Gay Damselflies and Hoses Up a Hillside

From out of the Pond, water pumps up the hillside.
Three (3 1/2?) pairs of damselfly doing their thing near our submerged water pipe.

      So the following excerpt was too good not to reproduce again here:



Damselfly Mating Game Turns Some Males Gay

James Owen
for National Geographic News
June 21, 2005
Disguises used by female damselflies to avoid unwanted sexual advances can cause males to seek out their own sex, a new study suggests.

Belgian researchers investigated why male damselflies often try to mate with each other. The scientists say the reason could lie with females that adopt a range of appearances to throw potential mates off their scent. In an evolutionary battle of the sexes, males become attracted to a range of different looks, with some actually preferring a more masculine appearance.

The study, published recently in the journal Biology Letters, says such evolutionary selection pressures could also explain homosexual behavior seen in males of other animals whose females assume a variety of guises. Such "polymorphic" species are seen in dragonflies, butterflies, hummingbirds, and lizards.

Female blue-tailed damselflies (Ischnura elegans) assume different color forms, or morphs, in adulthood: green-brown, yellow-brown, and blue. The blue form closely matches the male in both body coloration and pattern.

The study team found the sexual preference of male damselflies was influenced by the company they keep. Males that were housed together before being introduced to females tended to seek out their own gender afterward. But males kept in mixed-sex living quarters later preferred all three female forms when choosing a mate.

This suggests male damselflies are likely to become attracted to other males only when females are absent or scarce. Yet a minority of males still showed an innate preference for male mates.

The team's findings were reflected in mating behavior observed in the wild, says study author Hans Van Gossum, an evolutionary biologist at the University of Antwerp, Belgium.

Van Gossum says around 17 percent of males in wild populations appear to favor same-sex pairings, while about one in six males in the lab experiments showed the same tendency despite exposure to females. "This behavior can be considered homosexual," he said.

Sexual Selection

But why should any males choose to mate with each other instead of with females? Such behavior apparently goes against theories of sexual selection, which predicts the optimization of reproductive success. Homosexual damselflies, however, aren't going to sire too many babies.

Homosexuality has been recorded in a wide range of animals, including beetles, sheep, fruit bats, dolphins, and monkeys. In many such cases explanations have been put forward to explain this behavior.

Consider, for example, the beetle known as the sugarcane rootstalk borer weevil. U.S. and Israeli researchers suggest the reason why females of the species mount other females is that the behavior attracts big males with good genes. Puny males seem to shy away from such antics.

Female Japanese macaques also engage in intimate sexual acts with one another. U.S. primatologist Amy Parish and other researchers say female macaques may enhance their social position and form alliance partners through such intimacy which in turn can boost breeding success.

Van Gossum and his colleagues propose a new explanation for homosexuality in animals like the blue-tailed damselfly. When males face strong evolutionary pressures to be flexible about their idea of what a female should look like, males may end up also fancying their own sex.

Males damselflies need to be adaptable because their female counterparts are adaptable. Numbers of the three main female color forms, or morphs, fluctuate over time.

Van Gossum, the study author, says most researchers agree such polymorphism most likely results from sexual conflict, with females evolving traits to avoid excessive harassment. While plenty of sex might suit male damselflies, this isn't the case for females.

Joan Roughgarden is a professor of biological sciences at Stanford University in California. She writes, "Copulation ranges from over one hour to over six hours, averaging three hours. While a long copulation might seem like great fun, this can waste a whole day and be too much of a good thing, especially if carried out day after day over a life span that is only a few days long."

Roughgarden adds that female damselflies collect all the sperm they need to reproduce from a single mating.

Aviodance Tactics

"Males go for quantity and females for quality," Van Gossum said. "As a consequence, females may wish to avoid excessive male attention. One way of doing so is by looking different from what a male thinks a female to be."

The blue female form may accomplish this by mimicking the appearance of males. But Van Gossum says an alternative theory is that male harassment also leads to other morphs.

"The minority female morph in a population"—whether blue or another form—"is the one that benefits, by receiving less male harassment," he added.

In turn, it's likely that males have developed a flexible "search-image" that matches the majority female fashion of the day. This boosts a male's chances of finding a mate.

"Males with a search-image that can be changed if the minority female morph becomes the majority morph are probably out-competing males that are less flexible," Van Gossum said.

Such flexibility may also lead to genuinely homosexual damselflies.

Van Gossum says such behavior could arise when a male is still young. A preference developed in male damselflies before reaching maturity, he says, is probably less prone to change in later life.

The Belgian researcher adds that evolutionary pressures that shape damselfly mating behavior may also explain homosexuality seen in other male animals, including butterflies and hummingbirds, whose females similarly adopt a range of colorful guises.
http://news.nationalgeographic.com/news/pf/48026386.html



This excerpt is also too good not to copy and paste: 



     "Damselflies, like all odonates, have a very interesting breeding system. Before they actually copulate, males and females of many groups spend some considerable time in physical contact with one another, presumably in an effort to assess their potential mate. . . .  This physical contact is made by the male clasping the female's thorax with the four terminal appendages on the end of his abdomen.  [Note in our photograph above each male holding its potential mate with its terminal appendage (and in the one somewhat more interesting case, the male holding the other male's abdomen.]
     "The male's terminal abdominal appendages consist of two superior cerci and two inferior paraprocts. The [left] figure [below] is a computer generated model of the tenth abdominal segment of a male E. ebrium viewed from the posterior. These four appendages grasp the female's thorax while they are in tandem. The [right] figure is a computer generated model of the females thorax viewed from above. The male's paraprocts contact her prothorax and the male's cerci fit into the two plates on the anterior surface of her mesothorax - the mesothoracic plates. These mesothoracic plates are thought to be used by the female to assess the species identity and potentially the suitability of the male that is grasping her in tandem.
      "Field studies have shown that females discriminate among males based on cerci shape (Paulson 1974, Robertson and Paterson 1982, Fincke et al. 2006). Also, males with experimentally altered cerci are rejected by conspecific females (Robertson and Paterson 1982). Thus, the morphologies of these male and female structures seem to be critical for mate recognition, and so the evolution of these structures may play a vital role in speciation in Enallagma. These structures are akin to a lock-and-key mechanism, with each sex potenitially evaluating the fit between the male's cerci with the contours of the female's mesothoracic plates."





http://www.enallagma.com/cerci/damselflyMating.html

     Immature damselflies (known as naiads), live in the stream for a year or so until one emerges into the world of air and becomes the light-weight flying thing that resembles a dragonfly.  The adult version will live for a few weeks to a few months, during which time its only real purpose is to mate.  The articles above tell the first part of this story.  The other part begins with the male arching his long abdomen over to his own abdomen where he will deposit sperm on the underside of about the second segment.  (Some sources say that the male deposits his sperm onto this accessory sex organ before searching for a female.)  He then clasps onto the female behind her head and she arches her abdomen under and around to retrieve the sperm.  She, then, will lay her fertilized eggs on the surface of waters, bits of plant emerging from the water, in the mud, drilled into plant stems, or let go in the warm summer or autumn air itself .

  Here's a drawing of part of the Act:


From the Pond, past the 3 1/2 pairs of damselflies, across the Stonefield,
and to the old Ruth Berry pressure pump.

And then up Whitman's Rough.


     I focused mainly on the cedar elms along the east slope of Whitman's Rough above the home site.  Buckeyes, junipers, persimmons, and other trees are dying, too.  While I was sitting in a thin patch of shade beside the hose, a three-inch long lizard appeared on a water-spattered boulder.  He went from one wet spot to the next, "lapping" up moisture as if in a frenzy.  I don't know where he and other animals could possibly be getting enough water to survive.


With no creek flowing into it, the Pool warms and evaporates,
shrinking the universe for dozens of fish, tens of thousands of insects,
and gazillions of smaller invertebrates. 

Creek: Meditation on a Word


     It wasn't until about the age of the Pilgrims in America (the 1620s) that the word came refer to a small stream or brook.  Before that time, the word "creke" meant something like a narrow inlet in a coastline.  It's all a chain of etymological guesses, but it appears that this word is related to "crook," calling attention to this body of water that's full of bends and turns.
     As for "stream," it appears that this word derives from the Old French root "rheum," itself from "rheuma," the Greek word for stream or a current or anything flowing.  So we end up with other Greek words such as rhythmos, meaning rhythm or rhytos, meaning a liquid or fluid.  The Polish word for brook is strumyk.  "That which flows" is the Rhine.
     In the ancient Sanskrit, rivus meant "stream."  In the 1500's the Italian word rivoletto flowed from out of the Latin rivus (think of "rivulet" and "river") which directly copied the Sanskrit.  In the same century, this rivus led unexpectedly to our word "rival."  The idea here is that a rivalis was originally "one who uses the same stream" (or "one on the opposite side of the stream").
     And it's likely this root word led to another favorite word of ours: "rill." A rill is nothing more than a small brook.  
     As for a "brook," another kind of small stream, the German and Dutch equivalents (Bruch and broek) both have the sense of a marsh.  In parts of England, a brook means a "water-meadow."
     So a creek. Or brook.  Or stream.  Or rill, river, wash, rivulet, runnel, run, burn, beck, branch, kill, syke, bayou, and lick.  The modern Dutch word for things like creeks is kil, and from this we got part of the bizarre word for what was once the largest landfill in the world: Fresh Kills, on the western part of Staten Island, where about one third of the debris from Ground Zero was taken to be sorted through.  4257 pieces of human remains were found and identified there beside the Fresh Kills Estuary.
     A "lick."  This is something between being a stream and a rill, the latter being essentially the first stage of a stream when water is just beginning to erode a path through dirt or rock.  And this being the case, a lick is more of an ephemeral stream.  Hamilton Creek is an ephemeral stream if there was ever any doubt, but still it's not quite as temporary as a lick.
     Now, our humble Creek is all a creek should be except that it hasn't any water.
     So below we enjoy other streams.


Meandering Stream at Lanting, by Suzuki Fuyo  

Alfred Sisley

Albert Bierstadt

Alfred Britcher
Peder Mork Monsted

Another Albert Bierstadt

Paul Weber Gebirgsbach


Frederick Arthur Bridgman

Rain

While two of us are in Colorado, we hear that rain came yesterday to the little creek canyon.

Enough for one blog post.

The Un-Creek Journal

     At what hour the Creek ceased to flow is not known.  Maybe creeks are special about not having a moment of death capable of being witnessed by us.  
     A couple small pools and the main pool still have water and fish, but the flow has gone out of the stream, and with the loss of flow, so also the loss of a sound and a shine.


Looking southward down-unstream.

Exposed shale just up-unstream from the main pool.




Looking southward at the Pool.


A run of un-creek south of the Pool.



     Up along the row of blackberry vines on the unnaturally thriving snow-on-the-mountain plant we've been looking at for several blog posts, I found this beautiful wasp-look-alike insect that may be a robber fly (Lampria bicolor).  If you can correct this identification, please let us know.


     And here we have an exploration of cinematography for the patient stone-watcher inside each of us.  I stone-watched on the west side of the Un-Creek.
http://www.youtube.com/watch?v=ob_lEmey6Lw

http://www.youtube.com/watch?v=vCoGS4EGWB8


     Harlin sent the following photographs and notes a few days ago.


     We are in the realm of easily misidentified with these two plants, not to mention the non-spectacular.  Still, they are different from the other plants which have been added to the Hamilton Creek plant list previously and that in itself is progress.  HH




Canadian horseweed (Conyza canadensis)


Canadian horseweed (Conyza canadensis)

Fragrent flatsedge (Cyperus odoratus)

Fragrent flatsedge (Cyperus odoratus)

     These two [below] are not only more colorful than the last two plants, but they have distinctive characters that rule out a large number of wrong possibilities.  These characteristics are not guarantees, but finding something that seems to be rare is an enjoyable experience at the end of the find-a-name puzzle.  In the example of the bean family vine Strophostyles, the unusual shape is that thing in the middle of the flower.  I have a book about the legumes of Texas and the description for the genus Strophostyles says "keel strongly incurved."  My picture looks similar to


http://www.wildflower.org/gallery/result.php?id_image=15557


     The name "heterotheca" means something like "different cases" since the achenes for the ray flowers don't have the pappus of bristles and the disk flowers do have achenes with the bristly hair on top (along with some other differences).
     I've found that it is good to take a few non-pretty pictures along with the pictures that might look good.  In fact, I usually feel I should have taken more of them.  They help answer questions that my sometimes rushed preservation hasn't preserved.  I mention that since in this case I also wish I had taken better pictures of the wild bean's keel and looked for good examples of the camphor weed's two kinds of seeds.  Of course, I didn't even know what I was missing at the time.  HH  


Wild bean/Amberique-bean/Trailing fuzzybean (Strophostyles helvola)

Camphor weed (Heterotheca subaxillaris)

And here's something interesting on the wild bean:

Strophostyles helvola (L.) Elliot
Wild bean (trailing wild bean)
Fabaceae [Steyermark: Leguminosae, Popilionoideae]

       
Strophostyles seeds are generally found in sieve sizes greater than 2.0 mm. Occasionally, pods are found as well (see Fritz 1986). Strophostyles helvola is found in archaeobotanical samples from sites of both foraging and agricultural groups.

Description
       The modern seeds are oblong with square ends, 5-10 mm long and 2-3 mm wide, with a grayish brown scurfy outer coat (Figure 1). The linear marginal hilum is covered with white and bordered by a narrow black outline. The pods are 4-9 cm long (Figure 2). Strophostyles helvola is easily identified archaeologically due to its long, diagnostic hilum. It is also longer and narrower than other legumes. Smaller fragments of bean make identification more difficult because they can be easily confused with other legumes, including Phaseolus vulgaris L. and Phaseolus polystachios L.

Archaeological Distribution
       Strophostyles helvola is found from the Middle Archaic through historic times in the Eastern Woodlands. Archaeological wild bean has been recovered in Alabama,Oklahoma, the Arkansas Ozarks, and Illinois. It has been consistently recovered in the American Bottom area, generally in low numbers (Johannessen 1984).
The Modern Plant and Its Distribution
       There are three species: Strophostyles umbellata (Muhlenb. ex. Willd.) Britton,Strophostyles leiosperma (Torry & A. Gray) Piper, and Strophostyles helvola.Strophostyles helvola is a herbaceous annual vine found in a variety of habitats, including beaches, thickets, open woods, open areas and old fields. Smith (1992:261) records finding wild bean in association with Chenopodium berlandieri which is not surprising given Chenopodium's need for nitrogen rich soil. Fritz also finds this association archaeologically in the Ozarks (1986). Strophostyles’ modern distribution is wider than its archaeological distribution. It is found from Quebec to Minnesota,South Dakota and Colorado, and south from Florida to Texas. Beans are available in the late summer and early autumn months.

Discussion
       Although some archaeological occurrences of wild bean could be the result of natural seed dispersion, as it does grow in disturbed soils, "...it has been recorded in frequencies great enough that one can conclude with near certainty that it was used as a food" (Asch and Asch 1985:387). Wild bean is smaller than common bean (Phaseolus vulgaris), but it has similar nutritional value. "Furthermore, because it is substantially larger than indigenous starchy seed cultigens, it may have had subsistence value greater than its numbers would indicate" (Parker 1991:314). Wild beans were probably prepared in many of the same ways as cultivated beans. Although they could be eaten green, they were often dried. Ethnohistorically, the roots were boiled and mashed and used for food as well (Yanovsky 1936:38).
       The Houma used Strophostyles helvola as a disease remedy, with a decoction of bean being taken for typhoid. The Iroquois used it as a dermatological aid, with the leaves being rubbed on parts affected by poison ivy or warts (Moerman 1986).