a separate creation. While evolutionary ideas were beginning to be discussed by the beginning of the 19th century, nobody had worked out a system by which evolutionary change could occur. It was thought that since the descendants of any given species were always of the same species, the species were immutable. The chicken and egg problem is the classic example of this – a chicken is what lays an egg, but is also what hatches from one, so how does a non-chicken ever lay a chicken-producing egg? The answer to this was uncertain until the middle of the 19th century, and was the fundamental impediment to a workable theory of evolution.
In 1831, a young naturalist named Charles Darwin set off on a long sea voyage aboard HMS Beagle, a survey ship of the Royal Navy. Darwin was actually aboard primarily as a social companion to Captain FitzRoy, because English captains of the time were of a much higher social class than their crews, and forbidden to socialize with them. Darwin’s secondary function aboard the Beagle was to keep notes on geology and natural history, a position in which he excelled, and which would later bring him fame. As Darwin traveled around the world observing the plants and animals, he was able to see relationships between them – the data point that was directly in front of Linnaeus and many other earlier biologists, but that none had satisfactorily explained. It took him over 20 years from the first rough sketches of the idea of evolution to the publication of On the Origin of Species, a timeframe that seems less surprising when you consider that the Origin is so beautifully thought out and written that it is still referred to today, 152 years after its first publication in 1859.
Starting while he was still aboard the Beagle on the five-year voyage, and refining his ideas over many years at home in England, Darwin developed the theory of evolution by natural selection. Different members of a species are not identical – they possess slight, but important variations. According to Darwin, and to 150 years of biology since he published On the Origin of Species, individuals which have variations favorable to survival will be more likely to survive to reproductive age, and to leave offspring behind, which will carry the (initially randomly occurring) variation. This view of species as essentially mutable – individuals vary, and those which have variations which benefit their survival will leave more offspring, enhancing their contribution to the next generation – is diametrically opposite to Linnaeus’ view that each species is perfect and unchanging, created by God for a specific purpose.
In Darwin’s view, species diverge from a common ancestor when any of several circumstances occur. Two populations of the same species could become separated (one moves to a new habitat), where different variations lead to better survival. The variations are present in some members of both populations, but one form leads to better survival in one location, while a different form is advantageous in the other. Eventually, in the absence of contact between the populations, they might diverge into separate species. Alternatively, a change in environment for part of a population might mean that a different set of variations was most successful, leading to a distinct population that may eventually diverge far enough to form a new species. A third possibility is that species could diverge through competition with each other, rather than through environmental change. For example, a bird with a mid-sized beak could evolve towards a small-beaked and a large-beaked species even in the absence of environmental segregation, if the smallest-beaked birds could take advantage of one food source, and the largest-beaked ones another, while a bird with a mid-sized beak was a disadvantage in exploiting either source. All of these possibilities have been confirmed by research over the last 150 years.
Darwin built on Linnaeus’ classification of species, bringing relatedness to Linnaeus’s order. A Linnaean view would say “these two species in the same genus are similar, therefore they belong next to each other, like library books on a shelf”. Darwin found the mechanism to say “they’re not just similar, they’re related to each other and share an ancestor, and that’s why they’re next to each other”.
Darwin’s great insights were the importance of subtle variations and time. Until shortly before Darwin, the Earth was believed to be only a few thousand years old, leaving time for a fairly limited number of generations of most species. Geologists in the half-century before Darwin were revising the age of the Earth steadily upward, giving substantially more time for change to occur – in Darwin’s day, there wasn’t an agreed-upon age of the Earth, but estimates were from hundreds of thousands of years to hundreds of millions or more (the currently accepted estimate is slightly over 4.5 billion years).
An older Earth gave time for subtle variations to accumulate – a non-chicken didn’t have to lay an egg from which a chicken hatched. Over many generations, a near-chicken could lay an egg that produced a slightly nearer-chicken, and, even today, a chicken doesn’t lay an egg that produces exactly the same chicken (as a matter of fact, from the standards of what Linnaeus first named Gallus gallus (a chicken), some of what shows up on today’s large poultry farms may be perilously close to being non-chicken, a different species).
While Darwin was formulating his grand idea, there was no concept of genetics in the intellectual discourse at all. People had long known that children tended to look like their parents (and that children who looked exactly like the wandering peddler who passed through town nine months before their birth indicated something had gone on). Nobody had provided any mechanism for why this was true, however.
At almost exactly the same time Darwin was working out the mechanisms of evolution, an Austrian monk named Gregor Mendel was studying heredity. While Darwin was studying the world as it is on a broad scale, gathering ideas from a round-the-world voyage, Mendel was the great small-scale experimentalist. He planted thousands of pea plants over several years, keeping track of the parents of each plant, and of the characteristics of the offspring. Mendel worked out how characteristics are passed from generation to generation.
Mendel was the first to discover that every organism receives one copy of each gene from each parent, and that it is random which of a parent’s two copies a given offspring receives. He also developed the concepts of dominant and recessive traits – a dominant trait appears if you get at least one copy of its gene (from either parent), while a recessive trait is only visible if each parent contributes a copy of its gene (if one parent contributes the dominant version of the gene, and the other the recessive, the offspring will have the dominant appearance, not a blend of the two). Mendel had worked out most of the basic math of inheritance, at least for traits that are controlled by a single gene (many complex traits are influenced by several genes, which makes the situation more difficult).
Unfortunately, and unlike Darwin, who was one of the best-known scientists of the 19th century within his lifetime, Mendel’s work was largely forgotten until well after his death. He presented his work as primarily about hybridization, without going into the much larger implications of inheritance in general. As a monk, and later abbot of his monastery, he was not able to give his scientific work the wide publicity it deserved. Other scientists dismissed Mendel as a monk breeding peas in a garden, not realizing until many years after his death that he had discovered the first principles of the modern science of genetics.
Mendel’s genetics was promptly forgotten about for 35 years, as Darwin’s evolution raised firestorms of criticism, largely from a religious establishment that did not want to hear that humans are close relatives of apes, preferring instead to view humans as direct descendants of God. By Darwin’s death in 1882, the battle was essentially over, at least in scientific circles. Just about every biologist had accepted that Darwin was right – debate would continue, and still does, on the precise mechanisms of evolution, but Darwin’s basic idea of evolution through natural selection was, and still is, essentially unchallenged. Many religious scholars also came to accept Darwin’s ideas relatively quickly – he was buried at Westminster Abbey, with many of the senior clergy of Britain in attendance.
Mendel’s ideas would take much longer to achieve general acceptance – his great paper was published in an obscure location, and discussed at a local natural history society. Shortly afterwards, his work faded into obscurity, where it remained for 35 years. Around the turn of the 20th century, several biologists began to independently work out the laws of heredity, and, in the process rediscovered Mendel’s writings. It was quickly accepted that Mendel had, in fact, pioneered this work in the mid-19th century.
Through the first half of the 20th century, the thrust of evolutionary thought was applying Mendelian genetics to the study of Darwinian evolution, leading by the middle of the century to the understanding of evolution that, on a basic level, is current today.
Mendel’s work only said that some material was passed from parent to child that carried genetic information – it made no assumption as to what that material could be. That would have to wait for nearly a full century, until James Watson, Francis Crick and colleagues worked out the structure of DNA in the early 1950s. The structure of DNA (and with it, how genetic information was passed on a molecular level) caused another revolution in our broader-scale understanding of the relationships between organisms. Building on the original work on the structure of DNA, recent biologists have been able to decode significant portions of the genetic code, presenting a clearer picture of evolutionary relationships among species. As we have come to understand the genetic basis of relationships between species, the emphasis of taxonomy has shifted from groups of physically apparent relatives (how Linnaeus constructed his classifications nearly 300 years ago) to groups of genetically closest relatives, called clades. Clades can be nested within each other, just as Linnaeus’ genera nested within families, families within orders, and so on. Clades of roughly the same extent as Linnaean groups are still called by the Linnaean name, so a Linnaean family that more or less encompassed a molecularly defined clade would still be called a family.

Of Common and Latin Names

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Wednesday, July 20th, 2011

As Green Mountain Digital’s in-house naturalist/scientist, I spend an awful lot of time naming things… I am forever keeping up with changes in the Latin (otherwise known as scientific) names of various organisms, and trying to determine which common (or English) names are most widely used – birds have standardized English names, but nothing else does (I can think of one mammal, Puma concolor, with at least 8 common names in reasonably wide use).
The genius of Linnaeus’s system of Latin names is that they uniquely identify every species, whether it be animal, plant, fungus or more unusual still. When a new species is found, the name it is assigned fits it in with its closest relatives. While it may seem intimidating, the system is not, in fact, all that difficult to understand. It is based on levels, all nested within one another. Perhaps the easiest way to explain it is to trace us through our family tree…

Kingdom – Anamalia – animals (anything composed of multiple cells that actively seeks food, as opposed to obtaining nutrients from the sun or from decay). This is a huge group, which we share with everything from lobsters to sea anemones, mosquitoes to octopi

Phylum – Chordata (has a notochord or spinal cord) and subphylum Vertebrata (has a backbone) – Everything from fish to fowl, this group contains most things that people immediately think of as “animals” (fish, amphibians, reptiles, birds, mammals). There are a few odd creatures (sea squirts and relatives) that are chordates, but not vertebrates, but, for the most part, you can think of these creatures as things with backbones, most of which have recognizable faces.

Class: Mammalia (nurses its young, has hair – even the apparently hairless whales have a little bit of hair, especially when young). All the mammals from whales to wombats. Many of these creatures are as familiar as dogs or cats, while others are as exotic as anteaters or armadillos, but they’re all clearly more closely related to us than any fish, bird, reptile or amphibian.

Order: Primates (monkeys, apes and people, along with a few more primitive groups like lemurs). These animals all clearly look and act fairly human – they have hands, they tend to live in bands or groups, and most of them communicate in sophisticated ways.

Family: Hominidae (the great apes, including people). Now, we are in the group of our closest relatives – these are all large, highly intelligent, tailless apes that share almost all of their DNA. They all take care of their young for years, while teaching them complex skills they’ll need to know to live in a complex society. Next time you’re at the zoo, watch a gorilla or a chimp, and try to understand their facial expressions and gestures. It’s not hard – their gestures are ours…

Genus Homo (people) and species Homo sapiens (modern humans). No other member of our genus survives, but, from what we know from fossils, our extinct relatives at the genus level were pretty much human.

The levels of names speak directly to levels of evolutionary relatedness. Two organisms that share a genus are more closely related than two that share a family, and so on through the higher levels. For any given species, it shared a common ancestor more recently with other species it shares more of its names with. As an example, the common ancestor of humans and chimpanzees lived about 6 million years ago, while the common ancestor of all mammals probably lived closer to ~100 million years ago.
To avoid a seven-name tongue twister, scientists generally refer to species by the last two levels of their name (if you’re reading this, you’re a member of Homo sapiens). Each genus name is unique throughout life – our genus Homo in the primates is the only genus named Homo allowed to exist anywhere, and because of this, a two-part name uniquely identifies a single species. The higher five levels put the species in context in the evolutionary tree.
The English (or other non-Latin) names are given by people who are not scientists (again, with the exception of birds, where various scientific societies including the American Ornithologists’ Union have standardized names in a variety of languages), and have one advantage, and several disadvantages, compared to the Latin names. The advantage is that the common names may be easier to remember, not being in Latin. The most important disadvantage is that a common name may not always refer to the same thing. Perhaps the worst example is “dolphin”, which refers to a large number of closely related mammals, but also to one fish that has nothing to do with the mammals, and what is called an “elk,” in Europe is a “moose” in North America (despite the fact that there are also “elk” in North America, which are different. Common names are also often not specific (“skunk” and “squirrel” both refer to a range of species) and there are very often multiple common names for the same species, even one language (to say nothing of the range of common names for the same creature in different languages). Because of all of these disadvantages, common names also don’t tell us anything about evolution – a “dolphin” (mammal) is very closely related to a “killer whale”, which is a large dolphin, and only loosely a whale, but neither one is related in any meaningful way to a “dolphin” (fish). There is very little porpoise in trying to sort these critters out by common name (it’s much easier to remember that the dolphinish mammals are all in the same family, the Delphinidae)
Next time, I’ll delve further into how scientific names came to be, the rules for their assignment, and what happens when a bunch of taxonomists (practitioners of the specific branch of science that deals with the naming and classification of living things) get into an intellectual boxing match.

Snapshots from Monteverde: from Phebe Meyers

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Tuesday, June 28th, 2011

“Where the Nectar Lies”

There are not too many opportunities to see ten species of hummingbirds buzzing in one area at once, yet Monteverde, Costa Rica is a biodiversity hotspot. There are thirty species of hummingbirds in the area. I could hear hummingbirds before I could see them as I walked up the path to the hummingbird garden at the Monteverde Cloud Forest Reserve. Their squeaks and the drone of their wings moving eighty flaps per second filled the air.
In a way it was cheating going to a hummingbird garden, where the birds were lured by sugar water, and although I preferred to observe the birds in their forest and field edge habitat, a garden with multiple feeders enabled me to see many species, tiny and large, in action. Since hummingbirds suck the nectar from flowers, the sugar water imitates the naturally sweet, succulent, drink from which they draw their energy. Small insects and/or spiders account for their protein intake. A hummingbird must eat more than its weight per day. Amazingly for such small, intense birds, they live up to 12 years.
Many of the flowers that are pollinated by hummingbirds are tubular, and individual hummingbird species have adaptations to access the nectar in their favorite flowers. Flowers and hummingbirds have co-evolved to benefit each other, as the hummingbirds are significant pollinators of specific flowering plants. Species of hummingbirds that feed on short tubular flowers have short beaks. Long curved tubular flowers attract hummingbirds with long, narrow beaks. Some hummingbirds are nectar robbers, so named because they use their short sharp beaks to pierce the flower tube near its base and steal the nectar, bypassing the pollen.
There are over 330 species of hummingbirds, comprising the second largest avian family in the New World. Even though they range from Alaska to Tierra Del Fuego, they are most abundant in the tropics. The climate and abundance of food is more prevalent in warmer climates; however, many are neo-tropical migrants, summering in cooler climates, such as my hometown in Vermont. Mother’s Day usually marks the first appearance of a ruby-throated hummingbird at the feeder on our porch, after its long migration.
The rapid wing flapping fascinates me. Hovering in one spot, the hummingbirds move each entire wing in a unique rotation at the shoulder joint, moving their wings 40-80 beats per second. They also have the ability to fly backwards.
Peaceful as it may be to watch hummingbirds, their behavior and interactions with one another, can seem fairly violent. In the hummingbird garden, they spend their time chasing each other, dive bombing, or fighting for the spot on the feeder. Even while perching on a branch, they seek opportunities to obtain food and dominate a food source.
The iridescent violet hues and white tips on the tail feathers of the Violet Sabrewing contrast with the green surroundings. This is the largest of hummingbirds found in Monteverde, reaching a height of about 6” (15cm). Other species seen included the Fiery-Throated Hummingbird, which is endemic to Costa Rica and western Panama, the Green Violet Ear, the Magnificent Hummingbird, the Green-Crowned Brilliant, the Rufous-Tailed Hummingbird, the Ruby-Throated Hummingbird, and the Scintillant Hummingbird.
My patience and stillness in gardens and along the forest edge allowed the birds to be unfazed by my presence. The view was spectacular.

Snap Shots from Monteverde: from Phebe Meyers

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Tuesday, June 21st, 2011

EPIPHYTES- CROWNS OF THE TROPICS: Epiphytes and Orchids

Bosque Eternal de Los Ninos, Santa Elena, Costa Rica: They’re called Epiphytes right? Walking down to San Gerardo Biological Station, descending through life zones from the elfin and cloud forests to the heart of the Monteverde rain forest, the flora and fauna, was striking. The first distinction of the forest from my home deciduous forests of Vermont was the plethora of green plant growth covering most of the trees. The bark was invisible on most, where orchids, bromeliads, vines, moss, lichen, liverworts, and more clung to the canopy branches. About one third of all the plants in this mountain region of Costa Rica were epiphytes.
What is so special about Epiphytes? Unlike many plants, epiphytes grow on branches and trees, taking water and nutrients from the air and rain instead of the ground. Their seeds are dispersed either by the wind or birds, settling on a canopy branch, trunk, or pocket ponds that nestle in the leaves of other epiphytes. They lack a root system buried in the ground and anchor themselves to trees. A single tree can hold up to one ton of extra plant life on its branches.
Orchids can also be epiphytes. There are over 1,800 species of orchids in Costa Rica, and 500 alone in Monteverde. Their leaves of the canopy dwelling orchids lack veins in order to retain water. They range in size, often growing high up in the canopy, causing identification to be a challenge. In this rich forest, new species are discovered each year. The most miniature orchid here can only be seen through a microscope, and some smell like coconut, chocolate, blood, or chicken soup.
Tree crowns are magnificent colonies, supporting diverse communities of animal and plant species. The variation of plant shapes and sizes highlights how near impossible it is to count how many species of epiphytes or plant species are growing on a single tree in the deep rain forest. I picked up a tiny branch, no longer than my finger, and counted at least five different species, including two epiphytes, emerging from the moss. The vegetation creates a textured spectrum of green, punctuated by red, orange, purple, and yellow flowers and leaves, the brilliant color of an orchid or the glint of a bird. A paradise!

How Santa Cruz Got Its Fox Back

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Wednesday, June 15th, 2011

California’s Channel Islands comprise an archipelago west of Santa Barbara, most of them now uninhabited by humans. Our historical tenure there, though, laid the foundation for one of the most challenging, intricate contemporary conservation stories I know of, the subject of T.C. Boyle’s most recent work, When the Killing’s Done.

Spanish explorers used Santa Cruz Island as a coastal base in the mid-19th century, and introduced feral pigs as an easy, self-sufficient food reserve. In the absence of predators, the pig population flourished, and when the sheep ranchers who had used the island for decades finally abandoned it in the 1970s, these porcine invaders essentially had the island to themselves.

At the same time, DDT dumped offshore by the Montrose Chemical Corporation was filtering up the marine food web, accumulating in the tissues of fish and marine mammals, and eventually reaching the regional population of piscivorous bald eagles, Haliaeetus leucocephalus. As the bald eagle population crashed in the 1980s, the apex predator niche was opened to a new and ecologically different species, one not native to the island ecosystem. The golden eagle, Aquila chrysaetos, a large raptor native to the mainland ecosystem, had historically visited the Channel Islands, but because of competition with territorial bald eagles, never colonized the area. Attracted to the feral piglets, an abundant and reliable source of prey, these aggressive predators moved in. However, it soon became apparent that golden eagles weren’t on a strict pork diet.

From the day an ancestor rafted across the blue waves some 20,000 years ago, the island fox, Urocyon littoralis spp., has been the primary terrestrial carnivore on the Channel Islands. A descendent of the mainland gray fox, Urocyon cinereoargenteus, this small canid—adults weigh between 2 and 6 lbs—is endemic to the islands; each is home to its own subspecies, six in total. Around the time the first golden eagle nest was found on Santa Cruz in the mid-1990s, the island fox population began to decline steeply, as much as 95 percent between 1995 and 2000. At its lowest point, the Santa Cruz island fox population was down to 62 individuals (from a historical estimate of roughly 1500). Observing golden eagles hunting, monitoring their nests, and keeping tabs on fox populations around the island allowed biologists to identify predation by golden eagles as the cause of death in nearly 90 percent of fox mortalities between 2000 and 2004.

The imminent threat of extinction to the Santa Cruz island fox provoked a hugely controversial response by the National Park Service and the Nature Conservancy, which owns a substantial portion of the island. Recovery plans involved an elaborate scheme of helicopter-netting and relocating golden eagles, a fox captive-breeding program, New Zealand-based sharpshooters who exterminated roughly 5,000 feral pigs, and a bald eagle reintroduction program. Close to ten years later, the various pieces of the puzzle have come together. The first bald eagle chick hatched on the island in 2006, the pigs are gone, and though vagrant golden eagles may still cast their shadows on the scrubby hillsides, the fox population is self-sustaining and quickly approaching pre-crash numbers.

In his latest novel, T.C. Boyle embarks on a fictionalized retelling of this struggle over the Channel Islands’ ecological fate. With his inimitable, vividly eccentric style, he pits NPS biologists against dreadlocked animal rights activists in a tale of gunslinging and exotic species in the New West, presenting diverse perspectives on the morality of meddling with nature. He’s well-versed in the islands’ cultural and natural histories, and endows this epic with meticulous details from the lives of its characters to create a complex, compelling portrait of the havoc we wreak, and the lengths we go to in search of redemption.

Birding Tip Series #8: Sort the Oddity from the Flock

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Friday, June 3rd, 2011

Sort the oddity from the flock. Uncommon or out-of range birds will often join a flock of common, but closely related species. Large, mixed-species flocks of waterfowl, gulls or shorebirds are good places to look . Here in Vermont, winter aggregations of birds by the edge of ice on Lake Champlain often contain a rarity or two. Several years ago, I was sorting through a raft of ducks that included quite a few Common Goldeneye (expected on the lake in the winter), but, upon closer inspection, one of the “Common Goldeneye” proved to be a severely out-of-range Barrow’s Goldeneye. Looking at eBird data for Vermont, that’s how Barrow’s is reported – one or a few at a time, in winter, probably mixed in with a flock of other ducks. In a similar situation, an aggregation of a few hundred (mostly ring-billed) gulls on the lake proved to contain single individuals of both Glaucous and Iceland Gulls – both rare in Vermont.

Another trick is to watch eBird, birding lists and other sources for reports of a species you’d like to see – even if it’s nowhere near you. Some species appear out of their accustomed range in irruptions, significant numbers of birds that leave their accustomed range in the same year, probably for reasons of weather or prey density. Both Snowy and Great Gray Owls are known for this behavior. Snowy Owls are rare most places south of the US-Canadian border, except in the far upper Midwest. However, in an irruptive year, numerous birds can be seen as far south as Pennsylvania, and isolated specimens are found even farther south. If you hear of Snowy Owls south of their usual haunts in some places, it’s a fair chance that an irruption is going on, and one may show up closer to you.

Birding Tip Series # 6: from Zoe J. Sheldon

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Wednesday, June 1st, 2011

Hmmm, birding tips… My favorite advice was from my college natural history professor, Steve Trombulak. He told all of us as novice birders to really look at the whole bird and try to come up with its “gestalt” – the essence of its entire form – through identifying distinctive shapes. Once you can recognize the “essence” of a sparrow, a tanager, a buteo, or whatever you’re looking at, then you can quickly zero in on the traits that distinguish species from one another.

I think that this has worked for me – really makes birding an instinctive thing. I know it’s not super-precise as far as tips go, but I think it’s my most useful offering.

Otherwise, I’d say:

1. Do some research and invest in quality binoculars. Then learn how to use them.
2. When you’re out in the field, scan the whole landscape constantly, looking for movement that’ll cue you in to a bird or birds, don’t assume you know where they’ll be.

Nests: A Magical Mystery Tour

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Thursday, May 5th, 2011

There are certain aspects of other creatures’ lives that we’re rarely exposed to. Some species are more comfortable making their life histories public than others, but most leave us guessing about how the whole story unfolds.

In her new book, Nests: Fifty Nests and the Birds that Built Them, photographer Sharon Beals brings to light an often-secreted piece of the lives of birds. From the collections of the California Academy of Sciences, the Berkeley Museum of Vertebrate Zoology, and the Western Foundation of Vertebrate Zoology, she has selected some of most ecologically unique, visually stunning, and just plain ingenious nests built by birds both familiar and exotic, from the marsh wren (Cistothorus palustris) to Kauai’s akekee (Loxops caeuleirostris). The nests are, by turn, miraculously intricate, strikingly simple, sinister, strange, or sweet, but all are a testament to the resourcefulness of creatures who lack complex tools but have nonetheless evolved some of the most sophisticated, diverse architecture of any organisms on the planet.

The brown booby (Sula leucogaster) collects marine detritus, using seaweed, spent feathers, and often the skeletons of other birds’ unlucky young to assemble a somewhat morbid nursery for their own offspring, a memento mori for the newly hatched.

The house wren (Troglodytes aedon) protects its nestlings with the egg sacs of jumping spiders, which feed on parasitic mites that might otherwise do them harm. The Altamira oriole (Icterus gularis), like many orioles, uses grasses, horsehair, and similar materials to weave a hanging, gourd-shaped nest. The Caspian tern (Hydroprogne caspia) makes a colorful (if uncomfortable-looking) pile of scallops and other seashells in a sandy depression. It’s just about impossible to pick a favorite. I find myself leafing through the pages again and again, looking for a standout, but diversity makes each inimitable construction uniquely appealing.

What strikes me most as I peruse, though, is that these nests are relatable in ways that other animals’ homes aren’t. Insofar as dwellings give some indication of their builders’ intent and character, we recognize certain facets of our own homemaking tendencies in birds’ habits – inexorable work ethic, meticulous construction, a desire for privacy, safety, even beauty. Our human lives are materially implicated, too, in their opportunistic incorporation of plastic trinkets, yarn, or other discards.

Call nest-building a biological imperative, name that perfectly camouflaged, symmetrical orb the result of thousands of years of evolution, and you’d be right. But I think you’d also be missing something.

On a typical Point Reyes morning, a clearing in the foggy Douglas firs (Pseudotsuga menziesii) on Limantour Road revealed three massive nests perched in conifer snags hundreds of feet above the ground. Covered with Old Man’s Beard, a lichen that gives the coastal forests here an ancient, almost haunted demeanor, especially on foggy days, the nests looked like they’d been hosting mating pairs and their offspring for centuries. As we watched, an osprey (Pandion haliaetus) circled in from nearby Tomales Bay, proffering the fish in its talons to its waiting mate. Though ospreys are easily spotted near water the world around, their nests conspicuous, bulky tangles of sticks usually exposed in the open, this encounter was somehow uncommon.

Being the only human eyes to observe this pair carrying out a long-evolved ritual in a humid, green and gray hour felt like uncovering a small piece of the mystery, the ineffable thing that binds romance and reality, the space between the imagined and the actual. Beals’ beautiful photographs, a sampling of hundreds of nests carefully collected and preserved, are a testament to the power of these miniature masterpieces to inspire our imaginations and awaken our powers of observation.

Check out Beals’ work in Audubon magazine here.